Revolution in mitochondrial medicine (Q33705828)

28 July 2017

1 reference

title

Revolution in mitochondrial medicine (English)

1 reference

28 July 2017

Larsson NG

1

1 reference

28 July 2017

Luft R

series ordinal

2

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 July 1999

1 reference

28 July 2017

1 reference

28 July 2017

volume

455

1 reference

28 July 2017

issue

3

1 reference

28 July 2017

page(s)

199-202

1 reference

Molecular genetic aspects of human mitochondrial disorders

28 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

The development of mitochondrial medicine

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Mitochondrial diseases in man and mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

21 January 2018

Mitochondrial evolution

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

INTRAMITOCHONDRIAL FIBERS WITH DNA CHARACTERISTICS. I. FIXATION AND ELECTRON STAINING REACTIONS

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Sequence and gene organization of mouse mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Sequence and organization of the human mitochondrial genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Structure and function of the mitochondrial genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Demonstration of a new pathogenic mutation in human complex I deficiency: a 5-bp duplication in the nuclear gene encoding the 18-kD (AQDQ) subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Mutant NDUFV1 subunit of mitochondrial complex I causes leukodystrophy and myoclonic epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

SHY1, the yeast homolog of the mammalian SURF-1 gene, encodes a mitochondrial protein required for respiration

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

An autosomal locus predisposing to deletions of mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Human deafness dystonia syndrome is a mitochondrial disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Extension of Drosophila lifespan by overexpression of human SOD1 in motorneurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Mitochondrial genetics: a paradigm for aging and degenerative diseases?

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Aging-dependent functional alterations of mitochondrial DNA (mtDNA) from human fibroblasts transferred into mtDNA-less cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Nuclear-recessive mutations of factors involved in mitochondrial translation are responsible for age-related respiration deficiency of human skin fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

A mutation in succinate dehydrogenase cytochrome b causes oxidative stress and ageing in nematodes

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Structural and functional conservation of the Caenorhabditis elegans timing gene clk-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Yeast Clk-1 homologue (Coq7/Cat5) is a mitochondrial protein in coenzyme Q synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

SCID mice containing muscle with human mitochondrial DNA mutations. An animal model for mitochondrial DNA defects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

7 January 2021

Mitochondrial medicine

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Reference charts for respiratory chain activities in human tissues

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

Tissue-specific selection for different mtDNA genotypes in heteroplasmic mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2899%2900854-6

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0014-5793(99)00854-6

1 reference

28 July 2017

1 reference