Usher syndrome proteins ADGRV1 (USH2C) and CIB2 (USH1J) interact and share a common interactome containing TRiC/CCT-BBS chaperonins

The human Usher syndrome (USH) is the most common form of a sensory hereditary ciliopathy characterized by progressive vision and hearing loss. Mutations in the genes ADGRV1 and CIB2 have been associated with two distinct sub-types of USH, namely, USH2C and USH1J. The proteins encoded by the two gen...

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Detalles Bibliográficos
Autores principales: Linnert, Joshua, Knapp, Barbara, Güler, Baran E., Boldt, Karsten, Ueffing, Marius, Wolfrum, Uwe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10323441/
https://www.ncbi.nlm.nih.gov/pubmed/37427378
http://dx.doi.org/10.3389/fcell.2023.1199069

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10323441/
https://www.ncbi.nlm.nih.gov/pubmed/37427378
http://dx.doi.org/10.3389/fcell.2023.1199069

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