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Items: 1 to 20 of 82

1.

Common variants of FUT2 are associated with plasma vitamin B12 levels.

Hazra A, Kraft P, Selhub J, Giovannucci EL, Thomas G, Hoover RN, Chanock SJ, Hunter DJ.

Nat Genet. 2008 Oct;40(10):1160-2. doi: 10.1038/ng.210.

2.

Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway.

Hazra A, Kraft P, Lazarus R, Chen C, Chanock SJ, Jacques P, Selhub J, Hunter DJ.

Hum Mol Genet. 2009 Dec 1;18(23):4677-87. doi: 10.1093/hmg/ddp428.

3.

Gastric intrinsic factor deficiency with combined GIF heterozygous mutations and FUT2 secretor variant.

Chery C, Hehn A, Mrabet N, Oussalah A, Jeannesson E, Besseau C, Alberto JM, Gross I, Josse T, Gérard P, Guéant-Rodriguez RM, Freund JN, Devignes J, Bourgaud F, Peyrin-Biroulet L, Feillet F, Guéant JL.

Biochimie. 2013 May;95(5):995-1001. doi: 10.1016/j.biochi.2013.01.022.

PMID:
23402911
4.

Helicobacter pylori serologic status has no influence on the association between fucosyltransferase 2 polymorphism (FUT2 461 G->A) and vitamin B-12 in Europe and West Africa.

Oussalah A, Besseau C, Chery C, Jeannesson E, Guéant-Rodriguez RM, Anello G, Bosco P, Elia M, Romano A, Bronowicki JP, Gerard P, Paoli J, Avogbe PH, Chabi N, Sanni A, Amouzou E, Peyrin-Biroulet L, Guéant JL.

Am J Clin Nutr. 2012 Feb;95(2):514-21. doi: 10.3945/ajcn.111.016410.

5.

Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations.

Tanaka T, Scheet P, Giusti B, Bandinelli S, Piras MG, Usala G, Lai S, Mulas A, Corsi AM, Vestrini A, Sofi F, Gori AM, Abbate R, Guralnik J, Singleton A, Abecasis GR, Schlessinger D, Uda M, Ferrucci L.

Am J Hum Genet. 2009 Apr;84(4):477-82. doi: 10.1016/j.ajhg.2009.02.011. Erratum in: Am J Hum Genet. 2009 May;84(5):712.

6.

A genetic variant in vitamin B12 metabolic genes that reduces the risk of congenital heart disease in Han Chinese populations.

Wang J, Zhao JY, Wang F, Peng QQ, Hou J, Sun SN, Gui YH, Duan WY, Qiao B, Wang HY.

PLoS One. 2014 Feb 12;9(2):e88332. doi: 10.1371/journal.pone.0088332.

7.

Genome-wide association study identifies novel loci associated with serum level of vitamin B12 in Chinese men.

Lin X, Lu D, Gao Y, Tao S, Yang X, Feng J, Tan A, Zhang H, Hu Y, Qin X, Kim ST, Peng T, Li L, Mo L, Zhang S, Trent JM, Mo Z, Zheng SL, Xu J, Sun J.

Hum Mol Genet. 2012 Jun 1;21(11):2610-7. doi: 10.1093/hmg/dds062.

PMID:
22367966
8.

Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.

McGovern DP, Jones MR, Taylor KD, Marciante K, Yan X, Dubinsky M, Ippoliti A, Vasiliauskas E, Berel D, Derkowski C, Dutridge D, Fleshner P, Shih DQ, Melmed G, Mengesha E, King L, Pressman S, Haritunians T, Guo X, Targan SR, Rotter JI; International IBD Genetics Consortium..

Hum Mol Genet. 2010 Sep 1;19(17):3468-76. doi: 10.1093/hmg/ddq248.

9.

Common variant in FUT2 gene is associated with levels of vitamin B(12) in Indian population.

Tanwar VS, Chand MP, Kumar J, Garg G, Seth S, Karthikeyan G, Sengupta S.

Gene. 2013 Feb 15;515(1):224-8. doi: 10.1016/j.gene.2012.11.021.

PMID:
23201895
10.

FUT2: filling the gap between genes and environment in Behçet's disease?

Xavier JM, Shahram F, Sousa I, Davatchi F, Matos M, Abdollahi BS, Sobral J, Nadji A, Oliveira M, Ghaderibarim F, Shafiee NM, Oliveira SA.

Ann Rheum Dis. 2015 Mar;74(3):618-24. doi: 10.1136/annrheumdis-2013-204475.

PMID:
24326010
11.

ABO histo-blood group might modulate predisposition to Crohn's disease and affect disease behavior.

Forni D, Cleynen I, Ferrante M, Cassinotti A, Cagliani R, Ardizzone S, Vermeire S, Fichera M, Lombardini M, Maconi G, de Franchis R, Asselta R, Biasin M, Clerici M, Sironi M.

J Crohns Colitis. 2014 Jun;8(6):489-94. doi: 10.1016/j.crohns.2013.10.014.

PMID:
24268527
12.

Transcobalamin C776G genotype modifies the association between vitamin B12 and homocysteine in older Hispanics.

Garrod MG, Allen LH, Haan MN, Green R, Miller JW.

Eur J Clin Nutr. 2010 May;64(5):503-9. doi: 10.1038/ejcn.2010.20.

13.

FUT2 and FUT3 genotype determines CA19-9 cut-off values for detection of cholangiocarcinoma in patients with primary sclerosing cholangitis.

Wannhoff A, Hov JR, Folseraas T, Rupp C, Friedrich K, Anmarkrud JA, Weiss KH, Sauer P, Schirmacher P, Boberg KM, Stremmel W, Karlsen TH, Gotthardt DN.

J Hepatol. 2013 Dec;59(6):1278-84. doi: 10.1016/j.jhep.2013.08.005.

PMID:
23958938
14.

Identification of 14 new alleles at the fucosyltransferase 1, 2, and 3 loci in Styrian blood donors, Austria.

Matzhold EM, Helmberg W, Wagner T, Drexler C, Ulrich S, Winkler A, Lanzer G.

Transfusion. 2009 Oct;49(10):2097-108. doi: 10.1111/j.1537-2995.2009.02293.x.

PMID:
19572973
15.

Extended analysis of a genome-wide association study in primary sclerosing cholangitis detects multiple novel risk loci.

Folseraas T, Melum E, Rausch P, Juran BD, Ellinghaus E, Shiryaev A, Laerdahl JK, Ellinghaus D, Schramm C, Weismüller TJ, Gotthardt DN, Hov JR, Clausen OP, Weersma RK, Janse M, Boberg KM, Björnsson E, Marschall HU, Cleynen I, Rosenstiel P, Holm K, Teufel A, Rust C, Gieger C, Wichmann HE, Bergquist A, Ryu E, Ponsioen CY, Runz H, Sterneck M, Vermeire S, Beuers U, Wijmenga C, Schrumpf E, Manns MP, Lazaridis KN, Schreiber S, Baines JF, Franke A, Karlsen TH.

J Hepatol. 2012 Aug;57(2):366-75. doi: 10.1016/j.jhep.2012.03.031.

16.
17.

A natural history of FUT2 polymorphism in humans.

Ferrer-Admetlla A, Sikora M, Laayouni H, Esteve A, Roubinet F, Blancher A, Calafell F, Bertranpetit J, Casals F.

Mol Biol Evol. 2009 Sep;26(9):1993-2003. doi: 10.1093/molbev/msp108.

PMID:
19487333
18.

Associations between 2 polymorphisms in the methylenetetrahydrofolate reductase gene and placental abruption.

Ananth CV, Peltier MR, De Marco C, Elsasser DA, Getahun D, Rozen R, Smulian JC; New Jersey-Placental Abruption Study Investigators..

Am J Obstet Gynecol. 2007 Oct;197(4):385.e1-7.

19.

Fucosyltransferase 2 (FUT2) non-secretor status and blood group B are associated with elevated serum lipase activity in asymptomatic subjects, and an increased risk for chronic pancreatitis: a genetic association study.

Weiss FU, Schurmann C, Guenther A, Ernst F, Teumer A, Mayerle J, Simon P, Völzke H, Radke D, Greinacher A, Kuehn JP, Zenker M, Völker U, Homuth G, Lerch MM.

Gut. 2015 Apr;64(4):646-56. doi: 10.1136/gutjnl-2014-306930.

PMID:
25028398
20.

Fut2 genotype is a risk factor for dominant stenosis and biliary candida infections in primary sclerosing cholangitis.

Rupp C, Friedrich K, Folseraas T, Wannhoff A, Bode KA, Weiss KH, Schirmacher P, Sauer P, Stremmel W, Gotthardt DN.

Aliment Pharmacol Ther. 2014 Apr;39(8):873-82. doi: 10.1111/apt.12663.

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