L turski (5 resultados)
Acta Informatica: Vol. 36, Fasc. 9/10, 2000
Bauer, F. L.; Broy, M.; Dijkstra, E. W.; Gries, D.; Turski, W. M. (eds.)
Editorial: Springer, Heidelberg, 2000
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Librería: PsychoBabel & Skoob Books, Didcot, Reino UnidoPsychoBabel & Skoob Books
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Añadir al carritoPaperback. Condición: Very Good. Paperback journal with very few superficial marks and scores on covers, and lightly worn edges, leading corners and spine ends. Pages are clean and sound throughout; all content is clear. TS. Used.

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Librería: Antiquariat Thomas Haker GmbH & Co. KG, Berlin, AlemaniaAntiquariat Thomas Haker GmbH & Co. KG
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Hardcover. Condición: Wie neu. 1st ed. 268 S. Like new. Shrink wrapped. Sprache: Englisch Gewicht in Gramm: 825.

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Librería: 100POCKETS, Berkeley, CA, Estados Unidos de America100POCKETS
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Hardcover. Condición: Near Fine. Estado de la sobrecubierta: None (As Issued?). HARD COVER. Text/BRAND NEW & Bright. Black cloth boards/Fine. DJ/None (as Issued?). PO name to first title page. Schering Foundation Workshop 3, June 27-28, 1911, Berlin symposium. Mechanisms through which glutamate, the principal excitatory neurotransmitter in the mammalian central nervous system, modifies neuronal membrane functions and intraneuronal functions. 186 pgs. 12 chapters. Essays review conceptual approaches and experiments reference to links between excitation mediated by glutamate and second messenger systems.…

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Librería: Revaluation Books, Exeter, Reino UnidoRevaluation Books
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Hardcover. Condición: Brand New. 1st edition. 255 pages. 9.25x6.50x0.75 inches. In Stock.

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Librería: AHA-BUCH GmbH, Einbeck, AlemaniaAHA-BUCH GmbH
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Buch. Condición: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Today, biologists and medicinal chemists realize that there is a strong relationship between pharmacodynamic (what the drug does to the organism) and pharmacokinetic (what the organism does to the drug) effects. A significant contributing factor to the evolution in drug discovery was the methodological and technological revolution with the advent of combinatorial chemistry, high-throughput screening and profiling, and in silico prediction of target-based activity and ADMET (absorption, distribution, metabolism, excretion and toxicity) properties. High-throughput screening and in silico methods have accelerated the process towards drugability of new chemical structures. Another component of the revolution in drug discovery is the replacement of the disease (indication)-based approach by a target-based approach. A better understanding of pathophysiology of diseases and the underlying biological processes of diseases combined with explosive development of genomics and proteomics have been instrumental in the birth of this new paradigm. This volume summarizes discussions of these three aspects of modern drug discovery, i.e. priority for targets, early ADMET assessment, and in silico screening. We trust that readers from academia as well as from industry will benefit from these studies.…