Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse
about
Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retinaMutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in miceImpaired photoreceptor protein transport and synaptic transmission in a mouse model of Bardet-Biedl syndromeAutosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish originLocalization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGMThe role of primary cilia in the development and disease of the retinaA partial structural and functional rescue of a retinitis pigmentosa model with compacted DNA nanoparticlesBiology and therapy of inherited retinal degenerative disease: insights from mouse modelsThe cGMP-gated channel and related glutamic acid-rich proteins interact with peripherin-2 at the rim region of rod photoreceptor disc membranesPhotoreceptor renewal: a role for peripherin/rdsNonvisual light responses in the Rpe65 knockout mouse: rod loss restores sensitivity to the melanopsin system.Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathiesA monogenic dominant mutation in Rom1 generated by N-ethyl-N-nitrosourea mutagenesis causes retinal degeneration in micePeripherin/rds co-distributes with putative binding partners in basal rod outer segment disksA correlation between computer-predicted changes in secondary structure and the phenotype of retinal degeneration associated with mutations in peripherin/RDS.Differential requirements for retinal degeneration slow intermolecular disulfide-linked oligomerization in rods versus conesRole of the second intradiscal loop of peripherin/rds in homo and hetero associations.RDS/peripherin gene mutations are frequent causes of central retinal dystrophies.Initiation of rod outer segment disc formation requires RDS.Gene delivery to mitotic and postmitotic photoreceptors via compacted DNA nanoparticles results in improved phenotype in a mouse model of retinitis pigmentosa.Disulfide-mediated oligomerization of Peripherin/Rds and Rom-1 in photoreceptor disk membranes. Implications for photoreceptor outer segment morphogenesis and degeneration.Recent advances in the molecular basis of inherited photoreceptor degeneration.Deciphering the structure and function of Als2cr4 in the mouse retina.Interaction and localization of the retinitis pigmentosa protein RP2 and NSF in retinal photoreceptor cells.Pathways to photoreceptor cell death in inherited retinal degenerations.Predicted and measured disorder in peripherin/rds, a retinal tetraspanin.The complexities of ocular genetics.Gene therapy for retinal and choroidal diseases.The cell biology of visionIn situ visualization of protein interactions in sensory neurons: glutamic acid-rich proteins (GARPs) play differential roles for photoreceptor outer segment scaffoldingControl of myeloid activity during retinal inflammation.The role of subunit assembly in peripherin-2 targeting to rod photoreceptor disk membranes and retinitis pigmentosa.The tetraspanin protein peripherin-2 forms a complex with melanoregulin, a putative membrane fusion regulatorNumb regulates the polarized delivery of cyclic nucleotide-gated ion channels in rod photoreceptor ciliaRetinal Degeneration Slow (RDS) Glycosylation Plays a Role in Cone Function and in the Regulation of RDS·ROM-1 Protein Complex Formation.Simulation of human autosomal dominant retinitis pigmentosa in transgenic mice expressing a mutated murine opsin gene.Photoreceptors at a glance.Deficiency of rds/peripherin causes photoreceptor death in mouse models of digenic and dominant retinitis pigmentosaLocalization of peripherin/rds in the disk membranes of cone and rod photoreceptors: relationship to disk membrane morphogenesis and retinal degenerationCellular interactions implicated in the mechanism of photoreceptor degeneration in transgenic mice expressing a mutant rhodopsin gene.
P2860
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P2860
Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse
description
1991 nî lūn-bûn
@nan
1991 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Photoreceptor peripherin is th ...... degeneration in the rds mouse
@ast
Photoreceptor peripherin is th ...... degeneration in the rds mouse
@en
Photoreceptor peripherin is th ...... degeneration in the rds mouse
@nl
type
label
Photoreceptor peripherin is th ...... degeneration in the rds mouse
@ast
Photoreceptor peripherin is th ...... degeneration in the rds mouse
@en
Photoreceptor peripherin is th ...... degeneration in the rds mouse
@nl
prefLabel
Photoreceptor peripherin is th ...... degeneration in the rds mouse
@ast
Photoreceptor peripherin is th ...... degeneration in the rds mouse
@en
Photoreceptor peripherin is th ...... degeneration in the rds mouse
@nl
P2093
P2860
P356
P1476
Photoreceptor peripherin is th ...... degeneration in the rds mouse
@en
P2093
P2860
P356
10.1073/PNAS.88.3.723
P407
P577
1991-02-01T00:00:00Z