A simple polymerase chain reaction assay for genotyping the retinal degeneration mutation (Pdeb(rd1)) in FVB/N-derived transgenic mice.
about
Using mouse models of autism spectrum disorders to study the neurotoxicology of gene-environment interactionsLeber congenital amaurosis linked to AIPL1: a mouse model reveals destabilization of cGMP phosphodiesteraseRetinoid-related orphan nuclear receptor RORbeta is an early-acting factor in rod photoreceptor developmentDisruption of the retinitis pigmentosa 28 gene Fam161a in mice affects photoreceptor ciliary structure and leads to progressive retinal degenerationOverexpression of RPGR leads to male infertility in mice due to defects in flagellar assemblyDifferences in memory development among C57BL/6NCrl, 129S2/SvPasCrl, and FVB/NCrl mice after delay and trace fear conditioning.A transgenic mouse class-III beta tubulin reporter using yellow fluorescent protein.Reevaluating hippocampus-dependent learning in FVB/N mice.The Flk1-myr::mCherry mouse as a useful reporter to characterize multiple aspects of ocular blood vessel development and diseaseThe Leber congenital amaurosis protein, AIPL1, is needed for the viability and functioning of cone photoreceptor cellsTranscription coactivators p300 and CBP are necessary for photoreceptor-specific chromatin organization and gene expression.Apelin is required for non-neovascular remodeling in the retina.Brain phenotype of transgenic mice overexpressing cystathionine β-synthase.A converging-methods approach to fragile X syndrome.Testing for a gap junction-mediated bystander effect in retinitis pigmentosa: secondary cone death is not altered by deletion of connexin36 from cones.Anatomically defined neuron-based rescue of neurodegenerative Niemann-Pick type C disorder.Destructive Changes in the Neuronal Structure of the FVB/N Mouse RetinaChoroidal neovascularization is inhibited via an intraocular decrease of inflammatory cells in mice lacking complement component C3.Variable phenotypic expressivity in inbred retinal degeneration mouse lines: A comparative study of C3H/HeOu and FVB/N rd1 miceEvidence for baseline retinal pigment epithelium pathology in the Trp1-Cre mouse.Mouse behavioural analysis in systems biology.Dry age-related macular degeneration like pathology in aged 5XFAD mice: Ultrastructure and microarray analysis.Retinal horizontal cells lacking Rb1 sustain persistent DNA damage and survive as polyploid giant cells.IL10-driven STAT3 signalling in senescent macrophages promotes pathological eye angiogenesis.Survey of common eye diseases in laboratory mouse strains.Depleting Rac1 in mouse rod photoreceptors protects them from photo-oxidative stress without affecting their structure or functionARL3 regulates trafficking of prenylated phototransduction proteins to the rod outer segment.Cognitive and sensorimotor tasks for assessing functional impairments in mouse models of Alzheimer's disease and related disordersGenetic modifiers as relevant biological variables of eye disorders.Epithelial-mesenchymal transition of the retinal pigment epithelium causes choriocapillaris atrophy.A TgCRND8 Mouse Model of Alzheimer's Disease Exhibits Sexual Dimorphisms in Behavioral Indices of Cognitive Reserve.Behavioral assessments for pre-clinical pharmacovigilance.Role of neuronal activity and kinesin on tract tracing by manganese-enhanced MRI (MEMRI).Gene and mutation independent therapy via CRISPR-Cas9 mediated cellular reprogramming in rod photoreceptors.Phosphatidylinositol-3-phosphate is light-regulated and essential for survival in retinal rods.Elevated amounts of myocilin in the aqueous humor of transgenic mice cause significant changes in ocular gene expression.The eye of the laboratory mouse remains anatomically adapted for natural conditions.Macrophages engulf endothelial cell membrane particles preceding pupillary membrane capillary regression.Genetically modified neural stem cells for a local and sustained delivery of neuroprotective factors to the dystrophic mouse retina.Notch signaling in the pigmented epithelium of the anterior eye segment promotes ciliary body development at the expense of iris formation.
P2860
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P2860
A simple polymerase chain reaction assay for genotyping the retinal degeneration mutation (Pdeb(rd1)) in FVB/N-derived transgenic mice.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh-hant
name
A simple polymerase chain reac ...... FVB/N-derived transgenic mice.
@en
A simple polymerase chain reaction assay for genotyping the retinal degeneration mutation
@nl
type
label
A simple polymerase chain reac ...... FVB/N-derived transgenic mice.
@en
A simple polymerase chain reaction assay for genotyping the retinal degeneration mutation
@nl
prefLabel
A simple polymerase chain reac ...... FVB/N-derived transgenic mice.
@en
A simple polymerase chain reaction assay for genotyping the retinal degeneration mutation
@nl
P356
P1433
P1476
A simple polymerase chain reac ...... FVB/N-derived transgenic mice
@en
P2093
P304
P356
10.1258/0023677011911525
P577
2001-04-01T00:00:00Z