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Titlebook: Returning Islamist Foreign Fighters; Threats and Challeng Elena Pokalova Book 2020 The Editor(s) (if applicable) and The Author(s), under e

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发表于 2025-3-21 17:56:00 | 显示全部楼层 |阅读模式
书目名称Returning Islamist Foreign Fighters
副标题Threats and Challeng
编辑Elena Pokalova
视频video
概述Provides the first in-depth examination of foreign fighter returnees and the challenges they pose for their home countries.Offers a unique review of the multiple waves of Islamist foreign fighters, no
图书封面Titlebook: Returning Islamist Foreign Fighters; Threats and Challeng Elena Pokalova Book 2020 The Editor(s) (if applicable) and The Author(s), under e
描述This book examines the challenges foreign fighter returnees from Syria and Iraq pose to Western countries. A number of returnees have demonstrated that they are willing to use violence against their home countries, and some have already staged terrorist attacks on Western soil on apparent orders from ISIS. Through the historical context of previous waves of mobilizations of Islamist foreign fighters, the author tracks the experiences of returnees from previous conflicts and discusses the major security challenges associated with them. The book analyzes the major approaches implemented by Western countries in response to foreign fighter returnees, discusses the prosecution of returnees, and evaluates the corresponding challenges of prison radicalization.
出版日期Book 2020
关键词foreign fighters; women in jihad; returnees rehabilitation; Syria; Iraq; child returnees
版次1
doihttps://doi.org/10.1007/978-3-030-31478-1
isbn_softcover978-3-030-31480-4
isbn_ebook978-3-030-31478-1
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Switzerl
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发表于 2025-3-21 23:31:11 | 显示全部楼层
Elena Pokalovalecs, on their cell surface. These self-non-self discriminating machineries give not only an advantage to the host cells in innate immune system but also a disadvantage because they allow cancer cells to escape from the immune cells. Siglec7 is one of such machineries predominantly expressed in natu
发表于 2025-3-22 00:48:50 | 显示全部楼层
Elena Pokalovalycosylation is regulated by the cellular expression profile of enzymes regarding glycan and substrate synthesis and the cellular metabolism reflecting cellular status and microenvironments. In the disease process, the glycan synthesis pathway is altered, and aberrant glycans can be generated. Sialy
发表于 2025-3-22 08:06:34 | 显示全部楼层
Elena Pokalovarch directions.Ideal guide to the field for students and you.This book, now in an extensively revised second edition, provides a comprehensive summary of the latest knowledge regarding glycosignals and a thorough analysis of their involvement in not only cancers but also other refractory conditions
发表于 2025-3-22 10:11:35 | 显示全部楼层
Elena Pokalovaof glycolsphingolipids have been largely elucidated via glyco-remodeling cells and animals. The progress in these glycobiology techniques has enabled us to understand the roles of “tumor-specific” carbohydrates during these 3 decades. Tumor antigens recognized by host immune systems of cancer patien
发表于 2025-3-22 16:58:36 | 显示全部楼层
Elena Pokalovaof glycolsphingolipids have been largely elucidated via glyco-remodeling cells and animals. The progress in these glycobiology techniques has enabled us to understand the roles of “tumor-specific” carbohydrates during these 3 decades. Tumor antigens recognized by host immune systems of cancer patien
发表于 2025-3-22 18:06:02 | 显示全部楼层
Elena Pokaloval in the infant stages and requires much more research and knowledge of the biological functions of cell surface receptors. Extrinsic apoptosis is the cell death cascade initiated at the cell surface involving specific receptors, followed by recruitment of protein complexes and activation of protein
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Elena Pokalovaes of such alteration, our studies have focused on mammalian sialidases, which regulate the cellular sialic acid content by catalyzing the removal of sialic acid residues from glycoproteins and glycolipids. There are four types of mammalian sialidases, designated as NEU1, NEU2, NEU3, and NEU4, encod
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