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1 n sepsis-induced ALI were confirmed by using tissue factor pathway inhibitor.
2 tor Xa, unaffected by subsequent addition of tissue factor pathway inhibitor.
3 n hemophilia, possibly through inhibition of tissue factor pathway inhibitor.
4 urally deleted (Kunitz 1-domainless) form of tissue factor pathway inhibitor.
5 possible disruption of FXa inhibition by the tissue factor pathway inhibitor.
6 d abrogate the anticoagulant function of the tissue factor pathway inhibitor.
7 oduction of tissue plasminogen activator and tissue factor pathway inhibitor.
8 tant to inactivation by antithrombin III and tissue factor pathway inhibitor.
9 nction of the natural anticoagulant protein, tissue factor pathway inhibitor.
10 in-2, and the first two inhibitor domains of tissue factor pathway inhibitor.
11 t (6L15), amyloid beta-protein precursor, or tissue factor pathway inhibitor.
12 ect either protein expression or activity of tissue factor pathway inhibitors.
13 ion of the murine tissue factor (TF) gene or tissue factor pathway inhibitor 1 (TFPI) gene results in
15 th factor activator inhibitor type 2 (HAI2), tissue factor pathway inhibitor-1 (TFPI1), and tissue fa
17 ased strategy to identify the methylation of tissue factor pathway inhibitor 2 (TFPI2), a potential t
20 rt here that the serine proteinase inhibitor tissue factor pathway inhibitor-2 (TFPI-2) can function
28 ntial DAC/DP treatment induced expression of tissue factor pathway inhibitor-2 (TFPI-2), an inhibitor
29 ssue factor pathway inhibitor-1 (TFPI1), and tissue factor pathway inhibitor-2 (TFPI2), as well as E-
31 nhances the inhibition of factor Xa (FXa) by tissue factor pathway inhibitor-alpha (TFPI-alpha) in th
32 indirect mechanism by forming a complex with tissue factor pathway inhibitor-alpha (TFPIalpha), resul
35 fXa for binding to the non-serpin inhibitors tissue factor pathway inhibitor and recombinant tick ant
36 anticoagulant fusion proteins based on human tissue factor pathway inhibitor and the leech anticoagul
37 more sensitive to inhibition by cell surface tissue factor pathway inhibitor and the phospholipid bin
38 e 6- to 86-fold more active than recombinant tissue factor pathway inhibitor and tick anticoagulant p
39 in, high activated protein C, protein S, and tissue factor pathway inhibitor) and hyperfibrinolysis (
40 ith Spectrozyme Xa(TM), antithrombin III and tissue factor pathway inhibitor, and prothrombin than it
41 rs X, IX, II, V, and VIII and the inhibitors tissue factor pathway inhibitor, antithrombin-III, and p
43 agulation inhibitors activated protein C and tissue factor pathway inhibitor but also is also a physi
44 increased rate in binding to the two-domain tissue factor pathway inhibitor; Ca(2+) (+/-Na(+)) has n
45 h (p = 0.002) and correlated inversely with tissue factor pathway inhibitor concentration (r = -0.61
46 inhibitor (>10-fold), followed by the second tissue factor pathway inhibitor domain (1.7-fold) and th
47 tely abrogates the anticoagulant function of tissue factor pathway inhibitor, enhances fibrin clot st
48 allenged with CpG DNA, and tissue factor and tissue factor pathway inhibitor expression and activity
49 coagulants, antithrombin III and recombinant tissue factor pathway inhibitor, failed to do so, implyi
50 , phospholipid transfer protein, matrilin-3, tissue factor pathway inhibitor, fibrinogen-like 1, and
51 tion, resulting from loss of FVIIa-dependent tissue factor pathway inhibitor function and the absence
53 lood cells, and an endogenous DPP4 inhibitor tissue factor pathway inhibitor has been discovered, inc
54 c for an "anticoagulant" gene, such as human tissue factor pathway inhibitor, hirudin, or CD39, or la
56 urring soluble anticoagulant proteins, human tissue factor pathway inhibitor (hTFPI) and the leech pr
57 oagulation inhibitor (LACI-D1, also known as tissue-factor pathway inhibitor-I) displayed on bacterio
58 e factor, a key initiator of coagulation and tissue factor pathway inhibitor in human coronary artery
59 glish language relating to tissue factor and tissue factor pathway inhibitor in intravascular coagula
60 ently completed phase 3 trial of recombinant tissue factor pathway inhibitor in severe sepsis failed
62 25%, inhibition by antithrombin III and the tissue factor pathway inhibitor is approximately 20%, an
63 -45)-protein C were effectively inhibited by tissue factor pathway inhibitor (K1 < 200 nM) and, excep
64 clot formation, decreasing upon induction of tissue factor pathway inhibitor or treatment with hirudi
65 tial thromboplastin times and tissue factor, tissue factor pathway inhibitor, protein C, plasminogen
67 ssue factor (TF) inhibition with recombinant tissue factor pathway inhibitor (rTFPI) on acute thrombu
70 C57BL/6 and transgenic mice overexpressing tissue factor pathway inhibitor (SM22alpha-TFPI) were su
71 ated FVIII), monoclonal antibodies targeting tissue factor pathway inhibitor, small interfering RNA t
73 ompared to HC, as were MPs expressing TF and Tissue Factor Pathway Inhibitor (TFPI) (all p < 0.0001).
75 d matrix metalloproteinases (MMPs) to cleave tissue factor pathway inhibitor (TFPI) and alter its act
76 interact with target plasma fXa inhibitors, tissue factor pathway inhibitor (TFPI) and antithrombin.
79 activity, FVIII coagulant (FVIIIC) activity, tissue factor pathway inhibitor (TFPI) antigen, and thro
80 ependent inhibition of the enzyme complex by tissue factor pathway inhibitor (TFPI) are considered pr
81 thrombomodulin (TM), tissue factor (TF) and tissue factor pathway inhibitor (TFPI) are markers of en
82 functions of the first two Kunitz domains of tissue factor pathway inhibitor (TFPI) are well defined
83 C, protein S, antithrombin III (AT-III), and tissue factor pathway inhibitor (TFPI) as well as combin
84 n of tissue factor-mediated coagulation with tissue factor pathway inhibitor (TFPI) attenuates neoint
87 (aPTT), plasma anti-Xa and anti-IIa levels, tissue factor pathway inhibitor (TFPI) concentration, an
88 in time (aPTT), anti-factors IIa and Xa, and tissue factor pathway inhibitor (TFPI) concentrations we
91 fibrin formation was associated with reduced tissue factor pathway inhibitor (TFPI) expression and in
93 perties, the ability to cause the release of tissue factor pathway inhibitor (TFPI) from the endothel
95 hird phase III study examining the effect of tissue factor pathway inhibitor (TFPI) in sepsis is curr
107 e now show that the endogenous anticoagulant tissue factor pathway inhibitor (TFPI) is also highly se
122 ) library, a clone with sequence homology to tissue factor pathway inhibitor (TFPI) was identified.
123 in vitro thrombin generation, and levels of tissue factor pathway inhibitor (TFPI) were strongly inc
124 shares significant homology with apo(a), on tissue factor pathway inhibitor (TFPI), a major regulato
125 a process which required cell surface-bound tissue factor pathway inhibitor (TFPI), a potent inhibit
127 of the factor VIIa/tissue factor complex by tissue factor pathway inhibitor (TFPI), additional facto
128 ine whether treatment with recombinant human tissue factor pathway inhibitor (TFPI), an inhibitor of
129 sue factor complex inhibitors, DEGR VIIa and tissue factor pathway inhibitor (TFPI), and the selectiv
130 The effects of the stoichiometric inhibitors tissue factor pathway inhibitor (TFPI), antithrombin-III
131 ein Z-dependent protease inhibitor (ZPI) and tissue factor pathway inhibitor (TFPI), effectively inhi
132 It displays high sequence similarity with a tissue factor pathway inhibitor (TFPI), Ixolaris, from t
135 emains intact but is negatively regulated by tissue factor pathway inhibitor (TFPI), which inhibits b
137 nds our previous model by including: (a) the tissue factor pathway inhibitor (TFPI)-mediated inactiva
147 o-hemostatic factors (tissue factor [TF] and tissue factor pathway inhibitor [TFPI-1]) are limited an
149 r 9 shifted the balance of tissue factor and tissue factor pathway inhibitor toward procoagulant phen
150 Conversely, CpG DNA significantly reduced tissue factor pathway inhibitor transcription, secretion
151 n S, soluble endothelial protein C receptor, tissue factor pathway inhibitor, von Willebrand factor,
152 bitor from the mammalian anticoagulant TFPI (tissue factor pathway inhibitor), which is functionally
153 platelet factor V and, surprisingly, plasma tissue factor pathway inhibitor, which is significantly
154 mRNA level of TF but not of its counterpart-tissue factor pathway inhibitor, which was accompanied b
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