Maternally transmitted mitochondrial DNA mutations can reduce lifespan (Q34311406)

1 August 2017

Maternally transmitted mitochondrial DNA mutations can reduce lifespan (English)

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1 August 2017

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Jaime M Ross

1

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1 August 2017

Giuseppe Coppotelli

series ordinal

2

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1 August 2017

Barry J Hoffer

series ordinal

3

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1 August 2017

Lars Olson

series ordinal

4

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1 August 2017

language of work or name

English

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publication date

9 October 2014

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1 August 2017

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1 August 2017

4

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1 August 2017

6569

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Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International

1 August 2017

start time

9 October 2014

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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exact match

https://scigraph.springernature.com/pub.10.1038/srep06569

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cites work

NAD(+)-dependent activation of Sirt1 corrects the phenotype in a mouse model of mitochondrial disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Declining NAD(+) induces a pseudohypoxic state disrupting nuclear-mitochondrial communication during aging

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Germline mitochondrial DNA mutations aggravate ageing and can impair brain development

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Mitochondrial DNA mutations in mutator mice confer respiration defects and B-cell lymphoma development

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Universal heteroplasmy of human mitochondrial DNA.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Visualization of mitochondrial respiratory function using cytochrome c oxidase/succinate dehydrogenase (COX/SDH) double-labeling histochemistry

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Study of DNA damage via the comet assay and base excision repair activities in rat brain neurons and astrocytes during aging

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Ultra-deep sequencing of mouse mitochondrial DNA: mutational patterns and their origins

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Endurance exercise rescues progeroid aging and induces systemic mitochondrial rejuvenation in mtDNA mutator mice

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

High brain lactate is a hallmark of aging and caused by a shift in the lactate dehydrogenase A/B ratio

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Mitochondrial DNA mutations induce mitochondrial dysfunction, apoptosis and sarcopenia in skeletal muscle of mitochondrial DNA mutator mice

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Mitochondrial dysfunction, proteotoxicity, and aging: causes or effects, and the possible impact of NAD+-controlled protein glycation.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Age-dependent cardiomyopathy in mitochondrial mutator mice is attenuated by overexpression of catalase targeted to mitochondria.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Somatic mtDNA mutations cause aging phenotypes without affecting reactive oxygen species production

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Premature ageing in mice expressing defective mitochondrial DNA polymerase

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Aging: a theory based on free radical and radiation chemistry

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Does oxidative damage to DNA increase with age?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Deletion of Ku86 causes early onset of senescence in mice

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

The biologic clock: the mitochondria?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Cytochrome-c-oxidase deficient cardiomyocytes in the human heart--an age-related phenomenon. A histochemical ultracytochemical study.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Detection of a specific mitochondrial DNA deletion in tissues of older humans

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Rapid evolution of animal mitochondrial DNA

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190956

Detecting heteroplasmy from high-throughput sequencing of complete human mitochondrial DNA genomes

6 July 2018

1 reference

Mitoflash frequency in early adulthood predicts lifespan in Caenorhabditis elegans.

21 January 2018

1 reference

Somatic mtDNA mutations cause progressive hearing loss in the mouse.

21 January 2018

1 reference

In vivo levels of mitochondrial hydrogen peroxide increase with age in mtDNA mutator mice.

21 January 2018

1 reference

Hematopoietic stem cell quiescence attenuates DNA damage response and permits DNA damage accumulation during aging.

21 January 2018

1 reference

DNA deletions and clonal mutations drive premature aging in mitochondrial mutator mice

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25299268

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Purifying selection of mtDNA and its implications for understanding evolution and mitochondrial disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25299268

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Somatic Progenitor Cell Vulnerability to Mitochondrial DNA Mutagenesis Underlies Progeroid Phenotypes in Polg Mutator Mice

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25299268

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/SREP06569

1 reference

Dimensions Publication ID

1 August 2017

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1 reference

1 August 2017

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