Zobrazeno 1 - 10
of 133
pro vyhledávání: '"A O Carbonara"'
Publikováno v:
Scopus-Elsevier
Monoclonal antibodies detect a new polymorphic antigenic determinant shared by HLA-A2, 3, 28, 29, 30, 31 and w33. This was demonstrated by population and family studies, including an HLA-A,B recombinant family, and by lysostrip experiments. Competiti
Publikováno v:
Scopus-Elsevier
B lymphocyte enriched suspensions isolated by E rosette depletion (E-cells) or by nylon fiber adherence (adherent cells) were identified by their cellular composition using different T and B cell markers (SIg,E receptor, T3, T4, T8 and Ia-like antige
Publikováno v:
Tissue Antigens. 10:323-329
Of 28 unabsorbed sera from polytransfused individuals or multiparous women, which were not cytotoxic for total peripheral blood lymphocytes, 13 were found to react positively against B cell-enriched suspensions. These 13 sera were further characteriz
Publikováno v:
Tissue Antigens. 4:558-563
Feto-maternal symbiosis during pregnancy induces the production of antibodies against fetal alloantigens. In this study, the presence of antibodies in the sera from parous women was checked by Complement dependent Lysis (CdL) at 20°C and at 15°C, a
Autor:
Fernanda Cinque, Boccazzi C, Alfredo Brusco, A. van Leeuwen, Angelo O. Carbonara, G. G. de Lange, M DeMarchi, Silvia Saviozzi
Publikováno v:
European Journal of Immunogenetics. 25:349-355
The molecular bases of classical serological immunoglobulin allotypes are progressively uncovered through detailed characterization of the relevant genes. Here we describe two isoallotypic determinants of the G4 gene. In the first, Leu 309, as in G1
Publikováno v:
Human Evolution. 13:49-56
Four Immunoglobulin gamma heavy chain isotypes are present in humans; the true phylogenetic relationship between the genes are not known because of the complex concerted evolution of the Ig multigene locus. Here we present data obtained from Southern
Publikováno v:
International Journal of Clinical & Laboratory Research. 27:253-256
Multiples of medians of serum markers are assumed to be independent of gestational age: every algorithm used for Down’s syndrome risk evaluation is based on this hypothesis. However, our former observations suggested that multiples of medians of hu