Identification of the gene and the mutation responsible for the mouse nob phenotype
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Retinal dystrophies, genomic applications in diagnosis and prospects for therapyThe dynamic architecture of photoreceptor ribbon synapses: cytoskeletal, extracellular matrix, and intramembrane proteinsToluene inhalation exposure for 13 weeks causes persistent changes in electroretinograms of Long-Evans ratsTopological analysis of small leucine-rich repeat proteoglycan nyctalopinContribution of Kir4.1 to the mouse electroretinogramRod-driven OFF pathway responses in the distal retina: dark-adapted flicker electroretinogram in mouseNeuronal pentraxins mediate synaptic refinement in the developing visual systemLrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB)A naturally-occurring mutation in Cacna1f in a rat model of congenital stationary night blindnessGene therapy restores vision in rd1 mice after removal of a confounding mutation in Gpr179The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responsesLight-evoked responses of the mouse retinal pigment epithelium.Refractive index measurement of the mouse crystalline lens using optical coherence tomography.Nyctalopin expression in retinal bipolar cells restores visual function in a mouse model of complete X-linked congenital stationary night blindnessComparison of refractive development and retinal dopamine in OFF pathway mutant and C57BL/6J wild-type miceOligomeric state of purified transient receptor potential melastatin-1 (TRPM1), a protein essential for dim light vision.Primate Retinal Signaling Pathways: Suppressing ON-Pathway Activity in Monkey With Glutamate Analogues Mimics Human CSNB1-NYX Genetic Night Blindness.Rod bipolar cells and horizontal cells form displaced synaptic contacts with rods in the outer nuclear layer of the nob2 retinaA role for nyctalopin, a small leucine-rich repeat protein, in localizing the TRP melastatin 1 channel to retinal depolarizing bipolar cell dendritesNYX 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.Retinoblastoma (Rb) regulates laminar dendritic arbor reorganization in retinal horizontal neuronsON pathway mutations increase susceptibility to form-deprivation myopia.Defective retinal depolarizing bipolar cells in regulators of G protein signaling (RGS) 7 and 11 double null mice.LRIT3 is essential to localize TRPM1 to the dendritic tips of depolarizing bipolar cells and may play a role in cone synapse formation.Postreceptoral contributions to the light-adapted ERG of mice lacking b-waves.Early Functional and Morphologic Abnormalities in the Diabetic Nyxnob Mouse RetinaGeneration, identification and functional characterization of the nob4 mutation of Grm6 in the mouse.Refinement of the retinogeniculate pathway.Comparisons of structural and functional abnormalities in mouse b-wave mutants.Gene expression in the mouse eye: an online resource for genetics using 103 strains of mice.High susceptibility to experimental myopia in a mouse model with a retinal on pathway defectPresence of the Gpr179(nob5) allele in a C3H-derived transgenic mouse.Naturally occurring animal models with outer retina phenotypes.LRIT3 Differentially Affects Connectivity and Synaptic Transmission of Cones to ON- and OFF-Bipolar Cells.GPR179 is required for high sensitivity of the mGluR6 signaling cascade in depolarizing bipolar cells.Functional architecture of the retina: development and disease.The Transduction Cascade in Retinal ON-Bipolar Cells: Signal Processing and Disease.G protein signaling in the retina and beyond: the Cogan lectureMolecular and Biochemical Aspects of the Retina on Refraction.
P2860
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P2860
Identification of the gene and the mutation responsible for the mouse nob phenotype
description
2003 nî lūn-bûn
@nan
2003 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Identification of the gene and the mutation responsible for the mouse nob phenotype
@ast
Identification of the gene and the mutation responsible for the mouse nob phenotype
@en
Identification of the gene and the mutation responsible for the mouse nob phenotype
@nl
type
label
Identification of the gene and the mutation responsible for the mouse nob phenotype
@ast
Identification of the gene and the mutation responsible for the mouse nob phenotype
@en
Identification of the gene and the mutation responsible for the mouse nob phenotype
@nl
prefLabel
Identification of the gene and the mutation responsible for the mouse nob phenotype
@ast
Identification of the gene and the mutation responsible for the mouse nob phenotype
@en
Identification of the gene and the mutation responsible for the mouse nob phenotype
@nl
P2093
P3181
P356
P1476
Identification of the gene and the mutation responsible for the mouse nob phenotype
@en
P2093
Machelle T Pardue
Maureen A McCall
Neal S Peachey
Ronald G Gregg
Sherry L Ball
Sophie I Candille
Suparna Mukhopadhyay
P304
P3181
P356
10.1167/IOVS.02-0501
P407
P577
2003-01-01T00:00:00Z