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Human Molecular Genetics|December 8, 2007
Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's diseaseYonghong Li, Andrew Grupe, Charles Rowland, et al.Biorxiv : the Preprint Server for Biology|June 10, 2024
<i>LRRK2</i> G2019S variant is associated with transcriptional changes in Parkinson's disease human myeloid cells under proinflammatory environmentElisa Navarro, Anastasia G Efthymiou, Madison Parks, et al.Alzheimer'S & Dementia (New York, N. Y.)|March 12, 2024
New directions for Alzheimer's disease research from the Jackson Laboratory Center for Alzheimer's and Dementia Research 2022 workshopMaria A Telpoukhovskaia, Thomas J Murdy, Olivia J Marola, et al.Scientific Reports|January 17, 2023
Genetic studies of plasma analytes identify novel potential biomarkers for several complex traitsYuetiva Deming, Jian Xia, Yefei Cai, et al.Brain : a Journal of Neurology|October 23, 2015
Common polygenic variation enhances risk prediction for Alzheimer's diseaseValentina Escott-Price, Rebecca Sims, Christian Bannister, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|October 17, 2022
Metabolomic and lipidomic signatures in autosomal dominant and late-onset Alzheimer's disease brainsBrenna C Novotny, Maria Victoria Fernandez, Ciyang Wang, et al.Brain : a Journal of Neurology|September 22, 2018
White matter diffusion alterations precede symptom onset in autosomal dominant Alzheimer's diseaseMiguel Ángel Araque Caballero, Marc Suárez-Calvet, Marco Duering, et al.Brain : a Journal of Neurology|August 14, 2016
BDNF Val66Met moderates memory impairment, hippocampal function and tau in preclinical autosomal dominant Alzheimer's diseaseYen Ying Lim, Jason Hassenstab, Carlos Cruchaga, et al.American Journal of Medical Genetics|February 22, 2002
Full genome screen for Alzheimer disease: stage II analysisAmanda Myers, Fabienne Wavrant De-Vrieze, Peter Holmans, et al.Human Molecular Genetics|July 19, 2006
DAPK1 variants are associated with Alzheimer's disease and allele-specific expressionYonghong Li, Andrew Grupe, Charles Rowland, et al.Pageof 25