(Q34312609)

English

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

scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

mitochondrial DNA

0 references

author name string

J M Shoffner

1

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

M T Lott

2

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

A S Voljavec

3

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

S A Soueidan

4

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

D A Costigan

5

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

D C Wallace

6

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

language of work or name

0 references

publication date

1 October 1989

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

86

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

20

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

7952-7956

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Sequence and gene organization of mouse mitochondrial DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

Sequence and organization of the human mitochondrial genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

Complete sequence of bovine mitochondrial DNA. Conserved features of the mammalian mitochondrial genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

The frequency of matching sequences in DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

A comprehensive sequence analysis program for the IBM personal computer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

Characterization of mitochondrial DNA in chloramphenicol-resistant interspecific hybrids and a cybrid

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

Replication of animal mitochondrial DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

The complete nucleotide sequence of the Xenopus laevis mitochondrial genome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

Improvement of abnormal pyruvate metabolism and cardiac conduction defect with coenzyme Q10 in Kearns-Sayre syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

Deletions of mitochondrial DNA in Kearns-Sayre syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

DNA sequencing with Thermus aquaticus DNA polymerase and direct sequencing of polymerase chain reaction-amplified DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

Deletion of blood mitochondrial DNA in pancytopenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

Kearns-Sayre syndrome with muscle mitochondrial DNA deletion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with recurrent abdominal symptoms and coenzyme Q10 administration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

Mitochondrial DNA deletion in Pearson's marrow/pancreas syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

6 July 2018

Antioxidative effect of ubiquinones on mitochondrial membranes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298190

28 October 2018

Treatment of Kearns-Sayre syndrome with coenzyme Q10

1 reference

https://pubmed.ncbi.nlm.nih.gov/2554297

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical improvement after administration of coenzyme Q10 in a patient with mitochondrial encephalomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2554297

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2554297

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heteroplasmy in mice with deletion of a large coding region of mitochondrial DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/2554297

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and biochemical correlations in mitochondrial myopathies treated with coenzyme Q10

1 reference

https://pubmed.ncbi.nlm.nih.gov/2554297

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions of muscle mitochondrial DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/2554297

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2554297

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/2554297

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identical mitochondrial DNA deletion in blood and muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/2554297

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.86.20.7952

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

1989PNAS...86.7952S

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

ResearchGate publication ID

0 references

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