Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (9) GO Terms (22) Nucleotides (65) Proteins (40) Interactants (84) Wiki
XB-GENEPAGE-6035797

Papers associated with glra1



???displayGene.coCitedPapers???

???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest Sort Oldest To Newest

Temporal and spatial transcriptomic dynamics across brain development in Xenopus laevis tadpoles., Ta AC, Huang LC, McKeown CR, Bestman JE, Van Keuren-Jensen K, Cline HT., G3 (Bethesda). January 4, 2022; 12 (1):               


In silico re-engineering of a neurotransmitter to activate KCNQ potassium channels in an isoform-specific manner., Manville RW, Abbott GW., Commun Biol. January 1, 2019; 2 401.                    


Inter- and Intra-Subunit Butanol/Isoflurane Sites of Action in the Human Glycine Receptor., McCracken ML, Gorini G, McCracken LM, Mayfield RD, Harris RA, Trudell JR., Front Mol Neurosci. February 15, 2016; 9 45.              


Mutation of a zinc-binding residue in the glycine receptor α1 subunit changes ethanol sensitivity in vitro and alcohol consumption in vivo., McCracken LM, Blednov YA, Trudell JR, Benavidez JM, Betz H, Harris RA., J Pharmacol Exp Ther. February 1, 2013; 344 (2): 489-500.


Activity-dependent neurotransmitter-receptor matching at the neuromuscular junction., Borodinsky LN, Spitzer NC., Proc Natl Acad Sci U S A. January 2, 2007; 104 (1): 335-40.                  


Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease., Rees MI, Harvey K, Pearce BR, Chung SK, Duguid IC, Thomas P, Beatty S, Graham GE, Armstrong L, Shiang R, Abbott KJ, Zuberi SM, Stephenson JB, Owen MJ, Tijssen MA, van den Maagdenberg AM, Smart TG, Supplisson S, Harvey RJ., Nat Genet. July 1, 2006; 38 (7): 801-6.


Functional characterization of compound heterozygosity for GlyRalpha1 mutations in the startle disease hyperekplexia., Rea R, Tijssen MA, Herd C, Frants RR, Kullmann DM., Eur J Neurosci. July 1, 2002; 16 (2): 186-96.


Comparison of glycine and GABA actions on the zebrafish homomeric glycine receptor., Fucile S, de Saint Jan D, David-Watine B, Korn H, Bregestovski P., J Physiol. June 1, 1999; 517 ( Pt 2) 369-83.


Isoform-selective deficit of glycine receptors in the mouse mutant spastic., Becker CM, Schmieden V, Tarroni P, Strasser U, Betz H., Neuron. February 1, 1992; 8 (2): 283-9.

???pagination.result.page??? 1