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D Dayton

Showing results (141-150 of 164) with videos related to

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Critical Care Explorations|February 17, 2023
Annexin A2 Loss After Cardiopulmonary Bypass and Development of Acute Postoperative Respiratory Dysfunction in ChildrenDeyin D Hsing, Arabela C Stock, Bruce M Greenwald, et al.
Cancer Chemotherapy and Pharmacology|June 16, 2009
Plasma and cerebrospinal fluid pharmacokinetics of ABT-888 after oral administration in non-human primatesJodi A Muscal, Patrick A Thompson, Vincent L Giranda, et al.
Clinical Science (London, England : 1979)|August 24, 2002
Pharmacology of endothelin receptor antagonists ABT-627, ABT-546, A-182086 and A-192621: ex vivo and in vivo studiesJerry L Wessale, Andrew L Adler, Eugene I Novosad, et al.
Neurotoxicology|June 1, 2022
Histopathological evidence that diethylene glycol produces kidney and nervous system damage in ratsN Jamison Courtney, K Cuevas-Ocampo Areli, B Flowers Ashley, et al.
Journal of Medical Primatology|February 3, 2015
Initial gene vector dosing for studying symptomatology of amyotrophic lateral sclerosis in non-human primatesKasey L Jackson, Robert D Dayton, Jeanne M Fisher-Perkins, et al.
Journal of Medicinal Chemistry|February 16, 1996
Azole endothelin antagonists. 3. Using delta log P as a tool to improve absorptionT W von Geldern, D J Hoffman, J A Kester, et al.
Journal of Medicinal Chemistry|January 31, 1997
Potent and selective non-benzodioxole-containing endothelin-A receptor antagonistsA S Tasker, B K Sorensen, H S Jae, et al.
European Journal of Pharmacology|March 19, 1999
Pharmacology of A-216546: a highly selective antagonist for endothelin ET(A) receptorJ R Wu-Wong, D B Dixon, W J Chiou, et al.
Bioorganic & Medicinal Chemistry Letters|June 14, 2005
Identification of aminopiperidine benzamides as MCHr1 antagonistsAnil Vasudevan, Mary K Verzal, Derek Wodka, et al.
The Journal of Pharmacology and Experimental Therapeutics|February 1, 1996
Pharmacological characterization of A-127722: an orally active and highly potent ETA-selective receptor antagonistT J Opgenorth, A L Adler, S V Calzadilla, et al.
Pageof 17

Showing results (141-150 of 164) with videos related to

Sort By:
Pageof 17
Critical Care Explorations|February 17, 2023
Annexin A2 Loss After Cardiopulmonary Bypass and Development of Acute Postoperative Respiratory Dysfunction in ChildrenDeyin D Hsing, Arabela C Stock, Bruce M Greenwald, et al.
Cancer Chemotherapy and Pharmacology|June 16, 2009
Plasma and cerebrospinal fluid pharmacokinetics of ABT-888 after oral administration in non-human primatesJodi A Muscal, Patrick A Thompson, Vincent L Giranda, et al.
Clinical Science (London, England : 1979)|August 24, 2002
Pharmacology of endothelin receptor antagonists ABT-627, ABT-546, A-182086 and A-192621: ex vivo and in vivo studiesJerry L Wessale, Andrew L Adler, Eugene I Novosad, et al.
Neurotoxicology|June 1, 2022
Histopathological evidence that diethylene glycol produces kidney and nervous system damage in ratsN Jamison Courtney, K Cuevas-Ocampo Areli, B Flowers Ashley, et al.
Journal of Medical Primatology|February 3, 2015
Initial gene vector dosing for studying symptomatology of amyotrophic lateral sclerosis in non-human primatesKasey L Jackson, Robert D Dayton, Jeanne M Fisher-Perkins, et al.
Journal of Medicinal Chemistry|February 16, 1996
Azole endothelin antagonists. 3. Using delta log P as a tool to improve absorptionT W von Geldern, D J Hoffman, J A Kester, et al.
Journal of Medicinal Chemistry|January 31, 1997
Potent and selective non-benzodioxole-containing endothelin-A receptor antagonistsA S Tasker, B K Sorensen, H S Jae, et al.
European Journal of Pharmacology|March 19, 1999
Pharmacology of A-216546: a highly selective antagonist for endothelin ET(A) receptorJ R Wu-Wong, D B Dixon, W J Chiou, et al.
Bioorganic & Medicinal Chemistry Letters|June 14, 2005
Identification of aminopiperidine benzamides as MCHr1 antagonistsAnil Vasudevan, Mary K Verzal, Derek Wodka, et al.
The Journal of Pharmacology and Experimental Therapeutics|February 1, 1996
Pharmacological characterization of A-127722: an orally active and highly potent ETA-selective receptor antagonistT J Opgenorth, A L Adler, S V Calzadilla, et al.
Pageof 17