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1 asminogen activator inhibitor type-1 and the urokinase receptor.
2 A-dependent ERK signaling via an alternative urokinase receptor.
3 s were confirmed on cells expressing variant urokinase receptor.
4 occur through interactions with endothelial urokinase receptors.
7 ed growth factor, matrix metalloproteinases, urokinase receptor and varied small-molecule tyrosine ki
9 n of metastasis, these findings suggest that urokinase receptor antagonists may be useful therapeutic
15 he crystal structure at 1.9 angstroms of the urokinase receptor complexed with the urokinase amino-te
17 ocyte antigen, PLAUR (plasminogen activator, urokinase receptor) domain-containing (LYPD)-6B on alpha
18 xperiments using nuclear extract from a high urokinase receptor-expressing cell line (RKO) indicated
19 urokinase receptor promoter activity in low urokinase receptor-expressing GEO cells was increased by
20 ine if a constitutively active Src regulates urokinase receptor expression and 2) to identify require
21 elements and trans-acting factors activating urokinase receptor expression through a footprinted (-14
22 yristate 13-acetate treatment, which induces urokinase receptor expression, increased complex formati
23 eceptor promoter (-152/-135) in constitutive urokinase receptor expression, we determined its role fo
25 vely active Src protein manifested increased urokinase receptor gene expression and Src activity.
27 grins, but it remains unclear to what degree urokinase receptor/integrin binding is important to beta
29 state 13-acetate-inducible expression of the urokinase receptor is mediated partly through trans-acti
31 PLAP and the carboxy-terminal portion of the urokinase receptor (MP/uPAR) into which various amino ac
34 ecently implicated an upstream region of the urokinase receptor promoter (-152/-135) in constitutive
36 r of activator protein-2 function diminished urokinase receptor promoter activity, protein, and lamin
38 a-related factor and Sp1/Sp3 binding reduced urokinase receptor promoter stimulation by this agent.
40 vasiveness and because both Src activity and urokinase receptor protein are elevated in invasive colo
41 ants with a Src-inhibitor (PD173955) reduced urokinase receptor protein levels and laminin degradatio
47 provides insight into the flexibility of the urokinase receptor that enables its interaction with a w
48 inogen (Pg(-)(/-)), urokinase (u-PA(-)(/-)), urokinase receptor (u-PAR(-)(/-)), or tissue plasminogen
52 uantitative increases in urokinase PA (uPA), urokinase receptor (uPAR) and plasminogen activator inhi
53 s significantly increased levels of cellular urokinase receptor (uPAR) and release increased amounts
59 e that in EGFRvIII-expressing GBM cells, the urokinase receptor (uPAR) functions as a major activator
60 etermine the role of urokinase (uPA) and the urokinase receptor (uPAR) in retinal angiogenesis, and w
70 here we report the sequestration behavior of urokinase receptor (uPAR), a glycosylphosphatidylinosito
71 CDC91L1 also resulted in upregulation of the urokinase receptor (uPAR), a GPI-anchored protein, and i
72 , through unknown receptors, overexpress the urokinase receptor (uPAR), a key mediator of the plasmin
74 One such protein, the glycolipid-anchored urokinase receptor (uPAR), associates with and modifies
76 urokinase-type plasminogen activator (uPA), urokinase receptor (uPAR), tissue-type plasminogen activ
77 ted on the surface of many cell types, where urokinase receptor (uPAR)-bound urokinase (uPA) activate
83 eukocyte integrin Mac-1 (CD11b/CD18) and the urokinase receptor (uPAR, CD87) mediate complementary fu
85 R4 physically and functionally interact with urokinase receptors (uPAR) on neutrophil plasma membrane
86 beta2 integrins for substrate attachment and urokinase receptors (uPAR) to focus pericellular proteol
93 utagenesis, single amino acid mutants of the urokinase receptor were identified that fail to associat
94 tions on beta1 integrin function, endogenous urokinase receptors were first stably silenced in tumor
95 ffract in the co-crystal, and a site for the urokinase receptor, which overlaps with the PAI-1-bindin
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