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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
Autores principales:	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:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2016
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4873209/ https://www.ncbi.nlm.nih.gov/pubmed/27196396 http://dx.doi.org/10.1371/journal.pone.0155860

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