ライフサイエンスコーパス: crosstalk

1 ty without substantial attenuation of soleus crosstalk.

2 tem for further studies on understanding PTM crosstalk.

3 gm, explicitly designing against off-pathway crosstalk.

4 ys modulated by C3-triggered proinflammatory crosstalk.

5 ARAP reservoir, and centrosome-autophagosome crosstalk.

6 to the evolution of networks with extensive crosstalk.

7 ays and identify the molecular basis of this crosstalk.

8 ell as inter-liposomal communication without crosstalk.

9 gly contradictory reports of NF-kappaB-STAT3 crosstalk.

10 is achieved without nonlinear inter-channel crosstalk.

11 e possibility for ubiquitination-acetylation crosstalk.

12 ndom expression patterns or networks with no crosstalk.

13 odulation is achieved without such nonlinear crosstalk.

14 redundant and give rise to precise ECM-cell crosstalk.

15 h for identifying pairs of pathways that may crosstalk.

16 s and mechanisms that support the identified crosstalk.

17 ntensive, and often results in unanticipated crosstalk.

18 ecific interactions while avoiding undesired crosstalk.

19 in 1 (ANXA6/LRP1/TSP1) complex in tumor cell crosstalk.

20 h mode onto its designated detector with low crosstalk.

21 ays and to take advantage of their intricate crosstalk.

22 parallel using two fluorescent dyes with no crosstalk.

23 complexity in auxin, cytokinin, and ethylene crosstalk.

24 tosolic Ca(2+) mediates mitochondria-nucleus crosstalk.

25 h high contrast, and low spectral or spatial crosstalk.

26 Regulation is complex, with substantial crosstalk across these multiple pathways.

27 We explore the hypothesis that crosstalk allows different cell types, each expressing a

28 Our data provide compelling evidence for a crosstalk among adipocytes, immune cells, and the sympat

29 tween the transmitter and receiver may cause crosstalk among channels.

30 The differential crosstalk among genes expressed in lymphoid tissues was

31 th-defense trade-offs stem from antagonistic crosstalk among hormones rather than an identified metab

32 least partly explained by the highly complex crosstalk among probiotic bacteria, the host's microbiot

33 involved in responses to various signals and crosstalk among signaling pathways.

34 es and discuss the mechanisms underlying the crosstalk among these pathways.

35 cross-phase modulation and four-wave mixing crosstalks among the channels destroy signal quality.

36 rall, our study reveals a novel mechanism of crosstalk amongst SDHD, PTEN and autophagy pathways and

37 ircular polarization failed due to excessive crosstalk, "anaglyph" filtering by spectral content clea

38 We also find that crosstalk and differential expression can influence drug

39 s mechanisms for commensal-mediated gut-lung crosstalk and dual TCR-based autoimmunity.

40 ic REMORINs are proteins regulating hormonal crosstalk and host invasion.

41 hemokines are linked with peripheral-central crosstalk and may be important in mediating depressive b

42 a novel target of endothelial-cardiomyocyte crosstalk and plays an important role in the angiogenesi

43 f-healing after the obstructions, and assess crosstalk and power penalty when data is transmitted.

44 ortant activator of macrophage-myofibroblast crosstalk and profibrotic signaling in the setting of ma

45 ere compared with DAVID, GSEA, GSA, PathNet, Crosstalk and SPIA on 23 GEO data sets involving 19 tiss

46 nds to suffer from both strong intra-channel crosstalk and strong inter-channel crosstalk with other

47 and specific classification of tumor immune crosstalk and the resulting tumor-associated immune cell

48 eatment with CSF1R inhibitors disrupted this crosstalk and triggered a profound increase in granulocy

49 ate biological processes, signalling pathway crosstalk, and determine precise sequence of events at t

50 ler-induced airflows, power loss, intermodal crosstalk, and system bit error rate (BER).

51 ell relationship and associated bioenergetic crosstalk, and the rapid expansion of our knowledge of t

52 ant stereoscopic ability, control for system crosstalk, and use validated measures of performance.

53 ikely than expected to resist the effects of crosstalk ( approximately 20% for one crosstalk interact

54 e, the molecular mechanisms controlling such crosstalk are not defined.

55 Overall, these studies identify SHP1 and SYK crosstalk as a critical regulator of MyD88 post-translat

56 Here we report an epigenetic crosstalk at enhancers between the UTX (H3K27 demethylas

57 y variants that may be responsible for ceRNA crosstalk at the post-transcriptional level.

58 ere assessed for sensitivity, stability, and crosstalk before conducting in vitro measurements using

59 that there was neither optical nor chemical crosstalk between 2-NBDG and TMRE, TMRE uptake was signi

60 Extensive crosstalk between a diverse array of signaling pathways

61 proteins, hormones, microRNAs) that mediate crosstalk between a pair of pathways and the species and

62 Reduction of the crosstalk between adjacent photonic components has been

63 have two crucial functions: they must block crosstalk between adjacent regulatory domains and at the

64 Shedding light on the crosstalk between allergic response and cancer is paving

65 Importantly, the role of crosstalk between alloimmune responses and autoimmune re

66 hat enables systematic investigations of the crosstalk between an organ's mechanical stress environme

67 UGS, thus establishing reciprocal regulatory crosstalk between AR and GDNF signaling in prostate deve

68 y TRIM14-USP14 and provide insights into the crosstalk between autophagy and type I IFN signaling in

69 Crosstalk between auxin and cytokinin plays an important

70 ortant modeling efforts for establishing how crosstalk between auxin, cytokinin, and ethylene regulat

71 The crosstalk between bacterial communities and innate immun

72 the integral role of previously unrecognized crosstalk between BITC, p53/LKB1 and p73/LKB1 axes in br

73 Continuous crosstalk between cancer cells and local/distant host en

74 Agonist binding directs crosstalk between co-receptors upon DNA binding, stabili

75 A and dimerisation of these domains provides crosstalk between complexes.

76 ct states of the system, as well as to model crosstalk between components.

77 These findings suggest that crosstalk between connexin 43 and purinergic signaling c

78 This crosstalk between CXCR4 and CXCR2 contributed to EMT, mi

79 her there are other mechanisms of regulatory crosstalk between DELLAs and PIFs.

80 o associated embryopathies through signaling crosstalk between developing face and brain structures.

81 hestration of bone repair processes requires crosstalk between different cell populations, including

82 this protein has the potential to stimulate crosstalk between different chromatin modifications.

83 s mechanisms of synergistic and antagonistic crosstalk between different CLRs and with TLRs.

84 ) and benzoates (i.e., SA and BA) to mediate crosstalk between different metabolic pathways, broadeni

85 egulators and to develop novel insights into crosstalk between different pathways involved in cancer.

86 ontrolled by regulatory mechanisms involving crosstalk between different PTMs.

87 properties of the microenvironment instruct crosstalk between different tissues to control the devel

88 n the developing kidney, essential signaling crosstalk between distinct cell types of the developing

89 show that transcription factor RD26 mediates crosstalk between drought and BR signalling.

90 ter introducing a single term to account for crosstalk between each pair of signals, the model was ab

91 oaches, we demonstrate that there is a close crosstalk between early- and late-recruited coactivators

92 these studies failed to account for possible crosstalk between EMT and non-EMT cells that promotes di

93 ed lipid metabolites that originate from the crosstalk between endocannabinoid and cytochrome P450 (C

94 Our data add mechanistic insight into the crosstalk between epigenetic modifications and post-tran

95 entification of region- and lineage-specific crosstalk between epithelium and their neighboring mesen

96 in stability, which brings new insights into crosstalk between ethylene and other phytohormones, and

97 This study has identified intricate crosstalk between EVTs, SpA cells, and decidual immune c

98 To study effects of the crosstalk between fetuin-A, RSF and kidney, human renal

99 gyrus granule cells, in a process involving crosstalk between GABABRs and extrasynaptic delta-subuni

100 Together, the crosstalk between glutamine metabolism and the DNA repai

101 These results suggest that crosstalk between Hedgehog and retinoid signaling modula

102 Herein, we have identified novel crosstalk between HIPK2 and the cytoprotective transcrip

103 s a dose-dependent upstream regulator of the crosstalk between Hippo- and TGF-beta-mediated signaling

104 Crosstalk between histamine receptors and other membrane

105 Akt2 controls hepatic tumorigenesis through crosstalk between HNF1alpha and PPARgamma.

106 n of beta-catenin, suggesting there may be a crosstalk between IL-22/STAT3 and beta-catenin pathway.

107 Recent work has demonstrated that the crosstalk between ILCs and their environment has a signi

108 This process is orchestrated by dynamic crosstalk between immune cells and the epithelium; howev

109 Our findings reveal that signaling crosstalk between interferons and TNF is integrated at t

110 These findings provide a paradigm for crosstalk between light and hormone signaling pathways.

111 ns unclear whether IL-22 is critical for the crosstalk between liver lymphocytes and parenchymal cell

112 rst in vitro and in vivo evidence to support crosstalk between LKB1, Stat3 and pluripotency factors i

113 the lncRNA-disease associations based on the crosstalk between lncRNAs and miRNAs.

114 We have previously demonstrated that crosstalk between lysine-specific demethylase 1 (LSD1) a

115 ur study provides important insight into the crosstalk between macrophages and endogenous MSCs toward

116 In this study, we examined crosstalk between macrophages and HSCs following HCV inf

117 or tumor progression, the reciprocal dynamic crosstalk between mesenchymal cancer cells and the extra

118 fundamental functions of the cell, potential crosstalk between metabolic and DNA repair pathways is p

119 as become apparent that there is significant crosstalk between miRNAs and lncRNAs and that this creat

120 MSC effects on malignant cells through which crosstalk between MSCs and TGFbeta regulates tumour meta

121 Dynamic crosstalk between myocytes and non-myocytes plays a cruc

122 ion of chemokine signaling genes, suggesting crosstalk between neurons and microglia in Ctcf CKO hipp

123 athway, but also uncovers a new mechanism of crosstalk between NF-kappaB signaling and autophagy path

124 hese genes further revealed the existence of crosstalk between Notch and Wnt signaling pathways.

125 n by agonists, and to determine the possible crosstalk between Orai1, TRPC1, and CaV1.2.

126 nalling networks are complex, with extensive crosstalk between pathways.

127 These results reveal a crosstalk between PKA and PKG pathways to govern egress

128 to study protein acetylation and its role in crosstalk between post-translational modifications.

129 iated tumor angiogenesis by antagonizing the crosstalk between PTMs involving HIF1alpha protein degra

130 rved eukaryotic processes, and the potential crosstalk between PTMs, that together regulate the intri

131 The importance of the crosstalk between RLK and ROS signaling is discussed in

132 n cancer cells and a role for the reciprocal crosstalk between signaling and CME in cancer progressio

133 neate specific mechanisms for the reciprocal crosstalk between signaling and the regulation of CME, l

134 Our results present a route to characterize crosstalk between species and predict systems-level sign

135 Recently, Wang et al. (2017) showed that crosstalk between specific microbial components and inna

136 base that carefully and explicitly documents crosstalk between specific pairs of signaling pathways.

137 Crosstalk between strains containing the lux, las and rh

138 Our study identifies a crosstalk between stromal fibroblasts and epithelial cel

139 s that access to different conformations and crosstalk between structural elements are essential for

140 cesses and illuminate the molecular basis of crosstalk between synapses.

141 Our study uncovered a critical molecular crosstalk between TAMs and GSCs through the PTN-PTPRZ1 p

142 us studies, we found a surprising absence of crosstalk between TGFbeta and Wnt/beta-catenin.

143 axis is complex, involving multidirectional crosstalk between the CRH/ACTH pathways, autonomic nervo

144 that the repressors, JAZs and RMT1, mediate crosstalk between the CrMYC2 and BIS regulatory cascades

145 There has been mounting evidence of crosstalk between the drug metabolism pathway and the en

146 This work highlights a novel aspect of the crosstalk between the gut microbiota of C-IBS patients a

147 ition, recent studies have shown evidence of crosstalk between the Hippo pathway and other key signal

148 to habit memory, most likely through altered crosstalk between the hippocampus and dorsal striatum wi

149 The crosstalk between the host and the microbiota may help r

150 ogether, these findings demonstrate critical crosstalk between the IL-17 and NOTCH1 pathway, regulati

151 identify miR-223 as a novel mediator of the crosstalk between the IL23 signal pathway and CLDN8 in t

152 Identifying key molecules that regulate the crosstalk between the immune and the CNS can provide pot

153 nation suggest that UPF3B is involved in the crosstalk between the NMD machinery and the PTC-bound ri

154 PTPN12 by CDK2, which orchestrated signaling crosstalk between the oncogenic CDK2 and HER2 pathways.

155 rthermore, our results suggested a potential crosstalk between the pheromone response pathway and the

156 Furthermore, we hypothesize functional crosstalk between the pore region and carboxy terminus,

157 Mechanistically, ATM mediates crosstalk between the prosurvival MEK/ERK and AKT/mTOR p

158 This review critically evaluates the crosstalk between the three hormones in Arabidopsis root

159 Substantial crosstalk between the two pathways has recently been unr

160 To elucidate the functional crosstalk between the two pathways, we generated a model

161 Thus, PP2A-B55(Pab1) enables a crosstalk between the two TOR complexes that controls ce

162 Here, we report a crosstalk between the ubiquitin protease Ubp2 and the ub

163 We also propose that p62 mediates the crosstalk between the ubiquitin-proteasome system and au

164 Dysregulated crosstalk between the vasculature and retinal neurons is

165 oth regulatory classes, the interactions and crosstalk between them are largely unexplored.

166 on of the protein-coding isoform, indicating crosstalk between them.

167 r-kappaB activity with GLI1, we identified a crosstalk between these 2 pathways that can inform the d

168 R membrane ubiquitin ligase, participates in crosstalk between these critical signaling pathways.

169 Reciprocal crosstalk between these modifications is critical for th

170 tylation and phosphorylation, as well as the crosstalk between these modifications on the structure a

171 n-overlapping, recent evidence has uncovered crosstalk between these subsystems.

172 the present work, we addressed the potential crosstalk between these two signaling pathways, laminin-

173 Moreover, crosstalk between transcription factor hub expression mo

174 Our data highlight a precise crosstalk between transcriptional regulation by NRF1 and

175 er mechanistic investigations underlying the crosstalk between tumor and stromal cells revealed that

176 nd uncovered an unexpected complexity in the crosstalk between two different sirtuins.

177 ollectively, our results demonstrate complex crosstalk between UV-B and high-temperature signaling.

178 It involves dynamic interactions and crosstalk between various cell types, interaction with e

179 evidence supporting the key role of a novel crosstalk between WA, ERK/RSK, ELK1, and DR5 in HCC inhi

180 These findings reveal a novel "crosstalk" between the GABA receptor systems, which can

181 iately when substituted for Fab-7: it blocks crosstalk but does not support bypass.

182 Multimerized Pita sites block iab-6<-->iab-7 crosstalk but fail to support iab-6 regulation of Abd-B

183 ated increases monotonically with additional crosstalk, but is independent of the specific regulation

184 Pelvic organs exhibit neural crosstalk by convergence of visceral sensory pathways, a

185 Thus, HopBB1 fine-tunes host phytohormone crosstalk by precisely manipulating part of the JA regul

186 the dBFP allows us to analyze dual receptor crosstalk by quantifying the spatiotemporal requirements

187 mes to study asymmetric histone modification crosstalk by time-resolved NMR spectroscopy.

188 ogate the complexity in cAMP/PKA-MAPK/ERK1&2 crosstalk by using multi-parameter biosensing experiment

189 ovel molecular mechanism and glomerular cell crosstalk by which local upregulation of MIF and its rec

190 This complex crosstalk can lead to a physiological outcome of drought

191 suggest that myokine-mediated muscle-kidney crosstalk can suppress metabolic reprograming and fibrog

192 gs demonstrate the potential of cognate and "crosstalk" competitive quorum sensing inhibition using t

193 er (and different) inter-morphogenic pathway crosstalk connections than expected; even pathways that

194 nd in adult Sertoli line, TLR4\NOD1 and NOD2 crosstalk converged in NFkappaB activation and elicited

195 Furthermore, the channel crosstalk decreases with an increase in OAM mode spacing

196 Second, we demonstrate that reciprocal crosstalk does not occur at PX(S/T)P sites, i.e., at sit

197 aration of timescales, which helped separate crosstalk due to initial signal transduction from subseq

198 These findings support a role of NOS2/COX2 crosstalk during disease progression of aggressive cance

199 ating sinusoidal endothelial cell-hepatocyte crosstalk during liver regeneration.

200 Te2 and basolateral amygdala (BLA) and their crosstalk during the recall of recent and remote fear me

201 coding remains unchanged, it will generate a crosstalk effect between different shots.

202 This crosstalk effect can only be suppressed by employing suf

203 ) radius along the trap axis, and we measure crosstalk errors between 10(-2) and 4 x 10(-4) at distan

204 ite of inflammation, it is not known whether crosstalk exists between these 2 classes of inflammatory

205 vestigated, revealing distinct signatures of crosstalk for each species.

206 ay pairs and a set of 140 pairs that did not crosstalk, for which Xtalk achieved an area under the re

207 rturbations of protein folding and organelle crosstalk have been implicated in neurodegenerative proc

208 highlighting the importance of neuro-immune crosstalk in allergic inflammation at mucosal surfaces.

209 l hook and reveal the role of auxin-ethylene crosstalk in balancing these two processes.

210 respectively, promote feed-forward NOS2/COX2 crosstalk in both MDA-MB-468 (basal-like) and MDA-MB-231

211 , thus unveiling the direct role of GLI2/WNT crosstalk in cell invasion.

212 ours due to distinct cancer-microenvironment crosstalk in distant organs.

213 c finger 2 (GLI2)-WNT/beta-catenin signaling crosstalk in human keratinocytes.

214 l approach to blunting detrimental fat-liver crosstalk in obesity.

215 nts, less is known about the consequences of crosstalk in spatially distributed mixtures of species.

216 elial-pericyte and endothelial-cardiomyocyte crosstalk in the heart; and on the other hand, PDGF sign

217 te the energy metabolism and drug metabolism crosstalk in this study, we exposed HepG2 cells to varyi

218 sent study examined the effects of TGF-beta1 crosstalk in TME and its role in mediating tumor formati

219 lar factors that drive chaperome networks to crosstalk in tumours, the distinguishing factors of the

220 or proarrhythmic myofibroblast-cardiomyocyte crosstalk in vitro, which suggests that TGF-beta1 may pl

221 sy-to-use interface for scientists to browse crosstalk information by querying one or more pathways o

222 cts of crosstalk ( approximately 20% for one crosstalk interaction) and remain dynamically modular.

223 Analysis of signaling pathways and their crosstalk is a cornerstone of systems biology.

224 etic fate in early mesoderm when BMP and Wnt crosstalk is disturbed.

225 We showed that this crosstalk is mediated by a pyknon, a short 20 nucleotid

226 is hypothesized that microtubule-actomyosin crosstalk is required for a neuron's 'two-stroke' nucleo

227 These interactions involve a bidirectional crosstalk leading to both growth-supporting and inhibito

228 cardiac mechano-signaling and characterizes crosstalk logic imparting differential control of transc

229 on between sensing elements and results in a crosstalk lower than 1%.

230 Interfering with this Notch-dependent crosstalk may be a therapeutic approach to block metasta

231 s of glutamate antipsychotic drugs and their crosstalk mechanism through a heteromeric complex of G p

232 Here we report the first molecular crosstalk mechanism, in which MSH2-MSH3 is used as a com

233 We demonstrate two generic crosstalk mechanisms.

234 egrate a variety of experimental data into a crosstalk network, which reveals multiple layers of comp

235 ability of PHOCOS to recover multi-attribute crosstalk networks from cellular perturbation assays.

236 rate experimental data to construct hormonal crosstalk networks to formulate a systems view of root g

237 ts proarrhythmic myofibroblast-cardiomyocyte crosstalk observed in vitro.

238 NMR and X-ray studies demonstrate the crosstalk occurring between the fused, coplanar, and con

239 It is increasingly clear that active crosstalk occurs between nociceptor neurons and the immu

240 cult to predict where, when, or even whether crosstalk occurs.

241 ot known if these mutations cooperate or how crosstalk occurs.

242 nd ARF elevation hypothesizing the essential crosstalk of AKT/mTOR/YAP with ARF in prostate cancer.

243 Thus, we reported a novel crosstalk of ARF/beta-catenin dysregulated YAP in Hippo

244 essential for elucidating the complexity in crosstalk of auxin, cytokinin, and ethylene in root deve

245 nd prevents degradation of cartilage through crosstalk of bone-cartilage in osteoarthritic mice.

246 Coordinated crosstalk of effector function suggests that MARTX toxin

247 Thus, functional crosstalk of the RNA/RBP network regulates their own qua

248 ments delineate the structural basis for the crosstalk of the TF-FVIIa complex with integrin traffick

249 We characterize the effects of crosstalk on FFL dynamics by modeling the cross regulati

250 a possible explanation for the evolution of crosstalk, our work indicates that consideration of cell

251 manually curated a gold standard set of 132 crosstalking pathway pairs and a set of 140 pairs that d

252 lecular mechanisms underlying complement-TLR crosstalk pathways can, therefore, be used productively

253 tain pathogens can manipulate complement-TLR crosstalk pathways in ways that undermine host immunity

254 utational framework for inferring phenotypic crosstalk (PHOCOS) that is suitable for high-content mic

255 at vascular endothelial growth factor (VEGF) crosstalk potentiates endothelial network formation and

256 This tissue crosstalk provides a putative mechanism that allows musc

257 Here we develop a simple and efficient crosstalk reduction approach for silicon-based nanophoto

258 In addition, the crosstalk reduction technique is shown to be capable of

259 results demonstrate that the Mdm30-Ubp2-Rsp5 crosstalk regulates mitochondrial fusion by coordinating

260 me, yet the mechanistic underpinning of this crosstalk remains poorly understood.

261 complexity in auxin, cytokinin, and ethylene crosstalk requires a combined experimental and systems m

262 This crosstalk results in chronic low-grade inflammation, the

263 rve varied with the pathway, suggesting that crosstalk should be evaluated on a pathway-by-pathway le

264 Analytical modeling suggests that crosstalk should overwhelmingly affect individual protei

265 light the importance of CAF-endothelial cell crosstalk signaling in cancer chemoresistance and demons

266 ruption of DAGLbeta perturbed eCB-eicosanoid crosstalk specifically in microglia and suppressed neuro

267 We propose that cells implement crosstalk strategies and share machinery when a canonica

268 is an underappreciated modality of cell-cell crosstalk that enables cells to convey packages of compl

269 Given the extensive crosstalk that occurs between mTORC1 and mTORC2 signalin

270 he regulatory factors identified interact or crosstalk to orchestrate the myriad N responses plants t

271 the desired mode increases to 4.3 dB and the crosstalk to the other mode increases to -10 dB.

272 desired mode fluctuates by 2.1 dB, while the crosstalk to the other mode is -19 dB below the power on

273 The photon pairs have minimal crosstalk to the pump power due to their broad spacing i

274 system for analysis of histone modification crosstalk, using mass spectrometry to separately identif

275 Crosstalk was measured by the ability of one morphogenic

276 ways and the species and tissue in which the crosstalk was observed.

277 Our findings reveal an enhancer-specific crosstalk whereby NF-kappaB enables STAT3 binding at som

278 eds of cis-regulatory DNA elements, and by a crosstalk whereby Wnt negatively regulates BMP ligand ex

279 Escherichia coli (E. coli) appears to favor crosstalk wherein at least one of the cross-linked FFLs

280 ent, polarization, scattering signature, and crosstalk, which are critical to system miniaturization,

281 eviously reported to have multiple points of crosstalk, which either do not share (TGFbeta and Wnt/be

282 identify an important microRNA-mediated GPCR crosstalk, which plays a key role in vascular developmen

283 malignancies can be influenced by the active crosstalk with an altered bone marrow (BM) microenvironm

284 at N-BLR facilitates migration primarily via crosstalk with E-cadherin and ZEB1.

285 ell wall lipids, particularly mycolic acids, crosstalk with human PXR (hPXR) by interacting with its

286 of oligodendrocyte precursor cells through a crosstalk with microglial cells.

287 te depolarization resulted from electrotonic crosstalk with myofibroblasts as demonstrated by immedia

288 ver, the liver inflammatory cells, and their crosstalk with myofibroblasts.

289 We also discuss the potential for functional crosstalk with other DNA damage-induced post-translation

290 a-channel crosstalk and strong inter-channel crosstalk with other OAM channels.

291 ines that operate as hormones to mediate the crosstalk with other organs including the brain.

292 Lysine acetylation in histones and its crosstalk with other post-translational modifications in

293 at has been learned about its regulation and crosstalk with other signaling pathways, with a particul

294 TETs' role in the crosstalk with specific histone modifications, however,

295 encoded in distinct brain regions, but that crosstalk with the hippocampus may be necessary to integ

296 he orchestration of these pathways and their crosstalk with the redox system under shear stress is la

297 malignant B cells engaged in a bidirectional crosstalk with their supportive microenvironment in inva

298 TGFbeta promotes invasion and crosstalks with Eph signaling via N-cadherin to drive co

299 e loss of Krtap5-5, suggesting that Krtap5-5 crosstalks with keratin 18 in E0771 cells.

300 ation provides another dimension of cellular crosstalk, with the ability to assemble a "kit" of direc