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Ralf Hausmann

Showing results (21-30 of 45) with videos related to

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Life Sciences|November 3, 2022
Extracellular binding sites of positive and negative allosteric P2X4 receptor modulatorsStephanie Weinhausen, Jessica Nagel, Vigneshwaran Namasivayam, et al.
Toxicology and Applied Pharmacology|April 18, 2020
Mechanism underlying hooked resurgent-like tail currents induced by an insecticide in human cardiac Nav1.5Sarah Thull, Cristian Neacsu, Andrias O O'Reilly, et al.
Molecular Pharmacology|March 23, 2006
The suramin analog 4,4',4'',4'''-(carbonylbis(imino-5,1,3-benzenetriylbis (carbonylimino)))tetra-kis-benzenesulfonic acid (NF110) potently blocks P2X3 receptors: subtype selectivity is determined by location of sulfonic acid groupsRalf Hausmann, Jürgen Rettinger, Zoltan Gerevich, et al.
American Journal of Otolaryngology|May 23, 2002
Color duplex sonography in post-therapeutic neck evaluationErcole Di Martino, Gabriele A Krombach, Bernd Nowak, et al.
Neuropharmacology|July 18, 2015
Flexible subunit stoichiometry of functional human P2X2/3 heteromeric receptorsMaria Kowalski, Ralf Hausmann, Julia Schmid, et al.
Pflugers Archiv : European Journal of Physiology|August 13, 2018
Loss-of-function of Nav1.8/D1639N linked to human pain can be rescued by lidocaineLuisa Kaluza, Jannis E Meents, Martin Hampl, et al.
British Journal of Pharmacology|January 31, 2025
α-Adrenoreceptor blocker phentolamine inhibits voltage-gated sodium channels via the local anaesthetic binding siteIdil Toklucu, Vishal Sudha Bhagavath Eswaran, Raya Atlanta Bott, et al.
Journal of the American Heart Association|February 20, 2026
Incidence of Papaverine-Induced Ventricular ArrhythmiasSara Corradetti, Daniel Munhoz, Monika Kodeboina, et al.
Neuropharmacology|August 29, 2019
Identification of aurintricarboxylic acid as a potent allosteric antagonist of P2X1 and P2X3 receptorsAstrid S Obrecht, Nicole Urban, Michael Schaefer, et al.
Molecular Pharmacology|December 31, 2010
Molecular determinants of potent P2X2 antagonism identified by functional analysis, mutagenesis, and homology dockingChristian Wolf, Christiane Rosefort, Ghada Fallah, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Life Sciences|November 3, 2022
Extracellular binding sites of positive and negative allosteric P2X4 receptor modulatorsStephanie Weinhausen, Jessica Nagel, Vigneshwaran Namasivayam, et al.
Toxicology and Applied Pharmacology|April 18, 2020
Mechanism underlying hooked resurgent-like tail currents induced by an insecticide in human cardiac Nav1.5Sarah Thull, Cristian Neacsu, Andrias O O'Reilly, et al.
Molecular Pharmacology|March 23, 2006
The suramin analog 4,4',4'',4'''-(carbonylbis(imino-5,1,3-benzenetriylbis (carbonylimino)))tetra-kis-benzenesulfonic acid (NF110) potently blocks P2X3 receptors: subtype selectivity is determined by location of sulfonic acid groupsRalf Hausmann, Jürgen Rettinger, Zoltan Gerevich, et al.
American Journal of Otolaryngology|May 23, 2002
Color duplex sonography in post-therapeutic neck evaluationErcole Di Martino, Gabriele A Krombach, Bernd Nowak, et al.
Neuropharmacology|July 18, 2015
Flexible subunit stoichiometry of functional human P2X2/3 heteromeric receptorsMaria Kowalski, Ralf Hausmann, Julia Schmid, et al.
Pflugers Archiv : European Journal of Physiology|August 13, 2018
Loss-of-function of Nav1.8/D1639N linked to human pain can be rescued by lidocaineLuisa Kaluza, Jannis E Meents, Martin Hampl, et al.
British Journal of Pharmacology|January 31, 2025
α-Adrenoreceptor blocker phentolamine inhibits voltage-gated sodium channels via the local anaesthetic binding siteIdil Toklucu, Vishal Sudha Bhagavath Eswaran, Raya Atlanta Bott, et al.
Journal of the American Heart Association|February 20, 2026
Incidence of Papaverine-Induced Ventricular ArrhythmiasSara Corradetti, Daniel Munhoz, Monika Kodeboina, et al.
Neuropharmacology|August 29, 2019
Identification of aurintricarboxylic acid as a potent allosteric antagonist of P2X1 and P2X3 receptorsAstrid S Obrecht, Nicole Urban, Michael Schaefer, et al.
Molecular Pharmacology|December 31, 2010
Molecular determinants of potent P2X2 antagonism identified by functional analysis, mutagenesis, and homology dockingChristian Wolf, Christiane Rosefort, Ghada Fallah, et al.
Pageof 5