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J H Sheldon

Showing results (21-30 of 29) with videos related to

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Journal of Cardiovascular Pharmacology|March 1, 1992
Selective adenosine-2 agonist produces both direct and reflex tachycardia in normotensive ratsR W Lappe, J H Sheldon, B F Cox
The Journal of Pharmacology and Experimental Therapeutics|February 12, 1998
Inhibition of guinea pig detrusor contraction by NS-1619 is associated with activation of BKCa and inhibition of calcium currentsJ H Sheldon, N W Norton, T M Argentieri
The Journal of Urology|August 8, 2001
Efficacy of the beta3-adrenergic receptor agonist CL-316243 on experimental bladder hyperreflexia and detrusor instability in the ratM Woods, N Carson, N W Norton, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 1, 1994
Potentiation of the renal responses to bradykinin by inhibition of neutral endopeptidase 3.4.24.11 and angiotensin-converting enzyme in anesthetized dogsA A Seymour, J H Sheldon, P L Smith, et al.
Hypertension (Dallas, Tex. : 1979)|October 1, 1995
Atrial natriuretic peptide in chronically hypertensive dogsA A Seymour, M M Asaad, J H Sheldon, et al.
Bioorganic & Medicinal Chemistry Letters|August 22, 2001
Synthesis and potassium channel opening activity of substituted 10H-benzo[4,5]furo[3,2-b]indole-and 5,10-dihydro-indeno[1,2-b]indole-1-carboxylic acidsJ A Butera, S A Antane, B Hirth, et al.
The Journal of Pharmacology and Experimental Therapeutics|May 21, 1999
Comparison of the potassium channel openers, WAY-133537, ZD6169, and celikalim on isolated bladder tissue and In vivo bladder instability in ratA Wojdan, C Freeden, M Woods, et al.
Journal of Medicinal Chemistry|March 29, 2000
Design and SAR of novel potassium channel openers targeted for urge urinary incontinence. 1. N-Cyanoguanidine bioisosteres possessing in vivo bladder selectivityJ A Butera, M M Antane, S A Antane, et al.
Journal of Medicinal Chemistry|March 29, 2000
Design and SAR of novel potassium channel openers targeted for urge urinary incontinence. 2. Selective and potent benzylamino cyclobutenedionesA M Gilbert, M M Antane, T M Argentieri, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Journal of Cardiovascular Pharmacology|March 1, 1992
Selective adenosine-2 agonist produces both direct and reflex tachycardia in normotensive ratsR W Lappe, J H Sheldon, B F Cox
The Journal of Pharmacology and Experimental Therapeutics|February 12, 1998
Inhibition of guinea pig detrusor contraction by NS-1619 is associated with activation of BKCa and inhibition of calcium currentsJ H Sheldon, N W Norton, T M Argentieri
The Journal of Urology|August 8, 2001
Efficacy of the beta3-adrenergic receptor agonist CL-316243 on experimental bladder hyperreflexia and detrusor instability in the ratM Woods, N Carson, N W Norton, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 1, 1994
Potentiation of the renal responses to bradykinin by inhibition of neutral endopeptidase 3.4.24.11 and angiotensin-converting enzyme in anesthetized dogsA A Seymour, J H Sheldon, P L Smith, et al.
Hypertension (Dallas, Tex. : 1979)|October 1, 1995
Atrial natriuretic peptide in chronically hypertensive dogsA A Seymour, M M Asaad, J H Sheldon, et al.
Bioorganic & Medicinal Chemistry Letters|August 22, 2001
Synthesis and potassium channel opening activity of substituted 10H-benzo[4,5]furo[3,2-b]indole-and 5,10-dihydro-indeno[1,2-b]indole-1-carboxylic acidsJ A Butera, S A Antane, B Hirth, et al.
The Journal of Pharmacology and Experimental Therapeutics|May 21, 1999
Comparison of the potassium channel openers, WAY-133537, ZD6169, and celikalim on isolated bladder tissue and In vivo bladder instability in ratA Wojdan, C Freeden, M Woods, et al.
Journal of Medicinal Chemistry|March 29, 2000
Design and SAR of novel potassium channel openers targeted for urge urinary incontinence. 1. N-Cyanoguanidine bioisosteres possessing in vivo bladder selectivityJ A Butera, M M Antane, S A Antane, et al.
Journal of Medicinal Chemistry|March 29, 2000
Design and SAR of novel potassium channel openers targeted for urge urinary incontinence. 2. Selective and potent benzylamino cyclobutenedionesA M Gilbert, M M Antane, T M Argentieri, et al.
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