Overexpression of Rhodopsin or Its Mutants Leads to Energy Metabolism Dysfunction in 661w Cells

PURPOSE: Retinitis pigmentosa (RP) is a heterogeneous group of inherited disorders characterized by photoreceptor degeneration. The rhodopsin gene (RHO) is the most frequent cause of autosomal dominant RP (ADRP), yet it remains unclear how RHO mutations cause heterogeneous phenotypes. Energy failure...

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Detalles Bibliográficos
Autores principales: Liu, Yang, Wang, Xin, Gong, Ruowen, Xu, Gezhi, Zhu, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9730732/
https://www.ncbi.nlm.nih.gov/pubmed/36469028
http://dx.doi.org/10.1167/iovs.63.13.2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9730732/
https://www.ncbi.nlm.nih.gov/pubmed/36469028
http://dx.doi.org/10.1167/iovs.63.13.2

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