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Distinct tissue-specific requirements for the zebrafish tbx5 genes during heart, retina and pectoral fin development
The transcription factor Tbx5 is expressed in the developing heart, eyes and anterior appendages. Mutations in human TBX5 cause Holt–Oram syndrome, a condition characterized by heart and upper limb malformations. Tbx5-knockout mouse embryos have severely impaired forelimb and heart morphogenesis fro...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The Royal Society
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4043114/ https://ncbi.nlm.nih.gov/pubmed/24759614 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1098/rsob.140014 |
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