(Q77312887)

English

Single muscle fiber analysis in patients with 3243 mutation in mitochondrial DNA: comparison with the phenotype and the proportion of mutant genome

scientific article published on 01 August 1998

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9741403%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

Single muscle fiber analysis in patients with 3243 mutation in mitochondrial DNA: comparison with the phenotype and the proportion of mutant genome (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9741403%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

author name string

M Ozawa

1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9741403%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

I Nonaka

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9741403%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

Y Goto

3

1 reference

Europe PubMed Central

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4 December 2019

publication date

1 August 1998

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9741403%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

Journal of the Neurological Sciences

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9741403%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

159

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9741403%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

2

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4 December 2019

170-175

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9741403%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900152-X

7 January 2021

Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900152-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900152-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900152-X

7 January 2021

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900152-X

7 January 2021

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900152-X

7 January 2021

A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900152-X

7 January 2021

Chronic progressive external ophthalmoplegia: a correlative study of mitochondrial DNA deletions and their phenotypic expression in muscle biopsies

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900152-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900152-X

7 January 2021

Nondroplet ultrastructural demonstration of cytochrome oxidase activity with a polymerizing osmiophilic reagent, diaminobenzidine (DAB).

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900152-X

7 January 2021

Variability in the activity of respiratory chain enzymes in mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900152-X

7 January 2021

Detection and analysis of mitochondrial DNA and RNA in muscle by in situ hybridization and single-fiber PCR

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900152-X

7 January 2021

Myoclonus epilepsy associated with ragged-red fibers: a G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA(Lys) in two families.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900152-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900152-X

7 January 2021

Extremely high levels of mutant mtDNAs co-localize with cytochrome c oxidase-negative ragged-red fibers in patients harboring a point mutation at nt 3243

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900152-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900152-X

7 January 2021

Muscle histopathology in diabetes mellitus associated with mitochondrial tRNA(Leu(UUR)) mutation at position 3243

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900152-X

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%2FS0022-510X%2898%2900152-X

7 January 2021

Tissue-specific selection for different mtDNA genotypes in heteroplasmic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900152-X

7 January 2021

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Identifiers

10.1016/S0022-510X(98)00152-X

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9741403%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9741403%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

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