Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase.
about
Transcriptomic analysis of human retinal detachment reveals both inflammatory response and photoreceptor deathPapillorenal syndrome-causing missense mutations in PAX2/Pax2 result in hypomorphic alleles in mouse and humanA role for prenylated rab acceptor 1 in vertebrate photoreceptor developmentThe retinitis pigmentosa GTPase regulator, RPGR, interacts with the delta subunit of rod cyclic GMP phosphodiesteraseX-arrestin: a new retinal arrestin mapping to the X chromosomeCloning, chromosomal localization and functional expression of the gene encoding the alpha-subunit of the cGMP-gated channel in human cone photoreceptorsIsolation and characterization of the Drosophila retinal degeneration B (rdgB) geneDisruption of retinoid-related orphan receptor beta changes circadian behavior, causes retinal degeneration and leads to vacillans phenotype in miceEctopic expression of a microbial-type rhodopsin restores visual responses in mice with photoreceptor degenerationAIPL1, the protein that is defective in Leber congenital amaurosis, is essential for the biosynthesis of retinal rod cGMP phosphodiesteraseMutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosaGenomic organization and complete sequence of the human gene encoding the beta-subunit of the cGMP phosphodiesterase and its localisation to 4p 16.3HDAC4 regulates neuronal survival in normal and diseased retinasTauroursodeoxycholic acid preservation of photoreceptor structure and function in the rd10 mouse through postnatal day 30Bile acids in treatment of ocular diseaseInstability of GGL domain-containing RGS proteins in mice lacking the G protein beta-subunit Gbeta5In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouseFunctional redundancy of cryptochromes and classical photoreceptors for nonvisual ocular photoreception in miceUse of a dense single nucleotide polymorphism map for in silico mapping in the mouseRetinal Cell Degeneration in Animal ModelsMultiple Independent Oscillatory Networks in the Degenerating RetinaAAV-mediated gene therapy in mouse models of recessive retinal degenerationLentiviral expression of retinal guanylate cyclase-1 (RetGC1) restores vision in an avian model of childhood blindnessCLRN1 is nonessential in the mouse retina but is required for cochlear hair cell developmentRestoring the ON Switch in Blind Retinas: Opto-mGluR6, a Next-Generation, Cell-Tailored Optogenetic ToolPARP1 gene knock-out increases resistance to retinal degeneration without affecting retinal function.Pharmacological analysis of intrinsic neuronal oscillations in rd10 retinaFunction of human pluripotent stem cell-derived photoreceptor progenitors in blind miceCalcium Imaging of AM Dyes Following Prolonged Incubation in Acute Neuronal TissueMapping the Flv locus controlling resistance to flaviviruses on mouse chromosome 5Human cone-specific cGMP phosphodiesterase alpha' subunit: complete cDNA sequence and gene arrangementAutosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesteraseRecessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosaCharacterization of the MRP4- and MRP5-mediated transport of cyclic nucleotides from intact cellsFunctional screening of 2 Mb of human chromosome 21q22.2 in transgenic mice implicates minibrain in learning defects associated with Down syndromeNonvisual light responses in the Rpe65 knockout mouse: rod loss restores sensitivity to the melanopsin system.Review: the history and role of naturally occurring mouse models with Pde6b mutationsLight-induced fos expression in intrinsically photosensitive retinal ganglion cells in melanopsin knockout (opn4) mice.Impaired channel targeting and retinal degeneration in mice lacking the cyclic nucleotide-gated channel subunit CNGB1Exacerbation of retinal degeneration in the absence of alpha crystallins in an in vivo model of chemically induced hypoxia
P2860
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P2860
Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase.
description
1990 nî lūn-bûn
@nan
1990 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
Retinal degeneration in the rd ...... of rod cGMP-phosphodiesterase.
@ast
Retinal degeneration in the rd ...... of rod cGMP-phosphodiesterase.
@en
type
label
Retinal degeneration in the rd ...... of rod cGMP-phosphodiesterase.
@ast
Retinal degeneration in the rd ...... of rod cGMP-phosphodiesterase.
@en
prefLabel
Retinal degeneration in the rd ...... of rod cGMP-phosphodiesterase.
@ast
Retinal degeneration in the rd ...... of rod cGMP-phosphodiesterase.
@en
P2093
P356
P1433
P1476
Retinal degeneration in the rd ...... of rod cGMP-phosphodiesterase.
@en
P2093
P2888
P304
P356
10.1038/347677A0
P407
P577
1990-10-01T00:00:00Z
P6179
1033528083