1 | SLC2A10, SLC2A13, SLC2A5
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| The Solute Carrier Family 2 Genes Are Potential Prognostic Biomarkers in Acute Myeloid Leukemia.
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| Lai B, Lai Y, Zhang Y, Zhou M, Sheng L, OuYang G.
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| Technol Cancer Res Treat 19:1533033819894308. doi: 10.1177/1533033819894308.
2020
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2 | ATS, SLC2A10
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| Comprehensive in silico Study of GLUT10: Prediction of Possible Substrate Binding Sites and Interacting Molecules.
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| Hosen MJ, Hasan M, Chakraborty S, Abir RA, Zubaer A, Coucke P.
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| Curr Pharm Biotechnol 21(2):117-130. doi: 10.2174/1389201020666190613152030.
2020
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3 | ATS, SLC2A10
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| Arterial Tortuosity Syndrome: An Ascorbate Compartmentalization Disorder?
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| Boel A, Veszelyi K, Németh CE, Beyens A, Willaert A, Coucke P, Callewaert B, Margittai É.
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| Antioxid Redox Signal ntioxid Redox Signal. 2019 Nov 14. doi: 10.1089/ars.2019.7843. [Epub ahead of print]
2019
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4 | SLC2A10
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| GLUT10 maintains the integrity of major arteries through regulation of redox homeostasis and mitochondrial function.
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| Syu YW, Lai HW, Jiang CL, Tsai HY, Lin CC, Lee YC.
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| Hum Mol Genet 27(2):307-321. doi: 10.1093/hmg/ddx401.
2018
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5 | SLC2A10
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| Localization of Glucose Transporter 10 to Hair Cells' Cuticular Plate in the Mouse Inner Ear.
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| Chen B, Wang Y, Geng M, Lin X, Tang W.
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| Biomed Res Int 2018:7817453. doi: 10.1155/2018/7817453. eCollection 2018.
2018
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6 | ATS, SLC2A10
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| Arterial tortuosity syndrome: 40 new families and literature review.
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| Beyens A, Albuisson J, Boel A, Al-Essa M, Al-Manea W, Bonnet D, Bostan O, Boute O, Busa T, Canham N, Cil E, Coucke PJ, Cousin MA, Dasouki M, De Backer J, De Paepe A, De Schepper S, De Silva D, Devriendt K, De Wandele I, Deyle DR, Dietz H, Dupuis-Girod S, Fontenot E, Fischer-Zirnsak B, Gezdirici A, Ghoumid J, Giuliano F, Diéz NB, Haider MZ, Hardin JS, Jeunemaitre X, Klee EW, Kornak U, Landecho MF, Legrand A, Loeys B, Lyonnet S, Michael H, Moceri P, Mohammed S, Muińo-Mosquera L, Nampoothiri S, Pichler K, Prescott K, Rajeb A, Ramos-Arroyo M, Rossi M, Salih M, Seidahmed MZ, Schaefer E, Steichen-Gersdorf E, Temel S, Uysal F, Vanhomwegen M, Van Laer L, Van Maldergem L, Warner D, Willaert A, Collins TR, Taylor A, Davis EC, Zarate Y, Callewaert B.
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| Genet Med 20(10):1236-1245. doi: 10.1038/gim.2017.253. Epub 2018 Jan 11. Erratum in: Genet Med. 2018 Sep 10;:.
2018
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7 | SLC2A10
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| GLUT10-Lacking in Arterial Tortuosity Syndrome-Is Localized to the Endoplasmic Reticulum of Human Fibroblasts.
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| Gamberucci A, Marcolongo P, Németh CE, Zoppi N, Szarka A, Chiarelli N, Hegedűs T, Ritelli M, Carini G, Willaert A, Callewaert BL, Coucke PJ, Benedetti A, Margittai É, Fulceri R, Bánhegyi G, Colombi M.
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| Int J Mol Sci 18(8). pii: E1820. doi: 10.3390/ijms18081820.
2017
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8 | SLC2A10
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| Glucose transporter type 10-lacking in arterial tortuosity syndrome-facilitates dehydroascorbic acid transport.
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| Németh CE, Marcolongo P, Gamberucci A, Fulceri R, Benedetti A, Zoppi N, Ritelli M, Chiarelli N, Colombi M, Willaert A, Callewaert BL, Coucke PJ, Gróf P, Nagy SK, Mészáros T, Bánhegyi G, Margittai É.
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| FEBS Lett 590(11):1630-40. doi: 10.1002/1873-3468.12204. Epub 2016 May 27.
2016
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9 | ATS, SLC2A10
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| 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.
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| Ritelli M, Chiarelli N, Dordoni C, Reffo E, Venturini M, Quinzani S, Monica MD, Scarano G, Santoro G, Russo MG, Calzavara-Pinton P, Milanesi O, Colombi M.
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| BMC Med Genet 15:122. doi: 10.1186/s12881-014-0122-5. Review.
2014
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10 | SLC2A1, SLC2A10, SLC2A12, SLC2A9
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| Expression of conventional and novel glucose transporters, GLUT1, -9, -10, and -12, in vascular smooth muscle cells.
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| Pyla R, Poulose N, Jun JY, Segar L.
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| Am J Physiol Cell Physiol 304(6):C574-89. doi: 10.1152/ajpcell.00275.2012. Epub 2013 Jan 9.
2013
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11 | SLC2A10
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| GLUT10 is required for the development of the cardiovascular system and the notochord and connects mitochondrial function to TGFβ signaling.
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| Willaert A, Khatri S, Callewaert BL, Coucke PJ, Crosby SD, Lee JG, Davis EC, Shiva S, Tsang M, De Paepe A, Urban Z.
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| Hum Mol Genet 21(6):1248-59. doi: 10.1093/hmg/ddr555. Epub 2011 Nov 24.
2012
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12 | ATS, SLC2A10
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| Glucose transporter 10 and arterial tortuosity syndrome: the vitamin C connection.
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| Segade F.
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| FEBS Lett 584(14):2990-4. Epub 2010 Jun 12. Review.
2010
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13 | ATS, SLC2A10
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| Mitochondrial GLUT10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insight into arterial tortuosity syndrome.
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| Lee YC, Huang HY, Chang CJ, Cheng CH, Chen YT.
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| Hum Mol Genet 19(19):3721-33. Epub 2010 Jul 16.
2010
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14 | ATS, SLC2A10
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| Mutations in the SLC2A10 gene cause arterial abnormalities in mice.
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| Cheng CH, Kikuchi T, Chen YH, Sabbagha NG, Lee YC, Pan HJ, Chang C, Chen YT.
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| Cardiovasc Res 81(2):381-8. Epub 2008 Nov 21.
2009
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15 | ATS, SLC2A10
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| A novel non-sense mutation in the SLC2A10 gene of an arterial tortuosity syndrome patient of Kurdish origin.
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| Zaidi SH, Meyer S, Peltekova VD, Lindinger A, Teebi AS, Faiyaz-Ul-Haque M.
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| Eur J Pediatr 168(7):867-70. Epub 2008 Sep 26.
2009
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16 | ATS, SLC2A10
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| A novel missense and a recurrent mutation in SLC2A10 gene of patients affected with arterial tortuosity syndrome.
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| Faiyaz-Ul-Haque M, Zaidi SH, Al-Sanna N, Alswaid A, Momenah T, Kaya N, Al-Dayel F, Bouhoaigah I, Saliem M, Tsui LC, Teebi AS.
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| Atherosclerosis 203(2):466-71. Epub 2008 Aug 5.
2009
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17 | SLC2A10, ATS
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| Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families.
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| Callewaert BL, Willaert A, Kerstjens-Frederikse WS, De Backer J, Devriendt K, Albrecht B, Ramos-Arroyo MA, Doco-Fenzy M, Hennekam RC, Pyeritz RE, Krogmann ON, Gillessen-kaesbach G, Wakeling EL, Nik-zainal S, Francannet C, Mauran P, Booth C, Barrow M, Dekens R, Loeys BL, Coucke PJ, De Paepe AM.
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| Hum Mutat 29(1):150-8. 2008
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18 | CDH22, HNF4A, PREX1, PTPN1, SLC2A10
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| Bento JL, Palmer ND, Zhong M, Roh B, Lewis JP, Wing MR, Pandya H, Freedman BI, Langefeld CD, Rich SS, Bowden DW, Mychaleckyj JC.
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| Heterogeneity in gene loci associated with type 2 diabetes on human chromosome 20q13.
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| Genomics 92(4):226-34. Epub 2008 Aug 9.
2008
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19 | SLC2A10, ATS
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| Two novel SLC2A10/GLUT10 mutations in a patient with arterial tortuosity syndrome.
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| Drera B, Guala A, Zoppi N, Gardella R, Franceschini P, Barlati S, Colombi M.
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| Am J Med Genet A 143(2):216-8. No abstract available. 2007
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20 | SLC2A10, ATS
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| Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome.
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| Coucke PJ, Willaert A, Wessels MW, Callewaert B, Zoppi N, De Backer J, Fox JE, Mancini GM, Kambouris M, Gardella R, Facchetti F, Willems PJ, Forsyth R, Dietz HC, Barlati S, Colombi M, Loeys B, De Paepe A.
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| Nat Genet 38(4):452-7. Epub 2006 Mar 19. 2006
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21 | ATS, SLC2A10
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| A GLUT of sugar leads to a tortuous future.
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| Kang M.
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| Clin Genet 70(2):111-3. No abstract available. 2006
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22 | SLC2A10
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| Functional characterization of the promoter of the human glucose transporter 10 gene.
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| Segade F, Allred DC, Bowden DW.
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| Biochim Biophys Acta 1730(2):147-58. 2005
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23 | SLC2A10, SLC2A12
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| Expression of Class III facilitative glucose transporter genes (GLUT-10 and GLUT-12) in mouse and human adipose tissues.
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| Wood IS, Hunter L, Trayhurn P.
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| Biochem Biophys Res Commun 308(1):43-9. 2003
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24 | SLC2A10
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| 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.
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| McVie-Wylie AJ, Lamson DR, Chen YT.
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| Genomics 72(1):113-7. 2001
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