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Pathologie-Biologie|June 1, 1988
[Polymorphism of C4 and factor B in type I diabetes]J F Blickle, G Hauptmann, J Goetz, et al.The Journal of Pediatrics|December 1, 1995
Association of HLA class I antigen deficiency related to a TAP2 gene mutation with familial bronchiectasisL Donato, H de la Salle, D Hanau, et al.Tissue Antigens|July 1, 1982
Type I Glanzmann's thrombasthenia segregates independently of Ss and Duffy systems and the A, B, C, factor B, C2 and C4 loci of the HLA complexM M Tongio, P Lutz, G Hauptmann, et al.Revue Francaise De Transfusion Et Immuno-Hematologie|October 1, 1987
[Anti-HLA immunization following transfusions of leukocyte-poor blood]C Waller, A Urlacher, M Fischbach, et al.Scandinavian Journal of Rheumatology|January 1, 1977
Hereditary diffuse articular chondrocalcinosis. Dominant manifestation without close linkage with the HLA system in a large pedigreeA Gaucher, G Faure, P Netter, et al.European Journal of Immunology|May 6, 1999
Inefficient protection of human TAP-deficient fibroblasts from autologous NK cell-mediated lysis by cytokines inducing HLA class I expressionJ Zimmer, L Donato, D Hanau, et al.Rheumatology International|January 1, 1990
HLA-DR1 and DRw6 association in DR4-negative rheumatoid arthritis patientsB Lang, I Melchers, A Urlacher, et al.Revue Francaise De Transfusion Et Immuno-Hematologie|February 1, 1980
[HLA antigens and responsiveness to tetanic toxoid in man]M M Tongio, M Schwartz, J Klein, et al.Human Immunology|December 1, 1989
A T-cell clone recognizing an MLC stimulating epitope located on the DRw11 beta 1 chainA Urlacher, J M Tiercy, M Schlesier, et al.Pageof 10