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Broschiert; Condizione: Gut. 19 Seiten; Das hier angebotene Heft stammt aus einer teilaufgelösten wissenschaftlichen Bibliothek und trägt die entsprechenden Kennzeichnungen (Rückenschild, Instituts-Stempel.). Der Zustand ist ansonsten ordentlich und dem Alter entsprechend gut. Sprache: Deutsch Gewicht in Gramm: 50.

Condizione: Fair. Volume 2. This is an ex-library book and may have the usual library/used-book markings inside.This book has hardback covers. In fair condition, suitable as a study copy. No dust jacket. Please note the Image in this listing is a stock photo and may not match the covers of the actual item,3100grams, ISBN:9783540581093.

Hardcover. Condizione: Very Good. No Jacket. 3540589651. Blue cloth hardcover, from closed pharmaceutical company library, 517 pages, index, illustrated with charts, tables and diagrams. Contents clean, tight and bright. Text in English. Book.

gebundene Ausgabe. Condizione: Gut. 517 Seiten Der Erhaltungszustand des hier angebotenen Werks ist trotz seiner Bibliotheksnutzung sehr sauber und kann entsprechende Merkmale aufweisen (Rückenschild, Instituts-Stempel.). In ENGLISCHER Sprache. Sprache: Englisch Gewicht in Gramm: 970.

, 517 Seiten. Condizione: Sehr gut. 1st impression. 16 x 24 cm dunkelblauer Leinenband im Oktavformat; sehr gutes Exemplar mit zahlreichen Beiträgen & Abbildungen, garphischen Darstellungen (und mit Widmung von Heinz Knauf i. Vorsatz) Sprache: Englisch Gewicht in Gramm: 1.

hardcover. Condizione: Good. Connecting readers with great books since 1972! Used textbooks may not include companion materials such as access codes, etc. May have some wear or writing/highlighting. We ship orders daily and Customer Service is our top priority!

Hardcover. Condizione: Very Good. Quartos. 2527 pages in two volumes. Hardcovers bound in blue cloth and housed in a grey board slipcase. Light wear to the slipcase and to the bindings of the books. A sound set and clean within.

Couverture rigide. Condizione: Bon. Texte en anglais / text in english ! Vol.1 XXIV + 1214 p. 700 Figures. 84 Tables. -- Vol. 2. XXIV + pp. 1215-2527. 722 Figures. 189 Tables. Pagination continue. 2/2 volumes. Forts volumes ! 21x27,5 cm. 2527 p. Reliure éditeur. Bon état. Plats légèrement défraîchis. Nom de l'ancien propriétaire en page de titre (cachet). Fort in-4°.

Condizione: Wie Neu. 70 Ill. u. graph. Darst. (illustratore). Literaturangaben, Versandhinweis: Aufgrund aktueller EPR-Verpackungsregelungen ist der Versand in einzelne EU-Länder derzeit nicht möglich. Details siehe Händlerprofil. XI, 321 S., Wie neu. Neuwertiger Zustand ohne erkennbare Gebrauchsspuren. Der Einband ist sauber und unbeschädigt, keine Knicke oder Kratzer. Seiten sind vollständig, ohne Markierungen oder Anstreichungen. Wirkt ungelesen. 25 cm.

Condizione: Sehr gut. 2 Bände gebunden im Schuber. Sehr gut erhalten. Sprache: Englisch Gewicht in Gramm: 5750.

Condizione: New. In.

Condizione: New. In.

Condizione: Sehr gut. Zustand: Sehr gut | Seiten: 538 | Sprache: Englisch | Produktart: Bücher | Keine Beschreibung verfügbar.

Condizione: Sehr gut. Zustand: Sehr gut | Sprache: Englisch | Produktart: Bücher | Keine Beschreibung verfügbar.

Condizione: New.

Paperback. Condizione: Brand New. reprint edition. 538 pages. 9.25x6.10x1.20 inches. In Stock.

Taschenbuch. Condizione: Neu. Diuretics | Rainer F. Greger (u. a.) | Taschenbuch | xxi | Englisch | 2011 | Springer | EAN 9783642795671 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.

Taschenbuch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - The first edition of this handbook appeared exactly twenty-five years ago. Due to enormous changes in the area of diuretics, the second edition has had to be completely revised. Substantial progress has been made in the functional anatomy of the kidney and in the concepts of how substances and ions are specifically transported across the various nephron segments. No one could have foreseen twenty-five years ago that the late 1980s and the early 1990s have provided us with methodologies to study transport events not only at the single cell level, but even at the level of the single transporter molecule. Many of the transporters for ions and organic substances have been cloned meanwhile by the new methods of molecular biology, and their function can be described more precisely by new transport studies such as the patch-clamp technique. These new insights have also led to a new understanding of how the currently used diuretics act. Just a few months ago, the Na+Cl- co-transporter, which is the target of thiazides, the Na+2CI-K+ co-transporter, which is the target of furosemide, and the amiloride sensitive Na+ channel were cloned. Hence, the targets of diuretics have now been identified at the molecular level. In addition, during the past twenty-five years extensive studies have been performed on the pharmacokinetics of diuretics. We have learned how changes in liver metabolism and altered renal excretion influence the pharmacology of this class of compounds.

Taschenbuch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - Seven months after the report of the cloning of the CF gene by three North American groups, a workshop scheduled before that report was held in sestri Levante, a splendid city on the Ligu rian coast. For three days almost 100 scientists from Europe and North America had the opportunity to discuss the perspectives and the new research strategies opened up by the cloning of the gene. The issue of publishing these proceedings was discussed at length among the invited speakers of the workshop and the pre vailing opinion was that they would be worthwhile if accompanied by the transcripts of the discussions which followed each pre sentation. Thanks to the generous suppport of the Menarini Foun dation, represented at the meeting by Dr. Sergio Gorini, and thanks to the reviewing work done by the Chairpersons of each session, by many participants, by Dr. Donata Brugioni, by Mrs. Katherine Loparco and by my collaborators Drs. Marcella Devoto and Luis J. V. Galietta, that idea has generated this book, which should be a helpful tool at least for some years for all those interested in understanding how the CFTR gene works. Prof. G. Romeo CONTENTS Cystic Fibrosis - A Strategy for the Future . . . . . . . . . . . . . . . 1 R. Williamson Molecular Genetics of cystic Fibrosis . . . . . . . . . . . . . . . . . . . . . 9 L. -C. Tsui, J. Rommens, B. Kerem, R. Rozmahel, J. Zielenski, D. Kennedy, D. Markiewicz, N. Plavsic, J. -L. Chou, D. Bozon and M.

Hardcover. Condizione: Very Good. Dust Jacket may NOT BE INCLUDED.CDs may be missing. SHIPS FROM MULTIPLE LOCATIONS. book.

Taschenbuch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - Comprehensive Human Physiology is a significantly important publication on physiology, presenting state-of-the-art knowledge about both the molecular mechanisms and the integrative regulation of body functions. This is the first time that such a broad range of perspectives on physiology have been combined to provide a unified overview of the field. This groundbreaking two-volume set reveals human physiology to be a highly dynamic science rooted in the ever-continuing process of learning more about life. Each chapter contains a wealth of original data, clear illustrations, and extensive references, making this a valuable and easy-to-use reference. This is the quintessential reference work in the fields of physiology and pathophysiology, essential reading for researchers, lecturers and advanced students.

Handbook of Experimental Pharmacology, 117. - Berlin, Springer Verlag, 1995, 8°, XXI, 517 pp., Fig., Tab., orig. Leinenband; ExBibExpl.

Condizione: new. Questo è un articolo print on demand.

Condizione: new. Questo è un articolo print on demand.

Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Seven months after the report of the cloning of the CF gene by three North American groups, a workshop scheduled before that report was held in sestri Levante, a splendid city on the Ligu rian coast. For three days almost 100 scientists from Europe and North America had the opportunity to discuss the perspectives and the new research strategies opened up by the cloning of the gene. The issue of publishing these proceedings was discussed at length among the invited speakers of the workshop and the pre vailing opinion was that they would be worthwhile if accompanied by the transcripts of the discussions which followed each pre sentation. Thanks to the generous suppport of the Menarini Foun dation, represented at the meeting by Dr. Sergio Gorini, and thanks to the reviewing work done by the Chairpersons of each session, by many participants, by Dr. Donata Brugioni, by Mrs. Katherine Loparco and by my collaborators Drs. Marcella Devoto and Luis J. V. Galietta, that idea has generated this book, which should be a helpful tool at least for some years for all those interested in understanding how the CFTR gene works. Prof. G. Romeo CONTENTS Cystic Fibrosis - A Strategy for the Future . . . . . . . . . . . . . . . 1 R. Williamson Molecular Genetics of cystic Fibrosis . . . . . . . . . . . . . . . . . . . . . 9 L. -C. Tsui, J. Rommens, B. Kerem, R. Rozmahel, J. Zielenski, D. Kennedy, D. Markiewicz, N. Plavsic, J. -L. Chou, D. Bozon and M. 424 pp. Englisch.

Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -The first edition of this handbook appeared exactly twenty-five years ago. Due to enormous changes in the area of diuretics, the second edition has had to be completely revised. Substantial progress has been made in the functional anatomy of the kidney and in the concepts of how substances and ions are specifically transported across the various nephron segments. No one could have foreseen twenty-five years ago that the late 1980s and the early 1990s have provided us with methodologies to study transport events not only at the single cell level, but even at the level of the single transporter molecule. Many of the transporters for ions and organic substances have been cloned meanwhile by the new methods of molecular biology, and their function can be described more precisely by new transport studies such as the patch-clamp technique. These new insights have also led to a new understanding of how the currently used diuretics act. Just a few months ago, the Na+Cl- co-transporter, which is the target of thiazides, the Na+2CI-K+ co-transporter, which is the target of furosemide, and the amiloride sensitive Na+ channel were cloned. Hence, the targets of diuretics have now been identified at the molecular level. In addition, during the past twenty-five years extensive studies have been performed on the pharmacokinetics of diuretics. We have learned how changes in liver metabolism and altered renal excretion influence the pharmacology of this class of compounds. 544 pp. Englisch.

Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. The action of diuretics including cellular mechanisms of action, pharmacokinetics, and clinical usage, with much emphasis placed on the most recent findings on the pharmacodynamics of the respective drugs. During the past twenty-five years since volume 14 o.

Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Cystic Fibrosis - A Strategy for the Future.- Molecular Genetics of Cystic Fibrosis.- The CF Gene Product as a Member of a Membrane Transporter (TM6-NBF) Super Family.- Genetic Analysis of Cystic Fibrosis.- Molecular and Genetic Analyses at the CF Locus.- Identification of Cystic Fibrosis Mutations.- Mutation Analysis for Cystic Fibrosis in a North American Population.- Toward a Geographical History of the Predominant and Secondary Mutations in Europe.- Origin and Diffusion of the Major CF Mutation in Europe.- Present State of DNA-Diagnosis for Cystic Fibrosis and Attitudes Concerning a Heterozygote Screening in the GDR.- Pros and Cons of Neonatal Screening for Cystic Fibrosis.- Genotype-Phenotype Correlations in Cystic Fibrosis Patients.- Ion Transport in Normal and CF Airway Epithelia.- Aerosolized Amiloride as Treatment of Cystic Fibrosis Lung Disease: A Pilot Study.- Some Properties of Sodium and Chloride Channels in Respiratory Epithelia of CF- and Non-CF-Patients.- Roles of Ca and cAMP on Cl Channel Activity in Cystic Fibrosis Sweat Clear Cells as Studied by Microsuperfusion and Cell Volume Analysis.- Regulation of Absorption in the Human Sweat Duct.- Altered Biochemical Regulation of Secretion in Cystic Fibrosis Epithelial Cells.- Chloride Ion Transport in Transformed Normal and Cystic Fibrosis Epithelial Cells.- Conductance Pathways Involved in Chloride Secretion and Their Regulation.- Regulation of Epithelial Chloride Channels: Roles of Protein Kinases and Arachidonic Acid.- Cytosolic Inhibition and Excision Activation of Epithelial Chloride Channels.- Purification of the Epithelial Cl Channel.- Regulation of Expression of CFTR in Human Intestinal Epithelial Cells.- Cystic Fibrosis, the CFTR, and Rectifying Cl- Channels.- Regulation of Ion Conductance inHuman Skin Fibroblasts.- Chloride Transport in the Cystic Fibrosis Enterocyte.- Chloride Transport Pathways in Human Keratinocytes.- A Chloride Conductance Evoked by Hypotonic Shock in Epithelial Cells.- Regulation of Lymphocyte Chloride Channels.- Guanine Nucleotide Binding Proteins Regulate Epithelial Na+ Channels.- Attitudes of Parents of Cystic Fibrosis Children Towards Neonatal Screening and Antenatal Diagnosis.- DNA Analysis in CF Families by Biotinylated Probes and Polymerase Chain Reaction Technique.- Prevalence of the Major Mutation of the CF Gene in Belgian Patients.- Cystic Fibrosis in the Sicilian Population: Linkage Disequilibrium and Prenatal Diagnosis by Polimerase Chain Reaction.- Study of Reconstitution of the Rabbit Parotid Na+/K+/2Cl-Cotransporter.- Human Placental Membrane Vesicles as Models for Investigation of Cystic Fibrosis.- The DeltaF508 Mutation in Israeli CF Families.- The DeltaF508-Deletion in 99 CF Patients of Switzerland.- The Prevalence of the Deletion F508 in a Belgian Cystic Fibrosis Population.- Cystic Fibrosis Delta F508 Mutation in a French Population.- Frequency of the Delta-F508 Mutation and Flanking Marker Haplotypes at the Cystic Fibrosis Locus from 167 Czech Families.- The Response of Chloride Transport to Cyclic AMP, Calcium and Hypotonic Shock in Normal and Cystic Fibrosis Fibroblasts.- 2D-Electrophoresis of Mitochondrial Proteins from Cystic Fibrosis Patients.- Frequency of Cystic Fibrosis Mutations and Associated Haplotype Distribution in Slovak CF Patients.- Frequency of Cystic Fibrosis Mutations Among Italian Patients.- Cultured Human Placental Trophoblasts as Models for Investigating Defective Regulation of Chloride Transport and Protein Secretion in Cystic Fibrosis.- A Deletion Mutation of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Locus: DeltaI507.- DNA Technology for Prenatal Diagnosis of Cystic Fibrosis in Italy.- Incidence of Cystic Fibrosis at the Faroe Islands.Springer-Verlag KG, Sachsenplatz 4-6, 1201 Wien 424 pp. Englisch.

Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -The first edition of this handbook appeared exactly twenty-five years ago. Due to enormous changes in the area of diuretics, the second edition has had to be completely revised. Substantial progress has been made in the functional anatomy of the kidney and in the concepts of how substances and ions are specifically transported across the various nephron segments. No one could have foreseen twenty-five years ago that the late 1980s and the early 1990s have provided us with methodologies to study transport events not only at the single cell level, but even at the level of the single transporter molecule. Many of the transporters for ions and organic substances have been cloned meanwhile by the new methods of molecular biology, and their function can be described more precisely by new transport studies such as the patch-clamp technique. These new insights have also led to a new understanding of how the currently used diuretics act. Just a few months ago, the Na+Cl- co-transporter, which is the target of thiazides, the Na+2CI-K+ co-transporter, which is the target of furosemide, and the amiloride sensitive Na+ channel were cloned. Hence, the targets of diuretics have now been identified at the molecular level. In addition, during the past twenty-five years extensive studies have been performed on the pharmacokinetics of diuretics. We have learned how changes in liver metabolism and altered renal excretion influence the pharmacology of this class of compounds.Springer-Verlag KG, Sachsenplatz 4-6, 1201 Wien 544 pp. Englisch.

Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Volume 1 and Volume 2|The reference book for human physiologyThe first reference focusing on the integration of molecular, cellular and general physiologyLavishly illustrated with 1350 figures, almost 700 in colourComprehensive Human P.