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Semaphorin Signaling

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Cover of 'Semaphorin Signaling'

Table of Contents

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    Book Overview
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    Chapter 1 Semaphorins and their Signaling Mechanisms.
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    Chapter 2 Isolating Fc-Tagged SEMA4D Recombinant Protein from 293FT Cells.
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    Chapter 3 Expression and Purification of Class 7 Semaphorin and Its PlexinC1 Receptor Using Baculovirus-Mediated Mammalian Cell Gene Transduction.
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    Chapter 4 Immunoaffinity Purification of the Glycosylated Extracellular Fragment of Mouse Plexin A2 Produced in a Mammalian Expression System.
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    Chapter 5 Plate-Based Assay for Measuring Direct Semaphorin-Neuropilin Interactions.
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    Chapter 6 Characterizing Plexin GTPase Interactions Using Gel Filtration, Surface Plasmon Resonance Spectrometry, and Isothermal Titration Calorimetry.
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    Chapter 7 In Vitro Assay for the Rap GTPase-Activating Protein Activity of the Purified Cytoplasmic Domain of Plexin.
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    Chapter 8 Characterizing F-actin Disassembly Induced by the Semaphorin-Signaling Component MICAL.
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    Chapter 9 Characterizing ErbB-2-Mediated Tyrosine Phosphorylation and Activation of Plexins.
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    Chapter 10 Characterizing PKA-Mediated Phosphorylation of Plexin Using Purified Proteins.
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    Chapter 11 Using Heterologous COS-7 Cells to Identify Semaphorin-Signaling Components.
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    Chapter 12 Analysis of Semaphorin-Induced Growth Cone Collapse and Axon Growth Inhibition.
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    Chapter 13 Using Rotary Shadow Electron Microscopy to Characterize Semaphorin-Mediated Growth Cone Collapse.
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    Chapter 14 An Electrical Impedance-Based Method for Quantitative Real-Time Analysis of Semaphorin-Elicited Endothelial Cell Collapse.
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    Chapter 15 Regulation of Cortical Dendrite Morphology and Spine Organization by Secreted Semaphorins: A Primary Culture Approach.
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    Chapter 16 Semaphorin Signaling
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    Chapter 17 Performing Axon Orientation Assays with Secreted Semaphorins and Other Guidance Cues.
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    Chapter 18 Assays to Examine Transmembrane Semaphorin Function In Vitro.
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    Chapter 19 Micro-CALI to Study Localized Roles of the Semaphorin Signaling Component CRMP in Axon Growth.
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    Chapter 20 Visualizing and Characterizing Semaphorin Endocytic Events Using Quantum Dot-Conjugated Proteins.
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    Chapter 21 Visualization of Clathrin-Mediated Endocytosis During Semaphorin-Guided Axonal Growth.
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    Chapter 22 Semaphorin Signaling
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    Chapter 23 Antibody-Feeding Assay: A Method to Track the Internalization of Neuropilin-1 and Other Cell Surface Receptors.
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    Chapter 24 Photolithography-Based Substrate Microfabrication for Patterning Semaphorin 3A to Study Neuronal Development.
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    Chapter 25 Characterization of Semaphorin 6A-Mediated Effects on Angiogenesis Through Regulation of VEGF Signaling.
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    Chapter 26 Semaphorin Signaling
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    Chapter 27 Characterizing Semaphorin-Mediated Immune Responses Using an Antigen-Presentation Assay.
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    Chapter 28 Podocyte Shape Regulation by Semaphorin 3A and MICAL-1.
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    Chapter 29 In Vivo and In Vitro Knockdown Approaches in the Avian Embryo as a Means to Study Semaphorin Signaling.
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    Chapter 30 Semaphorin Signaling
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    Chapter 31 Characterization of the Effects of Semaphorin 4D Signaling on Angiogenesis.
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    Chapter 32 Characterizing Semaphorin-Mediated Effects on Sensory and Motor Axon Pathfinding and Connectivity During Embryonic Development.
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    Chapter 33 Experimental Approaches for Studying Semaphorin Signals in Tumor Growth and Metastasis in Mouse Models.
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    Chapter 34 Characterizing Semaphorin Signaling In Vivo Using C. elegans.
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Chapter title
Semaphorins and their Signaling Mechanisms.
Chapter number 1
Book title
Semaphorin Signaling
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6448-2_1
Pubmed ID
Book ISBNs
978-1-4939-6446-8, 978-1-4939-6448-2
Authors

Laura Taylor Alto, Jonathan R. Terman, Laura T. Alto

Editors

Jonathan R. Terman

Abstract

Semaphorins are extracellular signaling proteins that are essential for the development and maintenance of many organs and tissues. The more than 20-member semaphorin protein family includes secreted, transmembrane and cell surface-attached proteins with diverse structures, each characterized by a single cysteine-rich extracellular sema domain, the defining feature of the family. Early studies revealed that semaphorins function as axon guidance molecules, but it is now understood that semaphorins are key regulators of morphology and motility in many different cell types including those that make up the nervous, cardiovascular, immune, endocrine, hepatic, renal, reproductive, respiratory and musculoskeletal systems, as well as in cancer cells. Semaphorin signaling occurs predominantly through Plexin receptors and results in changes to the cytoskeletal and adhesive machinery that regulate cellular morphology. While much remains to be learned about the mechanisms underlying the effects of semaphorins, exciting work has begun to reveal how semaphorin signaling is fine-tuned through different receptor complexes and other mechanisms to achieve specific outcomes in various cellular contexts and physiological systems. These and future studies will lead to a more complete understanding of semaphorin-mediated development and to a greater understanding of how these proteins function in human disease.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 301 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 301 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 64 21%
Student > Master 38 13%
Researcher 36 12%
Student > Bachelor 35 12%
Student > Doctoral Student 23 8%
Other 26 9%
Unknown 79 26%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 84 28%
Neuroscience 49 16%
Medicine and Dentistry 32 11%
Agricultural and Biological Sciences 22 7%
Immunology and Microbiology 7 2%
Other 19 6%
Unknown 88 29%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 02 July 2022.
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#18,390,814
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Outputs from Methods in molecular biology
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Outputs of similar age from Methods in molecular biology
#691
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