Update on blood group terminology and molecular polymorphisms
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References
1. Reid ME, Lomas-Francis C, Olsson ML. The Blood Group Antigen FactsBook. 3rd ed. London, UK, Academic Press, 2012.
2. Storry JR, Castilho L, Chen Q, Daniels G, Denomme G, Flegel WA, et al. International society of blood transfusion working party on red cell immunogenetics and terminology: report of the Seoul and London meetings. ISBT Sci Ser. 2016;11:118-22.
3. Daniels G. The molecular genetics of blood group polymorphism. Transpl Immunol. 2005;14:143-53.
4. Wagner FF, Flegel WA. RHD gene deletion occurred in the Rhesus box. Blood. 2000;95:3662-8.
5. Yamamoto F, Clausen H, White T, Marken J, Hakomori S. Molecular genetic basis of the histo-blood group ABO system. Nature. 1990;345:229-33.
6. Yamamoto F, McNeill PD, Hakomori S. Human histo-blood group A2 transferase coded by A2 allele, one of the A subtypes, is characterized by a single base deletion in the coding sequence, which results in an additional domain at the carboxyl terminal. Biochem Biophys Res Commun. 1992;187:366-74.
7. Singleton BK, Green CA, Avent ND, Martin PG, Smart E, Daka A, et al. The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in africans with the Rh D-negative blood group phenotype. Blood. 2000;95:12-8.
8. Wagner FF, Gassner C, Muller TH, Schonitzer D, Schunter F, Flegel WA. Three molecular structures cause rhesus D category VI phenotypes with distinct immunohematologic features. Blood. 1998;91:2157-68.
9. Palacajornsuk P, Nathalang O, Tantimavanich S, Bejrachandra S, Reid ME. Detection of MNS hybrid molecules in the Thai population using PCR-SSP technique. Transfus Med. 2007;17:169-74.
10. Sriwanitchrak P, Sriwanitchrak K, Tubrod J, Kupatawintu P, Kaset C, Nathalang O. Genomic characterisation of the Jk(a-b-) phenotype in Thai blood donors. Blood Transfus. 2012;10:181-5.
11. Singleton BK, Burton NM, Green C, Brady RL, Anstee DJ. Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype. Blood. 2008;112:2081-8.
12. Garcia-Sanchez F, Pardi C, Kupatawintu P, Thornton N, Rodriguez MA, Lucea I, et al. Identification of new KLF1 and LU alleles during the resolution of Lutheran typing discrepancies. Transfusion. 2016;56:1413-8.
13. Hellberg A, Ringressi A, Yahalom V, Säfwenberg J, Reid ME, Olsson ML. Genetic heterogeneity at the glycosyltransferase loci underlying the GLOB blood group system and collection. Br J Haematol. 2004;125:528-36.
14. Ricci Hagman J, Hult AK, Westman JS, Hosseini-Maaf B, Jongruamklang P, Saipin J, et al. Multiple miscarriages in two sisters of Thai origin with the rare Pk phenotype caused by a novel nonsense mutation at the B3GALNT1 locus. Transfus Med. 2018. doi: 10.1111/tme.12544. Epub 2018 Jun 6.
15. McBean R, Liew YW, Wilson B, Kupatawintu P, Emthip M, Hyland C, et al. Genotyping confirms inheritance of the rare At(a-) type in a case of haemolytic disease of the newborn. J Pathol Clin Res. 2015;2:53-5.
16. Nathalang O, Intharanut K, Sasikarn W, Nathalang S, Kupatawintu P. A new polymerase chain reaction: sequence-specific primer method for the Augustine blood type. Blood Transfus. 2016;14:577-9.
17. Lopez GH, Wilson B, Liew YW, Kupatawintu P, Emthip M, Hyland CA, et al. An alloantibody in a homozygous GYP*Mur individual defines JENU (MNS49), a new high-frequency antigen on glycophorin B. Transfusion. 2017;57:716-7.
1. Reid ME, Lomas-Francis C, Olsson ML. The Blood Group Antigen FactsBook. 3rd ed. London, UK, Academic Press, 2012.
2. Storry JR, Castilho L, Chen Q, Daniels G, Denomme G, Flegel WA, et al. International society of blood transfusion working party on red cell immunogenetics and terminology: report of the Seoul and London meetings. ISBT Sci Ser. 2016;11:118-22.
3. Daniels G. The molecular genetics of blood group polymorphism. Transpl Immunol. 2005;14:143-53.
4. Wagner FF, Flegel WA. RHD gene deletion occurred in the Rhesus box. Blood. 2000;95:3662-8.
5. Yamamoto F, Clausen H, White T, Marken J, Hakomori S. Molecular genetic basis of the histo-blood group ABO system. Nature. 1990;345:229-33.
6. Yamamoto F, McNeill PD, Hakomori S. Human histo-blood group A2 transferase coded by A2 allele, one of the A subtypes, is characterized by a single base deletion in the coding sequence, which results in an additional domain at the carboxyl terminal. Biochem Biophys Res Commun. 1992;187:366-74.
7. Singleton BK, Green CA, Avent ND, Martin PG, Smart E, Daka A, et al. The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in africans with the Rh D-negative blood group phenotype. Blood. 2000;95:12-8.
8. Wagner FF, Gassner C, Muller TH, Schonitzer D, Schunter F, Flegel WA. Three molecular structures cause rhesus D category VI phenotypes with distinct immunohematologic features. Blood. 1998;91:2157-68.
9. Palacajornsuk P, Nathalang O, Tantimavanich S, Bejrachandra S, Reid ME. Detection of MNS hybrid molecules in the Thai population using PCR-SSP technique. Transfus Med. 2007;17:169-74.
10. Sriwanitchrak P, Sriwanitchrak K, Tubrod J, Kupatawintu P, Kaset C, Nathalang O. Genomic characterisation of the Jk(a-b-) phenotype in Thai blood donors. Blood Transfus. 2012;10:181-5.
11. Singleton BK, Burton NM, Green C, Brady RL, Anstee DJ. Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype. Blood. 2008;112:2081-8.
12. Garcia-Sanchez F, Pardi C, Kupatawintu P, Thornton N, Rodriguez MA, Lucea I, et al. Identification of new KLF1 and LU alleles during the resolution of Lutheran typing discrepancies. Transfusion. 2016;56:1413-8.
13. Hellberg A, Ringressi A, Yahalom V, Säfwenberg J, Reid ME, Olsson ML. Genetic heterogeneity at the glycosyltransferase loci underlying the GLOB blood group system and collection. Br J Haematol. 2004;125:528-36.
14. Ricci Hagman J, Hult AK, Westman JS, Hosseini-Maaf B, Jongruamklang P, Saipin J, et al. Multiple miscarriages in two sisters of Thai origin with the rare Pk phenotype caused by a novel nonsense mutation at the B3GALNT1 locus. Transfus Med. 2018. doi: 10.1111/tme.12544. Epub 2018 Jun 6.
15. McBean R, Liew YW, Wilson B, Kupatawintu P, Emthip M, Hyland C, et al. Genotyping confirms inheritance of the rare At(a-) type in a case of haemolytic disease of the newborn. J Pathol Clin Res. 2015;2:53-5.
16. Nathalang O, Intharanut K, Sasikarn W, Nathalang S, Kupatawintu P. A new polymerase chain reaction: sequence-specific primer method for the Augustine blood type. Blood Transfus. 2016;14:577-9.
17. Lopez GH, Wilson B, Liew YW, Kupatawintu P, Emthip M, Hyland CA, et al. An alloantibody in a homozygous GYP*Mur individual defines JENU (MNS49), a new high-frequency antigen on glycophorin B. Transfusion. 2017;57:716-7.
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Published
2018-12-13
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บทความฟื้นวิชา (Literature review)
