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1  expression was confirmed, as was neutrophil chemoattraction.
2 oad biologic activities, including leukocyte chemoattraction.
3 n or pannexin-3 knockdown prevented monocyte chemoattraction.
4 hed growth cone chemorepulsion but permitted chemoattraction.
5 ved in regulation of the immune response and chemoattraction.
6 nted for in future in vitro studies of sperm chemoattraction.
7 g the guidance path, Net-Fra is not used for chemoattraction.
8 ll secreted proteins that initiate leukocyte chemoattraction.
9 re required for the CTD role of EGL-15 in SM chemoattraction.
10  domain that is specifically required for SM chemoattraction.
11 b2 can bind directly to EGL-15 to mediate SM chemoattraction.
12 oting inflammation, catabolism, and monocyte chemoattraction.
13 ype I collagen results in increased monocyte chemoattraction.
14 trafficking, and cell metastasis, depends on chemoattraction.
15 rmis, but 5B is incapable of carrying out SM chemoattraction.
16 on of a critical mass of neutrophils through chemoattraction.
17  lines restored CCL2 production and NKT cell chemoattraction.
18 P-1/CCL2), a chemokine required for NKT cell chemoattraction.
19 nduce uveitis, lymphocyte proliferation, and chemoattraction.
20 s sperm velocity, motility, straightness and chemoattraction.
21 onizes platelet-derived growth factor (PDGF) chemoattraction.
22  growth within that tissue might depend upon chemoattraction.
23 and that this chemorepulsion is converted to chemoattraction after PKCalpha activation.
24  because PICK1-/- axons are not converted to chemoattraction after PKCalpha activation.
25 mmatory cytokines that function in leukocyte chemoattraction and activation and have recently been sh
26 , inhibitory cytokine pathways for leukocyte chemoattraction and activation have been identified, but
27 CR1-mediated mechanism may direct lymphocyte chemoattraction and adhesion within the healthy and dise
28  we show that MET is required for neutrophil chemoattraction and cytotoxicity in response to its liga
29  Some studies implicate mechanisms including chemoattraction and enhanced adherence to bone endotheli
30 -gamma]) that impressively blocks eosinophil chemoattraction and function, but the mechanism has rema
31 ne production in hypoxic TAMs and consequent chemoattraction and inhibition of NKT cells represents a
32 xis drives both the anti-tumor effector cell chemoattraction and pro-tumor infiltration of the lungs
33 he process of vascularization by stimulating chemoattraction and proliferation of angioblasts and end
34 nes, complement component 5a and IL-8 induce chemoattraction and repulsion in equal proportions, resu
35 s might coexist and involve both S1P-induced chemoattraction and SDF-1-mediated chemorepulsion or fug
36              Lipoprotein(a) induces monocyte chemoattraction and smooth muscle cell activation in vit
37     Examination of the relationships between chemoattraction and the ability to elicit pathology at t
38 educe significantly CX(3)CR1(+)-bearing cell chemoattraction and to protect against endothelial damag
39 okines such as interleukin-8 (IL-8) regulate chemoattraction, and are elevated in tracheal aspirates
40 oward the striatum in response to Nrg1/ErbB4 chemoattraction, and avoid migrating into the adjacent c
41 ll secreted factors on trophoblast motility, chemoattraction, and signaling pathways to determine the
42 pacity of FKN to mediate leukocyte adhesion, chemoattraction, and transmigration, its increased produ
43 -8 is a CXC chemokine involved in neutrophil chemoattraction, angiogenesis, and stem cell mobilizatio
44 d not alter systemic Ag-specific immunity or chemoattraction at extrapulmonary sites.
45                     In addition to mediating chemoattraction, BLC induces B cells to up-regulate memb
46 f cytokines and several chemokines linked to chemoattraction but not inflammation were also increased
47                              The efficacy of chemoattraction by CK beta-11/MIP-3 beta/ELC and tissue
48 ophilic inflammation, which are hallmarks of chemoattraction by CXCR2 ligands.
49          Pertussis toxin treatment abrogates chemoattraction by granulysin, indicating involvement of
50  intercellular adhesion molecule 1 [ICAM1]), chemoattraction (CCL20, CCL5, CXCL10), immune suppressio
51 ulation (CD80 and CTLA4), apoptosis (NLRP1), chemoattraction (CCR10), and dendritic cell function (CL
52 ur different mechanisms: contact attraction, chemoattraction, contact repulsion, and chemorepulsion.
53 ent mechanisms: contact-mediated attraction, chemoattraction, contact-mediated repulsion, and chemore
54 c cells signaling through CXCR4 and that the chemoattraction could be downmodulated by culture ex viv
55 he data demonstrate that besides its role in chemoattraction, CX3CR1 is a key regulator of myeloid ce
56  we provide experimental evidence that sperm chemoattraction directly affects the magnitude of fertil
57 ivate IGF-1R, and in so doing provoke T cell chemoattraction expression in fibroblasts, suggesting a
58 he protein, expressed in 3T3 cells, exhibits chemoattraction for both Xt and Xl sperm and cross react
59                      Interleukin-8 (IL-8), a chemoattraction for neutrophils, was 19 times higher tha
60 tumor cell immunogenicity and induces potent chemoattraction for T cells.
61 ields spatial distributions corresponding to chemoattraction (frontness pathways in-phase with the ex
62                First, Fra mediates canonical chemoattraction in response to netrin, and, second, it f
63 t in the repulsion that is observed when the chemoattraction is compromised.
64                                        Here, chemoattraction is found to provide a cheap evolutionary
65  levels and mediates chemorepulsion, whereas chemoattraction is PTEN-independent.
66 ch the cleavage event enhances MCP1-mediated chemoattraction is unknown; to investigate it, we use wi
67 f locomotion, and they reveal a mechanism of chemoattraction likely to function during both embryogen
68          This process of regulating Th1 cell chemoattraction may represent a mechanism for orchestrat
69 ed filamentous actin (F-actin) formation and chemoattraction, Mig potently blocks platelet activating
70 alpha (GRO-alpha) are chemokines involved in chemoattraction, neovascularization, and stimulation of
71 oxicity occurs at micromolar concentrations, chemoattraction occurs in the nanomolar range, and immun
72 eloped viruses, and other activities such as chemoattraction of a range of different cell types to th
73                 As a result, RANTES-mediated chemoattraction of CCR5(+) target cells was also severel
74 tumor-infiltrating host cells results in the chemoattraction of CCR6(+) B220(+) lymphocytes, which in
75 uding costimulation of T cell proliferation, chemoattraction of CD8+ T cells, and stimulation of lymp
76          Agents that disrupt CXCL12-mediated chemoattraction of CXCR4-expressing cells mobilize PMNs
77                              SDF-1-dependent chemoattraction of immature thymocytes is not significan
78 h inducing airway inflammatory responses and chemoattraction of inflammatory cells in asthma.
79  matrix destruction, which also includes the chemoattraction of inflammatory cells.
80 hat whereas cell-derived VEGF-C could induce chemoattraction of LECs across a membrane (which involve
81 ion gradient of CKbeta-11/MIP-3beta/ELC, and chemoattraction of mature SP thymocytes to CKbeta-11/MIP
82 in HIV-1 infection of macrophages, including chemoattraction of monocyte/macrophages (HIV-1 targets)
83 kine and adhesion molecule implicated in the chemoattraction of monocytes and in cell-mediated immuni
84 a proinflammatory cytokine implicated in the chemoattraction of monocytes and the development of athe
85 otic, annexin A1-externalizing cells induced chemoattraction of monocytes, which was clearly reduced
86 strongly expressed in the ceca, inhibits the chemoattraction of NCC to glial-derived neurotrophic fac
87  equivalent, indicating that CX3CL1 mediated chemoattraction of NK cells was relatively specific for
88 pletion of CXCR4/CXCR7 in mice abrogated the chemoattraction of SC to PCC.
89 thii, the sexual process is initiated by the chemoattraction of small sperm to a sexually competent f
90 emokines known to promote T-cell priming and chemoattraction of T cells and innate effector cells.
91 n of TGF-beta production and activation, and chemoattraction of T cells and nonspecific inflammatory
92 IL-2 to the tumor site and thereby achieving chemoattraction of T cells together with their activatio
93 latelet-derived mediators may play a role in chemoattraction of T lymphocytes.
94  domains of TrkA is essential for triggering chemoattraction of the growth cone in an NGF gradient.
95 -15(5A) isoform is necessary for the gonadal chemoattraction of the migrating sex myoblasts (SMs), wh
96                     We demonstrated that the chemoattraction of the trophoblast by dNK cells is impai
97 ase augmentation and indicate that selective chemoattraction of Tregs into diseased sites may offer a
98 y, it is now possible to achieve a selective chemoattraction of Tregs to periodontal tissues, attenua
99 trin-1 VI-V peptide, which fails to activate chemoattraction, or by pharmacological block of Src fami
100 panied by diminished macrophage infiltration/chemoattraction, phagocytosis, and activation of Toll-li
101 thermore, the data suggest that LRP-mediated chemoattraction represents a novel, non-classical signal
102 analyse four qualitative migration patterns: chemoattraction, -repulsion, -kinesis and -inhibition, u
103                                  Growth cone chemoattraction required PI(3,4,5)P3 production and Akt
104 tream into branchial arch 2 (ba2), is due to chemoattraction through neuropilin-1-vascular endothelia
105  jejuni 81-176 (wildtype) exhibited enhanced chemoattraction to and respiration of formate in compari
106  not other amphid sensory neurons, abolished chemoattraction to CAI-1.
107               The potential for LRP-mediated chemoattraction to mediate axonal regeneration was exami
108 mportant role for mechanotransduction during chemoattraction to netrin-1 and that mechanical activati
109 fic CXCL12 depletion exhibited diminished SC chemoattraction to pancreatic intraepithelial neoplasia
110                                              Chemoattraction toward a gradient of metallothionein II
111 reased function of CXCR4 including increased chemoattraction toward CXCR4-using-gp120.
112 eotides as possible mediators of immune cell chemoattraction toward muscle in the context of obesity.
113 cassette resulted in a mutant with decreased chemoattraction toward nutrient supplements.
114 ggests a mechanism for the chemorepulsion-to-chemoattraction transition observed in neurons.
115 branchial arch-mediated growth promotion and chemoattraction was not blocked by anti-HGF antibodies.
116 Moreover, astrocyte growth and EGF-dependent chemoattraction were inhibited by the mTOR-selective dru
117 primary monocytes lost responsiveness to p17 chemoattraction, whereas CXCR1-transfected Jurkat cells
118 P1 and LRP2 ligands that could induce axonal chemoattraction, which might have therapeutic potential.
119 ent PDAC cells inhibited their bidirectional chemoattraction with neural cells, and more specifically
120 s recognized as the prototypical effector of chemoattraction, with roles in both long- and short-rang

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