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Titlebook: Synapse Development; Methods and Protocol Alexandros Poulopoulos Book 2017 Springer Science+Business Media LLC 2017 Neurons.Nervous system

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Frank Herrmannsdörfer,Benjamin Flottmann,Siddarth Nanguneri,Varun Venkataramani,Heinz Horstmann,Thomivity. Similarly, poly(gamma-benzyl-.-glutamate) (PBLG) was found out to be an excellent choice in flexible transducer applications because of its stability and high piezoelectric coefficients. Finally, poly(methyl methacrylate) (PMMA) was proved to be an ideal polymeric material for energy storage
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Miquel Bosch,Jorge Castro,Mriganka Sur,Yasunori Hayashirtness represents an innovative, coordinated, green, open and shared development ecology. The concept of Smart Port and its construction reflect an inevitable trend of historical development. Meanwhile, Smart Port extends the functional concept of traditional port to waterless port, logistics zone,
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Cordelia Imig,Benjamin H. Coopersignificantly affected the ship inspection procedures and in particular the controls by the Port State Authorities and the inspections from energy companies, members of the Oil Companies International Marine Forum (OCIMF) Ship Inspection Report Programme (SIRE). These unforeseen conditions mandated
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A Cell Culture System to Investigate the Presynaptic Control of Subsynaptic Membrane Differentiation induce and maintain the subsynaptic muscle membrane. We provide here a detailed protocol through which acetylcholine receptor clusters are induced in cultured myotubes contacting laminin-attached agrin, enabling molecular, biochemical and cell biological analyses including high resolution microscop
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Isolation of Synaptosomes, Synaptic Plasma Membranes, and Synaptic Junctional Complexesof the nerve terminals, such as responses to depolarization and the uptake or release of signaling molecules, have also been characterized through the use of fluorescent dyes, tagged transmitters, and transporter substrates. In addition, isolated synaptosomes can serve as the starting material for t
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Optimized Protocol for Imaging Cleared Neural Tissues Using Light Microscopynds of cubic millimeters. This experimental pipeline involves three steps: tissue clearing, tissue imaging, and data analysis. In an attempt to streamline the process for researchers entering this field, we address important considerations for each of these stages and describe an integrated solution
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Structured Illumination Microscopy for the Investigation of Synaptic Structure and Functionlution technique, Structured Illumination Microscopy (SIM), has emerged as an attractive method to examine synapse structure and function. SIM requires little change in standard light microscopy sample preparation steps, but results in a twofold improvement in both lateral and axial resolutions comp
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