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Results: 1-23 |
Results: 23
IDENTIFICATION OF A DIHYDROPYRIDINE AS A POTENT ALPHA(1A) ADRENOCEPTOR-SELECTIVE ANTAGONIST THAT INHIBITS PHENYLEPHRINE-INDUCED CONTRACTIONOF THE HUMAN PROSTATE
Authors: WONG WC CHIU G WETZEL JM MARZABADI MR NAGARATHNAM D WANG D FANG J MIAO SW HONG XF FORRAY C VAYSSE PJJ BRANCHEK TA GLUCHOWSKI C TANG R LEPOR H
Citation: Wc. Wong et al., IDENTIFICATION OF A DIHYDROPYRIDINE AS A POTENT ALPHA(1A) ADRENOCEPTOR-SELECTIVE ANTAGONIST THAT INHIBITS PHENYLEPHRINE-INDUCED CONTRACTIONOF THE HUMAN PROSTATE, Journal of medicinal chemistry, 41(14), 1998, pp. 2643-2650
CLONED HUMAN AND RAT GALANIN GALR3 RECEPTORS - PHARMACOLOGY AND ACTIVATION OF G-PROTEIN INWARDLY RECTIFYING K+ CHANNELS
Authors: SMITH KE WALKER MW ARTYMYSHYN R BARD J BOROWSKY B TAMM JA YAO WJ VAYSSE PJJ BRANCHEK TA GERALD C JONES KA
Citation: Ke. Smith et al., CLONED HUMAN AND RAT GALANIN GALR3 RECEPTORS - PHARMACOLOGY AND ACTIVATION OF G-PROTEIN INWARDLY RECTIFYING K+ CHANNELS, The Journal of biological chemistry, 273(36), 1998, pp. 23321-23326
MODELING THE G-PROTEIN-COUPLED NEUROPEPTIDE-Y Y1 RECEPTOR AGONIST ANDANTAGONIST BINDING-SITES
Authors: DU P SALON JA TAMM JA HOU CF CUI WL WALKER MW ADHAM N DHANOA DS ISLAM I VAYSSE PJJ DOWLING B SHIFMAN Y BOYLE N RUEGER H SCHMIDLIN T YAMAGUCHI Y BRANCHEK TA WEINSHANK RL GLUCHOWSKI C
Citation: P. Du et al., MODELING THE G-PROTEIN-COUPLED NEUROPEPTIDE-Y Y1 RECEPTOR AGONIST ANDANTAGONIST BINDING-SITES, Protein engineering, 10(2), 1997, pp. 109-117
A STRUCTURE-ACTIVITY ANALYSIS OF THE CLONED RAT AND HUMAN Y4 RECEPTORS FOR PANCREATIC-POLYPEPTIDE
Authors: WALKER MW SMITH KE BARD J VAYSSE PJJ GERALD C DAOUTI S WEINSHANK RL BRANCHEK TA
Citation: Mw. Walker et al., A STRUCTURE-ACTIVITY ANALYSIS OF THE CLONED RAT AND HUMAN Y4 RECEPTORS FOR PANCREATIC-POLYPEPTIDE, Peptides, 18(4), 1997, pp. 609-612
MODELING AND MUTAGENESIS OF THE HUMAN ALPHA(1A)-ADRENOCEPTOR - ORIENTATION AND FUNCTION OF TRANSMEMBRANE HELIX-V SIDE-CHAINS
Authors: WETZEL JM SALON JA TAMM JA FORRAY C CRAIG D NAKANISHI H CUI W VAYSSE PJJ CHIU G WEINSHANK RL HARTIG PR BRANCHEK TA GLUCHOWSKI C
Citation: Jm. Wetzel et al., MODELING AND MUTAGENESIS OF THE HUMAN ALPHA(1A)-ADRENOCEPTOR - ORIENTATION AND FUNCTION OF TRANSMEMBRANE HELIX-V SIDE-CHAINS, Receptors & channels, 4(3), 1996, pp. 165-177
REEVALUATION OF GABA TRANSPORT IN NEURONAL AND GLIAL-CELL CULTURES - CORRELATION OF PHARMACOLOGY AND MESSENGER-RNA LOCALIZATION
Authors: BORDEN LA SMITH KE VAYSSE PJJ GUSTAFSON EL WEINSHANK RL BRANCHEK TA
Citation: La. Borden et al., REEVALUATION OF GABA TRANSPORT IN NEURONAL AND GLIAL-CELL CULTURES - CORRELATION OF PHARMACOLOGY AND MESSENGER-RNA LOCALIZATION, Receptors & channels, 3(2), 1995, pp. 129-146
PHARMACOLOGICAL EVALUATION OF UK-14,304 ANALOGS AT CLONED HUMAN ALPHA-ADRENERGIC RECEPTORS
Authors: JEON YT LUO C FORRAY C VAYSSE PJJ BRANCHEK TA GLUCHOWSKI C
Citation: Yt. Jeon et al., PHARMACOLOGICAL EVALUATION OF UK-14,304 ANALOGS AT CLONED HUMAN ALPHA-ADRENERGIC RECEPTORS, Bioorganic & medicinal chemistry letters, 5(19), 1995, pp. 2255-2258
THE 5-HT4 RECEPTOR - MOLECULAR-CLONING AND PHARMACOLOGICAL CHARACTERIZATION OF 2 SPLICE VARIANTS
Authors: GERALD C ADHAM N KAO HT OLSEN MA LAZ TM SCHECHTER LE BARD JA VAYSSE PJJ HARTIG PR BRANCHEK TA WEINSHANK RL
Citation: C. Gerald et al., THE 5-HT4 RECEPTOR - MOLECULAR-CLONING AND PHARMACOLOGICAL CHARACTERIZATION OF 2 SPLICE VARIANTS, EMBO journal, 14(12), 1995, pp. 2806-2815
DIVERSITY OF GABA TRANSPORTERS
Authors: BORDEN LA SMITH KE DHAR TGM VAYSSE PJJ GLUCHOWSKI C WEINSHANK RL BRANCHEK TA
Citation: La. Borden et al., DIVERSITY OF GABA TRANSPORTERS, Journal of neurochemistry, 65, 1995, pp. 2-2
EXPRESSION CLONING AND PHARMACOLOGICAL CHARACTERIZATION OF A HUMAN HIPPOCAMPAL NEUROPEPTIDE-Y PEPTIDE YY Y2 RECEPTOR SUBTYPE
Authors: GERALD C WALKER MW VAYSSE PJJ HE CG BRANCHEK TA WEINSHANK RL
Citation: C. Gerald et al., EXPRESSION CLONING AND PHARMACOLOGICAL CHARACTERIZATION OF A HUMAN HIPPOCAMPAL NEUROPEPTIDE-Y PEPTIDE YY Y2 RECEPTOR SUBTYPE, The Journal of biological chemistry, 270(45), 1995, pp. 26758-26761
CHARACTERIZATION OF THE FUNCTIONAL-RESPONSES MEDIATED BY 2 SPLICE VARIANTS OF THE CLONED RAT 5-HT4 RECEPTOR IN HETEROLOGOUS EXPRESSION SYSTEMS
Authors: ADHAM N GERALD C VAYSSE PJJ WEINSHANK RL BRANCHEK TA
Citation: N. Adham et al., CHARACTERIZATION OF THE FUNCTIONAL-RESPONSES MEDIATED BY 2 SPLICE VARIANTS OF THE CLONED RAT 5-HT4 RECEPTOR IN HETEROLOGOUS EXPRESSION SYSTEMS, British Journal of Pharmacology, 114, 1995, pp. 158-158
A CONVENIENT SYNTHESIS OF 2-AMINO-2-OXAZOLINES AND THEIR PHARMACOLOGICAL EVALUATION AT CLONED HUMAN ALPHA-ADRENERGIC RECEPTORS
Authors: WONG WC WANG D FORRAY C VAYSSE PJJ BRANCHEK TA GLUCHOWSKI C
Citation: Wc. Wong et al., A CONVENIENT SYNTHESIS OF 2-AMINO-2-OXAZOLINES AND THEIR PHARMACOLOGICAL EVALUATION AT CLONED HUMAN ALPHA-ADRENERGIC RECEPTORS, Bioorganic & medicinal chemistry letters, 4(19), 1994, pp. 2317-2322
GABA TRANSPORTERS IN NEURONAL AND GLIAL-CELL CULTURES - CORRELATION OF PHARMACOLOGICAL ACTIVITY WITH MESSENGER-RNA LOCALIZATION
Authors: BORDEN LA SMITH KE VAYSSE PJJ WEINSHANK RL BRANCHEK TA
Citation: La. Borden et al., GABA TRANSPORTERS IN NEURONAL AND GLIAL-CELL CULTURES - CORRELATION OF PHARMACOLOGICAL ACTIVITY WITH MESSENGER-RNA LOCALIZATION, The FASEB journal, 8(4), 1994, pp. 10000112-10000112
COMPARISON OF THE PHARMACOLOGICAL PROPERTIES OF THE CLONED BOVINE, HUMAN, AND RAT ALPHA(1C)-ADRENERGIC RECEPTORS
Authors: FORRAY C BARD JA LAZ TM SMITH KE VAYSSE PJJ WEINSHANK RL GLUCHOWSKI C BRANCHEK TA
Citation: C. Forray et al., COMPARISON OF THE PHARMACOLOGICAL PROPERTIES OF THE CLONED BOVINE, HUMAN, AND RAT ALPHA(1C)-ADRENERGIC RECEPTORS, The FASEB journal, 8(4), 1994, pp. 10000353-10000353
NPY BINDING TO THE HUMAN Y1-RECEPTOR INVOLVES CHARGED AMINO-ACIDS IN THE RECEPTOR
Authors: WALKER MW TAMM JA CUI W VAYSSE PJJ BRANCHEK TA GLUCHOWSKI C WEINSHANK RL HARTIG PR SALON JA
Citation: Mw. Walker et al., NPY BINDING TO THE HUMAN Y1-RECEPTOR INVOLVES CHARGED AMINO-ACIDS IN THE RECEPTOR, The FASEB journal, 8(4), 1994, pp. 10000377-10000377
STRUCTURAL AND FUNCTIONAL-STUDIES OF THE HUMAN ALPHA-1C-ADRENERGIC RECEPTOR - THE ORIENTATION OF TRANSMEMBRANE HELIX-5
Authors: WETZEL JM TAMM JA FORRAY C SALON JA NAKANISHI H CUI W CHIU G VAYSSE PJJ BRANCHEK TA WEINSHANK RL HARTIG PR GLUCHOWSKI C
Citation: Jm. Wetzel et al., STRUCTURAL AND FUNCTIONAL-STUDIES OF THE HUMAN ALPHA-1C-ADRENERGIC RECEPTOR - THE ORIENTATION OF TRANSMEMBRANE HELIX-5, The FASEB journal, 8(4), 1994, pp. 10000377-10000377
THE IMPORTANCE OF AROMATIC INTERACTIONS IN NPY BINDING TO THE HUMAN Y1-RECEPTOR
Authors: SALON JA CUI W TAMM JA WALKER MW VAYSSE PJJ BRANCHEK TA GLUCHOWSKI C HARTIG PR WEINSHANK RL
Citation: Ja. Salon et al., THE IMPORTANCE OF AROMATIC INTERACTIONS IN NPY BINDING TO THE HUMAN Y1-RECEPTOR, The FASEB journal, 8(4), 1994, pp. 10000377-10000377
THE N-TERMINUS OF THE HUMAN Y1-RECEPTOR IS NOT A MAJOR DETERMINANT FOR NPY BINDING
Authors: TAMM JA WALKER MW VAYSSE PJJ BRANCHEK TA WEINSHANK RL HARTIG PR SALON JA
Citation: Ja. Tamm et al., THE N-TERMINUS OF THE HUMAN Y1-RECEPTOR IS NOT A MAJOR DETERMINANT FOR NPY BINDING, The FASEB journal, 8(4), 1994, pp. 10000378-10000378
USE OF RECOMBINANT HUMAN ALPHA-ADRENERGIC RECEPTORS FOR THE PHARMACOLOGICAL EVALUATION OF ALPHA-ADRENERGIC OCULAR HYPOTENSIVE AGENTS
Authors: GLUCHOWSKI C JEON YT WETZEL JM VAYSSE PJJ BRANCHEK TA WEINSHANK RL BORDEN LA BARD JA HARTIG PR FORRAY C
Citation: C. Gluchowski et al., USE OF RECOMBINANT HUMAN ALPHA-ADRENERGIC RECEPTORS FOR THE PHARMACOLOGICAL EVALUATION OF ALPHA-ADRENERGIC OCULAR HYPOTENSIVE AGENTS, Investigative ophthalmology & visual science, 35(4), 1994, pp. 1399-1399
A SINGLE-POINT MUTATION INCREASES THE AFFINITY OF SEROTONIN 5-HT1D-ALPHA, 5-HT1D-BETA, 5-HT1E AND 5-HT1F RECEPTORS FOR BETA-ADRENERGIC ANTAGONISTS
Authors: ADHAM N TAMM JA SALON JA VAYSSE PJJ WEINSHANK RL BRANCHEK TA
Citation: N. Adham et al., A SINGLE-POINT MUTATION INCREASES THE AFFINITY OF SEROTONIN 5-HT1D-ALPHA, 5-HT1D-BETA, 5-HT1E AND 5-HT1F RECEPTORS FOR BETA-ADRENERGIC ANTAGONISTS, Neuropharmacology, 33(3-4), 1994, pp. 387-391
THE CLONED HUMAN 5-HT1E RECEPTOR COUPLES TO INHIBITION AND ACTIVATIONOF ADENYLYL-CYCLASE VIA 2 DISTINCT PATHWAYS IN TRANSFECTED BS-C-1 CELLS
Authors: ADHAM N VAYSSE PJJ WEINSHANK RL BRANCHEK TA
Citation: N. Adham et al., THE CLONED HUMAN 5-HT1E RECEPTOR COUPLES TO INHIBITION AND ACTIVATIONOF ADENYLYL-CYCLASE VIA 2 DISTINCT PATHWAYS IN TRANSFECTED BS-C-1 CELLS, Neuropharmacology, 33(3-4), 1994, pp. 403-410
THE RAT HOMOLOG OF THE BOVINE ALPHA(1C)-ADRENERGIC RECEPTOR SHOWS THEPHARMACOLOGICAL PROPERTIES OF THE CLASSICAL ALPHA(1A) SUBTYPE
Authors: LAZ TM FORRAY C SMITH KE BARD JA VAYSSE PJJ BRANCHEK TA WEINSHANK RL
Citation: Tm. Laz et al., THE RAT HOMOLOG OF THE BOVINE ALPHA(1C)-ADRENERGIC RECEPTOR SHOWS THEPHARMACOLOGICAL PROPERTIES OF THE CLASSICAL ALPHA(1A) SUBTYPE, Molecular pharmacology, 46(3), 1994, pp. 414-422
CELL-SPECIFIC COUPLING OF THE CLONED HUMAN 5-HT(1F) RECEPTOR TO MULTIPLE SIGNAL-TRANSDUCTION PATHWAYS
Authors: ADHAM N BORDEN LA SCHECHTER LE GUSTAFSON EL COCHRAN TL VAYSSE PJJ WEINSHANK RL BRANCHEK TA
Citation: N. Adham et al., CELL-SPECIFIC COUPLING OF THE CLONED HUMAN 5-HT(1F) RECEPTOR TO MULTIPLE SIGNAL-TRANSDUCTION PATHWAYS, Naunyn-Schmiedeberg's archives of pharmacology, 348(6), 1993, pp. 566-575
Risultati: 1-23 |