Abstract
The biological effect of chemical agents can only be the result of an interaction of the molecules of the active agent and particular molecules or molecular complexes present in the biological object. The same holds true for endogenous bioactive agents such as hormones, neurotransmitters, etc. Often these messengers have their molecular sites of action, referred to as their specific receptors, located on the outer cell membrane (Lefkowitz et al., 1976). They then transmit information from remote or nearby cells to the surface of the target cells where they trigger these cells, thus inducing certain changes in cell function. The interaction between the bioactive agent and its specific receptors initiates the transduction of information received from outside to the cell interior. An example is the generation of intracellular mediators such as cyclic AMP. Similarly, the hormone-receptor complex, in the case of the interaction of steroid hormones and their specific proteins in the cytoplasm, is involved in the transduction of information to the cell nucleus. The presence of specific receptor for the bioactive agents either on the outer cell membrane or in the cytoplasm of only particular tissue cells accounts for a selectivity in action on these tissues.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Albuquerque, E. X., Eldefrawi, A. T., Eldefrawi, M. E., Mansour, N. A., and Tsai, M. C., 1978, Amantadine: Neuromuscular blockade by suppression of ionic conductance of the acetylcholine receptor, Science 199:788.
Ariƫns, E. J., 1964, Molecular Pharmacology, Vol. I, Academic Press, New York.
AriĆ«ns, E. J., 1966a, Receptor theory and structure-action relationships, in: Advances in Drug Research, Vol. Ill (N. J. Harper and A. B. Simmonds, eds.), pp. 235ā285, Academic Press, New York.
AriĆ«ns, E. J., 1966b, Eine Molekulargrundlage fĆ¼r die Wirkung von Pharmaka, Arzneim.-Forsch. 16:1376.
AriĆ«ns, E. J., 1967, The structure-activity relationships of Ī²-adrenergic drugs and Ī²-adrenergic blocking drugs, Ann. NY Acad. Sci. 139:606.
AriĆ«ns, E. J., 1971a, A general introduction to the field of drug design, in: Drug Design, Vol. I (E. J. AriĆ«ns, ed.), pp. 1ā263, Academic Press, New York.
AriĆ«ns, E. J., 1971b, Modulation of pharmacokinetics by molecular manipulation, in Drug Design, Vol. II (E. J. AriĆ«ns, ed.), pp. 2ā127, Academic Press, New York.
Ariƫns, E. J., 1974, Drug levels in the target tissue and effect, Clin. Pharmacol. Ther. 16:155.
Ariƫns, E. J., 1976, Stereochemie und pharmakologische Wirkung, Schriftenr. Bundesapoth. Wiss. Fortbild. IV: 77.
Ariƫns, E. J., and Beld, A. J., 1977, The receptor concept in evolution, Biochem. Pharmacol. 26:913.
Ariƫns, E. J., and Simonis, A. M., 1960, Autonomie drugs and their receptors, Arch. Int. Pharmacodyn. Ther. 127:479.
Ariƫns, E. J., and Simonis, A. M., 1964, A molecular basis for drug action, J. Pharm. Pharmacol. 16:137.
Ariƫns, E. J., and Simonis, A. M., 1967, Cholinergic and anticholinergic drugs, do they act on common receptors?, Ann. NY Acad. Sci. 144:842.
Ariƫns, E. J., and Simonis, A. M., 1974, Design of bioactive compounds, Top. Current Chem. 52:3.
AriĆ«ns, E. J., and Simonis, A. M., 1976, Receptors and receptor mechanisms, in: Beta-Adrenoceptor Blocking Agents (P. R. Saxena and R. P. Forsyth, eds.), pp. 3ā27, North-Holland, Amsterdam.
AriĆ«ns, E. J., and Simonis, A. M., 1977, Chemical structure and toxic action. Avoidance of toxicity by molecular manipulation, in: Drug Design and Adverse Reactions (H. Bundgaard, P. Juul, and H. Kofod, eds.), pp. 317ā330, Munksgaard, Copenhagen.
Ariƫns, E. J., and Van Rossum, J. M., 1957, Affinity, intrinsic activity and the all-or-none response, Arch. Int. Pharmacodyn. Ther. 113:89.
Ariƫns, E. J., Van Rossum, J. M., and Simonis, A. M., 1956a, A theoretical basis of molecular pharmacology, Arzneim.-Forsch. 6:282.
Ariƫns, E. J., Van Rossum, J. M., and Simonis, A. M., 1956b, A theoretical basis of molecular pharmacology, part II, Arzneim.-Forsch. 6:611.
Ariƫns, E. J., Van Rossum, J. M., and Koopman, P. C., 1960, Receptor reserve and threshold phenomena, I. Theory and experiments with autonomic drugs tested on isolated organs, Arch. Int. Pharmacodyn. Ther. 127:459.
AriĆ«ns, E. J., Simonis, A. M., and Van Rossum, J. M., 1964, Drug-receptor interaction: Interaction of one or more drugs with different receptor systems, in: Molecular Pharmacology, Vol. 1 (E. J. AriĆ«ns, ed.), pp. 287ā393, Academic Press, New York.
Aronstam, R. S., Hoss, W., and Abood, L. G., 1977, Conversion between configurational states of the muscarinic receptor in rat brain, Eur. J. Pharmacol. 46:279.
Beld, A. J., and AriĆ«ns, E. J., 1974, Stereospecific binding as a tool in attempts to localize and isolate muscarinic receptors, part II. Binding of [+]-benzetimide, [ā]-benzetimide and atropine to a fraction from bovine tracheal smooth muscle and to bovine caudate nucleus, Eur. J. Pharmacol. 25:203.
Beld, A. J., Van den Hoven, S., Wouterse, A. C., and Zegers, M. A. P., 1975, Are muscarinic receptors in the central and peripheral nervous system different?, Eur. J. Pharmacol. 30:360.
Belleau, B., 1964, A molecular theory of drug action based on induced conformational perturbations of receptors, J. Med. Chem. 7:776.
Bennett, J. P., and Snyder, S. H., 1976, Serotonin and lysergic acid diethylamide binding in rat brain membranes: Relationship to postsynaptic serotonin receptors, Mol. Pharmacol. 12:373.
Berde, B., Cerletti, A., and Konzett, H., 1961a, The biological activity of a series of peptides related to oxytocin, in: Oxytocin (R. Cadeyro-Barcia and H. Heller, eds.), pp. 247ā265, Pergamon Press, Elmsford, N.Y.
Berde, B., Weidmann, H., and Cerletti, A., 1961b, Ćber Phenylalanin2-Lysin-Vasopressin, Helv. Physiol. Pharmacol. Acta 19:285.
Bregestovski, P. D., Iljin, V. I., Jurchenko, O. P., Veprintsev, B. N., and Vulfius, C. A., 1977, Acetylcholine receptor conformational transition on excitation masks disulphide bonds against reduction, Nature (London) 270:71.
Burgen, A. S. V., 1970, Receptor mechanisms, Annu. Rev. Pharmacol. 10:7.
Burgen, A. S. V., Hiley, C. R., and Young, J. M., 1974, The binding of [3H]-propylbenzilylcholine mustard by longitudinal muscle strips from guinea-pig small intestine, Br. J. Pharmacol. 50:145.
Burt, D. R., Creese, I., and Snyder, S. H., 1976, Properties of [3H]haloperidol and [3H]dopamine binding associated with dopamine receptors in calf brain membranes, Mol. Pharmacol. 12:800.
Carlsson, E., Ć blad, B., BrƤndstrƶm, A., and Carlsson, B., 1972, Differentiated blockade of the chronotropic effects of various adrenergic stimuli in the cat heart, Life Sci. 11:953.
Changeux, J. P., ThiƩry, J., Tung, Y., and Kittel, C., 1967, On the cooperativity of biological membranes, Proc. Natl. Acad. Sci. USA 57:335.
Clark, A. J., 1937, General Pharmacology, Handbuch der experimentellen Pharmakologie, Vol. 4, Springer, Berlin.
Colquhoun, D., 1973, The relation between classical and cooperative models for drug action, in: Drug Receptors (H. P. Rang, ed.), pp. 149ā182, Macmillan, New York.
Cools, A. R., 1977, Two functionally and pharmacologically distinct dopamine receptors in the rat brain, Adv. Biochem. Psychopharmacol. 16:215.
Cools, A. R., and Van Rossum, J. M., 1976, Excitation-mediating and inhibition-mediating dopamine-receptors. A new concept towards a better understanding of electrophysiological, biochemical, pharmacological, functional and clinical data, Psychopharmacologia 45:243.
Creese, I., Burt, D. R., and Snyder, S. H., 1976, Dopamine receptor binding predicts clinical and pharmacological potencies of antischizophrenic drugs, Science 192:481.
Cuatrecasas, P., 1974, Membrane receptors, Annu. Rev. Biochem. 43:169.
Cuatrecasas, P., 1975, Hormone-receptor interactions and the plasma membrane, in : Cell Membranes: Biochemistry, Cell Biology and Pathology (G. Weissmann and R. Claiborne, eds.), pp. 177ā184, H. P. Publishing, New York.
Cuatrecasas, P., Hollenberg, M. D., Chang, K. J., and Bennett, V., 1975, Hormone receptor complexes and their modulation of membrane function, Recent Prog. Horm. Res. 31:37.
Del Castillo, J., and Katz, B., 1955, On the localization of acetylcholine receptors, J. Physiol. (London) 128:157.
de Robertis, E., 1975a, Synaptic ReceptorsāIsolation and Molecular Biology, Dekker, New York,
de Robertis, E., 1975b, Synaptic receptor proteins; isolation and reconstitution in artificial membranes, Rev. Physiol. Biochem. Pharmacol. 73:9.
de Robertis, E., 1976, Synaptic receptor proteins and chemical excitable membranes, in: The Structural Basis of Membrane Function (Y. Hatefi and L. Djavadi Ohaniance, eds.), pp. 339ā361, Academic Press, New York.
Doxey, J. C., Smith, C. F. C., and Walker, J. M., 1977, Selectivity of blocking agents for pre- and postsynaptic a-adrenoceptors, Br. J. Pharmacol. 60:91.
Driel, C. van, Houthoff, H. J., and Baljet, B., 1973, The innervation of the myometrium, some histochemical observations in man and rat, Eur. J. Obstet. Gynecol. Reprod. Biol. 3:11.
Ellenbroek, B. W. J., 1964, Stereoisomerie en biologische aktiviteit, Ph.D. Thesis, University of Nijmegen, Nijmegen, The Netherlands.
Ellenbroek, B. W. J., Nivard, R. J. F., Van Rossum, J. M., and AriĆ«ns, E. J., 1965, Absolute configuration and parasympathetic action : Pharmacodynamics of enantiomorphic and diastereoisomeric esters of Ī²-methylcholine, J. Pharm. Pharmacol. 17:393.
Furchgott, R. F., 1954, Dibenamine blockade in strips of rabbit aorta and its use in differentiating receptors, J. Pharmacol. Exp. Ther. 111:265.
Gaddum, J. H., 1937, The quantitative effects of antagonistic drugs, J. Physiol. (London) 89:7P.
Goldberg, N. D., 1975, Cyclic nucleotides and cell function, in: Cell Membranes: Biochemistry, Cell Biology and Pathology (G. Weissmann and R. Claiborne, eds.), pp. 185ā202, H. P. Publishing, New York.
Gosselin, R. E., and Gosselin, R. S., 1973, Tachyphylaxis of guinea-pig ileum to histamine and furtrethonium, J. Pharmacol. Exp. Ther. 184:494.
Grana, E., Lucchelli, A., and Zonta, F., 1974, Selectivity of Ī²-adrenergic compounds, III. Classification of Ī²-reeeptors, Il Farmaco-Educ. Sci. 29:786.
Greaves, H. F., 1977, Membrane receptor-adenylate cyclase relationships, Nature (London) 265:681.
Greengard, P., 1976, Possible role for cyclic nucleotides and phosphorylated membrane proteins in postsynaptic actions of neurotransmitters, Nature (London) 260:101.
Grob, D., 1976, Myasthenia gravis, Ann. NY Acad. Sci. 274:1.
Harms, A. F., and Nauta, W. Th., 1960, The effects of alkyl substitution in drugs. I. Substituted dimethylaminoethyl benzhydryl ethers, J. Med. Pharm. Chem. 2:57.
Haydon, D. A., Hendry, B. M., and Levison, S. R., 1977, The molecular mechanisms of anaesthesia, Nature (London) 268:356.
Hechter, O., and Braun, Th., 1971, Peptide hormone-receptor interaction: an informational transaction, in: Structure-Activity Relationships of Protein and Polypeptide Hormones (M. Margoulies and F. C. Greenwood, eds.), pp. 212ā227, Excerpta Medica, Amsterdam.
Heidelberger, Ch., 1973, Current trends in chemical carcinogenesis, Fed. Proc. 32:2154.
Hitchings, G. H., 1964, Antimetabolites and chemotherapy: Integration of biochemistry and molecular manipulation, in: Chemotherapy of Cancer (P. A. Plattner, ed.), pp. 77ā87, Elsevier, Amsterdam.
Hofmann, K., 1960, Preliminary observations relating structures and function in some pituitary hormones, Brookhaven Symp. Biol. 13:184.
Jacobs, S., and Cuatrecasas, P., 1976, The mobile receptor hypothesis and ācooperativityā of hormone binding. Application to insulin, Biochim. Biophys. Acta 433:482.
Kachadorian, W. A., Wade, J. B., and DiScala, V. A., 1975, Vasopressin: Induced structural change in toad bladder luminal membrane, Science 190:67.
Karlin, A., 1967, On the application of āa plausible modelā of allosteric proteins to the receptor for acetylcholine, J. Theor. Biol. 16:306.
Lands, A. M., Luduena, F. P., and Buzzo, H. J., 1967, Differentiation of Ī²-receptors responsive to isoproterenol. Life Sci. 6:2241.
Lee, A. G., 1977, Local anesthesia: The interaction between phospholipids and chlorpromazine, propranolol, and practolol, Mol. Pharmacol. 13:474.
Lefkowitz, R. J., Caron, M. G., Limbird, L., Mukherjee, C., and Williams, L. T., 1976, Membrane-bound hormone receptors, in: The Enzymes of Biological Membranes, Vol. 4 (A. Martonosi, ed.), pp. 283ā310, Wiley, New York.
LĆ¼llmann, H., and Ziegler, A., 1973, A transient state concept of drug receptor interaction, Naunyn-Schmiedebergās Arch. Pharmakol. 280:1.
LĆ¼llmann, H., Preuner, J., and Schaube, H., 1974, A kinetic approach for an interpretation of the acetylcholine-d-tubocurarine interaction on chronically denervated skeletal muscle, Naunyn-Schmiedebergās Arch. Pharmakol. 281:415.
Maddy, A. H., and Dunn, M. J., 1976, The solubilization of membranes, in: Biochemical Analysis of Membranes (A. H. Maddy, ed.), pp. 177ā196, Chapman & Hall, London.
Maugh, T. H., 1976, Hormone receptors: New clues to the cause of diabetes, Science 193:220.
McGuire, W. L., Carbone, P. P., and Vollmer, E. P., 1975, Estrogen Receptors in Human Breast Cancer, Raven Press, New York.
Monod, J., WymĆ¢n, J., and Changeux, J. P., 1965, On the nature of allosteric transitions: A plausible model, J. Mol. Biol. 12:88.
Nickerson, M., 1956, Receptor occupancy and tissue response, Nature (London) 178:697.
Papadimitriou, A., and Worcel, M., 1974, Dose-response curves for angiotensin II and synthetic analogues in three types of smooth muscle: existence of different forms of receptor sites for angiotensin II, Br. J. Pharmacol. 50:291.
Paton, W. O. M., 1961, A theory of drug action based on the rate of drug receptor combination, Proc. Roy. Soc. London Ser. B 154:21.
Pert, C. B., 1976, The opiate receptor, in: Cell Membrane Receptors for Viruses, Antigens and Antibodies, Polypeptide Hormones and Small Molecules (R. F. Beers and E. G. Bassett, eds.), pp. 435ā448, Raven Press, New York.
Pert, C. B., and Snyder, S. H., 1974, Opiate receptor binding of agonists and antagonists affected differentially by sodium, Mol. Pharmacol. 10:868.
Pfeiffer, C. C., 1956, Optical isomerism and pharmacological action, a generalization, Science 124: 29.
Podleski, T. R., and Changeux, J. P., 1970, On the excitability and cooperativity of the electroplax membrane, in: Fundamental Concepts in Drug-Receptor Interactions (J. F. Danielli, J. F. Moran, and D. J. Triggle, eds.), pp. 93ā119, Academic Press, New York.
Raftery, M. A., 1975, Transductive coupling between acetylcholine, its receptor, and the postsynaptic membrane, in: Functional Linkage in Biomolecular Systems (F. O. Schmitt, D. M. Schneider, and D. M. Crothers, eds.), pp. 215ā223, Raven Press, New York.
Rang, H. P., and Ritter, J. M., 1970a, On the mechanism of desensitization at cholinergic receptors, Mol. Pharmacol. 6:357.
Rang, H. P., and Ritter, J. M., 1970b, The relationship between desensitization and the metaphilic effect at cholinergic receptors, Mol. Pharmacol. 6:383.
Raynaud, J. P., 1977a, A strategy for the design of potent hormones, in: Proceedings of the Vth International Symposium on Medicinal Chemistry, Paris, 1976, Elsevier, Amsterdam.
Raynaud, J. P., 1977b, Une stratĆ©gie de rĆ©cherche pour les hormones de synthĆØse: leurs interactions avec les rĆ©cepteurs hormonaux, in: ActualitĆ©s Pharmacologiques (J. Cheymol, J. R. Boissier, and P. Lechat, eds.), pp. 49ā64, Masson et Cie, Paris.
Reinhardt, D., and Wagner, J., 1974, Ī²-Adrenolytic antiarrhythmic and local anaesthetic effects of phenylephrine, Naunyn-Schmiedebergās Arch. Pharmakol. 284:245.
Rekker, R. F., Timmerman, H., Harms, A. F., and Nauta, W. Th., 1971, The antihistamine and anticholinergic activities of optically active diphenhydramine derivatives, Arzneim.-Forsch. 21:688.
Roach, P. J., 1977, Functional significance of enzyme cascade systems, Trends Biochem. Sci. 2:87.
Robison, G. A., Butcher, R. W., and Sutherland, E. W., 1971, Cyclic AMP, Academic Press, New York.
Rocha e Silva, M., 1970, A thermodynamic approach to problems of drug antagonism. II. A micro-physical model of the phenomenon of recovery, Physiol. Chem. Phys. 2:503.
Rocha e Silva, M., 1978, Kinetics of antagonist action, in: Histamine II and Anti-Histaminics (M. Rocha e Silva, ed.), Handbuch der experimentellen Pharmakologie, Vol. 18, No. 2, pp. 295ā332, Springer, Berlin.
Rodrigues de Miranda, J. F., Eikelboom, T. D., and Van Os, G. A. J., 1976, The extent of hydrophobic binding area studied by fatty acid binding to albumin, Mol. Pharmacol. 12:454.
Rosell, S., and Beifrage, E., 1975, Adrenergic receptors in adipose tissue and their relation to adrenergic innervation, Nature (London) 253:738.
Ross, E. M., and Gilman, A. G., 1977, Reconstitution of catecholamine-sensitive adenylate cyclase activity: Interaction of solubilized components with receptor-replete membranes, Proc. Natl. Acad. Sci. USA 74:3715.
Rudinger, J., Pliska, V., and Krejci, I., 1972, Oxytocin analogs in the analysis of some phases of hormone action, Recent Prog. Horm. Res. 28:131.
Ruffolo, R. R., Turowski, B. S., and Patil, P. N., 1977, Lack of cross-desensitization between structurally dissimilar a-adrenoceptor agonists, J. Pharm. Pharmacol. 29:378.
Scatchard, G., 1949, Attractions of proteins for small molecules and ions, Ann. NY Acad. Sci. 51:660.
Schaeffer, H. J., and Johnson, R. N., 1968, Enzyme inhibitors. XX. Studies on the hydrophobic and hydroxyl binding regions of adenosine deaminase. 9-(2-m-Bromoacetamidophenethyl)adenine, a new irreversible inhibitor of adenosine deaminase, J. Med. Chem. 11:21.
Schramm, M., Orly, J., Eimerl, S., and Korner, M., 1977, Coupling of hormone receptors to adenylate cyclase of different cells by cell fusion, Nature (London) 268:310.
Schueler, F. W., 1960, Chemobiodynamics and Drug Design, McGraw-Hill, New York.
Schwyzer, R., 1970, Programmierte Molekeln, Experientia 26:577.
Seelig, S., and Sayers, G., 1973, Isolated adrenal cortex cells: ACTH agonists, partial agonists, antagonists; Cyclic AMP and corticosterone production, Arch. Biochem. Biophys. 154:230.
Segura, E. T., and Biscardi, A. M., 1967, Changes in brain epinephrine and norepinephrine induced by afferent electrical stimulation in the isolated toad head, Life Sei. 6:1599.
Singer, S. J., and Nicolson, G. L., 1972, The fluid mosaic model of the structure of cell membranes, Science 175:720.
Sobel, A., Heidmann, T., Hofler, J., and Changeux, J. P., 1978, Distinct protein components from Torpedo marmorata membranes carry the acetylcholine receptor site and the binding site for local anesthetics and histrionicotoxin, Proc. Natl. Acad. Sci USA 75:510.
Steinhardt, J., and Reynolds, J. A., 1969, in: Multiple Equilibrium in Proteins (B. Horecker, N. O. Kaplan, J. Marmur, and H. A. Scheraga, eds.), Chap. II, p. 12, Academic Press, New York.
Struyker Boudier, H. A. J., de Boer, J., Smeets, G. M. W., Lien, E. J., and Van Rossum, J. M., 1975, Structure-activity relationships for central and peripheral a-adrenergic activity of imidazoline derivatives, Life Sci. 17:377.
Thron, C. D., 1973, On the analysis of pharmacological experiments in terms of an allosteric receptor model, Mol. Pharmacol. 9:1.
Triggle, D. J., 1965, Chemical Aspects of the Autonomic Nervous System, Academic Press, New York.
UāPrichard, D. C., Greenberg, D. A., and Snyder, S. H., 1977, Binding characteristics of a radiolabeled agonist and antagonist at central nervous system alpha noradrenergic receptors, Mol. Pharmacol. 13:454.
Van den Brink, F. G., 1973, The model of functional interaction, I and II, Eur. J. Pharmacol. 22:270 and 279.
Van Rossum, J. M., 1958, Pharmacodynamics of cholinomimetic and cholinolytic drugs, Ph.D. thesis, University of Nijmegen, Nijmegen, The Netherlands.
Van Rossum, J. M., 1966, Limitations of molecular pharmacology, in: Advances in Drug Research, Vol. Ill (N. J. Harper and A. B. Simmonds, eds.), pp. 189ā234, Academic Press, New York.
Van Rossum, J. M., 1968, Drug receptor theories, in: Recent Advances in Pharmacology (J. M. Robson and R. S. Stacey, eds.), pp. 99ā133, Churchill, London.
Van Rossum, J. M., 1977, Kinetics of Drug Action, Handbuch der experimentellen Pharmakologie, Vol. 47, Springer, Berlin.
Van Rossum, J. M., and Ariƫns, E. J., 1962, Receptor reserve and threshold phenomena, II. Theories on drugaction and a quantitative approach to spare receptors and threshold values, Arch. Int. Pharmacodyn. Ther. 136:385.
Waser, P. G., 1975, Cholinergic Mechanisms, Raven Press, New York.
Waud, D. R., 1968, Pharmacological receptors, Pharmacol. Rev. 20:49.
Waud, D. R., 1974, Adsorption isotherm vs. ion-exchange models for the drug-receptor reaction, J. Pharmacol. Exp. Ther. 188:520.
Waud, D. R., 1976, Analysis of dose-response relationships, in: Advances in General and Cellular Pharmacology, Vol. 1 (T. Narahashi and C. P. Bianchi, eds.), 145ā178, Plenum Press, New York.
Wick, H., 1972, unpublished data, Research Institute C. H. Boehringer Sohn, Ingelheim am Rhein, Germany.
Wyman, J., 1967, Allosteric linkage, J. Am. Chem. Soc. 89:2202.
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
Ā© 1979 Plenum Press, New York
About this chapter
Cite this chapter
AriĆ«ns, E.J., Beld, A.J., de Miranda, J.F.R., Simonis, A.M. (1979). The Pharmacon-Receptor-Effector Concept. In: OāBrien, R.D. (eds) General Principles and Procedures. The Receptors, vol 1. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-0979-6_2
Download citation
DOI: https://doi.org/10.1007/978-1-4684-0979-6_2
Publisher Name: Springer, Boston, MA
Print ISBN: 978-1-4684-0981-9
Online ISBN: 978-1-4684-0979-6
eBook Packages: Springer Book Archive