Relaxed replication of mtDNA: A model with implications for the expression of disease (Q43218359)

16 November 2017

Relaxed replication of mtDNA: A model with implications for the expression of disease (English)

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16 November 2017

1

P F Chinnery

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16 November 2017

D C Samuels

2

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PMC publication ID

1377840

16 November 2017

language of work or name

English

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publication date

1 April 1999

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American Journal of Human Genetics

16 November 2017

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16 November 2017

64

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16 November 2017

4

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16 November 2017

1158-1165

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Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice

16 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

Mammalian mitochondrial genetics: heredity, heteroplasmy and disease

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

mtDNA recombination: what do in vitro data mean?

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

Mitochondrial DNA mutations and pathogenesis

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

Misconceptions about mitochondria and mammalian fertilization: implications for theories on human evolution

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

Maternal inheritance and the evaluation of oxidative phosphorylation diseases

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

Molecular genetic aspects of human mitochondrial disorders

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

Mitochondrial DNA diseases: histological and cellular studies

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

Complementation and segregation behavior of disease-causing mitochondrial DNA mutations in cellular model systems

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

Mitochondrial DNA mutations in human degenerative diseases and aging

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

Diseases of the mitochondrial DNA.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF)

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

An essential guide to mtDNA maintenance.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

Clinical features, investigation, and management of patients with defects of mitochondrial DNA.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

Apparent Turnover of Mitochondrial Deoxyribonucleic Acid and Mitochondrial Phospholipids in the Tissues of the Rat

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377840

Mitochondrial DNA gets the drift

15 August 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/10090901

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10090901

12 December 2020

5-Bromodeoxyuridine labeling of monomeric and catenated circular mitochondrial DNA in hela cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/10090901

12 December 2020

Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/10090901

12 December 2020

Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions

1 reference

https://pubmed.ncbi.nlm.nih.gov/10090901

12 December 2020

Noninvasive diagnosis of the MELAS syndrome from blood DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/10090901

12 December 2020

Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)

1 reference

https://pubmed.ncbi.nlm.nih.gov/10090901

12 December 2020

Quantitation of mitochondrial DNA in human lymphoblasts by a competitive polymerase chain reaction method: application to the study of inhibitors of mitochondrial DNA content

1 reference

https://pubmed.ncbi.nlm.nih.gov/10090901

12 December 2020

Identifiers

DOI

10.1086/302311

1 reference

16 November 2017

1 reference

PMC publication ID

1377840

16 November 2017

PubMed publication ID

10090901

1 reference

PMC publication ID

1377840