Overview
- Fills the gap of what has not been discussed in protein review and protocol books
- Includes supplementary material: sn.pub/extras
Part of the book series: Protein Reviews (PRON, volume 4)
Access this book
Tax calculation will be finalised at checkout
Other ways to access
Table of contents (19 chapters)
-
Visualization of Protein Deposits In Vitro
-
Animal and Cell Models of Human Neurodegenerative Disorders
Keywords
About this book
This volume fills the gap in protein review and protocal literature while summarizing recent achievements in the understanding of the relationships between protein misfoldings, aggregation, and development of protein deposition disorders. It is devoted to the general questions of conformational disorders and includes discussion of involvement of such common factors as molecular chaperones, oxidative damage, proteasome, glycosoaminoglycans, serum amyloid protein P and several others in the development of different disorders. Some experimental techniques applicable for the visualization of protein deposition in vivo and in vitro are also present.
Editors and Affiliations
Bibliographic Information
Book Title: Protein Misfolding, Aggregation and Conformational Diseases
Book Subtitle: Part A: Protein Aggregation and Conformational Diseases
Editors: Vladimir N. Uversky, Anthony L. Fink
Series Title: Protein Reviews
DOI: https://doi.org/10.1007/b136464
Publisher: Springer New York, NY
eBook Packages: Biomedical and Life Sciences, Biomedical and Life Sciences (R0)
Copyright Information: Springer-Verlag US 2006
Hardcover ISBN: 978-0-387-25918-5Published: 13 June 2006
Softcover ISBN: 978-1-4419-3851-0Published: 29 November 2010
eBook ISBN: 978-0-387-25919-2Published: 24 November 2007
Edition Number: 1
Number of Pages: XVIII, 419
Topics: Life Sciences, general, Immunology, Cell Biology