M. S. Kava

Human cloned α1A-adrenoceptor isoforms display α1L-adrenoceptor pharmacology in functional studies

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

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.

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

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

Human cloned alpha1A-adrenoceptor isoforms display alpha1L-adrenoceptor pharmacology in functional studies.

J. Gever, A. Ford, D. V. Daniels, 1999, European journal of pharmacology.

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.

5-HT4 Receptors in Lower Urinary Tract Tissues

A. Ford, M. S. Kava, 1998 .

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.