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J Lotti

Showing results (81-90 of 124) with videos related to

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Neuroscience Letters|February 28, 1986
Thyrotropin-releasing hormone receptors in gut tissues resemble pituitary receptorsV J Lotti, R S Chang, D J Cerino, et al.
Journal of Medicinal Chemistry|January 1, 1981
Piperazinylquinoxalines with central serotoninmimetic activityW C Lumma, R D Hartman, W S Saari, et al.
Journal of Biological Regulators and Homeostatic Agents|July 14, 2017
Use of platelet rich plasma in human infertilityG V L Colombo, V Fanton, D Sosa, et al.
Journal of Medicinal Chemistry|February 1, 1990
Novel glutamic acid derived cholecystokinin receptor ligandsR M Freidinger, W L Whitter, N P Gould, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 1, 1984
R-enantiomer of timolol: a potential selective ocular antihypertensive agentN N Share, V J Lotti, P Gautheron, et al.
Molecular Pharmacology|June 1, 1989
Characterization of the binding of [3H]L-365,260: a new potent and selective brain cholecystokinin (CCK-B) and gastrin receptor antagonist radioligandR S Chang, T B Chen, M G Bock, et al.
Journal of Medicinal Chemistry|September 1, 1978
Synthesis and analgesic activity of 1,3-dihydro-3-(substituted phenyl)imidazo[4,5-b]pyridin-2-ones and 3-(substituted phenyl)-1,2,3-triazolo[4,5-b]pyridinesR L Clark, A A Pessolano, T Y Shen, et al.
Journal of Biological Regulators and Homeostatic Agents|July 14, 2017
Regenerative medicine in the treatment of gastro-esophageal reflux disease and laryngo-pharyngeal reflux. From research to cureS E Aragona, G Mereghetti, M Bianchetti, et al.
The Journal of Pharmacology and Experimental Therapeutics|May 1, 1985
Selectivity of (+)-4-propyl-9-hydroxynaphthoxazine [(+)-PHNO] for dopamine receptors in vitro and in vivoG E Martin, M Williams, D J Pettibone, et al.
Journal of Medicinal Chemistry|August 1, 1989
Cholecystokinin antagonists. Synthesis and biological evaluation of 3-substituted benzolactamsW H Parsons, A A Patchett, M K Holloway, et al.
Pageof 13

Showing results (81-90 of 124) with videos related to

Sort By:
Pageof 13
Neuroscience Letters|February 28, 1986
Thyrotropin-releasing hormone receptors in gut tissues resemble pituitary receptorsV J Lotti, R S Chang, D J Cerino, et al.
Journal of Medicinal Chemistry|January 1, 1981
Piperazinylquinoxalines with central serotoninmimetic activityW C Lumma, R D Hartman, W S Saari, et al.
Journal of Biological Regulators and Homeostatic Agents|July 14, 2017
Use of platelet rich plasma in human infertilityG V L Colombo, V Fanton, D Sosa, et al.
Journal of Medicinal Chemistry|February 1, 1990
Novel glutamic acid derived cholecystokinin receptor ligandsR M Freidinger, W L Whitter, N P Gould, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 1, 1984
R-enantiomer of timolol: a potential selective ocular antihypertensive agentN N Share, V J Lotti, P Gautheron, et al.
Molecular Pharmacology|June 1, 1989
Characterization of the binding of [3H]L-365,260: a new potent and selective brain cholecystokinin (CCK-B) and gastrin receptor antagonist radioligandR S Chang, T B Chen, M G Bock, et al.
Journal of Medicinal Chemistry|September 1, 1978
Synthesis and analgesic activity of 1,3-dihydro-3-(substituted phenyl)imidazo[4,5-b]pyridin-2-ones and 3-(substituted phenyl)-1,2,3-triazolo[4,5-b]pyridinesR L Clark, A A Pessolano, T Y Shen, et al.
Journal of Biological Regulators and Homeostatic Agents|July 14, 2017
Regenerative medicine in the treatment of gastro-esophageal reflux disease and laryngo-pharyngeal reflux. From research to cureS E Aragona, G Mereghetti, M Bianchetti, et al.
The Journal of Pharmacology and Experimental Therapeutics|May 1, 1985
Selectivity of (+)-4-propyl-9-hydroxynaphthoxazine [(+)-PHNO] for dopamine receptors in vitro and in vivoG E Martin, M Williams, D J Pettibone, et al.
Journal of Medicinal Chemistry|August 1, 1989
Cholecystokinin antagonists. Synthesis and biological evaluation of 3-substituted benzolactamsW H Parsons, A A Patchett, M K Holloway, et al.
Pageof 13