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Gene expression analysis of developing cell groups in the pretectal region of Xenopus laevis. , Morona R., J Comp Neurol. March 1, 2017; 525 (4): 715-752.
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.
Evolutionary structural and functional conservation of an ortholog of the GLUT2 glucose transporter gene ( SLC2A2) in zebrafish. , Castillo J., Am J Physiol Regul Integr Comp Physiol. November 1, 2009; 297 (5): R1570-81.
Inhibition of the intestinal glucose transporter GLUT2 by flavonoids. , Kwon O., FASEB J. February 1, 2007; 21 (2): 366-77.
QLS motif in transmembrane helix VII of the glucose transporter family interacts with the C-1 position of D-glucose and is involved in substrate selection at the exofacial binding site. , Seatter MJ., Biochemistry. February 3, 1998; 37 (5): 1322-6.
Structure-function analysis of liver-type ( GLUT2) and brain-type ( GLUT3) glucose transporters: expression of chimeric transporters in Xenopus oocytes suggests an important role for putative transmembrane helix 7 in determining substrate selectivity. , Arbuckle MI., Biochemistry. December 24, 1996; 35 (51): 16519-27.
Analysis of the structural requirements of sugar binding to the liver, brain and insulin-responsive glucose transporters expressed in oocytes. , Colville CA., Biochem J. September 15, 1993; 294 ( Pt 3) 753-60.
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.
Different mammalian facilitative glucose transporters expressed in Xenopus oocytes. , Keller K., Biomed Biochim Acta. January 1, 1990; 49 (12): 1201-3.