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1 chemokine (C-X-C motif) ligand 9 (CXCL9) and matrix metalloproteinase 13.
2 ng did not prevent collagen I degradation by matrix metalloproteinase 13.
3 ed with the expression profiles of DDR-2 and matrix metalloproteinase 13.
4 roteinase 1, matrix metalloproteinase 2, and matrix metalloproteinase 13.
5 such as transforming growth factor-beta2 and matrix metalloproteinase-13.
6 ey are heterogeneous regarding expression of matrix metalloproteinase-13.
7 shly isolated hepatic stellate cells express matrix metalloproteinase-13.
8 synovial fluid CSF1-R levels correlated with matrix metalloproteinase 13, a prognostic marker and mol
9 synovial fluid CSF1-R levels correlated with matrix metalloproteinase 13, a prognostic marker and mol
10 d expression of catabolic factors, including matrix metalloproteinase-13, accompanied by an increase
11 nally, nebulized hypertonic saline inhibited matrix -metalloproteinase-13 accumulation in the broncho
12 ention, sustained gene silencing and reduced matrix metalloproteinase 13 activity over 30 days, resul
13 mediated induction by KC of type X collagen, matrix metalloproteinase-13, alkaline phosphatase, and c
16 lagen breakdown via the direct activation of matrix metalloproteinase-13 and possibly other fibrillar
17 ramatic up-regulation and down-regulation of matrix metalloproteinase-13 and vascular endothelial gro
22 tinocytes use an alternative plasminogen and matrix metalloproteinase-13-dependent pathway for dissol
25 an optimized small interfering RNA targeting matrix metalloproteinase 13 for preferential delivery to
26 carrying small interfering RNA targeting the matrix metalloproteinase 13 gene (Mmp13), which breaks d
29 einases revealed significant upregulation of matrix metalloproteinase 13 in Col1a1(r/r) wounds, but m
31 necrosis factor alpha, IL-1beta, IL-10, and matrix metalloproteinase 13 in the joint to the same ext
33 tein receptor, retinoic acid receptor gamma, matrix metalloproteinase 13, Indian hedgehog, osteocalci
34 nt of beta-catenin cAct mice with a specific matrix metalloproteinase 13 inhibitor, ameliorated the m
35 hoalveolar lavage protein, shock vs. shock + matrix metalloproteinase-13 inhibitor CL-82198, p = .002
36 ic saline, p = .009) and pretreatment with a matrix metalloproteinase-13 inhibitor was sufficient to
37 midin-4-ones 9 as orally active and specific matrix metalloproteinase-13 inhibitors were discovered f
38 ifugation of co-cultured cells revealed that matrix metalloproteinase-13 is localized mainly within h
41 ether S100A4 can stimulate the production of matrix metalloproteinase 13 (MMP-13) by articular chondr
46 o found increased expression and activity of matrix metalloproteinase 13 (MMP-13) in the mutant mouse
47 ed to evaluate Smad3 and Runx2 regulation of matrix metalloproteinase 13 (MMP-13) messenger RNA (mRNA
48 The ability of S100B and HMGB-1 to stimulate matrix metalloproteinase 13 (MMP-13) production was also
49 on 740 (Y740A), and luciferase driven by the matrix metalloproteinase 13 (MMP-13) promoter were trans
50 age and to stimulate chondrocytes to produce matrix metalloproteinase 13 (MMP-13) through activation
53 d its novel role as an essential mediator of matrix metalloproteinase-13 (MMP-13) expression during t
59 reported that HDAC4 was a basal repressor of matrix metalloproteinase-13 (MMP-13) transcription and p
62 broblasts, we measured the effect of IL-6 on matrix metalloproteinase-13 (MMP-13), c-jun, junB, and c
63 ranslated region corresponding to the canine matrix metalloproteinase-13 (MMP-13), collagenase-3 gene
64 er (BIK), migration-inhibitory factor (MIF), matrix metalloproteinase-13 (MMP-13), fibroblast growth
67 o zebrafish model to show that the epidermal matrix-metalloproteinase 13 (MMP-13) induces degeneratio
68 nocytes, but not axons, and up-regulation of matrix-metalloproteinase 13 (MMP-13, collagenase 3) in t
70 and production of interstitial collagenase (matrix metalloproteinase-13; MMP-13), a critical enzyme
71 or 23 (FGF23) expression and FGFR1 activity; Matrix metalloproteinase 13 (MMP13) and Aggrecanase2 (AD
72 real-time PCR was used to measure COL2A1 and matrix metalloproteinase 13 (MMP13) gene expression; Wes
73 expression of type X collagen (Col10a1) and matrix metalloproteinase 13 (Mmp13) genes is decreased.
77 xtracellular matrix (ECM) by the collagenase matrix metalloproteinase 13 (MMP13) represents a key eve
78 xpress more bone-resorbing enzymes including Matrix metalloproteinase 13 (Mmp13) when they generate s
84 ddition to the 3'-untranslated region of the matrix metalloproteinases-13 (MMP13) gene, the different
85 his communication we show that expression of matrix metalloproteinase-13 mRNA is reciprocally modulat
86 late cells are co-cultured with hepatocytes, matrix metalloproteinase-13 mRNA is up-regulated and alp
88 pport the notion that alpha1(I) collagen and matrix metalloproteinase-13 mRNAs are reciprocally modul
90 sequence for HMMP13 is 86% identical to rat matrix metalloproteinases-13 (RMMP13); however, the regu
91 the immunoreactivity of type X collagen and matrix metalloproteinase-13 were seen between the groups