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 *

355 related articles for article (PubMed ID: 23521133)

  • 1. Molecular genetic analysis of ABO blood group variations reveals 29 novel ABO subgroup alleles.
    Cai X; Jin S; Liu X; Fan L; Lu Q; Wang J; Shen W; Gong S; Qiu L; Xiang D
    Transfusion; 2013 Nov; 53(11 Suppl 2):2910-6. PubMed ID: 23521133
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of a novel A1v-O1v hybrid allele with G829A mutation in a chimeric individual of AelBel phenotype.
    Sun CF; Chen DP; Tseng CP; Wang WT; Liu JP
    Transfusion; 2006 May; 46(5):780-9. PubMed ID: 16686846
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 4():17. PubMed ID: 14617382
    [TBL] [Abstract][Full Text] [Related]  

  • 4. New and unusual O alleles at the ABO locus are implicated in unexpected blood group phenotypes.
    Hosseini-Maaf B; Irshaid NM; Hellberg A; Wagner T; Levene C; Hustinx H; Steffensen R; Chester MA; Olsson ML
    Transfusion; 2005 Jan; 45(1):70-81. PubMed ID: 15647021
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genomic analysis of clinical samples with serologic ABO blood grouping discrepancies: identification of 15 novel A and B subgroup alleles.
    Olsson ML; Irshaid NM; Hosseini-Maaf B; Hellberg A; Moulds MK; Sareneva H; Chester MA
    Blood; 2001 Sep; 98(5):1585-93. PubMed ID: 11520811
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An extensive polymerase chain reaction-allele-specific polymorphism strategy for clinical ABO blood group genotyping that avoids potential errors caused by null, subgroup, and hybrid alleles.
    Hosseini-Maaf B; Hellberg A; Chester MA; Olsson ML
    Transfusion; 2007 Nov; 47(11):2110-25. PubMed ID: 17958541
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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; 23(2):173-6. PubMed ID: 16604489
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Systematic analysis of the ABO gene diversity within exons 6 and 7 by PCR screening reveals new ABO alleles.
    Seltsam A; Hallensleben M; Kollmann A; Burkhart J; Blasczyk R
    Transfusion; 2003 Apr; 43(4):428-39. PubMed ID: 12662274
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel B(weak) hybrid allele lacks three enhancer repeats but generates normal ABO transcript levels.
    Thuresson B; Hosseini-Maaf B; Hult AK; Hustinx H; Alan Chester M; Olsson ML
    Vox Sang; 2012 Jan; 102(1):55-64. PubMed ID: 21592135
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Weak blood group B phenotypes may be caused by variations in the CCAAT-binding factor/NF-Y enhancer region of the ABO gene.
    Seltsam A; Wagner FF; Grüger D; Gupta CD; Bade-Doeding C; Blasczyk R
    Transfusion; 2007 Dec; 47(12):2330-5. PubMed ID: 17764507
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nondeletional ABO*O alleles express weak blood group A phenotypes.
    Seltsam A; Das Gupta C; Wagner FF; Blasczyk R
    Transfusion; 2005 Mar; 45(3):359-65. PubMed ID: 15752153
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Molecular mechanism of an individual with weaken B phenotype in ABO blood group].
    Ying YL; Tao SD; He YM; Xu XG; Zhu FM; Lv HJ; Yan LX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Aug; 28(4):397-400. PubMed ID: 21811978
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A unique 502C>T mutation in exon 7 of ABO gene associated with the Bel phenotype in Taiwan.
    Lin PH; Li L; Lin-Tsai SJ; Lin KT; Chen JM; Chu DC
    Transfusion; 2003 Sep; 43(9):1254-9. PubMed ID: 12919428
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A weak blood group A phenotype caused by a new mutation at the ABO locus.
    Seltsam A; Hallensleben M; Eiz-Vesper B; Lenhard V; Heymann G; Blasczyk R
    Transfusion; 2002 Mar; 42(3):294-301. PubMed ID: 11961233
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [C742T mutation of α1, 3 N-acetyl-D-galactosaminyltransferase gene is responsible for A2 subgroup].
    Hong XZ; Yin YL; Xu XG; Ma KR; Lan XF; Liu Y; Zhu FM; Lü HJ; Yan LX
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2011 Jun; 19(3):702-5. PubMed ID: 21729554
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Two novel mutations p. L319V and p. L91P in ABO glycosyltransferases lead to A
    Lei H; Wang Z; Wang Y; Xiang D; Wang X; Cai X
    Blood Transfus; 2020 Nov; 18(6):471-477. PubMed ID: 32281923
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.