The cellular and molecular etiology of the craniofacial defects in the avian ciliopathic mutant talpid(2)

talpid(2) is an avian autosomal recessive mutant with a myriad of congenital malformations, including polydactyly and facial clefting. Although phenotypically similar to talpid(3), talpid(2) has a distinct facial phenotype and an unknown cellular, molecular and genetic basis. We set out to determine...

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Detalles Bibliográficos
Autores principales: Chang, Ching-Fang, Schock, Elizabeth N., O'Hare, Elizabeth A., Dodgson, Jerry, Cheng, Hans H., Muir, William M., Edelmann, Richard E., Delany, Mary E., Brugmann, Samantha A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists 2014
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197679/
https://www.ncbi.nlm.nih.gov/pubmed/25053433
http://dx.doi.org/10.1242/dev.105924

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197679/
https://www.ncbi.nlm.nih.gov/pubmed/25053433
http://dx.doi.org/10.1242/dev.105924

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