New In Vitro Cellular Model for Molecular Studies of Retinitis Pigmentosa

Retinitis pigmentosa (RP) is an inherited form of retinal degeneration characterized by primary rod photoreceptor cell death followed by cone loss. Mutations in several genes linked to the disease cause increased levels of cyclic guanosine monophosphate (cGMP) and calcium ion influxes. The purpose o...

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Detalles Bibliográficos
Autores principales: Huang, Li, Kutluer, Meltem, Adani, Elisa, Comitato, Antonella, Marigo, Valeria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8235468/
https://www.ncbi.nlm.nih.gov/pubmed/34208617
http://dx.doi.org/10.3390/ijms22126440

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8235468/
https://www.ncbi.nlm.nih.gov/pubmed/34208617
http://dx.doi.org/10.3390/ijms22126440

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