Showing results (21-30 of 40) with videos related to
Sort By:
Pageof 4
The Journal of Pharmacology and Experimental Therapeutics|July 1, 1995
A-61603, a potent alpha 1-adrenergic receptor agonist, selective for the alpha 1A receptor subtypeS M Knepper, S A Buckner, M E Brune, et al.Pharmacology|February 19, 1998
Cardiovascular activity of A-74283, a 5-hydroxytryptamine 1A agent, in the spontaneously hypertensive ratJ Y Lee, A A Hancock, R B Warner, et al.Diabetes Care|July 1, 1996
Impaired peripheral vasomotion in diabetesK B Stansberry, S A Shapiro, M A Hill, et al.Journal of Dairy Science|August 1, 1996
Treatment with recombinant bovine interferon-tau in utero attenuates secretion of prostaglandin F from cultured endometrial epithelial cellsM D Meyer, G D Desnoyers, B Oldick, et al.Journal of Diabetes and Its Complications|June 9, 1998
Normal blood flow response and vasomotion in the diabetic Charcot footS A Shapiro, K B Stansberry, M A Hill, et al.European Journal of Pain (London, England)|August 27, 2014
A selective α2 B adrenoceptor agonist (A-1262543) and duloxetine modulate nociceptive neurones in the medial prefrontal cortex, but not in the spinal cord of neuropathic ratsK L Chu, J Xu, J Frost, et al.European Journal of Pharmacology|April 20, 2000
The identification of novel structural compound classes exhibiting high affinity for neuronal nicotinic acetylcholine receptors and analgesic efficacy in preclinical models of painM D Meyer, M W Decker, L E Rueter, et al.Pharmaceutica Acta Helvetiae|May 17, 2000
Structural aspects of high affinity ligands for the alpha 4 beta 2 neuronal nicotinic receptorM J Dart, J T Wasicak, K B Ryther, et al.Journal of Dairy Science|September 1, 1995
Extension of corpus luteum lifespan and reduction of uterine secretion of prostaglandin F2 alpha of cows in response to recombinant interferon-tauM D Meyer, P J Hansen, W W Thatcher, et al.Journal of Medicinal Chemistry|March 28, 1997
Structure-activity studies for a novel series of N-(arylethyl)-N-(1,2,3,4-tetrahydronaphthalen-1-ylmethyl)-N-methylamine s possessing dual 5-HT uptake inhibiting and alpha2-antagonistic activitiesM D Meyer, A A Hancock, K Tietje, et al.Pageof 4