Expression of alternative oxidase in Drosophila ameliorates diverse phenotypes due to cytochrome oxidase deficiency. - Test2 - elhamkhani - TriplyDB

Expression of alternative oxidase in Drosophila ameliorates diverse phenotypes due to cytochrome oxidase deficiency.

Expression of alternative oxidase in Drosophila ameliorates diverse phenotypes due to cytochrome oxidase deficiency.

http://www.wikidata.org/entity/Q37649092

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Mitochondrial cytochrome c oxidase deficiency Practical Recommendations for the Use of the GeneSwitch Gal4 System to Knock-Down Genes in Drosophila melanogaster Phenotypic rescue of a Drosophila model of mitochondrial ANT1 disease.Expression of Ciona intestinalis AOX causes male reproductive defects in Drosophila melanogaster The alternative oxidase AOX does not rescue the phenotype of tko25t mutant flies Genetic mosaic analysis of a deleterious mitochondrial DNA mutation in Drosophila reveals novel aspects of mitochondrial regulation and function.Mitochondrial Dysfunction Plus High-Sugar Diet Provokes a Metabolic Crisis That Inhibits Growth β carbonic anhydrase is required for female fertility in Drosophila melanogaster.Diiron centre mutations in Ciona intestinalis alternative oxidase abolish enzymatic activity and prevent rescue of cytochrome oxidase deficiency in flies Ligand-Bound GeneSwitch Causes Developmental Aberrations in Drosophila that Are Alleviated by the Alternative Oxidase Broad AOX expression in a genetically tractable mouse model does not disturb normal physiology.Rare variants in drug target genes contributing to complex diseases, phenome-wide.Developmental arrest in Drosophila melanogaster caused by mitochondrial DNA replication defects cannot be rescued by the alternative oxidase

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P2860

Expression of alternative oxidase in Drosophila ameliorates diverse phenotypes due to cytochrome oxidase deficiency.

http://www.wikidata.org/entity/Q37649092

description

2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年學術文章

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name

Expression of alternative oxid ...... cytochrome oxidase deficiency.

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Expression of alternative oxid ...... cytochrome oxidase deficiency.

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type

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Expression of alternative oxid ...... cytochrome oxidase deficiency.

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Expression of alternative oxid ...... cytochrome oxidase deficiency.

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Expression of alternative oxid ...... cytochrome oxidase deficiency.

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Expression of alternative oxid ...... cytochrome oxidase deficiency.

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Human Molecular Genetics

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Expression of alternative oxid ...... cytochrome oxidase deficiency.

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Akbar Zeb

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Anna Popplestone

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Ashwin Sriram

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Juho Rinne

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Kia K Kemppainen

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Matti Lakanmaa

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Pierre Rustin

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Satpal Singh

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Tea Tuomela

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P2860

SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome

Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene

A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency

NDUFA4 is a subunit of complex IV of the mammalian electron transport chain

Cytochrome c oxidase subassemblies in fibroblast cultures from patients carrying mutations in COX10, SCO1, or SURF1

Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial disease

Human mtDNA haplogroups associated with high or reduced spermatozoa motility

Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics.

Age-associated mosaic respiratory chain deficiency causes trans-neuronal degeneration

Identification of a protein mediating respiratory supercomplex stability

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2078-2093

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