464 related articles for article (PubMed ID: 18776911)
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. PubMed ID: 18776911
[TBL] [Abstract][Full Text] [Related]
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; 18(23):4677-87. PubMed ID: 19744961
[TBL] [Abstract][Full Text] [Related]
3. GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians.
Nongmaithem SS; Joglekar CV; Krishnaveni GV; Sahariah SA; Ahmad M; Ramachandran S; Gandhi M; Chopra H; Pandit A; Potdar RD; H D Fall C; Yajnik CS; Chandak GR
Hum Mol Genet; 2017 Jul; 26(13):2551-2564. PubMed ID: 28334792
[TBL] [Abstract][Full Text] [Related]
4. The FUT2 secretor variant p.Trp154Ter influences serum vitamin B12 concentration via holo-haptocorrin, but not holo-transcobalamin, and is associated with haptocorrin glycosylation.
Velkova A; Diaz JEL; Pangilinan F; Molloy AM; Mills JL; Shane B; Sanchez E; Cunningham C; McNulty H; Cropp CD; Bailey-Wilson JE; Wilson AF; Brody LC
Hum Mol Genet; 2017 Dec; 26(24):4975-4988. PubMed ID: 29040465
[TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 23402911
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 22237057
[TBL] [Abstract][Full Text] [Related]
7. 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; 9(2):e88332. PubMed ID: 24533076
[TBL] [Abstract][Full Text] [Related]
8. Association of combined GIF290T>C heterozygous mutation/FUT2 secretor variant with neural tube defects.
Guéant-Rodriguez RM; Chery C; Caillierez-Fofou BM; Voirin J; Foliguet B; Josse T; Tramoy D; Feillet F; Guéant JL
Clin Genet; 2018 Jan; 93(1):191-193. PubMed ID: 28742214
[TBL] [Abstract][Full Text] [Related]
9. FUT2 Genetic Variants and Reported Respiratory and Gastrointestinal Illnesses During Infancy.
Barton SJ; Murray R; Lillycrop KA; Inskip HM; Harvey NC; Cooper C; Karnani N; Zolezzi IS; Sprenger N; Godfrey KM; Binia A
J Infect Dis; 2019 Feb; 219(5):836-843. PubMed ID: 30376117
[TBL] [Abstract][Full Text] [Related]
10. 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; 21(11):2610-7. PubMed ID: 22367966
[TBL] [Abstract][Full Text] [Related]
11. A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways.
Bustamante M; Standl M; Bassat Q; Vilor-Tejedor N; Medina-Gomez C; Bonilla C; Ahluwalia TS; Bacelis J; Bradfield JP; Tiesler CM; Rivadeneira F; Ring S; Vissing NH; Fink NR; Jugessur A; Mentch FD; Ballester F; Kriebel J; Kiefte-de Jong JC; Wolsk HM; Llop S; Thiering E; Beth SA; Timpson NJ; Andersen J; Schulz H; Jaddoe VW; Evans DM; Waage J; Hakonarson H; Grant SF; Jacobsson B; Bønnelykke K; Bisgaard H; Davey Smith G; Moll HA; Heinrich J; Estivill X; Sunyer J
Hum Mol Genet; 2016 Sep; 25(18):4127-4142. PubMed ID: 27559109
[TBL] [Abstract][Full Text] [Related]
12. Genetic determinants of serum vitamin B12 and their relation to body mass index.
Allin KH; Friedrich N; Pietzner M; Grarup N; Thuesen BH; Linneberg A; Pisinger C; Hansen T; Pedersen O; Sandholt CH
Eur J Epidemiol; 2017 Feb; 32(2):125-134. PubMed ID: 27995393
[TBL] [Abstract][Full Text] [Related]
13.
Chen CT; Liao WY; Hsu CC; Hsueh KC; Yang SF; Teng YH; Yu YL
Int J Med Sci; 2017; 14(9):885-890. PubMed ID: 28824326
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 19572973
[TBL] [Abstract][Full Text] [Related]
15. 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. PubMed ID: 24268527
[TBL] [Abstract][Full Text] [Related]
16. 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; 515(1):224-8. PubMed ID: 23201895
[TBL] [Abstract][Full Text] [Related]
17. Distinct single nucleotide polymorphism pattern at the FUT2 promoter among human populations.
Soejima M; Koda Y
Ann Hematol; 2008 Jan; 87(1):19-25. PubMed ID: 17805536
[TBL] [Abstract][Full Text] [Related]
18. Combinations of FUT2 gene polymorphisms and environmental factors are associated with oral cancer risk.
Su KJ; Ho CC; Lin CW; Chen MK; Su SC; Yu YL; Yang SF
Tumour Biol; 2016 May; 37(5):6647-52. PubMed ID: 26646561
[TBL] [Abstract][Full Text] [Related]
19. 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. PubMed ID: 23958938
[TBL] [Abstract][Full Text] [Related]
20. Association of MTHFR C677T polymorphism with elevated homocysteine level and disease development in vitiligo.
Bagheri Hamidi A; Namazi N; Mohammad Amoli M; Amani M; Gholami M; Youssefian L; Vahidnezhad H; Abdollahimajd F; Uitto J
Int J Immunogenet; 2020 Aug; 47(4):342-350. PubMed ID: 32064757
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
