The mutant mitochondrial genes in mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) were selectively amplified through generations (Q67581830)

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scientific article published on 01 January 1992

Language	Label	Description	Also known as
English	The mutant mitochondrial genes in mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) were selectively amplified through generations	scientific article published on 01 January 1992

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1434521%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

The mutant mitochondrial genes in mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) were selectively amplified through generations (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1434521%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

lactic acidosis

1 reference

based on heuristic

inferred from title

mitochondrial myopathy

1 reference

based on heuristic

inferred from title

author name string

Y. Kobayashi

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1434521

26 September 2022

K. Ichihashi

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1434521

26 September 2022

S. Ohta

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1434521

26 September 2022

K. Nihei

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1434521

26 September 2022

Y. Kagawa

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1434521

26 September 2022

M. Yanagisawa

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1434521

26 September 2022

M. Y. Momoi

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1434521

26 September 2022

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1434521

26 September 2022

publication date

1 January 1992

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1434521%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1434521%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

15

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1434521%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1434521%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

803-808

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1434521%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

Respiration-deficient cells are caused by a single point mutation in the mitochondrial tRNA-Leu (UUR) gene in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)

1 reference

https://pubmed.ncbi.nlm.nih.gov/1434521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Widespread tissue distribution of mitochondrial DNA deletions in Kearns-Sayre syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1434521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1434521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1434521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Kearns-Sayre syndrome: different amounts of deleted mitochondrial DNA are present in several autoptic tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/1434521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common mitochondrial DNA mutation in the t-RNA(Lys) of patients with myoclonus epilepsy associated with ragged-red fibers

1 reference

https://pubmed.ncbi.nlm.nih.gov/1434521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1434521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1434521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1434521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/1434521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/1434521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1434521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1434521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1434521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MELAS syndrome: Characteristic migrainous and epileptic features and maternal transmission

1 reference

https://pubmed.ncbi.nlm.nih.gov/1434521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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