Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene. - Wikidata - awgldk - TriplyDB

Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene.

Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene.

http://www.wikidata.org/entity/Q36926146

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Tauroursodeoxycholic acid preservation of photoreceptor structure and function in the rd10 mouse through postnatal day 30 Bile acids in treatment of ocular disease AAV-mediated gene therapy in mouse models of recessive retinal degeneration Neuronal remodeling in retinal circuit assembly, disassembly, and reassembly The role of mislocalized phototransduction in photoreceptor cell death of retinitis pigmentosa Function of human pluripotent stem cell-derived photoreceptor progenitors in blind mice Pax6-positive Müller glia cells express cell cycle markers but do not proliferate after photoreceptor injury in the mouse retina Restoration of vision in the pde6β-deficient dog, a large animal model of rod-cone dystrophy Review: the history and role of naturally occurring mouse models with Pde6b mutations Disruption of the retinitis pigmentosa 28 gene Fam161a in mice affects photoreceptor ciliary structure and leads to progressive retinal degeneration Early synaptic defects in tulp1-/- mice Caspase inhibition with XIAP as an adjunct to AAV vector gene-replacement therapy: improving efficacy and prolonging the treatment window Mouse model resources for vision research.Non-contact measurement of linear external dimensions of the mouse eye.Cone degeneration following rod ablation in a reversible model of retinal degeneration.Differential loss and preservation of glutamate receptor function in bipolar cells in the rd10 mouse model of retinitis pigmentosa Insights into the role of RD3 in guanylate cyclase trafficking, photoreceptor degeneration, and Leber congenital amaurosis.Acute and Protracted Cell Death in Light-Induced Retinal Degeneration in the Canine Model of Rhodopsin Autosomal Dominant Retinitis Pigmentosa.Self-complementary AAV5 vector facilitates quicker transgene expression in photoreceptor and retinal pigment epithelial cells of normal mouse.Constituents of bile, bilirubin and TUDCA, protect against oxidative stress-induced retinal degeneration Dominant cone-rod dystrophy: a mouse model generated by gene targeting of the GCAP1/Guca1a gene.Functional principal component analysis reveals discriminating categories of retinal pigment epithelial morphology in mice.Autosomal-recessive early-onset retinitis pigmentosa caused by a mutation in PDE6G, the gene encoding the gamma subunit of rod cGMP phosphodiesterase Intrinsic bursting of AII amacrine cells underlies oscillations in the rd1 mouse retina CX3CL1 (fractalkine) protein expression in normal and degenerating mouse retina: in vivo studies.PGC-1α determines light damage susceptibility of the murine retina Inhibition of ceramide biosynthesis preserves photoreceptor structure and function in a mouse model of retinitis pigmentosa.Different effects of valproic acid on photoreceptor loss in Rd1 and Rd10 retinal degeneration mice A profile of transcriptomic changes in the rd10 mouse model of retinitis pigmentosa.Long-term retinal function and structure rescue using capsid mutant AAV8 vector in the rd10 mouse, a model of recessive retinitis pigmentosa.shRNA knockdown of guanylate cyclase 2e or cyclic nucleotide gated channel alpha 1 increases photoreceptor survival in a cGMP phosphodiesterase mouse model of retinitis pigmentosa Degeneration modulates retinal response to transient exogenous oxidative injury.Overexpression of SOD in retina: need for increase in H2O2-detoxifying enzyme in same cellular compartment.NRF2 promotes neuronal survival in neurodegeneration and acute nerve damage.Retinal degeneration modulates intracellular localization of CDC42 in photoreceptors Spontaneous Oscillatory Rhythm in Retinal Activities of Two Retinal Degeneration (rd1 and rd10) Mice.Atypical retinal degeneration 3 in mice is caused by defective PDE6B pre-mRNA splicing.TUDCA slows retinal degeneration in two different mouse models of retinitis pigmentosa and prevents obesity in Bardet-Biedl syndrome type 1 mice.Variable phenotypic expressivity in inbred retinal degeneration mouse lines: A comparative study of C3H/HeOu and FVB/N rd1 mice Retinal Pigment Epithelium Atrophy 1 (rpea1): A New Mouse Model With Retinal Detachment Caused by a Disruption of Protein Kinase C, θ

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Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene.

http://www.wikidata.org/entity/Q36926146

description

2007 nî lūn-bûn

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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2007年论文

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2007年论文

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name

Two mouse retinal degeneration ...... d cGMP phosphodiesterase gene.

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Two mouse retinal degeneration ...... d cGMP phosphodiesterase gene.

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Two mouse retinal degeneration ...... d cGMP phosphodiesterase gene.

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J.VISRES.2006.11.020

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Vision Research

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Two mouse retinal degeneration ...... d cGMP phosphodiesterase gene.

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A M German

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A P Boyd

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B Chang

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J H Boatright

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J M Nickerson

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J R Heckenlively

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K Rengarajan

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M J Phillips

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M T Davisson

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M T Pardue

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P2860

Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosa

Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa

Retinal degeneration mutants in the mouse

Multiple cyclic nucleotide phosphodiesterases

Cyclic guanosine monophosphate: elevation in degenerating photoreceptor cells of the C3H mouse retina

Enzymic basis for cyclic GMP accumulation in degenerative photoreceptor cells of mouse retina

Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene.

The Inheritance of a Retinal Abnormality in White Mice.

Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesterase.

PCR analysis of DNA from 70-year-old sections of rodless retina demonstrates identity with the mouse rd defect

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10.1016/J.VISRES.2006.11.020

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5

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47

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2007-01-30T00:00:00Z

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6537537

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17267005

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2562796

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