Germ-line deletions of mtDNA in mitochondrial myopathy (Q35196394)

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English	Germ-line deletions of mtDNA in mitochondrial myopathy	scientific article

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instance of

scholarly article

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Europe PubMed Central

PubMed publication ID

2014792

retrieved

7 August 2017

title

Germ-line deletions of mtDNA in mitochondrial myopathy (English)

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stated in

Europe PubMed Central

PubMed publication ID

2014792

retrieved

7 August 2017

main subject

mitochondrial myopathy

1 reference

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inferred from title

author name string

Poulton J

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2014792

retrieved

7 August 2017

Deadman ME

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2014792

retrieved

7 August 2017

Ramacharan S

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2014792

retrieved

7 August 2017

Gardiner RM

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2014792

retrieved

7 August 2017

language of work or name

English

0 references

publication date

1 April 1991

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stated in

Europe PubMed Central

PubMed publication ID

2014792

retrieved

7 August 2017

published in

American Journal of Human Genetics

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stated in

Europe PubMed Central

PubMed publication ID

2014792

retrieved

7 August 2017

volume

48

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2014792

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7 August 2017

issue

4

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stated in

Europe PubMed Central

PubMed publication ID

2014792

retrieved

7 August 2017

page(s)

649-653

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Europe PubMed Central

PubMed publication ID

2014792

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7 August 2017

cites work

Sequence and organization of the human mitochondrial genome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682963

retrieved

13 July 2018

Maternal inheritance of human mitochondrial DNA

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682963

retrieved

13 July 2018

The clinical features of mitochondrial myopathy

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682963

retrieved

13 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682963

retrieved

13 July 2018

Nucleotide sequence preservation of human mitochondrial DNA.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682963

retrieved

13 July 2018

Deletion of blood mitochondrial DNA in pancytopenia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682963

retrieved

13 July 2018

Kearns-Sayre syndrome with muscle mitochondrial DNA deletion

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682963

retrieved

13 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682963

retrieved

13 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682963

retrieved

13 July 2018

Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682963

retrieved

13 July 2018

Heteroplasmy of mitochondrial genomes in clonal cultures from patients with Kearns-Sayre syndrome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682963

retrieved

13 July 2018

Unequal partitioning of bovine mitochondrial genotypes among siblings

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682963

retrieved

13 July 2018

A new mitochondrial disease associated with mitochondrial DNA heteroplasmy

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682963

retrieved

13 July 2018

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682963

retrieved

13 July 2018

The origins of replication of the yeast mitochondrial genome and the phenomenon of suppressivity

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682963

retrieved

26 September 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682963

retrieved

15 November 2018

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/2014792

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/2014792

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2014792

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2014792

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1682963

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2014792

retrieved

7 August 2017

PubMed publication ID

2014792

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2014792

retrieved

7 August 2017

 

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