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Saïd Bendahhou

Institut de Pharmacologie Moléculaire et Cellulaire


Université de Nice Sophia Antipolis



Name/email consistency: high



  • Institut de Pharmacologie Moléculaire et Cellulaire, UMR 6097 CNRS, Université de Nice Sophia Antipolis, France. 2005 - 2007
  • Université de Nice Sophia Antipolis, UMR 6097 CNRS, Institut de Pharmacologie Moléculaire et Cellulaire, 660 Route des Lucioles, France. 2005
  • Department of Human Molecular Biology and Genetics, University of Utah, Salt Lake City, Utah 84112, USA. 2003


  1. 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) [Pubmed]
  2. 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) [Pubmed]
  3. 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) [Pubmed]
  4. 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) [Pubmed]
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