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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Vydáno v:PLoS One
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Public Library of Science 2016
Témata:
Research Article
On-line přístup: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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