552 related articles for article (PubMed ID: 17465952)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. A novel blood group B subgroup: serological and genetic studies.
Estalote AC; Palatnik M; Chester MA; Olsson ML; Sant'Anna Gomes BM
Transfus Med; 2004 Apr; 14(2):173-80. PubMed ID: 15113382
[TBL] [Abstract][Full Text] [Related]
7. Aberrant intracellular trafficking of a variant B glycosyltransferase.
Seltsam A; Grüger D; Just B; Figueiredo C; Gupta CD; Deluca DS; Blasczyk R
Transfusion; 2008 Sep; 48(9):1898-905. PubMed ID: 18513251
[TBL] [Abstract][Full Text] [Related]
8. 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]
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
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
14. 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
[TBL] [Abstract][Full Text] [Related]
15. ABO blood group alleles and genetic recombination.
Suzuki K
Leg Med (Tokyo); 2005 Jul; 7(4):205-12. PubMed ID: 15949965
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Fifteen novel mutations in PKLR associated with pyruvate kinase (PK) deficiency: structural implications of amino acid substitutions in PK.
van Wijk R; Huizinga EG; van Wesel AC; van Oirschot BA; Hadders MA; van Solinge WW
Hum Mutat; 2009 Mar; 30(3):446-53. PubMed ID: 19085939
[TBL] [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; 45(1):50-5. PubMed ID: 15647018
[TBL] [Abstract][Full Text] [Related]
19. [Biochemical basis of the ABO system subgroups].
Schenkel-Brunner H
Wien Klin Wochenschr; 2001 Oct; 113(20-21):787-98. PubMed ID: 11732114
[TBL] [Abstract][Full Text] [Related]
20. 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; 34(4):437-42. PubMed ID: 15648786
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
