Ciliogenesis in Caenorhabditis elegans requires genetic interactions between ciliary middle segment localized NPHP-2 (inversin) and transition zone-associated proteins

The cystic kidney diseases nephronophthisis (NPHP), Meckel–Gruber syndrome (MKS) and Joubert syndrome (JBTS) share an underlying etiology of dysfunctional cilia. Patients diagnosed with NPHP type II have mutations in the gene INVS (also known as NPHP2), which encodes inversin, a cilia localizing pro...

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Detalhes bibliográficos
Main Authors: Warburton-Pitt, Simon R. F., Jauregui, Andrew R., Li, Chunmei, Wang, Juan, Leroux, Michel R., Barr, Maureen M.
Formato: Artigo
Idioma:Inglês
Publicado em: Company of Biologists 2012
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3403231/
https://ncbi.nlm.nih.gov/pubmed/22393243
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/jcs.095539
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