Mammalian mitochondrial genetics: heredity, heteroplasmy and disease (Q41653872)

6 October 2017

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title

Mammalian mitochondrial genetics: heredity, heteroplasmy and disease (English)

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6 October 2017

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2

Chinnery PF

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6 October 2017

Lightowlers RN

1

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PubMed ID

9385842

6 October 2017

Turnbull DM

series ordinal

3

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PubMed ID

9385842

6 October 2017

Howell N

series ordinal

4

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6 October 2017

1 November 1997

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6 October 2017

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6 October 2017

13

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6 October 2017

11

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6 October 2017

450-455

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Molecular genetic aspects of human mitochondrial disorders

6 October 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

Amounts of mitochondrial DNA and abundance of some mitochondrial gene transcripts in early mouse embryos

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

Number of mitochondria and some properties of mitochondrial DNA in the mouse egg

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

Mitochondrial DNA sequence heteroplasmy in the Grand Duke of Russia Georgij Romanov establishes the authenticity of the remains of Tsar Nicholas II

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

Rearranged mitochondrial genomes are present in human oocytes

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

MELAS- and kearns-sayre-type with myopathy and autoimmune polyendocrinopahy

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

Intracellular mitochondrial triplasmy in a patient with two heteroplasmic base changes

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

Mammalian mitochondria possess homologous DNA recombination activity

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

Human mitochondria: distinct organelles or dynamic network?

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

Dynamics of mitochondria in living cells: shape changes, dislocations, fusion, and fission of mitochondria

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

Human mitochondria and mitochondrial genome function as a single dynamic cellular unit

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

The interorganellar interaction between distinct human mitochondria with deletion mutant mtDNA from a patient with mitochondrial disease and with HeLa mtDNA

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

Voice fatigue in myasthenia gravis: the sinking pitch sign

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

Complementation of mutant and wild-type human mitochondrial DNAs coexisting since the mutation event and lack of complementation of DNAs introduced separately into a cell within distinct organelles

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

Organization of multiple nucleoids and DNA molecules in mitochondria of a human cell

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

In situ localization of mitochondrial DNA replication in intact mammalian cells

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

A near homoplasmic T8993G mtDNA mutation in a patient with atypic Leigh syndrome not present in the mother's tissues.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

Rapid segregation of heteroplasmic bovine mitochondria

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

A novel heteroplasmic tRNAleu(CUN) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapy.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

Reversal of a mitochondrial DNA defect in human skeletal muscle.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acids

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901266-3

7 January 2021

10.1016/S0168-9525(97)01266-3

Identifiers

DOI

1 reference

6 October 2017

1 reference

PubMed ID

9385842