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fras1 shapes endodermal pouch 1 and stabilizes zebrafish pharyngeal skeletal development

Lesions in the epithelially expressed human gene FRAS1 cause Fraser syndrome, a complex disease with variable symptoms, including facial deformities and conductive hearing loss. The developmental basis of facial defects in Fraser syndrome has not been elucidated. Here we show that zebrafish fras1 mu...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Talbot, Jared Coffin, Walker, Macie B., Carney, Thomas J., Huycke, Tyler R., Yan, Yi-Lin, BreMiller, Ruth A., Gai, Linda, DeLaurier, April, Postlethwait, John H., Hammerschmidt, Matthias, Kimmel, Charles B.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Company of Biologists 2012
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC3392706/
https://ncbi.nlm.nih.gov/pubmed/22782724
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dev.074906
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