(Q40284277)

19 September 2017

title

m.6267G>A: a recurrent mutation in the human mitochondrial DNA that reduces cytochrome c oxidase activity and is associated with tumors (English)

1 reference

Santiago Rodriguez de Córdoba

19 September 2017

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7

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19 September 2017

M Esther Gallardo

1

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19 September 2017

Raquel Moreno-Loshuertos

2

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19 September 2017

Celia López

3

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19 September 2017

Mercedes Casqueiro

4

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19 September 2017

Javier Silva

5

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19 September 2017

Felix Bonilla

6

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19 September 2017

José Antonio Enríquez

8

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19 September 2017

publication date

1 June 2006

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19 September 2017

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19 September 2017

volume

27

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19 September 2017

issue

6

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19 September 2017

page(s)

575-582

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Free radicals in the physiological control of cell function

19 September 2017

cites work

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https://api.crossref.org/works/10.1002%2FHUMU.20338

An intragenic suppressor in the cytochrome c oxidase I gene of mouse mitochondrial DNA.

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Sequence and organization of the human mitochondrial genome

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7 January 2021

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

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Biogenesis of mitochondria

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Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma

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Automated detection of point mutations using fluorescent sequence trace subtraction

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Mitochondrial defects in cancer

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Mitochondrial DNA mutations in primary leukemia cells after chemotherapy: clinical significance and therapeutic implications.

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Accumulation of mitochondrial DNA mutations in ageing, cancer, and mitochondrial disease: is there a common mechanism?

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7 January 2021

The bioenergetic signature of lung adenocarcinomas is a molecular marker of cancer diagnosis and prognosis

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7 January 2021

Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation

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7 January 2021

Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction

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7 January 2021

Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups

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7 January 2021

Respiration and growth defects in transmitochondrial cell lines carrying the 11778 mutation associated with Leber's hereditary optic neuropathy

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7 January 2021

Use of polarography to detect respiration defects in cell cultures

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7 January 2021

Alteration of the bioenergetic phenotype of mitochondria is a hallmark of breast, gastric, lung and oesophageal cancer.

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7 January 2021

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

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7 January 2021

Phylogeny of east Asian mitochondrial DNA lineages inferred from complete sequences

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7 January 2021

Mitochondrial diabetes: investigation and identification of a novel mutation

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7 January 2021

The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs

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7 January 2021

Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

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7 January 2021

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

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Phylogeny of mitochondrial DNA macrohaplogroup N in India, based on complete sequencing: implications for the peopling of South Asia

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7 January 2021

Inhibition of mitochondrial respiration: a novel strategy to enhance drug-induced apoptosis in human leukemia cells by a reactive oxygen species-mediated mechanism

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7 January 2021

mtDNA mutations increase tumorigenicity in prostate cancer

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7 January 2021

Somatic mutations of the mitochondrial genome in human colorectal tumours

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7 January 2021

Neurodegenerative disorders associated with diabetes mellitus

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7 January 2021

Human mtDNA haplogroups associated with high or reduced spermatozoa motility

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7 January 2021

Effects of purifying and adaptive selection on regional variation in human mtDNA.

1 reference

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7 January 2021

A critical reassessment of the role of mitochondria in tumorigenesis

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https://api.crossref.org/works/10.1002%2FHUMU.20338

7 January 2021

The epidemiology of mitochondrial disorders--past, present and future

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7 January 2021

Succinate links TCA cycle dysfunction to oncogenesis by inhibiting HIF-alpha prolyl hydroxylase

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7 January 2021

Positive contribution of pathogenic mutations in the mitochondrial genome to the promotion of cancer by prevention from apoptosis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20338

7 January 2021

Mitochondrial DNA mutations in human disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20338

7 January 2021

Mitochondrial DNA haplogroups do not play a role in the variable phenotypic presentation of the A3243G mutation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20338

7 January 2021

The whole structure of the 13-subunit oxidized cytochrome c oxidase at 2.8 A

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20338

7 January 2021

Identifiers

DOI

10.1002/HUMU.20338

1 reference

19 September 2017

1 reference