Osteogenic and Chondrogenic Master Genes Expression Is Dependent on the Kir2.1 Potassium Channel Through the Bone Morphogenetic Protein Pathway von Pini, Jonathan, Giuliano, Serena, Matonti, Julia, Gannoun, Lila, Simkin, Dina, Rouleau, Matthieu, Bendahhou, Saïd

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Keeping hyperactive voltage‐gated sodium channels in silent mode von Bendahhou, Saïd

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Bisphosphonates Targeting Ion Channels and Musculoskeletal Effects von Scala, Rosa, Maqoud, Fatima, Antonacci, Marina, Dibenedetto, Jacopo Raffaele, Perrone, Maria Grazia, Scilimati, Antonio, Castillo, Karen, Latorre, Ramón, Conte, Diana, Bendahhou, Saïd, Tricarico, Domenico

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New Structural insights into Kir channel gating from molecular simulations, HDX-MS and functional studies von Fagnen, Charline, Bannwarth, Ludovic, Oubella, Iman, Forest, Eric, De Zorzi, Rita, de Araujo, Aline, Mhoumadi, Yasmina, Bendahhou, Saïd, Perahia, David, Vénien-Bryan, Catherine

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First Evidence of Kv3.1b Potassium Channel Subtype Expression during Neuronal Serotonergic 1C11 Cell Line Development von Tabka, Hager, Cheikh, Amani, Maatoug, Sonia, Ayeb, Mohamed El, Bendahhou, Saïd, Benkhalifa, Rym

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TWIK1, a unique background channel with variable ion selectivity von Chatelain, Franck C., Bichet, Delphine, Douguet, Dominique, Feliciangeli, Sylvain, Bendahhou, Saïd, Reichold, Markus, Warth, Richard, Barhanin, Jacques, Lesage, Florian

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Integrative Study of the Structural and Dynamical Properties of a KirBac3.1 Mutant: Functional Implication of a Highly Conserved Tryptophan in the Transmembrane Domain von Fagnen, Charline, Bannwarth, Ludovic, Oubella, Iman, Zuniga, Dania, Haouz, Ahmed, Forest, Eric, Scala, Rosa, Bendahhou, Saïd, De Zorzi, Rita, Perahia, David, Vénien-Bryan, Catherine

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Cross Pharmacological, Biochemical and Computational Studies of a Human Kv3.1b Inhibitor from Androctonus australis Venom von Maatoug, Sonia, Cheikh, Amani, Khamessi, Oussema, Tabka, Hager, Landoulsi, Zied, Guigonis, Jean-Marie, Diochot, Sylvie, Bendahhou, Saïd, Benkhalifa, Rym

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Invalidation of TASK1 potassium channels disrupts adrenal gland zonation and mineralocorticoid homeostasis von Heitzmann, Dirk, Derand, Renaud, Jungbauer, Stefan, Bandulik, Sascha, Sterner, Christina, Schweda, Frank, Wakil, Abeer El, Lalli, Enzo, Guy, Nicolas, Mengual, Raymond, Reichold, Markus, Tegtmeier, Ines, Bendahhou, Saïd, Gomez-Sanchez, Celso E, Isabel Aller, M, Wisden, William, Weber, Achim, Lesage, Florian, Warth, Richard, Barhanin, Jacques

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Substitutions of the S4DIV R2 residue (R1451) in NaV1.4 lead to complex forms of paramyotonia congenita and periodic paralyses von Poulin, Hugo, Gosselin-Badaroudine, Pascal, Vicart, Savine, Habbout, Karima, Sternberg, Damien, Giuliano, Serena, Fontaine, Bertrand, Bendahhou, Saïd, Nicole, Sophie, Chahine, Mohamed

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The inward rectifier potassium channel Kir2.1 is required for osteoblastogenesis von Sacco, Sonia, Giuliano, Serena, Sacconi, Sabrina, Desnuelle, Claude, Barhanin, Jacques, Amri, Ez-zoubir, Bendahhou, Saïd

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Biological fractionation of lithium isotopes by cellular Na+/H+ exchangers unravels fundamental transport mechanisms von Poet, Mallorie, Vigier, Nathalie, Bouret, Yann, Jarretou, Gisèle, Gautier, Romain, Bendahhou, Saïd, Balter, Vincent, Montanes, Maryline, Thibon, Fanny, Counillon, Laurent

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Relationships between Plasma Pyrophosphate, Vascular Calcification and Clinical Severity in Patients Affected by Pseudoxanthoma Elasticum von Leftheriotis, Georges, Navasiolava, Nastassia, Clotaire, Laetitia, Duranton, Christophe, Le Saux, Olivier, Bendahhou, Saïd, Laurain, Audrey, Rubera, Isabelle, Martin, Ludovic

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A204E mutation in Nav1.4 DIS3 exerts gain- and loss-of-function effects that lead to periodic paralysis combining hyper- with hypo-kalaemic signs von Kokunai, Yosuke, Dalle, Carine, Vicart, Savine, Sternberg, Damien, Pouliot, Valérie, Bendahhou, Said, Fournier, Emmanuel, Chahine, Mohamed, Fontaine, Bertrand, Nicole, Sophie

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Modeling Andersen's Syndrome in Human Induced Pluripotent Stem Cells von Pini, Jonathan, Rouleau, Matthieu, Desnuelle, Claude, Sacconi, Sabrina, Bendahhou, Saïd

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Does Sumoylation Control K2P1/TWIK1 Background K + Channels? von Feliciangeli, Sylvain, Bendahhou, Saïd, Sandoz, Guillaume, Gounon, Pierre, Reichold, Markus, Warth, Richard, Lazdunski, Michel, Barhanin, Jacques, Lesage, Florian

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Dkk3 is a component of the genetic circuitry regulating aldosterone biosynthesis in the adrenal cortex von EL WAKIL, Abeer, BANDULIK, Sascha, GUY, Nicolas, BENDAHHOU, Saïd, ZENNARO, Maria-Christina, NIEHRS, Christof, MARI, Bernard, WARTH, Richard, BARHANIN, Jacques, LALLI, Enzo

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The K+ channel TASK1 modulates β‐adrenergic response in brown adipose tissue through the mineralocorticoid receptor pathway von Pisani, Didier F., Beranger, Guillaume E., Corinus, Alain, Giroud, Maude, Ghandour, Rayane A., Altirriba, Jordi, Chambard, Jean‐Claude, Mazure, Nathalie M., Bendahhou, Saïd, Duranton, Christophe, Michiels, Jean‐François, Frontini, Andrea, Rohner‐Jeanrenaud, Françoise, Cinti, Saverio, Christian, Mark, Barhanin, Jacques, Amri, Ez‐Zoubir

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Andersen’s syndrome mutants produce a knockdown of inwardly rectifying K+ channel in mouse skeletal muscle in vivo von Simkin, Dina, Robin, Gaëlle, Giuliano, Serena, Vukolic, Ana, Moceri, Pamela, Guy, Nicolas, Wagner, Kay-Dietrich, Lacampagne, Alain, Allard, Bruno, Bendahhou, Saïd

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Cryo-electron microscopy unveils unique structural features of the human Kir2.1 channel von Fernandes, Carlos A H, Zuniga, Dania, Fagnen, Charline, Kugler, Valérie, Scala, Rosa, Péhau-Arnaudet, Gérard, Wagner, Renaud, Perahia, David, Bendahhou, Saïd, Vénien-Bryan, Catherine

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