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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Bibliografski detalji
Izdano u:PLoS One
Glavni autori: 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
Format: Artigo
Jezik:Inglês
Izdano: Public Library of Science 2016
Teme:
Research Article
Online pristup: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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