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T Ashton

Showing results (161-170 of 169) with videos related to

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Journal of Medicinal Chemistry|August 19, 1994
Triazolinone biphenylsulfonamide derivatives as orally active angiotensin II antagonists with potent AT1 receptor affinity and enhanced AT2 affinityW T Ashton, L L Chang, K L Flanagan, et al.
Journal of Medicinal Chemistry|November 12, 1993
Nonpeptide angiotensin II antagonists derived from 1H-pyrazole-5-carboxylates and 4-aryl-1H-imidazole-5-carboxylatesW T Ashton, S M Hutchins, W J Greenlee, et al.
American Journal of Physiology. Renal Physiology|May 1, 2009
PPARgamma agonists inhibit vasopressin-mediated anion transport in the MDCK-C7 cell lineCharity Nofziger, Kathleen K Brown, Chari D Smith, et al.
Chembiochem : a European Journal of Chemical Biology|March 9, 2022
Linkage-Specific Synthesis of Di-ubiquitin Probes Enabled by the Incorporation of Unnatural Amino Acid ThzKHan Zhou, Tomaya Carpenter, Xuan Fu, et al.
Bioorganic & Medicinal Chemistry Letters|April 20, 2005
Dipeptidyl peptidase IV inhibitors derived from beta-aminoacylpiperidines bearing a fused thiazole, oxazole, isoxazole, or pyrazoleWallace T Ashton, Rosemary M Sisco, Hong Dong, et al.
Chembiochem : a European Journal of Chemical Biology|May 14, 2022
Corrigendum: Linkage-Specific Synthesis of Di-ubiquitin Probes Enabled by the Incorporation of Unnatural Amino Acid ThzKHan Zhou, Tomaya Carpenter, Xuan Fu, et al.
Bioorganic & Medicinal Chemistry Letters|June 27, 2001
Potent nonpeptide GnRH receptor antagonists derived from substituted indole-5-carboxamides and -acetamides bearing a pyridine side-chain terminusW T Ashton, R M Sisco, Y T Yang, et al.
Trends in Ecology & Evolution|August 19, 2017
Harnessing the Power of Genomics to Secure the Future of SeafoodLouis Bernatchez, Maren Wellenreuther, Cristián Araneda, et al.
Bioorganic & Medicinal Chemistry Letters|September 12, 2001
Orally bioavailable, indole-based nonpeptide GnRH receptor antagonists with high potency and functional activityW T Ashton, R M Sisco, G R Kieczykowski, et al.
Pageof 17

Showing results (161-170 of 169) with videos related to

Sort By:
Pageof 17
You have reached the last page of results.This site can display upto 169 results.
Journal of Medicinal Chemistry|August 19, 1994
Triazolinone biphenylsulfonamide derivatives as orally active angiotensin II antagonists with potent AT1 receptor affinity and enhanced AT2 affinityW T Ashton, L L Chang, K L Flanagan, et al.
Journal of Medicinal Chemistry|November 12, 1993
Nonpeptide angiotensin II antagonists derived from 1H-pyrazole-5-carboxylates and 4-aryl-1H-imidazole-5-carboxylatesW T Ashton, S M Hutchins, W J Greenlee, et al.
American Journal of Physiology. Renal Physiology|May 1, 2009
PPARgamma agonists inhibit vasopressin-mediated anion transport in the MDCK-C7 cell lineCharity Nofziger, Kathleen K Brown, Chari D Smith, et al.
Chembiochem : a European Journal of Chemical Biology|March 9, 2022
Linkage-Specific Synthesis of Di-ubiquitin Probes Enabled by the Incorporation of Unnatural Amino Acid ThzKHan Zhou, Tomaya Carpenter, Xuan Fu, et al.
Bioorganic & Medicinal Chemistry Letters|April 20, 2005
Dipeptidyl peptidase IV inhibitors derived from beta-aminoacylpiperidines bearing a fused thiazole, oxazole, isoxazole, or pyrazoleWallace T Ashton, Rosemary M Sisco, Hong Dong, et al.
Chembiochem : a European Journal of Chemical Biology|May 14, 2022
Corrigendum: Linkage-Specific Synthesis of Di-ubiquitin Probes Enabled by the Incorporation of Unnatural Amino Acid ThzKHan Zhou, Tomaya Carpenter, Xuan Fu, et al.
Bioorganic & Medicinal Chemistry Letters|June 27, 2001
Potent nonpeptide GnRH receptor antagonists derived from substituted indole-5-carboxamides and -acetamides bearing a pyridine side-chain terminusW T Ashton, R M Sisco, Y T Yang, et al.
Trends in Ecology & Evolution|August 19, 2017
Harnessing the Power of Genomics to Secure the Future of SeafoodLouis Bernatchez, Maren Wellenreuther, Cristián Araneda, et al.
Bioorganic & Medicinal Chemistry Letters|September 12, 2001
Orally bioavailable, indole-based nonpeptide GnRH receptor antagonists with high potency and functional activityW T Ashton, R M Sisco, G R Kieczykowski, et al.
Pageof 17