コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 n through the expression of the receptor for urokinase type plasminogen activator.
2 ly enhances the activation of plasminogen by urokinase type plasminogen activator.
3 oteins intercellular adhesion molecule-1 and urokinase-type plasminogen activator.
4 iation, and this cleavage may be mediated by urokinase-type plasminogen activator.
5 of endothelial cell integrin alphavbeta3 and urokinase-type plasminogen activator.
6 but not thrombin, coagulation factor Xa, or urokinase-type plasminogen activator.
7 th factor 1, leukemia inhibitory factor, and urokinase-type plasminogen activator.
8 quent cell movement and migration by binding urokinase-type plasminogen activator.
9 a more effective inactivator of tPA than of urokinase-type plasminogen activator.
10 nt hK2, which readily activated single chain urokinase-type plasminogen activator.
11 U1) by costimulation with phorbol esters and urokinase-type plasminogen activator.
12 any previously reported variants of t-PA or urokinase-type plasminogen activator.
13 activities of matrix metalloproteinase-2 and urokinase-type plasminogen activator.
14 is the main inhibitor of the tissue type and urokinase type plasminogen activators.
15 the reactions of PAI-1 with tissue-type and urokinase-type plasminogen activators.
16 comitant increased expression of its target, urokinase-type plasminogen activator, a known tumor-asso
18 filtrates induce a 3- to 10-fold increase in urokinase-type plasminogen activator activity in mammary
21 , leading to the up-regulation of macrophage urokinase type plasminogen activator and matrix metallop
23 ibrinolytic cascade by colocalizing with the urokinase type plasminogen activator and receptor comple
24 Pdef also results in the down-regulation of urokinase-type plasminogen activator and activation of t
25 d secretion of matrix metalloproteinases and urokinase-type plasminogen activator and an increase in
26 at the translational level by eIF3e included urokinase-type plasminogen activator and apoptotic regul
27 ement with these findings, reduced levels of urokinase-type plasminogen activator and elevated levels
28 turn induced expression of VEGF, MMP-9, and urokinase-type plasminogen activator and increased migra
30 ation of collagen IV, and their secretion of urokinase-type plasminogen activator and its receptor.
31 associated with expression of high levels of urokinase-type plasminogen activator and low levels of T
33 dative phenotype of macrophages via enhanced urokinase-type plasminogen activator and MMP-9 expressio
34 cultures stimulates their expression of both urokinase-type plasminogen activator and MMP-9, and the
36 the expression of matrix metalloproteinases, urokinase-type plasminogen activator, and cytokines in h
38 m via mechanisms involving both cell surface urokinase-type plasminogen activator, and interactions b
39 variant failed to activate the single-chain urokinase-type plasminogen activator, and the G221A and
40 sminogen, tissue-type plasminogen activator, urokinase-type plasminogen activator, and urokinase-type
41 the inhibition of interleukin (IL)-6, IL-8, urokinase-type plasminogen activator, and VEGF productio
42 activated receptor 2 (PAR2) and single-chain urokinase-type plasminogen activator are proteins that a
43 roduced plasminogen activators (i.e. tPA and urokinase-type plasminogen activator) are responsible fo
44 ng rate constant (klim) of RCL insertion for urokinase-type plasminogen activator at pH 6.2-8.0 and f
45 complex with the amino-terminal fragment of urokinase-type plasminogen activator (ATF), at the resol
46 n (FN)-1, plasminogen activator inhibitor-1, urokinase-type plasminogen activator, caveolin-1 and Slu
47 MMP-12 induction in plasminogen(Plg)-treated urokinase-type plasminogen activator-deficient macrophag
48 (6) integrin, called alpha(6)p, generated by urokinase-type plasminogen activator-dependent cleavage
49 promatrilysin to an active elastolysin via a urokinase-type plasminogen activator-dependent pathway.
51 mice carrying a mouse major urinary protein-urokinase-type plasminogen activator fusion transgene.
52 mmune-deficient transgenic mice carrying the urokinase-type plasminogen activator gene driven by the
53 upon activation of PepO-bound plasminogen by urokinase-type plasminogen activator, generated plasmin
54 ombinant PSA failed to activate single chain urokinase-type plasminogen activator, in contrast to the
55 he expression of its downstream target gene, urokinase-type plasminogen activator, in metastatic panc
56 al (Beas2B) cells decreased basal as well as urokinase-type plasminogen activator-induced PAI-1 expre
58 PAI-1), the primary inhibitor of tissue- and urokinase-type plasminogen activators, is considered a c
59 (ERK)1/2 activation, and decreases levels of urokinase-type plasminogen activator, known downstream e
60 immunodeficient BALB-DeltaRAG/gamma(c) -uPA (urokinase-type plasminogen activator) mice, freshly thaw
62 icellular proteolytic cascades by activating urokinase-type plasminogen activator on the cell surface
63 in absence of ADAMTS13, after activation by urokinase-type plasminogen activator or the thrombolytic
64 in(i) acts specifically; it does not inhibit urokinase-type plasminogen activator, plasmin, chymotryp
65 cluding very low density lipoprotein (VLDL), urokinase-type plasminogen activator:plasminogen activat
66 gen activator precursor (PLAT; 2.8-fold) and urokinase-type plasminogen activator precursor (PLAU; 2.
68 e epsilon readily converted single-chain pro-urokinase-type plasminogen activator (pro-uPA/scuPA) int
69 an effect on the expression/function of the urokinase-type plasminogen activator protease uPA/uPAR s
73 Relatively high plasma levels of soluble urokinase-type plasminogen activator receptor (suPAR) ha
76 ulin (beta-2 m), neopterin and suPAR soluble urokinase-type plasminogen activator receptor (suPAR) wa
84 s accompanied by increased expression of the urokinase-type plasminogen activator receptor (uPAR) and
85 adenovirus-mediated expression of antisense urokinase-type plasminogen activator receptor (uPAR) and
86 Because beta-catenin and its target genes urokinase-type plasminogen activator receptor (uPAR) and
87 ocytosis of multiple ligands, transports the urokinase-type plasminogen activator receptor (uPAR) and
88 elial growth factor results in clustering of urokinase-type plasminogen activator receptor (uPAR) and
91 Previous studies have indicated that the urokinase-type plasminogen activator receptor (uPAR) can
93 a serine proteinase that upon binding to the urokinase-type plasminogen activator receptor (uPAR) cat
95 at in adult mice with a null mutation in the urokinase-type plasminogen activator receptor (uPAR) gen
98 in the mid-1980s, the cell membrane-anchored urokinase-type plasminogen activator receptor (uPAR) has
99 explore the potential of PET imaging of the urokinase-type plasminogen activator receptor (uPAR) in
100 Moreover, ErbB2-mediated upregulation of urokinase-type plasminogen activator receptor (uPAR) is
105 ar accumulation of beta-catenin, and induces urokinase-type plasminogen activator receptor (uPAR) mRN
106 ely, increases in steady-state expression of urokinase-type plasminogen activator receptor (uPAR) mRN
107 cells, interaction between vitronectin with urokinase-type plasminogen activator receptor (uPAR) on
111 e glycosylphosphatidyl-inositol (GPI)-linked urokinase-type plasminogen activator receptor (uPAR) rev
114 ule (ARM) that is capable of recognizing the urokinase-type plasminogen activator receptor (uPAR), a
115 surface or secreted factors, including CD73, urokinase-type plasminogen activator receptor (uPAR), an
116 se partitioning, co-immunoprecipitation with urokinase-type plasminogen activator receptor (uPAR), an
117 ulin-like growth factor-II, plasminogen, and urokinase-type plasminogen activator receptor (uPAR), to
118 ling pathways downstream of the EGFR and the urokinase-type plasminogen activator receptor (uPAR); ho
120 dinated by many receptors, in particular the urokinase-type plasminogen activator receptor (uPAR, CD8
121 18, Mac-1) forms a physical complex with the urokinase-type plasminogen activator receptor (uPAR/CD87
122 through the interaction with a region of the urokinase-type plasminogen activator receptor (uPAR88-92
123 phosphatidylinositol-linked proteins such as urokinase-type plasminogen activator receptor and endoth
124 n of epidermal growth factor receptor and/or urokinase-type plasminogen activator receptor in a varie
125 ive action of cell surface-associated HS and urokinase-type plasminogen activator receptor in the acc
126 ncoding the antimicrobial peptides antigen-6/urokinase-type plasminogen activator receptor related pr
127 r, urokinase-type plasminogen activator, and urokinase-type plasminogen activator receptor, along wit
128 that high basal VEGF, glucose transporter-1, urokinase-type plasminogen activator receptor, and plasm
129 , including plasminogen, thrombomodulin, the urokinase-type plasminogen activator receptor, and to a
130 ated targets of note from this study include urokinase-type plasminogen activator receptor, serine/th
131 the rise of nephropathy biomarkers, soluble urokinase-type plasminogen activator receptor, suPAR and
132 in studies of SLURP (secreted mammalian Ly-6/urokinase-type plasminogen activator receptor-related pr
136 asis of the interaction between single-chain urokinase-type plasminogen activator (scuPA) and its rec
138 precursor of PSA (pro-PSA) and single chain urokinase-type plasminogen activator (scuPA, pro-uPA).
140 in vivo efficacy of mAb16-71 in "human liver urokinase-type plasminogen activator, severe combined im
141 nvestigate the expression of tissue-type and urokinase-type plasminogen activators (t-PA and u-PA, re
142 , cathepsin G, and plasma kallikrein but not urokinase-type plasminogen activator, tissue plasminogen
143 rine proteases thrombin, plasmin, factor Xa, urokinase-type plasminogen activator, tissue plasminogen
144 ty of C4BP, the activation of plasminogen by urokinase-type plasminogen activator to active plasmin w
146 ytes into the liver of mice that contain the urokinase-type plasminogen activator transgene (uPA) and
147 To test our hypothesis, we directed murine urokinase-type plasminogen activator transgene expressio
149 uantitative image analysis for assessment of urokinase-type plasminogen activator (u-PA) and PAI-1.
150 re, 1 min after PHx, but not sham operation, urokinase-type plasminogen activator (u-PA) and u-PA rec
151 Previous studies have shown that activity of urokinase-type plasminogen activator (u-PA) increases ve
152 Gene knockout mice studies indicate that urokinase-type plasminogen activator (u-PA) is important
154 tissue-type plasminogen activator (t-PA) and urokinase-type plasminogen activator (u-PA), by modifyin
157 r extent) were found to drastically increase urokinase type plasminogen activator (uPA) and matrix me
158 s of normal scars and keloids expressed both urokinase type plasminogen activator (uPA) and plasminog
159 ase (MAPK), cytosolic phospholipase A(2) and urokinase type plasminogen activator (uPA) are required
160 alization and degradation of cell-associated urokinase type plasminogen activator (uPA) through the a
163 tissue-type plasminogen activator (tPA) and urokinase-type plasminogen activator (uPA) activities in
164 Matrix metalloproteinase (MMP), plasmin, and urokinase-type plasminogen activator (uPA) activities we
165 ographic procedure that specifically detects urokinase-type plasminogen activator (uPA) activity in b
167 Although maspin does not directly inhibit urokinase-type plasminogen activator (uPA) activity, we
168 (MMP) detection and a colorimetric assay for urokinase-type plasminogen activator (uPA) analysis, we
171 specifically inhibit cell surface-associated urokinase-type plasminogen activator (uPA) and fibrinoge
172 nizes the N-terminal growth factor domain of urokinase-type plasminogen activator (uPA) and is expres
173 The high affinity interaction between the urokinase-type plasminogen activator (uPA) and its glyco
174 Pancreatic carcinomas express high levels of urokinase-type plasminogen activator (uPA) and its recep
179 assess whether preoperative plasma levels of urokinase-type plasminogen activator (uPA) and its solub
180 1) and diminishing the enzymatic activity of urokinase-type plasminogen activator (uPA) and matrix me
182 as reduced and extracellular accumulation of urokinase-type plasminogen activator (uPA) and plasminog
183 d the involvement of p53-mediated changes in urokinase-type plasminogen activator (uPA) and plasminog
184 models focus on the ability of uPAR to bind urokinase-type plasminogen activator (uPA) and promote p
185 tein, p53, and apoptosis with suppression of urokinase-type plasminogen activator (uPA) and the uPA r
186 sly demonstrated that the expression of both urokinase-type plasminogen activator (uPA) and the uPA r
188 activity capable of cleaving a substrate for urokinase-type plasminogen activator (uPA) and tissue pl
189 rpin inhibitor of the plasminogen activators urokinase-type plasminogen activator (uPA) and tissue pl
190 in, we investigated the upstream activators, urokinase-type plasminogen activator (uPA) and tissue-ty
191 ay regulate cardiac fibrosis by inactivating urokinase-type plasminogen activator (uPA) and ultimatel
193 F-induced invasion, UM-SCC-1 cells expressed urokinase-type plasminogen activator (uPA) and uPA recep
195 tor (VLDLr) binds diverse ligands, including urokinase-type plasminogen activator (uPA) and uPA-plasm
198 s cells produced more of the serine protease urokinase-type plasminogen activator (uPA) as compared w
199 his study identifies the extracellular PAI-1/urokinase-type plasminogen activator (uPA) balance as an
202 crystal structures of trypsin, thrombin, and urokinase-type plasminogen activator (uPA) bound with a
204 tissue-type plasminogen activator (tPA) and urokinase-type plasminogen activator (uPA) decreased und
205 t of peripheral tolerance) actually produced urokinase-type plasminogen activator (uPA) during tolera
208 ase C (PKC) activity leading to up-regulated urokinase-type plasminogen activator (uPA) expression.
211 tissue-type plasminogen activator (tPA) and urokinase-type plasminogen activator (uPA) in liver repa
216 tissue-type plasminogen activator (tPA) and urokinase-type plasminogen activator (uPA) is associated
221 hypothesized that Mp-specific expression of urokinase-type plasminogen activator (uPA) is sufficient
230 ree-domain clamp of Argos also resembles the urokinase-type plasminogen activator (uPA) receptor, whi
234 ave a significant reduction in expression of urokinase-type plasminogen activator (uPA) relative to t
237 Recent studies indicate that binding of the urokinase-type plasminogen activator (uPA) to its high-a
243 ssays and plasminogen zymography showed that urokinase-type plasminogen activator (uPA) was responsib
244 n with bovine trypsin, rat trypsin and human urokinase-type plasminogen activator (uPA) were investig
247 ession was inversely correlated with that of urokinase-type plasminogen activator (uPA), a prometasta
249 a receptor for the plasmin-producing enzyme urokinase-type plasminogen activator (uPA), and can also
250 increased inflammation, increased levels of urokinase-type plasminogen activator (uPA), and greater
251 such as matrix metalloproteinase (MMP)-9 and urokinase-type plasminogen activator (uPA), in human pro
252 ficient cells, which secreted high levels of urokinase-type plasminogen activator (uPA), invaded exte
254 tissue-type plasminogen activator (tPA) and urokinase-type plasminogen activator (uPA), is mediated
256 of tissue-type plasminogen activator (tPA), urokinase-type plasminogen activator (uPA), its receptor
257 we found that the expression of epiregulin, urokinase-type plasminogen activator (uPA), matrix metal
259 g factors, such as interleukin (IL)-8, IL-6, urokinase-type plasminogen activator (uPA), or uPA recep
260 Tobacco smoke induced the expression of urokinase-type plasminogen activator (uPA), resulting in
261 (such as Factor Xa (FXa), Factor XIa (FXIa), urokinase-type plasminogen activator (uPA), thrombin, an
262 Plasminogen can be activated to plasmin by urokinase-type plasminogen activator (uPA), tissue-type
263 ility of gene-targeted mice deficient in the urokinase-type plasminogen activator (uPA), urokinase re
264 processes by virtue of its interactions with urokinase-type plasminogen activator (uPA), vitronectin
265 site-directed mutant of the serine protease urokinase-type plasminogen activator (uPA), was produced
266 as applied to the screening of inhibitors of urokinase-type plasminogen activator (uPA), which is a p
267 ilencing expression of endogenously produced urokinase-type plasminogen activator (uPA), which is nec
269 face receptor capable of not only focalizing urokinase-type plasminogen activator (uPA)-mediated fibr
284 iring the proteolytic cascade of cathepsin B/urokinase-type plasminogen activator (uPA)/matrix metall
286 urthermore, when tyrosine phosphorylation or urokinase-type plasminogen activator (uPA)/uPAR function
287 ession in mice with targeted deficiencies in urokinase-type plasminogen activator (UPA-/-) and its in
290 sine phosphorylation of beta-catenin, induce urokinase-type plasminogen activator, uPAR, and cyclin D
291 studies have indicated that the receptor for urokinase-type plasminogen activator, uPAR, can form fun
292 amino acid sequence of the chicken and human urokinase-type plasminogen activators (uPAs) revealed th
293 t the active sites of trypsin, thrombin, and urokinase type plasminogen activator (urokinase or uPA)
294 Bound to BBA70, plasminogen activated by urokinase-type plasminogen activator was able to degrade
296 ould lead to drug-entrapped vascular grafts: urokinase-type plasminogen activator was entrapped withi
297 ctor that expresses a nonsecreted urokinase (urokinase-type plasminogen activator) was transduced int
298 by a compensatory increase in expression of urokinase-type plasminogen activator, which activates uP
299 The PLAU gene within this region encodes urokinase-type plasminogen activator, which converts pla
300 rix metalloproteinase-9 and the secretion of urokinase-type plasminogen activator while increasing ti
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。