BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 9031498)

  • 1. Two missense mutations of H type alpha(1,2)fucosyltransferase gene (FUT1) responsible for para-Bombay phenotype.
    Wang B; Koda Y; Soejima M; Kimura H
    Vox Sang; 1997; 72(1):31-5. PubMed ID: 9031498
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Two novel FUT1 alleles that cause para-Bombay phenotype in a Chinese individual.
    Lin FQ; Zhang KL; Li XF; Zhang X; Liu Y; Li JP
    Transfusion; 2020 Dec; 60(12):E55-E57. PubMed ID: 33175455
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of six new alleles at the FUT1 and FUT2 loci in ethnically diverse individuals with Bombay and Para-Bombay phenotypes.
    Storry JR; Johannesson JS; Poole J; Strindberg J; Rodrigues MJ; Yahalom V; Levene C; Fujita C; Castilho L; Hustinx H; Olsson ML
    Transfusion; 2006 Dec; 46(12):2149-55. PubMed ID: 17176328
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel FUT1 allele was identified in a Chinese individual with para-Bombay phenotype.
    Xu X; Tao S; Ying Y; Hong X; He Y; Zhu F; Lv H; Yan L
    Transfus Med; 2011 Dec; 21(6):385-93. PubMed ID: 21988368
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Missense mutation of FUT1 and deletion of FUT2 are responsible for Indian Bombay phenotype of ABO blood group system.
    Koda Y; Soejima M; Johnson PH; Smart E; Kimura H
    Biochem Biophys Res Commun; 1997 Sep; 238(1):21-5. PubMed ID: 9299444
    [TBL] [Abstract][Full Text] [Related]  

  • 6. FUT1 variants responsible for Bombay or para-Bombay phenotypes in a database.
    Soejima M; Koda Y
    Sci Rep; 2023 Oct; 13(1):17447. PubMed ID: 37838738
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular genetic analysis of para-Bombay phenotypes in Chinese: a novel non-functional FUT1 allele is identified.
    Yip SP; Chee KY; Chan PY; Chow EY; Wong HF
    Vox Sang; 2002 Oct; 83(3):258-62. PubMed ID: 12366770
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Analysis of alpha-1,2-fucosyltransferase gene mutations in a Chinese family with para-Bombay phenotype].
    Xu XG; Hong XZ; Liu Y; Ying YL; Tao SD; He YM; Zhu FM; Lv HJ; Yan LX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Jun; 27(3):250-4. PubMed ID: 20533259
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Novel mutations, including a novel G659A missense mutation, of the FUT1 gene are responsible for the para-Bombay phenotype.
    Sun CF; Lo MD; Lee CH; Chu DC
    Ann Clin Lab Sci; 2000 Oct; 30(4):387-90. PubMed ID: 11045762
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Mutational analysis for FUT1 gene in two cases with para-Bombay blood type].
    Xu DY; Deng G; Huang DD; Zhao WJ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):694-8. PubMed ID: 22161108
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sequence analysis of α-(1, 2)-fucosyltransferase gene in nine Chinese individuals with Para-Bombay phenotype.
    Lin J; Chen R; Zhu S; Qiu X; Huang Y; Wang X
    Gene; 2019 Feb; 685():21-23. PubMed ID: 30217757
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A new h allele detected in Europe has a missense mutationin alpha(1,2)-fucosyltransferase motif II.
    Wagner T; Vadon M; Staudacher E; Schmarda A; Gassner C; Helmberg W; Lanzer G; Flegel WA; Wagner FF
    Transfusion; 2001 Jan; 41(1):31-8. PubMed ID: 11161242
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Analysis on FUT1 and FUT2 gene of 10 para-Bombay individuals in China].
    Guo ZH; Xiang D; Zhu ZY; Wang JL; Zhang JM; Liu X; Shen W; Chen HP
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):417-21. PubMed ID: 15476160
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular basis of Bombay phenotype in Mashhad, Iran: identification of a novel FUT1 deletion.
    Zanjani DS; Afzal Aghaee M; Badiei Z; Mehrasa R; Roodsarabi A; Khayyami ME; Shahabi M
    Vox Sang; 2016 Jul; 111(1):88-92. PubMed ID: 26926997
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Para-Bombay phenotype caused by combined heterozygote of two bases deletion on fut1 alleles].
    Ma KR; Tao SD; Lan XF; Hong XZ; Xu XG; Zhu FM; Lü HJ; Yan LX
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2011 Feb; 19(1):223-6. PubMed ID: 21362257
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular basis for para-Bombay phenotypes in Chinese persons, including a novel nonfunctional FUT1 allele.
    Yan L; Zhu F; Xu X; Hong X; Lv Q
    Transfusion; 2005 May; 45(5):725-30. PubMed ID: 15847661
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Two prevalent h alleles in para-Bombay haplotypes among 250,000 Taiwanese.
    Chen DP; Tseng CP; Wang WT; Peng CT; Tsao KC; Wu TL; Lin KT; Sun CF
    Ann Clin Lab Sci; 2004; 34(3):314-8. PubMed ID: 15487706
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Study of a case with homozygous 35C>T and 658C>T mutations of FUT1 gene leading to a para-Bombay phenotype].
    Lin F; Sun C; Wang H; Zhang X; Li J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Dec; 32(6):834-6. PubMed ID: 26663060
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.