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Nature Communications|January 20, 2016
Genomic signals of migration and continuity in Britain before the Anglo-SaxonsRui Martiniano, Anwen Caffell, Malin Holst, et al.
Neurobiology of Aging|November 15, 2011
VCP mutations in familial and sporadic amyotrophic lateral sclerosisMax Koppers, Marka M van Blitterswijk, Lotte Vlam, et al.
Archives of Neurology|April 15, 2009
Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromesFrans Brugman, Jan H Veldink, Hessel Franssen, et al.
Human Molecular Genetics|May 18, 2013
ALS-associated mutations in FUS disrupt the axonal distribution and function of SMNEwout J N Groen, Katsumi Fumoto, Anna M Blokhuis, et al.
Genome Biology|April 30, 2020
ExpansionHunter Denovo: a computational method for locating known and novel repeat expansions in short-read sequencing dataEgor Dolzhenko, Mark F Bennett, Phillip A Richmond, et al.
Nature Communications|August 8, 2018
Genome-wide identification of directed gene networks using large-scale population genomics dataRené Luijk, Koen F Dekkers, Maarten van Iterson, et al.
Acta Neuropathologica|May 12, 2016
Comparative interactomics analysis of different ALS-associated proteins identifies converging molecular pathwaysAnna M Blokhuis, Max Koppers, Ewout J N Groen, et al.
Stroke|March 31, 2016
RNA Sequencing Analysis of Intracranial Aneurysm Walls Reveals Involvement of Lysosomes and Immunoglobulins in RuptureRachel Kleinloog, Bon H Verweij, Pieter van der Vlies, et al.
Cell Reports|December 2, 2020
Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk GeneJohnathan Cooper-Knock, Sai Zhang, Kevin P Kenna, et al.
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