(Q45878904)

17 December 2017

title

Inter-mitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA. (English)

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17 December 2017

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Nakada K

1

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17 December 2017

Inoue K

2

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17 December 2017

Ono T

3

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17 December 2017

Isobe K

4

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17 December 2017

Ogura A

5

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17 December 2017

Goto YI

6

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17 December 2017

Nonaka I

7

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17 December 2017

Hayashi JI

8

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17 December 2017

language of work or name

English

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publication date

1 August 2001

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17 December 2017

published in

Nature Medicine

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17 December 2017

volume

7

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17 December 2017

page(s)

934-940

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17 December 2017

issue

8

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17 December 2017

https://scigraph.springernature.com/pub.10.1038/90976

exact match

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cites work

Molecular genetic aspects of human mitochondrial disorders

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7 January 2021

Mitochondrial diseases in man and mouse

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7 January 2021

Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expression.

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7 January 2021

Mice with only rat mtDNA are required as models of mitochondrial diseases

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7 January 2021

Isolation of mitochondrial DNA-less mouse cell lines and their application for trapping mouse synaptosomal mitochondrial DNA with deletion mutations

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7 January 2021

Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes

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7 January 2021

Elimination of paternal mitochondrial DNA in intraspecific crosses during early mouse embryogenesis

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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

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7 January 2021

Mitochondria and ageing

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7 January 2021

Mitochondrial DNA deletion: a cause of chronic tubulointerstitial nephropathy

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7 January 2021

Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy

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7 January 2021

Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction

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7 January 2021

Transcription of the mammalian mitochondrial genome

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7 January 2021

Human cells are protected from mitochondrial dysfunction by complementation of DNA products in fused mitochondria

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7 January 2021

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

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7 January 2021

Functional integrity of mitochondrial genomes in human platelets and autopsied brain tissues from elderly patients with Alzheimer's disease

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7 January 2021

Nondroplet ultrastructural demonstration of cytochrome oxidase activity with a polymerizing osmiophilic reagent, diaminobenzidine (DAB).

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7 January 2021

Cytochrome C oxidase deficiency in two siblings with leigh encephalomyelopathy

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7 January 2021

Tissue specificity in cytochrome c oxidase deficient myopathy

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7 January 2021

Identifiers

DOI

10.1038/90976

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17 December 2017

Dimensions Publication ID

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17 December 2017