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RPGR protein complex regulates proteasome activity and mediates store-operated calcium entry

Ciliopathies are a group of genetically heterogeneous disorders, characterized by defects in cilia genesis or maintenance. Mutations in the RPGR gene and its interacting partners, RPGRIP1 and RPGRIP1L, cause ciliopathies, but the function of their proteins remains unclear. Here we show that knockdow...

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Detalles Bibliográficos
Autores principales:	Patnaik, Sarita Rani, Zhang, Xun, Biswas, Lincoln, Akhtar, Saeed, Zhou, Xinzhi, Kusuluri, Deva Krupakar, Reilly, James, May-Simera, Helen, Chalmers, Susan, McCarron, John G., Shu, Xinhua
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Impact Journals LLC 2018
Materias:	Research Paper
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955404/ https://www.ncbi.nlm.nih.gov/pubmed/29796181 http://dx.doi.org/10.18632/oncotarget.25259

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