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K Shiosaki

Showing results (31-40 of 39) with videos related to

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Journal of Medicinal Chemistry|November 1, 1990
Development of CCK-tetrapeptide analogues as potent and selective CCK-A receptor agonistsK Shiosaki, C W Lin, H Kopecka, et al.
Journal of Medicinal Chemistry|September 1, 1991
Boc-CCK-4 derivatives containing side-chain ureas as potent and selective CCK-a receptor agonistsK Shiosaki, C W Lin, H Kopecka, et al.
Journal of Medicinal Chemistry|February 19, 1993
Potent and selective inhibitors of an aspartyl protease-like endothelin converting enzyme identified in rat lungK Shiosaki, A S Tasker, G M Sullivan, et al.
Journal of Medicinal Chemistry|May 29, 1992
Development of potent and selective CCK-A receptor agonists from Boc-CCK-4: tetrapeptides containing Lys(N epsilon)-amide residuesK Shiosaki, C W Lin, H Kopecka, et al.
The American Journal of Physiology|July 11, 1992
Behavioral effects of A71623, a highly selective CCK-A agonist tetrapeptideK E Asin, L Bednarz, A L Nikkel, et al.
Journal of Medicinal Chemistry|March 4, 1994
Tetrapeptide CCK-A agonists: effect of backbone N-methylations on in vitro and in vivo CCK activityM W Holladay, H Kopecka, T R Miller, et al.
Molecular Pharmacology|March 1, 1991
Characterization of two novel cholecystokinin tetrapeptide (30-33) analogues, A-71623 and A-70874, that exhibit high potency and selectivity for cholecystokinin-A receptorsC W Lin, K Shiosaki, T R Miller, et al.
Revista Iberoamericana De Micologia|October 19, 2004
Biochemical markers in taxonomy of the genus CunninghamellaR K Shiosaki, K Okada, N Buarque de Gusmão, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 1, 1996
ABT-431: the diacetyl prodrug of A-86929, a potent and selective dopamine D1 receptor agonist: in vitro characterization and effects in animal models of Parkinson's diseaseK Shiosaki, P Jenner, K E Asin, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Journal of Medicinal Chemistry|November 1, 1990
Development of CCK-tetrapeptide analogues as potent and selective CCK-A receptor agonistsK Shiosaki, C W Lin, H Kopecka, et al.
Journal of Medicinal Chemistry|September 1, 1991
Boc-CCK-4 derivatives containing side-chain ureas as potent and selective CCK-a receptor agonistsK Shiosaki, C W Lin, H Kopecka, et al.
Journal of Medicinal Chemistry|February 19, 1993
Potent and selective inhibitors of an aspartyl protease-like endothelin converting enzyme identified in rat lungK Shiosaki, A S Tasker, G M Sullivan, et al.
Journal of Medicinal Chemistry|May 29, 1992
Development of potent and selective CCK-A receptor agonists from Boc-CCK-4: tetrapeptides containing Lys(N epsilon)-amide residuesK Shiosaki, C W Lin, H Kopecka, et al.
The American Journal of Physiology|July 11, 1992
Behavioral effects of A71623, a highly selective CCK-A agonist tetrapeptideK E Asin, L Bednarz, A L Nikkel, et al.
Journal of Medicinal Chemistry|March 4, 1994
Tetrapeptide CCK-A agonists: effect of backbone N-methylations on in vitro and in vivo CCK activityM W Holladay, H Kopecka, T R Miller, et al.
Molecular Pharmacology|March 1, 1991
Characterization of two novel cholecystokinin tetrapeptide (30-33) analogues, A-71623 and A-70874, that exhibit high potency and selectivity for cholecystokinin-A receptorsC W Lin, K Shiosaki, T R Miller, et al.
Revista Iberoamericana De Micologia|October 19, 2004
Biochemical markers in taxonomy of the genus CunninghamellaR K Shiosaki, K Okada, N Buarque de Gusmão, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 1, 1996
ABT-431: the diacetyl prodrug of A-86929, a potent and selective dopamine D1 receptor agonist: in vitro characterization and effects in animal models of Parkinson's diseaseK Shiosaki, P Jenner, K E Asin, et al.
Pageof 4