A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice - Wikidata - awgldk - TriplyDB

A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

http://www.wikidata.org/entity/Q33821006

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Mitochondria Mitonuclear interactions: evolutionary consequences over multiple biological scales A big development for a small RNA Retained features of embryonic metabolism in the adult MRL mouse Mitochondrial DNA disease and developmental implications for reproductive strategies Vestibular dysfunction, altered macular structure and trait localization in A/J inbred mice.Caspase-mediated apoptosis in the cochleae contributes to the early onset of hearing loss in A/J mice.Recognition and control of the progression of age-related hearing loss.High-frequency sensorineural hearing loss and its underlying genetics (Hfhl1 and Hfhl2) in NIH Swiss mice.Tympanometry assessment of 61 inbred strains of mice.Phenotype and genetics of progressive sensorineural hearing loss (Snhl1) in the LXS set of recombinant inbred strains of mice Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss Auditory brainstem responses in 10 inbred strains of mice.A locus on distal chromosome 11 (ahl8) and its interaction with Cdh23 ahl underlie the early onset, age-related hearing loss of DBA/2J mice Inheritance patterns of progressive hearing loss in laboratory strains of mice A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice.Progressive hearing loss and increased susceptibility to noise-induced hearing loss in mice carrying a Cdh23 but not a Myo7a mutation Multiple quantitative trait loci modify cochlear hair cell degeneration in the Beethoven (Tmc1Bth) mouse model of progressive hearing loss DFNA36.Genome-wide association study for age-related hearing loss (AHL) in the mouse: a meta-analysis Inner ear proteomics of mouse models for deafness, a discovery strategy.Mitochondrial DNA variant in COX1 subunit significantly alters energy metabolism of geographically divergent wild isolates in Caenorhabditis elegans Strain background effects and genetic modifiers of hearing in mice.Ahl2, a second locus affecting age-related hearing loss in mice Evolution meets disease: penetrance and functional epistasis of mitochondrial tRNA mutations.Disrupting mitochondrial-nuclear coevolution affects OXPHOS complex I integrity and impacts human health.An Incompatibility between a mitochondrial tRNA and its nuclear-encoded tRNA synthetase compromises development and fitness in Drosophila.Mito-nuclear co-evolution: the positive and negative sides of functional ancient mutations Association of a citrate synthase missense mutation with age-related hearing loss in A/J mice Somatic alterations in mitochondrial DNA produce changes in cell growth and metabolism supporting a tumorigenic phenotype.Identification of an mtDNA mutation hot spot in UV-induced mouse skin tumors producing altered cellular biochemistry.Revisiting the mouse mitochondrial DNA sequence Mitochondrial Involvement in Vertebrate Speciation? The Case of Mito-nuclear Genetic Divergence in Chameleons.Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia Mitochondrial deafness alleles confer misreading of the genetic code Beyond retrograde and anterograde signalling: mitochondrial-nuclear interactions as a means for evolutionary adaptation and contemporary disease susceptibility The mitochondrial paradigm for cardiovascular disease susceptibility and cellular function: a complementary concept to Mendelian genetics.Mitochondrial DNA polymorphisms specifically modify cerebral β-amyloid proteostasis Dissecting the effects of mtDNA variations on complex traits using mouse conplastic strains.Naturally occurring mitochondrial DNA heteroplasmy in the MRL mouse.Mitochondrial genetic background modulates bioenergetics and susceptibility to acute cardiac volume overload.

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A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

http://www.wikidata.org/entity/Q33821006

description

2001 nî lūn-bûn

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2001 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2001 թվականի փետրվարին հրատարակված գիտական հոդված

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2001年の論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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2001年论文

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name

A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

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A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

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A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

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A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

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A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

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A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

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Nature Genetics

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A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

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P2093

K R Johnson

http://www.w3.org/2001/XMLSchema#string

N Fischel-Ghodsian

http://www.w3.org/2001/XMLSchema#string

O Spirina

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Q Y Zheng

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Y Bykhovskaya

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P2860

A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase

mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw)

The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse

Sequence and gene organization of mouse mitochondrial DNA

Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses.

Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice

Sensorineural deafness inherited as a tissue specific mitochondrial disorder.

Mitochondrial deafness mutations reviewed.

The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression.

Candidate locus for a nuclear modifier gene for maternally inherited deafness

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10.1038/84831

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2

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27

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mitochondrial DNA

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2862214

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