Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesterase.
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Expression of ionotropic glutamate receptors in the retina of the rdta transgenic mouseTransnasal delivery of human A-beta peptides elicits impaired learning and memory performance in wild type mice.Recent advances in understanding the spectrum of canine generalised progressive retinal atrophyReview: the history and role of naturally occurring mouse models with Pde6b mutationsLeber congenital amaurosis linked to AIPL1: a mouse model reveals destabilization of cGMP phosphodiesteraseOverexpression of RPGR leads to male infertility in mice due to defects in flagellar assemblyMonoacylglycerol lipase inhibitor JZL184 improves behavior and neural properties in Ts65Dn mice, a model of down syndromeLrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB)Inner retinal photoreception independent of the visual retinoid cycle.Behavioral validation of the Ts65Dn mouse model for Down syndrome of a genetic background free of the retinal degeneration mutation Pde6b(rd1).Structures of endogenous nonecotropic murine leukemia virus (MLV) long terminal repeats in wild mice: implication for evolution of MLVsStructure and distribution of endogenous nonecotropic murine leukemia viruses in wild mice.Overexpression of Dyrk1A is implicated in several cognitive, electrophysiological and neuromorphological alterations found in a mouse model of Down syndromePerinatal choline supplementation improves cognitive functioning and emotion regulation in the Ts65Dn mouse model of Down syndromeOrigins of albino and hooded rats: implications from molecular genetic analysis across modern laboratory rat strains.Rod photoreceptor-specific gene expression in human retinoblastoma cells.Testing for a gap junction-mediated bystander effect in retinitis pigmentosa: secondary cone death is not altered by deletion of connexin36 from cones.Transcriptional activation of the human rod cGMP-phosphodiesterase beta-subunit gene is mediated by an upstream AP-1 element.Genetic etiology of renal agenesis: fine mapping of Renag1 and identification of Kit as the candidate functional geneIncreased efficiency of the GABAA and GABAB receptor-mediated neurotransmission in the Ts65Dn mouse model of Down syndromeVariable phenotypic expressivity in inbred retinal degeneration mouse lines: A comparative study of C3H/HeOu and FVB/N rd1 miceCyclic intensive light exposure induces retinal lesions similar to age-related macular degeneration in APPswe/PS1 bigenic miceThe Rd8 mutation of the Crb1 gene is present in vendor lines of C57BL/6N mice and embryonic stem cells, and confounds ocular induced mutant phenotypes.Survey of the nob5 mutation in C3H substrains.Long-term characterization of retinal degeneration in rd1 and rd10 mice using spectral domain optical coherence tomographyDeficits in cognition and synaptic plasticity in a mouse model of Down syndrome ameliorated by GABAB receptor antagonists.Bach1 overexpression in Down syndrome correlates with the alteration of the HO-1/BVR-a system: insights for transition to Alzheimer's disease.AAV-mediated gene therapy for retinal degeneration in the rd10 mouse containing a recessive PDEbeta mutation.An Anti-β-Amyloid Vaccine for Treating Cognitive Deficits in a Mouse Model of Down Syndrome.Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene.Survey of common eye diseases in laboratory mouse strains.Genetic complexity of absence seizures in substrains of C3H mice.Cell loss in retinal dystrophies by apoptosis--death by informed consent!Retinal degeneration in mice lacking the gamma subunit of the rod cGMP phosphodiesterase.Insights from Genetic Model Systems of Retinal Degeneration: Role of Epsins in Retinal Angiogenesis and VEGFR2 Signaling.Fragile X mental retardation protein is necessary for neurotransmitter-activated protein translation at synapsesStructural and molecular bases of rod photoreceptor morphogenesis and disease.Proximate causes for diet-induced obesity in laboratory mice: a case study.CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis Pigmentosa.Encapsidated adenovirus mini-chromosome-mediated delivery of genes to the retina: application to the rescue of photoreceptor degeneration.
P2860
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P2860
Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesterase.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
1993年论文
@zh
1993年论文
@zh-cn
name
Localization of a retroviral e ...... nit of cGMP phosphodiesterase.
@ast
Localization of a retroviral e ...... nit of cGMP phosphodiesterase.
@en
type
label
Localization of a retroviral e ...... nit of cGMP phosphodiesterase.
@ast
Localization of a retroviral e ...... nit of cGMP phosphodiesterase.
@en
prefLabel
Localization of a retroviral e ...... nit of cGMP phosphodiesterase.
@ast
Localization of a retroviral e ...... nit of cGMP phosphodiesterase.
@en
P2093
P2860
P356
P1476
Localization of a retroviral e ...... nit of cGMP phosphodiesterase.
@en
P2093
D B Farber
J M Coffin
M Danciger
M L Applebury
W N Frankel
P2860
P304
P356
10.1073/PNAS.90.7.2955
P407
P577
1993-04-01T00:00:00Z