(Q43887789)

27 November 2017

title

The nuclear genome is involved in heteroplasmy control in a mitochondrial mutant strain of Drosophila subobscura (English)

1 reference

27 November 2017

0 references

1 reference

Drosophila subobscura

object named as

Drosophila subobscura

1 reference

Géraldine Farge

1

1 reference

27 November 2017

Sylvie Touraille

2

1 reference

27 November 2017

Samuel Le Goff

3

1 reference

27 November 2017

Nathalie Petit

4

1 reference

27 November 2017

Monique Renoux

5

1 reference

27 November 2017

Frédéric Morel

6

1 reference

27 November 2017

Serge Alziari

7

1 reference

27 November 2017

language of work or name

English

0 references

publication date

1 February 2002

1 reference

27 November 2017

1 reference

27 November 2017

volume

269

1 reference

27 November 2017

issue

3

1 reference

27 November 2017

page(s)

998-1005

1 reference

Mitochondrial diseases in man and mouse

27 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Mitochondrial genetics and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Mitochondrial defects in cardiomyopathy and neuromuscular disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Families of mtDNA re-arrangements can be detected in patients with mtDNA deletions: duplications may be a transient intermediate form.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

An autosomal locus predisposing to deletions of mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

A third locus predisposing to multiple deletions of mtDNA in autosomal dominant progressive external ophthalmoplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Role of adenine nucleotide translocator 1 in mtDNA maintenance

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

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/10.1046%2FJ.0014-2956.2001.02737.X

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/10.1046%2FJ.0014-2956.2001.02737.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

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/10.1046%2FJ.0014-2956.2001.02737.X

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/10.1046%2FJ.0014-2956.2001.02737.X

Quantitative analysis, by ultrastructural in situ hybridization, of mitochondrial genomes and their expression in mid-gut and ovarian cells of a mutant strain of Drosophila subobscura.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Developmental changes in heteroplasmy level and mitochondrial gene expression in a Drosophila subobscura mitochondrial deletion mutant.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

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/10.1046%2FJ.0014-2956.2001.02737.X

Duplications of mitochondrial DNA in mitochondrial myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Replication of animal mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Mitochondrial DNA maintenance in vertebrates

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Mitochondrial DNA repair pathways.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Repair of mtDNA in vertebrates

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Maintenance and integrity of the mitochondrial genome: a plethora of nuclear genes in the budding yeast

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Mammalian mitochondria possess homologous DNA recombination activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

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/10.1046%2FJ.0014-2956.2001.02737.X

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Construction of transgenic mice with tissue-specific acceleration of mitochondrial DNA mutagenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Homologous and heterologous expression of a ribosomal protein gene in Podospora anserina requires an intron

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

Do sequence variants in the major non-coding region of the mitochondrial genome influence mitochondrial mutations associated with disease?

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0014-2956.2001.02737.X

10.1046/J.0014-2956.2001.02737.X

21 January 2018

Identifiers

DOI

1 reference

27 November 2017

1 reference