ARL13B, PDE6D, and CEP164 form a functional network for INPP5E ciliary targeting

Mutations affecting ciliary components cause a series of related genetic disorders in humans, including nephronophthisis (NPHP), Joubert syndrome (JBTS), Meckel-Gruber syndrome (MKS), and Bardet-Biedl syndrome (BBS), which are collectively termed “ciliopathies.” Recent protein–protein interaction st...

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Detalhes bibliográficos
Main Authors: Humbert, Melissa C., Weihbrecht, Katie, Searby, Charles C., Li, Yalan, Pope, Robert M., Sheffield, Val C., Seo, Seongjin
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2012
Assuntos:
Biological Sciences
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3511769/
https://ncbi.nlm.nih.gov/pubmed/23150559
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1210916109
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