ライフサイエンスコーパス: chemotaxis

1 zed cell motility under confinement and cell chemotaxis.

2 mated, quantitative assessment of neutrophil chemotaxis.

3 e diffusion, which may facilitate neutrophil chemotaxis.

4 ulation of IL-8 and epithelial secretome for chemotaxis.

5 aviors such as fission, fusion, movement and chemotaxis.

6 y the chemokine receptor CXCR4, facilitating chemotaxis.

7 effects of specific modulators of neutrophil chemotaxis.

8 ole for ErkB and its substrates in directing chemotaxis.

9 bition of filopodia dynamics and cancer cell chemotaxis.

10 t of SP-A genetic variation on apoptosis and chemotaxis.

11 vates the cytoskeleton of crawling cells for chemotaxis.

12 leak, bronchoconstriction, and effector cell chemotaxis.

13 required by planktonic bacteria for S signal chemotaxis.

14 taxis and solute-phospholipid-based negative chemotaxis.

15 sion of genes involved in murine immune cell chemotaxis.

16 tastatic microenvironment tissues and models chemotaxis.

17 om the egg investments in a process known as chemotaxis.

18 l migration or interstitial chemokinesis and chemotaxis.

19 sing a simple agent-based model of bacterial chemotaxis.

20 n post-exposure through associative learning chemotaxis.

21 s data define a broad panel of regulators of chemotaxis.

22 igate the components necessary for H. pylori chemotaxis.

23 lated genes involving bacterial motility and chemotaxis.

24 -bacterial coinfection as well as neutrophil chemotaxis.

25 fast and high-throughput screening bacterial chemotaxis.

26 before initiation of the CXCL12/SDF1-guided chemotaxis.

27 tor between receptor and cytoskeleton during chemotaxis.

28 bility of keratinocytes to induce neutrophil chemotaxis.

29 ses endothelial cell activation and monocyte chemotaxis.

30 CL8 to stimulate neutrophil shape change and chemotaxis.

31 ial organization using swimming motility and chemotaxis.

32 al responses that include Akt activation and chemotaxis.

33 acteria use the flagellum for locomotion and chemotaxis.

34 reduces CXCR4-mediated activation of FAK and chemotaxis.

35 ributing to complement C5a receptor-mediated chemotaxis.

36 2) activates the SFK Lyn to drive neutrophil chemotaxis.

37 albeit decreased cell velocity and impaired chemotaxis.

38 cellular space and contributes to purinergic chemotaxis.

39 romoting FA growth and cell migration during chemotaxis.

40 is a derivative of K-12 and a wild-type for chemotaxis.

41 on and cell behavior that affect mesenchymal chemotaxis.

42 6-Dox and Cl66-Pac cells enhanced neutrophil chemotaxis.

43 ising as a fundamental requirement for sperm chemotaxis.

44 ape change, integrin (CD11b) expression, and chemotaxis.

45 lycosylation (2 of 2), and normal neutrophil chemotaxis (1 of 1), and bactericidal activity (1 of 1)

46 icylate (MeSA) elicited the highest positive chemotaxis (70-80%), alpha-pinene, limonene and tridecan

47 end of the five components elicited positive chemotaxis (71-88%), whereas individual components elici

48 in systemic neutrophil function (NETosis and chemotaxis), a reduction in systemic neutrophil elastase

49 atic effect of MSCs since inhibition of this chemotaxis abolished increased neutrophil recruitment an

50 on (IL-18 and IL-6), lymphocytic and myeloid chemotaxis and activation (CCL3, CCL4, and CDCP1), and m

51 Regulation of neutrophil chemotaxis and activation plays crucial roles in immunit

52 effectors with executive roles in invasion, chemotaxis and adhesion downstream of the ROCK-LIMK-cofi

53 lpQ of Pseudomonas aeruginosa, thus inducing chemotaxis and biofilm formation.

54 bacteria enables their characteristics like chemotaxis and biomolecule secretion to outperform conve

55 ne surveillance via both facilitating T-cell chemotaxis and CD137L/CD40 induced NF-kappaB/PCAF activa

56 abolished C5a-induced Ca(2+) transients, but chemotaxis and cell spreading were preserved.

57 us might actively contribute to its fate via chemotaxis and change the behavior of an organism indepe

58 athways such as chemokine receptor activity, chemotaxis and cytokine biosynthesis, and angiogenesis a

59 GPP, PPP, and AGEP, converged on neutrophil chemotaxis and diapedesis and cytokines known to drive n

60 Enzyme chemotaxis and EED may be important in biology and could

61 to the site of infection by a combination of chemotaxis and galvanotaxis; after phagocytosis of bacte

62 sor cells of BLS-type DLBCL are attracted by chemotaxis and home to the bone marrow, where the microe

63 ression signatures specific for myeloid cell chemotaxis and homeostasis reappeared in BRAFi-resistant

64 ed to bacterial colonization, proliferation, chemotaxis and invasion, immune-diseases, oxidative stre

65 reatic cancer metastasis, with roles in both chemotaxis and matrix remodeling.

66 ults also showed remarkable up-regulation of chemotaxis and motility associated genes responding to x

67 ily of mostly secreted molecules involved in chemotaxis and other patho/physiological processes.

68 an phagocytes share mechanistic pathways for chemotaxis and phagocytosis; Dictyostelium chemotax towa

69 Besides its application to study chemotaxis and phototaxis, PiVR is a versatile tool desi

70 Firstly, Pf reduced chemotaxis and production of pro-inflammatory ROS, cytok

71 Part of the effects of BVR-A deletion on chemotaxis and RANTES expression were blocked in the pre

72 timulation of the Rac GTPases, which control chemotaxis and ROS.

73 regulator of MC response that coordinates MC chemotaxis and secretion through its actin-nucleating ac

74 ay between enzyme-catalysis-induced positive chemotaxis and solute-phospholipid-based negative chemot

75 or chemoattractant to chase bacteria through chemotaxis and then use phagocytic receptors coupled wit

76 reveals functions for GLR channels in sperm chemotaxis and transcriptional regulation.

77 target due to its involvement in immune cell chemotaxis and vascular integrity.

78 ation in response to gradients of chemicals (chemotaxis) and light (phototaxis).

79 uperoxide production, impaired fMLF-directed chemotaxis, and abnormal macropinocytosis.

80 ron signaling, cell-cell adhesion, leukocyte chemotaxis, and angiogenesis.

81 tion, including genes involved in migration, chemotaxis, and cell adhesion as well as induction of a

82 se, chemokine-mediated signaling, neutrophil chemotaxis, and chemokine activity and distinguished the

83 activity as measured by ERK phosphorylation, chemotaxis, and G(i/o)-mediated cAMP inhibition.

84 and time, automated quantitative analysis of chemotaxis, and high throughput.

85 also suppressed the primary human neutrophil chemotaxis, and interaction with HUVEC.

86 etween just three tasks: efficient swimming, chemotaxis, and low cell construction cost.

87 eutrophil functions, like respiratory burst, chemotaxis, and phagocytosis.

88 severity genes encompassing immune response, chemotaxis, and regulation of macroautophagy.

89 tions about nanoscale energy flow, molecular chemotaxis, and self-powered nanomachines.

90 icles as 'nano-tools' for electron transfer, chemotaxis, and storage units, and (iii) speculated bene

91 chronic inflammation by inducing neutrophil chemotaxis, and the reduction of these microvesicles by

92 sitive regulator of directional migration in chemotaxis, and the underlying mechanism.

93 eukocytes were defective in polarization and chemotaxis, and TIPE2-deficient mice were resistant to l

94 of genes associated with immunosuppression, chemotaxis, and tumor matrix remodeling.

95 orce, extracellular matrix (ECM) production, chemotaxis, and wound healing.

96 outline key principles we have learned about chemotaxis; and 3) to point to the most important outsta

97 key canonical pathways such as phagocytosis, chemotaxis, antigen presentation, and cell-to-cell signa

98 e report an alternative symmetry (P2) of the chemotaxis apparatus that emerges from a strict linear o

99 rdial roles in cell adhesion, migration, and chemotaxis as a mechanism for recruitment of leukocytes

100 g of germ cells in vivo Using a live-imaging chemotaxis assay in a 3D matrix, we show that a shallow

101 Root exudate chemotaxis assays demonstrate that knockdown of each tra

102 a combination of theory, simulations, and 3D chemotaxis assays on single metastatic breast cancer cel

103 Chemotaxis assays revealed that receptor-mediated adapta

104 dy of nanotoxicology, including nanomaterial chemotaxis assays, bioaccumulation and deleterious effec

105 In human immune cell-based chemotaxis assays, we find that CXCL12-stimulated CXCR4

106 nimal with only 302 neurons, using olfactory chemotaxis assays.

107 evosia to sense environmental signals and in chemotaxis at stressed habitats.

108 with tractable applications in development, chemotaxis, bacteria-host interactions, and allorecognit

109 b1/crh-1-null animals show defects in innate chemotaxis behavior.

110 CRH-1 while being dispensable for its innate chemotaxis behavior.

111 In turn, this inhibits tumor chemotaxis, blocks cell invasion, and prevents metastati

112 Migration is often guided by chemotaxis, but simple chemoattractant gradients between

113 bditis elegans lacking ADARs exhibit reduced chemotaxis, but the targets responsible for this phenoty

114 udies further suggest that the regulation of chemotaxis by c-di-GMP through MapZ orthologs/homologs i

115 how Drosophila adult flies perform negative chemotaxis by modulating their locomotor speed to avoid

116 promoting their barrier function, and (iii) chemotaxis by modulating their polarization and TNF-alph

117 We conclude that MYH9-RD mutations impair MK chemotaxis by multiple mechanisms to disrupt migration t

118 Here we identify an alternative role of chemotaxis by systematically examining the spatiotempora

119 nd Gna13 (Galpha(13)) had essentially normal chemotaxis, Ca(2+) signaling, and cell spreading, except

120 outcomes, and show that aberrant neutrophil chemotaxis can move an otherwise healthy outcome to one

121 transduction pathways that control monocyte chemotaxis can unravel potential targets for preventive

122 These chemotaxis capabilities are mediated in part by PAK1 whi

123 ed increases in CXCL8 (neutrophil/eosinophil chemotaxis), CCL24 (eosinophil recruitment), and CXCL12

124 nts regulate physiological processes such as chemotaxis, cell migration, and adhesion.

125 signaling complex in vitro with TlpD and the chemotaxis (Che) proteins CheW and CheA, enabling quanti

126 m does not transfer phosphoryl groups to the chemotaxis (Che) system.

127 -like domain protein, alpha/beta hydrolase), chemotaxis (cheB, luxR) and stress response (phoQ, uspA,

128 Notably, relative fitness benefit of chemotaxis could be observed not only in the presence of

129 APOE, and inhibits SDF-1alpha/CXCR4-mediated chemotaxis, culminating in an impaired response to beta-

130 Through an analysis of bacterial chemotaxis data, we highlight the JDD's ability to extra

131 ast, mutants lacking motility (DeltamotB) or chemotaxis (DeltacheY) did not accumulate at the injury

132 rplay between metabolite excretion and their chemotaxis-dependent reutilization is likely to play an

133 ose and radiation treatment followed by PBMC chemotaxis determination via fluorescence microscopy.

134 Fibroblast chemotaxis directed by a gradient of platelet-derived gr

135 Chemotaxis, directed motion in response to external grad

136 hed arrest, spreading, uropod formation, and chemotaxis due to defective actin polymerization and int

137 In bacterial chemotaxis, each chemoreceptor has multiple methylation

138 Cells undergoing chemotaxis exhibited a stronger chemotactic response whe

139 A chemotaxis experiment with 1 muM progesterone was perfor

140 asophil responses to IL-31 were assessed for chemotaxis, externalization of CD63 and CD203c as well a

141 rallel, CORM-401-dependent modulation of PMN chemotaxis, F-actin expression/distribution, and actin-r

142 In addition to the previously reported core chemotaxis gene cluster, we identify several other conse

143 tern recognition receptor, cell adhesion, or chemotaxis genes in macrophages.

144 Chemotaxis has been primarily studied as an average char

145 ol of directionality based on chemical cues (chemotaxis) has been difficult to achieve.

146 The mechanisms of bacterial chemotaxis have been extensively studied for several dec

147 Previous models of bacterial chemotaxis have suggested that the movement of migrating

148 Controlling the extent and direction of chemotaxis holds considerable potential for designing ce

149 ion (IL-6, IFN-gamma, IP-10, IL-1RA, IL-10), chemotaxis (IL-8), systemic and vascular inflammation (C

150 ort showed upregulation of genes involved in chemotaxis, IL (interleukin)-6, and NF-kappaB (nuclear f

151 ry model where cells search for resources by chemotaxis in a shallow, noisy gradient.

152 Our model simulates chemokinesis and chemotaxis in a variety of chemical and mechanical envir

153 bit keratinocyte migration and IGF-1-induced chemotaxis in association with inhibition of IGF1R phosp

154 biochemical link between oxygen sensing and chemotaxis in diverse prokaryotes, including anaerobes o

155 ilson Award and be recognized for my work on chemotaxis in eukaryotic cells.

156 e exported by ABC transporters that enhances chemotaxis in GSCs migrating towards low concentrations

157 Likewise, in vivo chemotaxis in NOD-scid-Il2rg(-/-) mice was reduced in IL

158 Chemotaxis in nutrient-replete conditions promotes the e

159 We describe neutrophil chemotaxis in response to a combination of a defined gra

160 s an important role in regulating macrophage chemotaxis in response to C5a via modulation of C5aR1 ex

161 uding chemokines (RANTES, IP-10), as well as chemotaxis in response to LPS and C5a in bone marrow-der

162 et mRNAs to the cell rear perturbs efficient chemotaxis in shallow cAMP gradients, without affecting

163 ty of the parent NPD1, inhibiting neutrophil chemotaxis in vitro and neutrophil tissue infiltration i

164 flammation yet was less potent at inhibiting chemotaxis in vitro with an IC50 of 21 nm Furthermore, w

165 CD44 mediates C1q induced hNSC signaling and chemotaxis in vitro, and hNSC migration and functional r

166 associated with poor prognosis and increased chemotaxis; in B-cell acute lymphoblastic leukemia, high

167 econds to minutes) by phagocytes and induces chemotaxis, increases cytokine/chemokine production, and

168 osinophil clearance from lung tissue through chemotaxis, independent of SP-A2 Q223K, and by inducing

169 ndings have direct impacts for the fields of chemotaxis, innate immunity, inflammation, carcinogenesi

170 ction of these two proteins was critical for chemotaxis, invasion, and gelatin degradation by breast

171 MCP-1-induced monocyte chemotaxis is a crucial event in inflammation and athero

172 How signals coordinate and direct chemotaxis is an issue that is actively investigated.

173 th theory and simulation, we show collective chemotaxis is limited by cell-to-cell variation in signa

174 Chemotaxis is often characterized by the accuracy, persi

175 of mTOR inhibitors (mTOR-I) that can inhibit chemotaxis just enough to facilitate such competition.

176 s two binding partners, the P2 domain of the chemotaxis kinase, CheA, or the 16-residue "target regio

177 donics and offer molecular insight into salt chemotaxis learning.

178 , enabling quantitative assays for potential chemotaxis ligands.

179 ause archaea share similar cell division and chemotaxis machinery with other domains of life, our gho

180 A. brasilense mutant derivatives lacking the chemotaxis master histidine kinase, CheA4, or the centra

181 ve migration is achieved with thresholds for chemotaxis matching those of polarization in the reactio

182 s also allowed S. aureus to evade neutrophil chemotaxis, mediated by the reduction in bacterial membr

183 cation in more complex situations, including chemotaxis, migration through complex 3D matrices, and c

184 A chemotaxis model demonstrated decreased neutrophil recru

185 lular aggregates evolve because they perform chemotaxis more efficiently than single cells.

186 We show here that it exhibits chemotaxis, moving preferentially toward algae embedded

187 ly analyzed swimming trajectories of various chemotaxis mutants of the monotrichous soil bacterium, A

188 hanges in movement, reminiscent of bacterial chemotaxis mutants.

189 ed invadopodia contain receptors involved in chemotaxis, namely GABA receptor and EGFR.

190 erent from that in bulk and lend support for chemotaxis near solid surface.

191 , talin1-deficient DCs exhibited compromised chemotaxis, NFkappaB activation, and proinflammatory cyt

192 ria of the plant cells, as well as motility, chemotaxis, nutrient consumption and communication in th

193 monocytes, migration of dendritic cells, and chemotaxis of antigen-presenting cells pointing to an im

194 factors released from starved cells induced chemotaxis of B cells, macrophages, and neutrophils, sug

195 ory concentration values for eotaxin-induced chemotaxis of blood eosinophils are in the low nanomolar

196 CCL14 induced chemotaxis of both dNK cells and decidual macrophages, w

197 , but not rPrP(c) by itself, cause increased chemotaxis of both uninfected and HIV-infected human mon

198 for screening of molecules that modulate the chemotaxis of different immune cells.

199 Chemotaxis of fibroblasts and other mesenchymal cells is

200 recombinant human Ang-1 induced significant chemotaxis of isolated mouse neutrophils in a Tie2- and

201 UCB35625 induced the chemotaxis of L1.2 cells expressing CCR2 or CCR5.

202 se in expression levels of genes involved in chemotaxis of leukocytes and anti-inflammatory genes suc

203 by 57% (P < 0.05), and it inhibited ex vivo chemotaxis of leukocytes toward PAR2 agonists.

204 Here we show both positive or negative chemotaxis of liposomal protocells.

205 CCL2 is known to promote chemotaxis of M0 or M2 phenotype macrophages to the infl

206 theless, the mutation impaired CCL2-mediated chemotaxis of macrophages and slowed revascularization o

207 nd our results indicate that LRRK2 modulates chemotaxis of microglia and macrophages.

208 for CCR2, CCR2i, which blocks CCR2-mediated chemotaxis of monocytes in a syngeneic mouse T-cell lymp

209 ult, neddylation inactivation exhibits lower chemotaxis of monocytes, thereby decreasing TAMs infiltr

210 tome of ERK3-deficient cells is defective in chemotaxis of neutrophils and monocytes both in vitro an

211 anced IL-1beta-mediated inflammation and the chemotaxis of neutrophils.

212 Moreover, EC1 mutations in CD53 prevent the chemotaxis of pre-B cells toward a chemokine that suppor

213 rations of H2O2 also impede chemokinesis and chemotaxis of previously activated human T cells to CXCL

214 decreased TNF-alpha secretion, and enhanced chemotaxis of RAW264.7 cells toward CCL2 MPs.

215 are exuded by germinating seeds, we assayed chemotaxis of S. meliloti towards betonicine, choline, g

216 ibitor to microbes by revealing the positive chemotaxis of Shewanella to As(V).

217 d cells and the droplet and also support the chemotaxis of the droplet.

218 mbinant human SAA1 (rhSAA1) directly induced chemotaxis of WT neutrophils in a dose-dependent manner

219 e, we investigate regulation of motility and chemotaxis, one of the most complex and costly bacterial

220 +) mice displayed a significant reduction in chemotaxis, opsonophagocytosis, and production of reacti

221 provide evidence that netrin1 may guide via chemotaxis or haptotaxis.

222 ular organisms use gradient sensing to move (chemotaxis) or grow (chemotropism) towards a favorable e

223 Shewanella genomes to identify S. oneidensis chemotaxis orthologs conserved in the genus.

224 genes related to diverse processes including chemotaxis, oxidative phosphorylation and carbon and nit

225 isruption of the Pumilio-binding sequence in chemotaxis pathway mRNAs, or mislocalization of Puf118 a

226 ow that the mRNAs and proteins of these four chemotaxis pathways and actin are preferentially enriche

227 T cell activation, proliferation and chemotaxis pathways were differentially affected.

228 c states, there is a reduction in neutrophil chemotaxis, phagocytosis, and reactive oxygen species (R

229 rmation, oxidized mitochondrial DNA release, chemotaxis, phagocytosis, degranulation, ability to harm

230 s on distinct physiologic functions, such as chemotaxis, phagocytosis, host defense, and the regulati

231 e chemosensory receptor proteins and perturb chemotaxis phenotypes in filarial worms.

232 l of diverse biological processes, including chemotaxis, platelet aggregation, and adaptive immunity.

233 proof-of-principle we employed the bacterial chemotaxis protein CheY as our receptor.

234 a challenging set of sequences-the bacterial chemotaxis protein CheY, the N-terminal receiver domain

235 ism and mediated by several methyl-accepting chemotaxis proteins (MCPs), rather than a specific MCP.

236 Chemokines are a group of chemotaxis proteins that regulate cell trafficking and p

237 asmic interactions among receptors and other chemotaxis proteins, whereas involvement of membrane-med

238 g SscL and SscS, homologous methyl-accepting chemotaxis proteins.

239 Chemotaxis provides a mechanism for directing the transp

240 Bacterial chemotaxis receptors form extended hexagonal arrays that

241 In summary, invadopodia contain chemotaxis receptors that can respond to microenvironmen

242 olymorphisms and stomach niches suggest that chemotaxis, regulatory functions and outer membrane prot

243 Expression of mcp and other chemotaxis related genes (cheA, cheY2 and fliG) was indu

244 n and regression slopes, indicating that the chemotaxis-related alkane accumulation in A. baylyi is d

245 biospectroscopy approach to characterize the chemotaxis-related alkane bioaccumulation, and has immen

246 In summary, complement C5a-mediated chemotaxis requires Galpha(i2) and Gbeta(2), but not Ca(

247 Efficient chemotaxis requires rapid coordination between different

248 d enhanced enzyme diffusion (EED) and enzyme chemotaxis, respectively, lead to a novel view of enzyme

249 oncentrations for mouse and human neutrophil chemotaxis, respectively.

250 The attractant chemotaxis response of Escherichia coli to norepinephrin

251 Here, we report the chemotaxis response toward arsenate (As(V)) by Shewanell

252 individual flagellar motors to determine the chemotaxis response.

253 ested in reduced in vitro and in vivo T cell chemotaxis resulting in attenuation of profibrotic periv

254 Strikingly, PIKfyve is necessary for chemotaxis, ROS production, and stimulation of the Rac G

255 ay 4 secondary endpoints included neutrophil chemotaxis, safety and tolerability, Sequential Organ Fa

256 ever, knowledge of the molecules detected by chemotaxis signal transduction systems is limited.

257 MAP kinase ErkB as a critical component for chemotaxis signaling in Dictyostelium.

258 e results suggest a greater diversity of the chemotaxis signaling system than previously thought.

259 rimental paradigm for reproduction and sperm chemotaxis studies, the composition and regulation of th

260 recruit beta-arrestin and induce neutrophil chemotaxis, supporting the previous notion that beta-arr

261 The prokaryotic chemotaxis system is arguably the best-understood signal

262 ocyte and T cell migration was detected in a chemotaxis system.

263 atory mediators, presenting a model for cell chemotaxis that is calibrated against experimentally obs

264 Bacterial chemotaxis, the directed migration of bacteria in a grad

265 Bacterial chemotaxis, the directed movement of cells along gradien

266 esence of light is enough to boost bacterial chemotaxis through the stomatal opening and toward photo

267 phils to fibrinogen and decreased neutrophil chemotaxis to a formyl-Met-Leu-Phe gradient.

268 Peroxide promoted chemotaxis to arachidonic acid without being chemotactic

269 ase-deficient eosinophils exhibited impaired chemotaxis to CCL19 that was restored by exogenous leuko

270 embrane chemoreceptor MCP2201, which governs chemotaxis to citrate and other organic compounds in Com

271 In Drosophila larvae, we use innate positive chemotaxis to compare behavior elicited by real- and vir

272 d excreted metabolites, and subsequently use chemotaxis to enhance the utilization of these compounds

273 t, enticing animals to reach the surface via chemotaxis to food, and quantifying the relative success

274 However, the basis of chemotaxis to indole is poorly understood.

275 Bacterial chemotaxis to prominent microbiota metabolites such as i

276 Often, they use chemotaxis to sense nutrient availability and dangerous

277 pr2/3 regulates CCL20-CCR6-mediated monocyte chemotaxis to sites of mucosal injury in the gut.

278 ty of motility patterns, often controlled by chemotaxis, to promote dispersal.

279 Chemotaxis, together with motility, helps bacteria forag

280 Impairing AM chemotaxis toward bacteria induced superfluous neutrophi

281 own of BVR-A resulted in enhanced macrophage chemotaxis toward C5a.

282 -gated (CNG) channel subunit tax-4 in larval chemotaxis toward host serum, and these ion channel subu

283 quito migration, and exposure of L3s reduces chemotaxis toward host-associated cues in vitro.

284 nd their master regulator KLF-2, and reduced chemotaxis toward S1P and CCL21.

285 says, we investigated MK distribution in BM, chemotaxis toward stromal-derived factor 1, NMIIA activi

286 ndothelial cell cytoplasmic membranes, (iii) chemotaxis towards chemoattractant formyl Met-Leu-Phe (f

287 hat a shallow gradient of 12-S-HETE enhances chemotaxis towards low concentrations of S1P and stimula

288 ipase A2 (PLA2) or lipoxygenase (Lox) blocks chemotaxis towards low concentrations of S1P.

289 cells are capable of slow but deterministic chemotaxis up a chemical gradient, in a biased random wa

290 athway, which is the main system controlling chemotaxis, utilizes the other 23 chemoreceptors.

291 ysiological importance of the homotrimer for chemotaxis was demonstrated with site-directed mutations

292 In addition, IL-17-induced neutrophil chemotaxis was dependent on CXCR2 signaling.

293 Applying our formalism to Escherichia coli chemotaxis, we find that its pathway is compatible with

294 s elegans AWA neurons, which are crucial for chemotaxis, we uncovered a Ca(2+) NFL leading to adaptat

295 Complement C5a-mediated chemokinesis and chemotaxis were almost completely abolished in macrophag

296 ving more genes linked to acid tolerance and chemotaxis, while bacteria on limestone were more likely

297 e genes and reduced hemolysis and neutrophil chemotaxis, while exhibiting increased survival in blood

298 Nutrient-limiting environments promote chemotaxis with aggressive morphologies characteristic o

299 roof-of-concept strain that illustrates cAMP-chemotaxis with four fluorescent reporters coded by one

300 ns to reveal that halophilic archaea achieve chemotaxis with power requirements one hundred-fold lowe