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Biopolymers|January 1, 1990
SV40 large T-antigen nuclear signal analogues: successful nuclear targeting with bovine serum albumin but not low molecular weight fluorescent conjugatesT J Lobl, M A Mitchell, L L MaggioraJournal of Medicinal Chemistry|October 16, 1992
A general method for the preparation of internally quenched fluorogenic protease substrates using solid-phase peptide synthesisL L Maggiora, C W Smith, Z Y ZhangJournal of Medicinal Chemistry|July 8, 1999
Apstatin analogue inhibitors of aminopeptidase P, a bradykinin-degrading enzymeL L Maggiora, A T Orawski, W H SimmonsPharmaceutical Research|January 1, 1991
Role of complements C3 and C5 in the phagocytosis of liposomes by human neutrophilsJ F Scieszka, L L Maggiora, S D Wright, et al.The Journal of Pharmacology and Experimental Therapeutics|December 1, 1995
Effect of a new aminopeptidase P inhibitor, apstatin, on bradykinin degradation in the rat lungM M Prechel, A T Orawski, L L Maggiora, et al.International Journal of Peptide and Protein Research|November 1, 1988
Peptides as potential virus inhibitors. Synthesis and bioassay of five respiratory syncytial virus peptide analogs with antimeasles activityT J Lobl, H E Renis, R M Epand, et al.The Journal of Biological Chemistry|August 25, 1991
Dissociative inhibition of dimeric enzymes. Kinetic characterization of the inhibition of HIV-1 protease by its COOH-terminal tetrapeptideZ Y Zhang, R A Poorman, L L Maggiora, et al.The Journal of Biological Chemistry|May 15, 1993
The specificity of UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase as inferred from a database of in vivo substrates and from the in vitro glycosylation of proteins and peptidesA P Elhammer, R A Poorman, E Brown, et al.Journal of Medicinal Chemistry|January 1, 1988
Design, structure-activity, and molecular modeling studies of potent renin inhibitory peptides having N-terminal Nin-For-Trp (Ftr): angiotensinogen congeners modified by P1-P1' Phe-Phe, Sta, Leu psi[CH(OH)CH2]Val or leu psi[CH2NH]Val substitutionsT K Sawyer, D T Pals, B Mao, et al.Journal of Medicinal Chemistry|May 7, 1999
Synthesis of a series of stromelysin-selective thiadiazole urea matrix metalloproteinase inhibitorsE J Jacobsen, M A Mitchell, S K Hendges, et al.Pageof 1