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

A M MacLeod

Showing results (181-190 of 197) with videos related to

Pageof 20
Sort By:
Journal of Medicinal Chemistry|October 1, 1990
Synthesis and biological activity of 1,2,4-oxadiazole derivatives: highly potent and efficacious agonists for cortical muscarinic receptorsL J Street, R Baker, T Book, et al.
Kidney International|October 1, 1994
Nitric oxide production by human proximal tubular cells: a novel immunomodulatory mechanism?J S McLay, P Chatterjee, A G Nicolson, et al.
Journal of Medicinal Chemistry|November 14, 1997
Selective, orally active 5-HT1D receptor agonists as potential antimigraine agentsA M MacLeod, L J Street, A J Reeve, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 7, 2001
Do the Y-set and double-bag systems reduce the incidence of CAPD peritonitis? A systematic review of randomized controlled trialsC D Daly, M K Campbell, A M MacLeod, et al.
Physical Review Letters|November 13, 2007
Benchmarking of electro-optic monitors for femtosecond electron bunchesG Berden, W A Gillespie, S P Jamison, et al.
Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Serine derived NK1 antagonists. 1: The effect of modifications to the serine substituentsJ M Elliott, M A Cascieri, G Chicchi, et al.
Bioorganic & Medicinal Chemistry Letters|November 27, 1999
Parallel synthesis of 3-aryloxy-2-propanolamines and evaluation as dual affinity 5-HT(1A) and 5-HT re-uptake ligandsM B van Niel, M S Beer, J L Castro, et al.
Neuropharmacology|January 1, 1996
Tachykinin NK1 receptor antagonists act centrally to inhibit emesis induced by the chemotherapeutic agent cisplatin in ferretsF D Tattersall, W Rycroft, B Francis, et al.
Journal of Medicinal Chemistry|May 4, 2001
3-(4-Fluoropiperidin-3-yl)-2-phenylindoles as high affinity, selective, and orally bioavailable h5-HT(2A) receptor antagonistsM Rowley, D J Hallett, S Goodacre, et al.
Journal of Medicinal Chemistry|March 3, 1999
3-(Piperazinylpropyl)indoles: selective, orally bioavailable h5-HT1D receptor agonists as potential antimigraine agentsM S Chambers, L J Street, S Goodacre, et al.
Pageof 20

Showing results (181-190 of 197) with videos related to

Sort By:
Pageof 20
Journal of Medicinal Chemistry|October 1, 1990
Synthesis and biological activity of 1,2,4-oxadiazole derivatives: highly potent and efficacious agonists for cortical muscarinic receptorsL J Street, R Baker, T Book, et al.
Kidney International|October 1, 1994
Nitric oxide production by human proximal tubular cells: a novel immunomodulatory mechanism?J S McLay, P Chatterjee, A G Nicolson, et al.
Journal of Medicinal Chemistry|November 14, 1997
Selective, orally active 5-HT1D receptor agonists as potential antimigraine agentsA M MacLeod, L J Street, A J Reeve, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 7, 2001
Do the Y-set and double-bag systems reduce the incidence of CAPD peritonitis? A systematic review of randomized controlled trialsC D Daly, M K Campbell, A M MacLeod, et al.
Physical Review Letters|November 13, 2007
Benchmarking of electro-optic monitors for femtosecond electron bunchesG Berden, W A Gillespie, S P Jamison, et al.
Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Serine derived NK1 antagonists. 1: The effect of modifications to the serine substituentsJ M Elliott, M A Cascieri, G Chicchi, et al.
Bioorganic & Medicinal Chemistry Letters|November 27, 1999
Parallel synthesis of 3-aryloxy-2-propanolamines and evaluation as dual affinity 5-HT(1A) and 5-HT re-uptake ligandsM B van Niel, M S Beer, J L Castro, et al.
Neuropharmacology|January 1, 1996
Tachykinin NK1 receptor antagonists act centrally to inhibit emesis induced by the chemotherapeutic agent cisplatin in ferretsF D Tattersall, W Rycroft, B Francis, et al.
Journal of Medicinal Chemistry|May 4, 2001
3-(4-Fluoropiperidin-3-yl)-2-phenylindoles as high affinity, selective, and orally bioavailable h5-HT(2A) receptor antagonistsM Rowley, D J Hallett, S Goodacre, et al.
Journal of Medicinal Chemistry|March 3, 1999
3-(Piperazinylpropyl)indoles: selective, orally bioavailable h5-HT1D receptor agonists as potential antimigraine agentsM S Chambers, L J Street, S Goodacre, et al.
Pageof 20