(Q36654770)

15 August 2017

1 reference

title

Neurological disease and mitochondrial genes (English)

1 reference

extrachromosomal inheritance

15 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1710848

5 November 2022

author name string

A. E. Harding

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1710848

5 November 2022

language of work or name

1 reference

1 April 1991

1 reference

full work available at URL

15 August 2017

https://api.elsevier.com/content/article/PII:0166223691900815?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

https://api.elsevier.com/content/article/PII:0166223691900815?httpAccept=text/plain

5 November 2022

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

5 November 2022

published in

Trends in Neurosciences

1 reference

15 August 2017

14

1 reference

15 August 2017

132-138

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15 August 2017

4

1 reference

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

15 August 2017

1 reference

24 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1126/SCIENCE.2814477

Sequence and organization of the human mitochondrial genome

1

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Mitochondrial DNA and human evolution

5 November 2022

3

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

The clinical features of mitochondrial myopathy.

5 November 2022

4

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

5 November 2022

Mitochondrial myopathies

5

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Mitochondrial inheritance in a mitochondrially mediated disease

5 November 2022

7

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

5 November 2022

8

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Deletions of mitochondrial DNA in Kearns-Sayre syndrome

5 November 2022

9

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.

5 November 2022

10

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA

5 November 2022

11

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Duplications of mitochondrial DNA in mitochondrial myopathy

5 November 2022

12

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA.

5 November 2022

13

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

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

5 November 2022

16

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

MITOCHONDRIAL DNA DELETION IN PEARSON'S MARROW/PANCREAS SYNDROME

5 November 2022

17

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction

5 November 2022

18

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Maternally inherited mitochondrial myopathy and myoclonic epilepsy.

5 November 2022

20

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

5 November 2022

21

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

5 November 2022

23

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Molecular defects of NADH-ubiquinone oxidoreductase (complex I) in mitochondrial diseases

5 November 2022

24

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

5 November 2022

25

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

New aspects of the genetic, etiologic, and clinical puzzle of Leber's disease

5 November 2022

26

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

5 November 2022

27

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.

5 November 2022

28

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

A defect in mitochondrial electron-transport activity (NADH-coenzyme Q oxidoreductase) in Leber's hereditary optic neuropathy.

5 November 2022

31

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Mitochondrial complex I deficiency in Parkinson's disease

5 November 2022

35

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Abnormalities of the electron transport chain in idiopathic Parkinson's disease

5 November 2022

36

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

MITOCHONDRIAL FUNCTION IN PARKINSON'S DISEASE

5 November 2022

37

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Mitochondrial DNA analysis in Parkinson's disease

5 November 2022

38

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Increase of deleted mitochondrial DNA in the striatum in Parkinson's disease and senescence

5 November 2022

39

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

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

5 November 2022

40

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Injection of mitochondria into human cells leads to a rapid replacement of the endogenous mitochondrial DNA.

5 November 2022

41

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

Mitochondrial diseases: gene mapping and gene therapy

5 November 2022

43

1 reference

https://api.crossref.org/works/10.1016/0166-2236(91)90081-5

5 November 2022

Identifiers

1 reference

15 August 2017

1 reference