Papers associated with brain (and slc1a3)

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	Leucine 434 is essential for docosahexaenoic acid-induced augmentation of L-glutamate transporter current., Takahashi K., J Biol Chem. January 1, 2023; 299 (1): 102793.
	A Focal Impact Model of Traumatic Brain Injury in Xenopus Tadpoles Reveals Behavioral Alterations, Neuroinflammation, and an Astroglial Response., Spruiell Eldridge SL., Int J Mol Sci. July 8, 2022; 23 (14):
	Trafficking of the glutamate transporter is impaired in LRRK2-related Parkinson's disease., Iovino L., Acta Neuropathol. July 1, 2022; 144 (1): 81-106.
	Transport rate of EAAT2 is regulated by amino acid located at the interface between the scaffolding and substrate transport domains., Duffield M., Neurochem Int. October 1, 2020; 139 104792.
	Nervous NDRGs: the N-myc downstream-regulated gene family in the central and peripheral nervous system., Schonkeren SL., Neurogenetics. October 1, 2019; 20 (4): 173-186.
	Heterogeneity of the astrocytic AMPA-receptor transcriptome., Mölders A., Glia. December 1, 2018; 66 (12): 2604-2616.
	Photoswitchable Inhibitor of a Glutamate Transporter., Cheng B., ACS Chem Neurosci. August 16, 2017; 8 (8): 1668-1672.
	Up-Regulation of Excitatory Amino Acid Transporters EAAT1 and EAAT2 by ß-Klotho., Warsi J., Neurosignals. January 1, 2015; 23 (1): 59-70.
	Differential regulation of the glutamate transporters GLT-1 and GLAST by GSK3β., Jiménez E., Neurochem Int. December 1, 2014; 79 33-43.
	Inhibition of dopamine transporter activity by G protein βγ subunits., Garcia-Olivares J., PLoS One. January 1, 2013; 8 (3): e59788.
	Elevated ammonium levels: differential acute effects on three glutamate transporter isoforms., Søgaard R., Am J Physiol Cell Physiol. March 15, 2012; 302 (6): C880-91.
	Hetero-oligomerization of neuronal glutamate transporters., Nothmann D., J Biol Chem. February 4, 2011; 286 (5): 3935-43.
	Specificity and actions of an arylaspartate inhibitor of glutamate transport at the Schaffer collateral-CA1 pyramidal cell synapse., Sun W., PLoS One. January 1, 2011; 6 (8): e23765.
	The position of an arginine residue influences substrate affinity and K+ coupling in the human glutamate transporter, EAAT1., Ryan RM., J Neurochem. July 1, 2010; 114 (2): 565-75.
	TWIK-1 and TREK-1 are potassium channels contributing significantly to astrocyte passive conductance in rat hippocampal slices., Zhou M., J Neurosci. July 1, 2009; 29 (26): 8551-64.
	Mutations in transmembrane domains 5 and 7 of the human excitatory amino acid transporter 1 affect the substrate-activated anion channel., Huang S., Biochemistry. August 28, 2007; 46 (34): 9685-92.
	Characterization of novel aryl-ether, biaryl, and fluorene aspartic acid and diaminopropionic acid analogs as potent inhibitors of the high-affinity glutamate transporter EAAT2., Dunlop J., Mol Pharmacol. October 1, 2005; 68 (4): 974-82.
	The chloride permeation pathway of a glutamate transporter and its proximity to the glutamate translocation pathway., Ryan RM., J Biol Chem. May 14, 2004; 279 (20): 20742-51.
	WAY-855 (3-amino-tricyclo[2.2.1.02.6]heptane-1,3-dicarboxylic acid): a novel, EAAT2-preferring, nonsubstrate inhibitor of high-affinity glutamate uptake., Dunlop J., Br J Pharmacol. November 1, 2003; 140 (5): 839-46.
	Cloning and characterization of excitatory amino acid transporters GLT-1 and EAAC1 in canine brain., Sato K., J Vet Med Sci. September 1, 2001; 63 (9): 997-1002.
	Pharmacological characterization of threo-3-methylglutamic acid with excitatory amino acid transporters in native and recombinant systems., Eliasof S., J Neurochem. April 1, 2001; 77 (2): 550-7.
	Differentiation of substrate and nonsubstrate inhibitors of the high-affinity, sodium-dependent glutamate transporters., Koch HP., Mol Pharmacol. December 1, 1999; 56 (6): 1095-104.
	Molecular basis for differential inhibition of glutamate transporter subtypes by zinc ions., Vandenberg RJ., Mol Pharmacol. July 1, 1998; 54 (1): 189-96.
	New beta-hydroxyaspartate derivatives are competitive blockers for the bovine glutamate/aspartate transporter., Lebrun B., J Biol Chem. August 15, 1997; 272 (33): 20336-9.
	Inhibition of the high-affinity brain glutamate transporter GLAST-1 via direct phosphorylation., Conradt M., J Neurochem. March 1, 1997; 68 (3): 1244-51.
	Interaction of L-cysteine with a human excitatory amino acid transporter., Zerangue N., J Physiol. June 1, 1996; 493 ( Pt 2) 419-23.
	Comparison of Na+-dependent glutamate transport activity in synaptosomes, C6 glioma, and Xenopus oocytes expressing excitatory amino acid carrier 1 (EAAC1)., Dowd LA., Mol Pharmacol. March 1, 1996; 49 (3): 465-73.
	Localization of N-glycosylation sites and functional role of the carbohydrate units of GLAST-1, a cloned rat brain L-glutamate/L-aspartate transporter., Conradt M., Eur J Biochem. May 1, 1995; 229 (3): 682-7.
	Differential modulation of human glutamate transporter subtypes by arachidonic acid., Zerangue N., J Biol Chem. March 24, 1995; 270 (12): 6433-5.
	Functional properties and substrate specificity of the cloned L-glutamate/L-aspartate transporter GLAST-1 from rat brain expressed in Xenopus oocytes., Klöckner U., J Neurosci. October 1, 1994; 14 (10): 5759-65.
	Functional comparisons of three glutamate transporter subtypes cloned from human motor cortex., Arriza JL., J Neurosci. September 1, 1994; 14 (9): 5559-69.
	Electrogenic L-glutamate uptake in Xenopus laevis oocytes expressing a cloned rat brain L-glutamate/L-aspartate transporter (GLAST-1)., Klöckner U., J Biol Chem. July 15, 1993; 268 (20): 14594-6.
	Structure, expression, and functional analysis of a Na(+)-dependent glutamate/aspartate transporter from rat brain., Storck T., Proc Natl Acad Sci U S A. November 15, 1992; 89 (22): 10955-9.

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