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Titlebook: Drebrin; From Structure and F Tomoaki Shirao,Yuko Sekino Book 2017 The Editor(s) (if applicable) and The Author(s), under exclusive license

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發(fā)表于 2025-3-21 18:15:39 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Drebrin
副標(biāo)題From Structure and F
編輯Tomoaki Shirao,Yuko Sekino
視頻videohttp://file.papertrans.cn/283/282822/282822.mp4
概述Offers the first comprehensive review of drebrin from its molecular structure and function to the physiological and pathological roles edited by the discoverer of drebrin.Presents a multidisciplinary
叢書名稱Advances in Experimental Medicine and Biology
圖書封面Titlebook: Drebrin; From Structure and F Tomoaki Shirao,Yuko Sekino Book 2017 The Editor(s) (if applicable) and The Author(s), under exclusive license
描述This book is the first comprehensive review of drebrin, which plays pivotal roles in various cellular events, via forming unique actin cytoskeletons, including synapse formation and in synaptic function. Particularly the loss of drebrin from dendritic spines is used as a marker of dementia in neurological disorders such as Alzheimer’s disease. Since drebrin was first identified by our group in 1985, many studies of drebrin have been done in various fields, including not only molecular biology, biophysics, cell biology, neuroscience, clinical studies, spermatogenesis, immunology, and cancer metastasis, but others as well. The structure of this book facilitates the understanding of the whole picture of studies on drebrin. The volume begins with a general introduction to drebrin, and then the chapters in the second part provide the basic knowledge for further understanding. The third part examines its function in the nervous system, and the fourth part discusses its function in the non-nervous system. This work will appeal to researchers who are interested in cytoskeletal dynamics at membrane-cytoskeletal interface as well as the number of them who use drebrin as a tool, such as a mar
出版日期Book 2017
關(guān)鍵詞Actin filament; Cell migration; Process formation; Synapse formation; Synaptic plasticity; Adherens junct
版次1
doihttps://doi.org/10.1007/978-4-431-56550-5
isbn_softcover978-4-431-56817-9
isbn_ebook978-4-431-56550-5Series ISSN 0065-2598 Series E-ISSN 2214-8019
issn_series 0065-2598
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Japan KK
The information of publication is updating

書目名稱Drebrin影響因子(影響力)




書目名稱Drebrin影響因子(影響力)學(xué)科排名




書目名稱Drebrin網(wǎng)絡(luò)公開度




書目名稱Drebrin網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Drebrin被引頻次




書目名稱Drebrin被引頻次學(xué)科排名




書目名稱Drebrin年度引用




書目名稱Drebrin年度引用學(xué)科排名




書目名稱Drebrin讀者反饋




書目名稱Drebrin讀者反饋學(xué)科排名




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沙發(fā)
發(fā)表于 2025-3-21 20:33:29 | 只看該作者
板凳
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Advances in Experimental Medicine and Biologyhttp://image.papertrans.cn/e/image/282822.jpg
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發(fā)表于 2025-3-22 06:49:47 | 只看該作者
Multi-sense Attention for Autonomous Agentsein, which is classified into two major isoforms produced by alternative splicing from a single . gene. The isoform predominantly expressed in the adult brain (drebrin A) is neuron specific, containing a neuron-specific sequence (Ins2) in the middle of the molecule. Drebrin A is highly concentrated
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發(fā)表于 2025-3-22 14:00:19 | 只看該作者
https://doi.org/10.1007/978-3-031-04386-4in in vivo, we must understand its molecular properties. In this chapter, I will focus on the purification and characterization of drebrin in vitro. Drebrin binds to F-actin with a stoichiometry of 1:5~6 with a .. of 1~3 × 10. M and strongly inhibits the binding of other actin-binding proteins such
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發(fā)表于 2025-3-23 02:56:15 | 只看該作者
Nikolaos Karagiannis,Debbie A. Mohammedyclonal and monoclonal antibodies. Immunoblot analysis demonstrated that the adult drebrin isoform (drebrin A) is restricted to neural tissues, while the embryonic drebrin isoforms (drebrin E1 and E2 in chicken and drebrin E in mammals) are found in a wide variety of tissues. In the developing brain
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發(fā)表于 2025-3-23 07:26:23 | 只看該作者
Nikolaos Karagiannis,Debbie A. Mohammedn is an F-actin-binding protein that increases noticeably during juvenile synaptogenesis. Electron microscopic analysis reveals that drebrin is highly enriched specifically on the postsynaptic side of excitatory synapses. Since dendritic spines are structures specialized for excitatory synaptic tran
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