Modeling human mitochondrial diseases in flies. - Wikidata - awgldk - TriplyDB

Modeling human mitochondrial diseases in flies.

Modeling human mitochondrial diseases in flies.

http://www.wikidata.org/entity/Q36522081

about

Modeling dietary influences on offspring metabolic programming in Drosophila melanogaster Mitochondrial genome deletions and minicircles are common in lice (Insecta: Phthiraptera)The alternative oxidase AOX does not rescue the phenotype of tko25t mutant flies An inventory of peroxisomal proteins and pathways in Drosophila melanogaster Identification of novel modulators of mitochondrial function by a genome-wide RNAi screen in Drosophila melanogaster Modeling mitochondrial encephalomyopathy in Drosophila.Invertebrate models for coenzyme q10 deficiency.A Drosophila model for the Zellweger spectrum of peroxisome biogenesis disorders.Drosophila melanogaster: An emerging model of transgenerational effects of maternal obesity.Mouse models for mitochondrial diseases.Mislocalization of mitochondria and compromised renal function and oxidative stress resistance in Drosophila SesB mutants.A novel histochemistry assay to assess and quantify focal cytochrome c oxidase deficiency.Feeding difficulties, a key feature of the Drosophila NDUFS4 mitochondrial disease model.

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P2860

Modeling human mitochondrial diseases in flies.

http://www.wikidata.org/entity/Q36522081

description

2006 nî lūn-bûn

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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2006年论文

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2006年论文

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Modeling human mitochondrial diseases in flies.

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Modeling human mitochondrial diseases in flies.

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Modeling human mitochondrial diseases in flies.

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Modeling human mitochondrial diseases in flies.

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Modeling human mitochondrial diseases in flies.

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Modeling human mitochondrial diseases in flies.

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J.BBABIO.2006.05.008

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Biochimica et Biophysica Acta

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Modeling human mitochondrial diseases in flies.

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P2093

Alvaro Sánchez-Martínez

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Cristina Adán

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Laurie S Kaguni

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Miguel Angel Fernández-Moreno

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Ningguang Luo

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Paula Clemente

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Pilar Ochoa

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Rafael Garesse

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Rosana Hernández-Sierra

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P2860

Role of adenine nucleotide translocator 1 in mtDNA maintenance

Targeted gene expression as a means of altering cell fates and generating dominant phenotypes

Shy1p occurs in a high molecular weight complex and is required for efficient assembly of cytochrome c oxidase in yeast.

Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin

Structure-function defects of human mitochondrial DNA polymerase in autosomal dominant progressive external ophthalmoplegia

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

Technical knockout, a Drosophila model of mitochondrial deafness

Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits

Constitutive knockout of Surf1 is associated with high embryonic lethality, mitochondrial disease and cytochrome c oxidase deficiency in mice

Inactivation of the Friedreich ataxia mouse gene leads to early embryonic lethality without iron accumulation

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10.1016/J.BBABIO.2006.05.008

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