Comparisons of structural and functional abnormalities in mouse b-wave mutants. - Wikidata - awgldk - TriplyDB

Comparisons of structural and functional abnormalities in mouse b-wave mutants.

Comparisons of structural and functional abnormalities in mouse b-wave mutants.

http://www.wikidata.org/entity/Q37226295

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GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness Mutations in TRPM1 are a common cause of complete congenital stationary night blindness Synaptic remodeling of neuronal circuits in early retinal degeneration The dynamic architecture of photoreceptor ribbon synapses: cytoskeletal, extracellular matrix, and intramembrane proteins Psychophysical testing in rodent models of glaucomatous optic neuropathy Class 5 transmembrane semaphorins control selective Mammalian retinal lamination and function Norrin, frizzled-4, and Lrp5 signaling in endothelial cells controls a genetic program for retinal vascularization.Different inner retinal pathways mediate rod-cone input in irradiance detection for the pupillary light reflex and regulation of behavioral state in mice Examination of VLC-PUFA-deficient photoreceptor terminals.Genetic disruption of the On visual pathway affects cortical orientation selectivity and contrast sensitivity in mice Autoantibodies in melanoma-associated retinopathy target TRPM1 cation channels of retinal ON bipolar cells Differential function of Gγ13 in rod bipolar and ON cone bipolar cells.ON pathway mutations increase susceptibility to form-deprivation myopia.Synaptic pathology and therapeutic repair in adult retinoschisis mouse by AAV-RS1 transfer.Assessing retinal structure in complete congenital stationary night blindness and Oguchi disease Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation.Inactivation of the microRNA-183/96/182 cluster results in syndromic retinal degeneration.Photoreceptor and postreceptor responses in congenital stationary night blindness.NGL-2 regulates pathway-specific neurite growth and lamination, synapse formation, and signal transmission in the retina.Sequence variations of GRM6 in patients with high myopia.Naturally occurring animal models with outer retina phenotypes.GPR179 is required for high sensitivity of the mGluR6 signaling cascade in depolarizing bipolar cells.Mouse b-wave mutants.Functional architecture of the retina: development and disease.A transient receptor potential-like channel mediates synaptic transmission in rod bipolar cells.Retinal ganglion cells in model organisms: development, function and disease.Developmental time course distinguishes changes in spontaneous and light-evoked retinal ganglion cell activity in rd1 and rd10 mice.

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Comparisons of structural and functional abnormalities in mouse b-wave mutants.

http://www.wikidata.org/entity/Q37226295

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on 24 July 2008

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Comparisons of structural and functional abnormalities in mouse b-wave mutants.

@en

Comparisons of structural and functional abnormalities in mouse b-wave mutants.

@nl

type

label

Comparisons of structural and functional abnormalities in mouse b-wave mutants.

@en

Comparisons of structural and functional abnormalities in mouse b-wave mutants.

@nl

prefLabel

Comparisons of structural and functional abnormalities in mouse b-wave mutants.

@en

Comparisons of structural and functional abnormalities in mouse b-wave mutants.

@nl

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JPHYSIOL.2008.159327

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The Journal of Physiology

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Comparisons of structural and functional abnormalities in mouse b-wave mutants

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Maureen A McCall

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Ronald G Gregg

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P2860

Essential role of Ca2+-binding protein 4, a Cav1.4 channel regulator, in photoreceptor synaptic function.

X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene

Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy

Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels

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

Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina

Role of the beta(2) subunit of voltage-dependent calcium channels in the retinal outer plexiform layer

Immunohistological studies of metabotropic glutamate receptor subtype 6-deficient mice show no abnormality of retinal cell organization and ganglion cell maturation

Molecular characterization of a novel retinal metabotropic glutamate receptor mGluR6 with a high agonist selectivity for L-2-amino-4-phosphonobutyrate

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