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Rheumatoid Arthritis

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Cover of 'Rheumatoid Arthritis'

Table of Contents

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    Book Overview
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    Chapter 1 Collagen-Induced Arthritis Models
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    Chapter 2 Human Xenograft Model
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    Chapter 3 Long-Term Constant Subcutaneous Drug Administration
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    Chapter 4 Clinical Scoring of Disease Activity in Animal Models
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    Chapter 5 Histological Analysis of Arthritic Joints
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    Chapter 6 Preparation of Joint Extracts
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    Chapter 7 Production of Immunizing Antigen Proteoliposome Using Cell-Free Protein Synthesis System
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    Chapter 8 Reconstruction of Protein/Liposome Complex
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    Chapter 9 Production of Neutralizing Antibody
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    Chapter 10 Autoantibody Profiling Using Human Autoantigen Protein Array and AlphaScreen
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    Chapter 11 Generation of Specific Aptamers
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    Chapter 12 Production of Lentiviral Particles
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    Chapter 13 RNA Interference Ex Vivo
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    Chapter 14 Lentiviral-Mediated Systemic RNA Interference In Vivo
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    Chapter 15 Mesenchymal Stem Cell Engineering
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    Chapter 16 Screening of Ca2+ Influx in Lymphocytes
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    Chapter 17 Single-Cell Ca2+ Imaging
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    Chapter 18 Electrophysiological Methods to Measure Ca2+ Current
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    Chapter 19 The Functional Assessment of T cells
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    Chapter 20 Release of Antibodies and Cytokines from B Cells
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    Chapter 21 Evaluation of Autoreactive Responses
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    Chapter 22 Bone Resorption Activity in Mature Osteoclasts
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    Chapter 23 Animal Models of Vasculitis
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    Chapter 24 Design an Intervention Study
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    Chapter 25 Assessment of Disease Activity, Structural Damage, and Function in Rheumatoid Arthritis
Attention for Chapter 16: Screening of Ca2+ Influx in Lymphocytes
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Chapter title
Screening of Ca2+ Influx in Lymphocytes
Chapter number 16
Book title
Rheumatoid Arthritis
Published in
Methods in molecular biology, September 2018
DOI 10.1007/978-1-4939-8802-0_16
Pubmed ID
Book ISBNs
978-1-4939-8801-3, 978-1-4939-8802-0
Authors

Erika Takemasa, Shuang Liu

Abstract

The Ca2+ ion is an important second messenger in lymphocytes, similarly to its function in other mammalian cells. The generation of long-lasting intracellular Ca2+ elevations is essential for Ca2+-dependent gene transcription, proliferation, differentiation, and cytokine production in lymphocytes. Since store-operated Ca2+ entry (SOCE) is considered the predominant mode of Ca2+ influx in lymphocytes, the activation and function of lymphocytes can be generally predicted by monitoring SOCE. A method suitable for dynamic monitoring of Ca2+ influx using fura-2 labeling in lymphocytes is introduced in this chapter. Using this technique, large-scale screening of the activation status of primary or cultured lymphocytes can be realized.

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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 %
Student > Bachelor 1 50%
Student > Postgraduate 1 50%
Readers by discipline Count As %
Nursing and Health Professions 1 50%
Unknown 1 50%