219 related articles for article (PubMed ID: 9016941)
1. Synthesis of glucose-chlorambucil derivatives and their recognition by the human GLUT1 glucose transporter.
Halmos T; Santarromana M; Antonakis K; Scherman D
Eur J Pharmacol; 1996 Dec; 318(2-3):477-84. PubMed ID: 9016941
[TBL] [Abstract][Full Text] [Related]
2. Synthesis of O-methylsulfonyl derivatives of D-glucose as potential alkylating agents for targeted drug delivery to the brain. Evaluation of their interaction with the human erythrocyte GLUT1 hexose transporter.
Halmos T; Santarromana M; Antonakis K; Scherman D
Carbohydr Res; 1997 Mar; 299(1-2):15-21. PubMed ID: 9129293
[TBL] [Abstract][Full Text] [Related]
3. Rapid substrate translocation by the multisubunit, erythroid glucose transporter requires subunit associations but not cooperative ligand binding.
Coderre PE; Cloherty EK; Zottola RJ; Carruthers A
Biochemistry; 1995 Aug; 34(30):9762-73. PubMed ID: 7626647
[TBL] [Abstract][Full Text] [Related]
4. Endofacial competitive inhibition of the glucose transporter 1 activity by gossypol.
Pérez A; Ojeda P; Valenzuela X; Ortega M; Sánchez C; Ojeda L; Castro M; Cárcamo JG; Rauch MC; Concha II; Rivas CI; Vera JC; Reyes AM
Am J Physiol Cell Physiol; 2009 Jul; 297(1):C86-93. PubMed ID: 19386788
[TBL] [Abstract][Full Text] [Related]
5. Glucose transporter function is controlled by transporter oligomeric structure. A single, intramolecular disulfide promotes GLUT1 tetramerization.
Zottola RJ; Cloherty EK; Coderre PE; Hansen A; Hebert DN; Carruthers A
Biochemistry; 1995 Aug; 34(30):9734-47. PubMed ID: 7626644
[TBL] [Abstract][Full Text] [Related]
6. Human erythrocyte sugar transport is incompatible with available carrier models.
Cloherty EK; Heard KS; Carruthers A
Biochemistry; 1996 Aug; 35(32):10411-21. PubMed ID: 8756697
[TBL] [Abstract][Full Text] [Related]
7. Nicotinamide is not a substrate of the facilitative hexose transporter GLUT1.
Reyes AM; Bustamante F; Rivas CI; Ortega M; Donnet C; Rossi JP; Fischbarg J; Vera JC
Biochemistry; 2002 Jun; 41(25):8075-81. PubMed ID: 12069599
[TBL] [Abstract][Full Text] [Related]
8. Genistein is a natural inhibitor of hexose and dehydroascorbic acid transport through the glucose transporter, GLUT1.
Vera JC; Reyes AM; Cárcamo JG; Velásquez FV; Rivas CI; Zhang RH; Strobel P; Iribarren R; Scher HI; Slebe JC
J Biol Chem; 1996 Apr; 271(15):8719-24. PubMed ID: 8621505
[TBL] [Abstract][Full Text] [Related]
9. The red blood cell glucose transporter presents multiple, nucleotide-sensitive sugar exit sites.
Cloherty EK; Levine KB; Carruthers A
Biochemistry; 2001 Dec; 40(51):15549-61. PubMed ID: 11747430
[TBL] [Abstract][Full Text] [Related]
10. WZB117 (2-Fluoro-6-(m-hydroxybenzoyloxy) Phenyl m-Hydroxybenzoate) Inhibits GLUT1-mediated Sugar Transport by Binding Reversibly at the Exofacial Sugar Binding Site.
Ojelabi OA; Lloyd KP; Simon AH; De Zutter JK; Carruthers A
J Biol Chem; 2016 Dec; 291(52):26762-26772. PubMed ID: 27836974
[TBL] [Abstract][Full Text] [Related]
11. Differentiation of erythrocyte-(GLUT1), liver-(GLUT2), and adipocyte-type (GLUT4) glucose transporters by binding of the inhibitory ligands cytochalasin B, forskolin, dipyridamole, and isobutylmethylxanthine.
Hellwig B; Joost HG
Mol Pharmacol; 1991 Sep; 40(3):383-9. PubMed ID: 1716731
[TBL] [Abstract][Full Text] [Related]
12. Cadmium increases GLUT1 substrate binding affinity in vitro while reducing its cytochalasin B binding affinity.
Lachaal M; Liu H; Kim S; Spangler RA; Jung CY
Biochemistry; 1996 Nov; 35(47):14958-62. PubMed ID: 8942661
[TBL] [Abstract][Full Text] [Related]
13. Properties of the human erythrocyte glucose transport protein are determined by cellular context.
Levine KB; Robichaud TK; Hamill S; Sultzman LA; Carruthers A
Biochemistry; 2005 Apr; 44(15):5606-16. PubMed ID: 15823019
[TBL] [Abstract][Full Text] [Related]
14. Glucose transporter oligomeric structure determines transporter function. Reversible redox-dependent interconversions of tetrameric and dimeric GLUT1.
Hebert DN; Carruthers A
J Biol Chem; 1992 Nov; 267(33):23829-38. PubMed ID: 1429721
[TBL] [Abstract][Full Text] [Related]
15. Caffeine inhibits glucose transport by binding at the GLUT1 nucleotide-binding site.
Sage JM; Cura AJ; Lloyd KP; Carruthers A
Am J Physiol Cell Physiol; 2015 May; 308(10):C827-34. PubMed ID: 25715702
[TBL] [Abstract][Full Text] [Related]
16. Activation of Glut1 glucose transporter in human erythrocytes.
Zhang JZ; Ismail-Beigi F
Arch Biochem Biophys; 1998 Aug; 356(1):86-92. PubMed ID: 9681995
[TBL] [Abstract][Full Text] [Related]
17. Chromatography on cells: analyses of solute interactions with the glucose transporter Glut1 in human red cells adsorbed on lectin-gel beads.
Gottschalk I; Li YM; Lundahl P
J Chromatogr B Biomed Sci Appl; 2000 Feb; 739(1):55-62. PubMed ID: 10744313
[TBL] [Abstract][Full Text] [Related]
18. The human erythrocyte sugar transporter presents two sugar import sites.
Hamill S; Cloherty EK; Carruthers A
Biochemistry; 1999 Dec; 38(51):16974-83. PubMed ID: 10606533
[TBL] [Abstract][Full Text] [Related]
19. Direct inhibition of the hexose transporter GLUT1 by tyrosine kinase inhibitors.
Vera JC; Reyes AM; Velásquez FV; Rivas CI; Zhang RH; Strobel P; Slebe JC; Núñez-Alarcón J; Golde DW
Biochemistry; 2001 Jan; 40(3):777-90. PubMed ID: 11170395
[TBL] [Abstract][Full Text] [Related]
20. The inhibition of GLUT1 glucose transport and cytochalasin B binding activity by tricyclic antidepressants.
Pinkofsky HB; Dwyer DS; Bradley RJ
Life Sci; 2000; 66(3):271-8. PubMed ID: 10666003
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
