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BENDAHHOU , S.

Last name: BENDAHHOU

First name: S.

    Recent uploads

  • 2002 (v1)
    Journal article
    Metadata-only
    Impairment of slow inactivation as a common mechanism for periodic paralysis in DIIS4-S5
    Bendahhou, S. Cummins, T.R. Kula, R.W.

    No description

    Uploaded on: December 2, 2022
  • 2002 (v1)
    Journal article
    Metadata-only
    Impairment of slow inactivation as a common mechanism for periodic paralysis in DIIS4-S5
    Bendahhou, S. Cummins, T.R. Kula, R.W.

    No description

    Uploaded on: October 11, 2023
  • 2004 (v1)
    Journal article
    Metadata-only
    ARF6-dependent interaction of the TWIK1 K(+) channel with EFA6, a GDP/GTP exchange factor for ARF6.
    Decressac, S. Franco, M. Bendahhou, S.

    No description

    Uploaded on: October 11, 2023
  • 2004 (v1)
    Journal article
    Metadata-only
    ARF6-dependent interaction of the TWIK1 K(+) channel with EFA6, a GDP/GTP exchange factor for ARF6.
    Decressac, S. Franco, M. Bendahhou, S.

    No description

    Uploaded on: December 2, 2022
  • August 2014 (v1)
    Journal article
    Metadata-only
    Revisiting CFTR inhibition: a comparative study of CFTR inh -172 and GlyH-101 inhibitors
    Melis, N Tauc, M. Cougnon, M.

    International audience

    Uploaded on: December 4, 2022
  • 2003 (v1)
    Journal article
    Metadata-only
    Defective potassium channel Kir2.1 trafficking underlies andersen-tawil syndrome
    Bendahhou, S. Donaldson, M.R. Plaster, N.M.

    No description

    Uploaded on: October 11, 2023
  • 2003 (v1)
    Journal article
    Metadata-only
    Defective potassium channel Kir2.1 trafficking underlies andersen-tawil syndrome
    Bendahhou, S. Donaldson, M.R. Plaster, N.M.

    No description

    Uploaded on: December 3, 2022
  • 2005 (v1)
    Journal article
    Metadata-only
    In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart.
    Bendahhou, S. Marionneau, C. Haurogne, K.

    No description

    Uploaded on: December 3, 2022
  • April 3, 2012 (v1)
    Journal article
    Metadata-only
    TWIK1, a unique background channel with variable ion selectivity
    Chatelain, Franck Bichet, D. Douguet, D.

    International audience

    Uploaded on: December 3, 2022
  • April 3, 2012 (v1)
    Journal article
    Metadata-only
    TWIK1, a unique background channel with variable ion selectivity
    Chatelain, Franck Bichet, D. Douguet, D.

    International audience

    Uploaded on: February 22, 2023
  • 2005 (v1)
    Journal article
    Metadata-only
    In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart.
    Bendahhou, S. Marionneau, C. Haurogne, K.

    No description

    Uploaded on: October 11, 2023
  • April 3, 2012 (v1)
    Journal article
    Metadata-only
    TWIK1, a unique background channel with variable ion selectivity
    Chatelain, Franck Bichet, D. Douguet, D.

    TWIK1 belongs to the family of background K(+) channels with two pore domains. In native and transfected cells, TWIK1 is detected mainly in recycling endosomes. In principal cells in the kidney, TWIK1 gene inactivation leads to the loss of a nonselective cationic conductance, an unexpected effect that was attributed to adaptive regulation of...

    Uploaded on: December 3, 2022
  • 2005 (v1)
    Journal article
    Metadata-only
    In vivo and in vitro functional characterization of Andersen's syndrome mutations.
    Bendahhou, S. Fournier, E. Sternberg, D.

    No description

    Uploaded on: December 2, 2022
  • 2005 (v1)
    Journal article
    Metadata-only
    In vivo and in vitro functional characterization of Andersen's syndrome mutations.
    Bendahhou, S. Fournier, E. Sternberg, D.

    No description

    Uploaded on: October 11, 2023
  • 2003 (v1)
    Journal article
    Metadata-only
    PIP(2) binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome
    Donaldson, M.R. Jensen, J.L. Tristani-Firouzi, M.

    No description

    Uploaded on: October 11, 2023
  • 2003 (v1)
    Journal article
    Metadata-only
    PIP(2) binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome
    Donaldson, M.R. Jensen, J.L. Tristani-Firouzi, M.

    No description

    Uploaded on: December 2, 2022
  • 2002 (v1)
    Journal article
    Metadata-only
    Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)
    Tristani-Firouzi, M. Jensen, J.L. Donaldson, M.R.

    No description

    Uploaded on: October 11, 2023
  • 2002 (v1)
    Journal article
    Metadata-only
    Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)
    Tristani-Firouzi, M. Jensen, J.L. Donaldson, M.R.

    No description

    Uploaded on: December 3, 2022
  • 2004 (v1)
    Journal article
    Metadata-only
    Proximal renal tubular acidosis in TASK2 K+ channel-deficient mice reveals a mechanism for stabilizing bicarbonate transport.
    Warth, R. Barriere, H. Meneton, P.

    No description

    Uploaded on: December 2, 2022
  • 2004 (v1)
    Journal article
    Metadata-only
    Proximal renal tubular acidosis in TASK2 K+ channel-deficient mice reveals a mechanism for stabilizing bicarbonate transport
    Warth, R. Barriere, H. Meneton, P.

    No description

    Uploaded on: December 3, 2022

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