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Acta Neuropathologica Communications|November 21, 2013
The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer's diseaseLauren D Stutzbach, Sharon X Xie, Adam C Naj, et al.
Archives of Neurology|April 17, 2008
Clinical and neuropathological features of the arctic APP gene mutation causing early-onset Alzheimer diseaseHans Basun, Nenad Bogdanovic, Martin Ingelsson, et al.
Bioinformatics (Oxford, England)|August 15, 2013
DRAW+SneakPeek: analysis workflow and quality metric management for DNA-seq experimentsChiao-Feng Lin, Otto Valladares, D Micah Childress, et al.
American Journal of Human Genetics|July 13, 2004
Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2Ellen M Wijsman, E Warwick Daw, Change-En Yu, et al.
American Journal of Medical Genetics|September 5, 2002
No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA networkBernie Devlin, Pamela Bennett, Edwin H Cook, et al.
Human Genetics|October 22, 2010
Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16Nicola H Chapman, Annette Estes, Jeff Munson, et al.
Annals of Neurology|March 19, 2011
Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotypeSuman Jayadev, David Nochlin, Parvoneh Poorkaj, et al.
Nucleic Acids Research|August 17, 2018
INFERNO: inferring the molecular mechanisms of noncoding genetic variantsAlexandre Amlie-Wolf, Mitchell Tang, Elisabeth E Mlynarski, et al.
Journal of Neurochemistry|September 27, 2003
Alteration in calcium channel properties is responsible for the neurotoxic action of a familial frontotemporal dementia tau mutationKatsutoshi Furukawa, Yue Wang, Pamela J Yao, et al.
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