M. Skoog

发表

Specificity of an HPETE peroxidase from rat PMN.

B. Harrison, J. Wiseman, J. Nichols, 1988, Prostaglandins.

Glutathione peroxidase is neither required nor kinetically competent for conversion of 5-HPETE to 5-HETE in rat PMN lysates.

B. Harrison, J. Wiseman, J. Nichols, 1986, Prostaglandins.

Inhibition of HIV‐1 reverse transcriptase and virus replication by a non‐nucleoside dipyridodiazepinone BI‐RG‐587 (nevirapine)

K. D. Hargrave, V. J. Merluzzi, J. Miglietta, 1992, Medicinal research reviews.

5-lipoxygenase from rat PMN lysate.

J. Wiseman, J. Nichols, M. Skoog, 1986, Prostaglandins.

Kinetics of leukotriene A4 synthesis by 5-lipoxygenase from rat polymorphonuclear leukocytes.

B. Harrison, J. Wiseman, J. Nichols, 1987, Biochemistry.

The specificity of two proteinases that cleave adjacent to arginine, C1 esterase and acrosin, for peptide p-nitroanilide substrates.

J. Wiseman, P. Bey, S. Mehdi, 1989, Biochimica et biophysica acta.

Inhibition of 5-lipoxygenase by substituted 3,4-dihydro-2H-1,4-thiazines.

E. Huber, J. Wiseman, P. Weintraub, 1989, Journal of pharmaceutical sciences.

Inhibition of human leukocyte elastase by N-substituted tripeptide trifluoromethyl ketones.

V. Fuchs, J. Skiles, M. Skoog, 1990, Research communications in chemical pathology and pharmacology.

Inhibition of HIV-1 replication by a nonnucleoside reverse transcriptase inhibitor.

J. Adams, K. Grozinger, J. Wu, 1990, Science.

Phosphoryl transfer between pyridines

W. Jencks, M. Skoog, 1983 .

Rhinovirus 3C protease catalyzes efficient cleavage of a fluorescein-labeled peptide affording a rapid and robust assay.

M. Emmanuel, P. Pallai, R. Betageri, 1991, Journal of biochemical and biophysical methods.

Rapid, sensitive and efficient HPLC assays for HIV-1 proteinase.

M. Emmanuel, D. Thibeault, R. Betageri, 1993, Journal of biochemical and biophysical methods.

Cleavage of synthetic peptides by purified poliovirus 3C proteinase.

K. Harris, M. Nicklin, P. Pallai, 1989, The Journal of biological chemistry.

Substituted naphthalenones as a new structural class of HIV-1 reverse transcriptase inhibitors.

R. Colonno, A. Patick, A. Meyers, 1993, Antiviral research.

Reactions of pyridines and primary amines with N-phosphorylated pyridines

W. Jencks, M. Skoog, 1984 .

α-hydroxyamide derived aminodiols as potent inhibitors of hiv protease

Ping Chen, S. Spergel, J. Barrish, 1995 .

Inhibition of human leukocyte elastase by N-substituted peptides containing alpha,alpha-difluorostatone residues at P1.

P. Mui, J. Keirns, S. Weldon, 1992, Journal of medicinal chemistry.

BI-RG-587 is active against zidovudine-resistant human immunodeficiency virus type 1 and synergistic with zidovudine

D. Richman, T. Chou, T C Chou, 1991, Antimicrobial Agents and Chemotherapy.

Activity of purified biosynthetic proteinase of human immunodeficiency virus on natural substrates and synthetic peptides.

E. Wimmer, H. Kräusslich, P. Pallai, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Mechanism and activation for allosteric adenosine 5'-monophosphate nucleosidase. Kinetic alpha-deuterium isotope effects for the enzyme-catalyzed hydrolysis of adenosine 5'-monophosphate and nicotinamide mononucleotide.

M. Skoog, 1986, The Journal of biological chemistry.

Activity of soybean lipoxygenase in the absence of lipid hydroperoxide.

J. Wiseman, C. Clapp, M. Skoog, 1988, Biochemistry.

Novel non-nucleoside inhibitors of HIV-1 reverse transcriptase. 1. Tricyclic pyridobenzo- and dipyridodiazepinones.

J. Proudfoot, U. Patel, K. Grozinger, 1991, Journal of medicinal chemistry.