Zobrazeno 1 - 10
of 56
pro vyhledávání: '"G. Juszczak"'
Autor:
S. Oudin, T. Tabary, B. Reveil, N. Gupta, P. Rouger, J.H.M. Cohen, F. Philbert, David Klatzmann, M. Tonye Libyh, G. Juszczak, Francine Bougy, P. Cornillet, D. Goossens, X. Dervillez
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Monomeric recombinant molecules prove generally unsatisfactory for in vivo use. Most biological systems are indeed multivalent either structurally, associating different chains, or functionally, when cross-linked by their ligands. Mimicking natural m
Two new alleles of the RHCE gene in Black individuals: the RHce allele ceMO and the RHcE allele cEMI
Autor:
F, Noizat-Pirenne, I, Mouro, P Y, Le Pennec, H, Ansart-Pirenne, G, Juszczak, C, Patereau, M, Verdier, J, Babinet, M, Roussel, P, Rouger, J P, Cartron
Publikováno v:
British journal of haematology. 113(3)
Six unrelated individuals of Afro-Caribbean origin, whose red cells have a marked reduction of the Rhe antigen expression, have been identified. All exhibited the same serological profile with anti-e monoclonal antibodies and lacked expression of the
Publikováno v:
Transfusion. 20:536-539
The H and I antigens were studied in the plasma and saliva of 52 group O subjects, by hemagglutination inhibition at continuous flow. H plasma substance was detected with one anti-H antibody from a Bh donor. Secretors have more H plasma substance tha
Publikováno v:
Revue Francaise de Transfusion et Immuno-hématologie. 23:233-248
Resume A partir de l'etude parallele de 20 familles ou est observe un phenotype deficitaire en H, la classification pratique suivante est proposee: A. — Les phenotypes Bombay Oh, OAh, OBh, OABh (10 familles) sont definis selon les criteres suivants
Autor:
Rafael Oriol, G. Juszczak, J.-P. Cartron, C. Salmon, Philippe Rouger, G. Liberge, J. Le Pendu
Publikováno v:
Vox Sanguinis. 44:360-365
alpha-2-L-fucosyltransferase activity was found in the sera of 4 H-deficient secretor individuals (Hz). This activity represented about 5-10% of the activity present in the serum of normal H phenotypes.
Publikováno v:
Revue Francaise de Transfusion et Immuno-hématologie. 21:21-27
Summary Hm phenotype represents a dissociation between a normal salivary expression of H substance and a very weakened expression of the antigen on red blood cells. Genetic analysis of the reported family reveals a dominant inheritance : Some members
Publikováno v:
European Journal of Immunogenetics. 10:333-335
SUMMARY Two murine monoclonal antibodies (E11-1 and MR4-130) agglutinated all samples of human red cells except those of the Ge (-1, -2, -3) phenotype. It was possible to demonstrate that these antibodies recognize two different epitopes of the Gerbi
Publikováno v:
Immunological communications. 9(2)
H and I substances are present in the plasma and the saliva. In the plasma there is no quantitative relationship between H and I substances, whereas in the saliva only non-secretors produce I substance [shown by anti-IS serum, (Sti.)]. The study of I
Publikováno v:
Revue francaise de transfusion et immuno-hematologie. 21(1)
Hm phenotype represents a dissociation between a normal salivary expression of H substance and a very weakened expression of the antigen on red blood cells. Genetic analysis of the reported family reveals a dominant inheritance: Some members (Marie K
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