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Annals of Neurology|October 1, 1990
HTLV-I sequences are not detected in peripheral blood genomic DNA or in brain cDNA of multiple sclerosis patientsJ R Oksenberg, R Mantegazza, K Sakai, et al.Journal of Neuroimmunology|July 1, 1993
Gamma delta T cell receptor repertoire in brain lesions of patients with multiple sclerosisJ Hvas, J R Oksenberg, R Fernando, et al.Human Immunology|June 1, 1988
Polymorphic markers of human T-cell receptor alpha and beta genes. Family studies and comparison of frequencies in healthy individuals and patients with multiple sclerosis and myasthenia gravisJ R Oksenberg, C N Gaiser, L L Cavalli-Sforza, et al.International Immunology|January 14, 1999
Differential display analysis of murine encephalitogenic mRNAM C Jeong, L Izikson, A Uccelli, et al.Critical Reviews in Immunology|January 1, 1992
T-cell receptors: germline polymorphism and patterns of usage in demyelinating diseasesK Usuku, N Joshi, S L HauserImmunogenetics|May 10, 2000
CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis. Multiple Sclerosis Genetics GroupL F Barcellos, A M Schito, J B Rimmler, et al.Annals of Neurology|September 1, 1993
The T-cell response to myelin basic protein in familial multiple sclerosis: diversity of fine specificity, restricting elements, and T-cell receptor usageN Joshi, K Usuku, S L HauserGenes and Immunity|October 30, 2009
Multiple sclerosis susceptibility alleles in African AmericansB A Johnson, J Wang, E M Taylor, et al.Human Molecular Genetics|July 21, 1998
Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics GroupJ L Haines, H A Terwedow, K Burgess, et al.Journal De Genetique Humaine|May 1, 1987
[An XX male newborn infant. A genetic and endocrinologic study]J L Nivelon, E Seboun, M Fellous, et al.Pageof 20