ライフサイエンスコーパス: intercellular signaling

1 ation, primary cilia are key participants in intercellular signaling.

2 which might mediate potassium cycling and/or intercellular signaling.

3 ical nature of the local microenvironment in intercellular signaling.

4 integration of asymmetric cell divisions and intercellular signaling.

5 t the extracellular environment and modulate intercellular signaling.

6 eptors required for cell-cell interaction or intercellular signaling.

7 t they also play a role in intracellular and intercellular signaling.

8 e synaptic activity and participate in brain intercellular signaling.

9 the technique has minimal (if any) impact on intercellular signaling.

10 d intraflagellar transport (IFT) to organize intercellular signaling.

11 esion molecules during synaptogenesis and in intercellular signaling.

12 nerve is a favorable system for the study of intercellular signaling.

13 es a transmembrane protein that functions in intercellular signaling.

14 em of small molecules to communicate through intercellular signaling.

15 pendence of oral-aboral ectoderm polarity on intercellular signaling.

16 sess the requirements of individual genes in intercellular signaling.

17 shing that the lin-36 pathway is involved in intercellular signaling.

18 ich in turn stimulates basal cell growth via intercellular signaling.

19 otential roles in neuronal cell adhesion and intercellular signaling.

20 y subcellular processes and in long distance intercellular signaling.

21 cally evaluate the nature and limitations of intercellular signaling.

22 liferation of basal keratinocytes likely via intercellular signaling.

23 transcriptional regulator, LAG-1, to mediate intercellular signaling.

24 on of connexin binding partners and sites of intercellular signaling.

25 l migration, differentiation, apoptosis, and intercellular signaling.

26 thms of each neuron are synchronized through intercellular signaling.

27 he endodermis, suggesting the involvement of intercellular signaling.

28 as not dependent on new protein synthesis or intercellular signaling.

29 he ER represents a new mode of regulation of intercellular signaling.

30 llular matrix components and disrupting host intercellular signaling.

31 an be implemented through cell autonomous or intercellular signaling.

32 ansport lipophilic cargos and participate in intercellular signaling.

33 g higher cognition must rely on a network of intercellular signaling.

34 ells and this distribution can be induced by intercellular signaling.

35 in the generation of a bystander signal and intercellular signaling.

36 s aiming at correcting the intracellular and intercellular signaling abnormalities may prove effectiv

37 The results indicate that intercellular signaling across gap junctions is an impor

38 We propose that Dlx proteins regulate intercellular signaling across the interface between neu

39 However, the nature of intercellular signaling across the network and how indiv

40 chaperonin 60, has been established to have intercellular signaling activity in addition to its esta

41 ormation in the mouse embryo and may possess intercellular signaling activity in vivo.

42 or release of chemical messengers to mediate intercellular signaling among human biological systems.

43 However, it remains unclear how intercellular signaling among somatic cells results in o

44 rotein signaling (RGS) proteins control both intercellular signaling and asymmetric cell divisions by

45 rane-bound NADPH oxidases necessary for both intercellular signaling and cell death.

46 soprenylcysteine methylation is required for intercellular signaling and development in Dictyostelium

47 Both intercellular signaling and engrailed expression play an

48 These cells play key roles in intercellular signaling and neuronal development, and th

49 hases (NOSs) produce nitric oxide to mediate intercellular signaling and protect against pathogens.

50 cell types in the kidney may participate in intercellular signaling and provide an enriched source o

51 s members of gap junctions, are important in intercellular signaling and wound repair.

52 syndecan-CASK interaction may be involved in intercellular signaling and/or cell adhesion.

53 protein composition of the plasma membrane, intercellular signaling, and cell polarity.

54 sed complex pathways that linked metabolism, intercellular signaling, and stress responses to environ

55 al root positioning and the implications for intercellular signaling are considered.

56 study tested the hypothesis that cooperative intercellular signaling between activated T cells and AS

57 mechanical interactions and/or unidentified intercellular signaling between constricted airways, the

58 Altered intercellular signaling between enteric glia and neurons

59 suggesting a role of activated NF-kappa B in intercellular signaling between epithelial and stromal c

60 at SED1 contributes, at least partly, to the intercellular signaling between luminal and myoepithelia

61 pment requires N-glycosylation regulation of intercellular signaling, but the requirements in synapto

62 These results suggest that intercellular signaling by a subset of vertebrate Wnts i

63 Intercellular signaling by a subset of Wnts is mediated

64 Intercellular signaling by bone morphogenetic proteins (

65 ients that characterize the spatial range of intercellular signaling by diffusing ligands.

66 Intercellular signaling by fibroblast growth factors pla

67 Cx37 supports transmembrane and intercellular signaling by forming functional hemichanne

68 ivo may effectively and efficiently modulate intercellular signaling by inositol phosphates.

69 Intercellular signaling by transforming growth factor-be

70 LINGO-1-mediated inhibition of OPCs through intercellular signaling by using a surface-bound LINGO-1

71 This modulation of intercellular signaling by Vj can play a crucial role in

72 e of small molecule and protein mediators of intercellular signaling, chemotaxis, vasoconstriction, a

73 isabled-1 protein in mouse is known to be an intercellular signaling component of the Reelin molecula

74 ditis elegans vulva serves as a paradigm for intercellular signaling during animal development.

75 findings that highlight novel mechanisms in intercellular signaling during development.

76 ially targetable driver of hypoxia-dependent intercellular signaling during tumor development.

77 on between HH and XCI and support a role for intercellular signaling during XCI.

78 Intercellular signaling dynamics critically influence th

79 ts provide important unique insight into the intercellular signaling environment necessary for in viv

80 nderstanding of the regulatory mechanisms of intercellular signaling events that coordinate cell fate

81 s in epithelial morphogenesis and regulating intercellular signaling events.

82 nducing signals from the mesoderm and to the intercellular signaling factor noggin.

83 ecreted antagonists regulate the activity of intercellular signaling factors, thereby modulating cell

84 Important contributions come from intercellular signaling, fibroblast transformation, remo

85 d measurements highlight the crucial role of intercellular signaling for generating regulated spatial

86 ling involves transformation of fibroblasts; intercellular signaling-for example between epithelial a

87 g the possibility that dachsous affected the intercellular signaling function of frizzled.

88 ell contact to facilitate their own evolving intercellular signaling functions.

89 rs, including its target gene Patched (Ptc), intercellular signaling genes Bone Morphogenetic Protein

90 acellular regions (ECRs) that likely mediate intercellular signaling; however, the precise roles of E

91 lly and display diverse functions, including intercellular signaling, immunomodulation, protein matur

92 e of effects on gene expression dependent on intercellular signaling, implicating the method of bioch

93 and uniformly all the changes resulting from intercellular signaling in both DC-->T cell and T cell--

94 (AP3) gene has distinct roles in regulating intercellular signaling in different tissues.

95 r vesicles (EVs) that play a central role in intercellular signaling in mammals by transporting prote

96 y have played a role in the establishment of intercellular signaling in metazoans.

97 in protein trafficking and intracellular and intercellular signaling in neuronal and non-neuronal cel

98 ation of release generates new insights into intercellular signaling in the brain.

99 of transmitter-laden vesicles enables rapid intercellular signaling in the central nervous system an

100 y projecting MNs, revealing a novel role for intercellular signaling in the establishment of neuronal

101 reveal a paracrine role for secreted cAMP in intercellular signaling in the myocardium, and we postul

102 ated partly by tissue-specific and partly by intercellular signaling initiated by phyA.

103 n of VPC fates is controlled by a network of intercellular signaling, intracellular signal transducti

104 Intercellular signaling is critical for many FR-HIR indu

105 Intercellular signaling is critical for the normal devel

106 f ~24 h rhythms in behavior in mice in which intercellular signaling is disrupted through loss of VIP

107 Evidence suggesting an important role for intercellular signaling is emphasized.

108 Intercellular signaling is essential for the coordinatio

109 Intercellular signaling is important for accurate circad

110 Intercellular signaling is particularly critical in plan

111 We show that intercellular signaling is required for the correct patt

112 e is the key transcriptional motivator of an intercellular signaling loop which drives endomesoderm s

113 aling pathway is an evolutionarily conserved intercellular signaling mechanism essential for embryoni

114 ling pathway is an evolutionarily conserved, intercellular signaling mechanism essential for proper e

115 The Notch signaling pathway is a conserved intercellular signaling mechanism that is essential for

116 Notch signaling is an ancient intercellular signaling mechanism that plays myriad role

117 led growth of neighboring neurons through an intercellular signaling mechanism that requires its glyc

118 e of [H(+)] buildup limits the speed of this intercellular signaling mechanism, but for tonic signals

119 re components of an evolutionarily conserved intercellular signaling mechanism.

120 re components of an evolutionarily conserved intercellular signaling mechanism.

121 Further studies on intracellular and intercellular signaling mechanisms modulating multinucle

122 in the female reproductive tract depends on intercellular signaling mechanisms that coordinate sperm

123 HSL quorum sensing has become a paradigm for intercellular signaling mechanisms.

124 control heterocyst pattern formation through intercellular signaling mechanisms.

125 ance of instructions from the egg; or mutual intercellular signaling mediated by cell contact or diff

126 The intercellular signaling mediated by endothelins and thei

127 ostimulatory molecules, and this cooperative intercellular signaling mediates the induction of proast

128 re, ATP rather than Ca or IP3 is the primary intercellular signaling messenger.

129 t that the EBV-encoded dUTPase may act as an intercellular signaling molecule capable of modulating t

130 e action of gamma-aminobutyrate (GABA) as an intercellular signaling molecule has been intensively st

131 likely reflects the importance of ATP as an intercellular signaling molecule in this system.

132 rotein that has been shown to function as an intercellular signaling molecule that can promote the mo

133 We suggest that norspermidine serves as an intercellular signaling molecule that mediates the attac

134 ne lactone, an acyl-homoserine lactone (AHL) intercellular signaling molecule used by many gram-negat

135 Intercellular signaling molecules and their receptors, w

136 veral members of the WNT family of paracrine intercellular signaling molecules are expressed in speci

137 A large number of intercellular signaling molecules have been identified t

138 Endocannabinoids are key intercellular signaling molecules in the brain, but the

139 ns constitute one of the largest families of intercellular signaling molecules in vertebrates with es

140 s) and their receptors (Fgfrs) are important intercellular signaling molecules that are essential to

141 a new role for Eph receptors and Ephrins as intercellular signaling molecules that establish cell po

142 ic amines such as serotonin and dopamine are intercellular signaling molecules that function widely a

143 One of the intercellular signaling molecules that is involved in th

144 Hedgehogs (Hhs) are intercellular signaling molecules that regulate tissue p

145 omoserine lactones (acyl-HSLs) are important intercellular signaling molecules used by many bacteria

146 Further investigation of these critical intercellular signaling molecules will provide important

147 pigments involve the opposing effects of two intercellular signaling molecules, alpha-melanocyte stim

148 eomelanin involve the opposing action of two intercellular signaling molecules, alpha-melanocyte-stim

149 idic acid (LPA) are now recognized widely as intercellular signaling molecules, the medicinal chemist

150 t use N-acyl-l-homoserine lactones (AHLs) as intercellular signaling molecules.

151 on may involve interplay of EphA4 with other intercellular signaling molecules.

152 ly synthesized, physiologically significant, intercellular signaling molecules.

153 activity that are also known to function as intercellular signaling molecules.

154 environment in silico as characterized by an intercellular signaling network comprising 5 types of ce

155 The intercellular signaling network underlying Caenorhabditi

156 array of soluble factors, forming a complex intercellular signaling network.

157 standing of the integrated intracellular and intercellular signaling networks that control plant grow

158 developmental precision is achieved through intercellular signaling networks, which establish patter

159 challenges through complex intracellular and intercellular signaling networks.

160 ndamental mechanism by which neurons control intercellular signaling, nutrient uptake, and synaptic t

161 thway suggests that previously unappreciated intercellular signaling occurs during myogenic different

162 me characteristics mediate hypoxia-dependent intercellular signaling of the highly malignant brain tu

163 lpha5 function plays an integral role in the intercellular signaling of this stage of development.

164 there is a hemichannel-mediated, purinergic intercellular signaling pathway between supporting cells

165 The Notch intercellular signaling pathway mediates the specificati

166 rstood, but there is evidence that the Notch intercellular signaling pathway plays a critical role.

167 The Notch intercellular signaling pathway regulates cell fate dete

168 and discs overgrown (dco) function within an intercellular signaling pathway that controls growth and

169 as ligand and receptor, respectively, for an intercellular signaling pathway that influences tissue p

170 are upstream components of a wound-induced, intercellular signaling pathway that involves both the b

171 as ligand and receptor, respectively, for an intercellular signaling pathway that regulates Hippo sig

172 ged1 ( JAG1 ), a conserved gene of the Notch intercellular signaling pathway, have been found to caus

173 our-jointed, Dachsous and Fat function in an intercellular signaling pathway, identify a normal role

174 JAG1 encodes a ligand in the Notch intercellular signaling pathway.

175 lying cell fate specification and elucidated intercellular signaling pathways [1].

176 Many niches and their intercellular signaling pathways are known, but for the

177 xtracellular proteins that play key roles in intercellular signaling pathways during vertebrate embry

178 Meristems require a myriad of intercellular signaling pathways for coordination of cel

179 sely investigated, with many of the critical intercellular signaling pathways identified, and well ch

180 ling pathway is one of several key conserved intercellular signaling pathways in animals, and plays f

181 rleukin 6 (IL-6) and its receptor (IL-6R) in intercellular signaling pathways in the olfactory mucosa

182 However, the intercellular signaling pathways that direct the synchro

183 critical roles in these circuits, and common intercellular signaling pathways that link diverse genes

184 The results presented have implications for intercellular signaling pathways that regulate embryonic

185 g requires the precise interplay of numerous intercellular signaling pathways to ensure that cells ar

186 cts, also observed in vivo, involve multiple intercellular signaling pathways, engaging Hmga2.

187 and imaginal development depends on the same intercellular signaling pathways.

188 inductions act via evolutionarily conserved intercellular signaling pathways.

189 oteoglycans with regulatory roles in several intercellular signaling pathways.

190 dest and most functionally diverse of animal intercellular signaling pathways.

191 3/ESR-related peptide family, participate in intercellular-signaling pathways.

192 ready contain the element is inhibited by an intercellular signaling peptide encoded by ICEBs1.

193 Downstream of intercellular signaling, pre- and postsynaptic scaffolds

194 hat the mybC gene product is required for an intercellular signaling process controlling maturation o

195 egulated exocytosis forms the basis for many intercellular signaling processes, for example, in hormo

196 ontrolling a wide array of developmental and intercellular signaling processes.

197 ne, is a cell-surface associated short-range intercellular signaling protein in Myxococcus xanthus.

198 C factor, an intercellular signaling protein, is required for aggrega

199 The hedgehog (Hh) family of intercellular signaling proteins is intricately linked t

200 The semaphorins are a family of intercellular signaling proteins that has grown to inclu

201 urrogates to investigate this superfamily of intercellular signaling proteins.

202 neral features for biochemical regulation of intercellular signaling: receptors are less frequent tar

203 ronment, but how biomechanics contributes to intercellular signaling remains unclear.

204 tuent that is believed to serve an important intercellular signaling role at certain excitatory synap

205 scriptional regulation (NF-kappaB, Gli), and intercellular signaling (Shh) to control bulge stem cell

206 DD), a molecule previously shown to regulate intercellular signaling, stress surveillance [6], and de

207 y serve as the endogenous ligands of a novel intercellular signaling system found widely throughout t

208 ns in genes that antagonize the ras-mediated intercellular signaling system responsible for vulval in

209 Thus our data identify an intercellular signaling system that restricts, directly

210 S uses a previously unknown peptide-mediated intercellular signaling system to control SpeB productio

211 There are three intercellular signaling systems employed by P. aeruginos

212 istic human pathogen which relies on several intercellular signaling systems for optimum population d

213 r in flowering plants, and several different intercellular signaling systems have evolved to elicit t

214 d its VPAC2 receptor form a key component of intercellular signaling systems in the SCN and criticall

215 Intracellular- and intercellular-signaling systems transduce this informati

216 (DA) in midbrain represents a novel form of intercellular signaling that inherently differs from cla

217 bodies, such as cell growth, migration, and intercellular signaling, that are required for primitive

218 Nitric oxide (NO) mediates intercellular signaling through activation of its recept

219 ant on cell surface proteoglycans, regulates intercellular signaling through its binding to various g

220 ing pathways, and the ability to investigate intercellular signaling through studies of cells remaini

221 Intercellular signaling through the Notch receptor and i

222 ellular addresses at specific times, and use intercellular signaling to coordinate multicellular even

223 at retinal precursors utilize Notch-mediated intercellular signaling to regulate their fates.

224 ain an intracellular molecular clock and use intercellular signaling to synchronize their timekeeping

225 volvement, and in particular the blocking of intercellular signaling transduction between neuron and

226 production of antibiotics, are controlled by intercellular signaling using small molecules.

227 Intercellular signaling via extracellular vesicles (EVs)

228 and of their Sfrp inhibitors, together with intercellular signaling via PCP proteins, polarize node

229 ptimum offer a physical basis for intra- and intercellular signaling via sound waves at interfaces, w

230 Intercellular signaling was initiated by pN-level forces

231 expression of neuropeptides critical for SCN intercellular signaling was significantly disturbed.

232 and electrophysiology with intracellular and intercellular signaling, we were able to develop the fir

233 -resistance transfer through manipulation of intercellular signaling, with implications in the clinic

234 Defective intercellular signaling within peripheral nerves might u