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Molecular and Cellular Biology|July 25, 2018
An Alzheimer's Disease-Linked Loss-of-Function CLN5 Variant Impairs Cathepsin D Maturation, Consistent with a Retromer Trafficking DefectYasir H Qureshi, Vivek M Patel, Diego E Berman, et al.
Neurogenetics|October 18, 2007
Age-at-onset linkage analysis in Caribbean Hispanics with familial late-onset Alzheimer's diseaseJoseph H Lee, Sandra Barral, Rong Cheng, et al.
Annals of Neurology|June 24, 2015
Rare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies lociBadri N Vardarajan, Mahdi Ghani, Amanda Kahn, et al.
Neurology. Genetics|August 31, 2017
Ultra-rare mutations in SRCAP segregate in Caribbean Hispanic families with Alzheimer diseaseBadri N Vardarajan, Giuseppe Tosto, Roger Lefort, et al.
Biorxiv : the Preprint Server for Biology|January 23, 2024
Rare genetic variation in Fibronectin 1 ( FN1 ) protects against APOEe4 in Alzheimer's diseasePrabesh Bhattarai, Tamil Iniyan Gunasekaran, Dolly Reyes-Dumeyer, et al.
Medrxiv : the Preprint Server for Health Sciences|June 6, 2025
Single-nucleus multiomics in brains from Hispanic individuals reveal APOE-ε4 -driven disruption of focal adhesion signaling in the presence of cerebrovascular pathologyElanur Yilmaz, Kevin W Chen, Elif Öykü Cakir, et al.
Annals of Clinical and Translational Neurology|September 5, 2015
F-box/LRR-repeat protein 7 is genetically associated with Alzheimer's diseaseGiuseppe Tosto, Hongjun Fu, Badri N Vardarajan, et al.
JAMA Neurology|August 18, 2016
The Role of Cardiovascular Risk Factors and Stroke in Familial Alzheimer DiseaseGiuseppe Tosto, Thomas D Bird, David A Bennett, et al.
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