196 results on '"Rodbell M"'
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2. G-Proteins Have Properties of Multimeric Proteins: An Explanation for the Role of GTPases in their Dynamic Behavior
3. G-Proteins Have Properties of Multimeric Proteins: An Explanation for the Role of GTPases in their Dynamic Behavior
4. Adenylate cyclase: actions and interactions of regulatory ligands
5. The Role of GTP in the Coupling of Hormone Receptors and Adenylate Cyclase
6. The Actions of Glucagon at Its Receptor: Regulation of Adenylate Cyclase
7. [7] Preparation of isolated fat cells and fat cell “ghost”; methods for assaying adenylate cyclase activity and levels of cyclic AMP
8. The Actions of Glucagon at Its Receptor: Regulation of Adenylate Cyclase
9. The Actions of Insulin and Catabolic Hormones on the Plasma Membrane of the Fat Cells
10. Signal transduction: evolution of an idea.
11. Bioinformatics: an emerging means of assessing environmental health.
12. The disaggregation theory of signal transduction revisited: further evidence that G proteins are multimeric and disaggregate to monomers when activated.
13. Glucagon induces disaggregation of polymer-like structures of the alpha subunit of the stimulatory G protein in liver membranes.
14. Carbachol-activated muscarinic (M1 and M3) receptors transfected into Chinese hamster ovary cells inhibit trafficking of endosomes.
15. Microsomal and cytosolic fractions of guinea pig hepatocytes contain 100-kilodalton GTP-binding proteins reactive with antisera against alpha subunits of stimulatory and inhibitory heterotrimeric GTP-binding proteins.
16. Octyl glucoside extracts GTP-binding regulatory proteins from rat brain "synaptoneurosomes" as large, polydisperse structures devoid of beta gamma complexes and sensitive to disaggregation by guanine nucleotides.
17. Isoproterenol stimulates shift of G proteins from plasma membrane to pinocytotic vesicles in rat adipocytes: a possible means of signal dissemination.
18. Adenosine receptor-mediated inhibition of rat cerebral cortical adenylate cyclase by a GTP-dependent process.
19. Simple model for hormone-activated adenylate cyclase systems.
20. Pertussis toxin induces structural changes in G alpha proteins independently of ADP-ribosylation.
21. Hydroxybenzylpindolol and hydroxybenzylpropranolol: partial beta adrenergic agonists of adenylate cyclase in the rat adipocyte.
22. Adenosine analogs inhibit adipocyte adenylate cyclase by a GTP-dependent process: basis for actions of adenosine and methylxanthines on cyclic AMP production and lipolysis.
23. Structure of the turkey erythrocyte adenylate cyclase system.
24. Proposed mechanism of insulin-resistant glucose transport in the isolated guinea pig adipocyte. Small intracellular pool of glucose transporters.
25. Activation of adenylate cyclase in hepatic membranes involves interactions of the catalytic unit with multimeric complexes of regulatory proteins.
26. Heterotrimeric G proteins in synaptoneurosome membranes are crosslinked by p-phenylenedimaleimide, yielding structures comparable in size to crosslinked tubulin and F-actin.
27. The Complex Regulation of Receptor-coupled G-Proteins
28. The hepatic adenylate cyclase system. II. Substrate binding and utilization and the effects of magnesium ion and pH
29. A reassessment of structure-function relationships in glucagon. Glucagon1-21 is a full agonist.
30. Glucagon1-6 binds to the glucagon receptor and activates hepatic adenylate cyclase.
31. The hepatic adenylate cyclase system. III. A mathematical model for the steady state kinetics of catalysis and nucleotide regulation
32. Preparation of 2-thioltryptophan-glucagon and (tryptophan-S-glucagon)2. Differences in binding to the glucagon receptor in the hepatic adenylate cyclase system.
33. The Coupling of Hormone Receptors and Adenylate Cyclase
34. Independent mechanisms of adenosine activation and inhibition of the turkey erythrocyte adenylate cyclase system.
35. The hepatic adenylate cyclase system. I. Evidence for transition states and structural requirements for guanine nucloetide activiation
36. A persistent active state of the adenylate cyclase system produced by the combined actions of isoproterenol and guanylyl imidodiphosphate in frog erythrocyte membranes.
37. On the mechanism of activation of fat cell adenylate cyclase by guanine nucleotides. An explanation for the biphasic inhibitory and stimulatory effects of the nucleotides and the role of hormones.
38. GTP stimulates and inhibits adenylate cyclase in fat cell membranes through distinct regulatory processes.
39. Solubilization and separation of the glucagon receptor and adenylate cyclase in guanine nucleotide-sensitive states.
40. The role of the guanine nucleotide exchange reaction in the regulation of the beta-adrenergic receptor and in the actions of catecholamines and cholera toxin on adenylate cyclase in turkey erythrocyte membranes.
41. Activation of hepatic adenylate cyclase by guanyl nucleotides. Modeling of the transient kinetics suggests an “excited” state of GTPase is a control component of the system.
42. Evidence for distinct guanine nucleotide sites in the regulation of the glucagon receptor and of adenylate cyclase activity.
43. Multiple inhibitory and activating effects of nucleotides and magnesium on adrenal adenylate cyclase.
44. The fat cell adenylate cyclase system. Characterization and manipulation of its bimodal regulation by GTP.
45. Selective effects of organic mercurials on the GTP-regulatory proteins of adenylate cyclase systems.
46. Programmable messengers: a new theory of hormone action
47. Cholera toxin modifies diverse GTP-modulated regulatory proteins
48. Characteristics of the guanine nucleotide regulatory component of adenylate cyclase in human erythrocyte membranes
49. Effects of GTP on binding of (3H) glucagon to receptors in rat hepatic plasma membranes.
50. Evidence for specific binding sites for guanine nucleotides in adipocyte and hepatocyte plasma membranes. A difference in fate of GTP and guanosine 5'-(beta, gamma-imino) triphosphate.
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