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1 generation of plasmin, it was independent of proteinase-activated receptor 1 (PAR-1) and instead refl
2  cardiomyocytes, and cardiac fibroblasts via proteinase-activated receptor 1 (PAR-1) and mammalian ta
3 f the major high-affinity thrombin receptor, proteinase-activated receptor 1 (PAR-1), during the deve
4 er integrity following the activation of the proteinase-activated receptor 1 (PAR1) by thrombin.
5 cantly increased, together with those of the proteinase-activated receptor 1 (PAR1), an inflammation-
6         The high-affinity thrombin receptor, proteinase-activated receptor 1 (PAR1), has been implica
7                         Thrombin-induced and proteinase-activated receptor 1 (PAR1)-mediated signalin
8 riginating in the G-protein-coupled receptor proteinase-activated receptor 1 (PAR1).
9                                              Proteinase-activated-receptor 1 (PAR-1) and epidermal gr
10 As thrombin binding to the G protein-coupled proteinase activated receptor-1 (PAR-1) induces endothel
11 he mechanisms of restoration of cell surface proteinase-activated receptor-1 (PAR-1) by investigating
12                                              Proteinase-activated receptor-1 (PAR-1) is protective ag
13 ility by the activation of G protein-coupled proteinase-activated receptor-1 (PAR-1).
14  the NH(2) terminus of the G protein-coupled proteinase-activated receptor-1 (PAR-1).
15 o transactivation of EGF receptor (EGFR) via proteinase-activated receptor 2 (PAR(2)) activation.
16                                              Proteinase-activated receptor 2 (PAR-2) is a recently ch
17                                          The proteinase-activated receptor 2 (PAR-2) is important for
18 al sequencing, while its ability to activate proteinase-activated receptor 2 (PAR-2) was determined u
19 ses activate the G protein-coupled receptor, proteinase-activated receptor 2 (PAR-2), via cleavage an
20                                              Proteinase-activated receptor 2 (PAR2 ) is a G protein-c
21                 NB thymosin beta (TMSNB) and proteinase-activated receptor 2 (PAR2) (both downregulat
22                        Thrombin receptor and proteinase-activated receptor 2 (PAR2) define a family o
23 ulation signaling via tissue factor (TF) and proteinase-activated receptor 2 (PAR2) in obesity-mediat
24                                              Proteinase-activated receptor 2 (PAR2) is a G protein-co
25                                              Proteinase-activated receptor 2 (PAR2) is a receptor for
26 ta), serine proteinases such as trypsin, and proteinase-activated receptor 2 (PAR2) promote tumor dev
27 ype III IFNs by ATP, UTP, histamine, and the proteinase-activated receptor 2 (PAR2) receptor agonist
28   We report that agonists of Galphaq-coupled proteinase-activated receptor 2 (PAR2) stimulate formati
29        Trypsin and mast cell tryptase cleave proteinase-activated receptor 2 (PAR2) to induce alterat
30                                              Proteinase-activated receptor 2 (PAR2), a seven-transmem
31  fibers of the respiratory tract by cleaving proteinase-activated receptor 2 (PAR2).
32   We then demonstrated that injection of the proteinase-activated receptor 2 activating peptide into
33                             Using a specific proteinase-activated receptor 2 activating peptide, we f
34  to noxious stimulation of the pancreas with proteinase-activated receptor 2 agonists.
35 ents after intrapancreatic administration of proteinase-activated receptor 2 agonists.
36 ctions was performed with antibodies against proteinase-activated receptor 2 and vanilloid receptor 1
37        Trypsin and mast cell tryptase cleave proteinase-activated receptor 2 and, by unknown mechanis
38              These observations suggest that proteinase-activated receptor 2 contributes to nocicepti
39 gnals, whereas serine protease activation of proteinase-activated receptor 2 is a negative signal reg
40                                          The proteinase-activated receptor 2 is expressed on a subset
41 Thus, tryptase inhibitors and antagonists of proteinase-activated receptor 2 may be useful anti-infla
42 1 (TRPA1)-deficient mice but not in c-kit or proteinase-activated receptor 2 mice.
43                                              Proteinase-activated receptor 2 was expressed by virtual
44 imary spinal afferent neurons, which express proteinase-activated receptor 2, also contain the proinf
45 ucts), which likely led to the initiation of proteinase-activated receptor 2-mediated pruritus and My
46                 Our findings suggest a novel proteinase-activated receptor 2-mediated role for trypsi
47      Preinfusion of the pancreatic duct with proteinase-activated receptor 2-specific activating pept
48                           Both trypsin and a proteinase-activated receptor 2-specific peptide agonist
49 an also activate nociceptive neurons via the proteinase-activated receptor 2.
50 te inflammatory edema induced by agonists of proteinase-activated receptor 2.
51  vasorelaxation in response to muscarinic or proteinase-activated-receptor 2 agonists.
52 orthern blot analysis completed with a human proteinase activated receptor-2 (PAR-2) cDNA as probe de
53 rk shows that the G-protein-coupled receptor proteinase activated receptor-2 activates signals that s
54 emarkably similar to the organization of the proteinase activated receptor-2 gene in which the putati
55 cally cleaved receptors that may include the proteinase activated receptor-2.
56                         We hypothesized that proteinase-activated receptor-2 (PAR(2)) modulates intes
57                                              Proteinase-Activated receptor-2 (PAR(2)), a G-protein-co
58                                              Proteinase-activated receptor-2 (PAR-2) is a G protein-c
59                                              Proteinase-activated receptor-2 (PAR-2) is a G protein-c
60                                              Proteinase-activated receptor-2 (PAR-2) is a G-protein-c
61                                          The proteinase-activated receptor-2 (PAR-2) is the second me
62                                              Proteinase-activated receptor-2 (PAR-2) may participate
63 e disruption approaches, we demonstrate that proteinase-activated receptor-2 (PAR-2) plays a pivotal
64 synthase kinase 3beta, protein kinase C, and proteinase-activated receptor-2 (PAR-2), which is consis
65                                              Proteinase-Activated Receptor-2 (PAR2 ) is a G protein-c
66                                              Proteinase-activated receptor-2 (PAR2), a G protein-coup
67 inases can signal by cleaving and activating proteinase-activated receptor-2 (PAR2), a G-protein-coup
68  of the following key proinflammatory genes: proteinase-activated receptor-2 (PAR2), tumor necrosis f
69 ctivated receptor-2, either through specific proteinase-activated receptor-2 activating peptides or t
70 contrast, Rho activity did not affect either proteinase-activated receptor-2 activity or mRNA and pro
71 ed 5,6-EET via a mechanism that involved the proteinase-activated receptor-2 and cytochrome epoxygena
72                New insights into the role of proteinase-activated receptor-2 in the pancreas add to t
73                                 We show that proteinase-activated receptor-2 mediated phagocytosis in
74        These data are the first to show that proteinase-activated receptor-2 mediated phagocytosis is
75                                              Proteinase-activated receptor-2 mediated Rho activation
76      We explored the signaling mechanisms of proteinase-activated receptor-2 mediated Rho activation
77 uman keratinocytes is Rho dependent and that proteinase-activated receptor-2 signals to activate Rho.
78 iated phagocytosis is Rho dependent and that proteinase-activated receptor-2 signals to Rho and cAMP
79 an keratinocytes and show that activation of proteinase-activated receptor-2, either through specific
80 trated markedly reduced capacity to activate proteinase-activated receptor-2.
81 ning GTPase activating protein 2) and F2rl2 (proteinase-activated receptor-3), 2 genes that were also
82 aggregation induced by low concentrations of proteinase-activated receptor 4-activating peptide, U466
83                                              Proteinase-activated receptors 4 (PAR(4)) is a class A G
84                                   A role for proteinase-activated receptor-4 (PAR-4) was recently sug
85 cornea are activation of thrombin-sensitive, proteinase-activated receptors and cleavage of fibrinoge
86                                              Proteinase-activated receptors and peroxisome proliferat
87                                              Proteinase-activated receptors are a family of seven-tra
88 reviously known to regulate inflammation via proteinase-activated receptors, can also play a substant
89                Binding and barrier assays in proteinase activated receptor (PAR)(2)-expressing and PA
90                        These targets include proteinase-activated receptor (PAR) 1 or histamine recep
91                                Proteases and proteinase-activated receptor (PAR) activation are invol
92                               Members of the proteinase-activated receptor (PAR) subfamily of G prote
93 diseases, is the increased expression of the proteinase-activated receptor (PAR) subtype PAR-2.
94  to examine whether HCECs express functional proteinase-activated receptor (PAR)-1 and -2 and evaluat
95 rmation of vasculature, we hypothesized that proteinase-activated receptor (Par)-2 (official name F2r
96 e use genetic epistasis analysis to identify proteinase-activated receptor (PAR)-2-dependent inflamma
97                                              Proteinase-activated receptor (PAR)-4 is a member of the
98 ochemistry, we confirmed renal expression of proteinase-activated receptor (PAR-2) and demonstrated i
99                                     A second proteinase-activated receptor (PAR-2) was cloned recentl
100                                            A proteinase-activated receptor (PAR-2)-specific agonist p
101 telet aggregation by coordinately activating proteinase-activated receptors (PARs) 1 and 4.
102                                              Proteinase-activated receptors (PARs) are a four-member
103                                              Proteinase-activated receptors (PARs) are novel G-protei
104                             Proteases cleave proteinase-activated receptors (PARs) to expose N-termin
105 ing/activating a G-protein-coupled family of proteinase-activated receptors (PARs).
106 or disarming signal transduction mediated by proteinase-activated receptors (PARs).
107 nicity and airway inflammation by activating proteinase-activated receptors (PARs).
108         Proteases regulate cells by cleaving proteinase-activated receptors (PARs).
109 ding prostaglandin subtypes, growth factors, proteinase-activated receptors, peroxisome proliferator-

 
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