(Q34456867)

2 August 2017

Animal models for respiratory chain disease (English)

1 reference

2 August 2017

Larsson NG

1

1 reference

PubMed ID

11733222

2 August 2017

Rustin P

series ordinal

2

1 reference

2 August 2017

1 December 2001

1 reference

Trends in Molecular Medicine

2 August 2017

1 reference

2 August 2017

7

1 reference

2 August 2017

578-581

1 reference

2 August 2017

12

1 reference

Molecular genetic aspects of human mitochondrial disorders

2 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

The genetics and pathology of oxidative phosphorylation

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

Clinical spectrum and diagnosis of mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

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

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

Genetic modification of survival in tissue-specific knockout mice with mitochondrial cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

Impaired insulin secretion and beta-cell loss in tissue-specific knockout mice with mitochondrial diabetes.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

Inactivation of the Friedreich ataxia mouse gene leads to early embryonic lethality without iron accumulation

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

Maternal germ-line transmission of mutant mtDNAs from embryonic stem cell-derived chimeric mice.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

Increased in vivo apoptosis in cells lacking mitochondrial DNA gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

Late-onset corticohippocampal neurodepletion attributable to catastrophic failure of oxidative phosphorylation in MILON mice.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902167-0

7 January 2021

10.1016/S1471-4914(01)02167-0

Identifiers

DOI

1 reference

2 August 2017

1 reference

PubMed ID

11733222