Molecular diagnostics in immunohaematology

Vox Sanguinis, Supplement

Volumn 87, Issue 2, 2004, Pages

  Van Der Schoot, C Ellen ^a  

^a SANQUIN RESEARCH   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; BLOOD GROUP TYPING; CLINICAL IMMUNOLOGY; CONFERENCE PAPER; DIAGNOSTIC PROCEDURE; DNA MICROARRAY; GENE AMPLIFICATION; GENOTYPE; HEMATOLOGY; HOMOZYGOSITY; HUMAN; IMMUNOHEMATOLOGY; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

ALLERGY AND IMMUNOLOGY; BLOOD DONORS; BLOOD TRANSFUSION; GENETIC TECHNIQUES; GENOTYPE; HEMATOLOGY; HLA ANTIGENS; HUMANS; NUCLEIC ACID HYBRIDIZATION; PHENOTYPE; POLYMERASE CHAIN REACTION;

EID: 4444364254     PISSN: 17416892     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

References (33)

1. Crew VK, Green CA, Daniels G, Anstee DJ: Renal failure associated with an inactivating mutation in the human CD 151 gene of three individuals lacking the MER2 blood group. Blood 2003; 102:4a
2. Roudier N, Ripoche P, Gane P, Le Pennec PY, Daniels G, Cartron JP, Bailly P: AQP3 deficiency in humans and the molecular basis of a novel blood group system, GIL. J Biol Chem 2002; 277:45854-9
3. Reid ME: Applications of DNA-based assays in blood group antigen and antibody identification. Transfusion 2003; 43:1748-57
4. Lyamichev V, Mast AL, Hall JG, Prudent JR, Kaiser MW, Takova T, Kwiatkowski RW, Sander TJ, de Arruda M, Arco DA: Polymorphism identification and quantitative detection of genomic DNA by invasive deavage of oligonudeotide probes. Nat Biotechnol 1999; 17:292-6
5. Maaskant-van Wijk PA, Faas BH, de Ruijter JA, Overbeeke MA, von dem Borne AE, van Rhenen DJ, van der School CE: Genotyping of RHD by multiplex polymerase chain reaction analysis of six RHD-specific exons. Transfusion 1998; 38:1015-21
6. Olsson ML, Hansson C, Avent ND, Akesson EE, Green CA, Daniels GL: A clinically applicable method for determining the three major alleles at the Duffy (FY) blood group locus using polymerase chain reaction with allele-specific primers. Transfusion 1998; 38:168-73
7. Liu W, Sommer SS: Detection of extremely rare alleles by bidirectional pyrophosphorolysis-activated polymerization allele-specific amplification (Bi-PAP-A). Biotechniques 2004; 36:2-10
8. Mouritzen P, Nielsen AT, Pfundheller HM, Choleva Y, Kongsbak L, Moller S: Single nucleotide polymorphism genotyping using locked nucleic acid (LNA). Expert Rev Mol Diagn 2003; 3:27-38
9. Igloi GL: Single-nucleotide polymorphism detection using peptide nucleic acids. Expert Rev Mol Diagn 2003; 3:17-26
10. Muller TH, Doscher A, Schunter F: Genotyping of the human platelet antigen-1 by ELISA detection of allele-specific amplicons. Vox Sang 1997; 73:185-8
11. Beiboer SHW, Wieringa-Jelsma T, Maaskant-van Wijk PA, van der Schoot CE, Roos D, den Dunnen JT, de Haas M: Rapid genotyping of blood group antigens by multiplex PCR and DNA microarray. Vox Sang 2004; 87(Suppl. 3):(Abstract P18.4)
12. Si-Louis M, Perreault J, Lemieux R: Extended blood grouping of blood donors with automatable PCR-ELISA genotyping. Transfusion 2003; 43:1126-32
13. Armstrong B, Stewart M, Mazumder A: Suspension arrays for high throughput, multiplexed single nucleotide polymorphism genotyping. Cytometry 2000; 40:102-8
14. Santacroce R, Ratti A, Carol F, Foglieni B, Ferraris A, Cremonesi L, Margaglione M, Seri M, Ravazzolo R, Restagno G, Dallapiccola B, Rappaport E, Pollak ES, Surrey S, Ferrari M, Fortina P: Analysis of clinically relevant single-nucleotide polymorphisms by use of microelectronic array technology. Clin Chem 2002; 48:2124-30
15. van Moorsel CHM, van Wijngaarden EE, Fokkema IF, den Dunnen JT, Roos D, van Zwieten R, Giordano PC, Harteveld CL: Alpha-globin mutation detection by tagged single-base extension and hybridization to universal glass and flow-through microarrays. Eur J Hum Gen 2004; in press
16. van Drunen J, Beckers EAM, Sintnicolaas K, van Rhenen DJ, Maaskant-van Wijk PA: Rapid pyrosequencing of blood group systems using the pyrosequencing technique. Vox Sang 2002; 83:104-5
17. Wagner FF, Flegel WA: RHD gene deletion occurred in the Rhesus box. Blood 2000; 95:3662-8
18. van der Schoot CE, Tax GH, Rijnders RJ, de Haas M, Christiaens GC: Prenatal typing of Rh and Kell blood group system antigens: The edge of a watershed. Transfus Med Rev 2003; 17:31-44
19. Finning KM, Martin PG, Soothill PW, Avent ND: Prediction of fetal D status from maternal plasma: Introduction of a new noninvasive fetal RHD genotyping service. Transfusion 2002; 42:1079-85
20. Faas BH, Beuling EA, von Christiaens GC, von dem Borne AE, van der Schoot CE: Detection of fetal RHD-specific sequences in maternal plasma. Lancet 1998; 352:1196-7
21. Dee R, Rijnders RJP, Bossers B, de Haas M, Christiaens LGCM, van der Schoot CE: RealTime PCR of biallelic insertion/ deletion polymorphisms as positive control for fetal plasma DNA. Vox Sang 2004; 87(Suppl. 3):(Abstract P18.24)
22. van der Schoot CE, Ait Soussan A, Dee R, Bonsel GJ, de Haas M: Screening for fetal RHD-genotype by plasma PCR in all D-negative pregnant women is feasible. Vox Sang 2004; 87(Suppl. 3): (Abstract Tu07.04)
23. Matheson KA, Denomme GA: Novel 3′ Rhesus box sequences confound RHD zygosity assignment. Transfusion 2002; 42:645-50
24. Tax MGHM, Maaskant-van Wijk PA, van Drunen J, van der School CE: The highly variable RH locus in non-whites highly hampers RHD zygosity determination. Vox Sang 2004; 87(Suppl. 3): (Abstract F18.23)
25. Castilho L, Rios M, Bianco C, Pellegrino J Jr, Alberto FL, Saad ST, Costa FF: DNA-based typing of blood groups for the management of multiply-transfused sickle cell disease patients. Transfusion 2002; 42:232-8
26. Rozman P, Dovc T, Gassner C: Differentiation of autologous ABO, RHD, RHCE, KEL, JK, and FY blood group genotypes by analysis of peripheral blood samples of patients who have recently received multiple transfusions. Transfusion 2000; 40:936-42
27. Reid ME, Rios M, Powell VI, Charles-Pierre D, Malavade V: DNA from blood samples can be used to genotype patients who have recently received a transfusion. Transfusion 2000; 40:48-53
28. Wenk RE, Chiafari PA: DNA typing of recipient blood after massive transfusion. Transfusion 1997; 37:1108-10
29. Wagner FF, Gassner C, Muller TH, Schonitzer D, Schunter F, Flegel WA: Molecular basis of weak D phenotypes. Blood 1999; 93:385-93
30. Olsson ML, Irshaid NM, Hosseini-Maaf B, Hellberg A, Moulds MK, Sareneva H, Chester MA: Genomic analysis of clinical samples with serologic ABO blood grouping discrepancies: Identification of 15 novel A and B subgroup alleles. Blood 2001; 98:1585-93
31. Hurd CM, Cavanagh G, Schuh A, Ouwehand WH, Metcalfe P: Genotyping for platelet-specific antigens: Techniques for the detection of single nucleotide polymorphisms. Vox Sang 2002; 83:1-12
32. Cheroutre G, Porcelijn L, Jongerius J, McBride S, Jaikaran E, Maaskant P, de Haas M: Automated human platelet antigen (HPA) genotyping to provide a completely typed donor population. Vox Sang 2004; 87(Suppl. 3):(Abstract o 18.2)
33. Rios M, Hue-Roye K, Lee AH, Chiofolo JT, Miller JL, Reid ME: DNA analysis for the Dombrock polymorphism. Transfusion 2001; 41:1143-6