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1 pha, interleukin (IL)-1beta, and IL-6 in the synovial membrane.
2 ) from measures of pathologic changes in the synovial membrane.
3 ve osteoclast precursor cells emerged in the synovial membrane.
4 pression in, and PGE(2) production from, the synovial membrane.
5 is a critical factor for GC formation in the synovial membrane.
6 y disease with primary manifestations in the synovial membrane.
7 ion of synovial cells and hyperplasia of the synovial membrane.
8 the expression of the immune response in the synovial membrane.
9 hocytes, macrophages and synoviocytes in the synovial membrane.
10 of the lining of the joint cavity called the synovial membrane.
11 and led to a reduced size selectivity of the synovial membrane.
12 ion in the target tissue of the disease, the synovial membrane.
13 ssa articular cartilage, articular disc, and synovial membrane.
14 form a protective lining barrier within the synovial membrane and actively participate in the remiss
17 g heterotypic signaling between cells of the synovial membrane and infiltrating lymphocytes in regula
18 lammatory phenotype in fibroblasts from both synovial membrane and infra-patellar fat pad and therefo
19 Strong immunohistochemical staining of the synovial membrane and subsynovial tissue was apparent in
20 rminal center response within the rheumatoid synovial membrane and the existence of similar structure
21 from the sprouted sympathetic fibers in the synovial membrane and upper dermis contribute to the pai
24 e IL-1alpha transcripts was also detected in synovial membranes and was coordinately up-regulated in
25 pression of COX-2 and PGE(2) in OA meniscus, synovial membrane, and osteophytic fibrocartilage explan
26 s of human OA articular cartilage, meniscus, synovial membrane, and osteophytic fibrocartilage were o
28 in the superficial and deeper layers of the synovial membrane as well as a proliferation of synovial
30 degradation of cartilage proteoglycans in OA synovial membrane-cartilage cocultures was blocked by th
38 onfirmed that PBEF immunolocalized in apical synovial membrane cells, endothelial cells, adipocytes,
40 IkappaBalpha were used to infect ex vivo RA synovial membrane cultures and synovial fibroblasts obta
42 n of TNFalpha and interleukin-1 (IL-1) in RA synovial membrane cultures reduced VEGF release by 45% (
43 primary human monocytes, macrophages, and RA synovial membrane cultures with p38 MAPK inhibitor compo
46 r the first time in a prospective study that synovial membrane cytokine mRNA expression is predictive
51 ow been demonstrated in rheumatoid arthritis synovial membrane, including members of the IL-1 superfa
52 and have demonstrated its expression in the synovial membrane lining layer by immunohistochemistry.
56 erent methods consistently demonstrated that synovial membrane mRNA levels of IL-1beta, TNFalpha, IL-
57 n (V(H)) genes of B cells recovered from the synovial membrane of five OA patients with marked B cell
58 mutations in p53 have been described in the synovial membrane of rheumatoid arthritis patients, the
63 as undertaken to analyze their expression in synovial membrane (SM) of patients with psoriatic arthri
64 fic for ADAMTS-4_v1 was found to bind to the synovial membrane surface on cryosections, and the prote
67 lts from a T cell-driven inflammation in the synovial membrane that is frequently associated with the
68 an recruit and activate T lymphocytes in the synovial membrane, thereby contributing to RA pathogenes
69 ohistochemistry in rheumatoid arthritis (RA) synovial membrane tissue and in paw tissue from arthriti
72 after gadolinium administration, to quantify synovial membrane volume (SV) as a measure of synovial p
74 l salivary gland, kidney cortex, dermis, and synovial membrane were completely restored, whereas only
76 nalytical improvements in synovial fluid and synovial membrane, with increasing regulatory macrophage