Structural features of phenol derivatives determining potency for activation of chloride currents via α 1 homomeric and α 1 β heteromeric glycine receptors
Author:
Publisher
Wiley
Subject
Pharmacology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1038/sj.bjp.0706254/fullpdf
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3. Interaction of positive allosteric modulators with human and Drosophila recombinant GABA receptors expressed in Xenopus laevis oocytes;BELELLI;Br. J. Pharmacol.,1996
4. A single glycine residue at the entrance of the first membrane-spanning domain of the γ-aminobutyric acid type A receptor β2 subunit affects allosteric sensitivity to GABA and anesthetics;CARLSON;Mol. Pharmacol.,2000
5. The actions of propofol on γ-aminobutyric acid-A and glycine receptors in acutely dissociated spinal dorsal horn neurons of the rat;DONG;Anesth. Analg.,2002
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3. Activation and modulation of recombinant glycine and GABAAreceptors by 4-halogenated analogues of propofol;British Journal of Pharmacology;2016-09-06
4. Employment of 4-(1,2,4-triazol-1-yl)phenol as a signal enhancer of the chemiluminescent luminol-H2O2-horseradish peroxidase reaction for detection of hepatitis C virus in real samples;Luminescence;2015-03-25
5. 4-Chloropropofol enhances chloride currents in human hyperekplexic and artificial mutated glycine receptors;BMC Neurology;2012-09-24
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