OFD1, as a Ciliary Protein, Exhibits Neuroprotective Function in Photoreceptor Degeneration Models

Ofd1 is a newly identified causative gene for Retinitis pigmentosa (RP), a photoreceptor degenerative disease. This study aimed to examine Ofd1 localization in retina and further to investigate its function in photoreceptor degeneration models. Ofd1 localization in rat retina was examined using immu...

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Detalles Bibliográficos
Publicado en:PLoS One
Main Authors: Wang, Juan, Chen, Xin, Wang, Fang, Zhang, Jieping, Li, Peng, Li, Zongyi, Xu, Jingying, Gao, Furong, Jin, Caixia, Tian, Haibin, Zhang, Jingfa, Li, Weiye, Lu, Lixia, Xu, Guo-Tong
Formato: Artigo
Idioma:Inglês
Publicado: Public Library of Science 2016
Assuntos:
Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4873209/
https://ncbi.nlm.nih.gov/pubmed/27196396
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0155860
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