(Q35080485)

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The co-occurrence of mtDNA mutations on different oxidative phosphorylation subunits, not detected by haplogroup analysis, affects human longevity and is population specific

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scholarly article

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6 August 2017

The co-occurrence of mtDNA mutations on different oxidative phosphorylation subunits, not detected by haplogroup analysis, affects human longevity and is population specific (English)

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Europe PubMed Central

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6 August 2017

phosphorylation

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Olivier Toussaint

29

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Olivier Toussaint

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Alberto Montesanto

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Alberto Montesanto

8

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Jukka S Moilanen

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Jukka S Moilanen

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Giuseppina Rose

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Giuseppina Rose

31

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Irene Maeve Rea

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Irene M Rea

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Peter Kristensen

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Peter Kristensen

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Thomas E Johnson

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Kaare Christensen

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Kaare Christensen

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Ewa Sikora

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33

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Markus Perola

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6 August 2017

Vladyslav Bezrukov

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Vladyslav Bezrukov

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Huanming Yang

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6 August 2017

35

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Lars Bolund

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Claudio Franceschi

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Claudio Franceschi

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Stefan Schreiber

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Stefan Schreiber

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6 August 2017

Efstathios S. Gonos

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Efstathios S Gonos

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Jean-Marie Robine

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Jean Marie Robine

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Michel Poulain

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James W Vaupel

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author name string

Nicola Raule

1

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6 August 2017

Federica Sevini

2

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6 August 2017

Shengting Li

3

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6 August 2017

Annalaura Barbieri

4

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6 August 2017

Federica Tallaro

5

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6 August 2017

Laura Lomartire

6

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6 August 2017

Dario Vianello

7

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6 August 2017

Hélène Blanché

11

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6 August 2017

Antti Hervonen

12

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Luca Deiana

14

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Tom B L Kirkwood

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Alberta Leon

18

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6 August 2017

Pier Giuseppe Pelicci

19

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6 August 2017

Josè Remacle

22

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6 August 2017

Peternella Eline Slagboom

26

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6 August 2017

Liana Spazzafumo

27

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6 August 2017

Maria Antonietta Stazi

28

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6 August 2017

Kari Majamaa

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Giuseppe Passarino

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6 August 2017

publication date

17 December 2013

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6 August 2017

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6 August 2017

13

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6 August 2017

401-407

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6 August 2017

Frailty and mortality are not influenced by mitochondrial DNA haplotypes in the very old.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

The role of mitochondria in aging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

The role of mitochondrial DNA mutations and free radicals in disease and ageing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Genome-wide linkage analysis for human longevity: Genetics of Healthy Aging Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

A high-performance computing toolset for relatedness and principal component analysis of SNP data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Global DNA methylation levels are modulated by mitochondrial DNA variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Design, recruitment, logistics, and data management of the GEHA (Genetics of Healthy Ageing) project

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Are mitochondrial haplogroups associated with extreme longevity? A study on a Spanish cohort

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Evidence for sub-haplogroup h5 of mitochondrial DNA as a risk factor for late onset Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Principal-component analysis for assessment of population stratification in mitochondrial medical genetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Ancient mtDNA genetic variants modulate mtDNA transcription and replication

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Mitochondrial DNA mutations and ageing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

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The diploid genome sequence of an Asian individual

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Mitochondrial DNA involvement in human longevity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Lineage-specific selection in human mtDNA: lack of polymorphisms in a segment of MTND5 gene in haplogroup J

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Mitochondrial DNA polymorphisms associated with longevity in a Finnish population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

The variability of the mitochondrial genome in human aging: a key for life and death?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Mitochondrial genotype associated with longevity and its inhibitory effect on mutagenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Human mtDNA haplogroups associated with high or reduced spermatozoa motility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Classification of European mtDNAs from an analysis of three European populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Mitochondrial DNA sequence analysis of four Alzheimer's and Parkinson's disease patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

A mitochondrial DNA clone is associated with increased risk for Alzheimer disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

8 July 2018

Mitochondrial DNA haplogroup distribution within Leber hereditary optic neuropathy pedigrees

1 reference

https://api.crossref.org/works/10.1111%2FACEL.12186

21 January 2018

Differences of sperm motility in mitochondrial DNA haplogroup U sublineages

1 reference

https://api.crossref.org/works/10.1111%2FACEL.12186

21 January 2018

mtDNA tree Build 17 (18 Feb 2016)

1 reference

https://api.crossref.org/works/10.1111%2FACEL.12186

21 January 2018

Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.

1 reference

https://api.crossref.org/works/10.1111%2FACEL.12186

21 January 2018

HAPLOFIND: a new method for high-throughput mtDNA haplogroup assignment

1 reference

https://api.crossref.org/works/10.1111%2FACEL.12186

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Mitochondrial DNA mutations in disease and aging.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

27 September 2018

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326891

25 October 2018

Mitochondrial DNA polymorphism: its role in longevity of the Irish population

1 reference

https://pubmed.ncbi.nlm.nih.gov/24341918

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inferred from PubMed ID database lookup

Paradoxes in longevity: sequence analysis of mtDNA haplogroup J in centenarians

1 reference

https://pubmed.ncbi.nlm.nih.gov/24341918

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial genotype associated with longevity

1 reference

https://pubmed.ncbi.nlm.nih.gov/24341918

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/24341918

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based on heuristic

inferred from PubMed ID database lookup

Association of the mitochondrial DNA haplogroup J with longevity is population specific

1 reference

https://pubmed.ncbi.nlm.nih.gov/24341918

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1111/ACEL.12186

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

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