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Titlebook: Cellular Adhesion; Molecular Definition Brian W. Metcalf,Barbara J. Dalton,Judy Schatz Book 1994 Springer Science+Business Media New York 1

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The Pathological Consequences of Bacterial Adhesion to Medical Deviceshe adhesion . to crypt cells in the intestine, have been largely controlled by modern antibiotics and by vaccines that are often designed to counteract their specific adhesion and toxigenic mechanisms. Modern bacterial pathogens, such as . aeruginosa and ., are ubiquitous in their distribution: the
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Peptide Mimetics as Adhesion Molecule Antagoniststide pharmacophore model for the design of novel nonpeptide mimetic ligands to GPIIb/IIIa. It will be instructive, however, to examine first the path that led to the discovery of small potent inhibitory peptide GPIIb/IIIa antagonists, focusing on the work at SmithKline Beecham.
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Open Innovation in the Financial Services, developmental and tissue-specific patterns of expression and display corresponding binding specificities. In this way, Cadherins are thought to influence cell sorting, morphogenesis, and the maintenance of adult tissues (Takeichi, 1988, 1991; Kemler .., 1989).
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The Uvomorulin—Catenin Complex developmental and tissue-specific patterns of expression and display corresponding binding specificities. In this way, Cadherins are thought to influence cell sorting, morphogenesis, and the maintenance of adult tissues (Takeichi, 1988, 1991; Kemler .., 1989).
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Limits of Complete Denture Rehabilitation, 1985) and toxins (van Heyningen, 1983) to their target cells. Each of these cases involves the recognition of specific carbohydrate structures. Recent progress in physical and structural characterization has greatly increased our understanding of these interactions at the molecular level.
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Banking for the Next Generation,o normal function, as well as into the diagnosis and treatment of disease. A deeper knowledge of these events may help to explain the aberrations of development that lead to birth defects and the alterations in adult organisms that lead to disease and degenerative states.
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The Biological Function of β3 Integrins and Other Vitronectin Receptorsr (a) complex (Hynes, 1987; Ruoslahti and Pierschbacher, 1987). In some cases, a given integrin heterodimer may recognize multiple ligands, or multiple integrins may recognize common ligands. The biological function underlying this intrinsic multiplicity and redundancy in ligand-integrin interaction is not well understood.
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