MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis

Meckel-Gruber syndrome (MKS), nephronophthisis (NPHP), and related ciliopathies present with overlapping phenotypes and display considerable allelism between at least twelve different genes of largely unexplained function. We demonstrate that the conserved C. elegans B9 domain (MKS-1, MKSR-1, and MK...

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Detalhes bibliográficos
Main Authors: Williams, Corey L., Li, Chunmei, Kida, Katarzyna, Inglis, Peter N., Mohan, Swetha, Semenec, Lucie, Bialas, Nathan J., Stupay, Rachel M., Chen, Nansheng, Blacque, Oliver E., Yoder, Bradley K., Leroux, Michel R.
Formato: Artigo
Idioma:Inglês
Publicado em: The Rockefeller University Press 2011
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3063147/
https://ncbi.nlm.nih.gov/pubmed/21422230
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1083/jcb.201012116
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