Amyloid, prions, and other protein aggregates. Part B /

The ability of polypeptides to form alternatively folded, polymeric structures such as amyloids and related aggregates is being increasingly recognized as a major new frontier in protein research. This new volume of Methods in Enzymology along with Part C (volume 413) on Amyloid, Prions and other Pr...

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Bibliographic Details
Other Authors: Kheterpal, Indu (Editor), Wetzel, Ronald (Editor)
Format: Manuscript Book
Language:English
Published: Amsterdam ; Boston : Elsevier/Academic, [2006]
Series:Methods in enzymology ; volume 412.
Subjects:
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245 0 0 |a Amyloid, prions, and other protein aggregates.  |n Part B /  |c edited by Indu Kheterpal, Ronald Wetzel. 
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490 1 |a Methods in enzymology ;  |v v. 412 
504 |a Includes bibliographical references and indexes. 
505 0 |a Front Cover; Amyloid, Prions, and Other Protein Aggregates; Copyright Page; Table of Contents; Contributors to Volume 412; Preface; Volumes in Series; Section I: Characterization of Protein Deposition In Vivo and Ex Vivo; Section II: Cell and Animal Models of Amyloid Formation and Toxicity; Section III: Computational Approaches and Theory; Author Index; Subject Index. 
520 |a The ability of polypeptides to form alternatively folded, polymeric structures such as amyloids and related aggregates is being increasingly recognized as a major new frontier in protein research. This new volume of Methods in Enzymology along with Part C (volume 413) on Amyloid, Prions and other Protein Aggregates continue in the tradition of the first volume (309) in containing detailed protocols and methodological insights, provided by leaders in the field, into the latest methods for investigating the structures, mechanisms of formation, and biological activities of this important class of. 
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