Keeping hyperactive voltage-gated sodium channels in silent mode

由 Bendahhou, Saïd
出版 2012

Skeletal Muscle Na(+) Channel Disorders

由 Simkin, Dina, Bendahhou, Saïd
出版 2011

Characterization of a new sodium channel mutation at arginine 1448 associated with moderate paramyotonia congenita in humans

由 Bendahhou, Saïd, Cummins, Theodore R, Kwiecinski, Hubert, Waxman, Stephen G, Ptácek, Louis J
出版 1999

Activation and Inactivation of the Voltage-Gated Sodium Channel: Role of Segment S5 Revealed by a Novel Hyperkalaemic Periodic Paralysis Mutation

由 Bendahhou, Saïd, Cummins, Theodore R., Tawil, Rabi, Waxman, Stephen G., Ptácek, Louis J.
發表在 J Neurosci (1999)

First Evidence of Kv3.1b Potassium Channel Subtype Expression during Neuronal Serotonergic 1C11 Cell Line Development

由 Tabka, Hager, Cheikh, Amani, Maatoug, Sonia, Ayeb, Mohamed El, Bendahhou, Saïd, Benkhalifa, Rym
發表在 Int J Mol Sci (2020)

Mechanisms underlying a life-threatening skeletal muscle Na(+) channel disorder

由 Simkin, Dina, Léna, Isabelle, Landrieu, Pierre, Lion-François, Laurence, Sternberg, Damien, Fontaine, Bertrand, Bendahhou, Saïd
出版 2011

A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivation

由 Bendahhou, Saïd, Cummins, Theodore R., Hahn, Angelika F., Langlois, Sylvie, Waxman, Stephen G., Ptácek, Louis J.
出版 2000

ARF6-dependent interaction of the TWIK1 K(+) channel with EFA6, a GDP/GTP exchange factor for ARF6

由 Decressac, Sonia, Franco, Michel, Bendahhou, Said, Warth, Richard, Knauer, Sebastian, Barhanin, Jacques, Lazdunski, Michel, Lesage, Florian
出版 2004

Potassium Channel Silencing by Constitutive Endocytosis and Intracellular Sequestration

由 Feliciangeli, Sylvain, Tardy, Magalie P., Sandoz, Guillaume, Chatelain, Franck C., Warth, Richard, Barhanin, Jacques, Bendahhou, Saïd, Lesage, Florian
出版 2010

TWIK1, a unique background channel with variable ion selectivity

由 Chatelain, Franck C., Bichet, Delphine, Douguet, Dominique, Feliciangeli, Sylvain, Bendahhou, Saïd, Reichold, Markus, Warth, Richard, Barhanin, Jacques, Lesage, Florian
出版 2012

A204E mutation in Na(v)1.4 DIS3 exerts gain- and loss-of-function effects that lead to periodic paralysis combining hyper- with hypo-kalaemic signs

由 Kokunai, Yosuke, Dalle, Carine, Vicart, Savine, Sternberg, Damien, Pouliot, Valérie, Bendahhou, Said, Fournier, Emmanuel, Chahine, Mohamed, Fontaine, Bertrand, Nicole, Sophie
發表在 Sci Rep (2018)

Defining a Mutational Panel and Predicting the Prevalence of Cystic Fibrosis in Oman

由 Fass, Uwe W., Al-Salmani, Majid, Bendahhou, Said, Shivalingam, Ganji, Norrish, Catherine, Hebal, Kallesh, Clark, Fiona, Heming, Thomas, Al-Khusaiby, Saleh
出版 2014

Substitutions of the S4DIV R2 residue (R1451) in Na(V)1.4 lead to complex forms of paramyotonia congenita and periodic paralyses

由 Poulin, Hugo, Gosselin-Badaroudine, Pascal, Vicart, Savine, Habbout, Karima, Sternberg, Damien, Giuliano, Serena, Fontaine, Bertrand, Bendahhou, Saïd, Nicole, Sophie, Chahine, Mohamed
發表在 Sci Rep (2018)

In vivo and in vitro functional characterization of Andersen's syndrome mutations

由 Bendahhou, Saïd, Fournier, Emmanuel, Sternberg, Damien, Bassez, Guillaume, Furby, Alain, Sereni, Carole, Donaldson, Matthew R, Larroque, Marie-Madeleine, Fontaine, Bertrand, Barhanin, Jacques
出版 2005

New Structural insights into Kir channel gating from molecular simulations, HDX-MS and functional studies

由 Fagnen, Charline, Bannwarth, Ludovic, Oubella, Iman, Forest, Eric, De Zorzi, Rita, de Araujo, Aline, Mhoumadi, Yasmina, Bendahhou, Saïd, Perahia, David, Vénien-Bryan, Catherine
發表在 Sci Rep (2020)

Unexpected Gating Behaviour of an Engineered Potassium Channel Kir

由 Fagnen, Charline, Bannwarth, Ludovic, Zuniga, Dania, Oubella, Iman, De Zorzi, Rita, Forest, Eric, Scala, Rosa, Guilbault, Samuel, Bendahhou, Saïd, Perahia, David, Vénien-Bryan, Catherine
發表在 Front Mol Biosci (2021)

Proximal renal tubular acidosis in TASK2 K(+) channel-deficient mice reveals a mechanism for stabilizing bicarbonate transport

由 Warth, Richard, Barrière, Hervé, Meneton, Pierre, Bloch, May, Thomas, Jörg, Tauc, Michel, Heitzmann, Dirk, Romeo, Elisa, Verrey, François, Mengual, Raymond, Guy, Nicolas, Bendahhou, Saïd, Lesage, Florian, Poujeol, Philippe, Barhanin, Jacques
出版 2004

Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)

由 Tristani-Firouzi, Martin, Jensen, Judy L., Donaldson, Matthew R., Sansone, Valeria, Meola, Giovanni, Hahn, Angelika, Bendahhou, Said, Kwiecinski, Hubert, Fidzianska, Anna, Plaster, Nikki, Fu, Ying-Hui, Ptacek, Louis J., Tawil, Rabi
出版 2002

A recessive Na(v)1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis

由 Habbout, Karima, Poulin, Hugo, Rivier, François, Giuliano, Serena, Sternberg, Damien, Fontaine, Bertrand, Eymard, Bruno, Morales, Raul Juntas, Echenne, Bernard, King, Louise, Hanna, Michael G., Männikkö, Roope, Chahine, Mohamed, Nicole, Sophie, Bendahhou, Said
發表在 Neurology (2016)

Task2 potassium channels set central respiratory CO(2) and O(2) sensitivity

由 Gestreau, Christian, Heitzmann, Dirk, Thomas, Joerg, Dubreuil, Véronique, Bandulik, Sascha, Reichold, Markus, Bendahhou, Saïd, Pierson, Patricia, Sterner, Christina, Peyronnet-Roux, Julie, Benfriha, Chérif, Tegtmeier, Ines, Ehnes, Hannah, Georgieff, Michael, Lesage, Florian, Brunet, Jean-Francois, Goridis, Christo, Warth, Richard, Barhanin, Jacques
出版 2010