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Loss of human disease protein retinitis pigmentosa GTPase regulator (RPGR) differentially affects rod or cone-enriched retina

It is unclear how genes, such as RPGR (retinitis pigmentosa guanine triphosphatase regulator) that are expressed in both rods and cones, cause variable disease pathogenesis. Using transcriptomic analysis, we show that loss of RPGR in a rod-dominant mouse retina (Rpgr(ko)) results in predominant alte...

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Dades bibliogràfiques
Publicat a:Hum Mol Genet
Autors principals: Rao, Kollu N., Li, Linjing, Zhang, Wei, Brush, Richard S., Rajala, Raju V.S., Khanna, Hemant
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2016
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4787904/
https://ncbi.nlm.nih.gov/pubmed/26908598
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw017
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