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Bioorganic & Medicinal Chemistry Letters|March 15, 2011
Design and synthesis of pyridin-2-yloxymethylpiperidin-1-ylbutyl amide CCR5 antagonists that are potent inhibitors of M-tropic (R5) HIV-1 replicationRenato Skerlj, Gary Bridger, Yuanxi Zhou, et al.
Biorxiv : the Preprint Server for Biology|August 4, 2020
Virus-Receptor Interactions of Glycosylated SARS-CoV-2 Spike and Human ACE2 ReceptorPeng Zhao, Jeremy L Praissman, Oliver C Grant, et al.
Cell Host & Microbe|August 26, 2020
Virus-Receptor Interactions of Glycosylated SARS-CoV-2 Spike and Human ACE2 ReceptorPeng Zhao, Jeremy L Praissman, Oliver C Grant, et al.
The Journal of Cell Biology|December 31, 2024
A truncated isoform of Connexin43 caps actin to organize forward delivery of full-length Connexin43Rachel Baum, Vu D Nguyen, Mario Maalouf, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2023
Fusion crystallization reveals the behavior of both the 1TEL crystallization chaperone and the TNK1 UBA domainSupeshala Nawarathnage, Yi Jie Tseng, Sara Soleimani, et al.
Journal of Acquired Immune Deficiency Syndromes (1999)|September 24, 2004
Safety, pharmacokinetics, and antiviral activity of AMD3100, a selective CXCR4 receptor inhibitor, in HIV-1 infectionCraig W Hendrix, Ann C Collier, Michael M Lederman, et al.
Biochemical Pharmacology|December 8, 2011
The molecular pharmacology of AMD11070: an orally bioavailable CXCR4 HIV entry inhibitorRenee M Mosi, Virginia Anastassova, Jennifer Cox, et al.
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