(Q33650029)

28 July 2017

title

Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases (English)

1 reference

28 July 2017

0 references

3

Ian J Wilson

1 reference

28 July 2017

4

Patrick F Chinnery

1 reference

28 July 2017

1

Gavin Hudson

1 reference

28 July 2017

Aurora Gomez-Duran

2

1 reference

28 July 2017

language of work or name

1 reference

22 May 2014

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28 July 2017

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28 July 2017

volume

10

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28 July 2017

issue

5

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28 July 2017

page(s)

e1004369

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Creative Commons Attribution 4.0 International

28 July 2017

copyright license

start time

22 May 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

ggplot2

object named as

ggplot2

ggplot

2 references

10 June 2022

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/efetch.fcgi?db=pmc&rettype=xml&id=4031051

CZ Software Mentions: A large dataset of software mentions in the biomedical literature

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Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy

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Failure to validate association between 12p13 variants and ischemic stroke

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Mitochondrial DNA haplogroups and risk of transient ischaemic attack and ischaemic stroke: a genetic association study

21 June 2018

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Cancer cell mitochondria confer apoptosis resistance and promote metastasis

21 June 2018

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Ancient mtDNA genetic variants modulate mtDNA transcription and replication

21 June 2018

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Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor

21 June 2018

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Mitochondrial variants in schizophrenia, bipolar disorder, and major depressive disorder

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21 June 2018

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Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

21 June 2018

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Investigation of the role of mitochondrial DNA in multiple sclerosis susceptibility

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Alzheimer's brains harbor somatic mtDNA control-region mutations that suppress mitochondrial transcription and replication

21 June 2018

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The epidemiology of primary biliary cirrhosis

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding region

21 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031051

Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene

21 June 2018

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Human mtDNA haplogroups associated with high or reduced spermatozoa motility

21 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031051

mtDNA haplogroups and frequency patterns in Europe

21 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031051

Classification of European mtDNAs from an analysis of three European populations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031051

The epidemiology of ankylosing spondylitis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031051

Pathological significance of the mtDNA COX III mutation at nucleotide pair 9438 in Leber hereditary optic neuropathy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031051

The power to detect disease associations with mitochondrial DNA haplogroups

21 June 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004369

Analysis of European mitochondrial haplogroups with Alzheimer disease risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004369

Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004369

Mutations in mitochondrial-encoded cytochrome c oxidase subunits I, II, and III genes detected in Alzheimer's disease using single-strand conformation polymorphism

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004369

Sporadic bilateral optic neuropathy in children: the role of mitochondrial abnormalities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004369

Incidence of multiple sclerosis in the United Kingdom : findings from a population-based cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004369

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004369

HaploGrep: a fast and reliable algorithm for automatic classification of mitochondrial DNA haplogroups.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004369

mtDNA tree Build 17 (18 Feb 2016)

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004369

Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004369

Mitochondrial DNA haplogroup H as a risk factor for idiopathic dilated cardiomyopathy in Spanish population

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004369

A missense mutation in the mitochondrial cytochrome b gene in a revisited case with histiocytoid cardiomyopathy

21 January 2018

1 reference

12 December 2020

A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome

1 reference

12 December 2020

Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis?

1 reference

12 December 2020

Molecular-clinical correlation in a family with a novel heteroplasmic Leigh syndrome missense mutation in the mitochondrial cytochrome c oxidase III gene

1 reference

12 December 2020

1 reference

12 December 2020

10.1371/JOURNAL.PGEN.1004369

Identifiers

DOI

1 reference

28 July 2017

1 reference

28 July 2017

1 reference