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  • 1
    UID:
    b3kat_BV037195478
    Umfang: 1 Online-Ressource (544 p.) , 80 b&w, ill
    ISBN: 1847558429 , 9781847558428
    Serie: Issues in toxicology v. 3
    Anmerkung: With contributions by a team of internationally respected scientists, this book provides up-to-date information on the extensively studied cytochrome P450 enzyme in a very accessible manner, During half a century, cytochrome P450 in its original uniqueness as an optically "wrong" cytochrome has attracted many investigators, who have contributed to the unveiling of a bewildering multiplicity of biologically important functions of the, by now very large, superfamily of cytochrome P 450 enzymes. With its discovery in 1958 and with the advent of more refined spectroscopic methodologies, through the double wavelength spectrophotometry, the mysterious enzyme system began to reveal its secrets in a swift stream of investigative successes. As one of the most extensively studied enzyme systems worldwide the interest in cytochromes P450 very much reflects its importance in the elimination of drugs and other chemicals from the body and its role in chemical toxicity and in the aetiology of diseases such as cancer. There has been significant progress in research in this area in recent years and current books on this subject are now out of date. This much needed, new, fully up-to-date publication fills this gap and emphasises the new relevant topics that have emerged during the last decade in an easily accessible manner. The enzyme system, cytochromes P450, comprises a number of families/subfamilies, and the focus of the book is to deal with each individually, furnishing information directly relevant to scientists involved in the development of chemicals, in particular in the evaluation of their safety. The book has contributions from internationally respected scientists who are research-active in the relevant areas. The authors have made extensive use of figures and tables so that the reader can access the necessary information without always having to read the text. In , addition, a very extensive, user-friendly index is a unique hallmark of the book. Part A of this monograph introduces the reader to the current knowledge of the evolutionary development of cytochrome P450 structure and function. Furthermore, it deals with the role of this enzyme in the formation of reactive intermediates. The shrewd and extensive utilisation of the molecular biology methodology very rapidly led to a vast body of enzymes calling for a classification of the plethora of different cytochromes P450 (the superfamily) into families and subfamilies. This is aptly exemplified by the ten chapters in Part B of this book, dealing with ten subfamilies and two families of cytochrome P450. Part C offers an insight into another aspect of cytochrome P450 research, namely its regulation through receptor-mediated stimuli - as opposed to enzyme induction or inhibition. The final chapter translates the current data on one of several drug metabolising systems into clinical application and highlights the role of cytochromes P450 in the treatment of neoplastic growth. The book deals extensively with each family/subfamily of the cytochromes P450 that contribute to the metabolism of xenobiotics. Essential and invaluable information is provided for the industrial research scientist working with fine chemicals, and especially those in the pharmaceutical industry, dealing with the safety evaluation of chemicals or being involved in the study of their metabolism, pharmacokinetics and toxicological properties. It should also prove of interest to Regulators concerned with the safety evaluation of chemicals, research pharmacologists and toxicologists, and postgraduate students studying drug metabolism and toxicology at an advanced level
    Sprache: Englisch
    Fachgebiete: Chemie/Pharmazie
    RVK:
    Schlagwort(e): Electronic books
    URL: Volltext  (Deutschlandweit zugänglich)
    URL: Volltext  (Deutschlandweit zugänglich)
    Mehr zum Autor: Ioannides, Costas
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Online-Ressource
    Online-Ressource
    Totowa, NJ :Humana Press :
    UID:
    almahu_9949251557502882
    Umfang: 1 online resource (XIV, 430 p. 89 illus., 10 illus. in color.)
    Ausgabe: 3rd ed. 2011.
    ISBN: 1-61779-160-1
    Serie: Methods in Molecular Biology, 756
    Inhalt: It is increasingly clear that signal transduction is a highly organized and integrated process.  Divided into two convenient sections, Signal Transduction Protocols, Third Edition focuses on experimental approaches to better understand the complexity of signal transduction.  Introductory chapters provide perspective on several of the challenges involved in signal transduction research and offer guidance on selecting the best approaches to various types of questions.  The individual chapters provide detailed experimental protocols covering various topics, from the effects of ligand binding on receptor conformation and effector coupling, to moving inside the cell in order to capture the spatial and temporal characteristics of signaling events. Written in the highly successful Methods in Molecular Biology™ series format, chapters contain introductions to their respective topics, lists of the necessary materials and reagents, step-by step, readily reproducible laboratory protocols, and notes on troubleshooting and avoiding known pitfalls.   Authoritative and accessible, Signal Transduction Protocols serves as an ideal guide to scientists of all backgrounds and is a valuable resource for future progress in the field of signal transduction research.
    Anmerkung: Bibliographic Level Mode of Issuance: Monograph , Refining Efficacy: Allosterism and Bias in G Protein-Coupled Receptor Signaling -- Imaging-based Approaches to Understanding G Protein-Coupled Receptor Signaling Complexes -- Improving Drug Discovery with Contextual Assays and Cellular Systems Analysis -- RGS-insensitive Ga Subunits: Probes of Ga Subtype-selective Signaling and Physiological Functions of RGS Proteins -- Bioinformatic Approaches to Metabolic Pathways Analysis -- Studying Ligand Efficacy at G Protein-Coupled Receptors Using FRET -- Using BRET to Detect Ligand-Specific Conformational Changes in Preformed Signaling Complexes -- Reconstitution of G Protein-Coupled Receptors into a Model Bilayer System: Reconstituted High Density Lipoprotein Particles (rHDL) -- Using Quantitative BRET to Assess G Protein-Coupled Receptor Homo- and Hetero-Dimerization -- Cell-Surface Protein-Protein Interaction Analysis with Time-Resolved FRET and Snap-tag Technologies: Application to G Protein-Coupled Receptor Oligomerization -- Analysis of GPCR/Ion Channel Interactions -- Multicolor BiFC Analysis of G Protein bg Complex Formation and Localization -- Real-Time BRET Assays to Measure G Protein/Effector Interactions -- Luminescent Biosensors for Real-Time Monitoring of Intracellular cAMP -- Simultaneous Real Time Imaging of Signal Oscillations Using Multiple Fluorescence-Based Reporters -- Using FRET-based Reporters to Visualize Subcellular Dynamics of Protein Kinase A Activity -- Genetically Encoded Fluorescent Reporters to Visualize Protein Kinase C Activation in Live Cells -- Visualizing Receptor Endocytosis and Trafficking -- Investigating G Protein-Coupled Receptor Endocytosis and Trafficking by TIR-FM -- Visualizing G Protein-Coupled Receptor Signalsomes Using Confocal Immunofluorescence Microscopy -- Detection and Characterization of Receptor Interactions with PDZ Domains -- Tandem Affinity Purification and Identification of Heterotrimeric G-Protein Associated Proteins -- Study of G Protein-Coupled Receptor/ßarrestin Interactions within Endosomes Using FRAP -- Disrupting Protein Complexes Using Tat-tagged Peptide Mimics -- Protein-fragment Complementation Assays for Large-Scale Analysis, Functional Dissection and Dynamic Studies of Protein-Protein Interactions in Living Cells. , English
    Weitere Ausg.: ISBN 1-61779-159-8
    Sprache: Englisch
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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