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Journal of Clinical Microbiology|April 10, 2009
Correlation of cefoxitin MICs with the presence of mecA in Staphylococcus sppJana M Swenson, William B Brasso, Mary Jane Ferraro, et al.Human Molecular Genetics|August 13, 1998
Pronounced impact of Th1/E47cs mutation compared with -491 AT mutation on neural APOE gene expression and risk of developing Alzheimer's diseaseJ C Lambert, C Berr, F Pasquier, et al.ACS Catalysis|August 8, 2024
Probing Ferryl Reactivity in a Nonheme Iron Oxygenase Using an Expanded Genetic CodeFlorence J Hardy, Matthew G Quesne, Emilie F Gérard, et al.Journal of Medical Genetics|December 14, 2004
Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's diseaseM Martinez, A Brice, J R Vaughan, et al.Neuroscience Letters|August 24, 1999
The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's diseaseB S Harhangi, M J Farrer, S Lincoln, et al.The Journal of Biological Chemistry|September 25, 1999
A loss of function mutation of presenilin-2 interferes with amyloid beta-peptide production and notch signalingH Steiner, K Duff, A Capell, et al.Brain Injury|September 29, 2020
Memory in repeat sports-related concussive injury and single-impact traumatic brain injuryMatthew J Wright, Martin M Monti, Evan S Lutkenhoff, et al.Neurology|May 29, 2003
Parkin-proven disease: common founders but divergent phenotypesS Lincoln, J Wiley, T Lynch, et al.Human Molecular Genetics|July 13, 1999
Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Abeta42 secretionC De Jonghe, M Cruts, E A Rogaeva, et al.Nature Communications|July 30, 2024
Structure of the MlaC-MlaD complex reveals molecular basis of periplasmic phospholipid transportPeter Wotherspoon, Hannah Johnston, David J Hardy, et al.Pageof 146