Zobrazeno 1 - 9
of 9
pro vyhledávání: '"T P O'Hanlon"'
Autor:
F W, Miller, W, Chen, T P, O'Hanlon, R G, Cooper, J, Vencovsky, L G, Rider, K, Danko, L R, Wedderburn, I E, Lundberg, L M, Pachman, A M, Reed, S R, Ytterberg, L, Padyukov, A, Selva-O'Callaghan, T R, Radstake, D A, Isenberg, H, Chinoy, W E R, Ollier, P, Scheet, B, Peng, A, Lee, J, Byun, J A, Lamb, P K, Gregersen, C I, Amos, Hemlata, Varsani
Publikováno v:
Genes & Immunity. 16:470-480
Autoimmune muscle diseases (myositis) comprise a group of complex phenotypes influenced by genetic and environmental factors. To identify genetic risk factors in patients of European ancestry, we conducted a genome-wide association study (GWAS) of th
Publikováno v:
The Journal of Immunology. 152:2569-2576
The idiopathic inflammatory myopathies (IIM) are a heterogeneous group of diseases in which autoreactive T cells are thought to play a pathogenetic role. We have determined the pattern of TCR-alpha beta gene expression by muscle-infiltrating lymphocy
Autor:
L G, Rider, E, Shamim, S, Okada, J P, Pandey, I N, Targoff, T P, O'Hanlon, H A, Kim, Y S, Lim, H, Han, Y W, Song, F W, Miller
Publikováno v:
Arthritis and rheumatism. 42(6)
To better understand genetic contributions to autoimmunity, immunogenetic markers were studied in two racially discrete and geographically isolated populations of patients with idiopathic inflammatory myopathy (IIM).Clinical characteristics, as well
Autor:
L G, Rider, R C, Gurley, J P, Pandey, I, Garcia de la Torre, A E, Kalovidouris, T P, O'Hanlon, L A, Love, R C, Hennekam, L L, Baumbach, H E, Neville, C A, Garcia, J, Klingman, M, Gibbs, M H, Weisman, I N, Targoff, F W, Miller
Publikováno v:
Arthritis and rheumatism. 41(4)
To describe the clinical, serologic, and immunogenetic features of familial idiopathic inflammatory myopathy (IIM) and to compare these with the features of sporadic IIM.Clinical signs and symptoms, autoantibodies, HLA-DRB1 and DQA1 alleles, and GM/K
Publikováno v:
Annals of internal medicine. 122(9)
The myositis syndromes, the most common forms of which are polymyositis and dermatomyositis, are defined by idiopathic chronic inflammation in skeletal muscle. Although initially described more than a century ago, these diseases are so rare and heter
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 152(5)
The idiopathic inflammatory myopathies (IIM) are a heterogeneous group of diseases in which autoreactive T cells are thought to play a pathogenetic role. We have determined the pattern of TCR-alpha beta gene expression by muscle-infiltrating lymphocy
Publikováno v:
Journal of Biological Chemistry. 264:17389-17394
The β-galactoside α-2,6-sialyItransferase represents a member of a family of sialyltransferases which catalyze the terminal addition of sialic acid to maturing carbohydrate chains. We surveyed rat tissues using cDNA probes complementary to coding a
Publikováno v:
Journal of Biological Chemistry. 264:1854-1859
The hepatic acute phase response is accompanied by increased levels of Gal beta 1-4GlcNAc alpha 2,6-sialyltransferase activity in liver and in circulation. Previous studies suggested that cytokines and glucocorticoids mediate the induction of this si
Publikováno v:
The Journal of biological chemistry. 264(29)
The beta-galactoside alpha-2,6-sialyltransferase represents a member of a family of sialyltransferases which catalyze the terminal addition of sialic acid to maturing carbohydrate chains. We surveyed rat tissues using cDNA probes complementary to cod