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505 related items for PubMed ID: 18680548

  • 1. 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
    [Abstract] [Full Text] [Related]

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  • 3. Structural basis for red cell phenotypic changes in newly identified, naturally occurring subgroup mutants of the human blood group B glycosyltransferase.
    Hosseini-Maaf B, Letts JA, Persson M, Smart E, LePennec PY, Hustinx H, Zhao Z, Palcic MM, Evans SV, Chester MA, Olsson ML.
    Transfusion; 2007 May; 47(5):864-75. PubMed ID: 17465952
    [Abstract] [Full Text] [Related]

  • 4. [C721T mutation of the alpha 1,3 galactosyltransferase gene responsible for Bw subgroup].
    Zhu F, Xu X, Hong X, Yan L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr; 22(2):138-41. PubMed ID: 15793772
    [Abstract] [Full Text] [Related]

  • 5. Amino-acid substitution in the disordered loop of blood group B-glycosyltransferase enzyme causes weak B phenotype.
    Yazer MH, Denomme GA, Rose NL, Palcic MM.
    Transfusion; 2005 Jul; 45(7):1178-82. PubMed ID: 15987364
    [Abstract] [Full Text] [Related]

  • 6. Identification of a novel A2 allele derived from the A transferase gene through a nucleotide substitution G539C.
    Chen DP, Tseng CP, Wang WT, Sun CF.
    Vox Sang; 2005 Apr; 88(3):196-9. PubMed ID: 15787730
    [Abstract] [Full Text] [Related]

  • 7. [Study on a 905A to G mutation of α 1,3 galactosyltransferase gene].
    Lin F, Zhang X, Li J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb; 31(1):82-4. PubMed ID: 24510570
    [Abstract] [Full Text] [Related]

  • 8. Two novel Jk(null) alleles derived from 222C>A in Exon 5 and 896G>A in Exon 9 of the JK gene.
    Liu HM, Lin JS, Chen PS, Lyou JY, Chen YJ, Tzeng CH.
    Transfusion; 2009 Feb; 49(2):259-64. PubMed ID: 18980618
    [Abstract] [Full Text] [Related]

  • 9. Missense mutations outside the catalytic domain of the ABO glycosyltransferase can cause weak blood group A and B phenotypes.
    Seltsam A, Blasczyk R.
    Transfusion; 2005 Oct; 45(10):1663-9. PubMed ID: 16181218
    [Abstract] [Full Text] [Related]

  • 10. [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
    [Abstract] [Full Text] [Related]

  • 11. [The molecular genetics basis for ABw07 phenotype of ABO subtype].
    Zhu H, Wu Y, Li X, Hong X, Xu X, Zhu F.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Dec; 25(6):678-80. PubMed ID: 19065531
    [Abstract] [Full Text] [Related]

  • 12. Cloning of a rat gene encoding the histo-blood group B enzyme: rats have more than one Abo gene.
    Turcot AL, Blancher A, Le Moullac-Vaidye B, Despiau S, Rocher J, Roubinet F, Szpirer C, Le Pendu J.
    Glycobiology; 2003 Dec; 13(12):919-28. PubMed ID: 12799344
    [Abstract] [Full Text] [Related]

  • 13. Weak A phenotypes associated with novel ABO alleles carrying the A2-related 1061C deletion and various missense substitutions.
    Hult AK, Yazer MH, Jørgensen R, Hellberg A, Hustinx H, Peyrard T, Palcic MM, Olsson ML.
    Transfusion; 2010 Jul; 50(7):1471-86. PubMed ID: 20456702
    [Abstract] [Full Text] [Related]

  • 14. Evolution of the O alleles of the human ABO blood group gene.
    Roubinet F, Despiau S, Calafell F, Jin F, Bertranpetit J, Saitou N, Blancher A.
    Transfusion; 2004 May; 44(5):707-15. PubMed ID: 15104652
    [Abstract] [Full Text] [Related]

  • 15. A novel cis-AB allele derived from the A transferase gene by nucleotide substitution C796A.
    Chen DP, Tseng CP, Wang WT, Wang MC, Tsao KC, Wu TL, Sun CF.
    Ann Clin Lab Sci; 2004 May; 34(4):437-42. PubMed ID: 15648786
    [Abstract] [Full Text] [Related]

  • 16. Association of ABO gene mutations resulting in a rare B subgroup.
    Sousa N, Anicchino-Bizzacchi JM, Leite EM, Locatelli MF, Albuquerque D, Costa FF, Barjas-Castro ML.
    Vox Sang; 2005 Jan; 88(1):31-4. PubMed ID: 15663720
    [Abstract] [Full Text] [Related]

  • 17. 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
    [Abstract] [Full Text] [Related]

  • 18. A novel cis-AB allele derived from a unique 796C>A mutation in exon 7 of ABO gene.
    Tzeng CH, Chen YJ, Lyou JY, Chen PS, Liu HM, Hu HY, Lin JS, Yu LC.
    Transfusion; 2005 Jan 17; 45(1):50-5. PubMed ID: 15647018
    [Abstract] [Full Text] [Related]

  • 19. [Study on molecular genetic structure of Ael blood subgroup].
    Yu Q, Wu GG, Liang YL, Deng ZH, Su YQ, Wang DM.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Apr 17; 23(2):173-6. PubMed ID: 16604489
    [Abstract] [Full Text] [Related]

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