Glucose Transport and Transporters in the Endomembranes
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G. Bánhegyi | A. Szarka | B. Lizák | Yejin Kim | Kyu-Sung Choi | Csilla E. Németh | P. Marcolongo | A. Benedetti | É. Margittai | C. E. Németh
[1] G. Juhász,et al. Autophagosome-lysosome fusion. , 2020, Journal of molecular biology.
[2] J. Vera,et al. GLUT1 and GLUT8 support lactose synthesis in Golgi of murine mammary epithelial cells , 2019, Journal of Physiology and Biochemistry.
[3] Yoshiro Nakano. Stories of spinster with various faces: from courtship rejection to tumor metastasis rejection , 2019, Journal of neurogenetics.
[4] K. Quinlan,et al. Characterization of Glucose Transporter 6 in Lipopolysaccharide-Induced Bone Marrow–Derived Macrophage Function , 2019, The Journal of Immunology.
[5] G. Bánhegyi,et al. Decreased Nuclear Ascorbate Accumulation Accompanied with Altered Genomic Methylation Pattern in Fibroblasts from Arterial Tortuosity Syndrome Patients , 2019, Oxidative medicine and cellular longevity.
[6] G. Bommer,et al. Failure to eliminate a phosphorylated glucose analog leads to neutropenia in patients with G6PT and G6PC3 deficiency , 2019, Proceedings of the National Academy of Sciences.
[7] Roberto Zoncu,et al. The lysosome as a cellular centre for signalling, metabolism and quality control , 2019, Nature Cell Biology.
[8] H. Kusuhara,et al. GLUT6 is a lysosomal transporter that is regulated by inflammatory stimuli and modulates glycolysis in macrophages , 2018, FEBS letters.
[9] Michael T. Zimmermann,et al. Assessing Human Genetic Variations in Glucose Transporter SLC2A10 and Their Role in Altering Structural and Functional Properties , 2018, Front. Genet..
[10] A. Sun. Lysosomal storage disease overview. , 2018, Annals of translational medicine.
[11] K. Hoehn,et al. Knockout of glucose transporter GLUT6 has minimal effects on whole body metabolic physiology in mice. , 2018, American journal of physiology. Endocrinology and metabolism.
[12] M. Maggiolini,et al. The Physiopathological Role of the Exchangers Belonging to the SLC37 Family , 2018, Front. Chem..
[13] K. Devriendt,et al. Arterial tortuosity syndrome: 40 new families and literature review , 2018, Genetics in Medicine.
[14] B. Scherlag,et al. Dysregulation of insulin-sensitive glucose transporters during insulin resistance-induced atrial fibrillation. , 2017, Biochimica et biophysica acta. Molecular basis of disease.
[15] T. Miyashita,et al. L-leucine and SPNS1 coordinately ameliorate dysfunction of autophagy in mouse and human Niemann-Pick type C disease , 2017, Scientific Reports.
[16] Palaniyandi Ravanan,et al. Autophagy: The spotlight for cellular stress responses. , 2017, Life sciences.
[17] G. Bánhegyi,et al. GLUT10—Lacking in Arterial Tortuosity Syndrome—Is Localized to the Endoplasmic Reticulum of Human Fibroblasts , 2017, International journal of molecular sciences.
[18] Daniel J Klionsky,et al. Autolysosome biogenesis and developmental senescence are regulated by both Spns1 and v-ATPase , 2017, Autophagy.
[19] Yoichi Chiba,et al. Glucose transporter 8 immunoreactivity in astrocytic and microglial cells in subependymal areas of human brains , 2017, Neuroscience Letters.
[20] J. Crowley,et al. SLC2A8 (GLUT8) is a mammalian trehalose transporter required for trehalose-induced autophagy , 2016, Scientific Reports.
[21] R. Gilmore,et al. N-linked glycosylation and homeostasis of the endoplasmic reticulum. , 2016, Current opinion in cell biology.
[22] T. Mészáros,et al. Glucose transporter type 10—lacking in arterial tortuosity syndrome—facilitates dehydroascorbic acid transport , 2016, FEBS letters.
[23] Nieng Yan,et al. GLUT, SGLT, and SWEET: Structural and mechanistic investigations of the glucose transporters , 2016, Protein science : a publication of the Protein Society.
[24] V. Lacombe,et al. Diabetes Alters the Expression and Translocation of the Insulin-Sensitive Glucose Transporters 4 and 8 in the Atria , 2015, PloS one.
[25] M. Ritelli,et al. GLUT10 deficiency leads to oxidative stress and non-canonical αvβ3 integrin-mediated TGFβ signalling associated with extracellular matrix disarray in arterial tortuosity syndrome skin fibroblasts , 2015, Human molecular genetics.
[26] G. Davis,et al. VCP-dependent muscle degeneration is linked to defects in a dynamic tubular lysosomal network in vivo , 2015, eLife.
[27] Lily S. Cheung,et al. Transport of sugars. , 2015, Annual review of biochemistry.
[28] M. Molinari,et al. Glycoprotein maturation and quality control. , 2015, Seminars in Cell and Developmental Biology.
[29] M. Molinari,et al. N-linked sugar-regulated protein folding and quality control in the ER. , 2015, Seminars in cell & developmental biology.
[30] A. Szarka,et al. In silico aided thoughts on mitochondrial vitamin C transport. , 2015, Journal of theoretical biology.
[31] J. Chou,et al. Type I glycogen storage diseases: disorders of the glucose-6-phosphatase/glucose-6-phosphate transporter complexes , 2015, Journal of Inherited Metabolic Disease.
[32] G. Scarano,et al. Arterial Tortuosity Syndrome: homozygosity for two novel and one recurrent SLC2A10 missense mutations in three families with severe cardiopulmonary complications in infancy and a literature review , 2014, BMC Medical Genetics.
[33] J. Lancaster,et al. Metabolic vulnerabilities in endometrial cancer. , 2014, Cancer research.
[34] G. Bánhegyi,et al. Subcellular compartmentation of ascorbate and its variation in disease states. , 2014, Biochimica et biophysica acta.
[35] Jenn-Kang Hwang,et al. CELLO2GO: A Web Server for Protein subCELlular LOcalization Prediction with Functional Gene Ontology Annotation , 2014, PloS one.
[36] Chih-Wen Che,et al. CELLO2GO: A Web Server for Protein subCELlular LOcalization Prediction with Functional Gene Ontology Annotation , 2014 .
[37] D. Klionsky,et al. Aberrant Autolysosomal Regulation Is Linked to The Induction of Embryonic Senescence: Differential Roles of Beclin 1 and p53 in Vertebrate Spns1 Deficiency , 2014, PLoS genetics.
[38] J. Vera,et al. Mitochondrial ascorbic acid transport is mediated by a low-affinity form of the sodium-coupled ascorbic acid transporter-2. , 2014, Free radical biology & medicine.
[39] J. Chou,et al. PHAGOCYTES , GRANULOCYTES , AND MYELOPOIESIS Molecular mechanisms of neutrophil dysfunction in glycogen storage disease type Ib , 2014 .
[40] K. Moley,et al. Glucose Transporter 8 (GLUT8) Mediates Fructose-induced de Novo Lipogenesis and Macrosteatosis* , 2014, The Journal of Biological Chemistry.
[41] J. Chou,et al. The SLC37 family of sugar-phosphate/phosphate exchangers. , 2014, Current topics in membranes.
[42] Mohammad M. Karimi,et al. Vitamin C induces Tet-dependent DNA demethylation and a blastocyst-like state in ES cells , 2013, Nature.
[43] William A. Pastor,et al. TETonic shift: biological roles of TET proteins in DNA demethylation and transcription , 2013, Nature Reviews Molecular Cell Biology.
[44] Andrea Ballabio,et al. Signals from the lysosome: a control centre for cellular clearance and energy metabolism , 2013, Nature Reviews Molecular Cell Biology.
[45] B. Thorens,et al. The SLC2 (GLUT) family of membrane transporters. , 2013, Molecular aspects of medicine.
[46] E. Wright,et al. Glucose transport families SLC5 and SLC50. , 2013, Molecular aspects of medicine.
[47] Y. Kohno,et al. Artery tortuosity syndrome exhibiting early‐onset emphysema with novel compound heterozygous SLC2A10 mutations , 2013, American journal of medical genetics. Part A.
[48] G. Bánhegyi,et al. Multiple roles of glucose-6-phosphatases in pathophysiology: state of the art and future trends. , 2013, Biochimica et biophysica acta.
[49] C. Corpe,et al. Intestinal Dehydroascorbic Acid (DHA) Transport Mediated by the Facilitative Sugar Transporters, GLUT2 and GLUT8* , 2013, The Journal of Biological Chemistry.
[50] W. Robinson,et al. Glucose as a fetal nutrient: dynamic regulation of several glucose transporter genes by DNA methylation in the human placenta across gestation. , 2013, The Journal of nutritional biochemistry.
[51] G. Bánhegyi,et al. The glucose‐6‐phosphate transport is not mediated by a glucose‐6‐phosphate/phosphate exchange in liver microsomes , 2012, FEBS letters.
[52] K. Moley,et al. Glucose transporter 8 (GLUT8) regulates enterocyte fructose transport and global mammalian fructose utilization. , 2012, Endocrinology.
[53] F. Zaccagna,et al. Adult presentation of arterial tortuosity syndrome in a 51‐year‐old woman with a novel homozygous c.1411+1G>A mutation in the SLC2A10 gene , 2012, American journal of medical genetics. Part A.
[54] Sharon Y. R. Dent,et al. Histone-modifying enzymes: regulators of developmental decisions and drivers of human disease. , 2012, Epigenomics.
[55] R. Grempler,et al. Functional characterisation of human SGLT‐5 as a novel kidney‐specific sodium‐dependent sugar transporter , 2012, FEBS letters.
[56] P. Coucke,et al. Arterial tortuosity syndrome: case report. , 2012, Genetic counseling.
[57] C. Klein,et al. G6PC3 mutations are associated with a major defect of glycosylation: a novel mechanism for neutrophil dysfunction. , 2011, Glycobiology.
[58] E. Baehrecke,et al. Spinster is required for autophagic lysosome reformation and mTOR reactivation following starvation , 2011, Proceedings of the National Academy of Sciences.
[59] K. Moley,et al. The amino acids upstream of NH(2)-terminal dileucine motif play a role in regulating the intracellular sorting of the Class III transporters GLUT8 and GLUT12 , 2011, Molecular membrane biology.
[60] J. Chou,et al. Glycogen storage disease type I and G6Pase-β deficiency: etiology and therapy , 2010, Nature Reviews Endocrinology.
[61] W. Frommer,et al. Sugar transporters for intercellular exchange and nutrition of pathogens , 2010, Nature.
[62] Yuan-Tsong Chen,et al. Mitochondrial GLUT10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insight into arterial tortuosity syndrome. , 2010, Human molecular genetics.
[63] W. Frommer,et al. Facilitative plasma membrane transporters function during ER transit , 2010, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[64] F. Segade. Glucose transporter 10 and arterial tortuosity syndrome: The vitamin C connection , 2010, FEBS letters.
[65] D. Hailey,et al. Autophagy termination and lysosome reformation regulated by mTOR , 2010, Nature.
[66] Oliver Kohlbacher,et al. YLoc—an interpretable web server for predicting subcellular localization , 2010, Nucleic Acids Res..
[67] R. Augustin. The protein family of glucose transport facilitators: It's not only about glucose after all , 2010, IUBMB life.
[68] D. Yin,et al. Insulin-stimulated translocation of glucose transporter (GLUT) 12 parallels that of GLUT4 in normal muscle. , 2009, The Journal of clinical endocrinology and metabolism.
[69] U. Jaeger,et al. Gene expression signature of chronic lymphocytic leukaemia with Trisomy 12 , 2009, European journal of clinical investigation.
[70] J. Mesonero,et al. Expression of GLUT8 in mouse intestine: Identification of alternative spliced variants , 2009, Journal of cellular biochemistry.
[71] L. Tsui,et al. A novel missense and a recurrent mutation in SLC2A10 gene of patients affected with arterial tortuosity syndrome. , 2009, Atherosclerosis.
[72] A. Schürmann,et al. GLUT8, the enigmatic intracellular hexose transporter. , 2009, American journal of physiology. Endocrinology and metabolism.
[73] A. Teebi,et al. A novel non-sense mutation in the SLC2A10 gene of an arterial tortuosity syndrome patient of Kurdish origin , 2009, European Journal of Pediatrics.
[74] S. Ambudkar,et al. The glucose‐6‐phosphate transporter is a phosphate‐linked antiporter deficient in glycogen storage disease type Ib and Ic , 2008, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[75] L. Tsui,et al. Identification of a p.Ser81Arg encoding mutation in SLC2A10 gene of arterial tortuosity syndrome patients from 10 Qatari families , 2008, Clinical genetics.
[76] W. Frommer,et al. GLUT1 and GLUT9 as major contributors to glucose influx in HepG2 cells identified by a high sensitivity intramolecular FRET glucose sensor. , 2008, Biochimica et biophysica acta.
[77] S. Rogers,et al. Mitogen-stimulated and rapamycin-sensitive glucose transporter 12 targeting and functional glucose transport in renal epithelial cells. , 2008, Endocrinology.
[78] S. Nik-Zainal,et al. Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families , 2008, Human mutation.
[79] S. Brunak,et al. Locating proteins in the cell using TargetP, SignalP and related tools , 2007, Nature Protocols.
[80] N. Zoppi,et al. Two novel SLC2A10/GLUT10 mutations in a patient with arterial tortuosity syndrome , 2007, American Journal of Medical Genetics. Part A.
[81] J. K. Oeser,et al. Deletion of the gene encoding the islet-specific glucose-6-phosphatase catalytic subunit-related protein autoantigen results in a mild metabolic phenotype , 2007, Diabetologia.
[82] J. Mandl,et al. Translocon pores in the endoplasmic reticulum are permeable to small anions. , 2006, American journal of physiology. Cell physiology.
[83] A. Schürmann,et al. Endocytosis of the glucose transporter GLUT8 is mediated by interaction of a dileucine motif with the β2-adaptin subunit of the AP-2 adaptor complex , 2006, Journal of Cell Science.
[84] H. Dietz,et al. Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome , 2006, Nature Genetics.
[85] W. Frommer,et al. Evidence for High-Capacity Bidirectional Glucose Transport across the Endoplasmic Reticulum Membrane by Genetically Encoded Fluorescence Resonance Energy Transfer Nanosensors , 2005, Molecular and Cellular Biology.
[86] K. Moley,et al. GLUT8 Contains a [DE]XXXL[LI] Sorting Motif and Localizes to a Late Endosomal/Lysosomal Compartment , 2005, Traffic.
[87] M. Widmer,et al. GLUT8 subcellular localization and absence of translocation to the plasma membrane in PC12 cells and hippocampal neurons. , 2005, Endocrinology.
[88] D. Golde,et al. Vitamin C enters mitochondria via facilitative glucose transporter 1 (Gluti) and confers mitochondrial protection against oxidative injury , 2005, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[89] A. Kania,et al. Aberrant lysosomal carbohydrate storage accompanies endocytic defects and neurodegeneration in Drosophila benchwarmer , 2005, The Journal of cell biology.
[90] P. Marcolongo,et al. Immunodetection of the expression of microsomal proteins encoded by the glucose 6-phosphate transporter gene. , 2005, The Biochemical journal.
[91] A. Wakamatsu,et al. SLC5A9/SGLT4, a new Na+-dependent glucose transporter, is an essential transporter for mannose, 1,5-anhydro-D-glucitol, and fructose. , 2005, Life sciences.
[92] B. Shin,et al. Glucose transporter GLUT8 translocation in neurons is not insulin responsive , 2004, Journal of neuroscience research.
[93] T. Rapoport,et al. The endoplasmic reticulum membrane is permeable to small molecules. , 2003, Molecular biology of the cell.
[94] M. Uldry,et al. The SLC2 family of facilitated hexose and polyol transporters , 2004, Pflügers Archiv.
[95] E. Wright,et al. A glucose sensor hiding in a family of transporters , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[96] D. Yamamoto,et al. HSpin1, a transmembrane protein interacting with Bcl-2/Bcl-xL, induces a caspase-independent autophagic cell death , 2003, Cell Death and Differentiation.
[97] T. Kuijpers,et al. Apoptotic neutrophils in the circulation of patients with glycogen storage disease type 1b (GSD1b). , 2003, Blood.
[98] W. Wonderlin,et al. The Permeability of the Endoplasmic Reticulum Is Dynamically Coupled to Protein Synthesis* , 2003, The Journal of Biological Chemistry.
[99] G. Davis,et al. Unrestricted Synaptic Growth in spinster—a Late Endosomal Protein Implicated in TGF-β-Mediated Synaptic Growth Regulation , 2002, Neuron.
[100] D. Gagnon,et al. Identification of a Novel Na+/myo-Inositol Cotransporter* , 2002, The Journal of Biological Chemistry.
[101] I. Gérin,et al. The glucose-6-phosphatase system. , 2002, The Biochemical journal.
[102] Yuan-Tsong Chen,et al. Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex. , 2002, Current molecular medicine.
[103] D. Yamamoto,et al. Zebrafish yolk‐specific not really started (nrs) gene is a vertebrate homolog of the Drosophila spinster gene and is essential for embryogenesis , 2002, Developmental dynamics : an official publication of the American Association of Anatomists.
[104] P. Dawson,et al. Sequence and functional analysis of GLUT10: a glucose transporter in the Type 2 diabetes-linked region of chromosome 20q12-13.1. , 2001, Molecular genetics and metabolism.
[105] A. Schürmann,et al. Targeting of GLUT6 (formerly GLUT9) and GLUT8 in rat adipose cells. , 2001, The Biochemical journal.
[106] J. Chatton,et al. Identification of a mammalian H+‐myo‐inositol symporter expressed predominantly in the brain , 2001, The EMBO journal.
[107] I. Gérin,et al. Novel arguments in favor of the substrate-transport model of glucose-6-phosphatase. , 2001, Diabetes.
[108] R. Ueda,et al. Mutations in the Novel Membrane Protein Spinster Interfere with Programmed Cell Death and Cause Neural Degeneration inDrosophila melanogaster , 2001, Molecular and Cellular Biology.
[109] Yuan-Tsong Chen,et al. Molecular cloning of a novel member of the GLUT family of transporters, SLC2a10 (GLUT10), localized on chromosome 20q13.1: a candidate gene for NIDDM susceptibility. , 2001, Genomics.
[110] H. Joost,et al. The extended GLUT-family of sugar/polyol transport facilitators: nomenclature, sequence characteristics, and potential function of its novel members , 2001, Molecular membrane biology.
[111] S. Norgren,et al. The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome , 2001, Human Genetics.
[112] I. Sandoval,et al. Distinct Reading of Different Structural Determinants Modulates the Dileucine-mediated Transport Steps of the Lysosomal Membrane Protein LIMPII and the Insulin-sensitive Glucose Transporter GLUT4* , 2000, The Journal of Biological Chemistry.
[113] A. Schürmann,et al. Activity and genomic organization of human glucose transporter 9 (GLUT9), a novel member of the family of sugar-transport facilitators predominantly expressed in brain and leucocytes. , 2000, The Biochemical journal.
[114] Ying Cui,et al. GLUT8 is a glucose transporter responsible for insulin-stimulated glucose uptake in the blastocyst. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[115] Andreas Brauers,et al. GLUT8, a Novel Member of the Sugar Transport Facilitator Family with Glucose Transport Activity* , 2000, The Journal of Biological Chemistry.
[116] M. Uldry,et al. GLUTX1, a Novel Mammalian Glucose Transporter Expressed in the Central Nervous System and Insulin-sensitive Tissues* , 2000, The Journal of Biological Chemistry.
[117] P. Marcolongo,et al. Mutations in the glucose‐6‐phosphate transporter (G6PT) gene in patients with glycogen storage diseases type 1b and 1c , 1999, FEBS letters.
[118] I. Gérin,et al. The putative glucose 6-phosphate translocase gene is mutated in essentially all cases of glycogen storage disease type I non-a , 1999, European Journal of Human Genetics.
[119] I. Gérin,et al. Structure of the gene mutated in glycogen storage disease type Ib. , 1999, Gene.
[120] K. Nakai,et al. PSORT: a program for detecting sorting signals in proteins and predicting their subcellular localization. , 1999, Trends in biochemical sciences.
[121] G. Bánhegyi,et al. Heterogeneity of glucose transport in rat liver microsomal vesicles. , 1998, Archives of biochemistry and biophysics.
[122] R. Burcelin,et al. Normal hepatic glucose production in the absence of GLUT2 reveals an alternative pathway for glucose release from hepatocytes. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[123] P. Marcolongo,et al. Structure and mutation analysis of the glycogen storage disease type 1b gene , 1998, FEBS letters.
[124] B. Annabi,et al. Transmembrane Topology of Glucose-6-Phosphatase* , 1998, The Journal of Biological Chemistry.
[125] M. Polymeropoulos,et al. The gene for glycogen-storage disease type 1b maps to chromosome 11q23. , 1998, American journal of human genetics.
[126] A. Podtelejnikov,et al. Linking genome and proteome by mass spectrometry: large-scale identification of yeast proteins from two dimensional gels. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[127] P. Marcolongo,et al. Permeability of liver microsomal membranes to glucose. , 1996, Biochemical and biophysical research communications.
[128] M. Chalfie,et al. Green fluorescent protein as a marker for gene expression. , 1994, Science.
[129] A. Burchell. The molecular basis of the type 1 glycogen storage diseases , 1992, BioEssays : news and reviews in molecular, cellular and developmental biology.
[130] G. Meissner,et al. Evidence for two types of rat liver microsomes with differing permeability to glucose and other small molecules. , 1981, The Journal of biological chemistry.
[131] C. Cori,et al. Glucose-6-phosphatase of the liver in glycogen storage disease. , 1952, The Journal of biological chemistry.