(Q34313597)

1 August 2017

Directly repeated sequences associated with pathogenic mitochondrial DNA deletions (English)

1 reference

1 August 2017

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D R Johns

1

1 reference

1 August 2017

S L Rutledge

series ordinal

2

1 reference

1 August 2017

O C Stine

series ordinal

3

1 reference

1 August 2017

O Hurko

series ordinal

4

1 reference

1 August 2017

language of work or name

English

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publication date

1 October 1989

1 reference

Proceedings of the National Academy of Sciences of the United States of America

1 August 2017

1 reference

1 August 2017

86

1 reference

1 August 2017

8059-8062

1 reference

1 August 2017

20

1 reference

Sequence and organization of the human mitochondrial genome

1 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298214

The structure and evolution of the human beta-globin gene family

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298214

Deficiency of the iron-sulfur clusters of mitochondrial reduced nicotinamide-adenine dinucleotide-ubiquinone oxidoreductase (complex I) in an infant with congenital lactic acidosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298214

Interspecific recombination of mitochondrial DNA molecules in hybrid somatic cells

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298214

Hypervariable 'minisatellite' regions in human DNA.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298214

Alu-Alu recombination deletes splice acceptor sites and produces secreted low density lipoprotein receptor in a subject with familial hypercholesterolemia.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298214

The clinical features of mitochondrial myopathy.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298214

Tandem duplications in animal mitochondrial DNAs: variation in incidence and gene content among lizards

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298214

Deletions of mitochondrial DNA in Kearns-Sayre syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298214

DNA typing from single hairs

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298214

Genetic studies on the Senegal population. I. Mitochondrial DNA polymorphisms

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298214

Kearns-Sayre syndrome with muscle mitochondrial DNA deletion

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298214

A deletion involving Alu sequences in the beta-hexosaminidase alpha-chain gene of French Canadians with Tay-Sachs disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298214

A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298214

Intrachromosomal gene conversion in yeast

6 July 2018

1 reference

12 December 2020

On the formation of spontaneous deletions: The importance of short sequence homologies in the generation of large deletions

1 reference

12 December 2020

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

12 December 2020

Deletions of muscle mitochondrial DNA

1 reference

12 December 2020

Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy

1 reference

12 December 2020

Two distinct mechanisms for deletion in mitochondrial DNA of Schizosaccharomyces pombe mutator strains. Slipped mispairing mediated by direct repeats and erroneous intron splicing

1 reference

12 December 2020

MTTOCHONDRIAL DNA DELETION IN ENCEPHALOMYOPATHY

1 reference

12 December 2020

Kearns-Sayre syndrome: biochemical studies of mitochondrial metabolism

1 reference

12 December 2020

Mitochondrial genetics. I. Methodology and phenomenology

1 reference

12 December 2020

Mitochondrial genetics. 3. Recombined molecules of mitochondrial DNA obtained from crosses between cytoplasmic petite mutants of Saccharomyces cerevisiae: physical and genetic characterization

1 reference

12 December 2020

Identical mitochondrial DNA deletion in blood and muscle

1 reference

12 December 2020

Structure of chi hotspots of generalized recombination

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.86.20.8059

1 reference

1 August 2017

0 references

1 reference

1 August 2017

1 reference