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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Kaur, Jasvir, Mencl, Stine, Sahaboglu, Ayse, Farinelli, Pietro, van Veen, Theo, Zrenner, Eberhart, Ekström, Per, Paquet-Durand, François, Arango-Gonzalez, Blanca
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Public Library of Science 2011
Gaiak:
Research Article
Sarrera elektronikoa: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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