(Q34657233)

3 August 2017

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

1 reference

3 August 2017

0 references

Liu VW

1

1 reference

3 August 2017

Zhang C

series ordinal

2

1 reference

3 August 2017

Nagley P

series ordinal

3

1 reference

3 August 2017

language of work or name

English

0 references

publication date

1 March 1998

1 reference

3 August 2017

Nucleic Acids Research

1 reference

3 August 2017

26

1 reference

3 August 2017

5

1 reference

3 August 2017

1268-1275

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147381

3 August 2017

1 reference

Mitochondrial oxidative phosphorylation changes in the life span. Molecular aspects and physiopathological implications

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147381

Evidence that specific mtDNA point mutations may not accumulate in skeletal muscle during normal human aging

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147381

Differential accumulations of 4,977 bp deletion in mitochondrial DNA of various tissues in human ageing.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147381

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147381

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147381

Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147381

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147381

Multiple mitochondrial DNA deletions in an elderly human individual.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147381

Mitochondrial genetics: a paradigm for aging and degenerative diseases?

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147381

Mitochondrial DNA mutation and the ageing process: bioenergy and pharmacological intervention

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147381

Mitochondrial DNA alterations as ageing-associated molecular events

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147381

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147381

Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147381

Human aging is associated with various point mutations in tRNA genes of mitochondrial DNA.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147381

Human cell mutants with very low mitochondrial DNA copy number (rho d).

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147381

Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac disease

26 October 2018

1 reference

12 December 2020

Independent occurrence of somatic mutations in mitochondrial DNA of human skin from subjects of various ages

1 reference

12 December 2020

DECLINE IN SKELETAL MUSCLE MITOCHONDRIAL RESPIRATORY CHAIN FUNCTION: POSSIBLE FACTOR IN AGEING

1 reference

12 December 2020

Liver mitochondrial respiratory functions decline with age

1 reference

12 December 2020

Mitochondrial gene mutation: the ageing process and degenerative diseases

1 reference

12 December 2020

Age-dependent increase in deleted mitochondrial DNA in the human heart: possible contributory factor to presbycardia

1 reference

12 December 2020

Accumulation of deletions in human mitochondrial DNA during normal aging: analysis by quantitative PCR

1 reference

12 December 2020

A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

A specific 4977-bp deletion of mitochondrial DNA in human ageing skin

1 reference

12 December 2020

Photoageing-associated mitochondrial DNA length mutations in human skin

1 reference

12 December 2020

Quantitative allele-specific PCR: demonstration of age-associated accumulation in human tissues of the A-->G mutation at nucleotide 3243 in mitochondrial DNA

1 reference

12 December 2020

Gross mosaic pattern of mitochondrial DNA deletions in skeletal muscle tissues of an individual adult human subject

1 reference

12 December 2020

Identifiers

DOI

10.1093/NAR/26.5.1268

1 reference

3 August 2017

1 reference

3 August 2017

1 reference