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Genomics|March 1, 1991
A centromere-based genetic map of the short arm of human chromosome 6H Blanché, H Y Zoghbi, E W Jabs, et al.Proceedings of the National Academy of Sciences of the United States of America|September 13, 1994
BY55 monoclonal antibody delineates within human cord blood and bone marrow lymphocytes distinct cell subsets mediating cytotoxic activityA Bensussan, E Gluckman, S el Marsafy, et al.Blood|August 1, 1988
The human T-cell V gamma gene locus: cloning of new segments and study of V gamma rearrangements in neoplastic T and B cellsZ Chen, M P Font, P Loiseau, et al.Tissue Antigens|February 1, 1980
Functional study and detection of HLA-D products on fractionated human bone marrow cellsD Fradelizi, E Gluckman, J Wiels, et al.Human Genetics|January 7, 1998
Exhaustive screening of the 21-hydroxylase gene in a population of hyperandrogenic womenH Blanché, P Vexiau, S Clauin, et al.International Immunology|May 18, 1999
IL-10 selectively induces HLA-G expression in human trophoblasts and monocytesP Moreau, F Adrian-Cabestre, C Menier, et al.La Nouvelle Presse Medicale|October 18, 1975
[Research of an association between HL-A antigens and systemic scleroderma]J Crouzet, M C Marbach, J P Camus, et al.Transplantation|May 1, 1978
Anti-B cell lymphocytotoxic antibodies in kidney transplant recipientsV Lepage, J C Gluckman, J Bedrossian, et al.Proceedings of the National Academy of Sciences of the United States of America|March 1, 1984
Class II HLA-DC beta-chain DNA restriction fragments differentiate among HLA-DR2 individuals in insulin-dependent diabetes and multiple sclerosisD Cohen, O Cohen, A Marcadet, et al.Human Genetics|December 1, 1986
Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiencyE Mornet, P Couillin, F Kutten, et al.Pageof 41