ライフサイエンスコーパス: chemoattractant

1 ellular migration, and can function as a PMN chemoattractant.

2 tility at a behavioral level by serving as a chemoattractant.

3 rogenitors in response to epithelium-derived chemoattractant.

4 mmatory mediators, including CCL20, a T-cell chemoattractant.

5 rientate poorly over broad dynamic ranges of chemoattractant.

6 d do not adapt to sustained stimulation with chemoattractant.

7 onally migrate over a large dynamic range of chemoattractant.

8 across intestinal epithelia in response to a chemoattractant.

9 cent FAs and protrusion orientation toward a chemoattractant.

10 ronments that contain wide-ranging levels of chemoattractant.

11 elative success animals have in reaching the chemoattractant.

12 FRC, and release CXCL1 protein, a neutrophil chemoattractant.

13 ement in the presence and absence of the EGF chemoattractant.

14 l, a previously undescribed bacterial-driven chemoattractant.

15 e cells' specific sensitivities to different chemoattractants.

16 sensitivity to multiple bacterially-secreted chemoattractants.

17 period that is shared with that generated by chemoattractants.

18 iral species and test their effectiveness as chemoattractants.

19 subunits and the lipid PIP(3) in response to chemoattractants.

20 sion and reduced cytokine-induced neutrophil chemoattractant 1 and interleukina-10 serum levels.

21 crophage colony-stimulating factor, monocyte chemoattractant 1, macrophage inflammatory protein 1alph

22 (TNF-alpha) and cytokine-induced neutrophil chemoattractant-1 (CINC-1).

23 ough the detection of an as-yet unidentified chemoattractant.(3-5) Similar H(2)O(2)-activated signali

24 Low levels of chemoattractants act as aroma-like cues in this process,

25 cial role for this structural determinant in chemoattractant activity.

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

27 al dissolution and autonomous release of the chemoattractant and killing agents result in long-range

28 kDa N-terminal Slit2 fragment (Slit2-N) is a chemoattractant and the ~110-kDa N-terminal Slit2 fragme

29 ping, and destroying pathogens by controlled chemoattractant and therapeutic agent release.

30 e contains a magnesium engine core and inner chemoattractant and therapeutic layers.

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

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

33 blood and tissues appears to be regulated by chemoattractants and chemorepellents.

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

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

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

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

40 This enhances chemoattractant biosynthesis in the growing cluster, whi

41 HOCl acts as a chemoattractant by reversibly oxidizing a conserved cyst

42 well as others, showed that the immune cell chemoattractant C-C motif chemokine ligand 21 (CCL21) is

43 oscope for their migration toward the potent chemoattractants C-X-C-motif ligand 2 (CXCL2) and CXCL8,

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

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

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

47 show using phosphoproteomics that different chemoattractants cause phosphorylation of the same core

48 nd increased migration toward the lymph node chemoattractant CCL19.

49 ibroblasts transiently produced the monocyte chemoattractants CCL2 and CCL7, thereby contributing to

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

51 T cell homing to the BM upregulated the Th17 chemoattractant CCL20, which recruited Th17 cells to the

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

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

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

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

56 ce of Pluronic concentration, gel height and chemoattractant choice to optimize assay performance.

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

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

59 The information from the egg chemoattractant concentration field is decoded into intr

60 ptor density constrains the steepness of the chemoattractant concentration gradient detectable by spe

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

62 DAG/active PKC polarization with respect to chemoattractant concentration while decreasing their who

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

64 and prioritize topographical, adhesive, and chemoattractant cues to choose one path among many.

65 locally elevated plasma levels of the T-cell chemoattractant CXCL-11.

66 of lung neutrophils by administration of the chemoattractant CXCL1 during RSV infection affected dise

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

68 Expression of the neutrophil chemoattractant CXCL1 was up-regulated in primary LSECs

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

70 Further, the chemokine and neutrophil chemoattractant, CXCL1, drove this reverse transendothel

71 ansporters SLC3A2 and SLC1A5, and the T-cell chemoattractants CXCL10, CXCL11, and RANTES.

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

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

74 ells preferentially expressed the neutrophil chemoattractant CXCL5, and blockade of CXCL5 or neutroph

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

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

77 We show that chemoattractant degradation creates steep local gradient

78 Using phosphoproteomics, they identify a chemoattractant-dependent ErkB targeted core set of sign

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

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

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

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

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

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

85 ew study shows how the dynamic alteration of chemoattractant flux by chemotaxing cells provides an ef

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

87 ood and ascites fluid, is both a mitogen and chemoattractant for cancer cells.

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

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

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

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

92 ll infiltration by serving as the ligand and chemoattractant for CXCR3(+) T-helper 1 (Th1) cells.

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

94 ining either the 223Q or the 223K allele was chemoattractant for eosinophils whereas only 223Q result

95 identified amidated PAM product serves as a chemoattractant for mating-type minus gametes but repels

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

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

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

99 C3aR and C5aR expressing MCs but also act as chemoattractants for MCs derived from different anatomic

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

101 oplasmic membranes, (iii) chemotaxis towards chemoattractant formyl Met-Leu-Phe (fMLP) coupled with t

102 d phagocytosis, neutrophils also utilize the chemoattractant GPCR/Gi signaling to mediate phagocytosi

103 This chemoattractant GPCR/Gi signaling works independently of

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

105 Through analyzing different chemoattractant gradient forms, we demonstrate for the f

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

107 ch independently sensing and responding to a chemoattractant gradient.

108 Perturbation of chemoattractant gradients and the increased hydraulic re

109 on is often guided by chemotaxis, but simple chemoattractant gradients between a source and sink cann

110 Chemoattractant gradients frequently guide migrating cel

111 We demonstrate that the slope of the chemoattractant gradients provides the coupling force be

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

113 red for the navigation of immune cells along chemoattractant gradients.

114 re cell movement under the influence of EGF (chemoattractant) gradients.

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

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

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

118 OE) increased the production of neutrophilic chemoattractant IL-8 in the absence or presence of M. pn

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

120 required the presence of at least one major chemoattractant in the medium.

121 bstantial evidence supporting a key role for chemoattractants in directed migration, however, less is

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

123 We observed increased levels of T cell chemoattractants in the BAL supernatant, consistent with

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

125 or CD44, interleukin 6 (IL-6), and other PMN chemoattractants including macrophage inflammatory prote

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

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

130 supercomplex formation is controlled by the chemoattractant-induced phosphorylation of Rho-GDP at S1

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

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

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

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

135 d found evidence that RANTES, another T-cell chemoattractant, is actively suppressed by Chlamydia.

136 ected migration of bacteria in a gradient of chemoattractant, is one of the most well-studied and wel

137 irected movement of cells along gradients of chemoattractants, is among the best-characterized subjec

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 rleukin-1beta [IL-1beta], IL-6, keratinocyte chemoattractant [KC], and IL-10) were measured in nasal

141 the pro-inflammatory cytokine and neutrophil chemoattractant, KC, resulting in reduced cellular infil

142 The dissolved chemoattractant (l-serine) significantly increases the a

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

144 AdA potently inhibited the formation of the chemoattractant leukotriene B(4) (LTB(4)), specifically

145 tment slowed the migration of PMN toward the chemoattractant leukotriene B4, decreased uptake of L. m

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

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

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

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

150 sates both precursor and mature forms of the chemoattractant LURE1(1), respectively blocking its secr

151 n, and promotes secretion of the pollen tube chemoattractant LURE1.2.

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

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

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

155 Chemoattractant-mediated recruitment of hematopoietic ce

156 icant reductions in expression of neutrophil chemoattractants MIP-2alpha and CXCL5 in AAA lesions or

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

158 In the sperm flagellum, a single chemoattractant molecule can trigger a Ca(2+) rise that

159 nses (monocyte and neutrophil activation and chemoattractant molecules) was observed at EoT in biopsy

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

161 the phagocytosis of Escherichia coli and the chemoattractant N-formyl-Met-Leu-Phe (fMLP)-coated beads

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

163 tility buffer that did not contain any major chemoattractants of E. coli, in contradiction to some pr

164 harmacological intervention of the MCP1-CCR2 chemoattractant pathway markedly reduced monocytic infil

165 pstream module triggered by the egg-released chemoattractant peptide, via receptor activation, cGMP s

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

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

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

169 Chemoattractants promote predominantly posterior movemen

170 global knockout of the receptor for monocyte chemoattractant protein (CCR2) prevented excess steatosi

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

172 levels of interleukin (IL)-6, IL-8, monocyte chemoattractant protein (MCP)-1, and osteoprotegerin (OP

173 ry protein (MIP)-1alpha, MIP-1beta, monocyte chemoattractant protein (MCP)-1, interferon gamma-induce

174 -gamma, IL-1RA, IL-6, IL-10, IL-19, monocyte chemoattractant protein (MCP)-1, MCP-2, MCP-3, CXCL9, CX

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

176 terleukin 6 (IL-6), interleukin 18, monocyte chemoattractant protein (MCP-1), autotaxin (ATX), and Ma

177 retion of CRS biomarkers, including monocyte chemoattractant protein 1 (MCP-1), interleukin (IL) 6, a

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

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

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

181 ylated tau, neurofilament light and monocyte chemoattractant protein 1 (MCP-1).

182 ling and promoted the production of monocyte chemoattractant protein 1 (MCP-1).

183 ha (P = .006), IL-1beta (P = .022), monocyte chemoattractant protein 1 (P = .028), RANTES (P = .005),

184 , interferon (IFN)-beta, IFN-gamma, monocyte chemoattractant protein 1 [MCP-1; chemokine (C-C motif)

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

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

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

188 erleukin 1beta, interleukin 10, and monocyte chemoattractant protein 1 in response to ZIKV, although

189 emokine (C-C motif) ligand (CCL) 2 (monocyte chemoattractant protein 1) and CCL3 (macrophage inflamma

190 , interleukin-6, interleukin-8, and monocyte chemoattractant protein 1), suggesting that mesenchymal

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

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

193 roinflammatory cytokines (including monocyte chemoattractant protein 1, tumor necrosis factor alpha,

194 f proinflammatory interleukin 6 and monocyte chemoattractant protein 1.

195 of tumor necrosis factor alpha and monocyte chemoattractant protein 1.

196 1, and C-C motif chemokine ligand 2/monocyte chemoattractant protein 1.

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

198 lar adhesion molecule-1], and MCP1 [monocyte chemoattractant protein 1]), increases inflammatory cell

199 2 (IL4 receptor [IL4R], IL13, CCL13/monocyte chemoattractant protein 4, CCL17/thymus and activation-r

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

201 lated with decreased levels of MCP (monocyte chemoattractant protein)-1 and IL (interleukin)-b1 in mi

202 nflammatory factors IL-1beta, IL-6, monocyte chemoattractant protein, and macrophage inflammatory pro

203 Chemerin, a novel chemoattractant protein, is closely associated with infl

204 CAA: 5.7 +/- 1 pg/mL; P = 0.01) and monocyte chemoattractant protein-1 (BCAA: -0.4% +/- 9%; low-BCAA:

205 SF levels of IL-10 (0.434, p<0.05), monocyte chemoattractant protein-1 (MCP-1) (0.798, p<0.005), tran

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

207 ine profile, defined as serum day 0 monocyte chemoattractant protein-1 (MCP-1) and peak interleukin-7

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

209 h directly stimulates expression of monocyte chemoattractant protein-1 (Mcp-1) by macrophages.

210 receptor 2 (CCR2) with its ligand, monocyte chemoattractant protein-1 (MCP-1) promotes cancer progre

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

212 amma- inducible protein 10 (IP-10), monocyte chemoattractant protein-1 (MCP-1), IFN-gamma, interleuki

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

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

215 if ligand chemokine-1 (CXCL1) and macrophage chemoattractant protein-1 (MCP1) are commonly upregulate

216 Monocyte chemoattractant protein-1 and C-C chemokine receptor 2 w

217 by inflammatory monocytes and serum monocyte chemoattractant protein-1 and interleukin-6 were signifi

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

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

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

221 ator of transcription 3 to increase monocyte chemoattractant protein-1 expression.

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

223 e marrow-derived fibrocytes and the monocyte chemoattractant protein-1 inflammatory pathway have been

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

225 domization suggest a role of MCP-1 (monocyte chemoattractant protein-1) in atherosclerosis and stroke

226 ess, expression of endothelin-1 and monocyte chemoattractant protein-1, and monocyte homing.

227 and immunostaining of IL-1beta and monocyte chemoattractant protein-1, decreased mRNA of inflammator

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

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

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

231 itory polypeptide, insulin, leptin, monocyte chemoattractant protein-1, pancreatic polypeptide, and p

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

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

234 strogliosis, interleukin-1beta, and monocyte chemoattractant protein-1, suggesting a paracrine mechan

235 gnificantly decreased production of monocyte chemoattractant protein-1, tumor necrosis factor alpha,

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

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

238 terleukin-1beta, interleukin-6, and monocyte chemoattractant protein-1.

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

240 ntly, our data demonstrate that the monocyte chemoattractant protein-1/C-C chemokine receptor 2 axis

241 The monocyte chemoattractant protein-1/CCR2 (chemokine receptor 2) ax

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

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

244 ate chemokine ligand CCL7 (formerly monocyte chemoattractant protein-3 (MCP-3)) using chimeras betwee

245 sm that results in release of MCPs (monocyte chemoattractant proteins) and monocyte mobilization.

246 ed by iMP recruitment of macrophages via the chemoattractants RANTES, MIF, CCL2, and CXCL12 and activ

247 stribution of CD4(+) T cells directed by the chemoattractant receptor Ebi2.

248 eosinophils (both resting and activated) and chemoattractant receptor homolog expressed on Th2 cells

249 through 2 GPCRs, d-type prostanoid 1 and the chemoattractant receptor homologous molecule expressed o

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

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

252 T2, the receptor for the cytokine IL-33, and chemoattractant receptor-homologous molecule expressed o

253 The prostaglandin (PG) D(2)-chemoattractant receptor-homologous molecule expressed o

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

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

256 urchin species-specific differences in sperm chemoattractant-receptor characteristics we show that re

257 Signaling from chemoattractant receptors activates the cytoskeleton of

258 Activated chemoattractant receptors also dock G protein-coupled re

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

260 However, chemoattractant receptors may couple to more than one ty

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

262 Ligand-engaged chemoattractant receptors trigger Galpha(i) subunit nucl

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

264 Compared with neutrophil chemoattractants, relatively little is known about neutr

265 female gamete by diffusive molecules, called chemoattractants, released from the egg investments in a

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

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

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

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

270 When urea (an identified chemoattractant sensed by TlpB) was microinjected into t

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

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

273 se is self-organized by neutrophil paracrine chemoattractant signaling (most notably of the inflammat

274 We then show that chemoattractant signaling between Hgf and Met is require

275 that prevents initiation of the feedforward chemoattractant signaling cascade that results in neutro

276 c map development in which the regulation of chemoattractant signaling in space and time guides axon

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

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

279 ection more frequently when moving away from chemoattractant sources.

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

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

282 maging in zebrafish revealed that neutrophil chemoattractant synthesis is triggered by a sustained ca

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

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

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

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

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

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

289 use G-protein-coupled receptors (GPCRs) for chemoattractant to chase bacteria through chemotaxis and

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

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

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

293 is, pollen tubes are guided by cysteine-rich chemoattractants to target the female gametophyte(1,2).

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

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

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

297 ecreted LOX functions as a potent macrophage chemoattractant via activation of the beta1 integrin-PYK

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 (SCS) of LNs abundantly expressed neutrophil chemoattractants, whereas LECs lining the medullary sinu