ライフサイエンスコーパス: chemoattractant

1 al groups (T-helper 1 and 2, regulatory, and chemoattractant).

2 , if their interactions are regulated by the chemoattractant.

3 become extremely migratory in response to a chemoattractant.

4 ling out these fast mediators as the primary chemoattractant.

5 e released LdTyrRS functions as a neutrophil chemoattractant.

6 on of CXCL16, which we show to be a monocyte chemoattractant.

7 enylacetate was confirmed to be a neutrophil chemoattractant.

8 across intestinal epithelia in response to a chemoattractant.

9 onally migrate over a large dynamic range of chemoattractant.

10 period that is shared with that generated by chemoattractants.

11 CFTR(inh)-172 blocked integrin activation by chemoattractants.

12 ction in macrophage chemotaxis to a range of chemoattractants.

13 gradient that amplifies the reach of primary chemoattractants.

14 e cells' specific sensitivities to different chemoattractants.

15 ontributes to local production of neutrophil chemoattractants.

16 L-759,656 and L-759,633 acted as macrophage chemoattractants.

17 k the transmigration of immune cells towards chemoattractants.

18 ing to calibrate cellular responses to local chemoattractants.

19 xide (H2O2) and CXCL8 are two key neutrophil chemoattractants.

20 sensitivity to multiple bacterially-secreted chemoattractants.

21 The potent eosinophil chemoattractant 5-oxo-6,8,11,14-eicosatetraenoic acid (5

22 ed ANXA1 as a potent CD14(+)CD16(-) monocyte chemoattractant, acting via ALX/FPR2.

23 1c(+) dendritic cells, mEar 11 has prominent chemoattractant activity for F4/80(+)CD11c(-) tissue mac

24 Chemoattractant activity is not dependent on full enzyma

25 cial role for this structural determinant in chemoattractant activity.

26 Unlike the response to chemoattractants, an intact actin cytoskeleton was essen

27 basic protein (PPBP) is a potent neutrophil chemoattractant and activator whose expression is repres

28 Chemerin is a chemoattractant and adipokine that circulates in blood a

29 NetrinB but not NetrinA serves as a chemoattractant and Unc5 contributes as a repellant Netr

30 ed as growth promoting (i.e., growth factors/chemoattractants and attractive guidance cues) or growth

31 In summary, DC-EV are naturally loaded with chemoattractants and can contribute to cell recruitment,

32 ed receptors (GPCRs) are known for detecting chemoattractants and directing cell migration, but their

33 ration was chemotactic toward many different chemoattractants and dose-dependent.

34 ent classes of inflammatory stimuli, namely, chemoattractants and growth factors.

35 mic analyses revealed pFUS upregulated local chemoattractants and increased MSC tropism to CLI muscle

36 The ability of macrophages to respond to chemoattractants and inflammatory signals is important f

37 nt induced proximal tubular cells to secrete chemoattractants and macrophages to express proinflammat

38 We investigated whether these chemoattractants and S100A9, through the receptor for ad

39 TAK1 control in neutrophils stimulated with chemoattractants and/or GM-CSF, namely, delayed apoptosi

40 to sensitize neutrophils towards the primary chemoattractant, and in a paracrine fashion to mediate t

41 s and chemokines, such as IL-6, keratinocyte chemoattractant, and MIP-2.

42 necrosis; levels of IL-1alpha, keratinocyte chemoattractant, and neutrophils in bronchoalveolar lava

43 We identify the chemoattractant as the complement component C3a, a facto

44 the expression of the cytokines, neutrophil chemoattractants, as well as the MPO activity in the lun

45 ntration c and the production rate j0 of the chemoattractant at the source surface.

46 ruitment and navigation to the regulation of chemoattractant availability and function by atypical he

47 ich allows bacteria to navigate gradients of chemoattractants by biasing their run-and-tumble motion.

48 contrasted with responses to an end agonist chemoattractant (C5a), for which a stable gradient led t

49 Thus, subcellular targeting of a chemoattractant can direct outgrowth to specific domains

50 unctionally, miR-146a impairs the neutrophil chemoattractant capacity of keratinocytes.

51 ng gradients in the concentration of soluble chemoattractants (CAs) to attract bacteria to the surfac

52 rferon transcriptional signatures and T-cell chemoattractant CCL2.

53 cognition receptor TLR7, the Langerhans cell chemoattractant CCL20, and proinflammatory cytokines int

54 press only low endogenous levels of the Th17 chemoattractant CCL20, and therefore, it is unclear how

55 to robust expression in the lung of the Th17 chemoattractant, CCL20.

56 A 5-fold increase was documented in the Treg chemoattractants CCL22 and CCL1 in melanoma-affected ski

57 MYC signaling and an increase in the T cell chemoattractant CCL5.

58 However, localization of the FGF chemoattractant changes from all muscle membranes to T-t

59 in coupled receptor chemR23, which binds the chemoattractant chemerin.

60 A wide array of chemoattractants, chemoattractant receptors, and adhesio

61 flammatory mediators, including the monocyte chemoattractant, chemokine (C-C motif) ligand (CCL) 2, a

62 CXCL10 and interferon-inducible T-cell alpha chemoattractant/chemokine (C-X-C motif) ligand 11 (ITAC/

63 ensitivity in terms of the ratio between the chemoattractant concentration c and the production rate

64 hese cellular defects of c2gapA(-) cells are chemoattractant concentration dependent.

65 Eukaryotic cells chemotax in a wide range of chemoattractant concentration gradients, and thus need i

66 ollective guidance that is robust to varying chemoattractant concentrations while not requiring stron

67 of bacteria; however, the role of neutrophil chemoattractant CXCL1 in bacterial clearance during seps

68 ils, and a reduction in levels of neutrophil chemoattractant CXCL1 in their lungs compared with wild-

69 CXCR7 antagonism reduced the most potent PMN chemoattractants CXCL1 and CXCL2/3.

70 -alpha, CCL3, CCL5, and keratinocyte-derived chemoattractant/CXCL1, relative to AC.

71 ll cells expressed high levels of the T cell chemoattractant CXCL12.

72 ion of several chemokines, among them B cell chemoattractant (CxCL13), both in a model T cell line an

73 ducts in the liver induced production of the chemoattractant CXCL16 by myeloid dendritic cells (mDCs)

74 However, production of the granulocyte chemoattractants CXCL8 and CCL11 was not induced.

75 Interleukin-16 (IL-16) is reported to be a chemoattractant cytokine and modulator of T-cell activat

76 associated with upregulation of prototypical chemoattractant cytokines mediating retention and homing

77 nt inflammatory molecule in the induction of chemoattractants, cytokines, and glandular apoptosis in

78 We show that chemoattractant degradation creates steep local gradient

79 ogenic hormogonium-repressing factor or as a chemoattractant, depending on its extracellular concentr

80 s of lymphatic biology, stromal variability, chemoattractant distribution, and fluid flow.

81 c inflammatory skin disorder associated with chemoattractants driving neutrophils into the epidermis.

82 ular and molecular mechanisms underlying the chemoattractant effect of endothelial cell-derived CD95L

83 SPARCL1 and HSP90B, as key mediators of this chemoattractant effect.

84 Eosinophils are recruited into the airway by chemoattractant eotaxins, which are expressed by endothe

85 We show that CatSper mediates the chemoattractant-evoked Ca(2+) influx and controls chemot

86 cellular motion to a 1D channel and control chemoattractant exposure, we observed directional memory

87 ynergistically increased monocyte and T-cell chemoattractants, expression of adhesion molecules on th

88 on molecules, their porcine ligands, and the chemoattractant factors that may promote the recruitment

89 hibited macrophage chemotaxis in response to chemoattractants fMLF and CCL2 by disrupting polarized d

90 Although PRL is an established chemoattractant for breast cancer cells, the precise mol

91 Ntn1 is an FP-derived long-range diffusible chemoattractant for CAs, but suggest a novel mechanism t

92 en thought to act as a long-range diffusible chemoattractant for commissural axons (CAs).

93 floor plate (FP) as a long-range diffusible chemoattractant for commissural axons in the embryonic s

94 etrin1 does not act as a long-range secreted chemoattractant for commissural spinal axons but instead

95 Here we report that DHMA is also a chemoattractant for EHEC.

96 Chemerin acts as a chemoattractant for monocytes and macrophages, whereas R

97 nding melanoma tissues, possibly acting as a chemoattractant for monocytes to modulate the melanoma m

98 rowth factor has been proposed to serve as a chemoattractant for the angioblasts and to regulate this

99 of norepinephrine produced by E. coli, is a chemoattractant for the nonpathogenic E. coli RP437 stra

100 erived growth factor (PDGF) is a mitogen and chemoattractant for vascular smooth muscle cells (VSMCs)

101 , which have been characterized as selective chemoattractants for CD11c(+) dendritic cells, mEar 11 h

102 ays showed that these two molecules serve as chemoattractants for CNB-1.

103 d medium from both conditions were tested as chemoattractants for human bronchial fibroblasts in the

104 beta-ketoadipate catabolic pathway serve as chemoattractants for Pseudomonas putida F1.

105 f the chemokines Ccl5 and Cxcl10, two potent chemoattractants for T lymphocytes.

106 ocytosis of bacteria, thereby representing a chemoattractant GPCR that mediates not only chasing but

107 o distinguish signals downstream of distinct chemoattractant GPCRs.

108 the tumor microenvironment in response to a chemoattractant gradient created from stromal, lymphoid,

109 ules diffuse away from the spot, a transient chemoattractant gradient is established across the spots

110 In chemoattractant gradients, abpG(-) cells display normal

111 global inhibition (LEGI) mechanism to sense chemoattractant gradients, the speed of the cell cluster

112 hanced further, to 99.4%, in the presence of chemoattractant gradients.

113 , we track sea urchin sperm navigating in 3D chemoattractant gradients.

114 diated release of signaling ligands, such as chemoattractants, growth factors, and cytokines is an at

115 T, the same PDGF-A/PDGFRalpha works as an NC chemoattractant, guiding their directional migration.

116 pt of polarized Rac1 activity in response to chemoattractants has always been apparent, our understan

117 Signal transduction pathways activated by chemoattractants have been extensively studied, but litt

118 -LOX), which is required to generate the PMN chemoattractant hepoxilin A3 (HXA3) from arachidonic aci

119 y, cancer-associated cytokines, keratinocyte chemoattractant, IL-22, and IL-6, in plasma.

120 utrophils to assess the contribution of each chemoattractant in driving neutrophil transepithelial mi

121 atory role of CFTR in integrin activation by chemoattractants in monocytes and identify CF as a new,

122 required for chemotaxis because of multiple chemoattractants in mouse neutrophils in vitro.

123 n inherent reduced ability to migrate toward chemoattractants in vitro, even after LPS activation.

124 cyte colony-stimulating factor, keratinocyte chemoattractant) in response to lipopolysaccharide.

125 sed levels of the chemokine CCL2, a monocyte chemoattractant, in serum, and this increase was abolish

126 We found that chemoattractant-induced activation of beta1 and beta2 in

127 Niacin showed a selected additive effect on chemoattractant-induced activation of ERK1/2, JNK and PI

128 cells show normal magnitude and kinetics of chemoattractant-induced activation of phosphoinositide 3

129 atases and found that activated PTPRG blocks chemoattractant-induced beta2 integrin activation.

130 distinct consequences for BCR signaling and chemoattractant-induced cell mobility.

131 lmitoylation avert its inhibitory effects on chemoattractant-induced cell motility.

132 t-term exposure to JWH-133 potently enhanced chemoattractant-induced eosinophil shape change, chemota

133 receptors are involved in the inhibition of chemoattractant-induced migration of macrophages by niac

134 a role for leukotriene B4 (LTB4 ), a potent chemoattractant involved in the inflammatory response, b

135 a role for leukotriene B4 (LTB4 ), a potent chemoattractant involved in the inflammatory response.

136 it is masked by feedback and redundancy when chemoattractant is used as the input, highlighting the v

137 The polarization of leukocytes toward chemoattractants is essential for the directed migration

138 Proinflammatory cytokines, keratinocyte chemoattractant (KC), and interleukin 6 (IL-6) were meas

139 ration of L. reuteri suppressed keratinocyte chemoattractant (KC), Il22, Il6, Tnf, and IL1alpha gene

140 y F-actin at the side of the cell facing the chemoattractant, leading to directed pseudopod extension

141 Here we demonstrate that the lipid chemoattractant leukotriene B4 (LTB4) was efficacious at

142 mechanism is robust against fluctuations of chemoattractant levels and expression patterns and expla

143 ta and IL-8; abolished chemotaxis to several chemoattractants like chemerin, fMLF, and MCP-1; and dou

144 In a shallow gradient of chemoattractant, local Ras activation triggers full exci

145 In the presence of the chemoattractant, longitudinal dispersion of PpG7 increas

146 increase in plasma levels of the neutrophil chemoattractant macrophage inflammatory protein-2 (MIP-2

147 of neutrophils, cytokine-induced neutrophil chemoattractant, matrix metalloproteinase 9, TNF-alpha,

148 es plus elevated TNFalpha and the macrophage chemoattractant MCP-1 in lung bronchoalveolar lavage flu

149 t GflB is an essential upstream regulator of chemoattractant-mediated cell polarity and cytoskeletal

150 ocyte is able to internalize particles via a chemoattractant-mediated engulfment process.

151 Chemoattractant-mediated recruitment of hematopoietic ce

152 conditions, individual Dictyostelium secrete chemoattractants, migrate, and aggregate.

153 atory cytokines (IL-6, IL-1beta), neutrophil chemoattractants (MIP-2, KC), neutrophil infiltration (M

154 these transients are positively regulated by chemoattractant molecules such as Netrin-1.

155 neutrophils, signal relay toward the primary chemoattractant N--formylmethionyl-leucyl-phenylalanine

156 We also demonstrate that the chemoattractant Netrin-1 elicits increases in the freque

157 hat E. coli cells respond to the gradient of chemoattractant not only by biasing their own random-wal

158 ted neutrophilia and induction of neutrophil chemoattractants over the background of cigarette smoke,

159 y role for LTA4H in degrading the neutrophil chemoattractant Pro-Gly-Pro (PGP) and rationalized that

160 utic antiviral T cells reliant on restricted chemoattractant production and interactions with apoptos

161 the epidermis than controls, whereas neither chemoattractant production in the epidermis nor macropha

162 Plasma leakage and keratinocyte chemoattractant production in the tibiotarsal joint, but

163 T mice, airway neutrophilia and keratinocyte chemoattractant production levels were higher in CysLTr1

164 Our analyses also suggest that the overall chemoattractant profile in the egg chamber is likely to

165 a pathway where the matrikine and neutrophil chemoattractant proline-glycine-proline (PGP) could be d

166 ed strong correlations with AHR and monocyte chemoattractant protein (MCP)-1 with asthma severity and

167 AM-1, IL-6, ICAM-1, E-selectin, and monocyte chemoattractant protein (MCP)-1.

168 D163) and soluble CD14 (sCD14), and monocyte chemoattractant protein 1 (CCL2) with subclinical athero

169 colony-stimulating factor (G-CSF), monocyte chemoattractant protein 1 (MCP-1), macrophage inflammato

170 gamma-inducible protein 10 (IP-10), monocyte chemoattractant protein 1 (MCP-1), macrophage inflammato

171 and inflammatory mediators such as monocyte chemoattractant protein 1 (MCP-1), TNF-alpha, and IL-6 a

172 ia increased expression of IL-6 and monocyte chemoattractant protein 1 (MCP-1).

173 okines (interleukin-6 [IL-6], IL-8, monocyte chemoattractant protein 1 [MCP-1], and IL-1beta) than do

174 IL-2, and IL-12 and the chemokines monocyte chemoattractant protein 1 and keratinocyte-derived chemo

175 nterferon-inducible protein 10, and monocyte chemoattractant protein 1 concentrations, whereas infarc

176 ted macrophages promoted IL-6 and macrophage chemoattractant protein 1 expression in primary human ad

177 of tumor necrosis factor-alpha and monocyte chemoattractant protein 1 in lumbar spinal cord of pacli

178 strongly correlated with increased monocyte chemoattractant protein 1 levels (r = 0.396, P = .0002)

179 -4, IL-5, IL-13, eotaxin, IL-8, and monocyte chemoattractant protein 1 production without affecting I

180 nflammation (tumor necrosis factor, monocyte chemoattractant protein 1, and chemokine [C-X-C motif] l

181 r were significantly reduced, while monocyte chemoattractant protein 1, macrophage inflammatory prote

182 y, higher levels of interleukin 22, monocyte chemoattractant protein 1, TNF-alpha, and IP-10 were obs

183 mouse melanoma cells in HDAC3- and monocyte chemoattractant protein 1-(MCP1)-dependent manner.

184 f proinflammatory interleukin 6 and monocyte chemoattractant protein 1.

185 [IFN-gamma], and IL-6), chemokines (monocyte chemoattractant protein 1/CCL-2, macrophage inflammatory

186 mine, cytokines, and the chemokines monocyte chemoattractant protein 1/CCL2, macrophage inflammatory

187 s (glial fibrillary acidic protein, monocyte chemoattractant protein 1/chemokine (C-C motif) ligand 2

188 rillary acidic protein (p = 0.002), monocyte chemoattractant protein 1/chemokine (C-C motif) ligand 2

189 served, certain chemokines (RANTES, monocyte chemoattractant protein 1[MCP-1], and IP-10) were increa

190 d proinflammatory cytokines (MCP-1 [monocyte chemoattractant protein 1], MIP-1alpha/beta [macrophage

191 The respective ligands, monocyte chemoattractant protein and C-C motif ligand 19, were bo

192 gnaling increased the expression of monocyte chemoattractant protein MCP-1, which in peripheral blood

193 inflammatory biomarkers, including monocyte chemoattractant protein-1 (adjusted OR 9.0 [95% CI 1.0-8

194 of 22.8 nM but was inactive against monocyte chemoattractant protein-1 (CCL2)-mediated calcium flux o

195 alpha-induced inflammatory factors, monocyte chemoattractant protein-1 (MCP-1) and interleukin-8 (IL-

196 sed levels of inflammatory cytokine monocyte chemoattractant protein-1 (MCP-1) and MCP-1 induced prot

197 ne impaired macrophage migration to monocyte chemoattractant protein-1 (MCP-1) as well as IL-17A, whi

198 These cells produced monocyte chemoattractant protein-1 (MCP-1) upon PIM treatment, an

199 reviously shown that the chemokine, monocyte chemoattractant protein-1 (MCP-1), is a mediator of PTH'

200 eract with the oligomeric chemokine Monocyte Chemoattractant Protein-1 (MCP-1)/CCL2 with different bi

201 ges showed reduced migration toward monocyte chemoattractant protein-1 and transmigration through col

202 C motif) ligand 5 and expression of monocyte chemoattractant protein-1 and vascular cell adhesion mol

203 -kappaB nuclear translocation and macrophage chemoattractant protein-1 and VCAM-1 levels in insulin-r

204 and two neuroinflammatory markers (monocyte chemoattractant protein-1 and YKL-40) were measured in C

205 e, markedly augmented the levels of monocyte chemoattractant protein-1 bound to RBCs, which in turn s

206 or-alpha, IL-1beta, IL-6, IL-8, and monocyte chemoattractant protein-1 by co-cultured dendritic cells

207 cular cell adhesion molecule -1 and monocyte chemoattractant protein-1 expressions.

208 limits neutrophils recruitment and monocyte chemoattractant protein-1 production, thus reducing clas

209 toll-like receptor 9), IFNG, MCP-1 (monocyte chemoattractant protein-1) and GM-CSF genes, and that th

210 ncreased renal expression of MCP-1 (monocyte chemoattractant protein-1) and VLA-4 (very-late antigen-

211 okines tumor necrosis factor-alpha, monocyte chemoattractant protein-1, and macrophage inflammatory p

212 mmatory mediators interleukin-6 and monocyte chemoattractant protein-1, fibroblast growth factor-2, a

213 drogenase, as well as expression of monocyte chemoattractant protein-1, IL-6, IL-1beta, and insulin-l

214 stimulation of Hmox1(+/+) SCs with monocyte chemoattractant protein-1, IL-6, IL-1beta, and is associ

215 tory response through alteration of monocyte chemoattractant protein-1, interleukin-1beta, and interl

216 Upregulation of monocyte chemoattractant protein-1, macrophage inflammatory prote

217 gamma inducible protein-10 [IP-10], monocyte chemoattractant protein-1, macrophage inflammatory prote

218 e 9, metalloproteinase inhibitor 1, monocyte chemoattractant protein-1, P-selectin, fibrinogen, recep

219 ded higher levels of interleukin-8, monocyte chemoattractant protein-1, resistin, soluble interleukin

220 phospholipase A2 mass and activity, monocyte chemoattractant protein-1, soluble endothelial cell adhe

221 nterleukin (IL)-1beta, IL-6, IL-10, monocyte chemoattractant protein-1, tumor necrosis factor-alpha,

222 llular cell adhesion molecule-1 and monocyte chemoattractant protein-1, were also determined.

223 In vitro, IL-6 markedly increased monocyte chemoattractant protein-1-driven monocyte-to-myeloid fib

224 llular cell adhesion molecule-1 and monocyte chemoattractant protein-1.

225 factor-beta, interferon-gamma, and monocyte chemoattractant protein-1.

226 ctor-alpha) and chemokines (such as monocyte chemoattractant protein-1/ chemokine (C-C motif) ligand

227 C-X-C motif chemokine ligand 8, and monocyte chemoattractant protein-1/chemokine ligand 2 in the MSC

228 otif chemokine ligand 8 P=0.04, and monocyte chemoattractant protein-1/chemokine ligand 2 P=0.01).

229 ental context entails silenced expression of chemoattractant proteins (chemokines), thereby preventin

230 s conclusively demonstrate that CB2 is not a chemoattractant receptor for murine macrophages.

231 The orphan chemoattractant receptor GPR15 mediates regulatory T cel

232 However, the ability of CB2 to act as a chemoattractant receptor in macrophages remains largely

233 ormyl peptide receptor 2 (FPR2), a classical chemoattractant receptor of G-protein-coupled receptors,

234 Formyl peptide receptor 2 (FPR2) is a chemoattractant receptor that recognizes proinflammatory

235 GPR15 is the chemoattractant receptor that regulates T-cell migration

236 oid receptors (DPs) DP1 and DP2 (also called chemoattractant receptor-homologous molecule expressed o

237 peT(H)2 cells were identified as chemoattractant receptor-homologous molecule expressed o

238 hymic stromal lymphopoietin, as well as oral chemoattractant receptor-homologous molecule expressed o

239 of CD203c(bright), CD63(+), and CD107a(+) on chemoattractant receptor-homologous molecule expressed o

240 D prostanoid receptor 2 (DP2; also known as chemoattractant receptor-homologous molecule expressed o

241 as tested by using TM30089, an antagonist of chemoattractant receptor-homologous molecule expressed o

242 Dexamethasone inhibited (P = .04) chemoattractant receptor-homologous molecule expressed o

243 roperties of a series of clinically relevant chemoattractant receptor-homologous molecules expressed

244 bitors that suppress inflammation (targeting chemoattractant receptor-homologous molecules expressed

245 or chemotaxis and phagocytosis indicate that chemoattractant receptor-signaling is not essential for

246 ecules such as thymic stromal lymphopoietin, chemoattractant-receptor homologous molecule expressed o

247 Chemoattractant receptors also control leukocyte egress

248 tivation and heterologous desensitization of chemoattractant receptors are involved in the inhibition

249 view recent advances in our understanding of chemoattractant receptors in disease pathogenesis, with

250 G-protein-coupled receptors that function as chemoattractant receptors in innate immune responses.

251 cking, we integrate a number of nonchemokine chemoattractant receptors into our discussion.

252 Leukocyte chemoattractant receptors play key roles in the pathogen

253 he innate immune system express adhesion and chemoattractant receptors that allow them to migrate dir

254 A wide array of chemoattractants, chemoattractant receptors, and adhesion molecules expres

255 S also sustained the release of keratinocyte chemoattractant, recruited polynuclear leukocytes and ma

256 Most chemoattractants rely on activation of the heterotrimeri

257 Production of epithelial chemoattractants required HRV replication.

258 dilator) and 12-hydroxyeicosatetraenoicacid (chemoattractant), respectively, increased after UVR (P <

259 ipheral T cell deficiency, and lacked T cell chemoattractant responses.

260 d peripheral CD4 and CD8 T cells had reduced chemoattractant responses.

261 signals and, unlike other ACKRs, it is not a chemoattractant-scavenging receptor, does not activate b

262 ecludes their capacity to migrate toward the chemoattractant SDF-1.

263 in-coupled receptor (GPCR) that recognizes a chemoattractant secreted by bacteria.

264 ptation of wild-type cells to high levels of chemoattractants sensed by only one of the major chemore

265 nds to optimal growth in the presence of the chemoattractant serine, pointing to a physiological rele

266 rosine phosphatase CD45 positively regulates chemoattractant signaling acting on SFK activity.

267 an essential role for RGS proteins in B cell chemoattractant signaling and for the proper position of

268 STIM1 is known to be involved in the chemoattractant signaling pathway for FPR1 in cell lines

269 oma to colonize the SVZ through secretion of chemoattractant signals toward which glioma cells home.

270 trated by mast cells and expressed mast cell chemoattractants similar to human counterparts.

271 ection more frequently when moving away from chemoattractant sources.

272 d-packed column containing a distribution of chemoattractant sources.

273 The chemoattractant sphingosine 1-phosphate (S1P) guides T c

274 l as decreased alpha5beta1-integrin-mediated chemoattractant-stimulated adhesion.

275 Chemoattractant-stimulated Homer3-knockdown cells also e

276 oughout the membrane and responds to uniform chemoattractant stimulation by transiently localizing to

277 s from an 'off' Ca(2+) response signifying a chemoattractant stimulation decrease and, thereby, a dro

278 ions of the bacterium by applying a stepwise chemoattractant stimulus while it is swimming forward or

279 igration of HPCs to a potent progenitor cell chemoattractant, stromal cell-derived factor 1alpha (CXC

280 s displayed increased in vitro chemotaxis to chemoattractants such as sphingosine-1-phosphate and CXC

281 pancreatic developmental axis constitutes a chemoattractant system essential for generating the hall

282 otif chemokine 13 (CXCL13) is a B lymphocyte chemoattractant that activates CXCR5.

283 extracellular signaling molecule is a strong chemoattractant that attracts distant cells to the food

284 ogen-elicited epithelial-produced neutrophil chemoattractant that directs transepithelial migration i

285 nuclear chromatin protein DEK is a secreted chemoattractant that is abundant in the synovia of patie

286 We determined that lactate is an H. pylori chemoattractant that is sensed via TlpC with a K D = 155

287 s accomplished through a tailored release of chemoattractants that recruit antiviral T cells, but few

288 on, including fibronectin, collagen III, and chemoattractants that were identified via single-cell an

289 Similarly to chemoattractants, the shear flow-induced signal transduc

290 hanges the role of H2O2 from an inflammatory chemoattractant to an activator signal that primes immun

291 o a chemotactic gradient release a secondary chemoattractant to enhance directional migration.

292 ne-dependent tumor suppressor by acting as a chemoattractant to recruit anticancer immune cells expre

293 focused ultrasound (pFUS) upregulates local chemoattractants to enhance homing of intravenously (IV)

294 d that HRV-infected epithelial cells release chemoattractants to recruit fibroblasts that could poten

295 tein-coupled receptor 15 (GPR15) as a T-cell chemoattractant/trafficking receptor for the colon.

296 ction analysis showed that, in CF monocytes, chemoattractant-triggered activation of RhoA and CDC42 R

297 individual cells can efficiently move toward chemoattractants using pili-based "twitching" motility a

298 A natural leukocyte chemoattractant was isolated from bovine serum by an est

299 howed that HMGB1 with reduced cysteines is a chemoattractant, whereas a disulfide bond makes it a pro

300 ygenase product that is a potent granulocyte chemoattractant, which induces the infiltration of eosin