These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

91 related articles for article (PubMed ID: 14674375)

  • 1. Identification of two new single-nucleotide polymorphisms in FUT3 associated with the Lewis-null phenotype.
    Cooling L; Gu Y
    Transfusion; 2003 Dec; 43(12):1760-1. PubMed ID: 14674375
    [No Abstract]   [Full Text] [Related]  

  • 2. Two novel FUT3 alleles responsible for Lewis-null phenotypes in Sri Lanka.
    Soejima M; Kimura H; Koda Y
    Transfusion; 2004 Oct; 44(10):1534-5. PubMed ID: 15383031
    [No Abstract]   [Full Text] [Related]  

  • 3. [FUT3 gene polymorphism associated with Lewis blood group in Chinese Zhejiang population].
    Xu XG; Zhu FM; Hong XZ; Wu JJ; Ma KR; Fu QH; Yan LX
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2006 Jun; 14(3):601-4. PubMed ID: 16800951
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular mechanisms of Lewis antigen expression.
    Soejima M; Koda Y
    Leg Med (Tokyo); 2005 Jul; 7(4):266-9. PubMed ID: 15946883
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lewis histo-blood group system phenotyping and genotyping reveal divergence in the association of Le(a-b-) phenotype and type 1 diabetes.
    Previato M; Borim MP; Liberatore RD; Pires AC; Dias MA; Brandão de Mattos CC; de Mattos LC
    Vox Sang; 2015 Apr; 108(3):281-6. PubMed ID: 25469787
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Homozygous expression of a missense mutation at nucleotide 385 in the FUT2 gene associates with the Le(a+b+) partial-secretor phenotype in an Indonesian family.
    Henry S; Mollicone R; Fernandez P; Samuelsson B; Oriol R; Larson G
    Biochem Biophys Res Commun; 1996 Feb; 219(3):675-8. PubMed ID: 8645240
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Lewis (FUT3) genotypes in Taiwanese, Thai, and Filipino populations.
    Liu TC; Chang JG; Lin SF; Chang WC; Yang TY; Lin CL; Wang NM; Tsai CH
    Ann Hematol; 2000 Nov; 79(11):599-603. PubMed ID: 11131918
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Detection of G to A missense mutation of Lewis-negative gene by PCR on genomic DNA.
    Koda Y; Soejima M; Kimura H
    Vox Sang; 1994; 67(3):327-8. PubMed ID: 7863639
    [No Abstract]   [Full Text] [Related]  

  • 9. The Lewis histo-blood group system: molecular analysis of the 59T>G, 508G>A, and 1067T>A polymorphisms in an Amazonian population.
    Corvelo TC; de Loiola Rdo S; Aguiar DC; de Matos Gde C; de Brito DC
    PLoS One; 2013; 8(7):e69908. PubMed ID: 23922852
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genotypic heterogeneity among Lewis negative individuals.
    Elmgren A; Rydberg L; Larson G
    Biochem Biophys Res Commun; 1993 Oct; 196(2):515-20. PubMed ID: 8240322
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Plasma alpha1,3-fucosyltransferase deficiency in schizophrenia.
    Yazawa S; Tanaka S; Nishimura T; Miyanaga K; Kochibe N
    Exp Clin Immunogenet; 1999; 16(3):125-30. PubMed ID: 10394050
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Distribution of Lewis (FUT3)genotype and allele: frequencies in a biethnic United States population.
    Cakir B; Pankow JS; Salomaa V; Couper D; Morris TL; Brantley KR; Hiller KM; Heiss G; Weston BW
    Ann Hematol; 2002 Oct; 81(10):558-65. PubMed ID: 12424536
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Lewis and Secretor gene effects on Lewis antigen and postnatal development of Lewis blood type.
    Ameno S; Kimura H; Ameno K; Zhang X; Kinoshita H; Kubota T; Ijiri I
    Biol Neonate; 2001 Feb; 79(2):91-6. PubMed ID: 11223649
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Advances in molecular genetics of alpha-2- and alpha-3/4-fucosyltransferases.
    Costache M; Cailleau A; Fernandez-Mateos P; Oriol R; Mollicone R
    Transfus Clin Biol; 1997 Jul; 4(4):367-82. PubMed ID: 9269717
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Correlation of a missense mutation in the human Secretor alpha 1,2-fucosyltransferase gene with the Lewis(a+b+) phenotype: a potential molecular basis for the weak Secretor allele (Sew).
    Yu LC; Yang YH; Broadberry RE; Chen YH; Chan YS; Lin M
    Biochem J; 1995 Dec; 312 ( Pt 2)(Pt 2):329-32. PubMed ID: 8526839
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Association of Ulcerative Colitis with FUT2 and FUT3 Polymorphisms in Patients from Southeast China.
    Hu D; Zhang D; Zheng S; Guo M; Lin X; Jiang Y
    PLoS One; 2016; 11(1):e0146557. PubMed ID: 26766790
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Heterogeneity of the human Secretor alpha(1,2)fucosyltransferase gene among Lewis(a+b-) non-secretors.
    Yu LC; Broadberry RE; Yang YH; Chen YH; Lin M
    Biochem Biophys Res Commun; 1996 May; 222(2):390-4. PubMed ID: 8670215
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Estimation of genetic variation in the Secretor and Lewis genes in Iranian hospitalized children.
    Farahmand M; Jalilvand S; Arashkia A; Izadi A; Forouzannia SM; Mollaei-Kandelous Y; Shoja Z
    Transfus Clin Biol; 2021 Feb; 28(1):11-15. PubMed ID: 33301983
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Function of fucosyltransferases].
    Kudo T; Narimatsu H
    Tanpakushitsu Kakusan Koso; 2003 Jun; 48(8 Suppl):940-6. PubMed ID: 12806991
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.