Loss of human disease protein retinitis pigmentosa GTPase regulator (RPGR) differentially affects rod or cone-enriched retina.
about
Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration.The K153Del PRPH2 mutation differentially impacts photoreceptor structure and function.Gelsolin dysfunction causes photoreceptor loss in induced pluripotent cell and animal retinitis pigmentosa models.Simple and complex retinal dystrophies are associated with profoundly different disease networksPrenylated retinal ciliopathy protein RPGR interacts with PDE6δ and regulates ciliary localization of Joubert syndrome-associated protein INPP5E.Primary cilia proteins: ciliary and extraciliary sites and functions.RPGR protein complex regulates proteasome activity and mediates store-operated calcium entry.
P2860
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P2860
Loss of human disease protein retinitis pigmentosa GTPase regulator (RPGR) differentially affects rod or cone-enriched retina.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Loss of human disease protein ...... s rod or cone-enriched retina.
@ast
Loss of human disease protein ...... s rod or cone-enriched retina.
@en
type
label
Loss of human disease protein ...... s rod or cone-enriched retina.
@ast
Loss of human disease protein ...... s rod or cone-enriched retina.
@en
prefLabel
Loss of human disease protein ...... s rod or cone-enriched retina.
@ast
Loss of human disease protein ...... s rod or cone-enriched retina.
@en
P2093
P2860
P356
P1476
Loss of human disease protein ...... s rod or cone-enriched retina.
@en
P2093
Kollu N Rao
Linjing Li
Raju V S Rajala
Richard S Brush
P2860
P304
P356
10.1093/HMG/DDW017
P577
2016-01-24T00:00:00Z