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Proceedings of the National Academy of Sciences of the United States of America|March 9, 2005
Characterization of functional and phenotypic changes in anti-Gag vaccine-induced T cell responses and their role in protection after HIV-1 infectionMichael R Betts, Barbara Exley, David A Price, et al.Brain : a Journal of Neurology|July 13, 2026
Cytomegalovirus-induced T cell responses accelerate Alzheimer's disease progression in miceMorgan Marsden, James E McLaren, Ryan J Bevan, et al.Marine Drugs|August 26, 2021
Identification of a New Antimicrobial, Desertomycin H, Utilizing a Modified Crowded Plate TechniqueOsama G Mohamed, Sadaf Dorandish, Rebecca Lindow, et al.Journal of the American College of Cardiology|July 21, 2004
A randomized trial of rescue angioplasty versus a conservative approach for failed fibrinolysis in ST-segment elevation myocardial infarction: the Middlesbrough Early Revascularization to Limit INfarction (MERLIN) trialAndrew G C Sutton, Philip G Campbell, Richard Graham, et al.Nature Chemical Biology|September 28, 2011
On-resin N-methylation of cyclic peptides for discovery of orally bioavailable scaffoldsTina R White, Chad M Renzelman, Arthur C Rand, et al.Nature Protocols|November 14, 2022
Metagenome-assembled genome extraction and analysis from microbiomes using KBaseDylan Chivian, Sean P Jungbluth, Paramvir S Dehal, et al.Protein Engineering, Design & Selection : PEDS|February 17, 2022
Immortalization and functional screening of natively paired human T cell receptor repertoiresAhmed S Fahad, Cheng-Yu Chung, Sheila N Lopez Acevedo, et al.Heart (British Cardiac Society)|September 16, 2005
One year results of the Middlesbrough early revascularisation to limit infarction (MERLIN) trialA G C Sutton, P G Campbell, R Graham, et al.Journal of Virology|March 16, 2012
Virus inhibition activity of effector memory CD8(+) T cells determines simian immunodeficiency virus load in vaccinated monkeys after vaccine breakthrough infectionTakuya Yamamoto, Matthew J Johnson, David A Price, et al.Nature Genetics|December 1, 1995
Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2N H Robin, G J Feldman, A L Aronson, et al.Pageof 261