Generation, identification and functional characterization of the nob4 mutation of Grm6 in the mouse. - Wikidata - awgldk - TriplyDB

Generation, identification and functional characterization of the nob4 mutation of Grm6 in the mouse.

Generation, identification and functional characterization of the nob4 mutation of Grm6 in the mouse.

http://www.wikidata.org/entity/Q37164641

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GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness Psychophysical testing in rodent models of glaucomatous optic neuropathy Speed, spatial, and temporal tuning of rod and cone vision in mouse Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB)Mouse Tmem135 mutation reveals a mechanism involving mitochondrial dynamics that leads to age-dependent retinal pathologies Missing optomotor head-turning reflex in the DBA/2J mouse.Quantitative trait locus analysis identifies Gabra3 as a regulator of behavioral despair in mice.Different inner retinal pathways mediate rod-cone input in irradiance detection for the pupillary light reflex and regulation of behavioral state in mice Sustained ocular hypertension induces dendritic degeneration of mouse retinal ganglion cells that depends on cell type and location.Non-centered spike-triggered covariance analysis reveals neurotrophin-3 as a developmental regulator of receptive field properties of ON-OFF retinal ganglion cells.Genetic disruption of the On visual pathway affects cortical orientation selectivity and contrast sensitivity in mice Nyctalopin expression in retinal bipolar cells restores visual function in a mouse model of complete X-linked congenital stationary night blindness Amyloid precursor protein is required for normal function of the rod and cone pathways in the mouse retina.Studying age-related macular degeneration using animal models.Guidance-cue control of horizontal cell morphology, lamination, and synapse formation in the mammalian outer retina Identification of a new mutant allele, Grm6(nob7), for complete congenital stationary night blindness LRIT3 is essential to localize TRPM1 to the dendritic tips of depolarizing bipolar cells and may play a role in cone synapse formation.Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation.Gbeta5-RGS complexes co-localize with mGluR6 in retinal ON-bipolar cells Postreceptoral contributions to the light-adapted ERG of mice lacking b-waves.Comparisons of structural and functional abnormalities in mouse b-wave mutants.Retina-specific GTPase accelerator RGS11/G beta 5S/R9AP is a constitutive heterotrimer selectively targeted to mGluR6 in ON-bipolar neurons Naturally occurring animal models with outer retina phenotypes.LRIT3 Differentially Affects Connectivity and Synaptic Transmission of Cones to ON- and OFF-Bipolar Cells.Mouse b-wave mutants.A missense mutation in Grm6 reduces but does not eliminate mGluR6 expression or rod depolarizing bipolar cell function.Defective ceramide synthases in mice cause reduced amplitudes in electroretinograms and altered sphingolipid composition in retina and cornea.Attenuation of oscillatory potentials in nob2 mice.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.Interpretation of the mouse electroretinogram.Effects of mGluR6-deficiency on photoreceptor ribbon synapse formation: comparison of electron microscopic analysis of serial sections with random sections.Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responses.Response properties of slow PIII in the Large (vls) mutant.

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P2860

Generation, identification and functional characterization of the nob4 mutation of Grm6 in the mouse.

http://www.wikidata.org/entity/Q37164641

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 January 2007

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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

Generation, identification and ...... mutation of Grm6 in the mouse.

@en

Generation, identification and ...... mutation of Grm6 in the mouse.

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type

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Generation, identification and ...... mutation of Grm6 in the mouse.

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Generation, identification and ...... mutation of Grm6 in the mouse.

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Generation, identification and ...... mutation of Grm6 in the mouse.

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Generation, identification and ...... mutation of Grm6 in the mouse.

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S0952523807070149

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Visual neuroscience

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Generation, identification and ...... mutation of Grm6 in the mouse

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Brandon Young

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Brett Glawe

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Chiaki Omura

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Dennis Maddox

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Donald R Cantrell

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Erin L McDearmon

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John B Troy

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Kazuhiro Shimomura

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Kirstan A Vessey

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Lawrence H Pinto

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P2860

Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6

Structural basis of glutamate recognition by a dimeric metabotropic glutamate receptor

Identification of the gene and the mutation responsible for the mouse nob phenotype

Stimulus size and intensity alter fundamental receptive-field properties of mouse retinal ganglion cells in vivo

The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses

Ion selectivity and activation of the M2 ion channel of influenza virus

Discharge patterns and functional organization of mammalian retina.

Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.

A naturally occurring mouse model of X-linked congenital stationary night blindness.

Localization of nyctalopin in the mammalian retina.

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111-123

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scholarly article

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10.1017/S0952523807070149

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1

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24

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Joseph S. Takahashi

Maureen A. McCall

Robert F. Mullins

Brandon M Invergo

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2007-01-01T00:00:00Z

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17430614

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3770726

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