Betz H - Search Results

1

The N-terminal domain of the GluN3A subunit determines the efficacy of glycine-activated NMDA receptors.

Mesic I, Madry C, Geider K, Bernhard M, Betz H, Laube B. Mesic I, et al. Among authors: betz h. Neuropharmacology. 2016 Jun;105:133-141. doi: 10.1016/j.neuropharm.2016.01.014. Epub 2016 Jan 9. Neuropharmacology. 2016. PMID: 26777280

2

Glycine receptors: recent insights into their structural organization and functional diversity.

Betz H, Laube B. Betz H, et al. J Neurochem. 2006 Jun;97(6):1600-10. doi: 10.1111/j.1471-4159.2006.03908.x. J Neurochem. 2006. PMID: 16805771 Free article. Review.

3

Principal role of NR3 subunits in NR1/NR3 excitatory glycine receptor function.

Madry C, Mesic I, Bartholomäus I, Nicke A, Betz H, Laube B. Madry C, et al. Among authors: betz h. Biochem Biophys Res Commun. 2007 Mar 2;354(1):102-8. doi: 10.1016/j.bbrc.2006.12.153. Epub 2006 Dec 28. Biochem Biophys Res Commun. 2007. PMID: 17214961

4

The N-terminal domains of both NR1 and NR2 subunits determine allosteric Zn2+ inhibition and glycine affinity of N-methyl-D-aspartate receptors.

Madry C, Mesic I, Betz H, Laube B. Madry C, et al. Among authors: betz h. Mol Pharmacol. 2007 Dec;72(6):1535-44. doi: 10.1124/mol.107.040071. Epub 2007 Sep 18. Mol Pharmacol. 2007. PMID: 17878266

5

Supralinear potentiation of NR1/NR3A excitatory glycine receptors by Zn2+ and NR1 antagonist.

Madry C, Betz H, Geiger JR, Laube B. Madry C, et al. Among authors: betz h. Proc Natl Acad Sci U S A. 2008 Aug 26;105(34):12563-8. doi: 10.1073/pnas.0805624105. Epub 2008 Aug 18. Proc Natl Acad Sci U S A. 2008. PMID: 18711142 Free PMC article.

6

Binding-site mutations in the alpha1 subunit of the inhibitory glycine receptor convert the inhibitory metal ion Cu2+ into a positive modulator.

Schumann T, Grudzinska J, Kuzmin D, Betz H, Laube B. Schumann T, et al. Among authors: betz h. Neuropharmacology. 2009 Jan;56(1):310-7. doi: 10.1016/j.neuropharm.2008.08.024. Epub 2008 Aug 28. Neuropharmacology. 2009. PMID: 18793654

7

Probing the pharmacological properties of distinct subunit interfaces within heteromeric glycine receptors reveals a functional ββ agonist-binding site.

Dutertre S, Drwal M, Laube B, Betz H. Dutertre S, et al. Among authors: betz h. J Neurochem. 2012 Jul;122(1):38-47. doi: 10.1111/j.1471-4159.2012.07755.x. Epub 2012 Apr 27. J Neurochem. 2012. PMID: 22486198 Free article.

8

Molecular determinants of ligand discrimination in the glutamate-binding pocket of the NMDA receptor.

Laube B, Schemm R, Betz H. Laube B, et al. Among authors: betz h. Neuropharmacology. 2004 Dec;47(7):994-1007. doi: 10.1016/j.neuropharm.2004.07.041. Neuropharmacology. 2004. PMID: 15555634

9

The beta subunit increases the ginkgolide B sensitivity of inhibitory glycine receptors.

Kondratskaya EL, Betz H, Krishtal OA, Laube B. Kondratskaya EL, et al. Among authors: betz h. Neuropharmacology. 2005 Nov;49(6):945-51. doi: 10.1016/j.neuropharm.2005.07.001. Epub 2005 Aug 24. Neuropharmacology. 2005. PMID: 16125206

10

Evidence for a tetrameric structure of recombinant NMDA receptors.

Laube B, Kuhse J, Betz H. Laube B, et al. Among authors: betz h. J Neurosci. 1998 Apr 15;18(8):2954-61. doi: 10.1523/JNEUROSCI.18-08-02954.1998. J Neurosci. 1998. PMID: 9526012 Free PMC article.

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