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Citation: Rj. Lefkowitz, RODBELL AND GILMAN WIN 1994 NOBEL-PRIZE FOR PHYSIOLOGY AND MEDICINE, Trends in pharmacological sciences, 15(12), 1994, pp. 442-444
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HAWES BE
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Citation: K. Touhara et al., SIMILARITY IN STRUCTURE AND FUNCTIONAL-EFFECTS OF THE G-BETA-GAMMA BINDING DOMAIN OF BETA-ADRENERGIC-RECEPTOR KINASE AND RETINAL PHOSDUCIN, The FASEB journal, 8(7), 1994, pp. 10001225-10001225
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Citation: Ca. Milano et al., ENHANCED MYOCARDIAL-FUNCTION IN TRANSGENIC MICE OVEREXPRESSING THE BETA(2)-ADRENERGIC RECEPTOR, Science, 264(5158), 1994, pp. 582-586
Authors:
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LEFKOWITZ RJ
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Citation: E. Reuveny et al., ACTIVATION OF THE CLONED MUSCARINIC POTASSIUM CHANNEL BY G-PROTEIN BETA-GAMMA-SUBUNITS, Nature, 370(6485), 1994, pp. 143-146
Citation: G. Pei et al., AN APPROACH TO THE STUDY OF G-PROTEIN-COUPLED RECEPTOR KINASES - AN IN VITRO-PURIFIED MEMBRANE ASSAY REVEALS DIFFERENTIAL RECEPTOR SPECIFICITY AND REGULATION BY G-BETA-GAMMA SUBUNITS, Proceedings of the National Academy of Sciences of the United Statesof America, 91(9), 1994, pp. 3633-3636
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Citation: J. Inglese et al., FUNCTIONALLY ACTIVE TARGETING DOMAIN OF THE BETA-ADRENERGIC-RECEPTOR KINASE - AN INHIBITOR OF G-BETA-GAMMA-MEDIATED STIMULATION OF TYPE-II ADENYLYL-CYCLASE, Proceedings of the National Academy of Sciences of the United Statesof America, 91(9), 1994, pp. 3637-3641
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Citation: G. Pei et al., A CONSTITUTIVELY ACTIVE MUTANT BETA(2)-ADRENERGIC RECEPTOR IS CONSTITUTIVELY DESENSITIZED AND PHOSPHORYLATED, Proceedings of the National Academy of Sciences of the United Statesof America, 91(7), 1994, pp. 2699-2702
Citation: Wj. Koch et al., DIRECT EVIDENCE THAT G(I)-COUPLED RECEPTOR STIMULATION OF MITOGEN-ACTIVATED PROTEIN-KINASE IS MEDIATED BY G(BETA-GAMMA) ACTIVATION OF P21(RAS), Proceedings of the National Academy of Sciences of the United Statesof America, 91(26), 1994, pp. 12706-12710
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DOLBER PC
ROCKMAN HA
BOND RA
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Citation: Ca. Milano et al., MYOCARDIAL EXPRESSION OF A CONSTITUTIVELY ACTIVE ALPHA(1B)-ADRENERGICRECEPTOR IN TRANSGENIC MICE INDUCES CARDIAC-HYPERTROPHY, Proceedings of the National Academy of Sciences of the United Statesof America, 91(21), 1994, pp. 10109-10113
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Citation: P. Samama et al., NEGATIVE ANTAGONISTS PROMOTE AN INACTIVE CONFORMATION OF THE BETA(2)-ADRENERGIC RECEPTOR, Molecular pharmacology, 45(3), 1994, pp. 390-394
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Citation: Dt. Price et al., LOCALIZATION OF MESSENGER-RNA FOR 3 DISTINCT ALPHA(1)-ADRENERGIC RECEPTOR SUBTYPES IN HUMAN TISSUES - IMPLICATIONS FOR HUMAN ALPHA-ADRENERGIC PHYSIOLOGY, Molecular pharmacology, 45(2), 1994, pp. 171-175
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KOCH WJ
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LEFKOWITZ RJ
Citation: Rt. Premont et al., IDENTIFICATION, PURIFICATION, AND CHARACTERIZATION OF GRK5, A MEMBER OF THE FAMILY OF G-PROTEIN-COUPLED RECEPTOR KINASES, The Journal of biological chemistry, 269(9), 1994, pp. 6832-6841
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Citation: Wj. Koch et al., CELLULAR EXPRESSION OF THE CARBOXYL-TERMINUS OF A G-PROTEIN-COUPLED RECEPTOR KINASE ATTENUATES G(BETA-GAMMA)-MEDIATED SIGNALING, The Journal of biological chemistry, 269(8), 1994, pp. 6193-6197
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TOUHARA K
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Citation: Be. Hawes et al., DETERMINATION OF THE G-BETA-GAMMA-BINDING DOMAIN OF PHOSDUCIN - A REGULATABLE MODULATOR OF G-BETA-GAMMA SIGNALING, The Journal of biological chemistry, 269(47), 1994, pp. 29825-29830
Citation: Rh. Stoffel et al., PALMITOYLATION OF G-PROTEIN-COUPLED RECEPTOR KINASE, GRK6 - LIPID MODIFICATION DIVERSITY IN THE GRK FAMILY, The Journal of biological chemistry, 269(45), 1994, pp. 27791-27794
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TIBERI M
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Citation: Ls. Barak et al., A HIGHLY CONSERVED TYROSINE RESIDUE IN G-PROTEIN-COUPLED RECEPTORS ISREQUIRED FOR AGONIST-MEDIATED BETA(2)-ADRENERGIC RECEPTOR SEQUESTRATION, The Journal of biological chemistry, 269(4), 1994, pp. 2790-2795