(Q41709851)

English

A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).

scientific article published on December 1990

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes). (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

lactic acidosis

1 reference

based on heuristic

inferred from title

mitochondrial myopathy

1 reference

based on heuristic

inferred from title

author name string

Kobayashi Y

1

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

Momoi MY

2

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

Tominaga K

3

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

Momoi T

4

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

Nihei K

5

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

Yanagisawa M

6

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

Kagawa Y

7

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

Ohta S

8

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

publication date

1 December 1990

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

Biochemical and Biophysical Research Communications

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

173

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

816-822

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

Mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

The clinical features of mitochondrial myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

Multiple deletions in mitochondrial DNA at direct repeats of non-D-loop regions in cases of familial mitochondrial myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

RAPID EXAMINATION OF MUSCLE TISSUE. AN IMPROVED TRICHROME METHOD FOR FRESH-FROZEN BIOPSY SECTIONS

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

Generation of human myogenic cell lines by the transformation of primary culture with origin-defective SV40 DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

Cytochrome c oxidase--deficient myogenic cell lines in mitochondrial myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

Sequence and organization of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

Complete sequence of bovine mitochondrial DNA. Conserved features of the mammalian mitochondrial genome

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

Sequence and gene organization of mouse mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

Compilation of tRNA sequences and sequences of tRNA genes

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

Mitochondrial DNA polymorphism in Japanese. II. Analysis with restriction enzymes of four or five base pair recognition

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

Termination of transcription in human mitochondria: identification and purification of a DNA binding protein factor that promotes termination

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980860-5

7 January 2021

Identifiers

10.1016/S0006-291X(05)80860-5

1 reference

https://api.fatcat.wiki/v0/release/2pfip6mfejahbepurayrxtr3hq

30 July 2022

based on heuristic

mapped directly with Wikidata item

release_2pfip6mfejahbepurayrxtr3hq

1 reference

https://api.fatcat.wiki/v0/release/2pfip6mfejahbepurayrxtr3hq

30 July 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

https://api.fatcat.wiki/v0/release/2pfip6mfejahbepurayrxtr3hq

30 July 2022

based on heuristic

mapped directly with Wikidata item

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