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 *

139 related articles for article (PubMed ID: 8526839)

  • 1. 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]  

  • 2. 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]  

  • 3. Molecular genetic analysis of the human Lewis histo-blood group system. II. Secretor gene inactivation by a novel single missense mutation A385T in Japanese nonsecretor individuals.
    Kudo T; Iwasaki H; Nishihara S; Shinya N; Ando T; Narimatsu I; Narimatsu H
    J Biol Chem; 1996 Apr; 271(16):9830-7. PubMed ID: 8621666
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Sequence and expression of a candidate for the human Secretor blood group alpha(1,2)fucosyltransferase gene (FUT2). Homozygosity for an enzyme-inactivating nonsense mutation commonly correlates with the non-secretor phenotype.
    Kelly RJ; Rouquier S; Giorgi D; Lennon GG; Lowe JB
    J Biol Chem; 1995 Mar; 270(9):4640-9. PubMed ID: 7876235
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Alpha (1,3/1,4)fucosyltransferase (FucT-III) gene is inactivated by a single amino acid substitution in Lewis histo-blood type negative individuals.
    Nishihara S; Yazawa S; Iwasaki H; Nakazato M; Kudo T; Ando T; Narimatsu H
    Biochem Biophys Res Commun; 1993 Oct; 196(2):624-31. PubMed ID: 8240337
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Wide variety of point mutations in the H gene of Bombay and para-Bombay individuals that inactivate H enzyme.
    Kaneko M; Nishihara S; Shinya N; Kudo T; Iwasaki H; Seno T; Okubo Y; Narimatsu H
    Blood; 1997 Jul; 90(2):839-49. PubMed ID: 9226185
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular basis for H blood group deficiency in Bombay (Oh) and para-Bombay individuals.
    Kelly RJ; Ernst LK; Larsen RD; Bryant JG; Robinson JS; Lowe JB
    Proc Natl Acad Sci U S A; 1994 Jun; 91(13):5843-7. PubMed ID: 7912436
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A newly identified nonsecretor allele of the human histo-blood group alpha(1,2)fucosyltransferase gene (FUT2).
    Yu LC; Lee HL; Chu CC; Broadberry RE; Lin M
    Vox Sang; 1999; 76(2):115-9. PubMed ID: 10085528
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Lewis histo-blood group system and associated secretory phenotypes.
    Henry S; Oriol R; Samuelsson B
    Vox Sang; 1995; 69(3):166-82. PubMed ID: 8578728
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular basis for secretor type alpha(1,2)-fucosyltransferase gene deficiency in a Japanese population: a fusion gene generated by unequal crossover responsible for the enzyme deficiency.
    Koda Y; Soejima M; Liu Y; Kimura H
    Am J Hum Genet; 1996 Aug; 59(2):343-50. PubMed ID: 8755920
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Molecular basis for Lewis alpha(1,3/1,4)-fucosyltransferase gene deficiency (FUT3) found in Lewis-negative Indonesian pedigrees.
    Mollicone R; Reguigne I; Kelly RJ; Fletcher A; Watt J; Chatfield S; Aziz A; Cameron HS; Weston BW; Lowe JB
    J Biol Chem; 1994 Aug; 269(33):20987-94. PubMed ID: 8063716
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular basis for erythrocyte Le(a+ b+) and salivary ABH partial-secretor phenotypes: expression of a FUT2 secretor allele with an A-->T mutation at nucleotide 385 correlates with reduced alpha(1,2) fucosyltransferase activity.
    Henry S; Mollicone R; Fernandez P; Samuelsson B; Oriol R; Larson G
    Glycoconj J; 1996 Dec; 13(6):985-93. PubMed ID: 8981090
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular characterization of secretor type alpha(1, 2)-fucosyltransferase gene deficiency in the Philippine population.
    Peng CT; Tsai CH; Lin TP; Perng LI; Kao MC; Yang TY; Wang NM; Liu TC; Lin SF; Chang JG
    Ann Hematol; 1999 Oct; 78(10):463-7. PubMed ID: 10550557
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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]  

  • 18. Molecular basis for plasma alpha(1,3)-fucosyltransferase gene deficiency (FUT6).
    Mollicone R; Reguigne I; Fletcher A; Aziz A; Rustam M; Weston BW; Kelly RJ; Lowe JB; Oriol R
    J Biol Chem; 1994 Apr; 269(17):12662-71. PubMed ID: 8175676
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular genetic analysis of the human Lewis histo-blood group system.
    Nishihara S; Narimatsu H; Iwasaki H; Yazawa S; Akamatsu S; Ando T; Seno T; Narimatsu I
    J Biol Chem; 1994 Nov; 269(46):29271-8. PubMed ID: 7961897
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Isolation of a novel human alpha (1,3)fucosyltransferase gene and molecular comparison to the human Lewis blood group alpha (1,3/1,4)fucosyltransferase gene. Syntenic, homologous, nonallelic genes encoding enzymes with distinct acceptor substrate specificities.
    Weston BW; Nair RP; Larsen RD; Lowe JB
    J Biol Chem; 1992 Feb; 267(6):4152-60. PubMed ID: 1740457
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.