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Scientific Reports|February 25, 2016
Impaired theta-gamma coupling in APP-deficient miceXiaomin Zhang, Wewei Zhong, Jurij Brankačk, et al.Hippocampus|May 16, 2020
Synchronicity of excitatory inputs drives hippocampal networks to distinct oscillatory patternsPascal Geschwill, Martin E Kaiser, Paul Grube, et al.Histochemistry and Cell Biology|January 19, 2016
KCC2 knockdown impairs glycinergic synapse maturation in cultured spinal cord neuronsChrysovalandis Schwale, Stefanie Schumacher, Claus Bruehl, et al.Nature Communications|January 15, 2025
Syntalos: a software for precise synchronization of simultaneous multi-modal data acquisition and closed-loop interventionsMatthias Klumpp, Lee Embray, Filippo Heimburg, et al.Pflugers Archiv : European Journal of Physiology|October 3, 2022
Breathing modulates gamma synchronization across speciesJoaquín González, Matias Cavelli, Alejandra Mondino, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 25, 2008
Amyloid beta oligomers (A beta(1-42) globulomer) suppress spontaneous synaptic activity by inhibition of P/Q-type calcium currentsVolker Nimmrich, Christiane Grimm, Andreas Draguhn, et al.Circulation. Arrhythmia and Electrophysiology|August 10, 2010
cAMP sensitivity of HCN pacemaker channels determines basal heart rate but is not critical for autonomic rate controlPatrick A Schweizer, Nana Duhme, Dierk Thomas, et al.Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|November 4, 2017
Local oxygen homeostasis during various neuronal network activity states in the mouse hippocampusJustus Schneider, Nikolaus Berndt, Ismini E Papageorgiou, et al.Combinatorial Chemistry & High Throughput Screening|December 12, 2012
Establishment of a secondary screening assay for P/Q-type calcium channel blockersDavid Hermann, Mario Mezler, Andrew M Swensen, et al.Pflugers Archiv : European Journal of Physiology|November 30, 2023
GPD1L-A306del modifies sodium current in a family carrying the dysfunctional SCN5A-G1661R mutation associated with Brugada syndromeFrancesca Semino, Fabrice F Darche, Claus Bruehl, et al.Pageof 14