(Q57420563)

English

Detection of Mitochondrial DNA Deletions in Human Skin Fibroblasts of Patients with Pearson's Syndrome by Two-color Fluorescence In Situ Hybridization

article by Mariëtte P.C. van de Corput et al published January 1997 in Journal of Histochemistry and Cytochemistry

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scholarly article

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Detection of Mitochondrial DNA Deletions in Human Skin Fibroblasts of Patients with Pearson's Syndrome by Two-color Fluorescence In Situ Hybridization (English)

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mitochondrial DNA

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1 reference

based on heuristic

inferred from title

object named as

Anton K. Raap

7

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author name string

Mariëtte P.C. van de Corput

1

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Johannes M.W. van den Ouweland

2

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Roeland W. Dirks

3

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Leen M. ‘t Hart

4

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G. Jan. Bruining

5

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J. Antonie Maassen

6

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publication date

January 1997

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Journal of Histochemistry and Cytochemistry

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45

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55-61

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1

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Sequence and organization of the human mitochondrial genome

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https://api.crossref.org/works/10.1177%2F002215549704500108

21 January 2018

Molecular basis of mitochondrial DNA disease

1 reference

https://api.crossref.org/works/10.1177%2F002215549704500108

21 January 2018

Replication of animal mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1177%2F002215549704500108

21 January 2018

A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues

1 reference

https://api.crossref.org/works/10.1177%2F002215549704500108

21 January 2018

Myopathology and a mitochondrial DNA deletion in the Pearson marrow and pancreas syndrome

1 reference

https://api.crossref.org/works/10.1177%2F002215549704500108

21 January 2018

Maternal inheritance of human mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1177%2F002215549704500108

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1177%2F002215549704500108

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1177%2F002215549704500108

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1177%2F002215549704500108

21 January 2018

Mitochondrial DNA diseases: histological and cellular studies

1 reference

https://api.crossref.org/works/10.1177%2F002215549704500108

21 January 2018

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

1 reference

https://api.crossref.org/works/10.1177%2F002215549704500108

21 January 2018

Mitochondrial DNA mutations in diseases of energy metabolism

1 reference

https://api.crossref.org/works/10.1177%2F002215549704500108

21 January 2018

Diseases of the mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1177%2F002215549704500108

21 January 2018

Mitochondrial DNA mutations and neuromuscular disease

1 reference

https://api.crossref.org/works/10.1177%2F002215549704500108

21 January 2018

Identifiers

10.1177/002215549704500108

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