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

L J Askonas

Showing results (1-10 of 8) with videos related to

Pageof 1
Sort By:
Biochemistry|December 10, 1991
Development of affinity labeling agents based on nonsteroidal anti-inflammatory drugs: labeling of the nonsteroidal anti-inflammatory drug binding site of 3 alpha-hydroxysteroid dehydrogenaseL J Askonas, T M Penning
Biochemistry|October 15, 1991
9-(5',6'-dideoxy-beta-D-ribo-hex-5'-ynofuranosyl)adenine, a novel irreversible inhibitor of S-adenosylhomocysteine hydrolaseR J Parry, A Muscate, L J Askonas
Biochemistry|January 24, 1995
Bromoacetamido analogs of indomethacin and mefenamic acid as affinity-labeling agents and mechanistic probes for prostaglandin H2 synthaseM S Tang, L J Askonas, T M Penning
Advances in Experimental Medicine and Biology|January 1, 1997
Bromoacetamido-analogs of indomethacin and mefenamic acid affinity-label prostaglandin H2 synthase at two sitesM S Tang, L J Askonas, T M Penning
The Biochemical Journal|September 15, 1991
The kinetic mechanism catalysed by homogeneous rat liver 3 alpha-hydroxysteroid dehydrogenase. Evidence for binary and ternary dead-end complexes containing non-steroidal anti-inflammatory drugsL J Askonas, J W Ricigliano, T M Penning
Steroids|April 1, 1986
Rat liver 3 alpha-hydroxysteroid dehydrogenaseT M Penning, T E Smithgall, L J Askonas, et al.
Protein Expression and Purification|October 1, 1993
High-level expression and purification of human leukotriene A4 hydrolase from insect cells infected with a baculovirus vectorJ K Gierse, V A Luckow, L J Askonas, et al.
Journal of Medicinal Chemistry|February 26, 2000
Structure-activity relationship studies on 1-[2-(4-Phenylphenoxy)ethyl]pyrrolidine (SC-22716), a potent inhibitor of leukotriene A(4) (LTA(4)) hydrolaseT D Penning, N S Chandrakumar, B B Chen, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Biochemistry|December 10, 1991
Development of affinity labeling agents based on nonsteroidal anti-inflammatory drugs: labeling of the nonsteroidal anti-inflammatory drug binding site of 3 alpha-hydroxysteroid dehydrogenaseL J Askonas, T M Penning
Biochemistry|October 15, 1991
9-(5',6'-dideoxy-beta-D-ribo-hex-5'-ynofuranosyl)adenine, a novel irreversible inhibitor of S-adenosylhomocysteine hydrolaseR J Parry, A Muscate, L J Askonas
Biochemistry|January 24, 1995
Bromoacetamido analogs of indomethacin and mefenamic acid as affinity-labeling agents and mechanistic probes for prostaglandin H2 synthaseM S Tang, L J Askonas, T M Penning
Advances in Experimental Medicine and Biology|January 1, 1997
Bromoacetamido-analogs of indomethacin and mefenamic acid affinity-label prostaglandin H2 synthase at two sitesM S Tang, L J Askonas, T M Penning
The Biochemical Journal|September 15, 1991
The kinetic mechanism catalysed by homogeneous rat liver 3 alpha-hydroxysteroid dehydrogenase. Evidence for binary and ternary dead-end complexes containing non-steroidal anti-inflammatory drugsL J Askonas, J W Ricigliano, T M Penning
Steroids|April 1, 1986
Rat liver 3 alpha-hydroxysteroid dehydrogenaseT M Penning, T E Smithgall, L J Askonas, et al.
Protein Expression and Purification|October 1, 1993
High-level expression and purification of human leukotriene A4 hydrolase from insect cells infected with a baculovirus vectorJ K Gierse, V A Luckow, L J Askonas, et al.
Journal of Medicinal Chemistry|February 26, 2000
Structure-activity relationship studies on 1-[2-(4-Phenylphenoxy)ethyl]pyrrolidine (SC-22716), a potent inhibitor of leukotriene A(4) (LTA(4)) hydrolaseT D Penning, N S Chandrakumar, B B Chen, et al.
Pageof 1