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Transport of Sugars
Open accessAbstract
Soluble sugars serve five main purposes in multicellular organisms: as sources of carbon skeletons, osmolytes, signals, and transient energy storage and as transport molecules. Most sugars are derived from photosynthetic organisms, particularly plants. In multicellular organisms, some cells specialize in providing sugars to other cells (e.g., intestinal and liver cells in animals, photosynthetic cells in plants), whereas others depend completely on an external supply (e.g., brain cells, roots and seeds). This cellular exchange of sugars requires transport proteins to mediate uptake or release from cells or subcellular compartments. Thus, not surprisingly, sugar transport is critical for plants, animals, and humans. At present, three classes of eukaryotic sugar transporters have been characterized, namely the glucose transporters (GLUTs), sodium-glucose symporters (SGLTs), and SWEETs. This review presents the history and state of the art of sugar transporter research, covering genetics, biochemistry, and physiology—from their identification and characterization to their structure, function, and physiology. In humans, understanding sugar transport has therapeutic importance (e.g., addressing diabetes or limiting access of cancer cells to sugars), and in plants, these transporters are critical for crop yield and pathogen susceptibility.
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“researchers asserted that besides its role in glucose reabsorption, SGLT may exhibit other distinct functions in CNS.13–15”
From Dapagliflozin Activates Neurons in the Central Nervous System and Regulates Cardiovascular Activity by Inhibiting SGLT-2 in Mice (2020) · cites this paper as [15]
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Sugar transporters for intercellular exchange and nutrition of pathogens
Chen, L., Hou, B., Lalonde, S., Takanaga, H., Hartung, M. L., Qu, X.-Q., Guo, W., Kim, J., Underwood, W. R., Chaudhuri, B., et al. (2010) · Nature · doi:10.1038/nature09606 · Cited by 1,629
Self-citationSequence and Structure of a Human Glucose Transporter
Mueckler, M. M., Caruso, C., Baldwin, S. A., Panico, M., Blench, I., Morris, H. R., Allard, W. J., Lienhard, G. E., & Lodish, H. F. (1985) · Science · doi:10.1126/science.3839598 · Cited by 1,529
Biology of Human Sodium Glucose Transporters
Wright, E. M., Loo, D. D. F., & Hirayama, B. A. (2011) · Physiological Reviews · doi:10.1152/physrev.00055.2009 · Cited by 1,430
Structure and Mechanism of the Lactose Permease of Escherichia coli
Abramson, J., Smirnova, I., Kasho, V. N., Verner, G., Kaback, H. R., & Iwata, S. (2003) · Science · doi:10.1126/science.1088196 · Cited by 1,389
Sucrose Efflux Mediated by SWEET Proteins as a Key Step for Phloem Transport
Chen, L., Qu, X.-Q., Hou, B., Sosso, D., Osorio, S., Fernie, A. R., & Frommer, W. B. (2011) · Science · doi:10.1126/science.1213351 · Cited by 1,384
Self-citationThe SLC2 (GLUT) family of membrane transporters
Mueckler, M., & Thorens, B. (2013) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2012.07.001 · Cited by 1,328
Regulated transport of the glucose transporter GLUT4
Bryant, N. J., Govers, R., & James, D. E. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm782 · Cited by 1,183
Coupled transport of sodium and organic solutes.
Schultz, S. G., & Curran, P. F. (1970) · Physiological Reviews · doi:10.1152/physrev.1970.50.4.637 · Cited by 1,175
Glucose transporters in the 21st Century
Thorens, B., & Mueckler, M. (2010) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00712.2009 · Cited by 1,013
Expression cloning and cDNA sequencing of the Na+/glucose co-transporter
Hediger, M. A., Coady, M. J., Ikeda, T. S., & Wright, E. M. (1987) · Nature · doi:10.1038/330379a0 · Cited by 1,004
Structure of a Glycerol-Conducting Channel and the Basis for Its Selectivity
Fu, D., Libson, A. M., Miercke, L. J. W., Weitzman, C., Nollert, P., Krucinski, J., & Stroud, R. M. (2000) · Science · doi:10.1126/science.290.5491.481 · Cited by 1,000
Mutation in hepatocyte nuclear factor–1β gene (TCF2) associated with MODY
Horikawa, Y., Iwasaki, N., Hara, M., Furuta, H., Hinokio, Y., Cockburn, B. N., Lindner, T. H., Yamagata, K., Ogata, M., Tomonaga, O., et al. (1997) · Nature Genetics · doi:10.1038/ng1297-384 · Cited by 878
Crystal structure of the human glucose transporter GLUT1
Deng, D., Xu, C., Sun, P., Wu, J., Yan, C., Hu, M., & Yan, N. (2014) · Nature · doi:10.1038/nature13306 · Cited by 777
Gorboulev, V., Schürmann, A., Vallon, V., Kipp, H., Jaschke, A., Klessen, D., Friedrich, A., Scherneck, S., Rieg, T., Cunard, R., et al. (2012) · Diabetes · doi:10.2337/db11-1029 · Cited by 687
Os8N3 is a host disease-susceptibility gene for bacterial blight of rice
Yang, B., Sugio, A., & White, F. F. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604088103 · Cited by 650
PHOSPHATE BOUND TO HISTIDINE IN A PROTEIN AS AN INTERMEDIATE IN A NOVEL PHOSPHO-TRANSFERASE SYSTEM
Kundig, W., Ghosh, S., & Roseman, S. (1964) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.52.4.1067 · Cited by 616
A common mechanism of action for three mood-stabilizing drugs
Williams, R. S. B., Cheng, L., Mudge, A. W., & Harwood, A. J. (2002) · Nature · doi:10.1038/417292a · Cited by 615
SGLT2 Mediates Glucose Reabsorption in the Early Proximal Tubule
Vallon, V., Platt, K. A., Cunard, R. A., Schroth, J., Whaley, J. M., Thomson, S. C., Koepsell, H., & Rieg, T. (2010) · Journal of the American Society of Nephrology · doi:10.1681/asn.2010030246 · Cited by 565
Fructose transporter in human spermatozoa and small intestine is GLUT5.
Burant, C., Takeda, J., Brot‐Laroche, E., Bell, G. I., & Davidson, N. O. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)42067-4 · Cited by 545
Crystal structure of a catalytic intermediate of the maltose transporter
Oldham, M. L., Khare, D., Quiocho, F. A., Davidson, A. L., & Chen, J. (2007) · Nature · doi:10.1038/nature06264 · Cited by 526
Faham, S., Watanabe, A., Mercado, G., Cascio, D., Specht, A., Hirayama, B. A., Wright, E. M., & Abramson, J. (2008) · Science · doi:10.1126/science.1160406 · Cited by 522
Riesmeier, J. W., Willmitzer, L., & Frommer, W. B. (1992) · The EMBO Journal · doi:10.1002/j.1460-2075.1992.tb05575.x · Cited by 504
Self-citationSequence of the lactose permease gene
Büchel, D. E., Gronenborn, B., & Müller‐Hill, B. (1980) · Nature · doi:10.1038/283541a0 · Cited by 500
NRT/PTR transporters are essential for translocation of glucosinolate defence compounds to seeds
Nour‐Eldin, H. H., Andersen, T. G., Burow, M., Madsen, S. R., Jørgensen, M. E., Olsen, C. E., Drèyer, I., Hedrich, R., Geiger, D., & Halkier, B. A. (2012) · Nature · doi:10.1038/nature11285 · Cited by 487
Crystal structure of a bacterial homologue of glucose transporters GLUT1–4
Sun, L., Zeng, X. W., Yan, C., Sun, X., Gong, X., Rao, Y., & Yan, N. (2012) · Nature · doi:10.1038/nature11524 · Cited by 483
TRANSPORT MECHANISMS FOR ORGANIC FORMS OF CARBON AND NITROGEN BETWEEN SOURCE AND SINK
Lalonde, S., Wipf, D., & Frommer, W. B. (2004) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.55.031903.141758 · Cited by 477
Self-citationCardiac and adipose tissue abnormalities but not diabetes in mice deficient in GLUT4
Katz, E. B., Stenbit, A. E., Hatton, K. S., DePinho, R. A., & Charron, M. J. (1995) · Nature · doi:10.1038/377151a0 · Cited by 467
Wallace, C., Newhouse, S., Braund, P. S., Zhang, F., Tobin, M. D., Falchi, M., Ahmadi, K. R., Dobson, R., Marçano, A. C. B., Hajat, C., et al. (2008) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2007.11.001 · Cited by 441
Chen, L., Lin, I. W., Qu, X.-Q., Sosso, D., McFarlane, H. E., Londoño, A., Samuels, L., & Frommer, W. B. (2015) · The Plant Cell · doi:10.1105/tpc.114.134585 · Cited by 437
Self-citationDeutscher, J., Aké, F. M., Derkaoui, M., Zébré, A. C., Cao, T. N., Bouraoui, H., Kentache, T., Mokhtari, A., Milohanic, E., & Joyet, P. (2014) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00001-14 · Cited by 432
Nectar secretion requires sucrose phosphate synthases and the sugar transporter SWEET9
Lin, I. W., Sosso, D., Chen, L., Gase, K., Kim, S.-G., Kessler, D., Klinkenberg, P. M., Gorder, M. K., Hou, B., Qu, X.-Q., et al. (2014) · Nature · doi:10.1038/nature13082 · Cited by 431
Self-citationEarly diabetes and abnormal postnatal pancreatic islet development in mice lacking Glut-2
Guillam, M., Hümmler, E., Schaerer, E., Wu, J.-Y., Birnbaum, M. J., Beermann, F., Schmidt, A., Dériaz, N., & Thorens, B. (1997) · Nature Genetics · doi:10.1038/ng1197-327 · Cited by 430
Human and rat beta cells differ in glucose transporter but not in glucokinase gene expression.
De Vos, A., Heimberg, H., Quartier, E., Huypens, P., Bouwens, L., Pipeleers, D., & Schuit, F. (1995) · Journal of Clinical Investigation · doi:10.1172/jci118308 · Cited by 425
Özcan, S., Dover, J., Rosenwald, A., Wölfl, S., & Johnston, M. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.22.12428 · Cited by 420
The Role of Energy Coupling in the Transport of β-Galactosides by Escherichia coli
Winkler, H. H., & Wilson, T. H. (1966) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)96607-x · Cited by 413
Coucke, P. J., Willaert, A., Wessels, M. W., Callewaert, B. L., Zoppi, N., Backer, J. F. A. D., Fox, J. E., Mancini, G. M. S., Kambouris, M., Gardella, R., et al. (2006) · Nature Genetics · doi:10.1038/ng1764 · Cited by 399
The protein family of glucose transport facilitators: It's not only about glucose after all
Augustin, R. (2010) · IUBMB Life · doi:10.1002/iub.315 · Cited by 398
Kayano, T., Burant, C., Fukumoto, H., Gould, G. W., Fan, Y. S., Eddy, R. L., Byers, M. G., Shows, T. B., Seino, S., & Bell, G. I. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)38295-x · Cited by 389
Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter
Turk, E., Zabel, B., Mundlos, S., Dyer, J., & Wright, E. M. (1991) · Nature · doi:10.1038/350354a0 · Cited by 379
Reifenberger, E., Boles, E., & Ciriacy, M. (1997) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1997.00324.x · Cited by 376
Inhibition of water and solute permeability in human red cells
Macey, R. L., & Farmer, R. E. L. (1970) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(70)90130-6 · Cited by 373
Fox, C., & Kennedy, E. P. (1965) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.54.3.891 · Cited by 372
Na+ -dependent transport in the intestine and other animal tissues.
Rk, C. (1966) · PubMed · Cited by 362
Frillingos, S., Sahin‐Tóth, M., Wu, J., & Kaback, H. R. (1998) · The FASEB Journal · doi:10.1096/fasebj.12.13.1281 · Cited by 360
SUT2, a Putative Sucrose Sensor in Sieve Elements
Barker, L., Kühn, C., Weise, A., Schulz, A., Gebhardt, C., Hirner, B., Hellmann, H. A., Schulze, W. X., Ward, J. M., & Frommer, W. B. (2000) · The Plant Cell · doi:10.1105/tpc.12.7.1153 · Cited by 357
Self-citationGuan, L., & Kaback, H. R. (2005) · Annual Review of Biophysics and Biomolecular Structure · doi:10.1146/annurev.biophys.35.040405.102005 · Cited by 356
Takanaga, H., Chaudhuri, B., & Frommer, W. B. (2008) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2007.11.015 · Cited by 338
Self-citationHolman, G. D., Kozka, I. J., CLARK, A. E., Flower, C. J., Saltis, J., Habberfield, A. D., Simpson, I. A., & Cushman, S. W. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)44734-x · Cited by 329
AtKUP1: An Arabidopsis Gene Encoding High-Affinity Potassium Transport Activity
Kim, E. J., Kwak, J. M., Uozumi, N., & Schroeder, J. I. (1998) · The Plant Cell · doi:10.1105/tpc.10.1.51 · Cited by 327
Klemens, P. A. W., Patzke, K., Deitmer, J. W., Spinner, L., Hir, R. L., Bellini, C., Bedu, M., Chardon, G., Krapp, A., & Neuhaus, H. E. (2013) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.224972 · Cited by 325
THE FATE OF SUGAR IN THE ANIMAL BODY
Cori, C. F. (1925) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)84780-9 · Cited by 321
Purification and reconstitution of functional lactose carrier from Escherichia coli.
Newman, M. J., Foster, D. L., Wilson, T. H., & Kaback, H. R. (1981) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)68477-2 · Cited by 311
A glucose sensor hiding in a family of transporters
Dı́ez-Sampedro, A., Hirayama, B. A., Osswald, C., Gorboulev, V., Baumgarten, K., Volk, C., Wright, E. M., & Koepsell, H. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1733027100 · Cited by 308
Imaging of the Dynamics of Glucose Uptake in the Cytosol of COS-7 Cells by Fluorescent Nanosensors
Fehr, M., Lalonde, S., Lager, I., Wolff, M. W., & Frommer, W. B. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m301333200 · Cited by 302
Self-citationYunus, S., Jonas, A. M., & Lakard, B. (2012) · Springer eBooks · doi:10.1007/978-3-642-16712-6 · Cited by 302
Comparative Genomic Analyses of the Bacterial Phosphotransferase System
Barabote, R. D., & Saier, M. H. (2005) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.69.4.608-634.2005 · Cited by 299
Functional role of oligomerization for bacterial and plant SWEET sugar transporter family
Xuan, Y., Hu, Y., Chen, L., Sosso, D., Ducat, D. C., Hou, B., & Frommer, W. B. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1311244110 · Cited by 289
Self-citationLeaf Fructose Content Is Controlled by the Vacuolar Transporter SWEET17 in Arabidopsis
Chardon, G., Bedu, M., Calenge, F., Klemens, P. A. W., Spinner, L., Clément, G., Chietera, G., Léran, S., Ferrand, M., Lacombe, B., et al. (2013) · Current Biology · doi:10.1016/j.cub.2013.03.021 · Cited by 284
Guo, W., Nagy, R., Chen, H., Pfrunder, S., Yu, Y.-C., Santelia, D., Frommer, W. B., & Martinoia, E. (2013) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.232751 · Cited by 282
Self-citationNiittylä, T., Fuglsang, A. T., Palmgren, M. B., Frommer, W. B., & Schulze, W. X. (2007) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m700164-mcp200 · Cited by 282
Self-citationStructure of a fucose transporter in an outward-open conformation
Dang, S., Sun, L., Huang, Y., Lu, F., Liu, Y., Gong, H., Wang, J., & Yan, N. (2010) · Nature · doi:10.1038/nature09406 · Cited by 272
New Observations on the Ultrastructure of the Membranes of Frog Peripheral Nerve Fibers
Robertson, J. D. (1957) · The Journal of Cell Biology · doi:10.1083/jcb.3.6.1043 · Cited by 259
Potato sucrose transporter expression in minor veins indicates a role in phloem loading.
Riesmeier, J. W., Hirner, B., & Frommer, W. B. (1993) · The Plant Cell · doi:10.1105/tpc.5.11.1591 · Cited by 255
Self-citationMembrane Transport of Sugars and Amino Acids
Reinhold, L., & Kaplan, A. (1984) · Annual Review of Plant Physiology · doi:10.1146/annurev.pp.35.060184.000401 · Cited by 254
Cohn, M. M., Bart, R. S., Shybut, M., Dahlbeck, D., Gómez, M. A. A., Morbitzer, R., Hou, B., Frommer, W. B., Lahaye, T., & Staskawicz, B. J. (2014) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-06-14-0161-r · Cited by 251
Self-citationLactose transport coupled to proton movements in escherichia coli
West, I. C. (1970) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(70)90063-x · Cited by 251
Proton‐driven sucrose symport and antiport are provided by the vacuolar transporters SUC4 and TMT1/2
Schulz, A., Beyhl, D., Marten, I., Wormit, A., Neuhaus, H. E., Poschet, G., Büttner, M., Schneider, S., Sauer, N., & Hedrich, R. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04672.x · Cited by 249
Alternating Access in Maltose Transporter Mediated by Rigid-Body Rotations
Khare, D., Oldham, M. L., Orelle, C., Davidson, A. L., & Chen, J. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.01.035 · Cited by 245
Sauer, N., Friedländer, K., & Gräml-Wicke, U. (1990) · The EMBO Journal · doi:10.1002/j.1460-2075.1990.tb07500.x · Cited by 238
Carpaneto, A., Geiger, D., Bamberg, E., Sauer, N., Fromm, J. H., & Hedrich, R. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m501785200 · Cited by 235
Structural determination of wild-type lactose permease
Guan, L., Mirza, O., Verner, G., Iwata, S., & Kaback, H. R. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0707688104 · Cited by 229
Quantitative Imaging with Fluorescent Biosensors
Okumoto, S., Jones, A. M., & Frommer, W. B. (2012) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042110-103745 · Cited by 224
Self-citationType 2 diabetes: Evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs
Ghosh, S., Watanabe, R. M., Hauser, E. R., Valle, T. T., Magnuson, V. L., Erdos, M. R., Langefeld, C. D., Balow, J. E., Ally, D. S., Kohtamäki, K., et al. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.5.2198 · Cited by 222
van den Heuvel, L. P., Assink, K., Willemsen, M. A. A. P., & Monnens, L. A. H. (2002) · Human Genetics · doi:10.1007/s00439-002-0820-5 · Cited by 220
An Arabidopsis senescence-associated protein SAG29 regulates cell viability under high salinity
Seo, P. J., Park, J. M., Kang, S. K., Kim, S., & Park, C. (2010) · Planta · doi:10.1007/s00425-010-1293-8 · Cited by 216
Crystal Structure of the Maltose Transporter in a Pretranslocation Intermediate State
Oldham, M. L., & Chen, J. (2011) · Science · doi:10.1126/science.1200767 · Cited by 214
Yamada, K., Osakabe, Y., Mizoi, J., Nakashima, K., Fujita, Y., Shinozaki, K., & Yamaguchi‐Shinozaki, K. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.054288 · Cited by 213
Will the original glucose transporter isoform please stand up!
Carruthers, A., Zutter, J. K. D., Ganguly, A., & Devaskar, S. U. (2009) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00496.2009 · Cited by 202
The yeast SNF3 gene encodes a glucose transporter homologous to the mammalian protein.
Celenza, J. L., Marshall-Carlson, L., & Carlson, M. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.7.2130 · Cited by 202
Höglund, P. J., Nordström, K. J. V., Schiöth, H. B., & Fredriksson, R. (2010) · Molecular Biology and Evolution · doi:10.1093/molbev/msq350 · Cited by 202
Snapshots of the maltose transporter during ATP hydrolysis
Oldham, M. L., & Chen, J. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1108858108 · Cited by 202
EVIDENCE OF ACTIVE TRANSFER OF CERTAIN NON-ELECTROLYTES ACROSS THE HUMAN RED CELL MEMBRANE
LeFevre, P. G. (1948) · The Journal of General Physiology · doi:10.1085/jgp.31.6.505 · Cited by 201
Tazawa, S., Yamato, T., Fujikura, H., Hiratochi, M., Itoh, F., Tomae, M., Takemura, Y., Maruyama, H., Sugiyama, T., Wakamatsu, A., et al. (2004) · Life Sciences · doi:10.1016/j.lfs.2004.10.016 · Cited by 200
BIHLER, I., & Crane, R. K. (1962) · Biochimica et Biophysica Acta · doi:10.1016/0006-3002(62)90699-6 · Cited by 197
The mechanism of sodium and substrate release from the binding pocket of vSGLT
Watanabe, A., Choe, S., Chaptal, V., Rosenberg, J. M., Wright, E. M., Grabe, M., & Abramson, J. (2010) · Nature · doi:10.1038/nature09580 · Cited by 194
Sugar, Amino Acid, and NA+ Cotransport in the Proximal Tubule
Ullrich, K. J. (1979) · Annual Review of Physiology · doi:10.1146/annurev.ph.41.030179.001145 · Cited by 192
Membrane Microdomains, Rafts, and Detergent-Resistant Membranes in Plants and Fungi
Malínský, J., Opekarová, M., Großmann, G., & Tanner, W. (2013) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-050312-120103 · Cited by 190
Self-citation[Galactoside-permease of Escherichia coli].
Buttin, G., Cohen, G. N., Monod, J., & Rickenberg, H. V. (1956) · PubMed · Cited by 176
Structural evidence for induced fit and a mechanism for sugar/H+ symport in LacY
Mirza, O., Guan, L., Verner, G., Iwata, S., & Kaback, H. R. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601028 · Cited by 174
Green Sperm. Identification of Male Gamete Promoters in Arabidopsis
Engel, M. L., Holmes‐Davis, R., & McCormick, S. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.054213 · Cited by 172
Structures of bacterial homologues of SWEET transporters in two distinct conformations
Xu, Y., Tao, Y., Cheung, L. S., Fan, C., Chen, L., Xu, S., Perry, K., Frommer, W. B., & Feng, L. (2014) · Nature · doi:10.1038/nature13670 · Cited by 171
Self-citationSignal transduction meets vesicle traffic: the software and hardware of GLUT4 translocation
Klip, A., Sun, Y., Chiu, T. T., & Foley, K. P. (2014) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00069.2014 · Cited by 170
Kasahara, M., & Hinkle, P. C. (1976) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.73.2.396 · Cited by 169
Sequence, tissue distribution, and functional characterization of the rat fructose transporter GLUT5
Rand, E. B., DePaoli, A. M., Davidson, N. O., Bell, G. I., & Burant, C. (1993) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1993.264.6.g1169 · Cited by 165
Leney, S. E., & Tavaré, J. M. (2009) · Journal of Endocrinology · doi:10.1677/joe-09-0037 · Cited by 163
Aluri, S., & Büttner, M. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610278104 · Cited by 163
The hexose carrier from Chlorella
Sauer, N., & Tanner, W. (1989) · FEBS Letters · doi:10.1016/0014-5793(89)81489-9 · Cited by 156
Self-citationRegulation of Calcium-Permeable TRPV2 Channel by Insulin in Pancreatic β-Cells
Hisanaga, E., Nagasawa, M., Ueki, K., Kulkarni, R. N., Mori, M., & Kojima, I. (2008) · Diabetes · doi:10.2337/db08-0862 · Cited by 154
A proton-cotransport system in a higher plant: Sucrose transport in Ricinus communis
Komor, E., Rotter, M., & Tanner, W. (1977) · Plant Science Letters · doi:10.1016/0304-4211(77)90093-1 · Cited by 152
Self-citationThe Hexose-Proton Cotransport System of Chlorella
Komor, E., & Tanner, W. (1974) · The Journal of General Physiology · doi:10.1085/jgp.64.5.568 · Cited by 150
Self-citationSistrom, W. R. (1958) · Biochimica et Biophysica Acta · doi:10.1016/0006-3002(58)90015-5 · Cited by 149
Sun, M.-X., Huang, X.-Y., Yang, J., Guan, Y., & Yang, Z. (2013) · Plant Reproduction · doi:10.1007/s00497-012-0208-1 · Cited by 146
Chaudhuri, B., Hörmann, F., Lalonde, S., Brady, S. M., Orlando, D. A., Benfey, P. N., & Frommer, W. B. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03652.x · Cited by 141
Self-citationStudies of the glucose-transport system in the rabbit erythrocyte
Regen, D. M., & Morgan, H. E. (1964) · Biochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects · doi:10.1016/0926-6577(64)90048-8 · Cited by 140
Proton‐coupled hexose transport in Chlorella vulgaris
Komor, E. (1973) · FEBS Letters · doi:10.1016/0014-5793(73)80501-0 · Cited by 139
The Hexose‐Proton Symport System of Chlorella vulgaris
Komor, E., & Tanner, W. (1974) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1974.tb03476.x · Cited by 136
Self-citationMaier, A., Völker, B., Boles, E., & Fuhrmann, G. F. (2002) · FEMS Yeast Research · doi:10.1111/j.1567-1364.2002.tb00121.x · Cited by 136
Structural basis for substrate transport in the GLUT-homology family of monosaccharide transporters
Quistgaard, E. M., Löw, C., Moberg, P., Tresaugues, L., & Nordlund, P. (2013) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2569 · Cited by 136
Doege, H., BOCIANSKI, A., Scheepers, A., Axer, H., Eckel, J., Joost, H., & Schürmann, A. (2001) · Biochemical Journal · doi:10.1042/0264-6021:3590443 · Cited by 135
Sugar Transport in Microorganisms
Cirillo, V. P. (1961) · Annual Review of Microbiology · doi:10.1146/annurev.mi.15.100161.001213 · Cited by 134
Transport Mechanism of the Cloned Potato H+/Sucrose Cotransporter StSUT1
Boorer, K. J., Loo, D. D. F., Frommer, W. B., & Wright, E. M. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.41.25139 · Cited by 132
Self-citationCrystal structure of a glucose/H + symporter and its mechanism of action
Iancu, C. V., Zamoon, J., Woo, S. B., Aleshin, A. E., & Choe, J. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1311485110 · Cited by 132
The permeability of plant protoplasts to non-electrolytes
Collander, R. (1937) · Transactions of the Faraday Society · doi:10.1039/tf9373300985 · Cited by 127
Kumar, H., Kasho, V. N., Смирнова, И. Н., Finer-Moore, J. S., Kaback, H. R., & Stroud, R. M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1324141111 · Cited by 126
Regulation of the human Na+-dependent glucose cotransporter hSGLT2
Ghezzi, C., & Wright, E. M. (2012) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00115.2012 · Cited by 124
Targeting of GLUT6 (formerly GLUT9) and GLUT8 in rat adipose cells
Lisinski, I., Schürmann, A., Joost, H., Cushman, S. W., & Al‐Hasani, H. (2001) · Biochemical Journal · doi:10.1042/0264-6021:3580517 · Cited by 123
The phospholipid requirement for activity of the lactose carrier of Escherichia coli.
Chen, C. C., & Wilson, T. H. (1984) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)90942-7 · Cited by 121
Optical sensors for monitoring dynamic changes of intracellular metabolite levels in mammalian cells
Hou, B., Takanaga, H., Großmann, G., Chen, L., Qu, X.-Q., Jones, A. M., Lalonde, S., Schweissgut, O., Wiechert, W., & Frommer, W. B. (2011) · Nature Protocols · doi:10.1038/nprot.2011.392 · Cited by 117
Self-citationFunctional architecture of MFS d -glucose transporters
Madej, M. G., Sun, L., Yan, N., & Kaback, H. R. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1400336111 · Cited by 115
Robertson, D. E., Kaczorowski, G. J., García, M. L., & Kaback, H. R. (1980) · Biochemistry · doi:10.1021/bi00566a005 · Cited by 115
The Alternating Access Transport Mechanism in LacY
Kaback, H. R., Смирнова, И. Н., Kasho, V. N., Nie, Y., & Zhou, Y. (2010) · The Journal of Membrane Biology · doi:10.1007/s00232-010-9327-5 · Cited by 114
Manolescu, A. R., Augustin, R., Moley, K. H., & Cheeseman, C. I. (2007) · Molecular Membrane Biology · doi:10.1080/09687680701298143 · Cited by 112
Topology of polytopic membrane protein subdomains is dictated by membrane phospholipid composition
Wang, X., Bogdanov, M. V., & Dowhan, W. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf571 · Cited by 110
GLUT4 translocation: The last 200 nanometers
Watson, R. T., & Pessin, J. E. (2007) · Cellular Signalling · doi:10.1016/j.cellsig.2007.06.003 · Cited by 109
GLUT‐1 glucose transporters in the blood–brain barrier: Differential phosphorylation
Devraj, K., Klinger, M., Myers, R. L., Mokashi, A. S., Hawkins, R. A., & Simpson, I. A. (2011) · Journal of Neuroscience Research · doi:10.1002/jnr.22738 · Cited by 104
Dutrochet, H. (1824) · Baillière eBooks · doi:10.5962/bhl.title.117365 · Cited by 102
LEWIS, D. A., & Bisson, L. F. (1991) · Molecular and Cellular Biology · doi:10.1128/mcb.11.7.3804-3813.1991 · Cited by 102
Evolution of ABC transporters by gene duplication and their role in human disease
Moitra, K., & Dean, M. C. (2011) · Biological Chemistry · doi:10.1515/bc.2011.006 · Cited by 96
Boorer, K. J., Loo, D. D. F., & Wright, E. M. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)32008-2 · Cited by 95
Mueckler, M. M., Weng, W., & Kruse, M. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)32026-4 · Cited by 95
Evolutionary mix-and-match with MFS transporters
Madej, M. G., Dang, S., Yan, N., & Kaback, H. R. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1303538110 · Cited by 93
Functioning and Evolutionary Significance of Nutrient Transceptors
Thevelein, J. M., & Voordeckers, K. (2009) · Molecular Biology and Evolution · doi:10.1093/molbev/msp168 · Cited by 92
Experiments on the absorption of organic solutes in the small intestine of rats
Höber, R., & Höber, J. (1937) · Journal of Cellular and Comparative Physiology · doi:10.1002/jcp.1030100402 · Cited by 92
Kusari, J., Verma, U. S., Buse, J. B., Henry, R. R., & Olefsky, J. M. (1991) · Journal of Clinical Investigation · doi:10.1172/jci115437 · Cited by 90
Chaptal, V., Kwon, S., Sawaya, M. R., Guan, L., Kaback, H. R., & Abramson, J. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1105687108 · Cited by 90
Crystal structure of a phosphorylation-coupled saccharide transporter
Cao, Y., Jin, X., Levin, E. J., Huang, H., Zong, Y., Quick, M., Weng, J., Pan, Y., Love, J. D., Punta, M., et al. (2011) · Nature · doi:10.1038/nature09939 · Cited by 86
Dynamic imaging of glucose flux impedance using FRET sensors in wild-type Arabidopsis plants
Chaudhuri, B., Hörmann, F., & Frommer, W. B. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/erq444 · Cited by 83
Self-citationThe GLUT5 hexose transporter is also localized to the basolateral membrane of the human jejunum
Blakemore, S. J., Aledo, J. C., James, J. L., Campbell, F. C., Lucocq, J. M., & Hundal, H. S. (1995) · Biochemical Journal · doi:10.1042/bj3090007 · Cited by 82
Role of sodium‐glucose transporters in glucose uptake of the intestine and kidney
Harada, N., & Inagaki, N. (2012) · Journal of Diabetes Investigation · doi:10.1111/j.2040-1124.2012.00227.x · Cited by 81
LEWIS, D. A., & Bisson, L. F. (1991) · Molecular and Cellular Biology · doi:10.1128/mcb.11.7.3804 · Cited by 78
Saier, M. H., Hvorup, R. N., & Barabote, R. D. (2005) · Biochemical Society Transactions · doi:10.1042/bst0330220 · Cited by 76
LA GALACTOSIDE-PERMÉASE D'ESCHERICHIA COLI
Rickenberg, H. V., Cohen, G. N., Buttin, G., & Monod, J. (1978) · Elsevier eBooks · doi:10.1016/b978-0-12-460482-7.50032-4 · Cited by 76
Stokes, A. J., Wakano, C., del Carmen, K. A., Koblan‐Huberson, M., & Turner, H. C. (2004) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20331 · Cited by 75
Lee, J., Lee, H.-K., Kim, J., Lee, S., Kim, D. H., Kim, S., & Hwang, I. (2011) · The Plant Cell · doi:10.1105/tpc.110.082230 · Cited by 74
Characterization of the active hexose transport system of chlorella vulgaris
Komor, E., & Tanner, W. (1971) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(71)90314-2 · Cited by 73
Self-citationHo, C.-H., & Frommer, W. B. (2014) · eLife · doi:10.7554/elife.01917 · Cited by 73
Self-citationXin, B., & Wang, H. (2010) · Clinical Genetics · doi:10.1111/j.1399-0004.2010.01440.x · Cited by 69
A Single Amino Acid Change Converts the Sugar Sensor SGLT3 into a Sugar Transporter
Bianchi, L. K., & Dı́ez-Sampedro, A. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010241 · Cited by 69
Clore, G. M., & Venditti, V. (2013) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2013.08.003 · Cited by 69
Structural insight into the PTS sugar transporter EIIC
McCoy, J. G., Levin, E. J., & Zhou, M. (2014) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2014.03.013 · Cited by 67
Facilitative plasma membrane transporters function during ER transit
Takanaga, H., & Frommer, W. B. (2010) · The FASEB Journal · doi:10.1096/fj.09-146472 · Cited by 66
Self-citationRegulation of transport across cell membranes by the serum- and glucocorticoid-inducible kinase SGK1
Lang, F., Stournaras, C., & Alesutan, I. (2014) · Molecular Membrane Biology · doi:10.3109/09687688.2013.874598 · Cited by 66
A possible mechanistic role of the membrane potential in proton—sugar cotransport of Chlorella
Schwab, W. G., & Komor, E. (1978) · FEBS Letters · doi:10.1016/0014-5793(78)80156-2 · Cited by 65
Cloning and functional characterization of the mouse fructose transporter, GLUT5
Corpe, C. P., Bovelander, F. J., Munoz, C. M., Hoekstra, J. H., Simpson, I. A., Kwon, O., Levine, M., & Burant, C. (2002) · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · doi:10.1016/s0167-4781(02)00284-1 · Cited by 64
Crystal structure of a bacterial homologue of SWEET transporters
Wang, J., Yan, C., Li, Y., Hirata, K., Yamamoto, M., Yan, N., & Hu, Q. (2014) · Cell Research · doi:10.1038/cr.2014.144 · Cited by 64
Imaging of glutamate in brain slices using FRET sensors
Dulla, C. G., Tani, H., Okumoto, S., Frommer, W. B., Reimer, R. J., & Huguenard, J. R. (2007) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2007.10.017 · Cited by 63
Self-citationResidues in the H+ Translocation Site Define the pKa for Sugar Binding to LacY
Смирнова, И. Н., Kasho, V. N., Sugihara, J., Choe, J., & Kaback, H. R. (2009) · Biochemistry · doi:10.1021/bi9011918 · Cited by 62
The β-galactoside permease ofEscherichia coli
Képès, A. (1971) · The Journal of Membrane Biology · doi:10.1007/bf02431964 · Cited by 61
Binding affinity of lactose permease is not altered by the H + electrochemical gradient
Guan, L., & Kaback, H. R. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0404936101 · Cited by 60
Kojima, I., Nakagawa, Y. S., Ohtsu, Y., Medina, A., & Nagasawa, M. (2014) · Endocrinology and Metabolism · doi:10.3803/enm.2014.29.1.12 · Cited by 59
The effect of intracellular pH on the rate of hexose uptake in Chlorella
Komor, E., Schwab, W. G. W., & Tanner, W. (1979) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(79)90406-1 · Cited by 58
Self-citationThe Active Hexose‐Uptake System of Chlorella vulgaris
Komor, E., Haass, D., Komor, B., & Tanner, W. (1973) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1973.tb03117.x · Cited by 56
Self-citationFluorescent sensors reporting the activity of ammonium transceptors in live cells
Michele, R. D., Ast, C., Loqué, D., Ho, C.-H., Andrade, S. L. A., Lanquar, V., Großmann, G., Gehne, S., Kumke, M. U., & Frommer, W. B. (2013) · eLife · doi:10.7554/elife.00800 · Cited by 55
Self-citationThe specificity of sugar transport by hamster intestine
Wilson, T. H., & Crane, R. K. (1958) · Biochimica et Biophysica Acta · doi:10.1016/0006-3002(58)90142-2 · Cited by 54
Conformational Dynamics of hSGLT1 during Na+/Glucose Cotransport
Loo, D. D. F., Hirayama, B. A., Karakossian, M. H., Meinild, A., & Wright, E. M. (2006) · The Journal of General Physiology · doi:10.1085/jgp.200609643 · Cited by 52
Yu, L., Lv, J., Zhou, S., Zhu, L., Hou, P., & Zhang, H. (2010) · Human Genetics · doi:10.1007/s00439-010-0927-z · Cited by 52
Respiratory increase and active hexose uptake of Chlorella vulgaris
DECKER, M. (1972) · Biochimica et Biophysica Acta · doi:10.1016/0006-3002(72)90009-1 · Cited by 50
Cloning and Characterization of a Novel Na+-dependent Glucose Transporter (NaGLT1) in Rat Kidney
Horiba, N., Masuda, S., Takeuchi, A., Takeuchi, D., Okuda, M., & Inui, K. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m212240200 · Cited by 50
RGA protein associates with a TRPV ion channel during biosynthesis and trafficking
Barnhill, J. C., Stokes, A. J., Koblan‐Huberson, M., Shimoda, L. M. N., Muraguchi, A., Adra, C. N., & Turner, H. C. (2004) · Journal of Cellular Biochemistry · doi:10.1002/jcb.10775 · Cited by 50
Sequence Determinants of GLUT1 Oligomerization
Zutter, J. K. D., Levine, K. B., Deng, D., & Carruthers, A. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.469023 · Cited by 44
The rate of absorption of a mixture of glucose and galactose.
Cori, C. F. (1926) · Experimental Biology and Medicine · doi:10.3181/00379727-23-2940 · Cited by 44
Daniel, E. D., Cheng, L., Maycox, P. R., & Mudge, A. W. (2006) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2006.01.015 · Cited by 35
Gene expression signature of chronic lymphocytic leukaemia with Trisomy 12
Porpaczy, E. A., Bilban, M., Heinze, G., Gruber, M., Vanura, K., Schwarzinger, I., Stilgenbauer, S., Streubel, B., Fonatsch, C., & Jaeger, U. (2009) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.2009.02146.x · Cited by 35
Widmer, M., Uldry, M., & Thorens, B. (2005) · Endocrinology · doi:10.1210/en.2005-0668 · Cited by 30
The Plasma Membrane, with Notes on the History of Botany
Smith, H. W. (1962) · Circulation · doi:10.1161/01.cir.26.5.987 · Cited by 28
Na+‐dependent fructose transport via rNaGLT1 in rat kidney
Horiba, N., Masuda, S., Ohnishi, C., Takeuchi, D., Okuda, M., & Inui, K. (2003) · FEBS Letters · doi:10.1016/s0014-5793(03)00600-8 · Cited by 27
Lin, W., Chuang, L., Chen, C. H., Yeh, J., Hsieh, P. S., Cheng, C.-H., & Chen, Y. (2006) · Diabetologia · doi:10.1007/s00125-006-0218-3 · Cited by 27
Tagoh, H., Kishi, H., & Muraguchi, A. (1996) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1996.0667 · Cited by 27
Komor, E., Loos, E., & Tanner, W. (1973) · The Journal of Membrane Biology · doi:10.1007/bf01869993 · Cited by 27
Self-citationKm mutants of the Chlorella monosaccharide/H+ cotransporter randomly generated by PCR.
Will, A., Caspari, T., & Tanner, W. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.21.10163 · Cited by 26
Self-citationKomor, B., Komor, E., & Tanner, W. (1974) · The Journal of Membrane Biology · doi:10.1007/bf01870184 · Cited by 24
Self-citationLi, J., & Tajkhorshid, E. (2011) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2011.09.011 · Cited by 24
Ernest Overton's Contribution to the Cell Membrane Concept: A Centennial Appreciation
Kleinzeller, A. (1997) · Physiology · doi:10.1152/physiologyonline.1997.12.1.49 · Cited by 24
SLC5 and SLC2 Transporters in Epithelia—Cellular Role and Molecular Mechanisms
Raja, M., Puntheeranurak, T., Hinterdorfer, P., & Kinne, R. K. H. (2012) · Current topics in membranes · doi:10.1016/b978-0-12-394316-3.00002-8 · Cited by 20
Differential regulation of glucose transport activity in yeast by specific cAMP signatures
Bermejo, C., Haerizadeh, F., Sadoine, M., Chermak, D., & Frommer, W. B. (2013) · Biochemical Journal · doi:10.1042/bj20121736 · Cited by 18
Self-citationThe Life and Times of Lac Permease: Crystals Ain’t Everything, but They Certainly Do Help
Madej, M. G., & Kaback, H. R. (2014) · Springer series in biophysics · doi:10.1007/978-3-642-53839-1_6 · Cited by 17
Metabolic sensor AMPK directly phosphorylates RAG1 protein and regulates V(D)J recombination
Um, J., Brown, A. L., Singh, S. K., Chen, Y., Guček, M., Lee, B.-S., Luckey, M. A., Kim, M. K., Park, J., Sleckman, B. P., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1307928110 · Cited by 17
Friedel, S., Antwerpen, B., HOCH, A., VOGEL, C., Grassl, W., Geller, F., Hebebrand, J., & Hinney, A. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb04316.x · Cited by 16
Neundlinger, I., Puntheeranurak, T., Wildling, L., Rankl, C., Wang, L., Gruber, H. J., Kinne, R. K.-H., & Hinterdorfer, P. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.529875 · Cited by 16
Eddy, A. A., Seaston, A., Gardner, D., & Hacking, C. (1980) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1980.tb47194.x · Cited by 15
The interaction between electron transfer, proton motive force and solute transport in bacteria
Konings, W. N., Hellingwerf, K. J., & Elferink, M. G. L. (1984) · Antonie van Leeuwenhoek · doi:10.1007/bf02386225 · Cited by 14
Zambon, A., Zoso, A., Luni, C., Frommer, W. B., & Elvassore, N. (2013) · Integrative Biology · doi:10.1039/c3ib40204e · Cited by 14
Self-citation(1961) · Nature · doi:10.1038/189629b0 · Cited by 14
The restrictions on possible mechanisms of intestinal transport of sugars
Crane, R. K. (1961) · Medical Entomology and Zoology · Cited by 14
Fingerprints of hSGLT5 sugar and cation selectivity
Ghezzi, C., Gorraitz, E., Hirayama, B. A., Loo, D. D. F., Grempler, R., Mayoux, E., & Wright, E. M. (2014) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00027.2014 · Cited by 10
Observations on an oligodynamic action of copper on human erythrocytes.
JACOBS, M. H., & STEWART, D. R. (1946) · PubMed · Cited by 9
Research works printed but not linked: 13
- Crane RK, 1965, Fed. Proc., 24, 1000
- Rickenberg HV, 1956, Ann. Inst. Pasteur, 91, 829
- Dutrochet BJH, 1824, Recherches anatomiques et physiologiques sur la structure intime des animaux et des végétaux
- Nägeli C, 1855, Pflanzenphysiologische Untersuchungen, Heft 1
- Kleinzeller A, 1997, News Physiol. Sci., 12, 49
- Overton E, 1895, Vierteljahr. Naturforsch. Ges. Zürich, 40, 159
- Jacobs MH, 1946, Am. J. Med. Sci., 211, 246
- Mitchell P, 1963, Biochem. Soc. Symp., 22, 142
- Maier A, 2002, FEMS Yeast Res., 2, 539
- 10.7554/eLife.00800 · DOI
- Zambon A, 2014, Integr. Biol. Quant. Biosci. Nano Macro, 6, 277
- 10.1073/pnas.1105687108 · DOI
- Fanconi G, 1949, Helv. Paediatr. Acta, 4, 359
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Metadata
- Authors
- Chen, L.-Q., Cheung, L. S., Feng, L., Tanner, W., & Frommer, W. B.
- Affiliations
- Carnegie Institution for Science (US)
- Stanford Medicine (US)
- University of Regensburg (DE)
- Venue
- Annual Review of Biochemistry
- Publisher
- Annual Reviews
- Published
- 2015-06-02
- Volume
- 84
- Issue
- 1
- Pages
- 865-894
- ISSN
- 0066-4154 (ISSN-L)
- 1545-4509
- OpenAlex
- W2116269912
- Cited by
- 507
- References
- 195
- Citations by year
- 2026: 33 · 2025: 64 · 2024: 64 · 2023: 56 · 2022: 68 · 2021: 51 · 2020: 36 · 2019: 37 · 2018: 30 · 2017: 39 · 2016: 19 · 2015: 10
- FWCI
- 3.39
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Annual Review of Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- University of Regensburg Publication Server (University of Regensburg) (submittedVersion)
- Funders
- National Science Foundation (1401855, 1258018)
- U.S. Department of Energy (DE‐FG02‐, FG02-04ER15542, DEFG0204ER15542)
- Bill and Melinda Gates Foundation (OPP1068450)
- Alfred P. Sloan Foundation
- Office of Science
- Basic Energy Sciences (DE-FG02-04ER15542, DE-FG02)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant nutrient uptake and metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion Transport and Channel Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- sugar transport, sugar transporters, glucose transporters, sodium-glucose cotransporter, sweets, sucrose transport, osmolytes, energy storage, diabetes mellitus, crop yield, pathogen susceptibility
- MeSH terms
- Animals, Biological Transport, Carbohydrates, Humans, Plants, Membrane Transport Proteins, Excitatory Amino Acid Transporter 2, Carbohydrate Metabolism, Plant Cells
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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