Saïd Bendahhou
Institut de Pharmacologie Moléculaire et Cellulaire
UMR 6097 CNRS
Université de Nice Sophia Antipolis
France
Name/email consistency: high
- Corticosteroid-exacerbated symptoms in an Andersen's syndrome kindred. Bendahhou, S., Fournier, E., Gallet, S., Ménard, D., Larroque, M.M., Barhanin, J. Hum. Mol. Genet. (2007)
- In vivo and in vitro functional characterization of Andersen's syndrome mutations. Bendahhou, S., Fournier, E., Sternberg, D., Bassez, G., Furby, A., Sereni, C., Donaldson, M.R., Larroque, M.M., Fontaine, B., Barhanin, J. J. Physiol. (Lond.) (2005)
- In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart. Bendahhou, S., Marionneau, C., Haurogne, K., Larroque, M.M., Derand, R., Szuts, V., Escande, D., Demolombe, S., Barhanin, J. Cardiovasc. Res. (2005)
- Defective potassium channel Kir2.1 trafficking underlies Andersen-Tawil syndrome. Bendahhou, S., Donaldson, M.R., Plaster, N.M., Tristani-Firouzi, M., Fu, Y.H., Ptácek, L.J. J. Biol. Chem. (2003)