(Q71852965)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7603511%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

review article

1 reference

title

Mitochondrial DNA mutation and muscle pathology in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7603511%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1 reference

mitochondrial myopathy

1 reference

S. Mita

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7603511

8 June 2024

M. Tokunaga

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7603511

8 June 2024

T. Kumamoto

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7603511

8 June 2024

M. Uchino

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7603511

8 June 2024

I. Nonaka

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7603511

8 June 2024

M. Ando

6

1 reference

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8 June 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7603511

8 June 2024

publication date

1 January 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7603511%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

21 October 2019

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fmus.880181423

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

https://onlinelibrary.wiley.com/doi/full/10.1002/mus.880181423

8 June 2024

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Muscle & nerve. Supplement

8 June 2024

published in

volume

3

page(s)

S113-8

publication date

1995

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7603511

8 June 2024

volume

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7603511%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

page(s)

S113-8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7603511%20AND%20SRC:MED&resulttype=core&format=json

Sequence and organization of the human mitochondrial genome

21 October 2019

cites work

1

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts

8 June 2024

2

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

MELAS: clinical features, biochemistry, and molecular genetics

8 June 2024

3

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature

8 June 2024

5

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation

8 June 2024

6

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

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

8 June 2024

7

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).

8 June 2024

8

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

A molecular genetic study of focal histochemical defects in mitochondrial encephalomyopathies

8 June 2024

9

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Strongly succinate dehydrogenase-reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes

8 June 2024

10

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

8 June 2024

11

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

A partial deficiency of cytochrome c oxidase in chronic progressive external ophthalmoplegia.

8 June 2024

12

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomes

8 June 2024

13

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Retinitis Pigmentosa, External Ophthalmoplegia, and Complete Heart Block

8 June 2024

14

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

8 June 2024

15

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Muscle histopathology in myoclonus epilepsy with ragged-red fibers (MERRF)

8 June 2024

16

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome

8 June 2024

18

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions

8 June 2024

20

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Mitochondrial angiopathy in cerebral blood vessels of mitochondrial encephalomyopathy

8 June 2024

21

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

8 June 2024

22

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Vascular involvement in mitochondrial myopathy.

8 June 2024

23

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Mitochondrial DNA mutations at nucleotide positions 3243 and 3271 in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes: a comparative study

8 June 2024

24

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

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

8 June 2024

25

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Biochimica et Biophysica Acta

8 June 2024

26

1101

206

Schon

1992

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

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

8 June 2024

27

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)

8 June 2024

28

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)

8 June 2024

29

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Mitochondrial DNA mutations and neuromuscular disease

8 June 2024

30

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy

8 June 2024

31

1 reference

https://api.crossref.org/works/10.1002/MUS.880181423

8 June 2024

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7603511%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1 reference