Reactive oxygen species and the segregation of mtDNA sequence variants (Q80220520)

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29 December 2019

title

Reactive oxygen species and the segregation of mtDNA sequence variants (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17460678%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

main subject

reactive oxygen species

1 reference

Brendan J Battersby

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17460678%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

Eric A Shoubridge

series ordinal

1 reference

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29 December 2019

publication date

1 May 2007

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29 December 2019

1 reference

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29 December 2019

volume

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29 December 2019

issue

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29 December 2019

page(s)

571-2; author reply 572

1 reference

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

29 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0507-571

7 January 2021

Tissue-specific selection for different mtDNA genotypes in heteroplasmic mice

1 reference

https://api.crossref.org/works/10.1038%2FNG0507-571

7 January 2021

Nuclear genetic control of mitochondrial DNA segregation

1 reference

https://api.crossref.org/works/10.1038%2FNG0507-571

7 January 2021

Differences in reactive oxygen species production explain the phenotypes associated with common mouse mitochondrial DNA variants

1 reference

https://api.crossref.org/works/10.1038%2FNG0507-571

7 January 2021

Selection of a mtDNA sequence variant in hepatocytes of heteroplasmic mice is not due to differences in respiratory chain function or efficiency of replication

1 reference

https://api.crossref.org/works/10.1038%2FNG0507-571

7 January 2021

Mitochondrial DNA segregation in hematopoietic lineages does not depend on MHC presentation of mitochondrially encoded peptides

1 reference

https://api.crossref.org/works/10.1038%2FNG0507-571

7 January 2021

Nuclear suppression of mitochondrial defects in cells without the ND6 subunit

1 reference

https://api.crossref.org/works/10.1038%2FNG0507-571

7 January 2021

Suppression of a mitochondrial tRNA gene mutation phenotype associated with changes in the nuclear background

1 reference

https://api.crossref.org/works/10.1038%2FNG0507-571

7 January 2021

A missense mutation of cytochrome oxidase subunit II causes defective assembly and myopathy

1 reference

https://api.crossref.org/works/10.1038%2FNG0507-571

7 January 2021

Identifiers

DOI

10.1038/NG0507-571

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17460678%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17460678%20AND%20SRC:MED&resulttype=core&format=json