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Journal of Neuroimmunology|August 30, 2001
No linkage or association of the nitric oxide synthase genes to multiple sclerosisH Modin, Y Dai, T Masterman, et al.Blood|September 15, 1992
Splice site mutations are a common cause of X-linked chronic granulomatous diseaseM de Boer, B G Bolscher, M C Dinauer, et al.The EMBO Journal|September 1, 1985
Heterogeneity of T-cell beta-chain gene rearrangements in human leukaemias and lymphomasT H Rabbitts, A Stinson, A Forster, et al.Biochemical and Biophysical Research Communications|June 11, 1999
Synergistic activation of the human Btk promoter by transcription factors Sp1/3 and PU.1S Müller, A Maas, T C Islam, et al.Journal of Immunology (Baltimore, Md. : 1950)|July 1, 1990
Subclass distribution of antigen-specific IgA antibodies in normal donors and individuals with homozygous C alpha 1 or C alpha 2 gene deletionsP E Engström, G Norhagen, A Bottaro, et al.The Journal of Rheumatology|January 27, 2000
Two edged role of mannose binding lectin in rheumatoid arthritis: a cross sectional studyP Garred, H O Madsen, H Marquart, et al.AIDS (London, England)|March 1, 1997
Heterozygosity for a deletion in the CKR-5 gene leads to prolonged AIDS-free survival and slower CD4 T-cell decline in a cohort of HIV-seropositive individualsJ Eugen-Olsen, A K Iversen, P Garred, et al.Investigative Ophthalmology & Visual Science|August 12, 1998
Human retinal pigment epithelial cell-induced apoptosis in activated T cellsA Jørgensen, A K Wiencke, M la Cour, et al.Human Molecular Genetics|April 1, 1995
Identification of Btk mutations in 20 unrelated patients with X-linked agammaglobulinaemia (XLA)H Jin, A D Webster, M Vihinen, et al.Clinical and Experimental Immunology|December 1, 1988
The antibody spectrum in individuals with defect expression of HLA class II and the LFA-1 glycoprotein family genesC I Smith, C Bremard-Oury, F Le Deist, et al.Pageof 54