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Pathogenic NPHP5 mutations impair protein interaction with Cep290, a prerequisite for ciliogenesis

Mutations in the human NPHP5 gene cause retinal and renal disease but the precise mechanisms by which NPHP5 functions are not understood. We report that NPHP5 is a centriolar protein whose depletion inhibits an early step of ciliogenesis, a phenotype reminiscent of Cep290 loss and contrary to IFT88...

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Détails bibliographiques
Auteurs principaux: Barbelanne, Marine, Song, Jenny, Ahmadzai, Mustafa, Tsang, William Y.
Format: Artigo
Langue:Inglês
Publié: 2013
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3797088/
https://ncbi.nlm.nih.gov/pubmed/23446637
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddt100
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