Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome (Q71925303)

From Wikidata

Jump to navigation Jump to search

scientific article published on 01 January 1995

Language	Label	Description	Also known as
English	Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome	scientific article published on 01 January 1995

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7623440%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7623440%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

mitochondrial myopathy

1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7623440%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

author name string

C Sewry

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7623440%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

C G Potter

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7623440%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

T Bougeron

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7623440%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

D Chretien

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7623440%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

F A Wijburg

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7623440%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

K J Morten

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7623440%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

G Brown

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7623440%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

publication date

1 January 1995

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7623440%20AND%20SRC:MED&resulttype=core&format=json

22 October 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:7623440%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

18

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7623440%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7623440%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

4-20

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7623440%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Sequence and organization of the human mitochondrial genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantification of specific mRNA by flatbed scintillation counting of dual-labeled dot blots

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic sequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscle mitochondrial density after exhaustive exercise in dogs: prolonged restricted activity and retraining.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the committee on human mitochondrial DNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

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/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure and variation of human ribosomal DNA: molecular analysis of cloned fragments

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital myotonic dystrophy: fiber type abnormalities in two cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The maturation of the inner membrane of foetal rat liver mitochondria

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defects of the mitochondrial respiratory chain complexes in three pediatric cases with hypotonia and cardiac involvement

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: A new approach to the study of mitochondrial myopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replication and Transcription of Vertebrate Mitochondrial DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fatal infantile liver failure associated with mitochondrial DNA depletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Accumulation of deletions in human mitochondrial DNA during normal aging: analysis by quantitative PCR

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Changes in volume densities and distribution of mitochondria in rat skeletal muscle after chronic hypoxia

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletion.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duplications of mitochondrial DNA in mitochondrial myopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytochrome c in Normal and Hypertrophied Heart

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deoxyribonucleic acid synthesis in the heart mitochondria after acute and exhaustive exercise

1 reference

https://pubmed.ncbi.nlm.nih.gov/7623440

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00711367

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7623440%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7623440%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q71925303&oldid=2221659217"