Mutations in cytochrome c oxidase subunit VIa cause neurodegeneration and motor dysfunction in Drosophila
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Mitochondrial cytochrome c oxidase deficiencySDHAF4 promotes mitochondrial succinate dehydrogenase activity and prevents neurodegeneration.Mitochondrial ROS and the Effectors of the Intrinsic Apoptotic Pathway in Aging Cells: The Discerning Killers!The ubiquitin-proteasome system in spongiform degenerative disordersBacteria, yeast, worms, and flies: exploiting simple model organisms to investigate human mitochondrial diseasesA cytoplasmic suppressor of a nuclear mutation affecting mitochondrial functions in Drosophila.Maintaining the brain: insight into human neurodegeneration from Drosophila melanogaster mutantsGenetic analysis in Drosophila reveals a role for the mitochondrial protein p32 in synaptic transmissionMitochondrial dysfunction precedes neurodegeneration in mahogunin (Mgrn1) mutant miceSevere infantile encephalomyopathy caused by a mutation in COX6B1, a nucleus-encoded subunit of cytochrome c oxidase.Expression of alternative oxidase in Drosophila ameliorates diverse phenotypes due to cytochrome oxidase deficiency.Engineering the alternative oxidase gene to better understand and counteract mitochondrial defects: state of the art and perspectives.Potassium channels in Drosophila: historical breakthroughs, significance, and perspectives.A mutation in Drosophila Aldolase causes temperature-sensitive paralysis, shortened lifespan, and neurodegeneration.LACK, a RACK1 ortholog, facilitates cytochrome c oxidase subunit expression to promote Leishmania major fitness.In utero and lactational exposure to low-doses of the pyrethroid insecticide cypermethrin leads to neurodevelopmental defects in male mice-An ethological and transcriptomic study.Inhibition of delayed rectifier potassium channels and induction of arrhythmia: a novel effect of celecoxib and the mechanism underlying it.Mito-Nuclear Interactions Affecting Lifespan and Neurodegeneration in a Drosophila Model of Leigh Syndrome.Early life benefits and later life costs of a two amino acid deletion in Drosophila simulans.
P2860
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P2860
Mutations in cytochrome c oxidase subunit VIa cause neurodegeneration and motor dysfunction in Drosophila
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Mutations in cytochrome c oxid ...... otor dysfunction in Drosophila
@ast
Mutations in cytochrome c oxid ...... otor dysfunction in Drosophila
@en
type
label
Mutations in cytochrome c oxid ...... otor dysfunction in Drosophila
@ast
Mutations in cytochrome c oxid ...... otor dysfunction in Drosophila
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prefLabel
Mutations in cytochrome c oxid ...... otor dysfunction in Drosophila
@ast
Mutations in cytochrome c oxid ...... otor dysfunction in Drosophila
@en
P2093
P2860
P1433
P1476
Mutations in cytochrome c oxid ...... otor dysfunction in Drosophila
@en
P2093
Alan J Siegel
Gunisha Kaur
Jeffery Benjamin
Patricia B Getman
Radhakrishnan Gnanasambandam
Randall D Shortridge
Satpal Singh
Wensheng Liu
P2860
P304
P356
10.1534/GENETICS.107.071688
P407
P577
2007-04-15T00:00:00Z