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1 onizes platelet-derived growth factor (PDGF) chemoattraction.
2  growth within that tissue might depend upon chemoattraction.
3  expression was confirmed, as was neutrophil chemoattraction.
4 oad biologic activities, including leukocyte chemoattraction.
5 stal module of its dCache domain, triggering chemoattraction.
6 to decreased chemokine expression and T cell chemoattraction.
7 ng neuronal migration through suppression of chemoattraction.
8  its sCache ligand binding domain, mediating chemoattraction.
9 g the guidance path, Net-Fra is not used for chemoattraction.
10 s sperm velocity, motility, straightness and chemoattraction.
11  of beta-arrestin recruitment and neutrophil chemoattraction.
12 n or pannexin-3 knockdown prevented monocyte chemoattraction.
13 hed growth cone chemorepulsion but permitted chemoattraction.
14 ved in regulation of the immune response and chemoattraction.
15 nted for in future in vitro studies of sperm chemoattraction.
16 ll secreted proteins that initiate leukocyte chemoattraction.
17 re required for the CTD role of EGL-15 in SM chemoattraction.
18  domain that is specifically required for SM chemoattraction.
19 b2 can bind directly to EGL-15 to mediate SM chemoattraction.
20 oting inflammation, catabolism, and monocyte chemoattraction.
21 ype I collagen results in increased monocyte chemoattraction.
22 trafficking, and cell metastasis, depends on chemoattraction.
23 rmis, but 5B is incapable of carrying out SM chemoattraction.
24 on of a critical mass of neutrophils through chemoattraction.
25  lines restored CCL2 production and NKT cell chemoattraction.
26 P-1/CCL2), a chemokine required for NKT cell chemoattraction.
27 nduce uveitis, lymphocyte proliferation, and chemoattraction.
28                            Inhibition of PMN chemoattraction, activation, and proteolytic function re
29 and that this chemorepulsion is converted to chemoattraction after PKCalpha activation.
30  because PICK1-/- axons are not converted to chemoattraction after PKCalpha activation.
31 mmatory cytokines that function in leukocyte chemoattraction and activation and have recently been sh
32 eceptors for C3a and C5a through which their chemoattraction and activation are mediated by anaphylat
33 , inhibitory cytokine pathways for leukocyte chemoattraction and activation have been identified, but
34 CR1-mediated mechanism may direct lymphocyte chemoattraction and adhesion within the healthy and dise
35  we show that MET is required for neutrophil chemoattraction and cytotoxicity in response to its liga
36 ession of cytokines that regulate macrophage chemoattraction and differentiation into M2 macrophage.
37  Some studies implicate mechanisms including chemoattraction and enhanced adherence to bone endotheli
38 -gamma]) that impressively blocks eosinophil chemoattraction and function, but the mechanism has rema
39 ne production in hypoxic TAMs and consequent chemoattraction and inhibition of NKT cells represents a
40 xis drives both the anti-tumor effector cell chemoattraction and pro-tumor infiltration of the lungs
41 he process of vascularization by stimulating chemoattraction and proliferation of angioblasts and end
42 nes, complement component 5a and IL-8 induce chemoattraction and repulsion in equal proportions, resu
43 s might coexist and involve both S1P-induced chemoattraction and SDF-1-mediated chemorepulsion or fug
44              Lipoprotein(a) induces monocyte chemoattraction and smooth muscle cell activation in vit
45     Examination of the relationships between chemoattraction and the ability to elicit pathology at t
46 educe significantly CX(3)CR1(+)-bearing cell chemoattraction and to protect against endothelial damag
47 okines such as interleukin-8 (IL-8) regulate chemoattraction, and are elevated in tracheal aspirates
48 oward the striatum in response to Nrg1/ErbB4 chemoattraction, and avoid migrating into the adjacent c
49 ll secreted factors on trophoblast motility, chemoattraction, and signaling pathways to determine the
50 pacity of FKN to mediate leukocyte adhesion, chemoattraction, and transmigration, its increased produ
51 -8 is a CXC chemokine involved in neutrophil chemoattraction, angiogenesis, and stem cell mobilizatio
52 d not alter systemic Ag-specific immunity or chemoattraction at extrapulmonary sites.
53                     In addition to mediating chemoattraction, BLC induces B cells to up-regulate memb
54 f cytokines and several chemokines linked to chemoattraction but not inflammation were also increased
55                              The efficacy of chemoattraction by CK beta-11/MIP-3 beta/ELC and tissue
56 ophilic inflammation, which are hallmarks of chemoattraction by CXCR2 ligands.
57          Pertussis toxin treatment abrogates chemoattraction by granulysin, indicating involvement of
58  intercellular adhesion molecule 1 [ICAM1]), chemoattraction (CCL20, CCL5, CXCL10), immune suppressio
59 ulation (CD80 and CTLA4), apoptosis (NLRP1), chemoattraction (CCR10), and dendritic cell function (CL
60 ur different mechanisms: contact attraction, chemoattraction, contact repulsion, and chemorepulsion.
61 ent mechanisms: contact-mediated attraction, chemoattraction, contact-mediated repulsion, and chemore
62 c cells signaling through CXCR4 and that the chemoattraction could be downmodulated by culture ex viv
63 he data demonstrate that besides its role in chemoattraction, CX3CR1 is a key regulator of myeloid ce
64  we provide experimental evidence that sperm chemoattraction directly affects the magnitude of fertil
65 ivate IGF-1R, and in so doing provoke T cell chemoattraction expression in fibroblasts, suggesting a
66 he protein, expressed in 3T3 cells, exhibits chemoattraction for both Xt and Xl sperm and cross react
67                      Interleukin-8 (IL-8), a chemoattraction for neutrophils, was 19 times higher tha
68 tumor cell immunogenicity and induces potent chemoattraction for T cells.
69 phage-infected Synechococcus elicited strong chemoattraction from Vibrio alginolyticus and Pseudoalte
70 ields spatial distributions corresponding to chemoattraction (frontness pathways in-phase with the ex
71 ults demonstrate that Pdgfab/Pdgfra-mediated chemoattraction guides the migration of sclerotome-deriv
72                         Eliminating monocyte chemoattraction in monocyte enriched PDGFB-driven GBM in
73                First, Fra mediates canonical chemoattraction in response to netrin, and, second, it f
74 t in the repulsion that is observed when the chemoattraction is compromised.
75 emorepulsion, but the magnitude of bacterial chemoattraction is controlled by indole levels.
76                                        Here, chemoattraction is found to provide a cheap evolutionary
77  levels and mediates chemorepulsion, whereas chemoattraction is PTEN-independent.
78 ch the cleavage event enhances MCP1-mediated chemoattraction is unknown; to investigate it, we use wi
79 f locomotion, and they reveal a mechanism of chemoattraction likely to function during both embryogen
80 d -extrinsic mechanisms, such as CD8+ T-cell chemoattraction, M1/M2 macrophage rebalancing, monocyte
81          This process of regulating Th1 cell chemoattraction may represent a mechanism for orchestrat
82 ed filamentous actin (F-actin) formation and chemoattraction, Mig potently blocks platelet activating
83                    While much is known about chemoattraction, much less is known about chemorepulsion
84 alpha (GRO-alpha) are chemokines involved in chemoattraction, neovascularization, and stimulation of
85 oxicity occurs at micromolar concentrations, chemoattraction occurs in the nanomolar range, and immun
86 eloped viruses, and other activities such as chemoattraction of a range of different cell types to th
87                 As a result, RANTES-mediated chemoattraction of CCR5(+) target cells was also severel
88 tumor-infiltrating host cells results in the chemoattraction of CCR6(+) B220(+) lymphocytes, which in
89 on epithelium increases CCL20 expression and chemoattraction of CCR6+ immune cells, contributing to g
90 uding costimulation of T cell proliferation, chemoattraction of CD8+ T cells, and stimulation of lymp
91                               In addition to chemoattraction of cells critical to the wound healing p
92          Agents that disrupt CXCL12-mediated chemoattraction of CXCR4-expressing cells mobilize PMNs
93                              SDF-1-dependent chemoattraction of immature thymocytes is not significan
94 h inducing airway inflammatory responses and chemoattraction of inflammatory cells in asthma.
95  matrix destruction, which also includes the chemoattraction of inflammatory cells.
96 orm in vivo proof-of-concept studies to show chemoattraction of invading glioblastoma cells in orthot
97 hat whereas cell-derived VEGF-C could induce chemoattraction of LECs across a membrane (which involve
98 N-gamma production by NK cells, resulting in chemoattraction of lymphocytes toward the respiratory ep
99 nts are neuronal chemorepellents and inhibit chemoattraction of many cell types, including neutrophil
100 ion gradient of CKbeta-11/MIP-3beta/ELC, and chemoattraction of mature SP thymocytes to CKbeta-11/MIP
101 in HIV-1 infection of macrophages, including chemoattraction of monocyte/macrophages (HIV-1 targets)
102 kine and adhesion molecule implicated in the chemoattraction of monocytes and in cell-mediated immuni
103 a proinflammatory cytokine implicated in the chemoattraction of monocytes and the development of athe
104 otic, annexin A1-externalizing cells induced chemoattraction of monocytes, which was clearly reduced
105 strongly expressed in the ceca, inhibits the chemoattraction of NCC to glial-derived neurotrophic fac
106 motes macrophage differentiation and induces chemoattraction of neutrophils.
107  equivalent, indicating that CX3CL1 mediated chemoattraction of NK cells was relatively specific for
108 pletion of CXCR4/CXCR7 in mice abrogated the chemoattraction of SC to PCC.
109 thii, the sexual process is initiated by the chemoattraction of small sperm to a sexually competent f
110 emokines known to promote T-cell priming and chemoattraction of T cells and innate effector cells.
111 n of TGF-beta production and activation, and chemoattraction of T cells and nonspecific inflammatory
112 IL-2 to the tumor site and thereby achieving chemoattraction of T cells together with their activatio
113 latelet-derived mediators may play a role in chemoattraction of T lymphocytes.
114  domains of TrkA is essential for triggering chemoattraction of the growth cone in an NGF gradient.
115 -15(5A) isoform is necessary for the gonadal chemoattraction of the migrating sex myoblasts (SMs), wh
116                     We demonstrated that the chemoattraction of the trophoblast by dNK cells is impai
117 ase augmentation and indicate that selective chemoattraction of Tregs into diseased sites may offer a
118 y, it is now possible to achieve a selective chemoattraction of Tregs to periodontal tissues, attenua
119 skeleton and pseudopods to induce neutrophil chemoattraction or chemorepulsion.
120 trin-1 VI-V peptide, which fails to activate chemoattraction, or by pharmacological block of Src fami
121 panied by diminished macrophage infiltration/chemoattraction, phagocytosis, and activation of Toll-li
122 thermore, the data suggest that LRP-mediated chemoattraction represents a novel, non-classical signal
123 analyse four qualitative migration patterns: chemoattraction, -repulsion, -kinesis and -inhibition, u
124                                  Growth cone chemoattraction required PI(3,4,5)P3 production and Akt
125           We find that AprA uses a subset of chemoattraction signal transduction pathways including R
126                                   Eukaryotic chemoattraction signal transduction pathways, such as th
127 s revealed enhancement in innate immune cell chemoattraction, survival, and phagocytosis, and diminis
128 apsules induced a potent monocyte-macrophage chemoattraction that could be used to direct the therapy
129 tream into branchial arch 2 (ba2), is due to chemoattraction through neuropilin-1-vascular endothelia
130  jejuni 81-176 (wildtype) exhibited enhanced chemoattraction to and respiration of formate in compari
131  not other amphid sensory neurons, abolished chemoattraction to CAI-1.
132 ing its smooth-swimming behavior, leading to chemoattraction to HOCl sources.
133               The potential for LRP-mediated chemoattraction to mediate axonal regeneration was exami
134 mportant role for mechanotransduction during chemoattraction to netrin-1 and that mechanical activati
135 fic CXCL12 depletion exhibited diminished SC chemoattraction to pancreatic intraepithelial neoplasia
136 XCR3 signaling in macrophages mediates their chemoattraction to the pancreas, enhances their prolifer
137                                              Chemoattraction toward a gradient of metallothionein II
138 reased function of CXCR4 including increased chemoattraction toward CXCR4-using-gp120.
139 eotides as possible mediators of immune cell chemoattraction toward muscle in the context of obesity.
140 cassette resulted in a mutant with decreased chemoattraction toward nutrient supplements.
141 tral migration of FBM neurons by suppressing chemoattraction towards Wnt5a in r3 and successfully tes
142 ggests a mechanism for the chemorepulsion-to-chemoattraction transition observed in neurons.
143                                              Chemoattraction via CXCL12/CXCR4 directs cellular migrat
144 branchial arch-mediated growth promotion and chemoattraction was not blocked by anti-HGF antibodies.
145                              Slit2-N-induced chemoattraction was unaffected by Ras inhibitors, revers
146 kine (CXCL) 13 for disease-associated B-cell chemoattraction, we found CXCL13 to be highly expressed
147 Moreover, astrocyte growth and EGF-dependent chemoattraction were inhibited by the mTOR-selective dru
148 primary monocytes lost responsiveness to p17 chemoattraction, whereas CXCR1-transfected Jurkat cells
149 n Celsr1 mutants results from Wnt5a-mediated chemoattraction, which is suppressed in wild-type embryo
150 P1 and LRP2 ligands that could induce axonal chemoattraction, which might have therapeutic potential.
151 ent PDAC cells inhibited their bidirectional chemoattraction with neural cells, and more specifically
152 s recognized as the prototypical effector of chemoattraction, with roles in both long- and short-rang

 
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