An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy.
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Mutations of the SCO1 gene in mitochondrial cytochrome c oxidase deficiency with neonatal-onset hepatic failure and encephalopathy.Mitochondrial cytochrome c oxidase deficiencyCytochrome c oxidase deficiencyThe R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathwayAssessment of cytochrome C oxidase dysfunction in the substantia nigra/ventral tegmental area in schizophrenia.The role of mitochondrial DNA copy number in mammalian fertility.Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene.Normal levels of wild-type mitochondrial DNA maintain cytochrome c oxidase activity for two pathogenic mitochondrial DNA mutations but not for m.3243A-->G.The impact of mitochondrial genetics on male infertility.Age-related increases in oxidatively damaged proteins of mouse kidney mitochondrial electron transport chain complexesCytochrome c oxidase dysfunction in oxidative stress.Pyrimidine nucleoside depletion sensitizes to the mitochondrial hepatotoxicity of the reverse transcriptase inhibitor stavudine.hCOA3 stabilizes cytochrome c oxidase 1 (COX1) and promotes cytochrome c oxidase assembly in human mitochondria.Novel Point Mutations and A8027G Polymorphism in Mitochondrial-DNA-Encoded Cytochrome c Oxidase II Gene in Mexican Patients with Probable Alzheimer Disease.The determination of complete human mitochondrial DNA sequences in single cells: implications for the study of somatic mitochondrial DNA point mutations.Postmortem studies on mitochondria in schizophrenia.Cytochrome c oxidase subunit IV is essential for assembly and respiratory function of the enzyme complex.In vivo regulation of oxidative phosphorylation in cells harboring a stop-codon mutation in mitochondrial DNA-encoded cytochrome c oxidase subunit I.Building the CuA site of cytochrome c oxidase: a complicated, redox-dependent process driven by a surprisingly large complement of accessory proteins.Mitochondrial DNA mutations as a fundamental mechanism in physiological declines associated with aging.Mutation in mitochondrial complex IV subunit COX5A causes pulmonary arterial hypertension, lactic acidemia, and failure to thrive.Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene.Mutations in COA3 cause isolated complex IV deficiency associated with neuropathy, exercise intolerance, obesity, and short stature.Mitochondrial cytochrome c oxidase subunit II variations predict adverse prognosis in cytogenetically normal acute myeloid leukaemia.Disease-related mutations in cytochrome c oxidase studied in yeast and bacterial models.Infantile cardioencephalopathy due to a COX15 gene defect: report and review.Hypoxia induces mitochondrial mutagenesis and dysfunction in inflammatory arthritis
P2860
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P2860
An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy.
description
1999 nî lūn-bûn
@nan
1999 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
An mtDNA mutation in the initi ...... tochondrial encephalomyopathy.
@ast
An mtDNA mutation in the initi ...... tochondrial encephalomyopathy.
@en
An mtDNA mutation in the initi ...... tochondrial encephalomyopathy.
@nl
type
label
An mtDNA mutation in the initi ...... tochondrial encephalomyopathy.
@ast
An mtDNA mutation in the initi ...... tochondrial encephalomyopathy.
@en
An mtDNA mutation in the initi ...... tochondrial encephalomyopathy.
@nl
prefLabel
An mtDNA mutation in the initi ...... tochondrial encephalomyopathy.
@ast
An mtDNA mutation in the initi ...... tochondrial encephalomyopathy.
@en
An mtDNA mutation in the initi ...... tochondrial encephalomyopathy.
@nl
P2093
P2860
P356
P1476
An mtDNA mutation in the initi ...... tochondrial encephalomyopathy.
@en
P2093
D M Turnbull
M A Johnson
P J Lamont
R M Andrews
R N Lightowlers
R W Taylor
Z M Chrzanowska-Lightowlers
P2860
P304
P356
10.1086/302361
P407
P577
1999-05-01T00:00:00Z