(Q34667108)

3 August 2017

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title

mtLOH (mitochondrial loss of heteroplasmy), aging, and 'surrogate self'. (English)

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3 August 2017

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Ekaterina Nekhaeva

1

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3 August 2017

Yevgenya Kraytsberg

series ordinal

2

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3 August 2017

Konstantin Khrapko

series ordinal

3

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3 August 2017

publication date

1 April 2002

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Mechanisms of Ageing and Development

3 August 2017

published in

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3 August 2017

volume

123

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3 August 2017

issue

8

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3 August 2017

page(s)

891-898

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Mitochondrial DNA deletion mutations are concomitant with ragged red regions of individual, aged muscle fibers: analysis by laser-capture microdissection

3 August 2017

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Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with age.

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

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A mitochondrial tRNA anticodon swap associated with a muscle disease

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Different in situ hybridization patterns of mitochondrial DNA in cytochrome c oxidase-deficient extraocular muscle fibres in the elderly

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7 January 2021

Clonally expanded mtDNA point mutations are abundant in individual cells of human tissues

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7 January 2021

What does it take to live to 100?

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7 January 2021

Human mitochondria: distinct organelles or dynamic network?

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7 January 2021

The effects of age and lifestyle factors on the accumulation of cytogenetic damage as measured by chromosome painting

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7 January 2021

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

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Mitochondrial DNA mutations and neuromuscular disease

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7 January 2021

Mitochondrial DNA deletion mutations colocalize with segmental electron transport system abnormalities, muscle fiber atrophy, fiber splitting, and oxidative damage in sarcopenia

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Identifiers

DOI

1 reference

3 August 2017

1 reference