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1 ferred to as T-lymphocyte-derived eosinophil chemotactic factor.
2  chamber assay using PDGF-BB (20 ng/ml) as a chemotactic factor.
3 ive tissue is a principal smooth muscle cell chemotactic factor.
4 ctivator, or the tripeptide fMLP, which is a chemotactic factor.
5 ndependent growth, while serving as a potent chemotactic factor.
6                DEP represents a new class of chemotactic factor.
7 t diseases involving leukocyte migration and chemotactic factors.
8 timulation of HMPS activity or glycolysis by chemotactic factors.
9 ng an activation by Fas ligand of neutrophil chemotactic factors.
10  platelet-activating factor, IL-8, or RANTES chemotactic factors.
11 lar endothelial cell expression of leukocyte chemotactic factors.
12 ctivated by various cytokines, stresses, and chemotactic factors.
13 enhance the respiratory burst in response to chemotactic factors.
14 sue deposition by altering the production of chemotactic factors.
15 y and profibrotic cytokines and myeloid cell chemotactic factors.
16 pid rafts, leading to expression of monocyte chemotactic factors.
17 n of major inflammatory cytokines, including chemotactic factors.
18 from infected rats was used as the source of chemotactic factors.
19 ially and temporally controlled gradients of chemotactic factors.
20 e chemotactic response of neutrophils to the chemotactic factors.
21 also inhibit leukocyte chemotaxis induced by chemotactic factors.
22 tly induced interleukin-10 (IL-10), monocyte chemotactic factor 1, IL-1beta, and tumor necrosis facto
23 nophil-derived cytokines include JE/monocyte chemotactic factor-1 and TGF-beta1, this cytokine networ
24 factor-alpha and cytokine-induced neutrophil chemotactic factor-1 in plasma were determined by enzyme
25 ta, basic fibroblast growth factor, monocyte chemotactic factor-1, and granulocyte CSF (G-CSF) had no
26 s cases are Ig light chain, AA, or leukocyte chemotactic factor 2 amyloidosis, but rare hereditary fo
27 ight chain (AL), heavy chain (AH), leukocyte chemotactic factor-2-type (ALECT2), secondary (AA), fibr
28  ability of IGF-I to serve additionally as a chemotactic factor affecting the mobility and invasive p
29 eri generated significantly higher levels of chemotactic factors after 24 h of incubation than did ex
30 hibit a hyperactive phenotype in response to chemotactic factors after cell "priming" with IL-5 famil
31 tion of reactive oxygen species and monocyte chemotactic factors after exposure of adipocytes to satu
32 ines (alveolar macrophage-derived neutrophil chemotactic factor [AMCF]-I/interleukin-8 and AMCF-II).
33 ion revealed that histamine acts as a T cell chemotactic factor and defective T cell trafficking was
34 broblast growth factor 1 (FGF-1) is a potent chemotactic factor and induces tyrosine phosphorylation
35 , cholesterol-containing diet showed reduced chemotactic factor and proinflammatory cytokine expressi
36 infection depends in part upon a gradient of chemotactic factors and adhesion molecules expressed by
37 rophils are mobilized rapidly in response to chemotactic factors and are among the first leukocytes r
38     Positive regulation of cell migration by chemotactic factors and downstream signaling pathways ha
39  contact with fibrinogen, endothelial cells, chemotactic factors and indomethacin, and treatment with
40                 Alterations in the levels of chemotactic factors and other proinflammatory cytokines
41 ts the production of MCP-1, a major monocyte chemotactic factor, and either decreases or minimally in
42 due to both the resistance of neutrophils to chemotactic factors, and reduced local production of neu
43                                              Chemotactic factors are postulated to direct emigration
44              Furthermore, DEK functions as a chemotactic factor, attracting neutrophils, CD8+ T lymph
45 sion of adhesion molecules and production of chemotactic factors, augmenting leukocyte adhesion and r
46     In neural precursors stimulated with the chemotactic factor BDNF, Numb binds to activated TrkB, t
47 r-like growth factor (HB-EGF), a mitogen and chemotactic factor, binds to two receptor tyrosine kinas
48 nt to plastic petri dishes with the purified chemotactic factors C5a and kallikrein increased their r
49 ols the expression of cell cycle and myeloid chemotactic factors, contributing to macrophage infiltra
50 n of Th17 cells and production of neutrophil chemotactic factor CXCL1 in vitro.
51 xes resulted in expression of the neutrophil chemotactic factors CXCL1/KC, CXCL5/LIX, and CXCL8/IL-8.
52 ous PKCalpha increased the production of the chemotactic factors cytokine-induced neutrophil chemoatt
53 rming Growth Factor-beta (TGF-beta), and the chemotactic factor derived from the conditioned culture
54                                          The chemotactic factors differed for the PMN and J774 cells,
55             Excess glucose and SFAs regulate chemotactic factor expression by a mechanism that involv
56 uitment and activation by inducing leukocyte chemotactic factor expression from VEC.
57 ertain SFAs, but not excess glucose, trigger chemotactic factor expression via a TLR4-dependent pathw
58 ctive oxygen species generation and monocyte chemotactic factor expression.
59  HDL, and methyl-beta-cyclodextrin inhibited chemotactic factor expression.
60 icates that exposure of human neutrophils to chemotactic factor FMLP as well as granulocyte-macrophag
61 the addition of IL-5 family cytokines or the chemotactic factors fMLP, CCL5, and CCL11.
62  to the surface of leukocytes serves as a co-chemotactic factor for C5a, significantly enhancing the
63           Thus, serum levels of IL-16, a key chemotactic factor for CD4(+) lymphocytes, were reduced
64 activity with HER4; and (iii) it is a potent chemotactic factor for cells overexpressing HER4.
65 noate (5-oxoETE) is gaining recognition as a chemotactic factor for eosinophilic (Eo) as well as neut
66  fold), a chemokine initially described as a chemotactic factor for eosinophils.
67 owth factor (HB-EGF) is a potent mitogen and chemotactic factor for fibroblasts, smooth muscle cells
68 c activity by itself; and (iii) it acts as a chemotactic factor for fibroblasts.
69 levated levels of circulating IL-8, a potent chemotactic factor for granulocytes and T lymphocytes, a
70 receptor CXCR3 and is known to function as a chemotactic factor for human T cells, particularly follo
71 -1alpha), is known to function in vitro as a chemotactic factor for lymphocytes, monocytes, and dendr
72 These results suggest that SDF-1 is a potent chemotactic factor for mature MKs.
73 amino-acid chemokine thought to be the major chemotactic factor for monocytes.
74 the delta subclass of chemokines, is a known chemotactic factor for monocytes/macrophages as well as
75 tivation of p38 and SYK signaling, acts as a chemotactic factor for myeloid cell migration and promot
76 e inflammatory protein 2 (MIP-2), a powerful chemotactic factor for neutrophils which is secreted by
77               Murine (Mu)Mig functioned as a chemotactic factor for resting memory and activated T ce
78 disease that, we show, also acts as a potent chemotactic factor for the migration of these leukocytes
79                              CXCL12 is a key chemotactic factor for the trafficking of CLL.
80 strated that IP-10 is a potent mitogenic and chemotactic factor for vascular smooth muscle cells, the
81 blastic and osteocytic cells contain soluble chemotactic factors for bone marrow mesenchymal progenit
82 f chemokines and triggered the production of chemotactic factors for macrophages and neutrophils.
83 is suggests neutrophils may be the source of chemotactic factors for monocytes.
84 FB103A, S100 proteins like S100A7, S100A12), chemotactic factors for neutrophils (e.g. CXCL5, CXCL8)
85         Although MLO-Y4 cells secrete potent chemotactic factors for osteoclast precursors, CCL7 was
86 he Trk receptor tyrosine kinases, are potent chemotactic factors for smooth muscle cells, and the exp
87    In vitro, HepG2 cells secreted functional chemotactic factors for tumor-derived lymphocytes that c
88  (CyPA) and CyPB have been well described as chemotactic factors for various leukocyte subsets, sugge
89 lar cyclophilins have been well described as chemotactic factors for various leukocyte subsets.
90 in accordance with tissue gene expression of chemotactic factors, for which receptors are differently
91 ther, chymase induced the release of various chemotactic factors from HLFs.
92 siRNA suppressed ROS generation and monocyte chemotactic factor gene expression induced by both gluco
93 ies (ROS) in adipocytes, leading to monocyte chemotactic factor gene expression.
94 ucose-stimulated ROS generation and monocyte chemotactic factor gene expression.
95 ellular spatial information in the form of a chemotactic factor gradient is transduced into intracell
96 ory reactions, the production and release of chemotactic factors guide the recruitment of selective l
97 e structure of a small-molecule, non-peptide chemotactic factor has been determined from activity pur
98                                       Unlike chemotactic factors, however, AA was fully active on cel
99 an genes than is porcine alveolar macrophage chemotactic factor-II.
100 capable of migrating toward the CD4-specific chemotactic factor IL-16, providing another function for
101  as TNF-alpha, IL-1 beta, and the neutrophil chemotactic factor IL-8 and inhibitors (e.g., soluble TN
102 lar adhesion molecule-1 [ICAM-1] and soluble chemotactic factors (IL-8).
103 say revealed the presence of a single active chemotactic factor in the supernatant from this incubati
104 d monocytes, indicating that CRAMP acts as a chemotactic factor in vivo.
105           FFAs induce expression of monocyte chemotactic factors in adipocytes via both transcription
106 oblast subsets abundantly express neutrophil chemotactic factors in psoriatic skin that are subsequen
107 he PDGFbeta receptor and VSMC sensitivity to chemotactic factors in serum, leading to altered migrato
108 ability of HepG2 cells to secrete lymphocyte chemotactic factors in vitro suggests that the tumor con
109 ncrease in eotaxin, but not other eosinophil chemotactic factors, in bronchoalveolar lavage fluid aft
110 jury and in VSMCs stimulated with growth and chemotactic factors including angiotensin II, basic fibr
111 in reduced expression of numerous macrophage chemotactic factors, including CCL5.
112 anner secreted an array of T cell-recruiting chemotactic factors, including IL-8, macrophage-derived
113 a concentrations of polarizing cytokines and chemotactic factors, including interleukin-12p70 (IL-12p
114 s ERK1/2, we also observed an enhancement of chemotactic factor-induced Akt phosphorylation after IL-
115 ation and vascular permeability in models of chemotactic factor-induced alveolitis.
116 uce HUVEC expression of the potent leukocyte chemotactic factor interleukin-8 (IL-8).
117 several cellular genes, including the potent chemotactic factor interleukin-8 (IL-8).
118 imals as compared to controls, levels of the chemotactic factors interleukin-5, macrophage inflammato
119                           The chemokine-like chemotactic factor leukocyte cell-derived chemotaxin 2 (
120 ficant inhibition of synthesis of the potent chemotactic factor leukotriene B4, and that process was
121 ation and renal expression of the neutrophil chemotactic factor macrophage inflammatory protein-2.
122 ha), and eotaxin, but not macrophage-derived chemotactic factor (MDC), than tissues from lymphoid hyp
123 de (ENA-78), and monocyte-derived neutrophil chemotactic factor (MDNCF).
124 duction of TNFalpha and the transcription of chemotactic factors (MIP-2, KC, S100A8/A9), vascular end
125 rotein-linked receptors for lipid or peptide chemotactic factors, neutrophils apparently also can uti
126 ed a receptor by which a non-serum-dependent chemotactic factor (NSCF) produced by C. albicans induce
127 l chemokine that can act either as a soluble chemotactic factor or as a transmembrane-anchored adhesi
128 ion also reduced the production of the mMDSC chemotactic factor osteopontin by tumor cells.
129 fied PDGF AA as the major stromal fibroblast chemotactic factor produced by tumor cells, and demonstr
130  CXCR2 chemokine receptor agonists and other chemotactic factors produced by tumors, neutrophils, and
131 CCL2, MIP-1alpha/CCL3, and RANTES/CCL5), and chemotactic factor receptors (CCR1, CCR2, and CCR5), but
132 onuclear neutrophils (PMNs) are recruited by chemotactic factors released by AMs to produce an intens
133                                              Chemotactic factors released by infected macrophages are
134 ainst LAM, suggesting that LAM is one of the chemotactic factors released by Mtb-infected alveolar ma
135 ions by preventing neutrophil activation via chemotactic factors released during reperfusion.
136                            Local delivery of chemotactic factors represents a novel approach to tissu
137  These responses, similar to those caused by chemotactic factors, resulted from a rise in the number
138 ression and release of an epithelium-derived chemotactic factor(s) for PMN.
139 ed influx suggests the local production of a chemotactic factor(s) such as interleukin-8 (IL-8).
140                                In search for chemotactic factor(s) that may mediate transmigration of
141              Chemokines are more than simple chemotactic factors, since they are also implicated in l
142                           In contrast, these chemotactic factors stimulate weak or indiscernible ERK
143  vitro and in vivo towards a gradient of the chemotactic factor stromal cell-derived factor-1 (SDF-1)
144 f IL-22 strongly decreased the expression of chemotactic factors such as CCL3 and CXCL3 and of biomar
145 yperalgesia produced by BMSCs required their chemotactic factors such as CCL4 and CCR2, the integrati
146 tivates endothelial cells (EC) to synthesize chemotactic factors, such as interleukin (IL)-8.
147  induce endothelial cells (EC) to synthesize chemotactic factors, such as interleukin 8 (IL-8).
148 oline induce endothelial cells to synthesize chemotactic factors, such as interleukin 8 (IL-8).
149         GRO alpha is an inducible neutrophil chemotactic factor synthesized in inflamed corneal tissu
150 ascular smooth muscle cell (SMC) mitogen and chemotactic factor that is expressed by endothelial cell
151 ctor-like growth factor (HB-EGF) is a potent chemotactic factor that is induced during ischemia/reper
152 een described as an eosinophil and mast cell chemotactic factor that mediates a number of inflammator
153 stream to a site of infection is mediated by chemotactic factors that are often host-derived.
154                                 The maternal chemotactic factors that direct trophoblast migration an
155  evaluate the entire picture of all monocyte chemotactic factors that potentially contribute to adipo
156 hat tumour hypoxia induces the expression of chemotactic factors that promote tolerance.
157 n of complement and generation of complement chemotactic factors that rapidly recruit macrophages.
158 secretion by cancer cells of proinflammatory chemotactic factors that recruit antitumor effector T ce
159  blockade; these also mediate an increase in chemotactic factors that recruit T cells.
160    In this study, it is shown that a classic chemotactic factor, the bacterial chemotactic peptide N-
161 chemotactic response by preincubation with a chemotactic factor to achieve deactivation, 5 x 10(-7) M
162                            The capacity of a chemotactic factor to stimulate glucose metabolism of hu
163                     Interleukin (IL)-15 is a chemotactic factor to T cells.
164                      Apoptotic cells secrete chemotactic factors to attract phagocytic cells, and we
165                                    The first chemotactic factors to be structurally defined were the
166              During stimulation with fMLP, a chemotactic factor, two Ca2+ waves traveling in opposite
167 es eosinophil responsiveness to a variety of chemotactic factors via a process called priming, althou
168 AC induces macrophage production of multiple chemotactic factors via NF-kappaB to promote monocyte mi
169                                          The chemotactic factor was concentrated by solid phase chrom
170 ic mAbs indicated that the serotonin-induced chemotactic factor was the previously characterized lymp
171                               The release of chemotactic factors was dose dependent and was initiated
172 lthough interleukin-6 (IL-6) is not itself a chemotactic factor, we found that medium from il-6-/- ne
173                                 Six monocyte chemotactic factors were found to be predominantly upreg
174 g clear that there is a complex interplay of chemotactic factors, which changes over time as the infl
175 ction in direct response to locally produced chemotactic factors, which signal through specific G pro

 
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