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American Journal of Human Genetics|October 13, 2015
A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar AtaxiaMarie Coutelier, Iulia Blesneac, Arnaud Monteil, et al.
Circulation Research|May 13, 2006
Bradycardia and slowing of the atrioventricular conduction in mice lacking CaV3.1/alpha1G T-type calcium channelsMatteo E Mangoni, Achraf Traboulsie, Anne-Laure Leoni, et al.
The Journal of Biological Chemistry|October 4, 2017
Calmodulin regulates Cav3 T-type channels at their gating brakeJean Chemin, Valentina Taiakina, Arnaud Monteil, et al.
The EMBO Journal|May 6, 2006
TREK-1, a K+ channel involved in polymodal pain perceptionAbdelkrim Alloui, Katharina Zimmermann, Julien Mamet, et al.
Frontiers in Pharmacology|October 20, 2025
Electrophysiological classification of CACNA1G gene variants associated with neurodevelopmental and neurological disordersAmaël Davakan, Leos Cmarko, Barbara Ribeiro Oliveira-Mendes, et al.
The Journal of Cell Biology|March 25, 2009
Akt regulates L-type Ca2+ channel activity by modulating Cavalpha1 protein stabilityDaniele Catalucci, Deng-Hong Zhang, Jaime DeSantiago, et al.
Circulation Research|December 4, 2025
L-Type Cav1.3 and HCN Channels Mediate Heart Rate Acceleration by CatecholaminesEleonora Torre, Mélanie Faure, Isabelle Bidaud, et al.
Nature Communications|August 22, 2014
Cardiac arrhythmia induced by genetic silencing of 'funny' (f) channels is rescued by GIRK4 inactivationPietro Mesirca, Jacqueline Alig, Angelo G Torrente, et al.
Scientific Reports|November 11, 2018
Lysosomal and network alterations in human mucopolysaccharidosis type VII iPSC-derived neuronsNeus Bayó-Puxan, Ana Paula Terrasso, Sophie Creyssels, et al.
Circulation|August 4, 2016
Peptidomimetic Targeting of Cavβ2 Overcomes Dysregulation of the L-Type Calcium Channel Density and Recovers Cardiac FunctionFrancesca Rusconi, Paola Ceriotti, Michele Miragoli, et al.
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