Pharmacology of P2X channels von Gever, Joel R, Cockayne, Debra A, Dillon, Michael P, Burnstock, Geoffrey, Ford, Anthony P D W

Volltext

Discovery and synthesis of a novel and selective drug-like P2X1 antagonist von JAIME-FIGUEROA, S, GREENHOUSE, R, PADILLA, F, DILLON, M. P, GEVER, J. R, FORD, A. P. D. W

Volltext

In vitroα1‐adrenoceptor pharmacology of Ro 70–0004 and RS‐100329, novel α1A‐adrenoceptor selective antagonists von Williams, T J, Blue, D R, Daniels, D V, Davis, B, Elworthy, T, Gever, J R, Kava, M S, Morgans, D, Padilla, F, Tassa, S, Vimont, R L, Chapple, C R, Chess‐Williams, R, Eglen, R M, Clarke, D E, Ford, A P D W

Volltext

Purinoceptors as therapeutic targets for lower urinary tract dysfunction von Ford, Anthony P D W., Gever, Joel R., Nunn, Philip A., Zhong, Yu, Cefalu, Joseph S., Dillon, Michael P., Cockayne, Debra A.

Volltext

Rice field surface microlayers: collection, composition and pesticide enrichment von Gever, J.R. (University of California, Davis, CA.), Mabury, S.A, Crosby, D.G

Volltext

Pharmacological characteristics of Ro 115–1240, a selective α 1A/1L ‐adrenoceptor partial agonist: a potential therapy for stress urinary incontinence von Blue, D.R., Daniels, D.V., Gever, J.R., Jett, M.F., O'Yang, C., Tang, H.M., Williams, T.J., Ford, A.P.D.W.

Volltext

Discovery and synthesis of a novel and selective drug-like P2X(1) antagonist von Jaime-Figueroa, S, Greenhouse, R, Padilla, F, Dillon, M P, Gever, J R, Ford, A P D W

Volltext

Antagonism of ATP responses at P2X receptor subtypes by the pH indicator dye, Phenol red von King, Brian F, Liu, Min, Townsend‐Nicholson, Andrea, Pfister, Jürg, Padilla, Fernando, Ford, Anthony P, Gever, Joel R, Oglesby, Ian B, Schorge, Stephanie, Burnstock, Geoffrey

Volltext

In vitro α 1 ‐adrenoceptor pharmacology of Ro 70–0004 and RS‐100329, novel α 1A ‐adrenoceptor selective antagonists von Williams, T J, Blue, D R, Daniels, D V, Davis, B, Elworthy, T, Gever, J R, Kava, M S, Morgans, D, Padilla, F, Tassa, S, Vimont, R L, Chapple, C R, Chess‐Williams, R, Eglen, R M, Clarke, D E, Ford, A P D W

Volltext

Pharmacological characteristics of Ro 115–1240, a selective α1A/1L‐adrenoceptor partial agonist: a potential therapy for stress urinary incontinence von Blue, D.R., Daniels, D.V., Gever, J.R., Jett, M.F., O'Yang, C., Tang, H.M., Williams, T.J., Ford, A.P.D.W.

Volltext

Pharmacological characteristics of Ro 115-1240, a selective alpha1A/1L-adrenoceptor partial agonist: a potential therapy for stress urinary incontinence von Blue, D R, Daniels, D V, Gever, J R, Jett, M F, O'Yang, C, Tang, H M, Williams, T J, Ford, A P D W

Volltext

Pharmacological pleiotropism of the human recombinant α1A‐adrenoceptor: implications for α1‐adrenoceptor classification von Ford, Anthony P D W, Daniels, Donald V, Chang, David J, Gever, Joel R, Jasper, Jeffrey R, Lesnick, John D, Clarke, David E

Volltext

Human cloned alpha1A-adrenoceptor isoforms display alpha1L-adrenoceptor pharmacology in functional studies von Daniels, D V, Gever, J R, Jasper, J R, Kava, M S, Lesnick, J D, Meloy, T D, Stepan, G, Williams, T J, Clarke, D E, Chang, D J, Ford, A P

Volltext

Human cloned α 1A-adrenoceptor isoforms display α1L-adrenoceptor pharmacology in functional studies von DANIELS, D. V, GEVER, J. R, FORD, A. P. D. W, JASPER, J. R, KAVA, M. S, LESNICK, J. D, MELOY, T. D, STEPAN, G, WILLIAMS, T. J, CLARKE, D. E, CHANG, D. J

Volltext

Pharmacological pleiotropism of the human recombinant alpha1A-adrenoceptor: implications for alpha1-adrenoceptor classification von Ford, A P, Daniels, D V, Chang, D J, Gever, J R, Jasper, J R, Lesnick, J D, Clarke, D E

Volltext

In vitro alpha1-adrenoceptor pharmacology of Ro 70-0004 and RS-100329, novel alpha1A-adrenoceptor selective antagonists von Williams, T J, Blue, D R, Daniels, D V, Davis, B, Elworthy, T, Gever, J R, Kava, M S, Morgans, D, Padilla, F, Tassa, S, Vimont, R L, Chapple, C R, Chess-Williams, R, Eglen, R M, Clarke, D E, Ford, A P

Volltext

Discovery and Synthesis of a Novel and Selective Drug‐Like P2X 1 Antagonist von Jaime‐Figueroa, S., Greenhouse, R., Padilla, F., Dillon, M. P., Gever, J. R., Ford, A. P. D. W.

Volltext

Discovery and Synthesis of a Novel and Selective Drug-Like P2X1 Antagonist von Jaime-Figueroa, S., Greenhouse, R., Padilla, F., Dillon, M. P., Gever, J. R., Ford, A. P. D. W.

Volltext

Regulated expression of the rat recombinant P2X(3) receptor in stably transfected CHO-K1 tTA cells von Lachnit, W G, Oglesby, I B, Gever, J R, Gever, M, Huang, C, Li, X C, Jin, H, McGivern, J G, Ford, A P

Volltext

Regulated expression of the rat recombinant P2X3 receptor in stably transfected CHO-K1 tTA cells: Purines and the autonomic nervous system: from controversy to clinic von LACHNIT, W. G, OGLESBY, I. B, GEVER, J. R, GEVER, M, HUANG, C.-C, XING CHENG LI, HONG JIN, MCGIVERN, J. G, FORD, A. P. D. W

Volltext