Nathalie Strutz-Seebohm
Affiliations: | 1998-2000 | Institute for Genetics of Cardiological Diseases | University Muenster |
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| Lübke M, Schreiber JA, Le Quoc T, et al. (2020) Rottlerin: Structure Modifications and KCNQ1/KCNE1 Ion Channel Activity. Chemmedchem |
| Bollmann E, Schreiber JA, Ritter N, et al. (2020) 4,4'-Diisothiocyanato-2,2'-Stilbenedisulfonic Acid (DIDS) Modulates the Activity of KCNQ1/KCNE1 Channels by an Interaction with the Central Pore Region. Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology. 54: 321-332 |
| Schreiber JA, Schepmann D, Frehland B, et al. (2019) A common mechanism allows selective targeting of GluN2B subunit-containing N-methyl-D-aspartate receptors. Communications Biology. 2: 420 |
| Schreiber JA, Schepmann D, Frehland B, et al. (2019) A common mechanism allows selective targeting of GluN2B subunit-containing -methyl-D-aspartate receptors. Communications Biology. 2: 420 |
| Peischard S, Ho HT, Theiss C, et al. (2019) A Kidnapping Story: How Coxsackievirus B3 and Its Host Cell Interact. Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology. 53: 121-140 |
| Amedonu E, Brenker C, Barman S, et al. (2019) An Assay to Determine Mechanisms of Rapid Autoantibody-Induced Neurotransmitter Receptor Endocytosis and Vesicular Trafficking in Autoimmune Encephalitis. Frontiers in Neurology. 10: 178 |
| Schreiber JA, Müller SL, Westphälinger SE, et al. (2018) Systematic variation of the benzoylhydrazine moiety of the GluN2A selective NMDA receptor antagonist TCN-201. European Journal of Medicinal Chemistry. 158: 259-269 |
| Möller M, Silbernagel N, Wrobel E, et al. (2018) In Vitro Analyses of Novel HCN4 Gene Mutations. Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology. 49: 1197-1207 |
| Dey S, Temme L, Schreiber JA, et al. (2017) Deconstruction - reconstruction approach to analyze the essential structural elements of tetrahydro-3-benzazepine-based antagonists of GluN2B subunit containing NMDA receptors. European Journal of Medicinal Chemistry. 138: 552-564 |
| Müller SL, Schreiber JA, Schepmann D, et al. (2017) Systematic variation of the benzenesulfonamide part of the GluN2A selective NMDA receptor antagonist TCN-201. European Journal of Medicinal Chemistry. 129: 124-134 |