The nuclear genome is involved in heteroplasmy control in a mitochondrial mutant strain of Drosophila subobscura (Q43887789)

27 November 2017

title

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

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27 November 2017

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Drosophila subobscura

object named as

Drosophila subobscura

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Géraldine Farge

1

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27 November 2017

Sylvie Touraille

2

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27 November 2017

Samuel Le Goff

3

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27 November 2017

Nathalie Petit

4

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27 November 2017

Monique Renoux

5

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27 November 2017

Frédéric Morel

6

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27 November 2017

Serge Alziari

7

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27 November 2017

language of work or name

English

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publication date

1 February 2002

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27 November 2017

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27 November 2017

volume

269

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27 November 2017

issue

3

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27 November 2017

page(s)

998-1005

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Mitochondrial diseases in man and mouse

27 November 2017

cites work

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Mitochondrial defects in cardiomyopathy and neuromuscular disease

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

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

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

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

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An autosomal locus predisposing to deletions of mitochondrial DNA

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

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Role of adenine nucleotide translocator 1 in mtDNA maintenance

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

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

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

21 January 2018

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

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

21 January 2018

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

21 January 2018

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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

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Duplications of mitochondrial DNA in mitochondrial myopathy

21 January 2018

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Replication of animal mitochondrial DNA.

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

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

21 January 2018

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Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

21 January 2018

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21 January 2018

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21 January 2018

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

21 January 2018

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Mammalian mitochondria possess homologous DNA recombination activity

21 January 2018

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

21 January 2018

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Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

21 January 2018

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21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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10.1046/J.0014-2956.2001.02737.X

21 January 2018

Identifiers

DOI

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27 November 2017

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