Showing results (141-150 of 182) with videos related to

Sort By:
Pageof 19
Molecular Psychiatry|May 29, 2026
Assessing the de novo paradigm in sporadic early-onset Alzheimer disease triosAline Zarea, Kevin Cassinari, François Lecoquierre, et al.
Nature Neuroscience|June 20, 2017
A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's diseaseKuan-Lin Huang, Edoardo Marcora, Anna A Pimenova, et al.
Translational Psychiatry|February 2, 2019
Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer's diseaseMaria Carolina Dalmasso, Luis Ignacio Brusco, Natividad Olivar, et al.
Acta Neuropathologica|March 14, 2020
PLCG2 protective variant p.P522R modulates tau pathology and disease progression in patients with mild cognitive impairmentLuca Kleineidam, Vincent Chouraki, Tomasz Próchnicki, et al.
The Lancet. Neurology|September 19, 2020
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association studyEmma Jones, Holger Hummerich, Emmanuelle Viré, et al.
Biorxiv : the Preprint Server for Biology|April 3, 2026
Non-microglial downregulation of <i>PLCG2</i> impairs synaptic function and elicits Alzheimer disease-related hallmarksAudrey Coulon, Florian Rabiller, Mari Takalo, et al.
Annals of Neurology|June 18, 2011
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortiumMyriam Fornage, Stephanie Debette, Joshua C Bis, et al.
Nature Reviews. Immunology|December 9, 2024
Neuroinflammation in Alzheimer diseaseMichael T Heneka, Wiesje M van der Flier, Frank Jessen, et al.
Journal of Alzheimer'S Disease : JAD|September 18, 2010
The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis studyJean-Charles Lambert, Kristel Sleegers, Antonio González-Pérez, et al.
Pageof 19