Chen Eitan
Rehovot, M 76100, Israel
Last Updated: 09/26/2026
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Found 10 publications
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis.
Journal: Neuron
Published: July 07, 2021
Rare variant burden analysis within enhancers identifies CAV1 as an ALS risk gene.
Journal: Cell reports
Published: February 03, 2021
Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk Gene.
Journal: Cell reports
Published: May 13, 2020
Spatiotemporal Proteomic Analysis of Stress Granule Disassembly Using APEX Reveals Regulation by SUMOylation and Links to ALS Pathogenesis.
Journal: Molecular cell
Published: January 31, 2020
Human genetics and neuropathology suggest a link between miR-218 and amyotrophic lateral sclerosis pathophysiology.
Journal: Science translational medicine
Published: September 26, 2018
CNS repair requires both effector and regulatory T cells with distinct temporal and spatial profiles.
Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience
Published: August 01, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026