Papers associated with brain (and mcts1)

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	The γ-hydroxybutyric acid (GHB) analogue NCS-382 is a substrate for both monocarboxylate transporters subtypes 1 and 4., Thiesen L., Eur J Pharm Sci. February 15, 2020; 143 105203.
	Conservation and divergence of protein pathways in the vertebrate heart., Federspiel JD., PLoS Biol. September 6, 2019; 17 (9): e3000437.
	Lack of evidence for synaptic high-affinity γ-hydroxybutyric acid (GHB) transport in rat brain synaptosomes and 11 Na+ -dependent SLC neurotransmitter transporters., Thiesen L., J Neurochem. April 1, 2019; 149 (2): 195-210.
	Energy Dynamics in the Brain: Contributions of Astrocytes to Metabolism and pH Homeostasis., Deitmer JW., Front Neurosci. March 15, 2019; 13 1301.
	Reference gene identification and validation for quantitative real-time PCR studies in developing Xenopus laevis., Mughal BB., Sci Rep. January 11, 2018; 8 (1): 496.
	In Vitro and In Vivo Evidence for Active Brain Uptake of the GHB Analog HOCPCA by the Monocarboxylate Transporter Subtype 1., Thiesen L., J Pharmacol Exp Ther. August 1, 2015; 354 (2): 166-74.
	Identification of key binding site residues of MCT1 for AR-C155858 reveals the molecular basis of its isoform selectivity., Nancolas B., Biochem J. February 15, 2015; 466 (1): 177-88.
	Functional characterization of 5-oxoproline transport via SLC16A1/MCT1., Sasaki S., J Biol Chem. January 23, 2015; 290 (4): 2303-11.
	The SLC16 gene family - structure, role and regulation in health and disease., Halestrap AP., Mol Aspects Med. January 1, 2013; 34 (2-3): 337-49.
	Significance of short chain fatty acid transport by members of the monocarboxylate transporter family (MCT)., Moschen I., Neurochem Res. November 1, 2012; 37 (11): 2562-8.
	Lactate flux in astrocytes is enhanced by a non-catalytic action of carbonic anhydrase II., Stridh MH., J Physiol. May 15, 2012; 590 (10): 2333-51.
	Rapid downregulation of the rat glutamine transporter SNAT3 by a caveolin-dependent trafficking mechanism in Xenopus laevis oocytes., Balkrishna S., Am J Physiol Cell Physiol. November 1, 2010; 299 (5): C1047-57.
	The inhibition of monocarboxylate transporter 2 (MCT2) by AR-C155858 is modulated by the associated ancillary protein., Ovens MJ., Biochem J. October 15, 2010; 431 (2): 217-25.
	AR-C155858 is a potent inhibitor of monocarboxylate transporters MCT1 and MCT2 that binds to an intracellular site involving transmembrane helices 7-10., Ovens MJ., Biochem J. January 15, 2010; 425 (3): 523-30.
	Studies on the DIDS-binding site of monocarboxylate transporter 1 suggest a homology model of the open conformation and a plausible translocation cycle., Wilson MC., J Biol Chem. July 24, 2009; 284 (30): 20011-21.
	Identity of SMCT1 (SLC5A8) as a neuron-specific Na+-coupled transporter for active uptake of L-lactate and ketone bodies in the brain., Martin PM., J Neurochem. July 1, 2006; 98 (1): 279-88.
	The role of charged residues in the transmembrane helices of monocarboxylate transporter 1 and its ancillary protein basigin in determining plasma membrane expression and catalytic activity., Manoharan C., Mol Membr Biol. January 1, 2006; 23 (6): 486-98.
	Facilitated lactate transport by MCT1 when coexpressed with the sodium bicarbonate cotransporter (NBC) in Xenopus oocytes., Becker HM., Biophys J. January 1, 2004; 86 (1 Pt 1): 235-47.
	Characterization of the high-affinity monocarboxylate transporter MCT2 in Xenopus laevis oocytes., Bröer S., Biochem J. August 1, 1999; 341 ( Pt 3) 529-35.
	cDNA cloning and functional characterization of rat intestinal monocarboxylate transporter., Takanaga H., Biochem Biophys Res Commun. December 5, 1995; 217 (1): 370-7.

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