PubMed for id: 68047

Year	Number of Results
1957	1
1988	2
1989	2
1991	3
1992	5
1993	4
1994	7
1995	5
1996	5
1997	5
1998	6
1999	5
2000	10
2001	9
2002	9
2003	11
2004	10
2005	12
2006	17
2007	24
2008	15
2009	28
2010	16
2011	21
2012	20
2013	15
2014	1
2024	0

1

Nervous glucose sensing regulates postnatal β cell proliferation and glucose homeostasis.

Tarussio D, Metref S, Seyer P, Mounien L, Vallois D, Magnan C, Foretz M, Thorens B. Tarussio D, et al. J Clin Invest. 2014 Jan;124(1):413-24. doi: 10.1172/JCI69154. Epub 2013 Dec 16. J Clin Invest. 2014. PMID: 24334455 Free PMC article.

2

Mouse embryonic stem cells established in physiological-glucose media express the high KM Glut2 glucose transporter expressed by normal embryos.

Jung JH, Wang XD, Loeken MR. Jung JH, et al. Stem Cells Transl Med. 2013 Dec;2(12):929-34. doi: 10.5966/sctm.2013-0093. Epub 2013 Oct 28. Stem Cells Transl Med. 2013. PMID: 24167319 Free PMC article.

3

Mutations in SLC2A2 gene reveal hGLUT2 function in pancreatic β cell development.

Michau A, Guillemain G, Grosfeld A, Vuillaumier-Barrot S, Grand T, Keck M, L'Hoste S, Chateau D, Serradas P, Teulon J, De Lonlay P, Scharfmann R, Brot-Laroche E, Leturque A, Le Gall M. Michau A, et al. J Biol Chem. 2013 Oct 25;288(43):31080-92. doi: 10.1074/jbc.M113.469189. Epub 2013 Aug 28. J Biol Chem. 2013. PMID: 23986439 Free PMC article.

4

N-Glycosylation modulates the membrane sub-domain distribution and activity of glucose transporter 2 in pancreatic beta cells.

Ohtsubo K, Takamatsu S, Gao C, Korekane H, Kurosawa TM, Taniguchi N. Ohtsubo K, et al. Biochem Biophys Res Commun. 2013 May 3;434(2):346-51. doi: 10.1016/j.bbrc.2013.03.076. Epub 2013 Mar 30. Biochem Biophys Res Commun. 2013. PMID: 23548572

5

Genetic variant SLC2A2 [corrected] Is associated with risk of cardiovascular disease – assessing the individual and cumulative effect of 46 type 2 diabetes related genetic variants.

Borglykke A, Grarup N, Sparsø T, Linneberg A, Fenger M, Jeppesen J, Hansen T, Pedersen O, Jørgensen T. Borglykke A, et al. PLoS One. 2012;7(11):e50418. doi: 10.1371/journal.pone.0050418. Epub 2012 Nov 21. PLoS One. 2012. PMID: 23185617 Free PMC article.

6

Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1.

Meier S, Mattheisen M, Vassos E, Strohmaier J, Treutlein J, Josef F, Breuer R, Degenhardt F, Mühleisen TW, Müller-Myhsok B, Steffens M, Schmael C, McMahon FJ; Bipolar Disorder Genome Study (BiGS) Consortium; Nöthen MM, Cichon S, Schulze TG, Rietschel M, Kelsoe JR, Greenwood TA, Nievergelt CM, Barrett TB, McKinney R, Shilling PD, Schork NJ, Smith EN, Bloss CS, Nurnberger J, Edenberg HJ, Foroud T, Koller DL, Gershon ES, Liu CY, Badner JA, Scheftner W, Lawson WB, Nwulia EA, Hipolito M, Coryell W, Rice J, Byerley W, McMahon F, Chen DT, Schulze TG, Berrettini W, Potash JB, Zandi PP, Mahon PB, McInnis M, Craig D, Szelinger S. Meier S, et al. Transl Psychiatry. 2012 Sep 25;2(9):e165. doi: 10.1038/tp.2012.81. Transl Psychiatry. 2012. PMID: 23010768 Free PMC article.

7

Fanconi-Bickel syndrome and autosomal recessive proximal tubulopathy with hypercalciuria (ARPTH) are allelic variants caused by GLUT2 mutations.

Mannstadt M, Magen D, Segawa H, Stanley T, Sharma A, Sasaki S, Bergwitz C, Mounien L, Boepple P, Thorens B, Zelikovic I, Jüppner H. Mannstadt M, et al. J Clin Endocrinol Metab. 2012 Oct;97(10):E1978-86. doi: 10.1210/jc.2012-1279. Epub 2012 Aug 3. J Clin Endocrinol Metab. 2012. PMID: 22865906 Free PMC article.

8

SLC2A2 mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretion.

Sansbury FH, Flanagan SE, Houghton JA, Shuixian Shen FL, Al-Senani AM, Habeb AM, Abdullah M, Kariminejad A, Ellard S, Hattersley AT. Sansbury FH, et al. Diabetologia. 2012 Sep;55(9):2381-5. doi: 10.1007/s00125-012-2595-0. Epub 2012 Jun 2. Diabetologia. 2012. PMID: 22660720

9

Mutation analysis of the GLUT2 gene in three unrelated Egyptian families with Fanconi-Bickel syndrome: revisited gene atlas for renumbering.

Al-Haggar M, Sakamoto O, Shaltout A, Al-Hawari A, Wahba Y, Abdel-Hadi D. Al-Haggar M, et al. Clin Exp Nephrol. 2012 Aug;16(4):604-10. doi: 10.1007/s10157-012-0603-9. Epub 2012 Feb 18. Clin Exp Nephrol. 2012. PMID: 22350464

10

Fanconi-Bickel syndrome: GLUT2 mutations associated with a mild phenotype.

Grünert SC, Schwab KO, Pohl M, Sass JO, Santer R. Grünert SC, et al. Mol Genet Metab. 2012 Mar;105(3):433-7. doi: 10.1016/j.ymgme.2011.11.200. Epub 2011 Dec 8. Mol Genet Metab. 2012. PMID: 22214819

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