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Journal of Immunology (Baltimore, Md. : 1950)|October 15, 1991
Ig H chain variable and C region genes in common variable immunodeficiency. Characterization of two new deletion haplotypesP G Olsson, M H Hofker, M A Walter, et al.
Nature Genetics|December 28, 1999
A humanized model for multiple sclerosis using HLA-DR2 and a human T-cell receptorL S Madsen, E C Andersson, L Jansson, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 24, 1998
Definition of MHC and T cell receptor contacts in the HLA-DR4restricted immunodominant epitope in type II collagen and characterization of collagen-induced arthritis in HLA-DR4 and human CD4 transgenic miceE C Andersson, B E Hansen, H Jacobsen, et al.
European Journal of Haematology|October 1, 1993
A 40-base-pair duplication in the gp91-phox gene leading to X-linked chronic granulomatous diseaseH Rabbani, M de Boer, A Ahlin, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 1, 1995
Prevalence, genetics and clinical presentation of chronic granulomatous disease in SwedenA Ahlin, M De Boer, D Roos, et al.
The Medical Journal of Australia|July 8, 1985
Gastrointestinal morbidity among World War II prisoners of war: 40 years onK J Goulston, O F Dent, P H Chapuis, et al.
Genes and Immunity|January 10, 2002
Linkage analysis suggests a region of importance for multiple sclerosis in 3p14-13Y Dai, C Xu, M Holmberg, et al.
Human Mutation|April 29, 1999
Mutations of the human BTK gene coding for bruton tyrosine kinase in X-linked agammaglobulinemiaM Vihinen, S P Kwan, T Lester, et al.
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|September 26, 2012
Controlling the formation of a monolayer of cytochrome P450 reductase onto Au surfacesJ H Convery, C I Smith, B Khara, et al.
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