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Annals of Neurology|February 22, 2008
TDP-43 A315T mutation in familial motor neuron diseaseMichael A Gitcho, Robert H Baloh, Sumi Chakraverty, et al.
Nature Biomedical Engineering|April 10, 2019
Comparison of three congruent patient-specific cell types for the modelling of a human genetic Schwann-cell disorderBipasha Mukherjee-Clavin, Ruifa Mi, Barbara Kern, et al.
Science Translational Medicine|October 25, 2013
Targeting RNA foci in iPSC-derived motor neurons from ALS patients with a C9ORF72 repeat expansionDhruv Sareen, Jacqueline G O'Rourke, Pratap Meera, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 3, 2023
MAPK/MAK/MRK overlapping kinase (MOK) controls microglial inflammatory/type-I IFN responses via Brd4 and is involved in ALSJesús A Pérez-Cabello, Lucía Silvera-Carrasco, Jaime M Franco, et al.
American Journal of Human Genetics|November 12, 2013
A dominant mutation in FBXO38 causes distal spinal muscular atrophy with calf predominanceCharlotte J Sumner, Constantin d'Ydewalle, Joe Wooley, et al.
Neuron|June 16, 2021
C9orf72 deficiency promotes microglial-mediated synaptic loss in aging and amyloid accumulationDeepti Lall, Ileana Lorenzini, Thomas A Mota, et al.
Neurology|March 10, 2019
Revised Airlie House consensus guidelines for design and implementation of ALS clinical trialsLeonard H van den Berg, Eric Sorenson, Gary Gronseth, et al.
Neuron|December 6, 2015
C9orf72 BAC Transgenic Mice Display Typical Pathologic Features of ALS/FTDJacqueline G O'Rourke, Laurent Bogdanik, A K M G Muhammad, et al.
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