Survey of common eye diseases in laboratory mouse strains.
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Review: the history and role of naturally occurring mouse models with Pde6b mutationsThe severity of retinal pathology in homozygous Crb1rd8/rd8 mice is dependent on additional genetic factors.Wounding the cornea to learn how it heals.Photoreceptor oxidative stress in hyperoxia-induced proliferative retinopathy accelerates rd8 degenerationStudying age-related macular degeneration using animal models.Retinal and nonocular abnormalities in Cyp27a1(-/-)Cyp46a1(-/-) mice with dysfunctional metabolism of cholesterol.Targeting channelrhodopsin-2 to ON-bipolar cells with vitreally administered AAV Restores ON and OFF visual responses in blind miceDeletion of placental growth factor prevents diabetic retinopathy and is associated with Akt activation and HIF1α-VEGF pathway inhibition.Apolipoprotein E promotes subretinal mononuclear phagocyte survival and chronic inflammation in age-related macular degenerationRAGE regulates immune cell infiltration and angiogenesis in choroidal neovascularization.A Novel, Real-Time, In Vivo Mouse Retinal Imaging SystemVariable phenotypic expressivity in inbred retinal degeneration mouse lines: A comparative study of C3H/HeOu and FVB/N rd1 miceRetinal Pigment Epithelium Atrophy 1 (rpea1): A New Mouse Model With Retinal Detachment Caused by a Disruption of Protein Kinase C, θThe Time Course of Deafness and Retinal Degeneration in a Kunming Mouse Model for Usher Syndrome.Survey of the nob5 mutation in C3H substrains.Age-related macular degeneration phenotypes are associated with increased tumor necrosis-alpha and subretinal immune cells in aged Cxcr5 knockout mice.Mthfr as a modifier of the retinal phenotype of Crb1(rd8/rd8) mice.Presence of the Gpr179(nob5) allele in a C3H-derived transgenic mouse.Correction of the Crb1rd8 allele and retinal phenotype in C57BL/6N mice via TALEN-mediated homology-directed repair.Analysis of MTHFR, CBS, Glutathione, Taurine, and Hydrogen Sulfide Levels in Retinas of Hyperhomocysteinemic Mice.Genetic modifiers as relevant biological variables of eye disorders.Mouse models of human ocular disease for translational research.Absence of Sigma 1 Receptor Accelerates Photoreceptor Cell Death in a Murine Model of Retinitis Pigmentosa.The Complement Regulatory Protein CD46 Deficient Mouse Spontaneously Develops Dry-Type Age-Related Macular Degeneration-Like Phenotype.Genetic modifier loci of mouse Mfrp(rd6) identified by quantitative trait locus analysis.Oral Monomethyl Fumarate Therapy Ameliorates Retinopathy in a Humanized Mouse Model of Sickle Cell Disease.Genetic Control of Rod Bipolar Cell Number in the Mouse Retina.Microtubule-Associated Protein 1 Light Chain 3B, (LC3B) Is Necessary to Maintain Lipid-Mediated Homeostasis in the Retinal Pigment EpitheliumSpontaneous Posterior Segment Vascular Disease Phenotype of a Mouse Model, rnv3, Is Dependent on the Crb1rd8 Allele
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Survey of common eye diseases in laboratory mouse strains.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 24 July 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Survey of common eye diseases in laboratory mouse strains.
@en
Survey of common eye diseases in laboratory mouse strains.
@nl
type
label
Survey of common eye diseases in laboratory mouse strains.
@en
Survey of common eye diseases in laboratory mouse strains.
@nl
prefLabel
Survey of common eye diseases in laboratory mouse strains.
@en
Survey of common eye diseases in laboratory mouse strains.
@nl
P2093
P2860
P356
P1476
Survey of common eye diseases in laboratory mouse strains.
@en
P2093
Jieping Wang
Patsy Nishina
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P304
P356
10.1167/IOVS.13-12289
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P577
2013-07-24T00:00:00Z