(Q35238386)

7 August 2017

Homopolymeric tract heteroplasmy in mtDNA from tissues and single oocytes: support for a genetic bottleneck (English)

1 reference

7 August 2017

1 reference

D R Marchington

1

1 reference

7 August 2017

G M Hartshorne

series ordinal

2

1 reference

7 August 2017

D Barlow

series ordinal

3

1 reference

7 August 2017

J Poulton

series ordinal

4

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 February 1997

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

60

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7 August 2017

2

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7 August 2017

408-416

1 reference

Drosophila Mitochondrial Genetics: Evolution of Heteroplasmy through Germ Line Cell Divisions

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712400

Comparison of the relative levels of the 3243 (A-->G) mtDNA mutation in heteroplasmic adult and fetal tissues

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712400

Length heteroplasmy in the first hypervariable segment of the human mtDNA control region

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712400

Different cellular backgrounds confer a marked advantage to either mutant or wild-type mitochondrial genomes.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712400

Length heterogeneity of a conserved displacement-loop sequence in human mitochondrial DNA.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712400

Nucleotide sequence preservation of human mitochondrial DNA.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712400

Rapid segregation of heteroplasmic bovine mitochondria

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712400

Intraspecific nucleotide sequence differences in the major noncoding region of human mitochondrial DNA.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712400

Replacement of bovine mitochondrial DNA by a sequence variant within one generation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712400

Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712400

Mitochondrial gene segregation in mammals: is the bottleneck always narrow?

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712400

Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712400

Noninvasive diagnosis of the MELAS syndrome from blood DNA

26 September 2018

1 reference

12 December 2020

Heterogeneous mitochondrial DNA D-loop sequences in bovine tissue

1 reference

12 December 2020

Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism

1 reference

12 December 2020

Mitochondrial DNA, diabetes and pancreatic pathology in Kearns-Sayre syndrome

1 reference

12 December 2020

A role for recombination junctions in the segregation of mitochondrial DNA in yeast

1 reference

12 December 2020

Do sequence variants in the major non-coding region of the mitochondrial genome influence mitochondrial mutations associated with disease?

1 reference

12 December 2020

Identifiers

PMCID

1712400

1 reference

7 August 2017

1 reference