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

W K Hagmann

Showing results (1-10 of 25) with videos related to

Pageof 3
Sort By:
Agents and Actions|March 1, 1990
Naphthalenes as inhibitors of myeloperoxidase: direct and indirect mechanisms of inhibitionR W Egan, W K Hagmann, P H Gale
Biochemistry|February 15, 1994
Studies on the kinetic and chemical mechanism of inhibition of stromelysin by an N-(carboxyalkyl)dipeptideM Izquierdo-Martin, K T Chapman, W K Hagmann, et al.
International Journal of Immunopharmacology|January 1, 1990
Steroidal glycolipid, L-644,257, is a potent enhancer of nonspecific host resistanceW K Hagmann, M M Ponpipom, J J Jackson, et al.
Journal of Medicinal Chemistry|February 1, 1990
Glycolipids as host resistance stimulatorsM M Ponpipom, W K Hagmann, L A O'Grady, et al.
Journal of Medicinal Chemistry|August 1, 1986
Synthesis and antiinflammatory/analgesic activities of 11H-dibenzo[b, e,][1,4]dioxepinacetic acidsW K Hagmann, C P Dorn, R A Frankshun, et al.
Biochemistry|May 19, 1992
Characterization of zinc-binding sites in human stromelysin-1: stoichiometry of the catalytic domain and identification of a cysteine ligand in the proenzymeS P Salowe, A I Marcy, G C Cuca, et al.
Biochemistry|December 7, 1993
Secondary structure and zinc ligation of human recombinant short-form stromelysin by multidimensional heteronuclear NMRP R Gooley, B A Johnson, A I Marcy, et al.
Journal of Biomolecular NMR|January 1, 1996
Comparison of the structure of human recombinant short form stromelysin by multidimensional heteronuclear NMR and X-ray crystallographyP R Gooley, J F O'Connell, A I Marcy, et al.
Journal of Medicinal Chemistry|January 24, 1992
Substituted 4,6-diaminoquinolines as inhibitors of C5a receptor bindingT J Lanza, P L Durette, T Rollins, et al.
Biochemistry|July 2, 1991
Human fibroblast stromelysin catalytic domain: expression, purification, and characterization of a C-terminally truncated formA I Marcy, L L Eiberger, R Harrison, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Agents and Actions|March 1, 1990
Naphthalenes as inhibitors of myeloperoxidase: direct and indirect mechanisms of inhibitionR W Egan, W K Hagmann, P H Gale
Biochemistry|February 15, 1994
Studies on the kinetic and chemical mechanism of inhibition of stromelysin by an N-(carboxyalkyl)dipeptideM Izquierdo-Martin, K T Chapman, W K Hagmann, et al.
International Journal of Immunopharmacology|January 1, 1990
Steroidal glycolipid, L-644,257, is a potent enhancer of nonspecific host resistanceW K Hagmann, M M Ponpipom, J J Jackson, et al.
Journal of Medicinal Chemistry|February 1, 1990
Glycolipids as host resistance stimulatorsM M Ponpipom, W K Hagmann, L A O'Grady, et al.
Journal of Medicinal Chemistry|August 1, 1986
Synthesis and antiinflammatory/analgesic activities of 11H-dibenzo[b, e,][1,4]dioxepinacetic acidsW K Hagmann, C P Dorn, R A Frankshun, et al.
Biochemistry|May 19, 1992
Characterization of zinc-binding sites in human stromelysin-1: stoichiometry of the catalytic domain and identification of a cysteine ligand in the proenzymeS P Salowe, A I Marcy, G C Cuca, et al.
Biochemistry|December 7, 1993
Secondary structure and zinc ligation of human recombinant short-form stromelysin by multidimensional heteronuclear NMRP R Gooley, B A Johnson, A I Marcy, et al.
Journal of Biomolecular NMR|January 1, 1996
Comparison of the structure of human recombinant short form stromelysin by multidimensional heteronuclear NMR and X-ray crystallographyP R Gooley, J F O'Connell, A I Marcy, et al.
Journal of Medicinal Chemistry|January 24, 1992
Substituted 4,6-diaminoquinolines as inhibitors of C5a receptor bindingT J Lanza, P L Durette, T Rollins, et al.
Biochemistry|July 2, 1991
Human fibroblast stromelysin catalytic domain: expression, purification, and characterization of a C-terminally truncated formA I Marcy, L L Eiberger, R Harrison, et al.
Pageof 3