Inhibition by folded isomers of L-2-(carboxycyclopropyl) glycine of glutamate uptake via the human glutamate transporter hGluT-1
- 28 April 1995
- journal article
- research article
- Published by Elsevier in European Journal of Pharmacology: Molecular Pharmacology
- Vol. 289 (2) , 387-390
- https://doi.org/10.1016/0922-4106(95)90118-3
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Cloning and Expression of a Human Glutamate TransporterBiochemical and Biophysical Research Communications, 1994
- Pharmacological characterization of a cloned rat glutamate transporter (GluT-1)Molecular Brain Research, 1994
- (2S,3S,4R)-2-(Carboxycyclopropyl)glycine, a potent and competitive inhibitor of both glial and neuronal uptake of glutamateNeuropharmacology, 1993
- Expression cloning of a rat glutamate transporterNeuroscience Research, 1993
- Subtypes of Sodium‐Dependent High‐Affinity L‐[3H]Glutamate Transport Activity: Pharmacologic Specificity and Regulation by Sodium and PotassiumJournal of Neurochemistry, 1993
- Cloning and expression of a rat brain L-glutamate transporterNature, 1992
- Primary structure and functional characterization of a high-affinity glutamate transporterNature, 1992
- Agonist analysis of 2‐(carboxycyclopropyl)glycine isomers for cloned metabotropic glutamate receptor subtypes expressed in Chinese hamster ovary cellsBritish Journal of Pharmacology, 1992
- 2-(carboxycyclopropyl)glycines: binding, neurotoxicity and induction of intracellular free Ca2+ increaseEuropean Journal of Pharmacology, 1992
- Potent NMDA‐like actions and potentiation of glutamate responses by conformational variants of a glutamate analogue in the rat spinal cordBritish Journal of Pharmacology, 1989