ライフサイエンスコーパス: chemotactic

1 nt alterations were attributed to the strong chemotactic ability of A. baylyi enhancing the affinity

2 infection site because of their unparalleled chemotactic ability, after which they unleash numerous a

3 to dissect with unprecedented resolution the chemotactic accumulation of marine bacteria around indiv

4 es the intrinsic bactericidal and neutrophil chemotactic activities of MNPs to generate a zone of def

5 can activate resting neutrophils and elicit chemotactic activity in a LTB4 receptor-dependent manner

6 receptor, and does not influence neutrophil chemotactic activity of CXCL8 in vitro.

7 After only 6 weeks on a HFD, in vivo chemotactic activity of monocytes was already significan

8 tional domains accounted for most of the pro-chemotactic activity of OPN-FL.

9 ations of the effect of glycosylation on the chemotactic activity of the chemokine (Ser-)CCL1 using h

10 e cVLPs containing GPI-CCL28 showed in-vitro chemotactic activity towards spleen and lung cells expre

11 Reduced neutrophil-like HL-60 cell chemotactic activity was observed in response to infecti

12 espiratory burst, acid phosphatase activity, chemotactic activity, and gene expression of PBL.

13 al fragment (OPN-CTF) did not have intrinsic chemotactic activity, but all potentiated CCL21-induced

14 OPN-CTF also possessed substantial pro-chemotactic activity, which was fully expressed upon thr

15 activity of CXCR4 without knocking down its chemotactic activity.

16 omes, thereby producing fragments with novel chemotactic activity.

17 CXCL1, CXCL8, CCL3, CCL5, and CCL20, potent chemotactic agents for activated leukocytes, and IL-36al

18 had fumigant activity, and 5 acted as stable chemotactic agents to M. incognita.

19 d pronounced defects in macropinocytosis and chemotactic aggregation that were rescued by V-1, but no

20 cer cells and stroma cells in tumors secrete chemotactic agonists that exacerbate invasive behavior,

21 motile than wild-type MEFs, as shown by both chemotactic analysis and wound-healing assays.

22 b-driven movement in Dictyostelium, which is chemotactic and controlled through PI3-kinase.

23 ne-containing trails, which may provide both chemotactic and haptotactic cues for efficient CD8(+) T

24 However, it is unclear how chemotactic and haptotactic pathways integrate with each

25 e complement system and in the production of chemotactic and inflammatory mediators, creating a condi

26 types with distinct adhesive, proliferative, chemotactic and matrix-degrading characteristics and dif

27 These results taken together suggest that chemotactic and mechanical stimuli trigger activation of

28 hich could explain why Pyk2 is important for chemotactic and migratory responses.

29 Furthermore, after migration, the highly chemotactic and non-chemotactic cells were retrieved and

30 ir infectivity status, frequency, as well as chemotactic and phagocytic functions.

31 ular polymers) and downregulated (ribosomal, chemotactic and primary biosynthetic enzymes) proteins i

32 CSCs exhibit marked chemotactic and proliferative responses when cocultured

33 P23 fusion protein significantly reduced the chemotactic and random migration induced by F. alocis Th

34 isplay great proliferative, differentiative, chemotactic, and immune-modulatory properties required t

35 ponder T cell proliferation were examined by chemotactic assays and lymphocyte proliferation assays,

36 Furthermore, we find that the chemotactic assembly of enzymes occurs even under cytoso

37 ibition of MMP-9 abrogated the difference in chemotactic attraction between serum from saline-treated

38 fic immunity and suggest inhibition of these chemotactic axes as a strategy for vitiligo stabilizatio

39 These chemotactic axes could be explored for the refinement of

40 In particular, it was found that chemotactic bacteria exhibited a distinct biased migrati

41 The use of chemotactic bacteria in bioremediation has the potential

42 in the literature to include predictions of chemotactic bacterial migration in response to multiple

43 activities that control the variability of a chemotactic behavior in response to an odor, providing a

44 Our results show a distinct chemotactic behavior of B. subtilis toward a particular

45 y similar to the widely known run-and-tumble chemotactic behavior of Escherichia coli bacteria, where

46 wed altered phagocytosis as a consequence of chemotactic behavior, including enhanced F-actin assembl

47 ing an integrin binding site and releasing a chemotactic C-terminal fragment.

48 crucial for haptotactic but dispensable for chemotactic CCL21 gradient sensing in vitro and confirm

49 signaling in cancer, which are essential for chemotactic cell migration and represent novel opportuni

50 whole-genome expression data and matched PPC chemotactic cell-surface receptors to cognate ligands ex

51 First, chemotactic cells moving up the oxygen gradient form a f

52 ng on the situations, while other non-neural chemotactic cells usually show uni-directional attractio

53 er migration, the highly chemotactic and non-chemotactic cells were retrieved and proved viable for l

54 nocyte (ccl2, ccl7, ccl8, cxcl3, and cxcl10) chemotactic chemokines and ccr1 and ccr5 receptor genes,

55 The model predicts that chemotactic, copiotrophic populations outcompete nonmoti

56 lear phagocytes (MPs) that responds to local chemotactic cues that are conserved among central neuron

57 tes, accumulate in the liver via coordinated chemotactic cues, and differentiate into ferroportin 1 (

58 hat stimulates P2Y2 receptors in response to chemotactic cues, and that P2Y2 receptors promote mTOR s

59 es to sense and respond to weak gradients of chemotactic cues.

60 te that intermediate progenitors release the chemotactic cytokine CXCL12 to promote intracortical int

61 ells, was identified as the most upregulated chemotactic cytokine in patients with newly diagnosed AN

62 8), proinflammatory (IL-6 and IL-1beta), and chemotactic cytokines (G-CSF, CXCL12, CXCL1, and CX3CL1)

63 Chemokines are chemotactic cytokines that control the migratory pattern

64 Chemokines are chemotactic cytokines that direct the traffic of leukocy

65 heir role within the innate immune system as chemotactic cytokines, signaling and recruiting host imm

66 erived dendritic cells exhibited significant chemotactic defects as well as reductions in chemokine-s

67 iction we quantify the directional biases in chemotactic Dictyostelium discoideum cells in a flow cha

68 egulation could lead to heritable control of chemotactic diversity.

69 erratia marcescens bacteria, we quantify the chemotactic drift of a large number of microswimmers tow

70 In addition, we find that their chemotactic drift velocity increases superquadratically

71 tions, we investigated the dependence of the chemotactic drift velocity on attractant concentration i

72 nstitutes the major factor that produces the chemotactic drift.

73 Current techniques used to study chemotactic driven cell invasion and metastasis utilize

74 and Interlukin-1 beta (IL-1beta), to predict chemotactic driven leukocyte migration into and within t

75 esults further suggest an important role for chemotactic-driven aggregation in spreading and survival

76 than the other B cell subsets, suggesting a chemotactic effect of eotaxin on these B cell subsets.

77 ured, 1,25-VitD3-treated arteries elicited a chemotactic effect on angiogenic myeloid cells, which wa

78 sels, and platelet-derived growth factor had chemotactic effect on Sox10(+) stem cells.

79 idney cells induced a significant neutrophil chemotactic effect, and a B1 receptor antagonist blocked

80 elix of CXCL14 had neither antimicrobial nor chemotactic effect.

81 equence in OPN-R was not involved in the pro-chemotactic effect.

82 ell migration, but few links from Galphai to chemotactic effectors are known.

83 ded for actin assembly or activation of core chemotactic effectors such as the Rac GTPase.

84 leavage site, and it demonstrated potent pro-chemotactic effects on CCL21-induced DC migration.

85 ty (of the cell body) was increased, whereas chemotactic efficiency was preserved, when compared with

86 adipose tissue exhibit higher levels of the chemotactic eicosanoid LTB4 in obese high-fat diet (HFD)

87 Hepoxilin A3 (HXA3) is a chemotactic eicosanoid shown to mediate the transepithel

88 at the wound margin and the generation of a chemotactic eicosanoid signal.

89 ry system, we predict the chemical gradients chemotactic Escherichia coli cells typically encounter i

90 s cases are Ig light chain, AA, or leukocyte chemotactic factor 2 amyloidosis, but rare hereditary fo

91 Thus, serum levels of IL-16, a key chemotactic factor for CD4(+) lymphocytes, were reduced

92 ion also reduced the production of the mMDSC chemotactic factor osteopontin by tumor cells.

93 f chemokines and triggered the production of chemotactic factors for macrophages and neutrophils.

94 Although MLO-Y4 cells secrete potent chemotactic factors for osteoclast precursors, CCL7 was

95 yperalgesia produced by BMSCs required their chemotactic factors such as CCL4 and CCR2, the integrati

96 stream to a site of infection is mediated by chemotactic factors that are often host-derived.

97 in reduced expression of numerous macrophage chemotactic factors, including CCL5.

98 n of major inflammatory cytokines, including chemotactic factors.

99 in the mobility of LPA receptor 2 (LPA2) on chemotactic fibroblasts.

100 d extracellular vesicles, which are potently chemotactic for cells of the innate immune system.

101 HRV-conditioned medium was chemotactic for fibroblasts.

102 duced from HRV-infected epithelial cells are chemotactic for fibroblasts.

103 iled to recruit neutrophils directly, it was chemotactic for gamma/delta T cells, and CCL8-responsive

104 tion following injury, molecules known to be chemotactic for HIV-target cells.

105 ter pulsing with a viral Ag; and 4) IL-27 is chemotactic for human DCs.

106 f elastin-derived peptides (EDPs), which are chemotactic for inflammatory cells such as monocytes.

107 bearing vesicles from hepatocytes, which are chemotactic for macrophages.

108 after chemotherapy, where it was selectively chemotactic for MRC1(+) TAMs.

109 pha6beta1-dependent neutrophil extravascular chemotactic function in vivo, effective through GATA-2-d

110 ing a chemokine from properly performing its chemotactic function.

111 e of the conformational dynamics of CheA for chemotactic function.

112 gic rhinitis based on a patient's neutrophil chemotactic function.

113 cancer patients, aberrant overexpression of chemotactic Gbetagamma effectors and recently identified

114 activation of the myeloid cell and phagocyte chemotactic genes and pathways, which we initially obser

115 the induction of antimicrobial peptides and chemotactic genes.

116 the capacity of leukocytes to follow a CXCL1 chemotactic gradient accurately in the interstitium.

117 r and adjacent nontumor tissues identified a chemotactic gradient for recruitment of TAMs and NKRs vi

118 ains how polarity can be maintained when the chemotactic gradient has faded.

119 at filopodia allow the interpretation of the chemotactic gradient in vivo by directing single-cell po

120 odia of pseudopods of invading cells under a chemotactic gradient of the chemokine CXCL12.

121 ss in which cells migrating in response to a chemotactic gradient release a secondary chemoattractant

122 atocyte growth factor (HGF) required for the chemotactic gradient responsible for sustained direction

123 standing of phospholipase C/PKC signaling in chemotactic gradient sensing and can guide the design of

124 vated Schwann cells and generate the initial chemotactic gradient that guides the transmigration of h

125 Under conditions lacking a chemotactic gradient, F. alocis-challenged neutrophils h

126 irectly illustrate the role of adaptation in chemotactic gradient-climbing.

127 n primary human blood monocytes migrating in chemotactic gradients and in various settings.

128 nes CXCL11 and CXCL12 to shape and terminate chemotactic gradients during development and immune resp

129 r which are responsible for invasion, nor if chemotactic gradients exist in real tumours.

130 eptor accessibility and activation, and that chemotactic gradients mediate cellular trafficking to th

131 extracellular matrix (ECM) environments and chemotactic gradients within microfluidic devices.

132 ge-related loss of its ability to migrate up chemotactic gradients, a functional defect that seems ca

133 Neutrophils respond to imposed chemotactic gradients, and migrate in response to Pseudo

134 cell movement and systematically controlled chemotactic gradients, leading to contradictory results

135 blebs, like pseudopods, can be orientated by chemotactic gradients.

136 cient directional extension of pseudopods in chemotactic gradients.

137 trinsic differences in cells responsible for chemotactic heterogeneity, we developed a single-cell mi

138 inant His-tagged trout CK12a (rCK12a) is not chemotactic in vitro but it increases the width of the n

139 become progressively insensitive to CIL in a chemotactic input-dependent manner.

140 ty of our model to quantitatively analyze 3D chemotactic invasion, both globally by tracking the prog

141 SH and the extent to which inhibition of the chemotactic ligand CXCL10 and its cognate receptor CXCR3

142 A library of significantly predicted chemotactic ligand-receptor pairs, as well as downstream

143 eukaryote Dictyostelium discoideum displays chemotactic locomotion in stages of its life cycle.

144 the localized assembly and stability of the chemotactic machinery, resulting in proper cell pole dev

145 chemokine array, indicating the presence of chemotactic mediators.

146 (TGF) beta signalling, which serves to drive chemotactic mesenchymal patterning when reaction-diffusi

147 ted the role of 5-lipoxygenase (5LO) and its chemotactic metabolite leukotriene B4 (LTB4) in KSHV bio

148 from patients with COPD at V1 had increased chemotactic migration in response to CXCL12 but not to C

149 Although the chemotactic migration is weak, computer simulations base

150 ommunication that significantly enhances the chemotactic migration of bacterial populations, a findin

151 Here, we show the chemotactic migration of dye molecules in response to th

152 Thus, chemotactic migration of effector T cells within periphe

153 CL21 acted in a paracrine fashion to mediate chemotactic migration of EMT cells toward lymphatic endo

154 Chemotactic migration of fibroblasts toward growth facto

155 The chemotactic migration of PBMCs was reduced by ANE treatm

156 wn of GMFG in monocytes resulted in impaired chemotactic migration toward formyl-Met-Leu-Phe (fMLP) a

157 ith LPS, display reduced CCR7 expression and chemotactic migration, impaired CD4(+) T cell alloprolif

158 rectly regulate their influx by altering the chemotactic milieu in the islets.

159 Our chemotactic model, calibrated from observed responses of

160 to link stimuli to actin polymerization and chemotactic motility and we distinguish the various mode

161 eurons immediately downstream of ASER encode chemotactic movement decisions.

162 Monocyte velocity, but not chemotactic navigation, was modestly dependent on Rho-RO

163 exposure, we observed directional memory in chemotactic neutrophil-like cells.

164 Leukotriene B4 (LTB4) is secreted by chemotactic neutrophils, forming a secondary gradient th

165 (P=0.003), impaired angiogenic (P=0.02) and chemotactic (P=0.003) response, and reduced CSC-mediated

166 Collectively, this study identified several chemotactic pathways that control the recruitment of leu

167 development and research tools for targeting chemotactic pathways universal to humans and other syste

168 ponses similar to those seen for the natural chemotactic peptide n-formyl-Met-Leu-Phe.

169 We show that buprenorphine reduces the chemotactic phenotype of monocytes.

170 e heterogeneous population sorted based upon chemotactic phenotype.

171 foundational step in designing microfluidic chemotactic platforms for point-of-care diagnostics.

172 10 mg/kg morphine for 3 d displayed reduced chemotactic potential for endothelial and breast cancer

173 trullinated C5a, achieved via lower level of chemotactic potential of the modified molecule, and weak

174 lysis of chemotaxis/haptotaxis, we propose a chemotactic precision index that is broadly applicable,

175 ith current chemotaxis models, we found that chemotactic precision-the strength of accumulation of ce

176 Despite the importance of this chemotactic process, the mechanisms controlling the dire

177 In addition to its chemotactic properties, we found that CCL22 activates Tr

178 il extracellular traps and neutralizes LL-37 chemotactic properties.

179 R4 and are Galphai full agonists with robust chemotactic properties.

180 Obvious down-regulation of monocyte chemotactic protein (MCP)-1 in the retina was found afte

181 tumor necrosis factor (TNF)-alpha, monocyte chemotactic protein (MCP)-1, nuclear factor (NF)-kappaB,

182 was associated with upregulation of monocyte chemotactic protein 1 (MCP-1) and inflammatory cytokine

183 it diminished migratory response to monocyte chemotactic protein 1 (MCP-1) and lipopolysaccharide com

184 Interleukin-6 (IL-6) and monocyte chemotactic protein 1 (MCP-1) expression were assessed u

185 F-alpha), interleukin 6 (IL-6), and monocyte chemotactic protein 1 (MCP-1).

186 , interleukin 1beta (IL-1beta), and monocyte chemotactic protein 1 (MCP-1).

187 Monocyte chemotactic protein 1 (MCP1) stimulates phosphorylation

188 Monocyte chemotactic protein 1 (MCP1) stimulates vascular smooth

189 to identify the RhoGEFs involved in monocyte chemotactic protein 1 (MCP1)-induced vascular wall remod

190 ct macrophages via the secretion of monocyte chemotactic protein 1 and promote endothelial cell proli

191 an inducer of hyperalgesic priming (monocyte chemotactic protein 1) is administered at the spinal cor

192 Proinflammatory cytokines macrophage chemotactic protein 1, C-X-C motif ligand 1, and IL-1bet

193 ells results in increased levels of monocyte chemotactic protein 1, IL-8, and IL-6 cytokines, which i

194 Serum macrophage chemotactic protein 1, interleukin-12p40, interferon (IF

195 lastogenesis-such as interleukin 6, monocyte-chemotactic protein 1, receptor activator of nuclear fac

196 rols included interleukin-2 (IL-2), monocyte chemotactic protein 2 (MCP-2), interferon gamma inducibl

197 Notably, ParP also stabilizes chemotactic protein complexes in the absence of ParC, in

198 cell adhesion molecule) and MCP-1 (monocyte chemotactic protein) were reduced in mice receiving perf

199 ating factor (GM-CSF), IL-8, IL-18, monocyte chemotactic protein-1 (CCL2) (MCP-1), tissue plasminogen

200 or activation by its primary ligand monocyte chemotactic protein-1 (MCP-1) is critical for monocyte i

201 sis in lighter skin and report that monocyte chemotactic protein-1 (MCP-1) is secreted by nonpigmente

202 by HPLC/MS/MS, and adiponectin and monocyte chemotactic protein-1 (MCP-1) levels in culture media we

203 S1P and monocyte chemotactic protein-1 (MCP-1) levels were significantly

204 of Toll-like receptor 4 (TLR4) and monocyte chemotactic protein-1 (MCP-1) that colocalize in neurons

205 Lung function, asthma control, and monocyte chemotactic protein-1 (MCP-1) were identified as the mos

206 Inhibition of monocyte chemotactic protein-1 (MCP-1) with the Spiegelmer emapti

207 Lower levels of interleukin-6, monocyte chemotactic protein-1 (MCP-1), and soluble CD40 ligand w

208 which was correlated with greater macrophage chemotactic protein-1 and hypoxia-inducible factor 1alph

209 sponse to proatherogenic cytokines (monocyte chemotactic protein-1 and macrophage colony-stimulating

210 ectly recruit MM cells through both monocyte chemotactic protein-1 and stromal cell-derived factor-1a

211 he secretion of TNFalpha, IL-8, and monocyte chemotactic protein-1 and the formation of PAI-1/tissue

212 r levels of the chemokines IL-8 and monocyte chemotactic protein-1 compared with mothers of GP contro

213 ges, we showed that mCAT suppressed monocyte chemotactic protein-1 expression by decreasing the activ

214 rowth differentiation factor-15 and monocyte chemotactic protein-1 in a murine macrophage cell line a

215 en by inducible protein-10, whereas monocyte chemotactic protein-1 was central in non-spinal cord inj

216 chemokines (HMGB1, TNFalpha, IL-8, monocyte chemotactic protein-1), and formation of PAI-1/tissue pl

217 rmal T cell expressed and secreted, monocyte chemotactic protein-1, and vascular endothelial growth f

218 d circulating TGF-beta1, TGF-beta2, monocyte chemotactic protein-1, C-reactive protein, intercellular

219 concentrations of proinflammatory (monocyte chemotactic protein-1, interleukin [IL]-8, IL-6, Fractal

220 lysaccharide-induced CXC chemokine, monocyte chemotactic protein-1, macrophage inflammatory protein-2

221 kin-6, tumor necrosis factor-alpha, monocyte chemotactic protein-1, P-selectin, and E-selectin in DBD

222 chemokine (C-C motif) ligand 5, and monocyte chemotactic protein-1, when cocultured with trophoblasts

223 dase (NOX) 2, NOX4, E-selectin, and monocyte chemotactic protein-1.

224 n into lesions, and lower levels of monocyte chemotactic protein-1.

225 okine ligand 10, interleukin 8, and monocyte chemotactic protein-1/CC chemokine ligand 2.

226 twork suggested that the chemokines monocyte chemotactic protein-1/CCL2 and monokine induced by gamma

227 Plasma levels of chemokines (monocyte chemotactic protein-1/CCL2, inducible protein-10/CXCL10,

228 esulting in decreased expression of monocyte chemotactic protein-1/chemokine (C-C motif) ligand 2 and

229 acterized by increased nasal lavage monocyte chemotactic protein-3, IFN-alpha2, and plasma IL-10 leve

230 Monocyte chemotactic protein-induced protein 1 (MCPIP1) is a zinc

231 In this study we investigate how monocyte chemotactic protein-induced protein 1 (MCPIP1; encoded b

232 MCPIP1 (monocyte chemotactic protein-induced protein 1) has been shown to

233 flamed tissues via interaction with monocyte chemotactic proteins.

234 ChemR23 is a chemotactic receptor expressed by APCs, such as dendriti

235 d heterodimers with CXCR2, a main neutrophil chemotactic receptor.

236 ins and microRNAs, control the expression of chemotactic receptors and molecules important for the fu

237 N-Formyl peptide (fMLF) receptors (FPRs) are chemotactic receptors involved in inflammation.

238 anoma cell lines is capable of affecting the chemotactic response and maturation of monocytes in vitr

239 estion, we developed a theory for describing chemotactic response based on a mathematical model of in

240 oate permease PcaK was shown to modulate the chemotactic response by facilitating the uptake of 4-hyd

241 The magnitude of chemotactic response depends on the structure of the mon

242 Tlp11 is required for the chemotactic response of C. jejuni to galactose, as shown

243 umulation and inflammation but did not alter chemotactic response of macrophages to adipocyte signals

244 eightened expression of CCR6 and a selective chemotactic response to the CCR6 ligand, CCL20.

245 ndicate that this Mcp is responsible for the chemotactic response towards As(III) and is regulated by

246 Unlike for chemotactic response, a long-term increase in swimming/m

247 ocytes and tumor cells to promote a monocyte chemotactic response.

248 Chemotactic responses in bacteria require large, highly

249 uantitatively and simultaneously compare the chemotactic responses of cells towards different chemoki

250 Transwell assays were used to test chemotactic responses of leukotriene C4 synthase-deficie

251 In addition, GPCR-dependent chemotactic responses often involve endosomal traffickin

252 CD38, and CD44, thereby positively affecting chemotactic responses to CXCL12.

253 Mrtf-null HSC/Ps were also defective in chemotactic responses to SDF-1.

254 ted by c-di-GMP is multifactorial, involving chemotactic responses, utilization of alternate substrat

255 terizing a Dictyostelium mutant defective in chemotactic responses, we identified a novel actin-bindi

256 ion in disease may be related to exaggerated chemotactic responses.

257 mic and hypoxic sites results from a lack of chemotactic responsiveness.

258 ir genomic composition, metabolic abilities, chemotactic sensitivity, and swimming speed, this fine-s

259 saccharides, transcriptional regulators, and chemotactic sensors emerge as key determinants for shapi

260 CXCL12 is not a chemotactic signal for endothelial cell migration, but r

261 While autophagy causes the release of ATP, a chemotactic signal for myeloid cells, polyploidization c

262 sters adjacent to the flagella--to which the chemotactic signal is transmitted--facilitates proper ch

263 to gradients, thereby provides insight into chemotactic signal relay in neutrophils during inflammat

264 re necessary for metallothionein II-mediated chemotactic signal transduction and that they may form p

265 blebbing independently of much of the known chemotactic signal transduction machinery, but involving

266 t activation of all tested components of the chemotactic signal transduction network, as well as acti

267 In contrast, we previously found that chemotactic signaling arrays in polarly flagellated vibr

268 roteins organize into large, highly ordered, chemotactic signaling arrays, which in Vibrio species ar

269 ost retina and an absence of data describing chemotactic signaling guiding migration of transplanted

270 To elucidate chemotactic signaling guiding transplanted cell migratio

271 aromatic compounds and initiates downstream chemotactic signaling in addition to its ability to trig

272 uses through the tissue to directly regulate chemotactic signaling in these cells.

273 define the portion or portions of eukaryotic chemotactic signaling networks that generate adaptation

274 capturing and preventing the dissociation of chemotactic signaling protein (CheA).

275 he extensive amplification characteristic of chemotactic signaling.

276 tered receptors involved in amplification of chemotactic signals are also necessary to produce the ob

277 ey play important functions in processing of chemotactic signals.

278 acellular matrix (ECM) fibers in response to chemotactic signals.

279 crucial readout of how the cluster processes chemotactic signals; both amplification and adaptation w

280 maintenance of immune responses, we examined chemotactic signatures in cultured vitiligo melanocytes

281 Such bio-hybrid microswimmers with chemotactic steering capability may find future applicat

282 attractant-evoked Ca(2+) influx and controls chemotactic steering; a concomitant alkalization serves

283 Th cells show an impaired response to chemotactic stimuli both in humans and in the pathogenic

284 In response to shallow gradients of chemotactic stimuli recognized by G protein-coupled rece

285 uses impairment of lymphocytes to respond to chemotactic stimuli, thus preventing their trafficking f

286 ell as the release of NETs, lactoferrin, and chemotactic stimuli.

287 y in PMN both at rest and in the presence of chemotactic stimuli.

288 sequently, bacteria have evolved a number of chemotactic strategies that consist of sequences of stra

289 We investigate bacterial chemotactic strategies using run-tumble and run-reverse-

290 ystemic release of biochemical mediators and chemotactic substances.

291 Such ChemR23-expressing M1 macrophages are chemotactic to chemerin, whereas M2 macrophages not expr

292 Blebbing cells are strongly chemotactic to cyclic-AMP, producing nearly all of their

293 mL pulse of Pseudomonas putida G7, which is chemotactic to naphthalene, and Pseudomonas putida G7 Y1

294 This preferential, vectorial migration was chemotactic toward many different chemoattractants and d

295 ssay, both wild-type and the fucP mutant are chemotactic towards fucose.

296 Recently, the chemotactic tripeptide Pro-Gly-Pro was identified as an

297 ptidase activity cleaves and inactivates the chemotactic tripeptide Pro-Gly-Pro.

298 In this study, to model 3D chemotactic tumor-stroma invasion in vitro, we developed

299 echanisms that control the efficiency of the chemotactic up-gradient motion.

300 al, anti-protist, insecticidal, spermicidal, chemotactic, wound healing, antioxidant and protease inh