(Q52533533)

2 May 2018

title

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

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2 May 2018

main subject

mitochondrial DNA

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dilated cardiomyopathy

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3

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2 May 2018

C. Ronald Kahn

8

object named as

Kahn CR

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2 May 2018

12

Larsson NG

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2 May 2018

author name string

Wang J

1

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2 May 2018

Wilhelmsson H

2

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2 May 2018

Li H

4

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2 May 2018

Oldfors A

5

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2 May 2018

Rustin P

6

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2 May 2018

Brüning JC

7

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2 May 2018

Clayton DA

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2 May 2018

Barsh GS

10

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2 May 2018

Thorén P

11

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2 May 2018

language of work or name

English

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publication date

1 January 1999

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2 May 2018

published in

Nature Genetics

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2 May 2018

volume

21

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2 May 2018

page(s)

133-137

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2 May 2018

issue

1

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2 May 2018

https://scigraph.springernature.com/pub.10.1038/5089

exact match

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cites work

Molecular genetic aspects of human mitochondrial disorders

1 reference

7 January 2021

Mitochondrial encephalomyopathies: clinical and molecular analysis

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7 January 2021

Mammalian mitochondrial genetics: heredity, heteroplasmy and disease

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7 January 2021

Mitochondrial genetics: a paradigm for aging and degenerative diseases?

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7 January 2021

Replication and Transcription of Vertebrate Mitochondrial DNA

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7 January 2021

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7 January 2021

Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice

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7 January 2021

Tissue-specific distribution and developmental regulation of M and B creatine kinase mRNAs

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7 January 2021

Biochemical correlates of cardiac hypertrophy. IV. Observations on the cellular organization of growth during myocardial hypertrophy in the rat

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7 January 2021

Constituents of the human ventricular myocardium: connective tissue hyperplasia accompanying muscular hypertrophy

1 reference

7 January 2021

Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase

1 reference

7 January 2021

A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions

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7 January 2021

Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres

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7 January 2021

Tissue-specific stability of nuclear- and mitochondrially encoded mRNAs

1 reference

7 January 2021

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

1 reference

7 January 2021

In situ hybridization of mitochondrial DNA in the heart of a patient with Kearns-Sayre syndrome and dilatative cardiomyopathy

1 reference

7 January 2021

Lumping or splitting? "Ophthalmoplegia-plus" or Kearns-Sayre syndrome?

1 reference

7 January 2021

Biochemical and molecular investigations in respiratory chain deficiencies

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7 January 2021

A PC-based on-line system for physiological in vivo and in vitro experiments.

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7 January 2021

In vivo echocardiographic detection of enhanced left ventricular function in gene-targeted mice with phospholamban deficiency

1 reference

7 January 2021

Identifiers

DOI

10.1038/5089

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2 May 2018

PubMed ID

9916807

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2 May 2018