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M A Levy

Showing results (51-60 of 78) with videos related to

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Molecular and Cellular Biology|March 1, 1991
Rapamycin sensitivity in Saccharomyces cerevisiae is mediated by a peptidyl-prolyl cis-trans isomerase related to human FK506-binding proteinY Koltin, L Faucette, D J Bergsma, et al.
The Journal of Steroid Biochemistry and Molecular Biology|February 1, 1994
Epristeride is a selective and specific uncompetitive inhibitor of human steroid 5 alpha-reductase isoform 2M A Levy, M Brandt, K M Sheedy, et al.
Journal of Medicinal Chemistry|March 1, 1990
Steroidal A ring aryl carboxylic acids: a new class of steroid 5 alpha-reductase inhibitorsD A Holt, M A Levy, D L Ladd, et al.
Bioorganic & Medicinal Chemistry|June 3, 1999
Structure-based design of non-peptide, carbohydrazide-based cathepsin K inhibitorsS K Thompson, S M Halbert, R L DesJarlais, et al.
Journal of Medicinal Chemistry|January 6, 1995
Benzophenone- and indolecarboxylic acids: potent type-2 specific inhibitors of human steroid 5 alpha-reductaseD A Holt, D S Yamashita, A L Konialian-Beck, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|April 18, 2002
SB-242235, a selective inhibitor of p38 mitogen-activated protein kinase. II: in vitro and in vivo metabolism studies and pharmacokinetic extrapolation to manK W Ward, J W Proksch, P D Gorycki, et al.
The Journal of Antibiotics|November 1, 1995
27-O-demethylrapamycin, an immunosuppressant compound produced by a new strain of Streptomyces hygroscopicusS J Box, P R Shelley, J W Tyler, et al.
Journal of Medicinal Chemistry|March 1, 1990
Inhibition of steroid 5 alpha-reductase by unsaturated 3-carboxysteroidsD A Holt, M A Levy, H J Oh, et al.
Pharmaceutical Research|October 31, 2001
SB-239063, a potent and selective inhibitor of p38 map kinase: preclinical pharmacokinetics and species-specific reversible isomerizationK W Ward, J W Proksch, L M Azzarano, et al.
Gene|February 1, 1992
The yeast cyclophilin multigene family: purification, cloning and characterization of a new isoformM M McLaughlin, M J Bossard, P L Koser, et al.
Pageof 8

Showing results (51-60 of 78) with videos related to

Sort By:
Pageof 8
Molecular and Cellular Biology|March 1, 1991
Rapamycin sensitivity in Saccharomyces cerevisiae is mediated by a peptidyl-prolyl cis-trans isomerase related to human FK506-binding proteinY Koltin, L Faucette, D J Bergsma, et al.
The Journal of Steroid Biochemistry and Molecular Biology|February 1, 1994
Epristeride is a selective and specific uncompetitive inhibitor of human steroid 5 alpha-reductase isoform 2M A Levy, M Brandt, K M Sheedy, et al.
Journal of Medicinal Chemistry|March 1, 1990
Steroidal A ring aryl carboxylic acids: a new class of steroid 5 alpha-reductase inhibitorsD A Holt, M A Levy, D L Ladd, et al.
Bioorganic & Medicinal Chemistry|June 3, 1999
Structure-based design of non-peptide, carbohydrazide-based cathepsin K inhibitorsS K Thompson, S M Halbert, R L DesJarlais, et al.
Journal of Medicinal Chemistry|January 6, 1995
Benzophenone- and indolecarboxylic acids: potent type-2 specific inhibitors of human steroid 5 alpha-reductaseD A Holt, D S Yamashita, A L Konialian-Beck, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|April 18, 2002
SB-242235, a selective inhibitor of p38 mitogen-activated protein kinase. II: in vitro and in vivo metabolism studies and pharmacokinetic extrapolation to manK W Ward, J W Proksch, P D Gorycki, et al.
The Journal of Antibiotics|November 1, 1995
27-O-demethylrapamycin, an immunosuppressant compound produced by a new strain of Streptomyces hygroscopicusS J Box, P R Shelley, J W Tyler, et al.
Journal of Medicinal Chemistry|March 1, 1990
Inhibition of steroid 5 alpha-reductase by unsaturated 3-carboxysteroidsD A Holt, M A Levy, H J Oh, et al.
Pharmaceutical Research|October 31, 2001
SB-239063, a potent and selective inhibitor of p38 map kinase: preclinical pharmacokinetics and species-specific reversible isomerizationK W Ward, J W Proksch, L M Azzarano, et al.
Gene|February 1, 1992
The yeast cyclophilin multigene family: purification, cloning and characterization of a new isoformM M McLaughlin, M J Bossard, P L Koser, et al.
Pageof 8