Mitochondrial DNA mutations and aging: a case closed? (Q80058835)

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28 December 2019

title

Mitochondrial DNA mutations and aging: a case closed? (English)

1 reference

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28 December 2019

Jan Vijg

1 reference

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28 December 2019

Konstantin Khrapko

1 reference

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28 December 2019

publication date

1 April 2007

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28 December 2019

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28 December 2019

volume

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28 December 2019

issue

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28 December 2019

page(s)

445-446

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Premature ageing in mice expressing defective mitochondrial DNA polymerase

28 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0407-445

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0407-445

7 January 2021

Mitochondrial mutations in mammalian aging: an over-hasty about-turn?

1 reference

https://api.crossref.org/works/10.1038%2FNG0407-445

7 January 2021

Does premature aging of the mtDNA mutator mouse prove that mtDNA mutations are involved in natural aging?

1 reference

https://api.crossref.org/works/10.1038%2FNG0407-445

7 January 2021

Mitochondrial point mutations do not limit the natural lifespan of mice.

1 reference

https://api.crossref.org/works/10.1038%2FNG0407-445

7 January 2021

Quantification of random genomic mutations.

1 reference

https://api.crossref.org/works/10.1038%2FNG0407-445

7 January 2021

Mutational spectrometry: means and ends.

1 reference

https://api.crossref.org/works/10.1038%2FNG0407-445

7 January 2021

Clonally expanded mtDNA point mutations are abundant in individual cells of human tissues

1 reference

https://api.crossref.org/works/10.1038%2FNG0407-445

7 January 2021

Origins of human mitochondrial point mutations as DNA polymerase gamma-mediated errors.

1 reference

https://api.crossref.org/works/10.1038%2FNG0407-445

7 January 2021

High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0407-445

7 January 2021

Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons

1 reference

https://api.crossref.org/works/10.1038%2FNG0407-445

7 January 2021

Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.

1 reference

https://api.crossref.org/works/10.1038%2FNG0407-445

7 January 2021

Mitochondrial DNA mutations in human colonic crypt stem cells

1 reference

https://api.crossref.org/works/10.1038%2FNG0407-445

7 January 2021

Identifiers

DOI

10.1038/NG0407-445

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17392805%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17392805%20AND%20SRC:MED&resulttype=core&format=json