Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases (Q69368213)

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1 October 2019

title

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

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1 October 2019

author name string

A W Linnane

1

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1 October 2019

S Marzuki

2

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1 October 2019

T Ozawa

3

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1 October 2019

M Tanaka

4

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1 October 2019

language of work or name

English

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publication date

1 March 1989

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1 October 2019

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1 October 2019

volume

1

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1 October 2019

page(s)

642-645

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1 October 2019

issue

8639

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Sequence and organization of the human mitochondrial genome

1 October 2019

cites work

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Genetics of mitochondrial biogenesis

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Maternal inheritance of human mitochondrial DNA

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Rapid evolution of animal mitochondrial DNA

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The biogenesis of mitochondria in microorganisms

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Mitochondrial genetics in perspective: The derivation of a genetic and physical map of the yeast mitochondrial genome

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Mitotic segregation of cytoplasmic determinants for chloramphenicol resistance in mammalian cells I: Fusions with mouse cell lines

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Carbomycin resistance in mouse L cells

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7 January 2021

Mitotic segregation of cytoplasmic determinants for chloramphenicol resistance in mammalian cells II: Fusions with human cell lines

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7 January 2021

The clinical features of mitochondrial myopathy.

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Mitochondrial myopathies

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7 January 2021

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

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7 January 2021

KEARNS-SAYRE SYNDROME WITH MUSCLE MITOCHONDRIAL DNA DELETION

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7 January 2021

Deletions of muscle mitochondrial DNA

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7 January 2021

Deletion of blood mitochondrial DNA in pancytopenia

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7 January 2021

Studies of sequence heterogeneity of mitochondrial DNA from rat and mouse tissues: evidence for an increased frequency of deletions/additions with aging.

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7 January 2021

Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy

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7 January 2021

MTTOCHONDRIAL DNA DELETION IN ENCEPHALOMYOPATHY

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7 January 2021

Mitochondrial DNA molecules and virtual number of mitochondria per cell in mammalian cells

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7 January 2021

Deficiency of subunits of Complex I and mitochondrial encephalomyopathy.

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7 January 2021

31P NMR study of improvement in oxidative phosphorylation by vitamins K3 and C in a patient with a defect in electron transport at complex III in skeletal muscle.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

10.1016/S0140-6736(89)92145-4

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2564461%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

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