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Journal Abstract Search

162 related items for PubMed ID: 17160941

  • 1. [278C > T variant of the alpha-1, 3-galactosyltransferase allele responsible for Bw subgroup].
    Xu XG, Hong XZ, Liu Y, Wu JJ, Ma KR, Zhu FM, Yan LX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Dec; 23(6):631-4. PubMed ID: 17160941
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  • 2. [Identification of a novel B variant allele in a Chinese Han individual with B subgroup].
    Yu Q, Wu G, Liang Y, Deng Z, Su Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr; 22(2):129-33. PubMed ID: 15793770
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  • 4. [Molecular genetic analysis of two individuals with Bw subtypes of ABO variant].
    Li GJ, Zhang X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Dec; 30(6):733-5. PubMed ID: 24327158
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  • 7. [Molecular genetic analysis of a new B112 allele of ABO blood group].
    Tao SD, He YM, Ying YL, Hong XZ, Xu XG, Zhu FM, Yan LX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Aug; 27(4):469-72. PubMed ID: 20677161
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  • 8. Identification of a novel B variant allele at the ABO locus in Chinese Han individuals with B subgroup.
    Deng ZH, Yu Q, Lian YL, Wu GG, Su YQ, Zhang X.
    Ann Clin Lab Sci; 2005 Aug; 35(3):265-9. PubMed ID: 16081582
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  • 9. [Study on BW.12 Subtype Caused by c.278C>T Mutation in Exon 6 of ABO Gene].
    Liu X, Wang LH, Xu XY, Shu J, LE F.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2022 Oct; 30(5):1557-1561. PubMed ID: 36208265
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  • 14. Molecular genetic analysis for the B subgroup revealing two novel alleles in the ABO gene.
    Cai XH, Jin S, Liu X, Shen W, Lu Q, Wang JL, Fan LF, Sun JL, Liu DZ, Xiang D.
    Transfusion; 2008 Nov; 48(11):2442-7. PubMed ID: 18680548
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  • 15. Identification of a novel B allele with a missense mutation (c.721C>G) in a Korean family with a weak B phenotype.
    Shin JG, Song SA, Jeong SY, Lee JY, Kim HR, Oh SH.
    Transfusion; 2017 Nov; 57(11):2809-2810. PubMed ID: 28833251
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  • 16. [Molecular genetic analysis of a family trio with weak B phenotype].
    Hu J, Nie Z, Gong J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Dec 10; 35(6):897-900. PubMed ID: 30512174
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  • 17. [A case of Bw39 subtype caused by 562C to T mutation of exon 7 of α -1,3-D-galactosyltransferase gene].
    Wang B, Shi L, Wang L, Liu Y, Ma L, Zhang R.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Jun 10; 34(3):427-430. PubMed ID: 28604971
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  • 18. ABO exon and intron analysis in individuals with the AweakB phenotype reveals a novel O1v-A2 hybrid allele that causes four missense mutations in the A transferase.
    Hosseini-Maaf B, Hellberg A, Rodrigues MJ, Chester MA, Olsson ML.
    BMC Genet; 2003 Nov 17; 4():17. PubMed ID: 14617382
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  • 19. [Indentification and Sequence Analysis of A Individual with B305 Blood Group Gene Subtypes of ABO Variant].
    Li GJ, Zhang X.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2016 Oct 17; 24(5):1563-1566. PubMed ID: 27784393
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  • 20. [Molecular genetic analysis for the A3 alleles].
    Yu Q, Liang YL, Deng ZH, Wu GG, Su YQ, Zhang X, Chen LH.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2005 Feb 17; 13(1):135-9. PubMed ID: 15748453
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