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 G Page

Showing results (41-50 of 48) with videos related to

Pageof 5
Sort By:
You have reached the last page of results.This site can display upto 48 results.
Journal of Combinatorial Chemistry|October 13, 2000
Rapid identification of substrates for novel proteases using a combinatorial peptide libraryG Rossé, E Kueng, M G Page, et al.
Journal of Medicinal Chemistry|July 6, 2000
Hydroxamic acid derivatives as potent peptide deformylase inhibitors and antibacterial agentsC Apfel, D W Banner, D Bur, et al.
Journal of Molecular Biology|March 19, 1999
The structure and function of the 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase from Haemophilus influenzaeM Hennig, G E Dale, A D'arcy, et al.
Journal of Molecular Biology|April 25, 1997
Structure and function of the dihydropteroate synthase from Staphylococcus aureusI C Hampele, A D'Arcy, G E Dale, et al.
Current Opinion in Cell Biology|August 1, 1992
Membrane transport proteins: implications of sequence comparisonsJ K Griffith, M E Baker, D A Rouch, et al.
Journal of Medicinal Chemistry|April 26, 1996
Synthesis and structure-activity relationship of (lactamylvinyl)cephalosporins exhibiting activity against staphylococci, pneumococci, and enterococciI Heinze-Krauss, P Angehrn, P Guerry, et al.
Journal of Medicinal Chemistry|October 10, 1998
Structure-based design of beta-lactamase inhibitors. 1. Synthesis and evaluation of bridged monobactamsI Heinze-Krauss, P Angehrn, R L Charnas, et al.
Journal of Molecular Biology|February 14, 1997
A single amino acid substitution in Staphylococcus aureus dihydrofolate reductase determines trimethoprim resistanceG E Dale, C Broger, A D'Arcy, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Journal of Combinatorial Chemistry|October 13, 2000
Rapid identification of substrates for novel proteases using a combinatorial peptide libraryG Rossé, E Kueng, M G Page, et al.
Journal of Medicinal Chemistry|July 6, 2000
Hydroxamic acid derivatives as potent peptide deformylase inhibitors and antibacterial agentsC Apfel, D W Banner, D Bur, et al.
Journal of Molecular Biology|March 19, 1999
The structure and function of the 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase from Haemophilus influenzaeM Hennig, G E Dale, A D'arcy, et al.
Journal of Molecular Biology|April 25, 1997
Structure and function of the dihydropteroate synthase from Staphylococcus aureusI C Hampele, A D'Arcy, G E Dale, et al.
Current Opinion in Cell Biology|August 1, 1992
Membrane transport proteins: implications of sequence comparisonsJ K Griffith, M E Baker, D A Rouch, et al.
Journal of Medicinal Chemistry|April 26, 1996
Synthesis and structure-activity relationship of (lactamylvinyl)cephalosporins exhibiting activity against staphylococci, pneumococci, and enterococciI Heinze-Krauss, P Angehrn, P Guerry, et al.
Journal of Medicinal Chemistry|October 10, 1998
Structure-based design of beta-lactamase inhibitors. 1. Synthesis and evaluation of bridged monobactamsI Heinze-Krauss, P Angehrn, R L Charnas, et al.
Journal of Molecular Biology|February 14, 1997
A single amino acid substitution in Staphylococcus aureus dihydrofolate reductase determines trimethoprim resistanceG E Dale, C Broger, A D'Arcy, et al.
Pageof 5