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Guiscard Seebohm

Showing results (81-90 of 189) with videos related to

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Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|May 23, 2012
Overlapping cardiac phenotype associated with a familial mutation in the voltage sensor of the KCNQ1 channelUlrike Henrion, Sven Zumhagen, Katja Steinke, et al.
Toxicon : Official Journal of the International Society on Toxinology|May 9, 2015
Solid phase synthesis, NMR structure determination of α-KTx3.8, its in silico docking to Kv1.x potassium channels, and electrophysiological analysis provide insights into toxin-channel selectivityBastian Kohl, Ina Rothenberg, Syed Abid Ali, et al.
The Journal of Physiology|November 17, 2007
Neutralization of a negative charge in the S1-S2 region of the KV7.2 (KCNQ2) channel affects voltage-dependent activation in neonatal epilepsyThomas V Wuttke, Johann Penzien, Michael Fauler, et al.
Nature Communications|February 1, 2018
Cardiogenic programming of human pluripotent stem cells by dose-controlled activation of EOMESMartin J Pfeiffer, Roberto Quaranta, Ilaria Piccini, et al.
Scientific Reports|July 12, 2018
Bioelectric-calcineurin signaling module regulates allometric growth and size of the zebrafish finJacob M Daane, Jennifer Lanni, Ina Rothenberg, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 1, 2021
Selective Inhibition of <i>N</i>-Methyl-d-aspartate Receptors with GluN2B Subunit Protects <i>β</i> Cells against Stress-Induced Apoptotic Cell DeathAnne Gresch, Héctor Noguera Hurtado, Laura Wörmeyer, et al.
Archiv Der Pharmazie|July 31, 2022
Phenol-benzoxazolone bioisosteres of GluN2B-NMDA receptor antagonists: Unexpected rearrangement during reductive alkylation with phenylcyclohexanoneAlexander Markus, Julian A Schreiber, Gunnar Goerges, et al.
Biochemical and Biophysical Research Communications|December 15, 2011
Activation of voltage gated K⁺ channel Kv1.5 by β-cateninCarlos Munoz, Roberta H Tóvolli, Mentor Sopjani, et al.
European Journal of Medicinal Chemistry|September 16, 2018
Systematic variation of the benzoylhydrazine moiety of the GluN2A selective NMDA receptor antagonist TCN-201Julian A Schreiber, Sebastian L Müller, Stefanie E Westphälinger, et al.
Biological Chemistry|October 10, 2022
Chemical, pharmacodynamic and pharmacokinetic characterization of the GluN2B receptor antagonist 3-(4-phenylbutyl)-2,3,4,5-tetrahydro-1<i>H</i>-3-benzazepine-1,7-diol - starting point for PET tracer developmentMarvin Korff, Ruben Steigerwald, Elena Bechthold, et al.
Pageof 19

Showing results (81-90 of 189) with videos related to

Sort By:
Pageof 19
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|May 23, 2012
Overlapping cardiac phenotype associated with a familial mutation in the voltage sensor of the KCNQ1 channelUlrike Henrion, Sven Zumhagen, Katja Steinke, et al.
Toxicon : Official Journal of the International Society on Toxinology|May 9, 2015
Solid phase synthesis, NMR structure determination of α-KTx3.8, its in silico docking to Kv1.x potassium channels, and electrophysiological analysis provide insights into toxin-channel selectivityBastian Kohl, Ina Rothenberg, Syed Abid Ali, et al.
The Journal of Physiology|November 17, 2007
Neutralization of a negative charge in the S1-S2 region of the KV7.2 (KCNQ2) channel affects voltage-dependent activation in neonatal epilepsyThomas V Wuttke, Johann Penzien, Michael Fauler, et al.
Nature Communications|February 1, 2018
Cardiogenic programming of human pluripotent stem cells by dose-controlled activation of EOMESMartin J Pfeiffer, Roberto Quaranta, Ilaria Piccini, et al.
Scientific Reports|July 12, 2018
Bioelectric-calcineurin signaling module regulates allometric growth and size of the zebrafish finJacob M Daane, Jennifer Lanni, Ina Rothenberg, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 1, 2021
Selective Inhibition of <i>N</i>-Methyl-d-aspartate Receptors with GluN2B Subunit Protects <i>β</i> Cells against Stress-Induced Apoptotic Cell DeathAnne Gresch, Héctor Noguera Hurtado, Laura Wörmeyer, et al.
Archiv Der Pharmazie|July 31, 2022
Phenol-benzoxazolone bioisosteres of GluN2B-NMDA receptor antagonists: Unexpected rearrangement during reductive alkylation with phenylcyclohexanoneAlexander Markus, Julian A Schreiber, Gunnar Goerges, et al.
Biochemical and Biophysical Research Communications|December 15, 2011
Activation of voltage gated K⁺ channel Kv1.5 by β-cateninCarlos Munoz, Roberta H Tóvolli, Mentor Sopjani, et al.
European Journal of Medicinal Chemistry|September 16, 2018
Systematic variation of the benzoylhydrazine moiety of the GluN2A selective NMDA receptor antagonist TCN-201Julian A Schreiber, Sebastian L Müller, Stefanie E Westphälinger, et al.
Biological Chemistry|October 10, 2022
Chemical, pharmacodynamic and pharmacokinetic characterization of the GluN2B receptor antagonist 3-(4-phenylbutyl)-2,3,4,5-tetrahydro-1<i>H</i>-3-benzazepine-1,7-diol - starting point for PET tracer developmentMarvin Korff, Ruben Steigerwald, Elena Bechthold, et al.
Pageof 19