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Brain : a Journal of Neurology
|
June 24, 2020
Epilepsy-causing STX1B mutations translate altered protein functions into distinct phenotypes in mouse neurons
Gülçin Vardar, Fabian Gerth, Xiao Jakob Schmitt, et al.
Journal of Natural Products
|
May 15, 2026
Proteotoxic Stress Bioreporter Enables Mechanism-Informed Antibiotic Discovery
Julian Schubert, Christian Geibel, Anne Berscheid, et al.
Pflugers Archiv : European Journal of Physiology
|
May 2, 2013
Regulation of ClC-2 gating by intracellular ATP
Gabriel Stölting, Georgeta Teodorescu, Birgit Begemann, et al.
Analytical Chemistry
|
October 25, 2025
High-Frequency Microfluidic Fractionation for Compound-Resolved Bioactivity-Based Metabolomics
Christian Geibel, Julian Schubert, Simon B Knoblauch, et al.
Epilepsy Research
|
June 20, 2015
Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?
Felicitas Becker, Julian Schubert, Sarah Weckhuysen, et al.
Epilepsia
|
September 16, 2017
Alterations in the α<sub>2</sub> δ ligand, thrombospondin-1, in a rat model of spontaneous absence epilepsy and in patients with idiopathic/genetic generalized epilepsies
Ines Santolini, Roberta Celli, Milena Cannella, et al.
Brain : a Journal of Neurology
|
January 8, 2019
Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability
Yuanyuan Liu, Julian Schubert, Lukas Sonnenberg, et al.
Human Mutation
|
October 25, 2017
Gain-of-function HCN2 variants in genetic epilepsy
Melody Li, Snezana Maljevic, A Marie Phillips, et al.
Journal of Neurology
|
January 10, 2013
PRRT2-related disorders: further PKD and ICCA cases and review of the literature
Felicitas Becker, Julian Schubert, Pasquale Striano, et al.
Ebiomedicine
|
September 11, 2022
Loss-of-function variants in the KCNQ5 gene are implicated in genetic generalized epilepsies
Johanna Krüger, Julian Schubert, Josua Kegele, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 25) with videos related to
Sort By:
Page
of 3
Brain : a Journal of Neurology
|
June 24, 2020
Epilepsy-causing STX1B mutations translate altered protein functions into distinct phenotypes in mouse neurons
Gülçin Vardar, Fabian Gerth, Xiao Jakob Schmitt, et al.
Journal of Natural Products
|
May 15, 2026
Proteotoxic Stress Bioreporter Enables Mechanism-Informed Antibiotic Discovery
Julian Schubert, Christian Geibel, Anne Berscheid, et al.
Pflugers Archiv : European Journal of Physiology
|
May 2, 2013
Regulation of ClC-2 gating by intracellular ATP
Gabriel Stölting, Georgeta Teodorescu, Birgit Begemann, et al.
Analytical Chemistry
|
October 25, 2025
High-Frequency Microfluidic Fractionation for Compound-Resolved Bioactivity-Based Metabolomics
Christian Geibel, Julian Schubert, Simon B Knoblauch, et al.
Epilepsy Research
|
June 20, 2015
Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?
Felicitas Becker, Julian Schubert, Sarah Weckhuysen, et al.
Epilepsia
|
September 16, 2017
Alterations in the α<sub>2</sub> δ ligand, thrombospondin-1, in a rat model of spontaneous absence epilepsy and in patients with idiopathic/genetic generalized epilepsies
Ines Santolini, Roberta Celli, Milena Cannella, et al.
Brain : a Journal of Neurology
|
January 8, 2019
Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability
Yuanyuan Liu, Julian Schubert, Lukas Sonnenberg, et al.
Human Mutation
|
October 25, 2017
Gain-of-function HCN2 variants in genetic epilepsy
Melody Li, Snezana Maljevic, A Marie Phillips, et al.
Journal of Neurology
|
January 10, 2013
PRRT2-related disorders: further PKD and ICCA cases and review of the literature
Felicitas Becker, Julian Schubert, Pasquale Striano, et al.
Ebiomedicine
|
September 11, 2022
Loss-of-function variants in the KCNQ5 gene are implicated in genetic generalized epilepsies
Johanna Krüger, Julian Schubert, Josua Kegele, et al.
Page
of 3