Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M A Levy

Showing results (61-70 of 78) with videos related to

Pageof 8
Sort By:
Chemistry & Biology|July 1, 1995
Structure-activity studies of rapamycin analogs: evidence that the C-7 methoxy group is part of the effector domain and positioned at the FKBP12-FRAP interfaceJ I Luengo, D S Yamashita, D Dunnington, 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. I: preclinical pharmacokineticsK W Ward, J W Proksch, K L Salyers, et al.
The Journal of Steroid Biochemistry and Molecular Biology|April 1, 1995
Cloning, expression and functional characterization of type 1 and type 2 steroid 5 alpha-reductases from Cynomolgus monkey: comparisons with human and rat isoenzymesM A Levy, M Brandt, K M Sheedy, et al.
Gene|July 30, 1993
The tyrosine89 residue of yeast FKBP12 is required for rapamycin bindingP L Koser, W K Eng, M J Bossard, et al.
The Journal of Biological Chemistry|May 24, 1996
Proteolytic activity of human osteoclast cathepsin K. Expression, purification, activation, and substrate identificationM J Bossard, T A Tomaszek, S K Thompson, et al.
Biochemistry|January 8, 2000
Mechanism of inhibition of cathepsin K by potent, selective 1, 5-diacylcarbohydrazides: a new class of mechanism-based inhibitors of thiol proteasesM J Bossard, T A Tomaszek, M A Levy, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|August 11, 2000
Inhibition of caspase-3-like activity prevents apoptosis while retaining functionality of human chondrocytes in vitroM E Nuttall, D P Nadeau, P W Fisher, et al.
Gene|December 1, 1991
The CYP2 gene of Saccharomyces cerevisiae encodes a cyclosporin A-sensitive peptidyl-prolyl cis-trans isomerase with an N-terminal signal sequenceP L Koser, D J Bergsma, R Cafferkey, et al.
American Journal of Veterinary Research|May 18, 1999
Synergistic effects of concurrent challenge with bovine respiratory syncytial virus and 3-methylindole in calvesH R Bingham, P S Morley, T E Wittum, et al.
Journal of Medicinal Chemistry|June 1, 2001
Potent and selective nonpeptide inhibitors of caspases 3 and 7D Lee, S A Long, J H Murray, et al.
Pageof 8

Showing results (61-70 of 78) with videos related to

Sort By:
Pageof 8
Chemistry & Biology|July 1, 1995
Structure-activity studies of rapamycin analogs: evidence that the C-7 methoxy group is part of the effector domain and positioned at the FKBP12-FRAP interfaceJ I Luengo, D S Yamashita, D Dunnington, 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. I: preclinical pharmacokineticsK W Ward, J W Proksch, K L Salyers, et al.
The Journal of Steroid Biochemistry and Molecular Biology|April 1, 1995
Cloning, expression and functional characterization of type 1 and type 2 steroid 5 alpha-reductases from Cynomolgus monkey: comparisons with human and rat isoenzymesM A Levy, M Brandt, K M Sheedy, et al.
Gene|July 30, 1993
The tyrosine89 residue of yeast FKBP12 is required for rapamycin bindingP L Koser, W K Eng, M J Bossard, et al.
The Journal of Biological Chemistry|May 24, 1996
Proteolytic activity of human osteoclast cathepsin K. Expression, purification, activation, and substrate identificationM J Bossard, T A Tomaszek, S K Thompson, et al.
Biochemistry|January 8, 2000
Mechanism of inhibition of cathepsin K by potent, selective 1, 5-diacylcarbohydrazides: a new class of mechanism-based inhibitors of thiol proteasesM J Bossard, T A Tomaszek, M A Levy, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|August 11, 2000
Inhibition of caspase-3-like activity prevents apoptosis while retaining functionality of human chondrocytes in vitroM E Nuttall, D P Nadeau, P W Fisher, et al.
Gene|December 1, 1991
The CYP2 gene of Saccharomyces cerevisiae encodes a cyclosporin A-sensitive peptidyl-prolyl cis-trans isomerase with an N-terminal signal sequenceP L Koser, D J Bergsma, R Cafferkey, et al.
American Journal of Veterinary Research|May 18, 1999
Synergistic effects of concurrent challenge with bovine respiratory syncytial virus and 3-methylindole in calvesH R Bingham, P S Morley, T E Wittum, et al.
Journal of Medicinal Chemistry|June 1, 2001
Potent and selective nonpeptide inhibitors of caspases 3 and 7D Lee, S A Long, J H Murray, et al.
Pageof 8