| fgf8 | Stage | Hours | ZFIN expression range | marginal blastomere | superficial blastomere | presumptive brain | presumptive neural plate | EVL | margin | forerunner cell group | axis | germ ring | shield | presumptive segmental plate | neural plate | presumptive cephalic mesoderm | mesoderm | ectoderm | neuroectoderm | hindbrain neural plate | midbrain hindbrain boundary neural plate | presumptive rhombomere 2 | presumptive rhombomere 4 | midbrain hindbrain boundary neural keel | neural keel | periderm | paraxial mesoderm | segmental plate | tail bud | notochord | tail | presumptive telencephalon | somite | forebrain neural rod | midbrain hindbrain boundary neural rod | neural rod | heart primordium | eye | floor plate | floor plate neural rod | neural tube | olfactory placode | pharyngeal endoderm | basal plate midbrain | floor plate diencephalon | floor plate rhombomere 1 | floor plate rhombomere 2 | floor plate rhombomere 3 | floor plate rhombomere 4 | floor plate rhombomere 5 | floor plate rhombomere 6 | floor plate rhombomere 7 | floor plate rhombomere 8 | floor plate telencephalon | rhombomere 1 | rhombomere 2 | rhombomere 4 | diencephalon | forebrain | midbrain | optic stalk | pharyngeal arch 3-7 skeleton | telencephalon | otic vesicle | forebrain midbrain boundary | midbrain hindbrain boundary | hypophysis | dorsal fin fold | median fin fold | cerebellum | fin | hypothalamus | pectoral fin bud | inner ear | retina | spinal cord | tegmentum | thyroid primordium | dorsal fin musculature | pectoral fin | peripheral olfactory organ | pharyngeal epithelium | retinal ganglion cell layer | apical ectodermal ridge pectoral fin | pectoral fin musculature | mandibular arch | unspecified |
| Zygote | 1-cell | 0 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cleavage | 2-cell | 0.75 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 4-cell | 1.0 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 8-cell | 1.25 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 16-cell | 1.5 | I | I | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 32-cell | 1.75 | I | I | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 64-cell | 2.0 | I | I | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Blastula | 124-cell | 2.25 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 256-cell | 2.5 | I | I | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 512-cell | 2.75 | I | I | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 1k-cell | 3.0 | I | I | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| High | 3.33 | I | I | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Oblong | 3.66 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sphere | 4.0 | ! | ! | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dome | 4.33 | ! | ! | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 30% epiboly | 4.66 | ! | ! | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Gastrula | 50%-epiboly | 5.25 | ! | ! | ! | ! | ! | ! | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Germ-ring | 5.66 | ! | ! | ! | ! | ! | ! | I | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Shield | 6.0 | ! | ! | ! | ! | ! | ! | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 75% epiboly stage | 8.0 | ! | ! | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 90% epiboly | 9.0 | ! | ! | ! | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| bud stage | 10.0 | ! | ! | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Segmentation | 1-4 somites | 10.33 | I | I | ! | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 5-9 somites | 11.66 | I | I | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 10-13 somites | 14.0 | ! | ! | ! | I | I | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 14-19 somites | 16.0 | ! | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 20-25 somites | 19.0 | I | ! | ! | ! | ! | ! | ! | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 26+ somites | 22.0 | I | ! | ! | ! | I | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Pharyngula | Prim-5 | 24.0 | X | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Prim-15 | 30.0 | X | X | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Prim-25 | 36.0 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| High-pec | 42.0 | I | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hatching | Long-pec | 48.0 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Pec-fin | 60.0 |
| Evidence for Interaction | Inhibition of Fgf signalling by microinjection of RNA encoding a dominant negative variant of zebrafish Fgfr1 (dn-fgfr1) causes a severe reduction or complete loss of spry2 expression. |
| Target Gene | spry2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | dominant negative |
| Time of Interaction in evidence | 4.33 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | overexpression of fgf8 RNA, either throughout the embryo or at the animal pole (which is far from its endogenous marginal expression) induces ectopic spry2 expression. |
| Target Gene | spry2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 4.33 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | Inhibition of Fgf signalling by microinjection of RNA encoding a dominant negative variant of zebrafish Fgfr1 (dn-fgfr1) causes expansion of ved expression domain. |
| Target Gene | ved |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | dominant negative |
| Time of Interaction in evidence | 4.66 |
| Location of Interaction in evidence | EVL |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | fgf8 overexpression abolishes the blastula stage expression of bmp4 in the ventral blastoderm. |
| Target Gene | bmp4 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 4.66 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | fgf8 overexpression abolishes the blastula stage expression of bmp4 in the ventral blastoderm. |
| Target Gene | bmp4 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 4.66 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | fgf8 overexpression abolishes the blastula stage expression of bmp4 in the ventral blastoderm. |
| Target Gene | bmp7 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 4.66 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | fgf8 overexpression abolishes the blastula stage expression of bmp7 in the ventral blastoderm. |
| Target Gene | bmp7 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 4.66 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | fgf8 overexpression abolishes the blastula stage expression of bmp7 in the ventral blastoderm. |
| Target Gene | bmp7 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 4.66 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | fgf8 overexpression abolishes the blastula stage expression of bmp7 in the ventral blastoderm. |
| Target Gene | bmp7 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 4.66 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | fgf8 overexpression abolishes the blastula stage expression of bmp2b in the ventral blastoderm. |
| Target Gene | bmp2b |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 4.66 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | Inhibition of Fgf signalling by injection of RNA encoding the Fgf-antagonist Spry2; dn-fgfr1; a dominant-negative variant of the signal transducer Ras or treatment with the pharmacological Fgfr antagonist SU5402, all results in expanded bmp2b expression. |
| Target Gene | bmp2b |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | drug konckdown, dominant negative, antagonist |
| Time of Interaction in evidence | 4.66 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | Injection of fgf8 RNA into the one-cell embryo led to an expansion of mkp3 expression. |
| Target Gene | dusp6 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression dominant negative |
| Time of Interaction in evidence | 4.66 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Igor B. Dawid |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2769 |
| Evidence for Interaction | This is the case, as injection of fgf8 RNA into the one-cell embryo led to an expansion of mkp3 expression. Conversely, inhibition of FGF signaling through the expression of a dominant-negative FGF receptor, XFD, resulted in suppression of mkp3 expression |
| Target Gene | dusp6 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression dominant negative |
| Time of Interaction in evidence | 4.66 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Igor B. Dawid |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2769 |
| Evidence for Interaction | Inhibition of Fgf signalling by microinjection of RNA encoding a dominant negative variant of zebrafish Fgfr1 (dn-fgfr1) causes a severe reduction or complete loss of spry2 expression. |
| Target Gene | spry2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | dominant negative |
| Time of Interaction in evidence | 4.66 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | activation of the FGF/ERK pathway disrupts endoderm formation in the embryo and antagonizes the ability of an activated form of Tar/Acvr1b to induce endoderm at the animal pole. |
| Target Gene | acvr1b |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 5.25 |
| Location of Interaction in evidence | mesendoderm |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Thierry Lepage |
| Journal | Development |
| Year | 2006 |
| Vol | 133 |
| Start Page | 2189 |
| Evidence for Interaction | overexpression of fgf8 elevated ntl expression in the entire embryo. |
| Target Gene | ntl |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 5.25 |
| Location of Interaction in evidence | mesendoderm |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Hiroyuki Takeda |
| Journal | Developmental Biology |
| Year | 2002 |
| Vol | 244 |
| Start Page | 9 |
| Evidence for Interaction | Fgf signalling is required in vivo to restrict early bmp2b expression to the ventral side of the embryo. This expansion of the bmp2b expression territory results in an increase of Bmp signalling activity as revealed by a strong spreading of ved expression |
| Target Gene | ved |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | dominant negative |
| Time of Interaction in evidence | 5.25 |
| Location of Interaction in evidence | EVL |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | overexpression of fgf8 elevated ntl expression in the entire embryo. |
| Target Gene | ntl |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 5.25 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Hiroyuki Takeda |
| Journal | Developmental Biology |
| Year | 2002 |
| Vol | 244 |
| Start Page | 9 |
| Evidence for Interaction | Injection of fgf8 mRNA induces ectopic sef expression |
| Target Gene | il17rd |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 5.25 |
| Location of Interaction in evidence | |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Igor B Dawid |
| Journal | brief communications |
| Year | 2002 |
| Vol | |
| Start Page |
| Evidence for Interaction | The fgf8 overexpression (10 pg) induced chd at the shield stage. |
| Target Gene | chordin |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 6 |
| Location of Interaction in evidence | mesendoderm |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Anming Meng |
| Journal | Developmental Biology |
| Year | 2004 |
| Vol | 271 |
| Start Page | 130 |
| Evidence for Interaction | fgf8 overexpression induced chd at the shield stage. |
| Target Gene | chordin |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 6 |
| Location of Interaction in evidence | mesendoderm |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Anming Meng |
| Journal | Developmental Biology |
| Year | 2004 |
| Vol | 271 |
| Start Page | 130 |
| Evidence for Interaction | The fgf8 overexpression (10 pg) induced chd at the shield stage. |
| Target Gene | chordin |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 6 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Anming Meng |
| Journal | Developmental Biology |
| Year | 2004 |
| Vol | 271 |
| Start Page | 130 |
| Evidence for Interaction | fgf8 overexpression induced chd at the shield stage. |
| Target Gene | chordin |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 6 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Anming Meng |
| Journal | Developmental Biology |
| Year | 2004 |
| Vol | 271 |
| Start Page | 130 |
| Evidence for Interaction | fgf8 overexpression (10 pg) inhibited eve1 at the shield stage. |
| Target Gene | eve1 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 6 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Anming Meng |
| Journal | Developmental Biology |
| Year | 2004 |
| Vol | 271 |
| Start Page | 130 |
| Evidence for Interaction | fgf8 overexpression inhibited eve1 at the shield stage. |
| Target Gene | eve1 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 6 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Anming Meng |
| Journal | Developmental Biology |
| Year | 2004 |
| Vol | 271 |
| Start Page | 130 |
| Evidence for Interaction | The fgf8 overexpression (10 pg) induced chd at the shield stage. |
| Target Gene | chordin |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 6 |
| Location of Interaction in evidence | epiblast |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Anming Meng |
| Journal | Developmental Biology |
| Year | 2004 |
| Vol | 271 |
| Start Page | 130 |
| Evidence for Interaction | fgf8 overexpression induced chd at the shield stage. |
| Target Gene | chordin |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 6 |
| Location of Interaction in evidence | epiblast |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Anming Meng |
| Journal | Developmental Biology |
| Year | 2004 |
| Vol | 271 |
| Start Page | 130 |
| Evidence for Interaction | fgf8 mis-expression caused a pronounced dorsoventral expansion of gbx2 in the injected half. |
| Target Gene | gbx2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | epiblast |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 129 |
| Start Page | 917 |
| Evidence for Interaction | In wild-type embryos, fgf8 mis-expression caused a strong dorsalization of the whole embryo, which is visible as a pronounced dorsoventral expansion of spry4 and gbx2 in the injected half. |
| Target Gene | gbx2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | epiblast |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 129 |
| Start Page | 917 |
| Evidence for Interaction | In wild-type embryos, fgf8 mis-expression caused a strong dorsalization of the whole embryo, which is visible as a pronounced dorsoventral expansion of spry4 and gbx2 in the injected half. |
| Target Gene | gbx2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | epiblast |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 129 |
| Start Page | 917 |
| Evidence for Interaction | Gbx2 is lost in both the mesendodermal and the euroectodermal germ layer in fgf8 mutant embryos. |
| Target Gene | gbx2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | mesendoderm |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 129 |
| Start Page | 917 |
| Evidence for Interaction | In embryos treated with the pharmacological Fgfr antagonist SU5402, the expression of sprouty4 is abolished. |
| Target Gene | spry4 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | drug knockdown |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2003 |
| Vol | 120 |
| Start Page | 919 |
| Evidence for Interaction | fgf8 mis-expression caused a pronounced dorsoventral expansion of spry4 in the injected half. |
| Target Gene | spry4 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 129 |
| Start Page | 917 |
| Evidence for Interaction | sprouty4 expression at tailbud in non-treatedembryos. In embryos treatedwith SU5402, the expression of sprouty4, an Fgf target, is abolished showing that the inhibition of Fgf signaling was efficient. |
| Target Gene | spry4 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | drug knockdown |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2003 |
| Vol | 120 |
| Start Page | 919 |
| Evidence for Interaction | In wild-type embryos, fgf8 mis-expression caused a strong dorsalization of the whole embryo , which is visible as a pronounced dorsoventral expansion of spry4 and gbx2 in the injected half . |
| Target Gene | spry4 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 129 |
| Start Page | 917 |
| Evidence for Interaction | The hindbrain domain of fgf8 becomes evident by 75% epiboly (8 hpf) in wild-type embryos but was only weakly expressed in most wnt8 morphants even as late as 90% epiboly (9 hpf). |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | The hindbrain domain of fgf8 was only weakly expressed in wnt8 morphants even as late as 90% epiboly. |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | The hindbrain domain of fgf8 becomes evident by 75% epiboly (8 hpf) in wild-type embryos but was only weakly expressed in most wnt8 morphants even as late as 90% epiboly (9 hpf). |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | MASO |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | The hindbrain domain of fgf8 was only weakly expressed in wnt8 morphants even as late as 90% epiboly. |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | MASO |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | Gbx2 is lost in both the mesendodermal and the euroectodermal germ layer in fgf8 mutant embryos. |
| Target Gene | gbx2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 129 |
| Start Page | 917 |
| Evidence for Interaction | The hindbrain domain of fgf8 becomes evident by 75% epiboly (8 hpf) in wild-type embryos but was only weakly expressed in most wnt8 morphants even as late as 90% epiboly (9 hpf). |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | The hindbrain domain of fgf8 was only weakly expressed in wnt8 morphants even as late as 90% epiboly. |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | The hindbrain domain of fgf8 becomes evident by 75% epiboly (8 hpf) in wild-type embryos but was only weakly expressed in most wnt8 morphants even as late as 90% epiboly (9 hpf). |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | MASO |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | The hindbrain domain of fgf8 was only weakly expressed in wnt8 morphants even as late as 90% epiboly. |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | MASO |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | Expressions of fgf8 was expanded laterally and ventrally in the embryos injected with 50 pg of GFP-kheper RNA, compared to the uninjected control embryos. |
| Target Gene | fgf8 |
| Upstream Gene | zfhx1 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Naomasa Miki |
| Journal | Developmental Biology |
| Year | 2000 |
| Vol | 228 |
| Start Page | 29 |
| Evidence for Interaction | Expressions of the neuroectodermal genes fgf8 was expanded laterally and ventrally in the embryos injected with 50 pg of GFP-kheper RNA, compared to the uninjected control embryos. |
| Target Gene | fgf8 |
| Upstream Gene | zfhx1 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Naomasa Miki |
| Journal | Developmental Biology |
| Year | 2000 |
| Vol | 228 |
| Start Page | 29 |
| Evidence for Interaction | fgf8 mis-expression caused a pronounced dorsoventral expansion of gbx2 in the injected half. |
| Target Gene | gbx2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 129 |
| Start Page | 917 |
| Evidence for Interaction | In wild-type embryos, fgf8 mis-expression caused a strong dorsalization of the whole embryo, which is visible as a pronounced dorsoventral expansion of spry4 and gbx2 in the injected half. |
| Target Gene | gbx2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 129 |
| Start Page | 917 |
| Evidence for Interaction | In wild-type embryos, fgf8 mis-expression caused a strong dorsalization of the whole embryo, which is visible as a pronounced dorsoventral expansion of spry4 and gbx2 in the injected half. |
| Target Gene | gbx2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 129 |
| Start Page | 917 |
| Evidence for Interaction | In embryos treated with the pharmacological Fgfr antagonist SU5402, the expression of sprouty4 is abolished. |
| Target Gene | spry4 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | drug knockdown |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2003 |
| Vol | 120 |
| Start Page | 919 |
| Evidence for Interaction | fgf8 mis-expression caused a pronounced dorsoventral expansion of spry4 in the injected half. |
| Target Gene | spry4 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 129 |
| Start Page | 917 |
| Evidence for Interaction | sprouty4 expression at tailbud in non-treatedembryos. In embryos treatedwith SU5402, the expression of sprouty4, an Fgf target, is abolished showing that the inhibition of Fgf signaling was efficient. |
| Target Gene | spry4 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | drug knockdown |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2003 |
| Vol | 120 |
| Start Page | 919 |
| Evidence for Interaction | In wild-type embryos, fgf8 mis-expression caused a strong dorsalization of the whole embryo , which is visible as a pronounced dorsoventral expansion of spry4 and gbx2 in the injected half . |
| Target Gene | spry4 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 129 |
| Start Page | 917 |
| Evidence for Interaction | The hindbrain domain of fgf8 becomes evident by 75% epiboly (8 hpf) in wild-type embryos but was only weakly expressed in most wnt8 morphants even as late as 90% epiboly (9 hpf). |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | The hindbrain domain of fgf8 was only weakly expressed in wnt8 morphants even as late as 90% epiboly. |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | The hindbrain domain of fgf8 becomes evident by 75% epiboly (8 hpf) in wild-type embryos but was only weakly expressed in most wnt8 morphants even as late as 90% epiboly (9 hpf). |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | MASO |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | The hindbrain domain of fgf8 was only weakly expressed in wnt8 morphants even as late as 90% epiboly. |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | MASO |
| Time of Interaction in evidence | 8 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | Onset of gbx2 expression is affected in the ace mutant, albeit in a different way. In ace mutants, expression of gbx2 is already absent at 90% of epiboly. |
| Target Gene | gbx2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | ectoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2003 |
| Vol | 120 |
| Start Page | 919 |
| Evidence for Interaction | In ace mutant s(fgf8 mutant) , gbx2 expression is already absent at 90% of epiboly. gbx1 expression is rescued by wild type cell transplantation into ace mutant |
| Target Gene | gbx2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | ectoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2003 |
| Vol | 120 |
| Start Page | 919 |
| Evidence for Interaction | In ace mutant s(fgf8 mutant) , gbx2 expression is already absent at 90% of epiboly. gbx1 expression is rescued by wild type cell transplantation into ace mutant |
| Target Gene | gbx2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | ectoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2003 |
| Vol | 120 |
| Start Page | 919 |
| Evidence for Interaction | Gbx2 is lost in both the mesendodermal and the euroectodermal germ layer in ace mutant embryos. |
| Target Gene | gbx2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | mesendoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 129 |
| Start Page | 917 |
| Evidence for Interaction | Gbx2 is lost in both the mesendodermal and the euroectodermal germ layer in ace mutant embryos. |
| Target Gene | gbx2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | mesendoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 129 |
| Start Page | 917 |
| Evidence for Interaction | overexpression of fgf17b caused the expression domain of the anterior neural marker otx1 to shrink substantially, whereas overexpression of fgf8 reduced the otx1 domain size to a lesser degree but clearly decreased its expression level. |
| Target Gene | otx1 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | mesendoderm |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Anming Meng |
| Journal | Developmental Biology |
| Year | 2004 |
| Vol | 271 |
| Start Page | 130 |
| Evidence for Interaction | overexpression of fgf8 or fgf3 reduced the otx2 domain size to a lesser degree but clearly decreased its expression level. |
| Target Gene | otx1 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | mesendoderm |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Anming Meng |
| Journal | Developmental Biology |
| Year | 2004 |
| Vol | 271 |
| Start Page | 130 |
| Evidence for Interaction | sprouty4 expression at tailbud in non-treatedembryos. In embryos treatedwith SU5402, the expression of sprouty4, an Fgf target, is abolished showing that the inhibition of Fgf signaling was efficient. |
| Target Gene | spry4 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | drug knockdown |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2003 |
| Vol | 120 |
| Start Page | 919 |
| Evidence for Interaction | sprouty4 expression at tailbud in non-treatedembryos. In embryos treatedwith SU5402, the expression of sprouty4, an Fgf target, is abolished showing that the inhibition of Fgf signaling was efficient. |
| Target Gene | spry4 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | drug knockdown |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | mesoderm |
| Evidence for Direct | |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2003 |
| Vol | 120 |
| Start Page | 919 |
| Evidence for Interaction | Gbx2 is lost in both the mesendodermal and the euroectodermal germ layer in ace mutant embryos. |
| Target Gene | gbx2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 129 |
| Start Page | 917 |
| Evidence for Interaction | Gbx2 is lost in both the mesendodermal and the euroectodermal germ layer in ace mutant embryos. |
| Target Gene | gbx2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 129 |
| Start Page | 917 |
| Evidence for Interaction | The expression of the posterior neuroectodermal marker hoxb1b was expanded, predominantly on the ventral side, by overexpression of any of the tested Fgf mRNAs. |
| Target Gene | hoxb1b |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Anming Meng |
| Journal | Developmental Biology |
| Year | 2004 |
| Vol | 271 |
| Start Page | 130 |
| Evidence for Interaction | The expression of the posterior neuroectodermal marker hoxb1b was expanded by overexpression of any of the tested fgf8 mRNAs. |
| Target Gene | hoxb1b |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Anming Meng |
| Journal | Developmental Biology |
| Year | 2004 |
| Vol | 271 |
| Start Page | 130 |
| Evidence for Interaction | overexpression of fgf17b caused the expression domain of the anterior neural marker otx1 to shrink substantially, whereas overexpression of fgf8 reduced the otx1 domain size to a lesser degree but clearly decreased its expression level. |
| Target Gene | otx1 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Anming Meng |
| Journal | Developmental Biology |
| Year | 2004 |
| Vol | 271 |
| Start Page | 130 |
| Evidence for Interaction | overexpression of fgf8 or fgf3 reduced the otx2 domain size to a lesser degree but clearly decreased its expression level. |
| Target Gene | otx1 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Anming Meng |
| Journal | Developmental Biology |
| Year | 2004 |
| Vol | 271 |
| Start Page | 130 |
| Evidence for Interaction | sprouty4 expression at tailbud in non-treatedembryos. In embryos treatedwith SU5402, the expression of sprouty4, an Fgf target, is abolished showing that the inhibition of Fgf signaling was efficient. |
| Target Gene | spry4 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | drug knockdown |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2003 |
| Vol | 120 |
| Start Page | 919 |
| Evidence for Interaction | The expression of the posterior neuroectodermal marker hoxb1b was expanded, predominantly on the ventral side, by overexpression of any of the tested Fgf mRNAs. |
| Target Gene | hoxb1b |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Anming Meng |
| Journal | Developmental Biology |
| Year | 2004 |
| Vol | 271 |
| Start Page | 130 |
| Evidence for Interaction | The expression of the posterior neuroectodermal marker hoxb1b was expanded by overexpression of any of the tested fgf8 mRNAs. |
| Target Gene | hoxb1b |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Anming Meng |
| Journal | Developmental Biology |
| Year | 2004 |
| Vol | 271 |
| Start Page | 130 |
| Evidence for Interaction | overexpression of fgf17b caused the expression domain of the anterior neural marker otx1 to shrink substantially, whereas overexpression of fgf8 reduced the otx1 domain size to a lesser degree but clearly decreased its expression level. |
| Target Gene | otx1 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Anming Meng |
| Journal | Developmental Biology |
| Year | 2004 |
| Vol | 271 |
| Start Page | 130 |
| Evidence for Interaction | overexpression of fgf8 or fgf3 reduced the otx2 domain size to a lesser degree but clearly decreased its expression level. |
| Target Gene | otx1 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Anming Meng |
| Journal | Developmental Biology |
| Year | 2004 |
| Vol | 271 |
| Start Page | 130 |
| Evidence for Interaction | sprouty4 expression at tailbud in non-treatedembryos. In embryos treatedwith SU5402, the expression of sprouty4, an Fgf target, is abolished showing that the inhibition of Fgf signaling was efficient. |
| Target Gene | spry4 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | drug knockdown |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2003 |
| Vol | 120 |
| Start Page | 919 |
| Evidence for Interaction | fgf8 expression is not affected in spg embryos at its onset of expression at the MHB, but soon becomes downregulated at around 90% of epiboly. In mutant embryos, fgf8 expression is strongly reduced within r1 and abolished within r2 and r4. |
| Target Gene | fgf8 |
| Upstream Gene | pou5f1 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 9 |
| Location of Interaction in evidence | r1 |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 129 |
| Start Page | 917 |
| Evidence for Interaction | In homozygous ace embryos erm expression levels is reduced in various expression domains. |
| Target Gene | erm |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | developing eye |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2001 |
| Vol | 107 |
| Start Page | 105 |
| Evidence for Interaction | In homozygous fgf8 embryos erm expression levels is reduced in various expression domains. |
| Target Gene | pea3 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | developing eye |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2001 |
| Vol | 107 |
| Start Page | 105 |
| Evidence for Interaction | Injection of fgf8 RNA drastically reduced the number of sox17-expressing cells. |
| Target Gene | sox17 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | endoderm |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Thierry Lepage |
| Journal | Development |
| Year | 2006 |
| Vol | 133 |
| Start Page | 2189 |
| Evidence for Interaction | Injection of fgf8 RNA drastically reduced the number of sox17-expressing cells. |
| Target Gene | sox17 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | endoderm |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Thierry Lepage |
| Journal | Development |
| Year | 2006 |
| Vol | 133 |
| Start Page | 2189 |
| Evidence for Interaction | triple knockdown of fgf8, Fgf17b and fgf24 resulted in a large increase in the number of endodermal precursors that formed. |
| Target Gene | sox17 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | MASO |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | endoderm |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Thierry Lepage |
| Journal | Development |
| Year | 2006 |
| Vol | 133 |
| Start Page | 2189 |
| Evidence for Interaction | In homozygous ace embryos erm expression levels is reduced in various expression domains. |
| Target Gene | erm |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | forebrain |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2001 |
| Vol | 107 |
| Start Page | 105 |
| Evidence for Interaction | In homozygous fgf8 embryos erm expression levels is reduced in various expression domains. |
| Target Gene | pea3 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | forebrain |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2001 |
| Vol | 107 |
| Start Page | 105 |
| Evidence for Interaction | Careful analyses of myocardial differentiation in fgf8 mutants and pharmacological inhibition studies of Fgf signaling suggest that fgf8 functions to regulate nkx2.5 expression during early somitogenesis. |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | myocardial precursors |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Didier Y. R. Stainier |
| Journal | Developmental Biology |
| Year | 2001 |
| Vol | 234 |
| Start Page | 330 |
| Evidence for Interaction | The most severe effect was detected for nkx2.5 expression, which was strongly reduced or absent between the 3-somite and 15-somite stages in acerebellar embryos. |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | cardiovascular system |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | Conversely, overexpression of fgf8 RNA, either throughout the embryo or at the animal pole (which is far from its endogenous marginal expression) induces ectopic spry2 expression. |
| Target Gene | spry2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | margin |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | The most severe effect was detected for nkx2.5 expression, which was strongly reduced or absent between the 3-somite and 15-somite stages in acerebellar embryos. |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | mesoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | Expression of pax8 is initiated weakly at the MHB at early somite stages in the mutant embryos and later lost in fgf8 mutants. |
| Target Gene | pax8 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 130 |
| Start Page | 6611 |
| Evidence for Interaction | In fgf8 mutant embryos, expression of spry2 is reduced in telencephalon, somites and tail bud, and completely lost at the level of the midbrain-hindbrain boundary (MHB). |
| Target Gene | spry2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | During gastrula stages, three parallel pathways (Pax,Wnt and Fgf) are activated around the otx2/gbx1 interface in response to patterning signals. |
| Target Gene | fgf8 |
| Upstream Gene | otx2 |
| Interaction Type | enhance |
| Altered model | response to patterning signals |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2003 |
| Vol | 120 |
| Start Page | 919 |
| Evidence for Interaction | During gastrula stages, three parallel pathways (Pax,Wnt and Fgf) are activated around the otx2/gbx3 interface in response to patterning signals. |
| Target Gene | fgf8 |
| Upstream Gene | otx2 |
| Interaction Type | enhance |
| Altered model | response to patterning signals |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2003 |
| Vol | 120 |
| Start Page | 919 |
| Evidence for Interaction | In homozygous ace embryos erm expression levels is reduced in various expression domains. |
| Target Gene | erm |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2001 |
| Vol | 107 |
| Start Page | 105 |
| Evidence for Interaction | We found that in homozygous ace embryos, erm expression levels is reduced in various expression domains. |
| Target Gene | erm |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2001 |
| Vol | 107 |
| Start Page | 105 |
| Evidence for Interaction | In homozygous ace embryos erm expression levels is reduced in various expression domains. |
| Target Gene | erm |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | olfactory placcodes |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2001 |
| Vol | 107 |
| Start Page | 105 |
| Evidence for Interaction | In homozygous fgf8 embryos erm expression levels is reduced in various expression domains. |
| Target Gene | pea3 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2001 |
| Vol | 107 |
| Start Page | 105 |
| Evidence for Interaction | We found that in homozygous ace embryos, both erm and pea3 expression levels are reduced or completely lost in various expression domains. |
| Target Gene | pea3 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2001 |
| Vol | 107 |
| Start Page | 105 |
| Evidence for Interaction | In homozygous fgf8 embryos erm expression levels is reduced in various expression domains. |
| Target Gene | pea3 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | olfactory placodes |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2001 |
| Vol | 107 |
| Start Page | 105 |
| Evidence for Interaction | During gastrula stages, three parallel pathways (Pax,Wnt and Fgf) are activated around the otx2/gbx1 interface in response to patterning signals. |
| Target Gene | fgf8 |
| Upstream Gene | gbx1 |
| Interaction Type | enhance |
| Altered model | response to patterning signals |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2003 |
| Vol | 120 |
| Start Page | 919 |
| Evidence for Interaction | During gastrula stages, three parallel pathways (Pax,Wnt and Fgf) are activated around the otx2/gbx1 interface in response to patterning signals. Towards the end of gastrulation, spg ( pou2) expression refines to theMHB territory.At the end of gastrulatio |
| Target Gene | fgf8 |
| Upstream Gene | gbx1 |
| Interaction Type | enhance |
| Altered model | response to patterning signals |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2003 |
| Vol | 120 |
| Start Page | 919 |
| Evidence for Interaction | Expression of fgf8 was also delayed in Dfw8 homozygotes, in which expression cannot be detected in the hindbrain until tailbud stage. |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | Wnt8 morphants reduced expression of fgf8 at tailbud stage. |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | Expression of fgf8 was also delayed in Dfw8 homozygotes, in which expression cannot be detected in the hindbrain until tailbud stage. |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | MASO |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | Wnt8 morphants reduced expression of fgf8 at tailbud stage. |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | MASO |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | Expression of fgf8 was also delayed in Dfw8 homozygotes, in which expression cannot be detected in the hindbrain until tailbud stage. |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | Wnt8 morphants reduced expression of fgf8 at tailbud stage. |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | Expression of fgf8 was also delayed in Dfw8 homozygotes, in which expression cannot be detected in the hindbrain until tailbud stage. |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | MASO |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | Wnt8 morphants reduced expression of fgf8 at tailbud stage. |
| Target Gene | fgf8 |
| Upstream Gene | wnt8a |
| Interaction Type | enhance |
| Altered model | MASO |
| Time of Interaction in evidence | 10 |
| Location of Interaction in evidence | presumptive brain |
| Evidence for Direct | 1, 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bruce B. Riley |
| Journal | Development |
| Year | 2003 |
| Vol | 131 |
| Start Page | 923 |
| Evidence for Interaction | We found that in homozygous ace embryos, both erm and pea3 expression levels are reduced or completely lost in various expression domains. |
| Target Gene | pea3 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | developing eye |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2001 |
| Vol | 107 |
| Start Page | 105 |
| Evidence for Interaction | We found that in homozygous ace embryos, both erm and pea3 expression levels are reduced or completely lost in various expression domains. |
| Target Gene | pea3 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | forebrain |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2001 |
| Vol | 107 |
| Start Page | 105 |
| Evidence for Interaction | Down-regulation of fgf8 was observed in fgf8 morphant. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | natural |
| Altered model | MASO |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | forebrain |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | At the three-somite stage, the expression levels of otx2, six3a, pax2.1, fgf8, and krox20 were not affected by MO-gbx2. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | natural |
| Altered model | MASO |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | forebrain |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | At the three-somite stage, the expression levels of otx2, six3a, pax2.1, fgf8, and krox20 were not affected by MO-gbx2. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | natural |
| Altered model | MASO |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | forebrain |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | Careful analyses of myocardial differentiation in ace/fgf8 mutants and pharmacological inhibition studies of Fgf signaling (Reifers et al., 2000) suggest that fgf8 functions to regulate nkx2.5 expression during early somitogenesis (i.e., after the myocard |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | myocardial precursors |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Didier Y. R. Stainier |
| Journal | Developmental Biology |
| Year | 2001 |
| Vol | 234 |
| Start Page | 330 |
| Evidence for Interaction | Careful analyses of myocardial differentiation in ace/fgf8 mutants and pharmacological inhibition studies of Fgf signaling (Reifers et al., 2000) suggest that fgf8 functions to regulate nkx2.5 expression during early somitogenesis (i.e., after the myocard |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | myocardial precursors |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Didier Y. R. Stainier |
| Journal | Developmental Biology |
| Year | 2001 |
| Vol | 234 |
| Start Page | 330 |
| Evidence for Interaction | Expression of the zinc-finger transcription factor gata4 is also clearly reduced in mutant embryos at the 3- to 6- somite stage . |
| Target Gene | gata4 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | cardiovascular system |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | The most severe effect was detected for nkx2.5 expression, which was strongly reduced or absent between the 3-somite and 15-somite stages in acerebellar embryos. |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | cardiovascular system |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | The most severe effect was detected for nkx2.5 expression, which was strongly reduced or absent between the 3-somite and 15-somite stages in acerebellar embryos. |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | cardiovascular system |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | Expression of the zinc-finger transcription factor gata4 is also clearly reduced in mutant embryos at the 3- to 6- somite stage . |
| Target Gene | gata4 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | mesoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | The most severe effect was detected for nkx2.5 expression, which was strongly reduced or absent between the 3-somite and 15-somite stages in acerebellar embryos. |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | mesoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | The most severe effect was detected for nkx2.5 expression, which was strongly reduced or absent between the 3-somite and 15-somite stages in acerebellar embryos. |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | mesoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | Down-regulation of fgf8 was observed in fgf8 morphant. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | natural |
| Altered model | MASO |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | midbrain |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | At the three-somite stage, the expression levels of otx2, six3a, pax2.1, fgf8, and krox20 were not affected by MO-gbx2. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | natural |
| Altered model | MASO |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | midbrain |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | At the three-somite stage, the expression levels of otx2, six3a, pax2.1, fgf8, and krox20 were not affected by MO-gbx2. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | natural |
| Altered model | MASO |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | midbrain |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | In fgf8/acerebellar mutant embryos, expression of spry2 is reduced in telencephalon, somites and tail bud, and completely lost at the level of the midbrain-hindbrain boundary (MHB) . |
| Target Gene | spry2 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Bernard Thisse |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2853 |
| Evidence for Interaction | Down-regulation of fgf8 was observed in fgf8 morphant. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | natural |
| Altered model | MASO |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | At the three-somite stage, the expression levels of otx2, six3a, pax2.1, fgf8, and krox20 were not affected by MO-gbx2. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | natural |
| Altered model | MASO |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | At the three-somite stage, the expression levels of otx2, six3a, pax2.1, fgf8, and krox20 were not affected by MO-gbx2. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | natural |
| Altered model | MASO |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | We found that in homozygous ace embryos, both erm and pea3 expression levels are reduced or completely lost in various expression domains. |
| Target Gene | pea3 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | olfactory placodes |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Mechanisms of Development |
| Year | 2001 |
| Vol | 107 |
| Start Page | 105 |
| Evidence for Interaction | Expressions of fgf8 was expanded laterally and ventrally in the embryos injected with 50 pg of GFP-kheper RNA, compared to the uninjected control embryos. |
| Target Gene | fgf8 |
| Upstream Gene | zfhx1 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Naomasa Miki |
| Journal | Developmental Biology |
| Year | 2000 |
| Vol | 228 |
| Start Page | 29 |
| Evidence for Interaction | Expressions of the neuroectodermal genes fgf8 was expanded laterally and ventrally in the embryos injected with 50 pg of GFP-kheper RNA, compared to the uninjected control embryos. |
| Target Gene | fgf8 |
| Upstream Gene | zfhx1 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 10.33 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Naomasa Miki |
| Journal | Developmental Biology |
| Year | 2000 |
| Vol | 228 |
| Start Page | 29 |
| Evidence for Interaction | Expression of the zinc-finger transcription factor gata4 is also clearly reduced in mutant embryos at the 3- to 6- somite stage. |
| Target Gene | gata4 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 11.66 |
| Location of Interaction in evidence | cardiovascular system |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | Expression of the zinc-finger transcription factor gata4 is also clearly reduced in mutant embryos at the 3- to 6- somite stage. |
| Target Gene | gata4 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 11.66 |
| Location of Interaction in evidence | mesoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | Expression of pax8 is initiated weakly at the MHB at early somite stages in the mutant embryos and later lost in ace mutants. |
| Target Gene | pax8 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 11.66 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2003 |
| Vol | 130 |
| Start Page | 6611 |
| Evidence for Interaction | Expression of spry4 is not initiated in the fgf8 mutants. |
| Target Gene | spry4 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 11.66 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 130 |
| Start Page | 6611 |
| Evidence for Interaction | In contrast to pax8, expression of spry4 is not initiated in the mutants. The arrowhead (I) marks the MHB expression domain of spry4 in the wild-type embryo. |
| Target Gene | spry4 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 11.66 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2003 |
| Vol | 130 |
| Start Page | 6611 |
| Evidence for Interaction | Increased fgf8 expression is detected in the telencephalon and midbrain/ hindbrain domains in IGF-1 injected embryos |
| Target Gene | fgf8 |
| Upstream Gene | igf1 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 11.66 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | LUCY BYRNES |
| Journal | Int. J. Dev. Biol. |
| Year | 2004 |
| Vol | 48 |
| Start Page | 1131 |
| Evidence for Interaction | Increased fgf8 expression is detected in the telencephalon and midbrain/ hindbrain domains in IGF-1 injected embryos |
| Target Gene | fgf8 |
| Upstream Gene | igf1 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 11.66 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | LUCY BYRNES |
| Journal | Int. J. Dev. Biol. |
| Year | 2004 |
| Vol | 48 |
| Start Page | 1131 |
| Evidence for Interaction | Increased fgf8 expression is detected in the telencephalon and midbrain/ hindbrain domains in IGF-1 injected embryos |
| Target Gene | fgf8 |
| Upstream Gene | igf1 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 11.66 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | LUCY BYRNES |
| Journal | Int. J. Dev. Biol. |
| Year | 2004 |
| Vol | 48 |
| Start Page | 1131 |
| Evidence for Interaction | Similarly, expression of fgf8 in noi -/ - mutants is initiated normally and disappears from the MHB by the 9-somite stage. |
| Target Gene | fgf8 |
| Upstream Gene | pax2a |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 11.66 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 1998 |
| Vol | 125 |
| Start Page | 3049 |
| Evidence for Interaction | Expression of fgf8 in noi -/ - mutants is initiated normally and disappears from the MHB by the 9-somite stage. |
| Target Gene | fgf8 |
| Upstream Gene | pax2a |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 11.66 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 1998 |
| Vol | 125 |
| Start Page | 3049 |
| Evidence for Interaction | Expression of fgf8 in noi -/ - mutants is initiated normally and disappears from the MHB by the 9-somite stage. |
| Target Gene | fgf8 |
| Upstream Gene | pax2a |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 11.66 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 1998 |
| Vol | 125 |
| Start Page | 3049 |
| Evidence for Interaction | Expression of dmbx1 is markedly expanded at early somitogenesis in the fgf8 mutant embryos at the 7- and 9-somite stage. |
| Target Gene | dmbx1 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 11.66 |
| Location of Interaction in evidence | mesencephalic tectum |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2003 |
| Vol | 130 |
| Start Page | 6611 |
| Evidence for Interaction | Expression of dmbx1 is markedly expanded at early somitogenesis in the fgf8 mutant embryos. |
| Target Gene | dmbx1 |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 11.66 |
| Location of Interaction in evidence | mesencephalic tectum |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 130 |
| Start Page | 6611 |
| Evidence for Interaction | Increased fgf8 expression is detected in the telencephalon and midbrain/ hindbrain domains in IGF-1 injected embryos |
| Target Gene | fgf8 |
| Upstream Gene | igf1 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 11.66 |
| Location of Interaction in evidence | telencephalon |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | LUCY BYRNES |
| Journal | Int. J. Dev. Biol. |
| Year | 2004 |
| Vol | 48 |
| Start Page | 1131 |
| Evidence for Interaction | Increased fgf8 expression is detected in the telencephalon and midbrain/ hindbrain domains in IGF-1 injected embryos |
| Target Gene | fgf8 |
| Upstream Gene | igf1 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 11.66 |
| Location of Interaction in evidence | telencephalon |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | LUCY BYRNES |
| Journal | Int. J. Dev. Biol. |
| Year | 2004 |
| Vol | 48 |
| Start Page | 1131 |
| Evidence for Interaction | Increased fgf8 expression is detected in the telencephalon and midbrain/ hindbrain domains in IGF-1 injected embryos |
| Target Gene | fgf8 |
| Upstream Gene | igf1 |
| Interaction Type | enhance |
| Altered model | overexpression |
| Time of Interaction in evidence | 11.66 |
| Location of Interaction in evidence | telencephalon |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | LUCY BYRNES |
| Journal | Int. J. Dev. Biol. |
| Year | 2004 |
| Vol | 48 |
| Start Page | 1131 |
| Evidence for Interaction | In fgf8 mutant embryos the anterior part of nkx2.5 expression is severely reduced and the expression in the posterior subdomain is completely absent. |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 14 |
| Location of Interaction in evidence | cardiovascular system |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | At the 11-somite stage the fgf8 expression domain partially overlaps the nkx2.5 domain and reaches further posterior at least to the level of rhombomere 5. In acerebellar mutant embryos the anterior part of nkx2.5 expression is severely reduced and the ex |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 14 |
| Location of Interaction in evidence | cardiovascular system |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | At the 11-somite stage the fgf8 expression domain partially overlaps the nkx2.5 domain and reaches further posterior at least to the level of rhombomere 5. In acerebellar mutant embryos the anterior part of nkx2.5 expression is severely reduced and the ex |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 14 |
| Location of Interaction in evidence | cardiovascular system |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | In fgf8 mutant embryos the anterior part of nkx2.5 expression is severely reduced and the expression in the posterior subdomain is completely absent. |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 14 |
| Location of Interaction in evidence | mesoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | At the 11-somite stage the fgf8 expression domain partially overlaps the nkx2.5 domain and reaches further posterior at least to the level of rhombomere 5. In acerebellar mutant embryos the anterior part of nkx2.5 expression is severely reduced and the ex |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 14 |
| Location of Interaction in evidence | mesoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | At the 11-somite stage the fgf8 expression domain partially overlaps the nkx2.5 domain and reaches further posterior at least to the level of rhombomere 5. In acerebellar mutant embryos the anterior part of nkx2.5 expression is severely reduced and the ex |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 14 |
| Location of Interaction in evidence | mesoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | The most severe effect was detected for nkx2.5 expression, which was strongly reduced or absent between the 3-somite and 15-somite stages in fgf8 embryos. |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 16 |
| Location of Interaction in evidence | cardiovascular system |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | The most severe effect was detected for nkx2.5 expression, which was strongly reduced or absent between the 3-somite and 15-somite stages in acerebellar embryos. |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 16 |
| Location of Interaction in evidence | cardiovascular system |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | The most severe effect was detected for nkx2.5 expression, which was strongly reduced or absent between the 3-somite and 15-somite stages in acerebellar embryos. |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 16 |
| Location of Interaction in evidence | cardiovascular system |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | The most severe effect was detected for nkx2.5 expression, which was strongly reduced or absent between the 3-somite and 15-somite stages in fgf8 embryos. |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 16 |
| Location of Interaction in evidence | mesoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | The most severe effect was detected for nkx2.5 expression, which was strongly reduced or absent between the 3-somite and 15-somite stages in acerebellar embryos. |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 16 |
| Location of Interaction in evidence | mesoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | The most severe effect was detected for nkx2.5 expression, which was strongly reduced or absent between the 3-somite and 15-somite stages in acerebellar embryos. |
| Target Gene | nkx2.5 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 16 |
| Location of Interaction in evidence | mesoderm |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2000 |
| Vol | 127 |
| Start Page | 225 |
| Evidence for Interaction | In DN-IGF- 1R injected embryo, an absence of fgf8 expression was detected in the anterior-most telencephalon region while expression was reduced in the midbrain-hindbrain boundary. |
| Target Gene | fgf8 |
| Upstream Gene | igf1rb |
| Interaction Type | enhance |
| Altered model | dominant negative |
| Time of Interaction in evidence | 16 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | LUCY BYRNES |
| Journal | Int. J. Dev. Biol. |
| Year | 2004 |
| Vol | 48 |
| Start Page | 1131 |
| Evidence for Interaction | Lateral view of DN-IGF- 1R injected embryo. An absence of fgf8 expression was detected in the anterior-most telencephalon region while expression was reduced in the midbrain-hindbrain boundary |
| Target Gene | fgf8 |
| Upstream Gene | igf1rb |
| Interaction Type | enhance |
| Altered model | dominant negative |
| Time of Interaction in evidence | 16 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | LUCY BYRNES |
| Journal | Int. J. Dev. Biol. |
| Year | 2004 |
| Vol | 48 |
| Start Page | 1131 |
| Evidence for Interaction | Markedly upregulated and expanded expression of wnt4 in fgf8 mutants. |
| Target Gene | wnt4a |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 19 |
| Location of Interaction in evidence | forebrain |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 130 |
| Start Page | 6611 |
| Evidence for Interaction | Enriched expression of wnt4 at the fore-midbrain region at the 20-somite stage in ace mutants. |
| Target Gene | wnt4a |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 19 |
| Location of Interaction in evidence | forebrain |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2003 |
| Vol | 130 |
| Start Page | 6611 |
| Evidence for Interaction | Markedly upregulated and expanded expression of wnt4 in fgf8 mutants. |
| Target Gene | wnt4a |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 19 |
| Location of Interaction in evidence | midbrain |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2002 |
| Vol | 130 |
| Start Page | 6611 |
| Evidence for Interaction | Enriched expression of wnt4 at the fore-midbrain region at the 20-somite stage in ace mutants. |
| Target Gene | wnt4a |
| Upstream Gene | fgf8 |
| Interaction Type | repress |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 19 |
| Location of Interaction in evidence | midbrain |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2003 |
| Vol | 130 |
| Start Page | 6611 |
| Evidence for Interaction | fgf8 expression in the anterior portion of the hindbrain was essentially intact, although it was downregulated in the dorsal telencephalon and anterior diencephalon. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 24 |
| Location of Interaction in evidence | diencephalon |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | In the embryos injected gbx2 mRNA data, fgf8 was suppressed. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 24 |
| Location of Interaction in evidence | diencephalon |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | In the embryos injected gbx2 mRNA data, fgf8 was suppressed. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 24 |
| Location of Interaction in evidence | diencephalon |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | The regulation of mkp3 expression by FGF is confirmed by the loss of mkp3 mRNA in the MHB of the zebrafish fgf8 mutant, acerebellar (ace), and in the pax2.1 mutant, no isthmus (noi), in which FGF activity within the MHB is lost . |
| Target Gene | dusp6 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 24 |
| Location of Interaction in evidence | MHB |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Igor B. Dawid |
| Journal | Development |
| Year | 2004 |
| Vol | 131 |
| Start Page | 2769 |
| Evidence for Interaction | fgf8 expression in the anterior portion of the hindbrain was essentially intact, although it was downregulated in the dorsal telencephalon and anterior diencephalon. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 24 |
| Location of Interaction in evidence | telencephalon |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | In the embryos injected gbx2 mRNA data, fgf8 was suppressed. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 24 |
| Location of Interaction in evidence | telencephalon |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | In the embryos injected gbx2 mRNA data, fgf8 was suppressed. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 24 |
| Location of Interaction in evidence | telencephalon |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | In the embryos injected gbx2 mRNA data, fgf8 was suppressed. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 28 |
| Location of Interaction in evidence | diencephalon |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | In the embryos injected gbx2 mRNA data, fgf8 was suppressed. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 28 |
| Location of Interaction in evidence | diencephalon |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | Zath1 expression is not detectable in the upper rhombic lips of ace (fgf8) mutants in comparison with wild-type embryos. |
| Target Gene | atoh1a |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 28 |
| Location of Interaction in evidence | upper rhombic |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Michael Brand |
| Journal | Development |
| Year | 2003 |
| Vol | 130 |
| Start Page | 6611 |
| Evidence for Interaction | In the embryos injected gbx2 mRNA data, fgf8 was suppressed. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 28 |
| Location of Interaction in evidence | telencephalon |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | In the embryos injected gbx2 mRNA data, fgf8 was suppressed. |
| Target Gene | fgf8 |
| Upstream Gene | gbx2 |
| Interaction Type | repress |
| Altered model | overexpression |
| Time of Interaction in evidence | 28 |
| Location of Interaction in evidence | telencephalon |
| Evidence for Direct | 2 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Kyo Yamasu |
| Journal | Developmental Dynamics |
| Year | 2003 |
| Vol | 228 |
| Start Page | 433 |
| Evidence for Interaction | Embryos treated with SU5402 show no expression of erm, confirming that other FGF genes are responsible for the remaining expression of both genes in acerebellar mutant embryos. |
| Target Gene | erm |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | drug knockdown |
| Time of Interaction in evidence | 30 |
| Location of Interaction in evidence | developing eye |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Christiane Nu¨ sslein-Volhard |
| Journal | Current Biology |
| Year | 2001 |
| Vol | 11 |
| Start Page | 503 |
| Evidence for Interaction | Embryos treated with SU5402 show no expression of erm, confirming that other FGF genes are responsible for the remaining expression of both genes in acerebellar mutant embryos. |
| Target Gene | erm |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | drug knockdown |
| Time of Interaction in evidence | 36 |
| Location of Interaction in evidence | forebrain |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Christiane Nu¨ sslein-Volhard |
| Journal | Current Biology |
| Year | 2001 |
| Vol | 11 |
| Start Page | 503 |
| Evidence for Interaction | Embryos treated with SU5402 show no expression of erm. |
| Target Gene | erm |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | drug knockdown |
| Time of Interaction in evidence | 36 |
| Location of Interaction in evidence | upper rhombic |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Christiane Nu¨ sslein-Volhard |
| Journal | Current Biology |
| Year | 2001 |
| Vol | 11 |
| Start Page | 503 |
| Evidence for Interaction | Embryos treated with SU5402 show no expression of pea3. |
| Target Gene | pea3 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | drug knockdown |
| Time of Interaction in evidence | 36 |
| Location of Interaction in evidence | upper rhombic |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Christiane Nu¨ sslein-Volhard |
| Journal | Current Biology |
| Year | 2001 |
| Vol | 11 |
| Start Page | 503 |
| Evidence for Interaction | Embryos treated with SU5402 show no expression of pea3, confirming that other FGF genes are responsible for the remaining expression of both genes in acerebellar mutant embryos. |
| Target Gene | pea3 |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | drug knockdown |
| Time of Interaction in evidence | 36 |
| Location of Interaction in evidence | |
| Evidence for Direct | |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Christiane Nu¨ sslein-Volhard |
| Journal | Current Biology |
| Year | 2001 |
| Vol | 11 |
| Start Page | 503 |
| Evidence for Interaction | Embryos treated with SU5402 show no expression of erm, confirming that other FGF genes are responsible for the remaining expression of both genes in acerebellar mutant embryos. |
| Target Gene | erm |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | drug knockdown |
| Time of Interaction in evidence | 36 |
| Location of Interaction in evidence | neuroectoderm |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Christiane Nu¨ sslein-Volhard |
| Journal | Current Biology |
| Year | 2001 |
| Vol | 11 |
| Start Page | 503 |
| Evidence for Interaction | Embryos treated with SU5402 show no expression of erm, confirming that other FGF genes are responsible for the remaining expression of both genes in acerebellar mutant embryos. |
| Target Gene | erm |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | drug knockdown |
| Time of Interaction in evidence | 36 |
| Location of Interaction in evidence | olfactory placcodes |
| Evidence for Direct | 3 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Christiane Nu¨ sslein-Volhard |
| Journal | Current Biology |
| Year | 2001 |
| Vol | 11 |
| Start Page | 503 |
| Evidence for Interaction | In fgf8 mutant embryos, pax2.1 expression is absent from the midhindbrain border and is reduced in the retina and otic vesicle. |
| Target Gene | pax2a |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 48 |
| Location of Interaction in evidence | midhindbrain border |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | David Kimelman |
| Journal | Developmental Biology |
| Year | 2003 |
| Vol | 264 |
| Start Page | 456 |
| Evidence for Interaction | In ace (fgf8) mutant embryos, pax2.1 expression is absent from the midhindbrain border and is reduced in the retina and otic vesicle. |
| Target Gene | pax2a |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 48 |
| Location of Interaction in evidence | midhindbrain border |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | David Kimelman |
| Journal | Developmental Biology |
| Year | 2003 |
| Vol | 264 |
| Start Page | 456 |
| Evidence for Interaction | In ace (fgf8) mutant embryos, pax2.1 expression is absent from the midhindbrain border and is reduced in the retina and otic vesicle. |
| Target Gene | pax2a |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 48 |
| Location of Interaction in evidence | midhindbrain border |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | David Kimelman |
| Journal | Developmental Biology |
| Year | 2003 |
| Vol | 264 |
| Start Page | 456 |
| Evidence for Interaction | In fgf8 mutant embryos, pax2.1 expression is absent from the midhindbrain border and is reduced in the retina and otic vesicle. |
| Target Gene | pax2a |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 48 |
| Location of Interaction in evidence | otic vesicle |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | David Kimelman |
| Journal | Developmental Biology |
| Year | 2003 |
| Vol | 264 |
| Start Page | 456 |
| Evidence for Interaction | In ace (fgf8) mutant embryos, pax2.1 expression is absent from the midhindbrain border and is reduced in the retina and otic vesicle. |
| Target Gene | pax2a |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 48 |
| Location of Interaction in evidence | otic vesicle |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | David Kimelman |
| Journal | Developmental Biology |
| Year | 2003 |
| Vol | 264 |
| Start Page | 456 |
| Evidence for Interaction | In ace (fgf8) mutant embryos, pax2.1 expression is absent from the midhindbrain border and is reduced in the retina and otic vesicle. |
| Target Gene | pax2a |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 48 |
| Location of Interaction in evidence | otic vesicle |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | David Kimelman |
| Journal | Developmental Biology |
| Year | 2003 |
| Vol | 264 |
| Start Page | 456 |
| Evidence for Interaction | In fgf8 mutant embryos, pax2.1 expression is absent from the midhindbrain border and is reduced in the retina and otic vesicle. |
| Target Gene | pax2a |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 48 |
| Location of Interaction in evidence | retina |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | David Kimelman |
| Journal | Developmental Biology |
| Year | 2003 |
| Vol | 264 |
| Start Page | 456 |
| Evidence for Interaction | In ace (fgf8) mutant embryos, pax2.1 expression is absent from the midhindbrain border and is reduced in the retina and otic vesicle. |
| Target Gene | pax2a |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 48 |
| Location of Interaction in evidence | retina |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | David Kimelman |
| Journal | Developmental Biology |
| Year | 2003 |
| Vol | 264 |
| Start Page | 456 |
| Evidence for Interaction | In ace (fgf8) mutant embryos, pax2.1 expression is absent from the midhindbrain border and is reduced in the retina and otic vesicle. |
| Target Gene | pax2a |
| Upstream Gene | fgf8 |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 48 |
| Location of Interaction in evidence | retina |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | David Kimelman |
| Journal | Developmental Biology |
| Year | 2003 |
| Vol | 264 |
| Start Page | 456 |
| Evidence for Interaction | 27 genes that are expressed in the dorsal margin in wild type, but lack margin expression in MZoep mutants. |
| Target Gene | fgf8 |
| Upstream Gene | oep |
| Interaction Type | enhance |
| Altered model | mutant embryos |
| Time of Interaction in evidence | 5.25 |
| Location of Interaction in evidence | blastomere |
| Evidence for Direct | 1 |
| Binding Site Sequence | |
| Location of Site | |
| Last Author | Schier, A. F. |
| Journal | Dev Biol |
| Year | 2007 |
| Vol | 304 |
| Start Page | 525 |