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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: 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.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: The Rockefeller University Press 2011
Pynciau:
Research Articles
Mynediad Ar-lein: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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