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Modes of metabolic compensation during mitochondrial disease using the Drosophila model of ATP6 dysfunctionGenetically encoded redox sensor identifies the role of ROS in degenerative and mitochondrial disease pathogenesisSmall mitochondrial-targeted RNAs modulate endogenous mitochondrial protein expression in vivo.The alternative oxidase AOX does not rescue the phenotype of tko25t mutant fliesThe ATP-sensitive K channel is seizure protective and required for effective dietary therapy in a model of mitochondrial encephalomyopathy.
P2860
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article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 21 May 2010
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Modeling mitochondrial encephalomyopathy in Drosophila.
@en
Modeling mitochondrial encephalomyopathy in Drosophila.
@nl
type
label
Modeling mitochondrial encephalomyopathy in Drosophila.
@en
Modeling mitochondrial encephalomyopathy in Drosophila.
@nl
prefLabel
Modeling mitochondrial encephalomyopathy in Drosophila.
@en
Modeling mitochondrial encephalomyopathy in Drosophila.
@nl
P2860
P1476
Modeling mitochondrial encephalomyopathy in Drosophila.
@en
P2093
Michael J Palladino
P2860
P356
10.1016/J.NBD.2010.05.009
P577
2010-05-21T00:00:00Z