Stabilization of negative activation voltages of Cav1.3 L-Type Ca(2+)-channels by alternative splicing

por Hofer, Nadja T., Pinggera, Alexandra, Nikonishyna, Yuliia V., Tuluc, Petronel, Fritz, Eva M., Obermair, Gerald J., Striessnig, Jörg
Publicado 2020

Biophysical classification of a CACNA1D de novo mutation as a high-risk mutation for a severe neurodevelopmental disorder

por Hofer, Nadja T., Tuluc, Petronel, Ortner, Nadine J., Nikonishyna, Yuliia V., Fernándes-Quintero, Monica L., Liedl, Klaus R., Flucher, Bernhard E., Cox, Helen, Striessnig, Jörg
Publicado 2020

RBP2 stabilizes slow Cav1.3 Ca(2+) channel inactivation properties of cochlear inner hair cells

por Ortner, Nadine J., Pinggera, Alexandra, Hofer, Nadja T., Siller, Anita, Brandt, Niels, Raffeiner, Andrea, Vilusic, Kristina, Lang, Isabelle, Blum, Kerstin, Obermair, Gerald J., Stefan, Eduard, Engel, Jutta, Striessnig, Jörg
Publicado 2019

β2-subunit alternative splicing stabilizes Cav2.3 Ca(2+) channel activity during continuous midbrain dopamine neuron-like activity

por Siller, Anita, Hofer, Nadja T, Tomagra, Giulia, Burkert, Nicole, Hess, Simon, Benkert, Julia, Gaifullina, Aisylu, Spaich, Desiree, Duda, Johanna, Poetschke, Christina, Vilusic, Kristina, Fritz, Eva Maria, Schneider, Toni, Kloppenburg, Peter, Liss, Birgit, Carabelli, Valentina, Carbone, Emilio, Ortner, Nadine Jasmin, Striessnig, Jörg
Publicado 2022

The human channel gating–modifying A749G CACNA1D (Cav1.3) variant induces a neurodevelopmental syndrome–like phenotype in mice

por Ortner, Nadine J., Sah, Anupam, Paradiso, Enrica, Shin, Josef, Stojanovic, Strahinja, Hammer, Niklas, Haritonova, Maria, Hofer, Nadja T., Marcantoni, Andrea, Guarina, Laura, Tuluc, Petronel, Theiner, Tamara, Pitterl, Florian, Ebner, Karl, Oberacher, Herbert, Carbone, Emilio, Stefanova, Nadia, Ferraguti, Francesco, Singewald, Nicolas, Roeper, Jochen, Striessnig, Jörg
Publicado 2023