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Molecular Pharmacology|August 11, 2011
The pharmacological profile of brain liver intestine Na+ channel: inhibition by diarylamidines and activation by fenamatesDominik Wiemuth, Stefan GründerThe Journal of Biological Chemistry|July 27, 2010
A single amino acid tunes Ca2+ inhibition of brain liver intestine Na+ channel (BLINaC)Dominik Wiemuth, Stefan GründerChannels (Austin, Tex.)|December 25, 2013
The bile acid-sensitive ion channel (BASIC), the ignored cousin of ASICs and ENaCDominik Wiemuth, Marc Assmann, Stefan GründerPflugers Archiv : European Journal of Physiology|October 25, 2018
Comparative electrophysiological analysis of the bile acid-sensitive ion channel (BASIC) from different species suggests similar physiological functionsPia Lenzig, Monika Wirtz, Dominik WiemuthBiomolecules|April 30, 2021
The Neuropeptide Nocistatin Is Not a Direct Agonist of Acid-Sensing Ion Channel 1a (ASIC1a)Sven Kuspiel, Dominik Wiemuth, Stefan GründerNeuropharmacology|May 28, 2026
Thyroid hormones are positive allosteric modulators of acid-sensing ion channels ASIC1a and ASIC3Lu Qin, Dominik Wiemuth, Stefan GründerScientific Reports|December 22, 2018
Screening of 109 neuropeptides on ASICs reveals no direct agonists and dynorphin A, YFMRFamide and endomorphin-1 as modulatorsAnna Vyvers, Axel Schmidt, Dominik Wiemuth, et al.Pflugers Archiv : European Journal of Physiology|September 22, 2021
The bile acid-sensitive ion channel (BASIC) mediates bile acid-dependent currents in bile duct epithelial cellsShari Wiegreffe, Daniel Löhrer, Monika Wirtz, et al.The Biochemical Journal|March 27, 2007
Epithelial sodium channel (ENaC) is multi-ubiquitinated at the cell surfaceDominik Wiemuth, Ying Ke, Meino Rohlfs, et al.Purinergic Signalling|May 18, 2019
Bile acids are potent inhibitors of rat P2X2 receptorsAxel Schmidt, Sylvia Joussen, Ralf Hausmann, et al.Pageof 3