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Protein Aggregation and Fibrillogenesis in Cerebral and Systemic Amyloid Disease

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Cover of 'Protein Aggregation and Fibrillogenesis in Cerebral and Systemic Amyloid Disease'

Table of Contents

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    Book Overview
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    Chapter 1 Introduction and Technical Survey: Protein Aggregation and Fibrillogenesis
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    Chapter 2 Fibril Formation by Short Synthetic Peptides
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    Chapter 3 In vitro Oligomerization and Fibrillogenesis of Amyloid-beta Peptides
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    Chapter 4 Tau Fibrillogenesis
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    Chapter 5 Prion Protein Aggregation and Fibrillogenesis In Vitro
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    Chapter 6 α-Synuclein Aggregation and Modulating Factors
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    Chapter 7 Pathological Self-Aggregation ofb 2 -Microglobulin: A Challenge for Protein Biophysics
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    Chapter 8 Islet Amyloid Polypeptide: Aggregation and Fibrillogenesisin vitroand Its Inhibition.
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    Chapter 9 Protein Aggregation and Fibrillogenesis in Cerebral and Systemic Amyloid Disease
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    Chapter 10 Fibrillogenesis of Huntingtin and Other Glutamine Containing Proteins
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    Chapter 11 Protein Aggregation and Fibrillogenesis in Cerebral and Systemic Amyloid Disease
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    Chapter 12 Experimental Inhibition of Peptide Fibrillogenesis by Synthetic Peptides, Carbohydrates and Drugs
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    Chapter 13 Experimental Inhibition of Fibrillogenesis and Neurotoxicity by amyloid-beta (Aβ) and Other Disease-Related Peptides/Proteins by Plant Extracts and Herbal Compounds
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    Chapter 14 Alzheimer's disease.
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    Chapter 15 Modeling the Polyglutamine Aggregation Pathway in Huntington’s Disease: From Basic Studies to Clinical Applications
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    Chapter 16 Parkinson’s Disease
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    Chapter 17 Human prion diseases: from kuru to variant creutzfeldt-jakob disease.
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    Chapter 18 Animal prion diseases.
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    Chapter 19 β(2)-Microglobulin Amyloidosis.
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    Chapter 20 Systemic AA Amyloidosis
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    Chapter 21 Familial amyloidotic polyneuropathy and transthyretin.
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    Chapter 22 The Challenge of Systemic Immunoglobulin Light-Chain Amyloidosis (AL)
Overall attention for this book and its chapters
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Title
Protein Aggregation and Fibrillogenesis in Cerebral and Systemic Amyloid Disease
Published by
Springer Netherlands, December 2012
DOI 10.1007/978-94-007-5416-4
ISBNs
978-9-40-075415-7, 978-9-40-075416-4
Editors

Harris, J. Robin

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X Demographics

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 565 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 3 <1%
France 1 <1%
Brazil 1 <1%
India 1 <1%
Colombia 1 <1%
Argentina 1 <1%
Russia 1 <1%
Spain 1 <1%
Greece 1 <1%
Other 0 0%
Unknown 554 98%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 102 18%
Student > Master 98 17%
Student > Ph. D. Student 76 13%
Researcher 52 9%
Student > Doctoral Student 26 5%
Other 71 13%
Unknown 140 25%
Readers by discipline Count As %
Agricultural and Biological Sciences 102 18%
Biochemistry, Genetics and Molecular Biology 89 16%
Medicine and Dentistry 58 10%
Neuroscience 47 8%
Chemistry 38 7%
Other 84 15%
Unknown 147 26%