S. Knepper

发表

A-61603, a potent alpha 1-adrenergic receptor agonist, selective for the alpha 1A receptor subtype.

J. Debernardis, A. Hancock, M. Brune, 1995, The Journal of pharmacology and experimental therapeutics.

Parallel production of oligonucleotide arrays using membranes and reagent jet printing.

D. Stimpson, P. Cooley, D. Wallace, 1998, BioTechniques.

Pharmacological characterization of A‐131701, a novel α1‐adrenoceptor antagonist selective for α1A‐ and α1D‐compared to α1B‐adrenoceptors

R. Chess-Williams, M. Williams, C. Chapple, 1998 .

Inhibition of norepinephrine transport into synaptic vesicles by amphetamine analogs.

S. Knepper, C. Rutledge, G. L. Grunewald, 1988, The Journal of pharmacology and experimental therapeutics.

Effects of calcium depletion on norepinephrine- and A23187-induced stimulation of inositol phosphate formation.

S. Knepper, C. Rutledge, 1987, Biochemical pharmacology.

Pharmacologic characterization of CHIR 2279, an N-substituted glycine peptoid with high-affinity binding for alpha 1-adrenoceptors.

D. Spellmeyer, R. Zuckermann, W. Moos, 1996, The Journal of pharmacology and experimental therapeutics.

Norepinephrine Stimulation of Phosphoinositide Hydrolysis in Rat Cerebral Cortex Is Associated with the Alpha1‐Adrenoceptor

D. Schoepp, S. Knepper, C. Rutledge, 1984, Journal of neurochemistry.

α1-Adrenoceptor-induced contractility in rat aorta is mediated by the α1D subtype

A. Hancock, S. Knepper, S. Buckner, 1996 .

Actions of terazosin and its enantiomers at subtypes of alpha 1- and alpha 2-adrenoceptors in vitro.

A. Hancock, S. Knepper, S. Buckner, 1995, Journal of receptor and signal transduction research.

Alpha 1-adrenoceptor-induced contractility in rat aorta is mediated by the alpha 1D subtype.

A. Hancock, S. Knepper, S. Buckner, 1996, European Journal of Pharmacology.

Synthesis and in vitro Characterization of N‐(5‐(4,5‐Dihydro‐1H‐ imidazol‐2‐yl)‐2‐hydroxy‐5,6,7,8‐tetrahydronaphthalen‐1‐yl) methanesulfonamide and Its Enantiomers: A Novel Selective α1A Receptor Agonist.

A. Hancock, M. Meyer, S. Knepper, 1997 .

Synthesis and in vitro characterization of N-[5-(4,5-dihydro-1H-imidazol-2-yl)-2-hydroxy-5,6,7,8- tetrahydronaphthalen-1-yl]methanesulfonamide and its enantiomers: a novel selective alpha 1A receptor agonist.

A. Hancock, M. Meyer, S. Knepper, 1996, Journal of medicinal chemistry.

Selective induction of nasal cavity tumors in rats by diallylnitrosamine

P. Pour, S. Knepper, C. Grandjean, 2005, Journal of Cancer Research and Clinical Oncology.