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Human Molecular Genetics|January 12, 2013
Loss and gain of Drosophila TDP-43 impair synaptic efficacy and motor control leading to age-related neurodegeneration by loss-of-function phenotypesDanielle C Diaper, Yoshitsugu Adachi, Ben Sutcliffe, et al.
Scientific Reports|December 12, 2025
Increased plasma fibronectin mirrors intimal phenotypic switching of vascular smooth muscle cells in moyamoya arteriopathyCaroline Asselman, Jozefien Meersschaut, Patrick Willems, et al.
American Journal of Human Genetics|September 22, 2005
Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sampleRosa Rademakers, Marc Cruts, Kristel Sleegers, et al.
Acta Neuropathologica Communications|September 24, 2015
Tau phosphorylation regulates the interaction between BIN1's SH3 domain and Tau's proline-rich domainYoann Sottejeau, Alexis Bretteville, François-Xavier Cantrelle, et al.
Epilepsia|May 14, 2016
Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasiaSarah Weckhuysen, Elise Marsan, Virginie Lambrecq, et al.
Scientific Reports|January 24, 2017
Developmental Expression of 4-Repeat-Tau Induces Neuronal Aneuploidy in Drosophila Tauopathy ModelsNicolas Malmanche, Pierre Dourlen, Marc Gistelinck, et al.
Annals of Neurology|May 4, 2004
A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaquesBart Dermaut, Samir Kumar-Singh, Sebastian Engelborghs, et al.
Neurobiology of Aging|December 11, 2007
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALSIlse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, et al.
Orphanet Journal of Rare Diseases|May 23, 2022
Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)Nika Schuermans, Dimitri Hemelsoet, Wim Terryn, et al.
Brain : a Journal of Neurology|February 24, 2006
A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLDJulie van der Zee, Rosa Rademakers, Sebastiaan Engelborghs, et al.
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