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Titlebook: Neurotransmitter Transporters; Structure, Function, Maarten E. A. Reith Book 2002Latest edition Springer Science+Business Media New York 20

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書目名稱Neurotransmitter Transporters
副標題Structure, Function,
編輯Maarten E. A. Reith
視頻videohttp://file.papertrans.cn/665/664578/664578.mp4
概述Includes supplementary material:
叢書名稱Contemporary Neuroscience
圖書封面Titlebook: Neurotransmitter Transporters; Structure, Function, Maarten E. A. Reith Book 2002Latest edition Springer Science+Business Media New York 20
描述Neurotransmission is a multicomponent process. Transmitters, released by neuronal activity, act on pre- and postsynaptic receptors, and many books detail advances in the receptor field. In addition, after their release from nerve endings, transmitters are removed from the neuronal vicinity by uptake into neuronal or glial cells by specific tra- porter proteins that have been studied intensely over the last 30 years; this information is scattered throughout numerous publishing vehicles. Therefore, the primary aim of this second edition of N- rotransmitter Transporters: Structure, Function, and Regulation is to offer a comprehensive picture of the characterization of neurotransmitter transporters and their biological roles. The transporter field has moved forward in stages. In the first phase, progress came from the use of substrate or blocker ligands selectively targeting transporters, the application of model systems allowing the study of transmitter tra- port shielded from storage, and the development of mathematical models for describing transport phenomena. In the second phase, roughly covering the last decade, advances in DNA techniques allowed the cloning of numerous genes cod
出版日期Book 2002Latest edition
關鍵詞Glutamat; biochemistry; cells; imaging techniques; physiology
版次2
doihttps://doi.org/10.1007/978-1-59259-158-9
isbn_softcover978-1-61737-267-4
isbn_ebook978-1-59259-158-9
copyrightSpringer Science+Business Media New York 2002
The information of publication is updating

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Family of Sodium-Coupled Transporters for GABA, Glycine, Proline, Betaine, Taurine, and Creatine,inal cord, and non-neural tissues for the biogenic amine neurotransmitters as described in Chapters 3 and 4, as well as the inhibitory neurotransmitters γ-amino butyric acid (GABA) and glycine. In addition, transport proteins have been cloned for several other small mol wt compounds, including proline, betaine, taurine, and creatine.
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Book 2002Latest editionail advances in the receptor field. In addition, after their release from nerve endings, transmitters are removed from the neuronal vicinity by uptake into neuronal or glial cells by specific tra- porter proteins that have been studied intensely over the last 30 years; this information is scattered
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Neurotransmitter-Transporter Proteins,these neurotransmitter transporters have been cloned (.). The cloned transporters contain consensus sequences for multiple N-linked glycosylation sites in the large extracellular loop (EL) between transmembrane regions 3 and 4. Consensus sites for phosphorylation by several protein kinases are located in the putative cytosolic domains.
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