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132 in total

1. Characterization of the binding of two novel glycine site antagonists to cloned NMDA receptors: evidence for two pharmacological classes of antagonists.

Authors: B Chopra; P L Chazot; F A Stephenson
Journal: Br J Pharmacol Date: 2000-05 Impact factor: 8.739

2. Selective mGluR1 antagonist EMQMCM inhibits the kainate-induced excitotoxicity in primary neuronal cultures and in the rat hippocampus.

Authors: Maria Śmiałowska; Krystyna Gołembiowska; Małgorzata Kajta; Barbara Zięba; Anna Dziubina; Helena Domin
Journal: Neurotox Res Date: 2011-12-06 Impact factor: 3.911

3. The ability of new non-competitive glutamate receptor blockers to weaken motor disorders in animals.

Authors: N I Rukoyatkina; L V Gorbunova; V E Gmiro; N Ya Lukomskaya
Journal: Neurosci Behav Physiol Date: 2003-03

4. Involvement of NMDA receptor in the modulation of excitatory and inhibitory amino acid neurotransmitters release in cortical neurons.

Authors: E López; J Hernandez; C Arce; S Cañadas; M J Oset-Gasque; M P González
Journal: Neurochem Res Date: 2010-06-12 Impact factor: 3.996

5. Stacking interaction and its role in kynurenic acid binding to glutamate ionotropic receptors.

Authors: Alexander V Zhuravlev; Gennady A Zakharov; Boris F Shchegolev; Elena V Savvateeva-Popova
Journal: J Mol Model Date: 2011-08-12 Impact factor: 1.810

6. Alterations in brain extracellular dopamine and glycine levels following combined administration of the glycine transporter type-1 inhibitor Org-24461 and risperidone.

Authors: Katalin Nagy; Bernadett Marko; Gabriella Zsilla; Peter Matyus; Katalin Pallagi; Geza Szabo; Zsolt Juranyi; Jozsef Barkoczy; Gyorgy Levay; Laszlo G Harsing
Journal: Neurochem Res Date: 2010-08-20 Impact factor: 3.996

10. Modulators of the glycine site on NMDA receptors, D-serine and ALX 5407, display similar beneficial effects to clozapine in mouse models of schizophrenia.

Authors: Tatiana Lipina; Viviane Labrie; Ina Weiner; John Roder
Journal: Psychopharmacology (Berl) Date: 2005-03-10 Impact factor: 4.530

Glycine and N-methyl-D-aspartate receptors: physiological significance and possible therapeutic applications.