ライフサイエンスコーパス: signal-dependent

1 ter elements identified for genes that are C-signal dependent.

2 -Golgi network in secretory pathway could be signal dependent.

3 ion in human bone marrow cells is also Stat3 signaling-dependent.

4 cellular event that was MyD88- and p38 MAPK-signalling dependent.

5 ventionally thought to be required for Stat3 signal-dependent activation and seems to play an essenti

6 namic MAPK movement either markedly impaired signal-dependent activation and/or resulted in improper

7 We report that the signal-dependent activation of gene transcription by nuc

8 tanding of mechanisms underlying priming and signal-dependent activation of macrophages and discuss t

9 OCT4 in a kidney cell line is sufficient for signal-dependent activation of otherwise unresponsive ge

10 lases, including LSD1, to permit ligand- and signal-dependent activation of regulated gene expression

11 Signal-dependent activation of Relish, including cleavag

12 ss an inducible transcriptional modulator by signal-dependent activation of specialized mechanisms th

13 e is controlled by a collaboration involving signal-dependent activation of transcription factors, tr

14 se element and an AP-1 motif, which mediated signal-dependent activation.

15 These findings suggest that Pak1 signaling-dependent activation of ER-S305 leads to an en

16 stration of a positive feedback loop linking signaling-dependent alternative splicing to mitogenic pr

17 olecular mechanism underlying SMAR1-mediated signal-dependent and -independent regulation of alternat

18 anscriptional coactivation in the context of signal-dependent and cell-type-specific gene regulation.

19 that a single coregulator can function as a signal-dependent and coordinated regulator of transcript

20 -cell proliferation but are TGFbeta receptor signaling dependent and independent, respectively.

21 sport proteins in an ETR1 and EIN2 (ethylene signaling)-dependent and TIR1 (auxin receptor)-dependent

22 umor cell proliferation/survival (Raf kinase signaling-dependent and signaling-independent mechanisms

23 o what extent beta-catenin activation is Wnt-signaling-dependent and the potential cell source of Wnt

24 EGFR expression on Th2 cells was TCR-signaling dependent, and therefore, our data reveal a me

25 nuclear function of p53 in regulating Ca(2+) signal-dependent apoptosis.

26 ly significantly influence the regulation of signal-dependent but not signal-independent turnover of

27 These responses are IL-1 signaling-dependent, but independent of PARP1, which als

28 osphorylation and augmentation of outside-in signaling-dependent c-Src activation.

29 ings suggest myocardin participates in a BMP signaling-dependent cardiac gene transcriptional program

30 nsport-receptor-facilitated translocation of signal-dependent cargo molecules.

31 ortin beta concentrations, about half of the signal-dependent cargos that interacted with an NPC were

32 Soluble nuclear transport receptors bind signal-dependent cargos to form transport complexes that

33 of two types primarily: classical Flt3-Flt3L signaling-dependent, CD103(+)CD11b(-) DCs and macrophage

34 xport, class IIa HDACs such as HDAC7 mediate signal-dependent changes in gene expression that are imp

35 lation of the BMP-regulated R-SMAD, MAD, and signal-dependent changes in levels and sub-cellular dist

36 tion between these states requires important signaling-dependent changes in actin cytoskeletal dynami

37 Subsequently, Notch signaling-dependent changes in apicobasal epithelial thi

38 llular signaling roles that are sensitive to signaling-dependent changes in endoplasmic reticulum Ca(

39 Flower opening, by contrast, requires JA-Ile signaling-dependent changes in primary metabolism, which

40 3 (eIF3) translation initiation complex in a signal-dependent, choreographed fashion.

41 2 expression level, which in turn depends on signaling-dependent chromatin accessibility at mesendode

42 d substrate specificity are likely driven by signal-dependent colocalization events.

43 ling, thus serving as an early trigger of Wg signaling-dependent competition.

44 ion, offering a conceptual means of dynamic, signal-dependent control of RNA granule assembly.

45 Here, we review the evidence for signaling-dependent control of the dynamic changes in pr

46 In addition, the signal-dependent cooperation between TCR and coreceptor

47 suggested a potential role of cpRNPs in the signal-dependent coregulation of chloroplast genes.

48 Signal-dependent CREB phosphorylation at Ser(133) (pCREB

49 To determine whether this stop signal-dependent decrease in the efficiency of translati

50 odel, we show that DSBs promote a DNA damage signaling-dependent decrease in gene expression in prima

51 here, RPW8.2 activates a salicylic acid (SA) signaling-dependent defense strategy that concomitantly

52 Our results indicate that signal-dependent degradation of EZH2 is a prerequisite f

53 Signal-dependent delivery to lysosomes has been suggeste

54 embryonic kidney cells by executing a damage-signal-dependent dephosphorylation of an H2AX carboxy-te

55 ression by signal-independent repression and signal-dependent derepression.

56 Here, we used the stereotyped, Wnt signaling-dependent development of the Caenorhabditis el

57 ROS and membrane signalling-dependent differences in bystander foci induc

58 expression can either enhance or inhibit the signal-dependent differentiation of a CD4(+)/CD8(+) cell

59 kinase (SYK) in tonic B-cell receptor (BCR) signal-dependent diffuse large B-cell lymphomas (DLBCLs)

60 igm in RNA biology: nondegradative ubiquitin signaling-dependent disassembly of mRNP promoted by the

61 nt IRF3 activation by UV is due to apoptotic signaling-dependent disruption of ULK1 (Unc51-like kinas

62 e regulation but also suggest that targeted, signal-dependent dissociation of multisubunit enzyme com

63 tective role of insulin thus derives from IR signaling-dependent downregulation of ADDL binding sites

64 inducible genes and that Crt1 functions as a signal-dependent dual-transcription activator and repres

65 such as the anorexigenic GPCR NPY2R undergo signal-dependent ectocytosis in wild-type cells.

66 Mirroring signal-dependent retrieval, signal-dependent ectocytosis is a selective and effectiv

67 Our data show that signal-dependent ectocytosis regulates ciliary signaling

68 d T cells as expected, but exerts unexpected signal-dependent effects during T cell differentiation i

69 phosphorous deficiency have opposing, auxin signalling-dependent effects on lateral root GSA in Arab

70 Here, we will discuss the recent advances in signaling-dependent epigenomic regulation of gene transc

71 Signal-dependent erasure of H4K20me3 is required for eff

72 y programs of gene expression is achieved by signal-dependent exchange of coregulator complexes that

73 el mechanism by which Mks underwent FGF-FGFR signaling dependent expansion to accelerate rapid FGF pr

74 family of transcription regulators modulate signal-dependent expression of genes involved in carbon

75 on extracellular matrix, and display normal signal-dependent expression of surface P-selectin and an

76 n widely studied, little is known about TrkB signaling-dependent expression of BDNF.

77 closely related cells with a similar set of signal-dependent factors to generate differential and pe

78 borative fashion and facilitating binding of signal-dependent factors.

79 face receptors trigger entotic invasion in a signal-dependent fashion has not been investigated.

80 AF6 or IkappaB kinase (IKK) in an activation signal-dependent fashion.

81 platelets synthesize numerous proteins in a signal-dependent fashion.

82 inating enzyme complex, which bound IRF-3 in signal-dependent fashion.

83 ersal by blocking the activation of retinoid-signaling-dependent feminization genes.

84 erase and methylesterase and why motors show signal-dependent FliM turnover.

85 t MrpC2 binds to sequences upstream of the C-signal-dependent fmgA promoter.

86 ere, we demonstrate that regulation of the C-signal-dependent fmgBC operon is under similar combinato

87 Ac-CIN85 complex and decreased alphaIIbbeta3 signaling dependent functions such as platelet spreading

88 eK1-null background, and we found that all C-signal-dependent fusions assayed also required SdeK for

89 ate molecular mechanisms to rapidly activate signal-dependent gene expression.

90 We have found that a third C-signal-dependent gene, herein named fmgD, is subject to

91 Several C-signal-dependent genes have been shown to be regulated b

92 This site is unique among the C-signal-dependent genes studied so far.

93 ide further insight into the regulation of C-signal-dependent genes, demonstrating both shared and un

94 the dev operon, like that of several other C-signal-dependent genes, is subject to combinatorial cont

95 similar to the promoter regions of several C-signal-dependent genes, where these sequences are crucia

96 ingly similar to promoter regions of other C-signal-dependent genes.

97 s found in the regulatory regions of other C-signal-dependent genes.

98 vation of p44/p42 MAPK mediates an anchorage signal-dependent growth pathway.

99 The signal-dependent, HILDA complex coordinates the function

100 The role of signal-dependent increases in U-STAT3 expression in regu

101 letion of Integrator subunits diminishes the signal-dependent induction of enhancer RNAs (eRNAs) and

102 a novel mechanism of T cell homeostasis and signal-dependent induction of mRNA degradation.

103 distinctions in the Toll-like receptor (TLR) signaling-dependent induction for the rapidly expressed

104 induced peritonitis, which is a typical IL-1 signaling-dependent inflammation animal model.

105 n of HOS in proliferating cells with mitogen-signaling-dependent inhibition of cell differentiation a

106 We conclude that signal-dependent interaction of Foxo4 with myocardin cou

107 on in response to IL-1, probably through its signal-dependent interaction with IRAK4, IRAK, and the t

108 d on its DNA-binding ability and evidence of signaling dependent interactions between the two protein

109 ient to induce cGAS-, STING-, and interferon signaling-dependent ISG15 monomer and conjugate protein

110 saccharide (LPS)-Toll-like receptor 4 (TLR4) signaling dependent Kupffer cell (KC) activation as an e

111 propriate ligand induces the expression of a signal-dependent lacZ reporter gene.

112 a in WHIM syndrome is caused by CXCL12-CXCR4 signaling-dependent leukocyte sequestration, and support

113 We show that PalH is phosphorylated in a signal dependent manner, resembling mammalian GPCRs, alt

114 y regulates CREB-mediated transcription in a signal dependent manner.

115 ng to NF-kappaB, associates with CARD11 in a signal-dependent manner and can compete with the require

116 Integrator is recruited to the IEGs in a signal-dependent manner and is required to engage and re

117 phosphorylation events of Akt in a time- and signal-dependent manner in neurons.

118 sphorylation of TFII-I can be regulated in a signal-dependent manner in various cell types.

119 osomes carrying microbial antigens, and in a signal-dependent manner under the control of Toll-like r

120 kA receptors, which predominantly recycle in signal-dependent manner, have unique biological properti

121 tuates between two stable conformations in a signal-dependent manner.

122 rgo into Golgi export carriers in an unusual signal-dependent manner.

123 controls transcription at specific loci in a signal-dependent manner.

124 5 on target inflammatory gene promoters in a signal-dependent manner.

125 TFII-I promotes growth arrest of cells in a signal-dependent manner.

126 suggesting that the interaction occurs in a signal-dependent manner.

127 reby derepressing specific target genes in a signal-dependent manner.

128 ther cardiac transcriptional activators in a signal-dependent manner.

129 ucleus and the cytoplasm in a cell type- and signal-dependent manner.

130 a expression was strongly induced in an IL-1 signaling-dependent manner during disease, expression of

131 gnature cytokine, was induced in a TGF-beta1 signaling-dependent manner in single-cell suspensions of

132 determined that hdm2 was expressed in a Ras-signaling-dependent manner in various pancreatic cancer

133 increased the abundance of Tregs, in a B7.2 signaling-dependent manner, along with IL-10 production

134 im)CD8(bright) T cells, likely through a Wnt signaling-dependent manner, and that these cells are ass

135 ity of the ADAM12 metalloprotease in a Notch signaling-dependent manner, leading to increased ectodom

136 HuR proteins in a nondegradative, ubiquitin signaling-dependent manner, revealing a novel mechanism

137 vator NURF-trithorax remodeling complex in a signaling-dependent manner.

138 t resistance against insects in a JA- and JA-signaling-dependent manner.

139 influence blood vessel formation in a Notch signaling-dependent manner.

140 epatocytes are desensitized by LPS in a TLR4 signaling-dependent manner.

141 on from macrophages in an autocrine and TLR4 signaling-dependent manner.

142 umor cell-specific behaviors in an ErbB2-ERK signaling-dependent manner.

143 s so in an alpha interferon receptor (IFNAR) signaling-dependent manner.

144 iltrating T cells in an IFN-gamma/IFN-gammaR signalling-dependent manner, which may serve as a potent

145 quitinated Ag-BCR complexes are formed via a signaling-dependent mechanism and restricted to plasma m

146 BCR complexes occurs by an Src family kinase signaling-dependent mechanism that is restricted to lipi

147 TGF increased procollagen by a TGF-beta/Smad signaling-dependent mechanism without involving Smad2/3.

148 h between an adhesion- versus a beta-catenin signaling-dependent mechanism, chimeric cadherin constru

149 gulate proinflammatory cytokines via a Wnt5a signaling-dependent mechanism.

150 n kinase A at early time points in a TGFbeta signaling-dependent mechanism.

151 f the adult midgut, are specified by a Notch signaling-dependent mechanism.

152 gulate dendritic spine density through a Ras signaling-dependent mechanism.

153 ulated by two distinct T-cell receptor (TCR) signaling-dependent mechanisms.

154 fy a Raptor-mTORC1-dependent pathway linking signal-dependent metabolic reprogramming to quiescence e

155 r Miro proteins are important for regulating signaling-dependent mitochondrial dynamics in astrocytic

156 lls, we confirm that NRP-1 modulates VEGFR-2 signaling-dependent mitogenic functions of VEGF.

157 Taken together, these data suggest mTOR signaling-dependent, mitogenic conditioning of AECII is

158 i-IL-2 treatment, further supporting an IL-2 signaling-dependent modulation.

159 Class IIa histone deacetylases (HDACs) are signal-dependent modulators of transcription with establ

160 Here, we engineered signal-dependent motility in Escherichia coli via the tr

161 Both planning noise and signal-dependent motor noise (together called accumulati

162 state pursuit can be attributed primarily to signal-dependent motor noise that arises downstream from

163 oise components due to 1) planning noise, 2) signal-dependent motor noise, and 3) signal-dependent pr

164 back gain and an increase of planning and/or signal-dependent motor noise.

165 granule convergence, a dynein- and integrin signal-dependent movement of lysosome-related organelles

166 hat Rab22 promotes nerve growth factor (NGF) signaling-dependent neurite outgrowth and gene expressio

167 h activity plays an important part in Reelin-signal-dependent neuronal migration.

168 around the time of saccades, as a result of signal dependent noise and of sensorimotor delays.

169 in noise spectrum deviating from broadband, signal dependent noise.

170 f instability arising from task geometry and signal-dependent noise (SDN) in the neuromuscular system

171 ses, perceptual inference in the presence of signal-dependent noise accounts for ubiquitous features

172 istributes work across effectors to minimize signal-dependent noise and effort.

173 gment angle variance increase due to greater signal-dependent noise associated with an increased acti

174 Three sources of noise were assessed: signal-dependent noise exemplified by the slope of the r

175 ow that accuracy demands alone, coupled with signal-dependent noise, lead to qualitatively the same b

176 n the initiation of pursuit, as expected for signal-dependent noise.

177 erence was correlated with lateralization of signal-dependent noise: the direction of force for which

178 The proposed mechanism reconciles signal-dependent nuclear accumulation of Smad2 with its

179 Through signal-dependent nuclear export, class IIa HDACs such as

180 se findings represent the first evidence for signal-dependent nuclear translocation of PCAF and hGCN5

181 ctions leads to a decrease in the range of a signal dependent on the HetN protein that is one of the

182 reduced cell proliferation and growth factor signaling dependent on a galectin lattice.

183 may exert reciprocating effects on cellular signaling dependent on duration of administration.

184 Cytokine signaling dependent on JAK3 and JAK1 is critically impor

185 stress effects on social affiliation and OT signaling dependent on odor context with particularly st

186 acetate skin carcinogenesis and identify Rho signaling dependent on RhoA and RhoB as a potent driver

187 ontrolling dsDNA-mediated IRF3 and NF-kappaB signaling dependent on STING.

188 -like phenotype, whereas non-canonical Notch signaling dependent on the adaptor Rictor activated the

189 tivated extracellular loop I with downstream signaling dependent on transmembrane region II.

190 We established that biosynthesis of, and signaling dependent on, the foliar defense phytohormone

191 I3K and MEK/ERK signaling, dependent on PI3K signaling, dependent on MEK/ERK signaling, and dependent

192 Thus, the regulation of intracellular Ca(2+) signaling, dependent on Miro1-mediated mitochondrial pos

193 at, whereas differentiation requires intense signaling, dependent on multiple reinforcing ligands, le

194 ere defined: independent of PI3K and MEK/ERK signaling, dependent on PI3K signaling, dependent on MEK

195 nds not only to nutritional cues but also to signals dependent on other macromolecular pathways of th

196 henotypes reflect interference with putative signals dependent on phenylpropanoid biosynthesis.

197 In the second part of the loop, ureteric bud signals dependent on Ret control stromal cell patterning

198 nger times and potentially amplifying Ca(2+) signals dependent on RyR channel activity.

199 result from interference with normal "stop" signals dependent on signaling by gradients of NGF.

200 ld modulate alternative splicing in either a signal-dependent or -independent manner remain enigmatic

201 n with a CD40L blocking antibody and by CD40 signaling-dependent p38 mitogen-activated protein kinase

202 ssing of extant p100; PKC deficiency impairs signal-dependent p52 accumulation because of defects in

203 acute lung injury is an example of thrombin signaling-dependent pathology.

204 le by osmotic stress through an IP3 receptor signaling-dependent pathway, indicating active regulatio

205 y of adherens junctions in a PI3K, Rac/Cdc42 signaling-dependent pathway.

206 posed to be induced in cell-autonomous, then signal-dependent phases.

207 overlaps the H-NS-binding motif required for signal-dependent phoP repression in high Mg2+ conditions

208 e checkpoint function of NCoR is relieved by signal-dependent phosphorylation of c-Jun, which directs

209 erns of two related cellular responses, both signal-dependent phosphorylation of the BMP-regulated R-

210 Activation of IRF3 requires signal-dependent phosphorylation, but little is known ab

211 we found that nitration of TCoB antagonizes signaling-dependent phosphorylation of TCoB, whereas opt

212 cient BDNF levels necessary for various TrkB signaling-dependent physiological outcomes in neurons.

213 the presence of functional spliceosomes and signal-dependent pre-mRNA splicing in the cytoplasm of p

214 ise, 2) signal-dependent motor noise, and 3) signal-dependent premotor noise entering within an inter

215 This signal-dependent process is controlled in part by the be

216 ts CCA cells from TRAIL cytotoxicity by a Hh-signaling-dependent process.

217 pressor/coactivator complexes in integrating signal-dependent programs of transcriptional responses a

218 These sequences are present in other C-signal-dependent promoter regions, indicating a general

219 as well as the C box, are present in other C-signal-dependent promoters, suggesting some similarity i

220 ly to be important for expression of other C-signal-dependent promoters.

221 wn to be important for expression of other C-signal-dependent promoters.

222 s 5'-CAYYCCY-3', which is found in several C-signal-dependent promoters.

223 on of the immunological synapse requires TCR signal-dependent protein redistribution.

224 ion analysis to investigate the mechanism of signaling-dependent protein-protein interactions in inta

225 (BRET)-based biosensor, capable of detecting signal-dependent PTEN conformational changes in live cel

226 regulating the activation of PKC and through signal-dependent recruiting of both PKC and CARD11 to li

227 elongation and mRNA processing, through the signal-dependent recruitment of P-TEFb.

228 to target genes and marks the chromatin for signal-dependent recruitment of the SWI/SNF core to musc

229 These results indicate that signal-dependent recycling is a more common property of

230 ne phosphorylation, suggesting metabolic and signal-dependent regulation of RBP function.

231 ractions provides an efficient mechanism for signal-dependent regulation of the epigenetic events con

232 etylase 7 (HDAC7) is a T-cell receptor (TCR) signal-dependent regulator of differentiation that is hi

233 These results reveal a role for MITR as a signal-dependent regulator of muscle differentiation.

234 ortion of secretory proteins might occur via signal-dependent regulatory mechanisms as demonstrated f

235 opy that Pelle functions to downregulate the signal-dependent relocalization of Tube.

236 teosome machinery that normally mediates the signal-dependent removal of corepressor complexes requir

237 of TLR target genes, where they prevent the signal-dependent removal of NCoR corepressor complexes r

238 CD4(+)/CD8(+) thymocytes and functions as a signal-dependent repressor of gene transcription during

239 We report that class I HDACs function as signal-dependent repressors of cardiac hypertrophy via i

240 drive both cell-specific gene expression and signal-dependent responses.

241 Mirroring signal-dependent retrieval, signal-dependent ectocytosis

242 We conclude that c-di-GMP can mediate signal-dependent RNA processing and that macromolecular

243 hat target the constitutively active Akt/PKB signaling-dependent SCLC cells.

244 Wnt/beta-catenin signaling-dependent secreted factors from keratinocytes

245 mbrane domain (TMD) length in modulating the signal-dependent segregation of membrane proteins to dis

246 A1.2 loss in these cells triggers DNA damage signaling-dependent senescence, a hallmark of RS.

247 an Eph receptor A (EphA) and ephrin A (Efna) signalling-dependent shift in the allocation of clonally

248 Histone deacetylase 4 (HDAC4) undergoes signal-dependent shuttling between the cytoplasm and nuc

249 Signal-dependent sorting of proteins in the early secret

250 together, our data redefine the AVRs as Tie2 signaling-dependent specialized hybrid vessels and provi

251 Signal-dependent splicing is a novel function of platele

252 Surprisingly, TOR is also required for light signal dependent stem cell activation.

253 , all three mutants dramatically reduced the signaling-dependent stimulation of cell spreading, indic

254 data further indicate that the SSD allows a signal-dependent structural change in Hmg2 that promotes

255 presented in this work clearly show that the signal dependent subcellular localization of HDAC7 is es

256 n-proteasome pathway can be achieved through signal-dependent, subunit-specific regulation of the pro

257 We propose that Snu114p serves as a signal-dependent switch that transduces signals to Brr2p

258 e peroxisome proliferator-activated receptor signaling-dependent switch from glycolysis to fatty acid

259 Without manipulating chemotaxis, signal-dependent switching of motility, either on or off

260 Signal-dependent synthesis of an active cytokine over se

261 Calcium (Ca2+) signaling-dependent systems, such as the epidermal diffe

262 Furthermore, IL-12 signaling-dependent T-bet expression was also found to b

263 t threonines 91/93 in c-Jun is essential for signal-dependent target gene activation.

264 s, so does the size of the NDR, the level of signal-dependent TF binding, and gene activation.

265 as broader principles of gene regulation and signal-dependent TFs.

266 tivator protein-1 (AP-1) sites to Jun family signal-dependent TFs.

267 g in developmental patterning defects in Shh signaling-dependent tissues such as the limb and neural

268 enetic tuning model, we demonstrate that the signal-dependent transcription factor (TF) STAT5 is crit

269 The signal-dependent transcription factor activator protein

270 , TFII-I is a direct substrate of JAK2 and a signal-dependent transcription factor that integrates si

271 We hypothesized that access of signal-dependent transcription factors (TFs) to enhancer

272 ancers/SEs are enriched in binding sites for signal-dependent transcription factors and dependent on

273 criptional programs, regulated by binding of signal-dependent transcription factors and their associa

274 herefore, our data suggest an active role of signal-dependent transcription factors in chromatin and

275 es are beginning to provide a picture of how signal-dependent transcription factors regulate the infl

276 on state driven by NF-kappaB, AP1, and other signal-dependent transcription factors that play crucial

277 matory signals is likely to be used by other signal-dependent transcription factors that regulate div

278 me cell-specific enhancers, thereby enabling signal-dependent transcription factors to bind and funct

279 The impact of signal-dependent transcription factors, such as glucocor

280 e prototypic of similar mechanisms for other signal-dependent transcription factors.

281 factor and these differentiation-initiating, signal-dependent transcription factors.

282 Under classical models for signal-dependent transcription in eukaryotes, DNA-bindin

283 date and a resource for understanding rapid signal-dependent transcription in other systems.

284 lR-like factors to DNA, and it suggests that signal-dependent transcription regulation is accomplishe

285 together, our data define TFII-I as a growth signal-dependent transcriptional activator that is criti

286 l are likely maintained by a balance between signal-dependent transcriptional induction and proteolys

287 transcription factors to mediate lineage and signal-dependent transcriptional repression.

288 cers are exploited to institute alternative, signal-dependent transcriptional responses remains poorl

289 Signal-dependent translation in activated neutrophils ma

290 in, demonstrating new biologic roles for the signal-dependent translation pathway controlled by this

291 ution of nuclear TFII-I, suggesting that the signal-dependent translocation is reversible.

292 yoblast fusion, inhibited the nuclear export signal-dependent translocation of p204 to the cytoplasm.

293 Cilia lacking IFT25 have defects in the signal-dependent transport of multiple Hedgehog componen

294 nists to inhibit the growth of hedgehog (HH) signaling-dependent tumors.

295 Derepression requires signal-dependent turnover of the nuclear receptor corepr

296 Signal-dependent ubiquitylation of DREDD is required for

297 imulate two types of InsP(3)-mediated Ca(2+) signal dependent upon feedback inhibition, producing two

298 phocyte activation requires sustained Ca(2+) signaling dependent upon capacitative Ca(2+) entry (CCE)

299 ccomplished through receptor tyrosine kinase signaling dependent vertical cell divisions within the l

300 promoter regions of several genes that are A-signal dependent, whereas sequences located upstream of