Relevant bibliographies by topics / GluTR

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'GluTR'

Author: Grafiati
Published: 4 June 2021
Last updated: 8 February 2022

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Journal articles on the topic "GluTR"

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Stuart, Charles A., Deling Yin, Mary E. A. Howell, Rhesa J. Dykes, John J. Laffan, and Arny A. Ferrando. "Hexose transporter mRNAs for GLUT4, GLUT5, and GLUT12 predominate in human muscle." American Journal of Physiology-Endocrinology and Metabolism 291, no. 5 (2006): E1067—E1073. http://dx.doi.org/10.1152/ajpendo.00250.2006.

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In the past few years, 8 additional members of the facilitative hexose transporter family have been identified, giving a total of 14 members of the SLC2A family of membrane-bound hexose transporters. To determine which of the new hexose transporters were expressed in muscle, mRNA concentrations of 11 glucose transporters (GLUTs) were quantified and compared. RNA from muscle from 10 normal volunteers was subjected to RT-PCR. Primers were designed that amplified 78- to 241-base fragments, and cDNA standards were cloned for GLUT1, GLUT2, GLUT3, GLUT4, GLUT5, GLUT6, GLUT8, GLUT9, GLUT10, GLUT11, G
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Inukai, Kouichi, Annette M. Shewan, Wendy S. Pascoe, Shigehiro Katayama, David E. James, and Yoshitomo Oka. "Carboxy Terminus of Glucose Transporter 3 Contains an Apical Membrane Targeting Domain." Molecular Endocrinology 18, no. 2 (2004): 339–49. http://dx.doi.org/10.1210/me.2003-0089.

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Abstract We previously demonstrated that distinct facilitative glucose transporter isoforms display differential sorting in polarized epithelial cells. In Madin-Darby canine kidney (MDCK) cells, glucose transporter 1 and 2 (GLUT1 and GLUT2) are localized to the basolateral cell surface whereas GLUTs 3 and 5 are targeted to the apical membrane. To explore the molecular mechanisms underlying this asymmetric distribution, we analyzed the targeting of chimeric glucose transporter proteins in MDCK cells. Replacement of the carboxy-terminal cytosolic tail of GLUT1, GLUT2, or GLUT4 with that from GLU
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Pyla, Rajkumar, Ninu Poulose, John Y. Jun, and Lakshman Segar. "Expression of conventional and novel glucose transporters, GLUT1, -9, -10, and -12, in vascular smooth muscle cells." American Journal of Physiology-Cell Physiology 304, no. 6 (2013): C574—C589. http://dx.doi.org/10.1152/ajpcell.00275.2012.

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Intimal hyperplasia is characterized by exaggerated proliferation of vascular smooth muscle cells (VSMCs). Enhanced VSMC growth is dependent on increased glucose uptake and metabolism. Facilitative glucose transporters (GLUTs) are comprised of conventional GLUT isoforms (GLUT1–5) and novel GLUT isoforms (GLUT6–14). Previous studies demonstrate that GLUT1 overexpression or GLUT10 downregulation contribute to phenotypic changes in VSMCs. To date, the expression profile of all 14 GLUT isoforms has not been fully examined in VSMCs. Using the proliferative and differentiated phenotypes of human aor
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Ali, Raafay S., Morag F. Dick, Saad Muhammad, et al. "Glucose transporter expression and regulation following a fast in the ruby-throated hummingbird, Archilochus colubris." Journal of Experimental Biology 223, no. 20 (2020): jeb229989. http://dx.doi.org/10.1242/jeb.229989.

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ABSTRACTHummingbirds, subsisting almost exclusively on nectar sugar, face extreme challenges to blood sugar regulation. The capacity for transmembrane sugar transport is mediated by the activity of facilitative glucose transporters (GLUTs) and their localisation to the plasma membrane (PM). In this study, we determined the relative protein abundance of GLUT1, GLUT2, GLUT3 and GLUT5 via immunoblot using custom-designed antibodies in whole-tissue homogenates and PM fractions of flight muscle, heart and liver of ruby-throated hummingbirds (Archilochus colubris). The GLUTs examined were detected i
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Rayner, D. V., Moira E. A. Thomas, and Paul Trayhurn. "Glucose transporters (GLUTs 1–4) and their mRNAs in regions of the rat brain: insulin-sensitive transporter expression in the cerebellum." Canadian Journal of Physiology and Pharmacology 72, no. 5 (1994): 476–79. http://dx.doi.org/10.1139/y94-069.

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Major regions of the rat brain have been examined for the presence of glucose transporters (GLUTs 1–4) and their mRNAs. Both the mRNA and immunoreactive protein for GLUT1 and GLUT3 were found in each brain region (medulla, pons, cerebellum, midbrain, hypothalamus, thalamus, hippocampus, parietal cortex). The mRNA and protein for GLUT4 were identified in the cerebellum, but not elsewhere in the brain. GLUT2 protein and mRNA were not detected in any region of the brain. Although GLUT1 and GLUT3 are the major brain glucose transporters, the presence of GLUT4 in the cerebellum suggests that insuli
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LISINSKI, Ivonne, Annette SCHÜRMANN, Hans-Georg JOOST, Samuel W. CUSHMAN, and Hadi AL-HASANI. "Targeting of GLUT6 (formerly GLUT9) and GLUT8 in rat adipose cells." Biochemical Journal 358, no. 2 (2001): 517–22. http://dx.doi.org/10.1042/bj3580517.

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The subcellular targeting of the two recently cloned novel mammalian glucose transporters, GLUT6 {previously referred to as GLUT9 [Doege, Bocianski, Joost and Schürmann (2000) Biochem. J. 350, 771–776]} and GLUT8, was analysed by expression of haemagglutinin (HA)-epitope-tagged GLUTs in transiently transfected primary rat adipose cells. Similar to HA-GLUT4, both transporters, HA-GLUT6 and HA-GLUT8, were retained in intracellular compartments in non-stimulated cells. In contrast, mutation of the N-terminal dileucine motifs in both constructs led to constitutive expression of the proteins on the
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Chin, Edward, A. Musa Zamah, Daniel Landau, et al. "Changes in Facilitative Glucose Transporter Messenger Ribonucleic Acid Levels in the Diabetic Rat Kidney*." Endocrinology 138, no. 3 (1997): 1267–75. http://dx.doi.org/10.1210/endo.138.3.5015.

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Abstract Facilitative glucose transporter (GLUTs 1, 2, 4, and 5) messenger RNAs (mRNAs) are differentially distributed in the rat nephron: GLUT1 is widely expressed, GLUT4 is selectively concentrated in thick ascending limbs, and GLUT2 and 5 are exclusively localized in proximal tubules, consistent with differential roles for these transporters in renal glucose handling. In the present study, quantitative in situ hybridization was used to evaluate changes in these mRNA levels during acute (2 and 7 days) and chronic (30, 90, and 180 days) streptozotocin-induced diabetes mellitus (STZ-DM). Medul
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Zhang, Shihai, Qing Yang, Man Ren, et al. "Effects of isoleucine on glucose uptake through the enhancement of muscular membrane concentrations of GLUT1 and GLUT4 and intestinal membrane concentrations of Na+/glucose co-transporter 1 (SGLT-1) and GLUT2." British Journal of Nutrition 116, no. 4 (2016): 593–602. http://dx.doi.org/10.1017/s0007114516002439.

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AbstractKnowledge of regulation of glucose transport contributes to our understanding of whole-body glucose homoeostasis and human metabolic diseases. Isoleucine has been reported to participate in regulation of glucose levels in many studies; therefore, this study was designed to examine the effect of isoleucine on intestinal and muscular GLUT expressions. In an animal experiment, muscular GLUT and intestinal GLUT were determined in weaning pigs fed control or isoleucine-supplemented diets. Supplementation of isoleucine in the diet significantly increased piglet average daily gain, enhanced G
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Navarrete Santos, Anne, Sarah Tonack, Michaela Kirstein, Silke Kietz, and Bernd Fischer. "Two insulin-responsive glucose transporter isoforms and the insulin receptor are developmentally expressed in rabbit preimplantation embryos." Reproduction 128, no. 5 (2004): 503–16. http://dx.doi.org/10.1530/rep.1.00203.

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Glucose is the most important energy substrate for mammalian blastocysts. Its uptake is mediated by glucose transporters (GLUT). In muscle and adipocyte cells insulin stimulates glucose uptake by activation of the insulin receptor (IR) pathway and translocation of GLUT4. GLUT4 is expressed in bovine preimplantation embryos. A new insulin-responsive isoform, GLUT8, was recently described in mouse blastocysts. Thus, potentially, two insulin-responsive isoforms are expressed in early embryos. The mechanism of insulin action on embryonic cells, however, is still not clear. In the present study exp
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Dominguez, J. H., K. Camp, L. Maianu, and W. T. Garvey. "Glucose transporters of rat proximal tubule: differential expression and subcellular distribution." American Journal of Physiology-Renal Physiology 262, no. 5 (1992): F807—F812. http://dx.doi.org/10.1152/ajprenal.1992.262.5.f807.

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In the late proximal tubule, glucose reabsorption progressively lowers the concentration of luminal glucose, and concentrative glucose influx increases to ensure complete glucose reabsorption. The change in glucose influx is effected by luminal Na(+)-dependent glucose transporters (Na(+)-GLUT), which exhibit higher Na(+)-to-glucose stoichiometric ratios in the late proximal tubule. In this work, the corresponding changes in the axial distribution of basolateral glucose efflux transporters (GLUTs) were examined. mRNAs encoding high-affinity facilitative basolateral transporter GLUT1, low-affini
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Dissertations / Theses on the topic "GluTR"

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Sandrin, Gauer Julia. "Effect of polyphenols on sugar transport by human GLUT2, GLUT5 and GLUT7." Thesis, University of Leeds, 2017. http://etheses.whiterose.ac.uk/18935/.

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Background: High dietary sugar intake is controversially associated with an increase in prevalence of type 2 diabetes globally. This has been attributed to the impact that sugars have in the development of disease risk factors linked to diabetes, cardiovascular disease and others. (Poly)phenols present in our daily diet may affect these processes by multiple mechanisms, including effects on the digestion, uptake and post-prandial distribution of glucose and fructose. Aim: Study the expression of GLUT7 in Caco-2/TC7 intestinal cells and identify novel inhibitors of sugar transporters by determi
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Apitz, Janina. "Charakterisierung von Arabidopsis HEMA-Mutanten und in vivo-Analyse funktioneller Domänen der pflanzlichen Glutamyl-tRNA-Reduktasen." Doctoral thesis, Humboldt-Universität zu Berlin, Lebenswissenschaftliche Fakultät, 2016. http://dx.doi.org/10.18452/17527.

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Die Tetrapyrrolbiosynthese (TBS) führt zu wichtigen Endprodukten wie Häm und Chlorophyll. Das gemeinsame Vorstufenmolekül aller Tetrapyrrole ist die 5-Aminolävulinsäure (ALA), die in Pflanzen über den C5-Weg aus Glutamat synthetisiert wird. Das erste spezifische Enzym der ALA-Synthese und somit auch der TBS ist die Glutamyl-tRNA Reduktase (GluTR). Sie unterliegt als Schlüsselenzym einer strengen Regulation. Aufgrund der unterschiedlichen Expression der HEMA-Gene in Arabidopsis wird ein differenzieller Beitrag der GluTR-Isoformen zu den Endprodukten der TBS vermutet. Analysen von knockout-Muta
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Marín, Juez Rubén. "Studies on the function and regulation of glucose transporters GLUT2 and GLUT4 in teleost fish / Estudios sobre la función y regulación de los transportadores de glucosa GLUT2 y GLUT4 en peces teleósteos." Doctoral thesis, Universitat de Barcelona, 2012. http://hdl.handle.net/10803/104147.

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The aim of this thesis was to study the function and regulation of two of the major players in the carbohydrate metabolism regulated by insulin, the facilitative glucose transporters GLUT2 and GLUT4, in teleost fish. In order to investigate the role of factors exerting a control on the transcription of the GLUT4 gene, we cloned the GLUT4 promoter in Fugu. The 5 ́-flanking region of the Fugu GLUT4 gene showed similar features to that in mammals. Structurally, comparative analysis between the cloned promoter sequence and that of other fish promoters revealed a high degree of conservation amo
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Marin, Juez Rubén. "Studies on the function and regulation of glucose transporters GLUT2 and GLUT4 in teleost fish / Estudios sobre la función y regulación de los transportadores de glucosa GLUT2 y GLUT4 en peces teleósteos." Doctoral thesis, Universitat de Barcelona, 2012. http://hdl.handle.net/10803/104147.

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The aim of this thesis was to study the function and regulation of two of the major players in the carbohydrate metabolism regulated by insulin, the facilitative glucose transporters GLUT2 and GLUT4, in teleost fish. In order to investigate the role of factors exerting a control on the transcription of the GLUT4 gene, we cloned the GLUT4 promoter in Fugu. The 5 ́-flanking region of the Fugu GLUT4 gene showed similar features to that in mammals. Structurally, comparative analysis between the cloned promoter sequence and that of other fish promoters revealed a high degree of conservation among
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Becker, Christoph. "Subzelluläre Kompartimentierungen und Trafficking der Glucosetransporter GLUT4 und GLUT1 in isolierten Herzmuskelzellen adulter Ratten /." Aachen : Mainz, 2000. http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&doc_number=009382963&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA.

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Yang, Jing. "Studies on subcellular trafficking of glucose transporters-GLUT1 and GLUT4 in 3T3-L1 cells." Thesis, University of Bath, 1993. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.357945.

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Yamamoto, Yuji. "Constitutively Active Mitogen-Activated Protein Kinase Kinase Increases GLUT1 Expression and Recruits Both GLUT1 and GLUT4 at the Cell Surface in 3T3-L1 Adipocytes." Kyoto University, 2001. http://hdl.handle.net/2433/150590.

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Sireesha, Dommaraju. "An Investigation of the Nano-Organization of Glucose Transporters, Glut1 and Glut3, in the Mammalian Plasma Membrane." Thesis, University of Skövde, School of Life Sciences, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-2330.

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<p>Glucose is a monosaccharide and fuel for body, it cannot pass through membrane by simple diffusion so, integral transmembrane proteins named glucose transporters (Gluts) are involved in the regulation of the movement of glucose between the extracellular and intracellular spaces within the body. GLUT1 and GLUT3 have previously been shown by cold detergent extraction methods to reside in distinct plasma membrane domains in non-polarized mammalian cells, with GLUT1, but not GLUT3, residing  in detergent-resistant membrane (DRM) domains. To confirm this observation under less invasive condition
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Ximenes, da Silva Adriana. "Métabolisme énergétique cérébral : effet d'une déficience en acides gras polyinsaturés." Paris 6, 2001. http://www.theses.fr/2001PA066493.

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HAINAULT, ISABELLE. "Regulation differentielle de l'expression des transporteurs de glucose glut1 et glut4 dans les adipocytes du jeune rat zucker obese et dans les adipocytes 3t3-f442a." Paris 7, 1994. http://www.theses.fr/1994PA077148.

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Nous avons etudie l'expression des genes et des proteines de glut1 et glut4 dans l'adipocyte du jeune rat zucker obese. A 30 jours, l'augementation du transport insulinostimule est uniquement attribuable a une augmentation de l'expression de glut4, glut1 etant inchange. L'augmentation des arnm de glut4 dans le tissu adipeux de rats obeses suggere une regulation a un niveau pretraductionnel. Chez le raton de 16 jours, normoinsulinemique, on observe deja une surexpression specifique du gene glut4 mais avec une amplitude moindre. Par contre, le contenu en arnm de glut4 dans le muscle n'est pas af
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Books on the topic "GluTR"

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Davidson, Susan. Robert Rauschenberg: Gluts. Guggenheim Museum Publications, 2009.

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Rauschenberg, Robert. Robert Rauschenberg: Gluts. Galerie Isy Brachot, 1988.

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Asefaw, Senai. Stimulation of myocardial AMP-activated protein kinase by AICAR increases cardiac glucose uptake and causes GLUT4 and GLUT1 translocation in vivo. s.n.], 1999.

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A glut of plums. Merehurst, 1988.

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Ritzel, Ulrich. Die schwarzen Ränder der Glut. Libelle, 2001.

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Glut und Asche: Eine Liebesgeschichte. Knaus, 1985.

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Struck, Karin. Glut und Asche: Eine Liebesgeschichte. Albrecht Knaus, 1985.

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Carr, Ann. A glut of apples & pears. Merehurst Press, 1988.

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Landrum, Roger. Flexo folder gluer: Maintenance and calibration procedures. TAPPI press, 1996.

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Hoffbauer, Jochen. Glut aus der Asche: Schlesische Erzahlungen. Husum-Druck, 1987.

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Book chapters on the topic "GluTR"

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Wagner, Peter, Frank C. Mooren, Hidde J. Haisma, et al. "GLUT4." In Encyclopedia of Exercise Medicine in Health and Disease. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-540-29807-6_2444.

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Ohtsubo, Kazuaki. "GLUT2." In Glycoscience: Biology and Medicine. Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54836-2_58-1.

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Deng, Dong, and Nieng Yan. "Crystallization and Structural Determination of the Human Glucose Transporters GLUT1 and GLUT3." In Methods in Molecular Biology. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7507-5_2.

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Vannucci, Susan J., Lisa B. Willing, and Robert C. Vannucci. "Developmental Expression of Glucose Transporters, Glut1 and Glut3, in Postnatal Rat Brain." In Frontiers in Cerebral Vascular Biology. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2920-0_1.

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Defries, Danielle M. "GLUT." In Encyclopedia of Signaling Molecules. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-67199-4_101958.

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Defries, Danielle M. "GLUT." In Encyclopedia of Signaling Molecules. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4614-6438-9_101958-1.

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Maher, Fran, Ian A. Simpson, and Susan J. Vannucci. "Alterations in Brain Glucose Transporter Proteins, Glut1 and Glut3, in Streptozotocin Diabetic Rats." In Frontiers in Cerebral Vascular Biology. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2920-0_2.

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Odrich, Peter. "Winterliche Glut." In Berichte aus dem japanischen Alltag. Birkhäuser Basel, 1987. http://dx.doi.org/10.1007/978-3-0348-6580-7_3.

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Kapsner, Andreas. "Gaps, Gluts and Paraconsistency." In Trends in Logic. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-05206-9_4.

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Timson, David J., Richard J. Reece, James B. Thoden, et al. "Glut-1 Deficiency Syndrome." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_708.

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Conference papers on the topic "GluTR"

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Kocdor, M., H. Kocdor, J. Pereira, J. Vanegas, I. Russo, and J. Russo. "Stage-Specific Expressions of GLUT-1, GLUT-3 and GLUT-12 in Estrogen-Induced Breast Cancer." In Abstracts: Thirty-Second Annual CTRC‐AACR San Antonio Breast Cancer Symposium‐‐ Dec 10‐13, 2009; San Antonio, TX. American Association for Cancer Research, 2009. http://dx.doi.org/10.1158/0008-5472.sabcs-09-5152.

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Silva, Jiviane Beatriz Cunha Barretto, and Ana Paula Dias Demasi. "EXPRESSÃO DE PROTEÍNAS DO METABOLISMO DA GLICOSE NA ERITROPOESE." In I Congresso Brasileiro de Hematologia Clínico-laboratorial On-line. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/629.

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Introdução: Evidências indicam que o metabolismo orienta o destino das células-tronco hematopoéticas entre a auto renovação e a diferenciação. Particularmente para células eritróides, que perdem núcleo e organelas em estágios terminais, a via glicolítica deve ser crucial durante todo o processo de desenvolvimento. As principais proteínas envolvidas nessa via, como o transportador de glicose 1 (Glut1), a enzima glicolítica lactato desidrogenase (LDH) e a enzima reguladora metabólica piruvato desidrogenase quinase 1 (PDK1), podem ser úteis para a avaliação da eritropoese. Objetivos: Verificar a
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PUCCIARELLI, Valentina, Marina CODARI, Chiara INVERNIZZI, et al. "Three-Dimensional Craniofacial Features of Glut1 Deficiency Syndrome Patients." In 6th International Conference on 3D Body Scanning Technologies, Lugano, Switzerland, 27-28 October 2015. Hometrica Consulting - Dr. Nicola D'Apuzzo, 2015. http://dx.doi.org/10.15221/15.061.

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Gehrmann, Sebastian, Hendrik Strobelt, and Alexander Rush. "GLTR: Statistical Detection and Visualization of Generated Text." In Proceedings of the 57th Annual Meeting of the Association for Computational Linguistics: System Demonstrations. Association for Computational Linguistics, 2019. http://dx.doi.org/10.18653/v1/p19-3019.

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Mafakheri, S., R. Flörke, S. Kanngießer, et al. "Regulation of recombinant TBC1D1, the RabGAP involved in GLUT4 translocation." In Diabetes Kongress 2019 – 54. Jahrestagung der DDG. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1688318.

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Wu, Xiangping, Xiaofang Liu, Wenglong Xu, Dandan Yan, and Yongli Chen. "Particle filtering for tracking of GLUT4 vesicles in TIRF microscpy." In Sixth International Symposium on Multispectral Image Processing and Pattern Recognition, edited by Jianguo Liu, Kunio Doi, Aaron Fenster, and S. C. Chan. SPIE, 2009. http://dx.doi.org/10.1117/12.831433.

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Labak, Collin M., Maheedhara R. Guda, Neha Jain, et al. "Abstract 3594: GLUT1 as a metabolic target in glioblastoma therapy." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-3594.

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Labak, Collin M., Maheedhara R. Guda, Neha Jain, et al. "Abstract 3594: GLUT1 as a metabolic target in glioblastoma therapy." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-3594.

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Koester, Anna Magdalena, Gwyn Gould, Godfrey Smith, and Nikolaj Gadegaard. "OP6 Investigating spatio-temporal dynamics of GLUT4 dispersal in cardiomyocytes." In Scottish Cardiovascular Forum – 23rd annual meeting, University of Strathclyde, Saturday 1st February 2020. BMJ Publishing Group Ltd and British Cardiovascular Society, 2020. http://dx.doi.org/10.1136/heartjnl-2020-scf.6.

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Yun, H. S., R. Harris, H. Hong, A. M. K. Choi, H. Stout-Delgado, and S. J. Cho. "GLUT1-Dependent Glycolysis Regulates Exacerbation of Fibrosis Via AIM2 Inflammasome Activation." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a5240.

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Reports on the topic "GluTR"

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Dooley, Michael, David Folkerts-Landau, and Peter Garber. Savings Gluts and Interest Rates: The Missing Link to Europe. National Bureau of Economic Research, 2005. http://dx.doi.org/10.3386/w11520.

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Seybold, Andrew. Mobile Web and Video Clog the Internet; Tablet Glut. Patricia Seybold Group, 2011. http://dx.doi.org/10.1571/psgp01-09-11cc.

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Choi, Horag, Nelson Mark, and Donggyu Sul. Endogenous Discounting, the World Saving Glut and the U.S. Current Account. National Bureau of Economic Research, 2007. http://dx.doi.org/10.3386/w13571.

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Justiniano, Alejandro, Giorgio Primiceri, and Andrea Tambalotti. The Effects of the Saving and Banking Glut on the U.S. Economy. National Bureau of Economic Research, 2013. http://dx.doi.org/10.3386/w19635.

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Mian, Atif, Ludwig Straub, and Amir Sufi. The Saving Glut of the Rich and the Rise in Household Debt. National Bureau of Economic Research, 2020. http://dx.doi.org/10.3386/w26941.

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Chinn, Menzie, and Hiro Ito. Current Account Balances, Financial Development and Institutions: Assaying the World "Savings Glut". National Bureau of Economic Research, 2005. http://dx.doi.org/10.3386/w11761.

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7

Borenstein, Severin, and Ryan Kellogg. The Incidence of an Oil Glut: Who Benefits from Cheap Crude Oil in the Midwest? National Bureau of Economic Research, 2012. http://dx.doi.org/10.3386/w18127.

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Laibson, David, and Johanna Mollerstrom. Capital Flows, Consumption Booms and Asset Bubbles: A Behavioural Alternative to the Savings Glut Hypothesis. National Bureau of Economic Research, 2010. http://dx.doi.org/10.3386/w15759.

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