Edor Kabashi

FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis.

Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansions.

Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders.

Sqstm1 knock-down causes a locomotor phenotype ameliorated by rapamycin in a zebrafish model of ALS/FTLD.

Defining the genetic connection linking amyotrophic lateral sclerosis (ALS) with frontotemporal dementia (FTD).

Depdc5 knockdown causes mTOR-dependent motor hyperactivity in zebrafish.

Transcriptomic Analysis of Zebrafish TDP-43 Transgenic Lines.

Functional Characterization of Neurofilament Light Splicing and Misbalance in Zebrafish.

TDP-43 Regulation of AChE Expression Can Mediate ALS-Like Phenotype in Zebrafish.

Autophagy and ALS: mechanistic insights and therapeutic implications.