Drosophila expressing human SOD1 successfully recapitulates mitochondrial phenotypic features of familial amyotrophic lateral sclerosis
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文摘

Expression of SOD1G93A in Drosophila thoracic muscles causes FALS phenotype.

24B-GAL4-SOD1G93A flies show impaired motor behavior and decreased lifespan.

24B-GAL4-SOD1G93A flies successful mimic mitochondrial dysfunction in FALS.

24B-GAL4-SOD1G93A represents novel therapeutic opportunities in FALS.

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