(Q37382577)

20 August 2017

The low abundance of clonally expanded mitochondrial DNA point mutations in aged substantia nigra neurons (English)

1 reference

20 August 2017

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1 reference

1 reference

Robert William Taylor

6

object named as

Robert W Taylor

1 reference

20 August 2017

Amy K Reeve

1

1 reference

20 August 2017

Kim J Krishnan

2

1 reference

20 August 2017

Geoffrey Taylor

3

1 reference

20 August 2017

Joanna L Elson

4

1 reference

20 August 2017

Andreas Bender

5

1 reference

20 August 2017

Christopher M Morris

7

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20 August 2017

Doug M Turnbull

8

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20 August 2017

31 May 2009

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20 August 2017

1 reference

20 August 2017

8

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20 August 2017

4

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20 August 2017

496-498

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What causes mitochondrial DNA deletions in human cells?

20 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759982

Prevalence of mitochondrial DNA disease in adults

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759982

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759982

mtDB: Human Mitochondrial Genome Database, a resource for population genetics and medical sciences

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759982

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759982

Mitochondrial DNA mutations in human disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759982

Premature ageing in mice expressing defective mitochondrial DNA polymerase

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759982

Mitochondrial DNA mutations in human colonic crypt stem cells

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759982

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759982

The determination of complete human mitochondrial DNA sequences in single cells: implications for the study of somatic mitochondrial DNA point mutations

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759982

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759982

Mutations in mitochondrial DNA accumulate differentially in three different human tissues during ageing

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759982

Sequence and organization of the human mitochondrial genome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759982

Reactive oxygen species and the central nervous system

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759982

Insensitivity of cultured rat cortical neurons to mitochondrial DNA synthesis inhibitors: evidence for a slow turnover of mitochondrial DNA.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759982

Exaggerated status of "novel" and "pathogenic" mtDNA sequence variants due to inadequate database searches

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759982

Nature of mitochondrial DNA deletions in substantia nigra neurons

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759982

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

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759982

Role of mitochondrial DNA mutations in human aging: implications for the central nervous system and muscle

2 September 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Quantification and sequencing of somatic deleted mtDNA in single cells: evidence for partially duplicated mtDNA in aged human tissues

1 reference

12 December 2020

Ageing muscle: clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial function

1 reference

12 December 2020

10.1111/J.1474-9726.2009.00492.X

Identifiers

DOI

1 reference

release_mwcdzbqqj5dutm34vhrmoz4aey

20 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/mwcdzbqqj5dutm34vhrmoz4aey

24 November 2022

mapped directly with Wikidata item

1 reference

20 August 2017

PubMed publication ID

19489744

1 reference