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Innate Antiviral Immunity

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Cover of 'Innate Antiviral Immunity'

Table of Contents

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    Book Overview
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    Chapter 1 The Application of Humanized Mouse Models for the Study of Human Exclusive Viruses
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    Chapter 2 Zebrafish as a Model for the Study of Host-Virus Interactions
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    Chapter 3 Northern Blot Detection of Virus-Derived Small Interfering RNAs in Caenorhabditis elegans Using Nonradioactive Oligo Probes
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    Chapter 4 Extraction and qPCR-Based Detection of miRNAs from Cultured PBMCs of Bubaline Origin
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    Chapter 5 Visualizing Virus-Derived dsRNA Using Antibody-Independent and -Dependent Methods
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    Chapter 6 RNA PAMPs as Molecular Tools for Evaluating RIG-I Function in Innate Immunity
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    Chapter 7 Methods to Visualize MAVS Subcellular Localization
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    Chapter 8 Purification of Cyclic GMP-AMP from Viruses and Measurement of Its Activity in Cell Culture
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    Chapter 9 cGAMP Quantification in Virus-Infected Human Monocyte-Derived Cells by HPLC-Coupled Tandem Mass Spectrometry
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    Chapter 10 Methods of Assessing STING Activation and Trafficking
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    Chapter 11 Genome-Wide CRISPR/Cas9 Screening for High-Throughput Functional Genomics in Human Cells
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    Chapter 12 High-Throughput Screening for Identification of Novel Innate Immune Activators
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    Chapter 13 Chromosome Conformation Capture for Research on Innate Antiviral Immunity
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    Chapter 14 Discovery of Variants Underlying Host Susceptibility to Virus Infection Using Whole-Exome Sequencing
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    Chapter 15 Isolation, Purification, and Culture of Primary Murine Sensory Neurons
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    Chapter 16 Isolation of Group 2 Innate Lymphoid Cells from Mouse Lungs
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    Chapter 17 Epidemiological Methods
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    Chapter 18 Erratum to: Purification of Cyclic GMP-AMP from Viruses and Measurement of Its Activity in Cell Culture
Attention for Chapter 15: Isolation, Purification, and Culture of Primary Murine Sensory Neurons
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Chapter title
Isolation, Purification, and Culture of Primary Murine Sensory Neurons
Chapter number 15
Book title
Innate Antiviral Immunity
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-7237-1_15
Pubmed ID
Book ISBNs
978-1-4939-7236-4, 978-1-4939-7237-1
Authors

Sarah Katzenell, Jorge R. Cabrera, Brian J. North, David A. Leib, Katzenell, Sarah, Cabrera, Jorge R., North, Brian J., Leib, David A.

Abstract

Cultured primary neurons have been of extraordinary value for the study of neuronal anatomy, cell biology, and physiology. While use of neuronal cell lines has ease and utility, there are often caveats that arise due to their mitotic nature. This methods article presents detailed methodology for the preparation, purification, and culture of adult murine sensory neurons for the study of herpes simplex virus lytic and latent infections. While virology is the application for our laboratory, these cultures also have broad utility for neurobiologists and cell biologists. While these primary cultures have been highly informative, the methodology is challenging to many investigators. Through publication of this highly detailed protocol, it is our hope that the use of this culture system can spread in the field to allow more rapid progress in furthering our understanding of neurotropic virus infection.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 56 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 56 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 18 32%
Researcher 8 14%
Student > Postgraduate 4 7%
Student > Master 4 7%
Student > Bachelor 3 5%
Other 6 11%
Unknown 13 23%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 15 27%
Agricultural and Biological Sciences 9 16%
Neuroscience 5 9%
Immunology and Microbiology 4 7%
Pharmacology, Toxicology and Pharmaceutical Science 4 7%
Other 5 9%
Unknown 14 25%