193 related articles for article (PubMed ID: 15318868)
1. ABO sequence analysis in a family with weak expression of blood group B.
Yazer MH; Blajchman MA; DiTomasso J; Denomme GA
Transfusion; 2004 Sep; 44(9):1394-5. PubMed ID: 15318868
[No Abstract] [Full Text] [Related]
2. Polymorphism and recombination events at the ABO locus: a major challenge for genomic ABO blood grouping strategies.
Olsson ML; Chester MA
Transfus Med; 2001 Aug; 11(4):295-313. PubMed ID: 11532186
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Multiplex ABO genotyping by minisequencing.
Ferri G; Pelotti S
Methods Mol Biol; 2009; 496():51-8. PubMed ID: 18839104
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. 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]
7. A weak blood group A phenotype caused by a translation-initiator mutation in the ABO gene.
Seltsam A; Das Gupta C; Bade-Doeding C; Blasczyk R
Transfusion; 2006 Mar; 46(3):434-40. PubMed ID: 16533287
[TBL] [Abstract][Full Text] [Related]
8. Demonstration of A antigen and A allele of ABO histo-blood group in nail in a case with the absence of A antigen and anti-A antibody in blood.
Michino J; Hata Y; Matsui K; Takizawa H; Kominato Y; Tabata S; Nishino K; Yasumura S; Kitajima I
Leg Med (Tokyo); 2005 May; 7(3):194-7. PubMed ID: 15847830
[TBL] [Abstract][Full Text] [Related]
9. Detection of a new weak A blood-group allele (Aw11).
Pruss A; Heymann GA; Braun J; Kiesewetter HH; Salama A
Vox Sang; 2006 Apr; 90(3):195-7. PubMed ID: 16507020
[TBL] [Abstract][Full Text] [Related]
10. A 425T>C mutation in the B allele for the ABO transferase is associated with the B3 phenotype in Han Chinese persons.
Zhu F; Xu X; Hong X; He J; Yan L
Transfusion; 2008 Nov; 48(11):2476-7. PubMed ID: 19054377
[No Abstract] [Full Text] [Related]
11. [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]
12. The serological and genetic basis of the cis-AB blood group in Korea.
Cho D; Kim SH; Jeon MJ; Choi KL; Kee SJ; Shin MG; Shin JH; Suh SP; Yazer MH; Ryang DW
Vox Sang; 2004 Jul; 87(1):41-3. PubMed ID: 15260821
[TBL] [Abstract][Full Text] [Related]
13. Analysis of the gene polymorphism of ABO blood group specific transferases helps diagnosis of acquired B status.
Fischer GF; FaƩ I; Dub E; Pickl WF
Vox Sang; 1992; 62(2):113-6. PubMed ID: 1355622
[TBL] [Abstract][Full Text] [Related]
14. A case of para-Bombay phenotype Bhm (OBHm).
Maeda H; Ohshima T; Takayasu T; Tanaka N
Nihon Hoigaku Zasshi; 1985 Jun; 39(3):209-13. PubMed ID: 3936956
[No Abstract] [Full Text] [Related]
15. Blood grouping discrepancies between ABO genotype and phenotype caused by O alleles.
Yazer MH; Hosseini-Maaf B; Olsson ML
Curr Opin Hematol; 2008 Nov; 15(6):618-24. PubMed ID: 18832934
[TBL] [Abstract][Full Text] [Related]
16. Novel A group allele with a 556A>G substitution previously found in a B subgroup allele.
Yu Q; Deng ZH; Wu GG; Liang YL; Su YQ
Transfus Med; 2006 Feb; 16(1):75-6. PubMed ID: 16480444
[No Abstract] [Full Text] [Related]
17. 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
[TBL] [Abstract][Full Text] [Related]
18. ABO genotyping by minisequencing analysis.
Ferri G; Bini C; Ceccardi S; Pelotti S
Transfusion; 2004 Jun; 44(6):943-4. PubMed ID: 15157266
[No Abstract] [Full Text] [Related]
19. Nondeletional ABO*O alleles frequently cause blood donor typing problems.
Wagner FF; Blasczyk R; Seltsam A
Transfusion; 2005 Aug; 45(8):1331-4. PubMed ID: 16078922
[TBL] [Abstract][Full Text] [Related]
20. [ABO polymorphism in blood donors in Morocco].
Habti N; Nourichafi N; Benchemsi N
Transfus Clin Biol; 2004 Apr; 11(2):95-7. PubMed ID: 15120106
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]