Calpain and PARP Activation during Photoreceptor Cell Death in P23H and S334ter Rhodopsin Mutant Rats

Retinitis pigmentosa (RP) is a heterogeneous group of inherited neurodegenerative diseases affecting photoreceptors and causing blindness. Many human cases are caused by mutations in the rhodopsin gene. An important question regarding RP pathology is whether different genetic defects trigger the sam...

Descripción completa

Detalles Bibliográficos
Autores principales: Kaur, Jasvir, Mencl, Stine, Sahaboglu, Ayse, Farinelli, Pietro, van Veen, Theo, Zrenner, Eberhart, Ekström, Per, Paquet-Durand, François, Arango-Gonzalez, Blanca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3134478/
https://www.ncbi.nlm.nih.gov/pubmed/21765948
http://dx.doi.org/10.1371/journal.pone.0022181

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3134478/
https://www.ncbi.nlm.nih.gov/pubmed/21765948
http://dx.doi.org/10.1371/journal.pone.0022181

Ejemplares similares