ライフサイエンスコーパス: chemotactic

1 Bacterial chemotactic ability is a major player in infiltration, a

2 However, other characteristics such as the chemotactic ability of a spermatozoon might influence th

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

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

5 t is robust to population ratio, density and chemotactic ability, and is observed in both laboratory

6 were defined by their energy efficiency and chemotactic ability.

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

8 plain this result and to propose that cells' chemotactic accuracy and persistence are mutually constr

9 in both experiments and simulations that the chemotactic accuracy, but not the persistence or speed,

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

11 that was coupled with reduced phagocytic and chemotactic activity compared to controls.

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

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

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

15 Notably, plant MDLs exert dose-dependent chemotactic activity toward human monocytes and T cells.

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

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

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

19 omes, thereby producing fragments with novel chemotactic activity.

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

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

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

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

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

25 Altogether, these processes create chemotactic and immunomodulatory cues for incoming and r

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

27 ified that LXR activation reduces neutrophil chemotactic and killing abilities in vitro.

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

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

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

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

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 that Strongylocentrotus purpuratus sperm are chemotactic and this response is consistent with frequen

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

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

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

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

39 tant and killing agents result in long-range chemotactic attraction, trapping, and destruction of mot

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

41 These chemotactic axes could be explored for the refinement of

42 ases is mediated primarily via the CCL2-CCR2 chemotactic axis.

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

44 The use of chemotactic bacteria in bioremediation has the potential

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

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

47 e find that S. putrefaciens CN-32 exhibits a chemotactic behavior toward As(V) and diverse electron a

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

49 old nanoswimmers with a positive, macroscale chemotactic behavior.

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

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

52 y consists of 46 protein ligands that induce chemotactic cell migration by activating a family of 23

53 and explores its functional significance on chemotactic cell migration.

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

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

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

57 have not previously been reported to act as chemotactic/chemoattractive agents.

58 We spatially modulated the diffusion/chemotactic coefficients of T cells (to mimic physical b

59 The model predicts that chemotactic, copiotrophic populations outcompete nonmoti

60 Inflammatory responses modified the chemotactic cues along the perivascular homing paths, le

61 ew drug, targeting specific tissues based on chemotactic cues and modulating secretion of instructive

62 may act as context-dependent integrators of chemotactic cues in directional cell migration and may s

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

64 Migration may depend on perception of chemotactic cues, which could stem from co-infecting par

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

66 cells base their directional choices on the chemotactic cues.

67 activation suppresses the transactivation of chemotactic cytokine ligand 2 (CCL2).

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

69 CXCL1) and CC chemokine ligand 2 (CCL2), the chemotactic cytokines for neutrophils and monocytes, res

70 Chemokines are chemotactic cytokines that direct the traffic of leukocy

71 Chemokines, a family of small secreted chemotactic cytokines, and their G protein-coupled seven

72 less inflammation, lower proinflammatory and chemotactic cytokines, less interleukin-17 production, a

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

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

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

76 nstitutes the major factor that produces the chemotactic drift.

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

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

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

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

81 elix of CXCL14 had neither antimicrobial nor chemotactic effect.

82 exchange factor 1 (P-REX1), a key Gbetagamma chemotactic effector, is directly controlled by Rho-acti

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

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

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

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

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

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

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

90 FB103A, S100 proteins like S100A7, S100A12), chemotactic factors for neutrophils (e.g. CXCL5, CXCL8)

91 CXCR2 chemokine receptor agonists and other chemotactic factors produced by tumors, neutrophils, and

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

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

94 a concentrations of polarizing cytokines and chemotactic factors, including interleukin-12p70 (IL-12p

95 n of major inflammatory cytokines, including chemotactic factors.

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

97 HRV-conditioned medium was chemotactic for fibroblasts.

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

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

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

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

102 study, we have demonstrated that CK11 is not chemotactic for unstimulated leukocyte populations from

103 bility to inhibit CCL8, CCL7, CCL2, and CCL3 chemotactic function in vitro We show that local as well

104 ing a chemokine from properly performing its chemotactic function.

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

106 the induction of antimicrobial peptides and chemotactic genes.

107 peptide receptor-1 (FPR1) is a member of the chemotactic GPCR-7TM formyl peptide receptor family, who

108 By augmenting the local chemotactic gradient as well as the antigenic load, this

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

110 lls expressing FliC(N87K) sensed ascending a chemotactic gradient in liquid but did not spread on a s

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

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

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

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

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

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

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

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

119 ceptors (ACKRs), which function to establish chemotactic gradients for directed cell migration.

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

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

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

123 cient directional extension of pseudopods in chemotactic gradients.

124 ct M over distances that exceed the range of chemotactic gradients.

125 enabling formation of dynamic spatiotemporal chemotactic gradients.

126 ly following global directional cues such as chemotactic gradients.

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

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

129 ses the conventional view about arsenic as a chemotactic inhibitor to microbes by revealing the posit

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

131 Chemotactic interactions are ubiquitous in nature and ca

132 e designed with controllable, non-reciprocal chemotactic interactions to generate emergent self-organ

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

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

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

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

137 This chemotactic loop drives collagen remodeling, tumor invas

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

139 creased secretion of neutrophil and monocyte chemotactic mediators in the lungs.

140 chemokine array, indicating the presence of chemotactic mediators.

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

142 rangements that occur during MC secretion or chemotactic migration and identify the underlying mechan

143 diaphanous-related formin 1 (mDia1) inhibits chemotactic migration and its typical actin rearrangemen

144 ith higher CCR6 expression revealed a higher chemotactic migration for CCL20.

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

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

147 Consistent with this in vivo finding, chemotactic migration of cultured macrophages through a

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

149 Thus, chemotactic migration of effector T cells within periphe

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

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

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

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

154 Our chemotactic model, calibrated from observed responses of

155 current study, we demonstrate virus-packaged chemotactic modulation of prey behavior.IMPORTANCE Virus

156 creased levels of inflammatory cytokines and chemotactic molecules that were attenuated by Bay 11-708

157 onizes and limits repair at damage sites via chemotactic motility that requires the TlpB chemorecepto

158 nus gold nanoswimmers display a collectively chemotactic motion along the concentration gradient of a

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

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

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

162 the mechanism of front-rear coordination in chemotactic neutrophils.

163 chemotaxis to arachidonic acid without being chemotactic on its own.

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

165 hils surrounding ruptured spherules, but the chemotactic pathways that draw neutrophils into the infe

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

167 TL and SKF inhibited chemotactic peptide fMLP-induced response linked to TRPV

168 Our results suggest that key aspects of chemotactic performance are inherently limited regardles

169 e the links among these different aspects of chemotactic performance.

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

171 e heterogeneous population sorted based upon chemotactic phenotype.

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

173 ers of our model, cellular proliferation and chemotactic potential of conditioned media.

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

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

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

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

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

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

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

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

182 stromal-derived factor 1 (Sdf1) or monocyte chemotactic protein 1 (Mcp1) enhanced (when silencing Sd

183 Monocyte chemotactic protein 1 (MCP1) stimulates phosphorylation

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

185 hat tumor necrosis factor alpha and monocyte chemotactic protein 1 expression was only elevated in ki

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

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

188 hypoxia-inducible factor 1 (HIF-1), monocyte chemotactic protein 1, transforming growth factor beta 1

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

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

191 45.4 pg/mL; P = .012) and decreased monocyte chemotactic protein-1 (MCP-1) (513.3 pg/mL vs 809.5 pg/m

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

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

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

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

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

197 < .001), interleukin-10 (P = .041), monocyte chemotactic protein-1 (P = .046), placental growth facto

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

199 rence-mediated knockdown assays and monocyte chemotactic protein-1 and intercellular adhesion molecul

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

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

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

203 er plasma sRAGE, interleukin-6, and monocyte chemotactic protein-1 concentrations.

204 products, plasma interleukin-6, and monocyte chemotactic protein-1 were sampled preextracorporeal mem

205 n M2-like phenotype, using MCP-1 (macrophage chemotactic protein-1) and IL-4 (interleukin-4), respect

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

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

208 ntly lower levels of interleukin-6, monocyte chemotactic protein-1, monocyte chemotactic protein-3, a

209 examined, such as IL-6, IL-10, and monocyte chemotactic protein-1, showed no consistent differences.

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

211 dy, we report that immune regulator Monocyte chemotactic protein-1-induced protein 1 (MCPIP1) can red

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

213 -6, monocyte chemotactic protein-1, monocyte chemotactic protein-3, and granulocyte-colony stimulatin

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

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

216 -dependent Rac exchange factor 1 (P-REX1), a chemotactic Rac guanine exchange factor (RacGEF).

217 t high expression of the monocyte-macrophage chemotactic receptor CCR2 is associated with severe COVI

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

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

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

221 ely suggest an added mechanistic pathway for chemotactic regulation.

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

223 n defect and a strongly reduced motility and chemotactic response by MKL1-deficient neutrophils.

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

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

226 dle, flow-free microfluidic chip to test the chemotactic response of spermatozoa made out of a hybrid

227 ls (a marker of LXR activation) and impaired chemotactic response toward CXCL8 compared with cells fr

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

229 s undergoing chemotaxis exhibited a stronger chemotactic response when exposed to lower average chemo

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

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

232 white blood cells showed a severely impaired chemotactic response.

233 Chemotactic responses in bacteria require large, highly

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

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

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

237 g di-iron protein (ODP) acts as a sensor for chemotactic responses to both iron and oxygen in the hum

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

239 ver, Fpr2/3(-/-) monocytes were defective in chemotactic responses to the chemokine CC chemokine liga

240 Unlike most chemotactic responses, ErkB phosphorylations are persist

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

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

243 ferences between ligands may lead to diverse chemotactic responses.

244 stance (barotaxis), in some cases overriding chemotactic responses.

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

246 del, reveal that strong heterogeneity in the chemotactic sensitivity coefficient exists even within c

247 in the T-maze originates primarily from the chemotactic sensitivity coefficient, arising from a dist

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

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

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

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

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

253 Moreover, we reveal that the chemotactic signal transduction pathway is conserved in

254 Newly arriving CTLs augment the chemotactic signal, further accelerating mass recruitmen

255 Ca(2+) transient elevations, and served as a chemotactic signal.

256 by mediators of the innate immune system and chemotactic signaling (interleukin-1 receptor antagonist

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

258 pectedly, phosphorylation is not promoted by chemotactic signaling but is greatly stimulated by cell:

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

260 To elucidate chemotactic signaling guiding transplanted cell migratio

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

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

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

264 antly, functional antiviral and proleukocyte chemotactic signaling pathways were significantly upregu

265 bone marrow after SCI is linked to aberrant chemotactic signaling that can be reversed by post-injur

266 integrates dynamic autophosphorylation with chemotactic signaling through G-protein-coupled receptor

267 by mediators of the innate immune system and chemotactic signaling was associated with both tuberculo

268 Here we show how chemotactic signalling between microscale oil droplets o

269 cells co-opt innate RNA sensing to induce a chemotactic signalling pathway in endothelium that drive

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

271 ng from fibroblast remodelling activities or chemotactic signals are neither required nor sufficient

272 echanisms by which the LTB4-BLT1 axis relays chemotactic signals during intravascular neutrophil resp

273 The eicosanoid leukotriene B4 (LTB4) relays chemotactic signals to direct neutrophil migration to in

274 ey play important functions in processing of chemotactic signals.

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

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

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

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

279 ung changes benefited in vivo responses, two chemotactic stimuli (a CXCL1 chemokine and a live Pseudo

280 through complex environments in response to chemotactic stimuli and motivate improved algorithms for

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

282 AK1 knockdown rendered cells unresponsive to chemotactic stimuli present in the stroma, resulting in

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

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

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

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

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

288 Many microorganisms have evolved chemotactic strategies to exploit the microscale heterog

289 ystemic release of biochemical mediators and chemotactic substances.

290 t an imbalance between nutrient efficacy and chemotactic superiority accelerates invasion.

291 Previously it was shown that droplet-based chemotactic systems when interfaced with biological syst

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

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 We model chemotactic transport of bacteria within a leaf tissue i

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