(Q52558334)

3 May 2018

title

Biochemical and molecular consequences of massive mitochondrial gene loss in different tissues of a mutant strain of Drosophila subobscura. (English)

1 reference

3 May 2018

main subject

Drosophila subobscura

object named as

Drosophila subobscura

1 reference

1 reference

Béziat F

1

1 reference

3 May 2018

Touraille S

2

1 reference

3 May 2018

Debise R

3

1 reference

3 May 2018

Morel F

4

1 reference

3 May 2018

Petit N

5

1 reference

3 May 2018

Lécher P

6

1 reference

3 May 2018

Alziari S

7

1 reference

3 May 2018

language of work or name

English

0 references

publication date

1 September 1997

1 reference

3 May 2018

Journal of Biological Chemistry

published in

1 reference

3 May 2018

volume

272

1 reference

3 May 2018

issue

36

1 reference

3 May 2018

page(s)

22583-22590

1 reference

3 May 2018

Mitochondrial DNA sequence variation in human evolution and disease.

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

Mitochondrial DNA mutations in human degenerative diseases and aging

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

Complementation and segregation behavior of disease-causing mitochondrial DNA mutations in cellular model systems

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

An autosomal locus predisposing to deletions of mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

Stable heteroplasmy for a large-scale deletion in the coding region of Drosophila subobscura mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

Mitochondrial genome expression in a mutant strain of D. subobscura, an animal model for large scale mtDNA deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

Biochemical consequences of a large deletion in the mitochondrial genome of a Drosophila subobscura strain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

Tissular distribution of heteroplasmy and ultrastructural studies of mitochondria from a Drosophila subobscura mitochondrial deletion mutant.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

Kearns-Sayre syndrome: different amounts of deleted mitochondrial DNA are present in several autoptic tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

In vitro incorporation of (35S)-methionine in mitochondrial proteins of Drosophila melanogaster.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

7 Preparation and properties of dihydroubiquinone: Cytochrome c oxidoreductase (complex III)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

8 Preparation and properties of complex IV (Ferrocytochrome c: Oxygen oxidoreductase EC 1.9.3.1)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

Rearranged mitochondrial genomes are present in human oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

The pattern of transcription of the human mitochondrial rRNA genes reveals two overlapping transcription units

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

A site-specific deletion in mitochondrial DNA of Podospora is under the control of nuclear genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

KEARNS-SAYRE SYNDROME WITH MUSCLE MITOCHONDRIAL DNA DELETION

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

Mitochondrial encephalomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

Preparation and properties of NADH: ubiquinone oxidoreductase (complexI), EC 1.6.5.3

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

A sensitive colorimetric assay for mitochondrial alpha-glycerophosphate dehydrogenase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

A luminometric method for the determination of ATP and phosphocreatine in single human skeletal muscle fibres

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.36.22583

21 January 2018

Identifiers

DOI

10.1074/JBC.272.36.22583

1 reference

3 May 2018

1 reference

3 May 2018