(Q33826111)

English

The age-related accumulation of a mitochondrial DNA control region mutation in muscle, but not brain, detected by a sensitive PNA-directed PCR clamping based method

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scholarly article

1 reference

Europe PubMed Central

29 July 2017

The age-related accumulation of a mitochondrial DNA control region mutation in muscle, but not brain, detected by a sensitive PNA-directed PCR clamping based method (English)

1 reference

Europe PubMed Central

29 July 2017

mitochondrial DNA

0 references

author name string

D G Murdock

1

1 reference

Europe PubMed Central

29 July 2017

N C Christacos

2

1 reference

Europe PubMed Central

29 July 2017

D C Wallace

3

1 reference

Europe PubMed Central

29 July 2017

language of work or name

0 references

publication date

1 November 2000

1 reference

Europe PubMed Central

29 July 2017

Nucleic Acids Research

1 reference

Europe PubMed Central

29 July 2017

28

1 reference

Europe PubMed Central

29 July 2017

4350-4355

1 reference

Europe PubMed Central

29 July 2017

21

1 reference

Europe PubMed Central

29 July 2017

Cloning of neuronal mtDNA variants in cultured cells by synaptosome fusion with mtDNA-less cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

The frequency of heteroplasmy in the HVII region of mtDNA differs across tissue types and increases with age.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

Facile detection of mitochondrial DNA mutations in tumors and bodily fluids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

Mitochondrial defects in cardiomyopathy and neuromuscular disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

Mitochondrial disease in mouse results in increased oxidative stress

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

Mitochondrial diseases in man and mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

Somatic mutations of the mitochondrial genome in human colorectal tumours

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

Human brain contains high levels of heteroplasmy in the noncoding regions of mitochondrial DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

Single base pair mutation analysis by PNA directed PCR clamping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

PNA hybridizes to complementary oligonucleotides obeying the Watson-Crick hydrogen-bonding rules

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

Marked increase in the number and variety of mitochondrial DNA rearrangements in aging human skeletal muscle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

Marked increase in mitochondrial DNA deletion levels in the cerebral cortex of Huntington's disease patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

Nucleotide sequence preservation of human mitochondrial DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

Studies of sequence heterogeneity of mitochondrial DNA from rat and mouse tissues: evidence for an increased frequency of deletions/additions with aging.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

Multiple mitochondrial DNA deletions in an elderly human individual.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

Transcription and replication of animal mitochondrial DNAs.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

4 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=113143

29 October 2018

Nucleotide sequence preservation of human leukemic mitochondrial DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/11058135

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial gene mutation: the ageing process and degenerative diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/11058135

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11058135

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel mitochondrial DNA deletion found in a renal cell carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/11058135

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial gene mutation, but not large-scale deletion, is a feature of colorectal carcinomas with mitochondrial microsatellite instability

1 reference

https://pubmed.ncbi.nlm.nih.gov/11058135

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The point mutation of mitochondrial DNA characteristic for MERRF disease is found also in healthy people of different ages

1 reference

https://pubmed.ncbi.nlm.nih.gov/11058135

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11058135

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA rearrangements in aging human brain and in situ PCR of mtDNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/11058135

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/NAR/28.21.4350

1 reference

Europe PubMed Central

29 July 2017

1 reference

Europe PubMed Central

29 July 2017

1 reference

Europe PubMed Central

29 July 2017

ResearchGate publication ID

0 references

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