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XB-GENEPAGE-5755356
Papers associated with slc2a1
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A Protein Kinase C Phosphorylation Motif in GLUT1 Affects Glucose Transport and is Mutated in GLUT1 Deficiency Syndrome., Lee EE, Ma J, Sacharidou A, Mi W, Salato VK, Nguyen N, Jiang Y, Pascual JM, North PE, Shaul PW, Mettlen M, Wang RC., Mol Cell. June 4, 2015; 58 (5): 845-53. |
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Functional characterization of the human facilitative glucose transporter 12 (GLUT12) by electrophysiological methods., Pujol-Giménez J, Pérez A, Reyes AM, Loo DD, Lostao MP., Am J Physiol Cell Physiol. June 15, 2015; 308 (12): C1008-22. |
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New fluorinated fructose analogs as selective probes of the hexose transporter protein GLUT5., Soueidan OM, Trayner BJ, Grant TN, Henderson JR, Wuest F, West FG, Cheeseman CI., Org Biomol Chem. June 21, 2015; 13 (23): 6511-21. |
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Spemann organizer transcriptome induction by early beta-catenin, Wnt, Nodal, and Siamois signals in Xenopus laevis., Ding Y, Ploper D, Sosa EA, Colozza G, Moriyama Y, Benitez MD, Zhang K, Merkurjev D, De Robertis EM., Proc Natl Acad Sci U S A. April 11, 2017; 114 (15): E3081-E3090.  |
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Tunable GLUT-Hexose Binding and Transport via Modulation of Hexose C-3 Hydrogen-Bonding Capabilities., Kumar Kondapi VP, Soueidan OM, Cheeseman CI, West FG., Chemistry. June 12, 2017; 23 (33): 8073-8081. |
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The SLC2A14 gene, encoding the novel glucose/dehydroascorbate transporter GLUT14, is associated with inflammatory bowel disease., Amir Shaghaghi M, Zhouyao H, Tu H, El-Gabalawy H, Crow GH, Levine M, Bernstein CN, Eck P., Am J Clin Nutr. December 1, 2017; 106 (6): 1508-1513. |
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Human Mutations in SLC2A9 (Glut9) Affect Transport Capacity for Urate., Ruiz A, Gautschi I, Schild L, Bonny O., Front Physiol. January 1, 2018; 9 476.  |
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Gain-of-function HCN2 variants in genetic epilepsy., Li M, Maljevic S, Phillips AM, Petrovski S, Hildebrand MS, Burgess R, Mount T, Zara F, Striano P, Schubert J, Thiele H, Nürnberg P, Wong M, Weisenberg JL, Thio LL, Lerche H, Scheffer IE, Berkovic SF, Petrou S, Reid CA., Hum Mutat. February 1, 2018; 39 (2): 202-209. |
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Development of a rapid functional assay that predicts GLUT1 disease severity., Zaman SM, Mullen SA, Petrovski S, Maljevic S, Gazina EV, Phillips AM, Jones GD, Hildebrand MS, Damiano J, Auvin S, Lerche H, Weber YG, Berkovic SF, Scheffer IE, Reid CA, Petrou S., Neurol Genet. December 6, 2018; 4 (6): e297.  |
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Functional and structural analysis of rare SLC2A2 variants associated with Fanconi-Bickel syndrome and metabolic traits., Enogieru OJ, Ung PMU, Yee SW, Schlessinger A, Giacomini KM., Hum Mutat. July 1, 2019; 40 (7): 983-995. |
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Structural comparison of GLUT1 to GLUT3 reveal transport regulation mechanism in sugar porter family., Custódio TF, Paulsen PA, Frain KM, Pedersen BP., Life Sci Alliance. February 3, 2021; 4 (4):  |
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Identification of Structural Determinants of the Transport of the Dehydroascorbic Acid Mediated by Glucose Transport GLUT1., Villagrán M, Burgos CF, Rivas CI, Mardones L., Molecules. January 5, 2023; 28 (2):  |
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Mitochondrial leak metabolism induces the Spemann-Mangold Organizer via Hif-1α in Xenopus., MacColl Garfinkel A, Mnatsakanyan N, Patel JH, Wills AE, Shteyman A, Smith PJS, Alavian KN, Jonas EA, Khokha MK., Dev Cell. November 20, 2023; 58 (22): 2597-2613.e4.  |
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