The carboxyl terminal mutational hotspot of the ciliary disease protein RPGRORF15 (retinitis pigmentosa GTPase regulator) is glutamylated in vivo
about
RPGR, a prenylated retinal ciliopathy protein, is targeted to cilia in a prenylation- and PDE6D-dependent manner.Codon-Optimized RPGR Improves Stability and Efficacy of AAV8 Gene Therapy in Two Mouse Models of X-Linked Retinitis Pigmentosa.BBSome function is required for both the morphogenesis and maintenance of the photoreceptor outer segment.Identification of DmTTLL5 as a Major Tubulin Glutamylase in the Drosophila Nervous System.Glutamylation Regulates Transport, Specializes Function, and Sculpts the Structure of Cilia.
P2860
The carboxyl terminal mutational hotspot of the ciliary disease protein RPGRORF15 (retinitis pigmentosa GTPase regulator) is glutamylated in vivo
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
The carboxyl terminal mutation ...... lator) is glutamylated in vivo
@en
type
label
The carboxyl terminal mutation ...... lator) is glutamylated in vivo
@en
prefLabel
The carboxyl terminal mutation ...... lator) is glutamylated in vivo
@en
P2860
P356
P1433
P1476
The carboxyl terminal mutation ...... lator) is glutamylated in vivo
@en
P2093
Kollu N Rao
Manisha Anand
P2860
P304
P356
10.1242/BIO.016816
P577
2016-03-03T00:00:00Z