Publicação: Association of ABO gene mutations resulting in a rare B subgroup
dc.contributor.author | Sousa, N. | |
dc.contributor.author | Anicchino-Bizzacchi, J. M. | |
dc.contributor.author | Leite, E. M. | |
dc.contributor.author | Locatelli, M. F. | |
dc.contributor.author | Albuquerque, D. | |
dc.contributor.author | Costa, F. F. | |
dc.contributor.author | Castro, M. L. | |
dc.contributor.institution | Universidade Estadual de Campinas (UNICAMP) | |
dc.contributor.institution | Universidade Estadual Paulista (Unesp) | |
dc.date.accessioned | 2014-05-20T13:24:25Z | |
dc.date.available | 2014-05-20T13:24:25Z | |
dc.date.issued | 2005-01-01 | |
dc.description.abstract | Background and Objectives B subgroups are rare and the genetic analysis reported to date has been limited.Materials and Methods Serological and molecular investigations were performed in blood from a B-subgroup donor.Results Red cells did not react with anti-B and anti-AB reagents. However, cells absorbed anti-B. Red cells presented positive reactions with anti-H, and saliva secreted H substance. The molecular study demonstrated a B allele with the substitutions 467C>T, 646T>A, 681G>A, 771C>T, 796C>A, 803G>C, 829G>A and an 0 allele with the sequence of 002.Conclusions It is probable that the presence in exon 7 of some of the 002 substitutions could have weakened the enzymatic activity of the encoded B transferase. | en |
dc.description.affiliation | Univ Estadual Campinas, Hemoctr, BR-13083970 Campinas, SP, Brazil | |
dc.description.affiliation | Univ Estadual Campinas, FCM, Dept Farmacol, BR-13083970 Campinas, SP, Brazil | |
dc.description.affiliation | UNESP, Fac Ciências Farmaceut, Araraquara, Brazil | |
dc.description.affiliationUnesp | UNESP, Fac Ciências Farmaceut, Araraquara, Brazil | |
dc.format.extent | 31-34 | |
dc.identifier | http://dx.doi.org/10.1111/j.1423-0410.2005.00583.x | |
dc.identifier.citation | Vox Sanguinis. Oxford: Blackwell Publishing Ltd, v. 88, n. 1, p. 31-34, 2005. | |
dc.identifier.doi | 10.1111/j.1423-0410.2005.00583.x | |
dc.identifier.issn | 0042-9007 | |
dc.identifier.uri | http://hdl.handle.net/11449/7561 | |
dc.identifier.wos | WOS:000226931200005 | |
dc.language.iso | eng | |
dc.publisher | Blackwell Publishing | |
dc.relation.ispartof | Vox Sanguinis | |
dc.relation.ispartofjcr | 2.107 | |
dc.relation.ispartofsjr | 1,003 | |
dc.rights.accessRights | Acesso restrito | |
dc.source | Web of Science | |
dc.subject | ABO | pt |
dc.subject | B subgroup | pt |
dc.subject | blood group | pt |
dc.subject | genotyping | pt |
dc.subject | molecular biology | pt |
dc.title | Association of ABO gene mutations resulting in a rare B subgroup | en |
dc.type | Artigo | |
dcterms.license | http://olabout.wiley.com/WileyCDA/Section/id-406071.html | |
dcterms.rightsHolder | Blackwell Publishing Ltd | |
dspace.entity.type | Publication |
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