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Article

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

Investigative ophthalmology & visual science - 1 Nov 1998

Pardue M T, McCall M A, LaVail M M, Gregg R G, Peachey N S

Abstract excerpt

PURPOSE: To describe a naturally occurring X-linked recessive mutation, no b-wave (nob), that compromises visual transmission between photoreceptors and second-order neurons in mice. METHODS: Affected mice were identified by recording the light-evoked response of the retina, the electroretinogram (ERG). To evaluate visual transmission, cortical potentials were recorded with a scalp electrode. The inheritance...

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PMID: 9804152

Genes

ERG

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

A naturally occurring mouse model of X-linked congenital stationary night blindness.PMID 9804152Read ↗

Comparisons of structural and functional abnormalities in mouse b-wave mutants.Semantic proximity Read ↗

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

Identification of the gene and the mutation responsible for the mouse nob phenotype.Semantic proximity Read ↗

Localization of the mouse nob (no b-wave) gene to the centromeric region of the X chromosome.Semantic proximity Read ↗

Identification of a new mutant allele, Grm6(nob7), for complete congenital stationary night blindness.Semantic proximity Read ↗

Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responses.Semantic proximity Read ↗

Lrit3 Deficient Mouse (nob6): A Novel Model of Complete Congenital Stationary Night Blindness (cCSNB)Semantic proximity Read ↗

Novel Grm6 Variant in a no b-wave (nob) Mouse Model: Phenotype Characterization and Gene Therapy.Semantic proximity Read ↗

Generation, identification and functional characterization of the nob4 mutation of Grm6 in the mouse.Semantic proximity Read ↗

Attenuation of oscillatory potentials in nob2 mice.Semantic proximity Read ↗

Photoreceptor degeneration in two mouse models for congenital stationary night blindness type 2.Semantic proximity Read ↗

Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina.Semantic proximity Read ↗

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