Statistical coassembly of glycine receptor α1 wildtype and the hyperekplexia mutant α1(P250T) in HEK 293 cells: impaired channel function is not dominant in the recombinant system-Reference-Cited by-同舟云学术

Statistical coassembly of glycine receptor α1 wildtype and the hyperekplexia mutant α1(P250T) in HEK 293 cells: impaired channel function is not dominant in the recombinant system

Published:2002-10 Issue:1 Volume:331 Page:21-24
ISSN:0304-3940
Container-title:Neuroscience Letters
language:en
Short-container-title:Neuroscience Letters

Author:

Breitinger Hans-Georg,Becker Cord-Michael

Publisher

Elsevier BV

Subject

General Neuroscience

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4. Familial hyperekplexia: startle disease. Clinical, electrophysiological and genetic study of a family;Bernasconi;Rev. Neurol. (Paris),1996

5. Structure and functions of inhibitory and excitatory glycine receptors;Betz;Ann. N.Y. Acad. Sci.,1999

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1. Impaired Glycine Receptor Trafficking in Neurological Diseases;Frontiers in Molecular Neuroscience;2018-08-21

2. Synergistic Inhibition of Glycinergic Transmission In Vitro and In Vivo by Flavonoids and Strychnine;Toxicological Sciences;2010-08-18

3. Recessive hyperekplexia mutations of the glycine receptor α1 subunit affect cell surface integration and stability;Journal of Neurochemistry;2009-09-01

4. Occupancy of a Single Anesthetic Binding Pocket Is Sufficient to Enhance Glycine Receptor Function;Journal of Biological Chemistry;2006-02

5. Molecular Structure and Function of the Glycine Receptor Chloride Channel;Physiological Reviews;2004-10