R. Vimont

发表

In vitroα1‐adrenoceptor pharmacology of Ro 70–0004 and RS‐100329, novel α1A‐adrenoceptor selective antagonists

J. Gever, A. Ford, D. V. Daniels, 1999 .

α1L‐Adrenoceptor mediation of smooth muscle contraction in rabbit bladder neck: a model for lower urinary tract tissues of man

A. Ford, D. Clarke, D. Blue, 1998, British journal of pharmacology.

RS-17053 (N-[2-(2-cyclopropylmethoxyphenoxy)ethyl]-5-chloro-alpha, alpha-dimethyl-1H-indole-3-ethanamine hydrochloride), a selective alpha 1A-adrenoceptor antagonist, displays low affinity for functional alpha 1-adrenoceptors in human prostate: implications for adrenoceptor classification.

T. Stamey, A. Ford, J. McNeal, 1996, Molecular pharmacology.

Functional evidence equating the pharmacologically‐defined α1A‐ and cloned α1C‐adrenoceptor: studies in the isolated perfused kidney of rat

A. Ford, N. Sharif, D. Clarke, 1995 .

Functional evidence equating the pharmacologically-defined alpha 1A- and cloned alpha 1C-adrenoceptor: studies in the isolated perfused kidney of rat.

A. Ford, N. Sharif, T. Williams, 1995, British Journal of Pharmacology.

Evidence for a noradrenergic innervation to α1A‐adrenoceptors in rat kidney

D. Clarke, D. Blue, R. Vimont, 1992 .

In vitro alpha1-adrenoceptor pharmacology of Ro 70-0004 and RS-100329, novel alpha1A-adrenoceptor selective antagonists.

J. Gever, A. Ford, R. Chess-Williams, 1999, British Journal of Pharmacology.

Vascular alpha1-adrenoceptors in rat kidney: agonist and antagonist [prazosin, idazoxan, WB 4101, (+)-niguldipine] characterization☆

D. Clarke, D. Blue, R. Vimont, 1990 .

N-arylpiperazinyl-N'-propylamino derivatives of heteroaryl amides as functional uroselective alpha 1-adrenoceptor antagonists.

A. Ford, T. Williams, M. S. Kava, 1997, Journal of medicinal chemistry.