Associated Papers
Amyotrophic Lateral Sclerosis Modifiers in Drosophila Reveal the Phospholipase D Pathway as a Potential Therapeutic Target.
Kankel MW et al.
Genetics, 2020
Understanding the role of TDP-43 and FUS/TLS in ALS and beyond.
Da Cruz S et al.
Current Opinion in Neurobiology, 2011
Cytoplasmic mislocalization of TDP-43 is toxic to neurons and enhanced by a mutation associated with familial amyotrophic lateral sclerosis.
Barmada SJ et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience, 2010
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