Nadja T. Hofer

β2-subunit alternative splicing stabilizes Cav2.3 Ca2+ channel activity during continuous midbrain dopamine neuron-like activity

B. Liss, P. Kloppenburg, T. Schneider, 2022, eLife.

Impaired chromaffin cell excitability and exocytosis in autistic Timothy syndrome TS2‐neo mouse rescued by L‐type calcium channel blockers

G. Bett, M. Sassoè-Pognetto, G. Obermair, 2019, The Journal of physiology.

Stabilization of negative activation voltages of Cav1.3 L-Type Ca2+-channels by alternative splicing

G. Obermair, Yuliia V Nikonishyna, Alexandra Pinggera, 2020, Channels.

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

B. Flucher, K. Liedl, Yuliia V Nikonishyna, 2020, Molecular Autism.

RBP2 stabilizes slow Cav1.3 Ca2+ channel inactivation properties of cochlear inner hair cells

G. Obermair, J. Engel, Alexandra Pinggera, 2019, Pflügers Archiv - European Journal of Physiology.

Alternative splicing of auxiliary β2-subunits stabilizes Cav2.3 Ca2+ channel activity in continuously active midbrain dopamine neurons

B. Liss, P. Kloppenburg, T. Schneider, 2021, bioRxiv.

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

N. Stefanova, A. Sah, N. Singewald, 2023, JCI insight.