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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 d expression of catabolic factors, including matrix metalloproteinase-13, accompanied by an increase
9 nally, nebulized hypertonic saline inhibited matrix -metalloproteinase-13 accumulation in the broncho
10 mediated induction by KC of type X collagen, matrix metalloproteinase-13, alkaline phosphatase, and c
11                 ATRA increased the levels of matrix metalloproteinase 13 and aggrecanase activity in
12 pression of matrix-degrading enzymes such as matrix metalloproteinase 13 and aggrecanase.
13 lagen breakdown via the direct activation of matrix metalloproteinase-13 and possibly other fibrillar
14 ramatic up-regulation and down-regulation of matrix metalloproteinase-13 and vascular endothelial gro
15                        These cells delivered matrix metalloproteinases-13 and -9, respectively, into
16 the activation of the fibrillar collagenase, matrix metalloproteinase-13, by keratinocytes.
17                                              Matrix metalloproteinase-13 (collagenase-3), a member of
18 tinocytes use an alternative plasminogen and matrix metalloproteinase-13-dependent pathway for dissol
19 -1 and -2, suggesting that plasmin activates matrix metalloproteinase-13 directly.
20 uce chondrocyte hypertrophy and ADAMTS-4 and matrix metalloproteinase 13 expression.
21 ly upregulated procollagen, fibronectin, and matrix metalloproteinase-13 genes.
22                                        Human matrix metalloproteinases-13 (HMMP13) shows a wide subst
23 einases revealed significant upregulation of matrix metalloproteinase 13 in Col1a1(r/r) wounds, but m
24  necrosis factor alpha, IL-1beta, IL-10, and matrix metalloproteinase 13 in the joint to the same ext
25                            The activation of matrix metalloproteinase-13 in normal keratinocytes was
26 tein receptor, retinoic acid receptor gamma, matrix metalloproteinase 13, Indian hedgehog, osteocalci
27 nt of beta-catenin cAct mice with a specific matrix metalloproteinase 13 inhibitor, ameliorated the m
28 hoalveolar lavage protein, shock vs. shock + matrix metalloproteinase-13 inhibitor CL-82198, p = .002
29 ic saline, p = .009) and pretreatment with a matrix metalloproteinase-13 inhibitor was sufficient to
30 midin-4-ones 9 as orally active and specific matrix metalloproteinase-13 inhibitors were discovered f
31 ifugation of co-cultured cells revealed that matrix metalloproteinase-13 is localized mainly within h
32                               Collagenase-3 (matrix metalloproteinase-13) is expressed by osteoblasts
33 ion of collagen I protein with no changes in matrix metalloproteinase 13 (MMP 13).
34 ether S100A4 can stimulate the production of matrix metalloproteinase 13 (MMP-13) by articular chondr
35                                              Matrix metalloproteinase 13 (MMP-13) expression was dete
36                                              Matrix metalloproteinase 13 (MMP-13) has attracted atten
37                                              Matrix metalloproteinase 13 (MMP-13) has been shown to b
38           Alterations in type X collagen and matrix metalloproteinase 13 (MMP-13) in articular chondr
39 o found increased expression and activity of matrix metalloproteinase 13 (MMP-13) in the mutant mouse
40 ed to evaluate Smad3 and Runx2 regulation of matrix metalloproteinase 13 (MMP-13) messenger RNA (mRNA
41 The ability of S100B and HMGB-1 to stimulate matrix metalloproteinase 13 (MMP-13) production was also
42 on 740 (Y740A), and luciferase driven by the matrix metalloproteinase 13 (MMP-13) promoter were trans
43 age and to stimulate chondrocytes to produce matrix metalloproteinase 13 (MMP-13) through activation
44                         Expression of DDR-2, matrix metalloproteinase 13 (MMP-13), and MMP-derived ty
45 nd selective inhibitors (10d and (S)-17b) of matrix metalloproteinase 13 (MMP-13).
46 d its novel role as an essential mediator of matrix metalloproteinase-13 (MMP-13) expression during t
47          Osteoarthritic chondrocytes secrete matrix metalloproteinase-13 (MMP-13) in response to inte
48                                              Matrix metalloproteinase-13 (MMP-13) is a zinc-dependent
49                                              Matrix metalloproteinase-13 (MMP-13) is an important enz
50                              The collagenase matrix metalloproteinase-13 (MMP-13) plays an important
51 reported that HDAC4 was a basal repressor of matrix metalloproteinase-13 (MMP-13) transcription and p
52      Previously we reported that PTH induces matrix metalloproteinase-13 (MMP-13) transcription in os
53                                              Matrix metalloproteinase-13 (MMP-13), a catabolic cartil
54 broblasts, we measured the effect of IL-6 on matrix metalloproteinase-13 (MMP-13), c-jun, junB, and c
55 ranslated region corresponding to the canine matrix metalloproteinase-13 (MMP-13), collagenase-3 gene
56 er (BIK), migration-inhibitory factor (MIF), matrix metalloproteinase-13 (MMP-13), fibroblast growth
57                        One of these genes is matrix metalloproteinase-13 (MMP-13), which is involved
58 of basic fibroblast growth factor (bFGF) and matrix metalloproteinase-13 (MMP-13).
59 nocytes, but not axons, and up-regulation of matrix-metalloproteinase 13 (MMP-13, collagenase 3) in t
60                               Collagenase-3 (matrix metalloproteinase 13, MMP-13) was employed as a s
61  and production of interstitial collagenase (matrix metalloproteinase-13; MMP-13), a critical enzyme
62 real-time PCR was used to measure COL2A1 and matrix metalloproteinase 13 (MMP13) gene expression; Wes
63  expression of type X collagen (Col10a1) and matrix metalloproteinase 13 (Mmp13) genes is decreased.
64                 PTH stimulates expression of matrix metalloproteinase 13 (MMP13) in bone.
65                  The major metalloproteinase matrix metalloproteinase 13 (MMP13) is also associated w
66 xtracellular matrix (ECM) by the collagenase matrix metalloproteinase 13 (MMP13) represents a key eve
67                                We identified matrix metalloproteinase 13 (MMP13), receptor activator
68                                              Matrix metalloproteinase 13 (Mmp13, collagenase-3) plays
69                                              Matrix metalloproteinase-13 (MMP13) is a Zn(2+)-dependen
70              This study investigated whether matrix metalloproteinase-13 (MMP13) is involved in P. ae
71 ddition to the 3'-untranslated region of the matrix metalloproteinases-13 (MMP13) gene, the different
72 his communication we show that expression of matrix metalloproteinase-13 mRNA is reciprocally modulat
73 late cells are co-cultured with hepatocytes, matrix metalloproteinase-13 mRNA is up-regulated and alp
74 tocytes with galactosamine further increased matrix metalloproteinase-13 mRNA production.
75 pport the notion that alpha1(I) collagen and matrix metalloproteinase-13 mRNAs are reciprocally modul
76 imultaneously produce alpha1(I) collagen and matrix metalloproteinase-13 mRNAs.
77  sequence for HMMP13 is 86% identical to rat matrix metalloproteinases-13 (RMMP13); however, the regu
78  the immunoreactivity of type X collagen and matrix metalloproteinase-13 were seen between the groups

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