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Titlebook: Membrane Receptors, Dynamics, and Energetics; K. W. A. Wirtz Book 1987 Springer Science+Business Media New York 1987 Chloroplast.Lipid.pro

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Calcium and Guanosine Nucleotide Modulation of Melanotropin Receptor Function and Adenylate Cyclase s (Parker, 1981), Both .- and .-melanotropins (.-MSH, .-MSH) are thought to regulate melanin synthesis in these cells via cAMP-dependent stimulation of the enzyme, tyrosinase (monophenol monooxygenase), in direct correlation with adenylate cyclase (AC) activity (Johnson and Pastan, 1972; Varga ., 19
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Structure-Function Studies of Growth-Factor Receptors probably comprised of at least four .-helices followed by turns of conserved lengths and β-strands. In the human and drosphila EGF and c-erb-2 receptors these homologous domains are each followed by a series of smaller cystine rich domains (S) to give a gene duplicafied structure L.S.S.S.L.S.S.S..
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Molecular Interactions of Ganglioside Receptors with Tetanotoxin on Solid Supports, Aqueous Solutionmacologically active agents which interact with specific cell surface determinants. The molecular details by which the message generated from these interactions is transduced through the lipid milieu to affect cell function are unclear.
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Interaction of Cholera Toxin with its Receptor the Monosialoganglioside GM1: A Fluorescence Studyt is an oligomeric protein (Mr ~ 84,000) composed of two structural and functional distinct subunits CT A and CT B (Mr ~ 29,000 and 55,000 respectively). CT B contains five identical polypeptide chains (Mr = 11,600), most likely arranged in a ring-like pentameric configuration and CT A consists of t
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Incorporation of GABA/Benzodiazepine Receptors into Natural Brain Lipid Liposomes: Biochemical Charatinct receptor subtypes designed GABA. and GABA.. Interaction of GABA with the former opens anion channels, located in cell membranes, which allow the passage of chloride ions down their electrochemical gradient; this generally leads to membrane hyperpolarisation. This receptor is therefore amenable
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Solubilization of the Fusicoccin Receptor and a Protein Kinase from Highly Purified Plasma Membrane brane (PM) protein. A highly purified preparation of plasma membrane vesicles has been prepared from oat roots and used to study the FC-binding protein (receptor). In these right-side out vesicles the FC-binding site is protected from trypsin degradation, but disruption of the vesicle integrity with
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