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Frontiers in Neurology|February 4, 2020
An Up-to-Date Overview of the Complexity of Genotype-Phenotype Relationships in Myotonic ChannelopathiesFernando Morales, Michael PuschThe Journal of General Physiology|November 19, 2020
Large transient capacitive currents in wild-type lysosomal Cl-/H+ antiporter ClC-7 and residual transport activity in the proton glutamate mutant E312AMichael Pusch, Giovanni ZifarelliThe Journal of General Physiology|August 13, 2003
Conformational changes in the pore of CLC-0Alessio Accardi, Michael PuschFrontiers in Pharmacology|August 12, 2011
Molecular Pharmacology of Kidney and Inner Ear CLC-K Chloride ChannelsAntonella Gradogna, Michael PuschNeuropharmacology|January 14, 2015
Biophysical properties of acid-sensing ion channels (ASICs)Stefan Gründer, Michael PuschEMBO Reports|August 29, 2009
Intracellular regulation of human ClC-5 by adenine nucleotidesGiovanni Zifarelli, Michael PuschChemistry & Biology|November 27, 2012
A kick-start for CLC antiporters' pharmacologyGiovanni Zifarelli, Michael PuschThe Journal of General Physiology|January 30, 2008
The muscle chloride channel ClC-1 is not directly regulated by intracellular ATPGiovanni Zifarelli, Michael PuschCell Calcium|December 3, 2014
ClC-5: Physiological role and biophysical mechanismsMichael Pusch, Giovanni ZifarelliEuropean Biophysics Journal : EBJ|January 10, 2009
The role of protons in fast and slow gating of the Torpedo chloride channel ClC-0Giovanni Zifarelli, Michael PuschPageof 13