Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa
about
The whole nucleotide sequence and chromosomal localization of the gene for human metabotropic glutamate receptor subtype 6On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic interventionInterconversion of red opsin isoforms by the cyclophilin-related chaperone protein Ran-binding protein 2Synaptogenesis and outer segment formation are perturbed in the neural retina of Crx mutant miceRhodopsin mutant P23H destabilizes rod photoreceptor disk membranesInactivation of VCP/ter94 suppresses retinal pathology caused by misfolded rhodopsin in DrosophilaBiology and therapy of inherited retinal degenerative disease: insights from mouse modelsThe chaperone environment at the cytoplasmic face of the endoplasmic reticulum can modulate rhodopsin processing and inclusion formationUpdate on the molecular genetics of retinitis pigmentosaFunctional analysis of the rod photoreceptor cGMP phosphodiesterase alpha-subunit gene promoter: Nrl and Crx are required for full transcriptional activityChemistry of the retinoid (visual) cyclePhenotype of transgenic mice overexpressed with inducible nitric oxide synthase in the retinaThe photoreceptor-specific nuclear receptor Nr2e3 interacts with Crx and exerts opposing effects on the transcription of rod versus cone genesTubby is required for trafficking G protein-coupled receptors to neuronal ciliaThe proteome of the mouse photoreceptor sensory cilium complexChemistry and biology of the initial steps in vision: the Friedenwald lecture.Severe retinal degeneration caused by a novel rhodopsin mutation.Apoptotic photoreceptor cell death in mouse models of retinitis pigmentosa.Differential requirements for retinal degeneration slow intermolecular disulfide-linked oligomerization in rods versus conesCone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathyIsolation of a zebrafish rod opsin promoter to generate a transgenic zebrafish line expressing enhanced green fluorescent protein in rod photoreceptors.Barrier to autointegration factor interacts with the cone-rod homeobox and represses its transactivation function.Kruppel-like factor 15, a zinc-finger transcriptional regulator, represses the rhodopsin and interphotoreceptor retinoid-binding protein promotersTransport of truncated rhodopsin and its effects on rod function and degeneration.An empty E1, E3, E4 adenovirus vector protects photoreceptors from light-induced degenerationLoss of responses to visual but not electrical stimulation in ganglion cells of rats with severe photoreceptor degeneration.Q344ter mutation causes mislocalization of rhodopsin molecules that are catalytically active: a mouse model of Q344ter-induced retinal degeneration.Cone survival despite rod degeneration in XOPS-mCFP transgenic zebrafishRestoration of visual function in P23H rhodopsin transgenic rats by gene delivery of BiP/Grp78Diverse cell type-specific mechanisms localize G protein-coupled receptors to Caenorhabditis elegans sensory ciliaMutations of the opsin gene (Y102H and I307N) lead to light-induced degeneration of photoreceptors and constitutive activation of phototransduction in mice.Modulation of cellular signaling pathways in P23H rhodopsin photoreceptors.Chaperoning G protein-coupled receptors: from cell biology to therapeuticsRescue of photoreceptor degeneration by curcumin in transgenic rats with P23H rhodopsin mutation.Molecular ophthalmology: an update on animal models for retinal degenerations and dystrophiesXenopus laevis P23H rhodopsin transgene causes rod photoreceptor degeneration that is more severe in the ventral retina and is modulated by light.GCAP1 rescues rod photoreceptor response in GCAP1/GCAP2 knockout miceGene augmentation for adRP mutations in RHO.Suppression and replacement gene therapy for autosomal dominant disease in a murine model of dominant retinitis pigmentosaRhodopsin expression level affects rod outer segment morphology and photoresponse kinetics
P2860
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P2860
Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa
description
1992 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 1992
@ast
im November 1992 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1992/11/01)
@sk
vědecký článek publikovaný v roce 1992
@cs
wetenschappelijk artikel (gepubliceerd op 1992/11/01)
@nl
наукова стаття, опублікована в листопаді 1992
@uk
научни чланак (објављен 1992/11/01)
@sr
name
Transgenic mice with a rhodops ...... dominant retinitis pigmentosa
@ast
Transgenic mice with a rhodops ...... dominant retinitis pigmentosa
@en
Transgenic mice with a rhodops ...... dominant retinitis pigmentosa
@nl
type
label
Transgenic mice with a rhodops ...... dominant retinitis pigmentosa
@ast
Transgenic mice with a rhodops ...... dominant retinitis pigmentosa
@en
Transgenic mice with a rhodops ...... dominant retinitis pigmentosa
@nl
prefLabel
Transgenic mice with a rhodops ...... dominant retinitis pigmentosa
@ast
Transgenic mice with a rhodops ...... dominant retinitis pigmentosa
@en
Transgenic mice with a rhodops ...... dominant retinitis pigmentosa
@nl
P2093
P3181
P1433
P1476
Transgenic mice with a rhodops ...... dominant retinitis pigmentosa
@en
P2093
B. S. Pawlyk
E. L. Berson
G. S. Cowley
J. E. Olsson
J. W. Gordon
R. S. Molday
T. P. Dryja
P304
P3181
P356
10.1016/0896-6273(92)90236-7
P407
P577
1992-11-01T00:00:00Z