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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.Stroke|January 19, 2023
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical HeterogeneityMark K Bakker, Jos P Kanning, Gad Abraham, 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.Pageof 28