Variation in germline mtDNA heteroplasmy is determined prenatally but modified during subsequent transmission (Q36382138)

13 August 2017

Variation in germline mtDNA heteroplasmy is determined prenatally but modified during subsequent transmission (English)

1 reference

13 August 2017

1 reference

Timothy Wai

7

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Lynsey M Cree

Lynsey M Cree

2

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Christoph Freyer

Christoph Freyer

1

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James Bruce Stewart

James B Stewart

4

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Arnaud Mourier

Arnaud Mourier

3

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David C. Samuels

David C Samuels

12

0 references

Nils-Göran Larsson

13

Nils-Göran Larsson

1 reference

13 August 2017

14

Patrick F Chinnery

1 reference

13 August 2017

Camilla Koolmeister

5

1 reference

13 August 2017

Dusanka Milenkovic

6

1 reference

13 August 2017

Vasileios I Floros

8

1 reference

13 August 2017

Erik Hagström

9

1 reference

13 August 2017

Emmanouella E Chatzidaki

10

1 reference

13 August 2017

Rudolf J Wiesner

11

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13 August 2017

language of work or name

English

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publication date

7 October 2012

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13 August 2017

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13 August 2017

44

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13 August 2017

11

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13 August 2017

1282-1285

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MTERF4 regulates translation by targeting the methyltransferase NSUN4 to the mammalian mitochondrial ribosome

13 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

Maintenance of respiratory chain function in mouse hearts with severely impaired mtDNA transcription

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

Previous estimates of mitochondrial DNA mutation level variance did not account for sampling error: comparing the mtDNA genetic bottleneck in mice and humans

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

Methylation of 12S rRNA is necessary for in vivo stability of the small subunit of the mammalian mitochondrial ribosome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

The mitochondrial DNA genetic bottleneck results from replication of a subpopulation of genomes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

The distribution of mitochondrial DNA heteroplasmy due to random genetic drift

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

Strong purifying selection in transmission of mammalian mitochondrial DNA

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

Premature ageing in mice expressing defective mitochondrial DNA polymerase

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

Random genetic drift determines the level of mutant mtDNA in human primary oocytes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

Blue native electrophoresis for isolation of membrane protein complexes in enzymatically active form

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

Mapping of mitochondrial DNA of individual sheep and goats: rapid evolution in the D loop region

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

Reassessing evidence for a postnatal mitochondrial genetic bottleneck.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

The mitochondrial bottleneck occurs without reduction of mtDNA content in female mouse germ cells.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

Generation of stella-GFP transgenic mice: a novel tool to study germ cell development.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

A Standard Reference Material to determine the sensitivity of techniques for detecting low-frequency mutations, SNPs, and heteroplasmies in mitochondrial DNA.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492742

Nucleotide sequence evidence for rapid genotypic shifts in the bovine mitochondrial DNA D-loop

21 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.2427

Purifying selection of mtDNA and its implications for understanding evolution and mitochondrial disease

21 January 2018

1 reference

12 December 2020

The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?

1 reference

12 December 2020

Identification of a mutation in the mitochondrial tRNA(Cys) gene associated with mitochondrial encephalopathy

1 reference

12 December 2020

Mitochondrial tRNACys gene mutation (A5814G): a second family with mitochondrial encephalopathy

1 reference

12 December 2020

Identifiers

DOI

10.1038/NG.2427

1 reference

Dimensions Publication ID

13 August 2017

0 references

1 reference

13 August 2017

PubMed publication ID

23042113

1 reference