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International Journal of Molecular Sciences|August 27, 2021
TRPM2 Oxidation Activates Two Distinct Potassium Channels in Melanoma Cells through Intracellular Calcium IncreaseLoretta Ferrera, Raffaella Barbieri, Cristiana Picco, et al.Journal of Hypertension|March 19, 2016
Kidney CLC-K chloride channels inhibitors: structure-based studies and efficacy in hypertension and associated CLC-K polymorphismsAntonella Liantonio, Paola Imbrici, Giulia Maria Camerino, et al.Cell Death Discovery|June 22, 2024
Interactomic exploration of LRRC8A in volume-regulated anion channelsVeronica Carpanese, Margherita Festa, Elena Prosdocimi, et al.ACS Chemical Neuroscience|December 5, 2023
Basic Residues at Position 11 of α-Conotoxin LvIA Influence Subtype Selectivity between α3β2 and α3β4 Nicotinic Receptors via an Electrostatic MechanismYves Haufe, Veeresh Kuruva, Ziyana Samanani, et al.Proceedings of the National Academy of Sciences of the United States of America|July 16, 2008
Divergent sodium channel defects in familial hemiplegic migraineKristopher M Kahlig, Thomas H Rhodes, Michael Pusch, et al.Lancet (London, England)|August 2, 2005
Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraineMartin Dichgans, Tobias Freilinger, Gertrud Eckstein, et al.Pflugers Archiv : European Journal of Physiology|January 7, 2014
Structural basis of PI(4,5)P2-dependent regulation of GluA1 by phosphatidylinositol-5-phosphate 4-kinase, type II, alpha (PIP5K2A)Guiscard Seebohm, Eva Wrobel, Michael Pusch, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 30, 2020
Pathobiologic Mechanisms of Neurodegeneration in Osteopetrosis Derived From Structural and Functional Analysis of 14 ClC-7 MutantsEleonora Di Zanni, Eleonora Palagano, Laura Lagostena, et al.Neurology. Genetics|February 3, 2026
Functional Characterization of a De Novo SCN2A Mixed Variant Linked to Early Infantile Developmental and Epileptic EncephalopathyAnna Corradi, Antonella Riva, Bruno Sterlini, et al.Proceedings of the National Academy of Sciences of the United States of America|April 4, 2022
Gain of function due to increased opening probability by two KCNQ5 pore variants causing developmental and epileptic encephalopathyMario Nappi, Vincenzo Barrese, Lidia Carotenuto, et al.Pageof 13