Gain-of-function mutation in TASK-4 channels and severe cardiac conduction disorder

por Friedrich, Corinna, Rinné, Susanne, Zumhagen, Sven, Kiper, Aytug K, Silbernagel, Nicole, Netter, Michael F, Stallmeyer, Birgit, Schulze-Bahr, Eric, Decher, Niels
Publicado 2014

Functional mutagenesis screens reveal the ‘cap structure’ formation in disulfide-bridge free TASK channels

por Goldstein, Matthias, Rinné, Susanne, Kiper, Aytug K., Ramírez, David, Netter, Michael F., Bustos, Daniel, Ortiz-Bonnin, Beatriz, González, Wendy, Decher, Niels
Publicado 2016

An N-terminal deletion variant of HCN1 in the epileptic WAG/Rij strain modulates HCN current densities

por Wemhöner, Konstantin, Kanyshkova, Tatyana, Silbernagel, Nicole, Fernandez-Orth, Juncal, Bittner, Stefan, Kiper, Aytug K., Rinné, Susanne, Netter, Michael F., Meuth, Sven G., Budde, Thomas, Decher, Niels
Publicado 2015

Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy

por Rinné, Susanne, Stallmeyer, Birgit, Pinggera, Alexandra, Netter, Michael F., Matschke, Lina A., Dittmann, Sven, Kirchhefer, Uwe, Neudorf, Ulrich, Opp, Joachim, Striessnig, Jörg, Decher, Niels, Schulze-Bahr, Eric
Publicado 2022

The molecular basis for an allosteric inhibition of K(+)-flux gating in K(2P) channels

por Rinné, Susanne, Kiper, Aytug K, Vowinkel, Kirsty S, Ramírez, David, Schewe, Marcus, Bedoya, Mauricio, Aser, Diana, Gensler, Isabella, Netter, Michael F, Stansfeld, Phillip J, Baukrowitz, Thomas, Gonzalez, Wendy, Decher, Niels
Publicado 2019

A Specific Two-pore Domain Potassium Channel Blocker Defines the Structure of the TASK-1 Open Pore

por Streit, Anne K., Netter, Michael F., Kempf, Franca, Walecki, Magdalena, Rinné, Susanne, Bollepalli, Murali K., Preisig-Müller, Regina, Renigunta, Vijay, Daut, Jürgen, Baukrowitz, Thomas, Sansom, Mark S. P., Stansfeld, Phillip J., Decher, Niels
Publicado 2011