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Programmed Necrosis

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Cover of 'Programmed Necrosis'

Table of Contents

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    Book Overview
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    Chapter 1 Tools in the Art of Studying Necroptosis
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    Chapter 2 Loss-of-Function RNAi Screen to Identify Necrosis-Signaling Molecules
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    Chapter 3 Chemical Library Screens to Identify Pharmacological Modulators of Necroptosis
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    Chapter 4 Distinguishing Necroptosis from Apoptosis
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    Chapter 5 Methods for Studying TNF-Mediated Necroptosis in Cultured Cells
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    Chapter 6 Analysis of Necroptosis in Bone Marrow-Derived Macrophages
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    Chapter 7 Generation and Use of Chimeric RIP Kinase Molecules to Study Necroptosis
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    Chapter 8 Detection of MLKL Oligomerization During Programmed Necrosis
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    Chapter 9 Analysis of Cytokine- and Influenza A Virus-Driven RIPK3 Necrosome Formation
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    Chapter 10 Detection of RIPK1 in the FADD-Containing Death Inducing Signaling Complex (DISC) During Necroptosis
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    Chapter 11 Use of RIP1 Kinase Small-Molecule Inhibitors in Studying Necroptosis
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    Chapter 12 Analyzing Necroptosis Using an RIPK1 Kinase Inactive Mouse Model of TNF Shock
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    Chapter 13 Assessment of In Vivo Kidney Cell Death: Acute Kidney Injury
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    Chapter 14 Assessment of In Vivo Kidney Cell Death: Glomerular Injury
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    Chapter 15 Detection of Necroptosis by Phospho-RIPK3 Immunohistochemical Labeling
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    Chapter 16 Characterization of the TNFR1-SC Using “Modified Tandem Affinity Purification” in Conjunction with Liquid Chromatography–Mass Spectrometry (LC-MS)
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    Chapter 17 Monitoring RIPK1 Phosphorylation in the TNFR1 Signaling Complex
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    Chapter 18 Analysis of CYLD Proteolysis by CASPASE 8 in Bone Marrow-Derived Macrophages
Attention for Chapter 2: Loss-of-Function RNAi Screen to Identify Necrosis-Signaling Molecules
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Chapter title
Loss-of-Function RNAi Screen to Identify Necrosis-Signaling Molecules
Chapter number 2
Book title
Programmed Necrosis
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-8754-2_2
Pubmed ID
Book ISBNs
978-1-4939-8753-5, 978-1-4939-8754-2
Authors

David Mark Moquin, Francis Ka-Ming Chan

Abstract

Over the recent years, genome-wide RNA interference (RNAi) library screens have been instrumental in the identification of key regulators of various biological pathways. The prolific use of this technique is attributed to its amenability to a high-throughput format. Here, we present the step-by-step method to conduct a siRNA screen to identify genes involved in necroptosis, a nonapoptotic form of proinflammatory cell death. The method described here uses MTS cell proliferation assay to measure necroptosis, which is compatible with high-throughput format screening on multiwell microtiter plates. This ensures that the screen can be performed in a timely and efficient manner.

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Mendeley readers

The data shown below were compiled from readership statistics for 2 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 2 100%

Demographic breakdown

Readers by professional status Count As %
Unspecified 1 50%
Student > Master 1 50%
Readers by discipline Count As %
Unspecified 1 50%
Biochemistry, Genetics and Molecular Biology 1 50%