Deletions of the mitochondrial genome (Q35848675)

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scientific article published on January 1, 1992

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Language	Label	Description	Also known as
English	Deletions of the mitochondrial genome	scientific article published on January 1, 1992

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528008

retrieved

10 August 2017

review article

1 reference

stated in

Europe PubMed Central

title

Deletions of the mitochondrial genome (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528008

retrieved

10 August 2017

main subject

chromosomal deletion syndrome

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528008

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1528008

retrieved

5 October 2022

author name string

A. E. Harding

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528008

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1528008

retrieved

5 October 2022

S. R. Hammans

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528008

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1528008

retrieved

5 October 2022

language of work or name

English

1 reference

stated in

National Center for Biotechnology Information

PubMed publication ID

1528008

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1528008

retrieved

5 October 2022

publication date

1 January 1992

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528008

retrieved

10 August 2017

published in

Journal of Inherited Metabolic Disease

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528008

retrieved

10 August 2017

volume

15

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528008

retrieved

10 August 2017

issue

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528008

retrieved

10 August 2017

page(s)

480-486

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528008

retrieved

10 August 2017

cites work

Replication-competent human mitochondrial DNA lacking the heavy-strand promoter region

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1007%2FBF01799606

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1007%2FBF01799606

retrieved

21 January 2018

Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial myopathy: a genetic study of 71 cases

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germ-line deletions of mtDNA in mitochondrial myopathy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Different copy numbers of apparently identically deleted mitochondrial DNA in tissues from a patient with Kearns-Sayre syndrome detected by PCR.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial inheritance in a mitochondrially mediated disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA polymorphism in mitochondrial myopathy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular insight into the asymmetric distribution of pathogenetic human mitochondrial DNA deletions

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions of muscle mitochondrial DNA in mitochondrial myopathies: sequence analysis and possible mechanisms.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial complex I deficiency in Parkinson's disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions of mitochondrial DNA in Kearns-Sayre syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscle development in the human fetus as exemplified by m. sartorius: a quantitative study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The clinical features of mitochondrial myopathy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative determination of deleted mitochondrial DNA relative to normal DNA in parkinsonian striatum by a kinetic PCR analysis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA analysis in Parkinson's disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial myopathies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A molecular genetic study of focal histochemical defects in mitochondrial encephalomyopathies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duplications of mitochondrial DNA in mitochondrial myopathy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biogenesis of mitochondria

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528008

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF01799606

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528008

retrieved

10 August 2017

PubMed publication ID

1528008

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528008

retrieved

10 August 2017

 

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