about
Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindnessTRPM1 is required for the depolarizing light response in retinal ON-bipolar cellsLrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB)Estimating ON and OFF contributions to the photopic hill: normative data and clinical applications.RGS7 and -11 complexes accelerate the ON-bipolar cell light response.Nyctalopin expression in retinal bipolar cells restores visual function in a mouse model of complete X-linked congenital stationary night blindnessWhole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindnessInvestigating mechanisms of myopia in mice.Rod bipolar cells and horizontal cells form displaced synaptic contacts with rods in the outer nuclear layer of the nob2 retinaTRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.R9AP stabilizes RGS11-G beta5 and accelerates the early light response of ON-bipolar cellsPhotoreceptor ablation initiates the immediate loss of glutamate receptors in postsynaptic bipolar cells in retina.NYX mutations in four families with high myopia with or without CSNB1TRPM1 forms complexes with nyctalopin in vivo and accumulates in postsynaptic compartment of ON-bipolar neurons in mGluR6-dependent manner.The Effect of PKCα on the Light Response of Rod Bipolar Cells in the Mouse RetinaTULP1 mutations causing early-onset retinal degeneration: preserved but insensitive macular cones.LRIT3 is essential to localize TRPM1 to the dendritic tips of depolarizing bipolar cells and may play a role in cone synapse formation.Gbeta5-RGS complexes co-localize with mGluR6 in retinal ON-bipolar cellsGeneration, identification and functional characterization of the nob4 mutation of Grm6 in the mouse.Two R7 regulator of G-protein signaling proteins shape retinal bipolar cell signaling.Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.Electroretinographic findings in a patient with congenital stationary night blindness due to a novel NYX mutation.Novel TRPM1 mutations in two Chinese families with early-onset high myopia, with or without complete congenital stationary night blindness.High susceptibility to experimental myopia in a mouse model with a retinal on pathway defectRetinal NMDA receptor function and expression are altered in a mouse lacking D-amino acid oxidaseNaturally occurring animal models with outer retina phenotypes.Sensory experience shapes the development of the visual system's first synapse.The Transduction Cascade in Retinal ON-Bipolar Cells: Signal Processing and Disease.Molecular and Biochemical Aspects of the Retina on Refraction.Congenital stationary night blindness with hypoplastic discs, negative electroretinogram and thinning of the inner nuclear layer.Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness.Diverse strategies engaged in establishing stereotypic wiring patterns among neurons sharing a common input at the visual system's first synapse.Asymmetrical growth of the photopic hill during the light adaptation effect.Synaptogenesis and synaptic protein localization in the postnatal development of rod bipolar cell dendrites in mouse retina.Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responses.Differential epitope masking reveals synapse-specific complexes of TRPM1.A novel missense mutation in the NYX gene associated with high myopia.
P2860
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P2860
description
2006 nî lūn-bûn
@nan
2006 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի մարտին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Localization of nyctalopin in the mammalian retina.
@ast
Localization of nyctalopin in the mammalian retina.
@en
Localization of nyctalopin in the mammalian retina.
@nl
type
label
Localization of nyctalopin in the mammalian retina.
@ast
Localization of nyctalopin in the mammalian retina.
@en
Localization of nyctalopin in the mammalian retina.
@nl
prefLabel
Localization of nyctalopin in the mammalian retina.
@ast
Localization of nyctalopin in the mammalian retina.
@en
Localization of nyctalopin in the mammalian retina.
@nl
P1476
Localization of nyctalopin in the mammalian retina
@en
P2093
Gaoying Ren
Lakshmi Akileswaran
P304
P356
10.1111/J.1460-9568.2006.04647.X
P407
P50
P577
2006-03-01T00:00:00Z