(Q71925303)

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

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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: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

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22 October 2019

author name string

C Sewry

2

1 reference

Europe PubMed Central

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22 October 2019

C G Potter

3

1 reference

Europe PubMed Central

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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

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22 October 2019

D Chretien

5

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22 October 2019

F A Wijburg

6

1 reference

Europe PubMed Central

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22 October 2019

K J Morten

7

1 reference

Europe PubMed Central

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22 October 2019

G Brown

8

1 reference

Europe PubMed Central

PubMed publication ID

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22 October 2019

publication date

1 January 1995

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Europe PubMed Central

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22 October 2019

Journal of Inherited Metabolic Disease

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Europe PubMed Central

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22 October 2019

18

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22 October 2019

1

1 reference

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22 October 2019

4-20

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22 October 2019

https://scigraph.springernature.com/pub.10.1007/bf00711367

0 references

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

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