Papers associated with brain (and slc2a1)

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	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.
	Spemann organizer transcriptome induction by early beta-catenin, Wnt, Nodal, and Siamois signals in Xenopus laevis., Ding Y., Proc Natl Acad Sci U S A. April 11, 2017; 114 (15): E3081-E3090.
	A Protein Kinase C Phosphorylation Motif in GLUT1 Affects Glucose Transport and is Mutated in GLUT1 Deficiency Syndrome., Lee EE., Mol Cell. June 4, 2015; 58 (5): 845-53.
	Left-right patterning in Xenopus conjoined twin embryos requires serotonin signaling and gap junctions., Vandenberg LN., Int J Dev Biol. January 1, 2014; 58 (10-12): 799-809.
	FGT-1 is the major glucose transporter in C. elegans and is central to aging pathways., Feng Y., Biochem J. December 1, 2013; 456 (2): 219-29.
	FGT-1 is a mammalian GLUT2-like facilitative glucose transporter in Caenorhabditis elegans whose malfunction induces fat accumulation in intestinal cells., Kitaoka S., PLoS One. June 4, 2013; 8 (6): e68475.
	Implications of aberrant temperature-sensitive glucose transport via the glucose transporter deficiency mutant (GLUT1DS) T295M for the alternate-access and fixed-site transport models., Cunningham P., J Membr Biol. June 1, 2013; 246 (6): 495-511.
	Glucose transporter 1 deficiency in the idiopathic generalized epilepsies., Arsov T., Ann Neurol. November 1, 2012; 72 (5): 807-15.
	GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy., Striano P., Neurology. February 21, 2012; 78 (8): 557-62.
	Water transport by glucose transporter type 3 expressed in Xenopus oocytes., Tomioka S., Neuroreport. January 4, 2012; 23 (1): 21-5.
	Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndrome., Flatt JF., Blood. November 10, 2011; 118 (19): 5267-77.
	Facilitative glucose transporter Glut1 is actively excluded from rod outer segments., Gospe SM., J Cell Sci. November 1, 2010; 123 (Pt 21): 3639-44.
	Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1., Suls A., Brain. July 1, 2008; 131 (Pt 7): 1831-44.
	Structural signatures and membrane helix 4 in GLUT1: inferences from human blood-brain glucose transport mutants., Pascual JM., J Biol Chem. June 13, 2008; 283 (24): 16732-42.
	GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak., Weber YG., J Clin Invest. June 1, 2008; 118 (6): 2157-68.
	Xenopus glucose transporter 1 (xGLUT1) is required for gastrulation movement in Xenopus laevis., Suzawa K., Int J Dev Biol. January 1, 2007; 51 (3): 183-90.
	Mammalian glucose permease GLUT1 facilitates transport of arsenic trioxide and methylarsonous acid., Liu Z., Biochem Biophys Res Commun. December 15, 2006; 351 (2): 424-30.
	Sequence and functional analysis of GLUT10: a glucose transporter in the Type 2 diabetes-linked region of chromosome 20q12-13.1., Dawson PA., Mol Genet Metab. January 1, 2001; 74 (1-2): 186-99.
	Cysteine scanning mutagenesis of helices 2 and 7 in GLUT1 identifies an exofacial cleft in both transmembrane segments., Olsowski A., Biochemistry. March 14, 2000; 39 (10): 2469-74.
	GLUTX1, a novel mammalian glucose transporter expressed in the central nervous system and insulin-sensitive tissues., Ibberson M., J Biol Chem. February 18, 2000; 275 (7): 4607-12.
	Selective expression of the large neutral amino acid transporter at the blood-brain barrier., Boado RJ., Proc Natl Acad Sci U S A. October 12, 1999; 96 (21): 12079-84.
	Cysteine-scanning mutagenesis of flanking regions at the boundary between external loop I or IV and transmembrane segment II or VII in the GLUT1 glucose transporter., Olsowski A., Biochemistry. July 28, 1998; 37 (30): 10738-45.
	Role of facilitative glucose transporters in diffusional water permeability through J774 cells., Loike JD., J Gen Physiol. November 1, 1993; 102 (5): 897-906.
	Kinetic analysis of the liver-type (GLUT2) and brain-type (GLUT3) glucose transporters in Xenopus oocytes: substrate specificities and effects of transport inhibitors., Colville CA., Biochem J. March 15, 1993; 290 ( Pt 3) 701-6.
	Mammalian facilitative glucose transporters: evidence for similar substrate recognition sites in functionally monomeric proteins., Burant CF., Biochemistry. October 27, 1992; 31 (42): 10414-20.
	A possible role for a mammalian facilitative hexose transporter in the development of resistance to drugs., Vera JC., Mol Cell Biol. July 1, 1991; 11 (7): 3407-18.
	Different mammalian facilitative glucose transporters expressed in Xenopus oocytes., Keller K., Biomed Biochim Acta. January 1, 1990; 49 (12): 1201-3.

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