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J M Schaeffer

Showing results (51-60 of 60) with videos related to

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Bioorganic & Medicinal Chemistry|April 1, 1996
Ophiobolin M and analogues, noncompetitive inhibitors of ivermectin binding with nematocidal activityA Tsipouras, A A Adefarati, J S Tkacz, et al.
Neurogastroenterology and Motility|September 17, 2009
Somatostatin receptor subtypes 2 and 5 mediate inhibition of egg yolk-induced gall bladder emptying in miceP Kaczmarek, V Singh, D E Cashen, et al.
Bioorganic & Medicinal Chemistry Letters|February 24, 2001
Nipecotic and iso-nipecotic amides as potent and selective somatostatin subtype-2 receptor agonistsC Zhou, L Guo, G Morriello, et al.
Bioorganic & Medicinal Chemistry Letters|March 26, 1999
Potent, orally bioavailable somatostatin agonists: good absorption achieved by urea backbone cyclizationA Pasternak, Y Pan, D Marino, et al.
Bioorganic & Medicinal Chemistry Letters|January 15, 2000
Modeling directed design and biological evaluation of quinazolinones as non-peptidic growth hormone secretagoguesZ Ye, Y Gao, R K Bakshi, et al.
Science (New York, N.Y.)|October 23, 1998
Rapid identification of subtype-selective agonists of the somatostatin receptor through combinatorial chemistryS P Rohrer, E T Birzin, R T Mosley, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 2, 1998
Synthesis and biological activities of potent peptidomimetics selective for somatostatin receptor subtype 2L Yang, S C Berk, S P Rohrer, et al.
Bioorganic & Medicinal Chemistry Letters|April 25, 2006
The discovery of tetrahydrofluorenones as a new class of estrogen receptor beta-subtype selective ligandsR R Wilkening, R W Ratcliffe, E C Tynebor, et al.
Journal of Medicinal Chemistry|April 13, 2001
A potent, nonpeptidyl 1H-quinolone antagonist for the gonadotropin-releasing hormone receptorR J DeVita, T F Walsh, J R Young, et al.
Science (New York, N.Y.)|August 16, 1996
A receptor in pituitary and hypothalamus that functions in growth hormone releaseA D Howard, S D Feighner, D F Cully, et al.
Pageof 6

Showing results (51-60 of 60) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
Bioorganic & Medicinal Chemistry|April 1, 1996
Ophiobolin M and analogues, noncompetitive inhibitors of ivermectin binding with nematocidal activityA Tsipouras, A A Adefarati, J S Tkacz, et al.
Neurogastroenterology and Motility|September 17, 2009
Somatostatin receptor subtypes 2 and 5 mediate inhibition of egg yolk-induced gall bladder emptying in miceP Kaczmarek, V Singh, D E Cashen, et al.
Bioorganic & Medicinal Chemistry Letters|February 24, 2001
Nipecotic and iso-nipecotic amides as potent and selective somatostatin subtype-2 receptor agonistsC Zhou, L Guo, G Morriello, et al.
Bioorganic & Medicinal Chemistry Letters|March 26, 1999
Potent, orally bioavailable somatostatin agonists: good absorption achieved by urea backbone cyclizationA Pasternak, Y Pan, D Marino, et al.
Bioorganic & Medicinal Chemistry Letters|January 15, 2000
Modeling directed design and biological evaluation of quinazolinones as non-peptidic growth hormone secretagoguesZ Ye, Y Gao, R K Bakshi, et al.
Science (New York, N.Y.)|October 23, 1998
Rapid identification of subtype-selective agonists of the somatostatin receptor through combinatorial chemistryS P Rohrer, E T Birzin, R T Mosley, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 2, 1998
Synthesis and biological activities of potent peptidomimetics selective for somatostatin receptor subtype 2L Yang, S C Berk, S P Rohrer, et al.
Bioorganic & Medicinal Chemistry Letters|April 25, 2006
The discovery of tetrahydrofluorenones as a new class of estrogen receptor beta-subtype selective ligandsR R Wilkening, R W Ratcliffe, E C Tynebor, et al.
Journal of Medicinal Chemistry|April 13, 2001
A potent, nonpeptidyl 1H-quinolone antagonist for the gonadotropin-releasing hormone receptorR J DeVita, T F Walsh, J R Young, et al.
Science (New York, N.Y.)|August 16, 1996
A receptor in pituitary and hypothalamus that functions in growth hormone releaseA D Howard, S D Feighner, D F Cully, et al.
Pageof 6