Strain background effects and genetic modifiers of hearing in mice. - Wikidata - wikimedia - TriplyDB

Strain background effects and genetic modifiers of hearing in mice.

Strain background effects and genetic modifiers of hearing in mice.

http://www.wikidata.org/entity/Q33804884

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PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair.Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.Identification of genetic and chemical modulators of zebrafish mechanosensory hair cell death Development of sensory, motor and behavioral deficits in the murine model of Sanfilippo syndrome type B The R109H variant of fascin-2, a developmentally regulated actin crosslinker in hair-cell stereocilia, underlies early-onset hearing loss of DBA/2J mice Population genomics of wild and laboratory zebrafish (Danio rerio)Espins and the actin cytoskeleton of hair cell stereocilia and sensory cell microvilli.A short splice form of Xin-actin binding repeat containing 2 (XIRP2) lacking the Xin repeats is required for maintenance of stereocilia morphology and hearing function Age-related changes in auditory nerve-inner hair cell connections, hair cell numbers, auditory brain stem response and gap detection in UM-HET4 mice.Vestibular dysfunction, altered macular structure and trait localization in A/J inbred mice.FVB/NJ mice demonstrate a youthful sensitivity to noise-induced hearing loss and provide a useful genetic model for the study of neural hearing loss Pathophysiology of age-related hearing loss (peripheral and central).Digenic inheritance of deafness caused by 8J allele of myosin-VIIA and mutations in other Usher I genes A new mouse mutant of the Cdh23 gene with early-onset hearing loss facilitates evaluation of otoprotection drugs.Polygenic inheritance of sensorineural hearing loss (Snhl2, -3, and -4) and organ of Corti patterning defect in the ALR/LtJ mouse strain Roles of the espin actin-bundling proteins in the morphogenesis and stabilization of hair cell stereocilia revealed in CBA/CaJ congenic jerker mice.Modifiers of hearing impairment in humans and mice.Interactions of hearing loss and diabetes mellitus in the middle age CBA/CaJ mouse model of presbycusis.Neurobehavioral abnormalities in the dysbindin-1 mutant, sandy, on a C57BL/6J genetic background.Hearing loss in a mouse model of Muenke syndrome A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice.Genetic dependence of cochlear cells and structures injured by noise.Production of germline transgenic prairie voles (Microtus ochrogaster) using lentiviral vectors Mutations in CLDN14 are associated with different hearing thresholds.Discovery Genetics - The History and Future of Spontaneous Mutation Research.Longitudinal fundus and retinal studies with SD-OCT: a comparison of five mouse inbred strains.Validation of simple sequence length polymorphism regions of commonly used mouse strains for marker assisted speed congenics screening.Association of a citrate synthase missense mutation with age-related hearing loss in A/J mice A QTL on Chr 5 modifies hearing loss associated with the fascin-2 variant of DBA/2J mice Mutation profile of the CDH23 gene in 56 probands with Usher syndrome type I.Wild-derived mouse stocks: an underappreciated tool for aging research.Sirt1 deficiency protects cochlear cells and delays the early onset of age-related hearing loss in C57BL/6 mice.A new Atp2b2 deafwaddler allele, dfw(i5), interacts strongly with Cdh23 and other auditory modifiers.Hearing impairment in hypothyroid dwarf mice caused by mutations of the thyroid peroxidase gene Does age matter? The impact of rodent age on study outcomes New treatment options for hearing loss.Vesicular glutamate transporter 3 in age-dependent optic neuropathy Reduced spiral ganglion neuronal loss by adjunctive neurotrophin-3 in experimental pneumococcal meningitis.Genetic rodent models of brain disorders: Perspectives on experimental approaches and therapeutic strategies.

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Strain background effects and genetic modifiers of hearing in mice.

http://www.wikidata.org/entity/Q33804884

description

2006 nî lūn-bûn

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2006 թուականի Մարտին հրատարակուած գիտական յօդուած

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2006 թվականի մարտին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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Strain background effects and genetic modifiers of hearing in mice.

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Strain background effects and genetic modifiers of hearing in mice.

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Strain background effects and genetic modifiers of hearing in mice.

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J.BRAINRES.2006.02.021

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Strain background effects and genetic modifiers of hearing in mice.

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Kenneth R Johnson

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Konrad Noben-Trauth

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Qing Yin Zheng

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P2860

The effect of an age-related hearing loss gene (Ahl) on noise-induced hearing loss and cochlear damage from low-frequency noise

Genetics of age-related hearing loss in mice. III. Susceptibility of inbred and F1 hybrid strains to noise-induced hearing loss

Genetic basis for susceptibility to noise-induced hearing loss in mice

Modification of human hearing loss by plasma-membrane calcium pump PMCA2

Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans

Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family.

Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance

The genetic structure of recombinant inbred mice: high-resolution consensus maps for complex trait analysis

Microtubule-associated protein 1A is a modifier of tubby hearing (moth1).

A large deletion including most of GJB6 in recessive non syndromic deafness: a digenic effect?

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