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Summary Anatomy Item Literature (1720) Expression Attributions Wiki
XB-ANAT-1495

Papers associated with portion of organism substance (and slc2a1)

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Glucose transporter 1 deficiency in the idiopathic generalized epilepsies., Arsov T., Ann Neurol. November 1, 2012; 72 (5): 807-15.

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.

Glut1 deficiency: inheritance pattern determined by haploinsufficiency., Rotstein M., Ann Neurol. December 1, 2010; 68 (6): 955-8.

SLC2A9 is a high-capacity urate transporter in humans., Caulfield MJ., PLoS Med. October 7, 2008; 5 (10): e197.          

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.

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.

Synthesis and biologic evaluation of (11)c-methyl-d-glucoside, a tracer of the sodium-dependent glucose transporters., Bormans GM., J Nucl Med. July 1, 2003; 44 (7): 1075-81.

Changes in glucose transport and water permeability resulting from the T310I pathogenic mutation in Glut1 are consistent with two transport channels per monomer., Iserovich P., J Biol Chem. August 23, 2002; 277 (34): 30991-7.  

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.

Role of facilitative glucose transporters in diffusional water permeability through J774 cells., Loike JD., J Gen Physiol. November 1, 1993; 102 (5): 897-906.

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