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Ophthalmology|November 1, 1991
Phthalocyanine photodynamic therapy of experimental iris neovascularizationJ W Miller, W G Stinson, W A Gregory, et al.Proceedings of the National Academy of Sciences of the United States of America|November 8, 1994
Spermine potentiation of recombinant N-methyl-D-aspartate receptors is affected by subunit compositionL Zhang, X Zheng, M C Paupard, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 22, 2001
Global ischemia-induced increases in the gap junctional proteins connexin 32 (Cx32) and Cx36 in hippocampus and enhanced vulnerability of Cx32 knock-out miceK Oguro, T Jover, H Tanaka, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 15, 1997
Global ischemia induces downregulation of Glur2 mRNA and increases AMPA receptor-mediated Ca2+ influx in hippocampal CA1 neurons of gerbilJ A Gorter, J J Petrozzino, E M Aronica, et al.Journal of Perinatology : Official Journal of the California Perinatal Association|December 23, 2016
Effects of delivery room quality improvement on premature infant outcomesW Lapcharoensap, M V Bennett, R J Powers, et al.Nature Neuroscience|March 29, 2001
Protein kinase C modulates NMDA receptor trafficking and gatingJ Y Lan, V A Skeberdis, T Jover, et al.Antimicrobial Agents and Chemotherapy|November 1, 1987
Oxazolidinones, a new class of synthetic antibacterial agents: in vitro and in vivo activities of DuP 105 and DuP 721A M Slee, M A Wuonola, R J McRipley, et al.Journal of Medicinal Chemistry|September 1, 1985
Preparation and antiarthritic and analgesic activity of 4,5-diaryl-2-(substituted thio)-1H-imidazoles and their sulfoxides and sulfonesT R Sharpe, S C Cherkofsky, W E Hewes, et al.Journal of Medicinal Chemistry|September 1, 1990
Antibacterials. Synthesis and structure-activity studies of 3-aryl-2-oxooxazolidines. 2. The "A" groupW A Gregory, D R Brittelli, C L Wang, et al.Journal of Medicinal Chemistry|August 1, 1989
Antibacterials. Synthesis and structure-activity studies of 3-aryl-2-oxooxazolidines. 1. The "B" groupW A Gregory, D R Brittelli, C L Wang, et al.Pageof 18