(Q35067263)

6 August 2017

title

Somatic mtDNA mutation spectra in the aging human putamen (English)

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6 August 2017

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3

Stephan Züchner

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6 August 2017

2

Deborah C Mash

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6 August 2017

Siôn L Williams

1

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6 August 2017

Carlos T Moraes

series ordinal

4

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6 August 2017

publication date

5 December 2013

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6 August 2017

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6 August 2017

volume

9

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6 August 2017

issue

12

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6 August 2017

page(s)

e1003990

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Creative Commons Attribution 3.0 Unported

6 August 2017

copyright license

start time

5 December 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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Two direct repeats cause most human mtDNA deletions

8 July 2018

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

8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?

8 July 2018

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mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region

8 July 2018

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8 July 2018

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Human aging is associated with stochastic somatic mutations of mitochondrial DNA.

8 July 2018

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Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

8 July 2018

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A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA.

8 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3854840

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

8 July 2018

1 reference

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3854840

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

8 July 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003990

Mechanisms of formation and accumulation of mitochondrial DNA deletions in aging neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003990

Population prevalence of the MELAS A3243G mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003990

Different effects of novel mtDNA G3242A and G3244A base changes adjacent to a common A3243G mutation in patients with mitochondrial disorders.

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003990

The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation--implications for diagnosis and management.

21 January 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3854840

The acquisition of an inheritable 50-bp deletion in the human mtDNA control region does not affect the mtDNA copy number in peripheral blood cells

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3854840

Occurrence of a particular base substitution (3243 A to G) in mitochondrial DNA of tissues of ageing humans

16 November 2018

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12 December 2020

Ageing-associated tandem duplications in the D-loop of mitochondrial DNA of human muscle

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12 December 2020

Conserved sequence box II directs transcription termination and primer formation in mitochondria

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12 December 2020

MitoTool: A web server for the analysis and retrieval of human mitochondrial DNA sequence variations

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12 December 2020

10.1371/JOURNAL.PGEN.1003990

Identifiers

DOI

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6 August 2017

1 reference

6 August 2017

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