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Programmed Cell Death

Overview of attention for book
Cover of 'Programmed Cell Death'

Table of Contents

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    Book Overview
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    Chapter 1 Detection of Apoptotic Versus Autophagic Cell Death by Flow Cytometry
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    Chapter 2 In Vivo Apoptosis Imaging Using Site-Specifically 68 Ga-Labeled Annexin V
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    Chapter 3 Detection of Active Caspases During Apoptosis Using Fluorescent Activity-Based Probes
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    Chapter 4 Detection of Initiator Caspase Induced Proximity in Single Cells by Caspase Bimolecular Fluorescence Complementation
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    Chapter 5 In Vitro Use of Peptide Based Substrates and Inhibitors of Apoptotic Caspases
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    Chapter 6 Programmed Cell Death
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    Chapter 7 Analysis of Cell Death Induction in Intestinal Organoids In Vitro
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    Chapter 8 In Vitro Differentiation of Mouse Granulocytes
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    Chapter 9 Programmed Cell Death
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    Chapter 10 Isolation of Cardiomyocytes and Cardiofibroblasts for Ex Vivo Analysis
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    Chapter 11 Programmed Cell Death
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    Chapter 12 Programmed Cell Death
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    Chapter 13 Modeling Metazoan Apoptotic Pathways in Yeast
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    Chapter 14 Characterizing Bcl-2 Family Protein Conformation and Oligomerization Using Cross-Linking and Antibody Gel-Shift in Conjunction with Native PAGE
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    Chapter 15 Using Förster-Resonance Energy Transfer to Measure Protein Interactions Between Bcl-2 Family Proteins on Mitochondrial Membranes
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    Chapter 16 Preparing Samples for Crystallization of Bcl-2 Family Complexes
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    Chapter 17 Programmed Cell Death
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    Chapter 18 Programmed Cell Death
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    Chapter 19 Programmed Cell Death
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    Chapter 20 Proteomic Profiling of Cell Death: Stable Isotope Labeling and Mass Spectrometry Analysis
Attention for Chapter 8: In Vitro Differentiation of Mouse Granulocytes
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Chapter title
In Vitro Differentiation of Mouse Granulocytes
Chapter number 8
Book title
Programmed Cell Death
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3581-9_8
Pubmed ID
Book ISBNs
978-1-4939-3579-6, 978-1-4939-3581-9
Authors

Ramona Reinhart, Simone Wicki, Thomas Kaufmann, Reinhart, Ramona, Wicki, Simone, Kaufmann, Thomas

Abstract

Granulocytes are central players of the immune system and, once activated, a tightly controlled balance between effector functions and cell removal by apoptosis guarantees maximal host benefit with least possible collateral damage to healthy tissue.Granulocytes are terminally differentiated cells that cannot be maintained in culture for prolonged times. Isolating primary granulocytes is inefficient and challenging when working with mice, and especially so for the lowly abundant eosinophil and basophil subtypes. Here we describe an in vitro protocol to massively expand mouse derived myeloid progenitors and to differentiate them "on demand" and in large numbers into mature neutrophils or basophils.

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Mendeley readers

The data shown below were compiled from readership statistics for 55 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 55 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 11 20%
Student > Master 8 15%
Student > Bachelor 6 11%
Student > Doctoral Student 5 9%
Researcher 5 9%
Other 8 15%
Unknown 12 22%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 12 22%
Agricultural and Biological Sciences 10 18%
Immunology and Microbiology 8 15%
Medicine and Dentistry 7 13%
Engineering 3 5%
Other 4 7%
Unknown 11 20%