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

D C Waters

Showing results (21-30 of 23) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 23 results.
The Journal of Pharmacology and Experimental Therapeutics|November 1, 1995
Pharmacological characterization of LY303870: a novel, potent and selective nonpeptide substance P (neurokinin-1) receptor antagonistB D Gitter, R F Bruns, J J Howbert, et al.
Molecular Plant-Microbe Interactions : MPMI|January 19, 2012
Quantitative variation in effector activity of ToxA isoforms from Stagonospora nodorum and Pyrenophora tritici-repentisKar-Chun Tan, Margo Ferguson-Hunt, Kasia Rybak, et al.
Journal of Medicinal Chemistry|February 2, 1996
3-Aryl-1,2-diacetamidopropane derivatives as novel and potent NK-1 receptor antagonistsP A Hipskind, J J Howbert, R F Bruns, et al.
Pageof 3

Showing results (21-30 of 23) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 23 results.
The Journal of Pharmacology and Experimental Therapeutics|November 1, 1995
Pharmacological characterization of LY303870: a novel, potent and selective nonpeptide substance P (neurokinin-1) receptor antagonistB D Gitter, R F Bruns, J J Howbert, et al.
Molecular Plant-Microbe Interactions : MPMI|January 19, 2012
Quantitative variation in effector activity of ToxA isoforms from Stagonospora nodorum and Pyrenophora tritici-repentisKar-Chun Tan, Margo Ferguson-Hunt, Kasia Rybak, et al.
Journal of Medicinal Chemistry|February 2, 1996
3-Aryl-1,2-diacetamidopropane derivatives as novel and potent NK-1 receptor antagonistsP A Hipskind, J J Howbert, R F Bruns, et al.
Pageof 3