Metabolic consequences of a novel missense mutation of the mtDNA CO I gene
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Mitochondrial cytochrome c oxidase deficiencyMitochondrial genomic variation associated with higher mitochondrial copy number: the Cache County Study on Memory Health and AgingProduction of transmitochondrial cybrids containing naturally occurring pathogenic mtDNA variants.Epistatic interactions modulate the evolution of mammalian mitochondrial respiratory complex components.Sympatric Drosophila simulans flies with distinct mtDNA show age related differences in mitochondrial metabolism.Mitochondrial DNA sequence variation in Finnish patients with matrilineal diabetes mellitus.Mitochondrial dysfunction and organic aciduria in five patients carrying mutations in the Ras-MAPK pathway.Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus.Mitochondrial mutations are associated with atherosclerotic lesions in the human aortaAssociation of mitochondrial genetic variation with carotid atherosclerosisComplex IV subunit 1 defect predicts postoperative survival in hepatocellular carcinoma.Yeast cytochrome c oxidase: a model system to study mitochondrial forms of the haem-copper oxidase superfamily.Review: quantifying mitochondrial dysfunction in complex diseases of aging.Mitochondrial epilepsy in pediatric and adult patients.The role of mitochondria in epilepsy: implications for neurodegenerative diseases.Mitochondrial myopathy and rhabdomyolysis associated with a novel nonsense mutation in the gene encoding cytochrome c oxidase subunit I.High prevalence of the COII/tRNA(Lys) intergenic 9-bp deletion in mitochondrial DNA of Taiwanese patients with MELAS or MERRF syndrome.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.Characterization and prognostic significance of mitochondrial DNA variations in acute myeloid leukemia
P2860
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P2860
Metabolic consequences of a novel missense mutation of the mtDNA CO I gene
description
2002 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի օգոստոսին հրատարակված գիտական հոդված
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artículu científicu espublizáu en 2002
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im August 2002 veröffentlichter wissenschaftlicher Artikel
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scientific journal article
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vedecký článok (publikovaný 2002/08/01)
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vědecký článek publikovaný v roce 2002
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wetenschappelijk artikel (gepubliceerd op 2002/08/01)
@nl
наукова стаття, опублікована в серпні 2002
@uk
مقالة علمية (نشرت في أغسطس 2002)
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name
Metabolic consequences of a novel missense mutation of the mtDNA CO I gene
@ast
Metabolic consequences of a novel missense mutation of the mtDNA CO I gene
@en
Metabolic consequences of a novel missense mutation of the mtDNA CO I gene
@nl
type
label
Metabolic consequences of a novel missense mutation of the mtDNA CO I gene
@ast
Metabolic consequences of a novel missense mutation of the mtDNA CO I gene
@en
Metabolic consequences of a novel missense mutation of the mtDNA CO I gene
@nl
prefLabel
Metabolic consequences of a novel missense mutation of the mtDNA CO I gene
@ast
Metabolic consequences of a novel missense mutation of the mtDNA CO I gene
@en
Metabolic consequences of a novel missense mutation of the mtDNA CO I gene
@nl
P2093
P356
P1476
Metabolic consequences of a novel missense mutation of the mtDNA CO I gene
@en
P2093
Albert Becker
Alexei P. Kudin
Armin Heils
Christian E. Elger
Dagmar Kunz
Dmitry A. Varlamov
Johannes Rebstock
Karsten Haug
Robert Sassen
Rolf Schröder
P304
P356
10.1093/HMG/11.16.1797
P577
2002-08-01T00:00:00Z