Hasil Pencarian - Michael F. Netter

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  1. 1
    Gain‐of‐function mutation in TASK‐4 channels and severe cardiac conduction disorder

    Gain‐of‐function mutation in TASK‐4 channels and severe cardiac conduction disorder oleh Corinna Friedrich, Susanne Rinné, Sven Zumhagen, Aytug K Kiper, Nicole Silbernagel, Michael F Netter, Birgit Stallmeyer, Eric Schulze‐Bahr, Niels Decher

    Diterbitkan 2014-06-01
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  2. 2
    Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene <i>CACNA1D</i> Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy

    Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene <i>CACNA1D</i> Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy oleh Susanne Rinné, Birgit Stallmeyer, Alexandra Pinggera, Michael F. Netter, Lina A. Matschke, Sven Dittmann, Uwe Kirchhefer, Ulrich Neudorf, Joachim Opp, Jörg Striessnig, Niels Decher, Eric Schulze-Bahr

    Diterbitkan 2022-11-01
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  3. 3
    The molecular basis for an allosteric inhibition of K+-flux gating in K2P channels

    The molecular basis for an allosteric inhibition of K+-flux gating in K2P channels oleh Susanne Rinné, Aytug K Kiper, Kirsty S Vowinkel, David Ramírez, Marcus Schewe, Mauricio Bedoya, Diana Aser, Isabella Gensler, Michael F Netter, Phillip J Stansfeld, Thomas Baukrowitz, Wendy Gonzalez, Niels Decher

    Diterbitkan 2019-02-01
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  4. 4
    An N-terminal deletion variant of HCN1 in the epileptic WAG/Rij strain modulates HCN current densities

    An N-terminal deletion variant of HCN1 in the epileptic WAG/Rij strain modulates HCN current densities oleh Konstantin eWemhöner, Tatyana eKanyshkova, Nicole eSilbernagel, Juncal eFernandez-Orth, Stefan eBittner, Aytug K Kiper, Susanne eRinné, Michael F Netter, Sven G Meuth, Thomas eBudde, Niels eDecher

    Diterbitkan 2015-11-01
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