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...

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Detalhes bibliográficos
Main Authors: Kaur, Jasvir, Mencl, Stine, Sahaboglu, Ayse, Farinelli, Pietro, van Veen, Theo, Zrenner, Eberhart, Ekström, Per, Paquet-Durand, François, Arango-Gonzalez, Blanca
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2011
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3134478/
https://ncbi.nlm.nih.gov/pubmed/21765948
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0022181
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