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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Detaylı Bibliyografya
Asıl Yazarlar: Kaur, Jasvir, Mencl, Stine, Sahaboglu, Ayse, Farinelli, Pietro, van Veen, Theo, Zrenner, Eberhart, Ekström, Per, Paquet-Durand, François, Arango-Gonzalez, Blanca
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2011
Konular:
Research Article
Online Erişim: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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