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Prions

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Cover of 'Prions'

Table of Contents

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    Book Overview
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    Chapter 1 Purification and Fibrillation of Full-Length Recombinant PrP
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    Chapter 2 Method for Folding of Recombinant Prion Protein to Soluble β-Sheet Secondary Structure
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    Chapter 3 Analysis of Prion Protein Conformation Using Circular Dichroism Spectroscopy
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    Chapter 4 Analysis of Prion Protein Structure Using Nuclear Magnetic Resonance Spectroscopy
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    Chapter 5 Immunodetection of PrP Sc Using Western Immunoblotting Techniques
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    Chapter 6 Analysis of miRNA Signatures in Neurodegenerative Prion Disease
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    Chapter 7 Cell Biology Approaches to Studying Prion Diseases
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    Chapter 8 Expression of Heterologous PrP and Prion Propagation in RK13 Cells
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    Chapter 9 Generation of Infectious Prions and Detection with the Prion-Infected Cell Assay
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    Chapter 10 Analysis of Cellular Prion Protein Endoproteolytic Processing
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    Chapter 11 Cellular Analysis of Adult Neural Stem Cells for Investigating Prion Biology
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    Chapter 12 Neurotoxicity of Prion Peptides on Cultured Cerebellar Neurons
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    Chapter 13 Methods of Protein Misfolding Cyclic Amplification
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    Chapter 14 RT-QuIC Assays for Prion Disease Detection and Diagnostics
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    Chapter 15 A Quick Method to Evaluate the Effect of the Amino Acid Sequence in the Misfolding Proneness of the Prion Protein
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    Chapter 16 Insights into Mechanisms of Transmission and Pathogenesis from Transgenic Mouse Models of Prion Diseases
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    Chapter 17 In Vivo-Near Infrared Imaging of Neurodegeneration
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    Chapter 18 Strain Typing of Prion Diseases Using In Vivo Mouse Models
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    Chapter 19 Preparation and Immunostaining of the Myenteric Plexus of Prion-Infected Mice
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    Chapter 20 Cell Culture Methods for Screening of Prion Therapeutics
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    Chapter 21 Real-Time Quaking-Induced Conversion for Diagnosis of Prion Disease
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    Chapter 22 Methods for Molecular Diagnosis of Human Prion Disease
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    Chapter 23 Molecular Subtyping of PrPres in Human Sporadic CJD Brain Tissue
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    Chapter 24 Intercellular Prion-Like Conversion and Transmission of Cu/Zn Superoxide Dismutase (SOD1) in Cell Culture
Attention for Chapter 20: Cell Culture Methods for Screening of Prion Therapeutics
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Chapter title
Cell Culture Methods for Screening of Prion Therapeutics
Chapter number 20
Book title
Prions
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-7244-9_20
Pubmed ID
Book ISBNs
978-1-4939-7242-5, 978-1-4939-7244-9
Authors

Hilary E. McMahon, McMahon, Hilary E.

Abstract

It is currently difficult to predict the number of asymptomatic prion carriers who will potentially go on to develop a prion disease or who will unknowingly transmit the prion agent to another individual. As prion therapeutic clinical trials have lacked success, there is a continuous need for novel therapeutics that have the potential to prevent, as for inherited prion disorders; slow, as for all prion disorders; and ultimately stop disease progression. Prion-infected cell models provide an ideal tool to search for new treatment avenues. This chapter describes the use of prion cell culture systems in the identification of prion therapeutics. It also deals with the methods required to validate the potential of an antiprion agent through cell viability and impact on cell growth rate.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 7 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 7 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 2 29%
Professor 1 14%
Student > Bachelor 1 14%
Student > Ph. D. Student 1 14%
Unknown 2 29%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 2 29%
Immunology and Microbiology 1 14%
Neuroscience 1 14%
Unknown 3 43%