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Plos One|November 9, 2013
SMG1 identified as a regulator of Parkinson's disease-associated alpha-synuclein through siRNA screeningAdrienne Henderson-Smith, Donald Chow, Bessie Meechoovet, et al.Physiological Genomics|February 14, 2008
Altered neuronal gene expression in brain regions differentially affected by Alzheimer's disease: a reference data setWinnie S Liang, Travis Dunckley, Thomas G Beach, et al.Neurobiology of Aging|June 24, 2008
Neuronal gene expression in non-demented individuals with intermediate Alzheimer's Disease neuropathologyWinnie S Liang, Travis Dunckley, Thomas G Beach, et al.Physiological Genomics|November 2, 2006
Gene expression profiles in anatomically and functionally distinct regions of the normal aged human brainWinnie S Liang, Travis Dunckley, Thomas G Beach, et al.Journal of Medicinal Chemistry|September 30, 2024
Discovery and Functional Characterization of a Potent, Selective, and Metabolically Stable PROTAC of the Protein Kinases DYRK1A and DYRK1BGerrit Wilms, Kevin Schofield, Shayna Maddern, et al.Proceedings of the National Academy of Sciences of the United States of America|March 12, 2008
Alzheimer's disease is associated with reduced expression of energy metabolism genes in posterior cingulate neuronsWinnie S Liang, Eric M Reiman, Jon Valla, et al.Neuroimage|October 5, 2010
Association between GAB2 haplotype and higher glucose metabolism in Alzheimer's disease-affected brain regions in cognitively normal APOEε4 carriersWinnie S Liang, Kewei Chen, Wendy Lee, et al.Neurobiology of Aging|October 26, 2005
Gene expression correlates of neurofibrillary tangles in Alzheimer's diseaseTravis Dunckley, Thomas G Beach, Keri E Ramsey, et al.BMC Genomics|January 14, 2010
High-content siRNA screening of the kinome identifies kinases involved in Alzheimer's disease-related tau hyperphosphorylationDavid O Azorsa, RiLee H Robeson, Danielle Frost, et al.Proceedings of the National Academy of Sciences of the United States of America|July 27, 2004
Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of functionErik G Puffenberger, Diane Hu-Lince, Jennifer M Parod, et al.Pageof 4