(Q70765918)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8513327%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

title

A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies (English)

1 reference

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13 October 2019

2

Sweeney MG

1 reference

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13 October 2019

John A. Morgan-Hughes

4

object named as

Morgan-Hughes JA

1 reference

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13 October 2019

author name string

Brockington M

1

1 reference

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13 October 2019

Hammans SR

3

1 reference

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13 October 2019

Harding AE

5

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13 October 2019

publication date

1 May 1993

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13 October 2019

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8513327%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

volume

4

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13 October 2019

issue

1

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13 October 2019

page(s)

67-71

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https://scigraph.springernature.com/pub.10.1038/ng0593-67

13 October 2019

exact match

0 references

cites work

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

A molecular genetic study of focal histochemical defects in mitochondrial encephalomyopathies

1 reference

7 January 2021

Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions

1 reference

7 January 2021

Duplications of mitochondrial DNA in mitochondrial myopathy

1 reference

7 January 2021

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

1 reference

7 January 2021

PCR analysis of platelet mtDNA: lack of specific changes in Parkinson's disease

1 reference

7 January 2021

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

1 reference

7 January 2021

Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy

1 reference

7 January 2021

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

1 reference

7 January 2021

Sequence and organization of the human mitochondrial genome

1 reference

7 January 2021

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

1 reference

7 January 2021

Nuclear gadgets in mitochondrial DNA replication and transcription

1 reference

7 January 2021

Length heterogeneity of a conserved displacement-loop sequence in human mitochondrial DNA.

1 reference

7 January 2021

Initiation of transcription from each of the two human mitochondrial promoters requires unique nucleotides at the transcriptional start sites

1 reference

7 January 2021

Identification of transcriptional regulatory elements in human mitochondrial DNA by linker substitution analysis

1 reference

7 January 2021

Nucleus-driven mutations of human mitochondrial DNA

1 reference

7 January 2021

Families of mtDNA re-arrangements can be detected in patients with mtDNA deletions: duplications may be a transient intermediate form.

1 reference

7 January 2021

DNA sequencing with chain-terminating inhibitors

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG0593-67

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8513327%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference