(Q46623419)

23 December 2017

title

Growing old: the most common mitochondrial disease of all? (English)

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23 December 2017

main subject

mitochondrial disease

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Harding AE

1

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23 December 2017

language of work or name

English

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publication date

1 December 1992

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23 December 2017

published in

Nature Genetics

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23 December 2017

volume

2

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23 December 2017

issue

4

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23 December 2017

page(s)

251-252

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23 December 2017

Diseases of the mitochondrial DNA.

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-251

Mitochondrial mutations may increase oxidative stress: implications for carcinogenesis and aging?

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG1292-251

Widespread tissue distribution of mitochondrial DNA deletions in Kearns-Sayre syndrome

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG1292-251

Regulation of mitochondrial gene expression in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-251

Quantitation of a mitochondrial DNA deletion in Parkinson's disease

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG1292-251

Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG1292-251

7 January 2021

Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain

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7 January 2021

DECLINE IN SKELETAL MUSCLE MITOCHONDRIAL RESPIRATORY CHAIN FUNCTION: POSSIBLE FACTOR IN AGEING

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https://api.crossref.org/works/10.1038%2FNG1292-251

7 January 2021

Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases

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https://api.crossref.org/works/10.1038%2FNG1292-251

7 January 2021

An introduction to the free radical hypothesis in Parkinson's disease

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https://api.crossref.org/works/10.1038%2FNG1292-251

7 January 2021

Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome

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https://api.crossref.org/works/10.1038%2FNG1292-251

7 January 2021

Human brain glucose utilization and cognitive function in relation to age

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https://api.crossref.org/works/10.1038%2FNG1292-251

7 January 2021

Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA

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https://api.crossref.org/works/10.1038%2FNG1292-251

7 January 2021

Mitochondrial genetics: a paradigm for aging and degenerative diseases?

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https://api.crossref.org/works/10.1038%2FNG1292-251

7 January 2021

Mitochondrial complex I deficiency in Parkinson's disease

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https://api.crossref.org/works/10.1038%2FNG1292-251

7 January 2021

Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-251

7 January 2021

Decreased ferritin levels in brain in Parkinson's disease

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https://api.crossref.org/works/10.1038%2FNG1292-251

7 January 2021

Increase of deleted mitochondrial DNA in the striatum in Parkinson's disease and senescence

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https://api.crossref.org/works/10.1038%2FNG1292-251

7 January 2021

Detection of point mutations in codon 331 of mitochondrial NADH dehydrogenase subunit 2 in Alzheimer's brains

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7 January 2021

Identifiers

DOI

10.1038/NG1292-251

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23 December 2017

Dimensions Publication ID

1022947255

0 references

1 reference

23 December 2017