Christiane K. Bauer
Hamburg, HH 20246, Germany
Last Updated: 09/26/2026
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Found 15 publications
KCNH3 Loss-of-Function Variant Associated with Epilepsy and Neurodevelopmental Delay Enhances Kv12.2 Channel Inactivation.
Journal: International journal of molecular sciences
Published: April 10, 2025
Loss-of-function variant in KCNH3 is associated with global developmental delay, autistic behavior, insomnia, and nocturnal seizures.
Journal: Seizure
Published: January 10, 2025
Clinically Relevant KCNQ1 Variants Causing KCNQ1-KCNE2 Gain-of-Function Affect the Ca2+ Sensitivity of the Channel.
Journal: International journal of molecular sciences
Published: July 28, 2022
Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca2+-Activated K+ Channel SK3 Cause Zimmermann-Laband Syndrome.
Journal: American journal of human genetics
Published: February 12, 2019
Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome.
Journal: American journal of human genetics
Published: July 06, 2018
Ether-à-go-go K+ channels: effective modulators of neuronal excitability.
Journal: The Journal of physiology
Published: October 26, 2017
Effects of Temperature on Heteromeric Kv11.1a/1b and Kv11.3 Channels.
Journal: Biophysical journal
Published: February 16, 2016
Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome.
Journal: Nature genetics
Published: October 29, 2014
Easy method to examine single nerve fiber excitability and conduction parameters using intact nonanesthetized earthworms.
Journal: Advances in physiology education
Published: September 03, 2014
"Alcohol and nicotine"--Concept and evaluation of an interdisciplinary elective course with OSPE in preclinical medical education.
Journal: GMS Zeitschrift fur medizinische Ausbildung
Published: June 14, 2013
Effects of the small molecule HERG activator NS1643 on Kv11.3 channels.
Journal: PloS one
Published: September 22, 2012
Last Updated: 09/26/2026