"synopsis" may belong to another edition of this title.
Shipping:
US$ 4.25
Within U.S.A.
Book Description Hardcover. Condition: new. New Copy. Customer Service Guaranteed. Seller Inventory # think3540661204
Book Description Hardcover. Condition: new. New. Seller Inventory # Wizard3540661204
Book Description Condition: new. Seller Inventory # FrontCover3540661204
Book Description Condition: New. New. In shrink wrap. Looks like an interesting title! 1.8. Seller Inventory # Q-3540661204
Book Description Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. With contributions by numerous experts|Dieser Band vermittelt einen umfassenden Ueberblick ueber das Gebiet der Glutamat Rezeptoren and ihrer Rolle in der erregenden synaptischen Uebertragung.Section I: Molecula r Structure of Glutamate Receptors.- 1 Struc. Seller Inventory # 4897530
Book Description Hardcover. Condition: new. Seller Inventory # 9783540661207
Book Description Condition: New. PRINT ON DEMAND Book; New; Fast Shipping from the UK. No. book. Seller Inventory # ria9783540661207_lsuk
Book Description Buch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -It is now widely accepted that glutamate is the major excitatory neurotrans mitter in the mammalian central nervous system. The main criteria for accept ing a molecule as a chemical transmitter appear to be fulfilled at several synapses: Glutamate mimics the action of the natural transmitter in the post synaptic neuron (CURTIS et al. 1959), glutamate is present in presynaptic ele ments (OTTERSEN and STORM-MATHISEN 1984), and glutamate is released from central neurons in an activity-dependent manner (BRADFORD 1970). The postsynaptic receptors that mediate the effects of glutamate are markedly diverse. Based on their activation by agonists that act more selec tively than the natural transmitter itself, a-amino-3-hydroxy-5-methyl- isoxazolepropionate (AMPA) receptors, kainate receptors, and N-methyl-D aspartate (NMDA) receptors can be distinguished. Molecular cloning has revealed additional structural diversity. To date, almost 20 glutamate receptor subunit genes have been identified, and an even larger number of splice vari ants and edited versions are present in the mammalian brain. Analysis of synaptic transmission revealed that 'the' excitatory synapse does not exist. Glutamatergic synapses in different circuitries differ substan tially in their signaling properties, although they use the same transmitter. We have learned that cellular, subcellular, and molecular factors determine synap tic function, and that glutamate receptor subunit diversity is of direct relevance in shaping the unique signaling properties of a glutamatergic synapse. 560 pp. Englisch. Seller Inventory # 9783540661207
Book Description Buch. Condition: Neu. Druck auf Anfrage Neuware - Printed after ordering - It is now widely accepted that glutamate is the major excitatory neurotrans mitter in the mammalian central nervous system. The main criteria for accept ing a molecule as a chemical transmitter appear to be fulfilled at several synapses: Glutamate mimics the action of the natural transmitter in the post synaptic neuron (CURTIS et al. 1959), glutamate is present in presynaptic ele ments (OTTERSEN and STORM-MATHISEN 1984), and glutamate is released from central neurons in an activity-dependent manner (BRADFORD 1970). The postsynaptic receptors that mediate the effects of glutamate are markedly diverse. Based on their activation by agonists that act more selec tively than the natural transmitter itself, a-amino-3-hydroxy-5-methyl- isoxazolepropionate (AMPA) receptors, kainate receptors, and N-methyl-D aspartate (NMDA) receptors can be distinguished. Molecular cloning has revealed additional structural diversity. To date, almost 20 glutamate receptor subunit genes have been identified, and an even larger number of splice vari ants and edited versions are present in the mammalian brain. Analysis of synaptic transmission revealed that 'the' excitatory synapse does not exist. Glutamatergic synapses in different circuitries differ substan tially in their signaling properties, although they use the same transmitter. We have learned that cellular, subcellular, and molecular factors determine synap tic function, and that glutamate receptor subunit diversity is of direct relevance in shaping the unique signaling properties of a glutamatergic synapse. Seller Inventory # 9783540661207