SOD1 activity threshold and TOR signalling modulate VAP(P58S) aggregation via reactive oxygen species-induced proteasomal degradation in a Drosophila model of amyotrophic lateral sclerosis

Familial amyotrophic lateral sclerosis (ALS) is an incurable, late-onset motor neuron disease, linked strongly to various causative genetic loci. ALS8 codes for a missense mutation, P56S, in VAMP-associated protein B (VAPB) that causes the protein to misfold and form cellular aggregates. Uncovering...

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Main Authors: Kriti Chaplot (Author), Lokesh Pimpale (Author), Balaji Ramalingam (Author), Senthilkumar Deivasigamani (Author), Siddhesh S. Kamat (Author), Girish S. Ratnaparkhi (Author)
Format: Book
Published: The Company of Biologists, 2019-02-01T00:00:00Z.
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