ライフサイエンスコーパス: signal-dependent

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

2 SsrB requirement for PhoP/PhoQ activation is 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 unique nanoscale architecture of a flexible, signal-dependent actin structure.

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

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

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

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

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

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

12 Signal-dependent activation of Relish, including cleavag

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

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

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

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

17 In addition, the loss of Eph leads to a Rho signaling-dependent activation of the PI3K-Akt1 pathway,

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

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

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

21 s were independently required for subsequent signal-dependent and co-dependent events: NF-kappaB recr

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

23 r results demonstrate how cross talk between signal-dependent and lineage-determining factors promote

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

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

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

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

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

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

30 cidated the molecular mechanisms behind TrkB signaling-dependent BDNF mRNA induction and show that CR

31 d place aversion (considered a beta-arrestin signaling-dependent behavior), consistent with the augme

32 duced hypolocomotion and analgesia-G protein signaling-dependent behaviors; a ventral striatal-specif

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

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

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

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

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

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

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

40 f IgE-mediated food allergy revealed an IL-4 signaling-dependent cell-intrinsic effect on SI MMC9 acc

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

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

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

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

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

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

47 3 (eIF3) translation initiation complex in a signal-dependent, choreographed fashion.

48 2 expression level, which in turn depends on signaling-dependent chromatin accessibility at mesendode

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

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

51 atory elements conferring spatiotemporal and signal-dependent control of gene expression.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

68 Finally, we show that signal-dependent down-regulation of RAG gene expression

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

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

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

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

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

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

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

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

77 Signal-dependent erasure of H4K20me3 is required for eff

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

79 yndrome (BBS) proteins, are required for the signal-dependent exit of ciliary GPCRs, but the function

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

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

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

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

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

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

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

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

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

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

90 In vivo, signal-dependent fluctuations in NS levels are required

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

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

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

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

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

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

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

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

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

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

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

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

103 me the same role, maintaining classical IL-6 signaling-dependent GVHD responses.

104 The signal-dependent, HILDA complex coordinates the function

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

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

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

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

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

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

111 To evaluate such flexible, signal-dependent interactions and their contribution tow

112 static relationships, exist depending on the signal-dependent interactions between the Galpha and Gbe

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

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

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

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

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

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

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

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

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

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

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

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

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

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

127 5 on target inflammatory gene promoters in a signal-dependent manner.

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

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

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

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

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

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

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

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

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

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

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

139 n-1 and Card9- and type I and III interferon signaling-dependent manner, respectively.

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

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

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

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

144 moted gastric cancer progression in a Ca(2+) signaling-dependent manner.

145 S2) (encodes COX-2) expression in a TGF-beta signaling-dependent manner.

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

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

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

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

150 d-type NSCs in a cell-cell contact and Notch signaling-dependent manner.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

183 tor planning variability and not exclusively signal-dependent noise.

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

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

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

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

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

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

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

191 Cytokine signaling dependent on JAK3 and JAK1 is critically impor

192 (DAMGO) causes differences in spatiotemporal signaling dependent on MOR distribution at the plasma me

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

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

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

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

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

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

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

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

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

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

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

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

205 ng of the vascular plexus is orchestrated by signals dependent on the pharyngeal ECM microenvironment

206 We find that IE1 controls the signal-dependent Opening Step that makes CARD11 accessib

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

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

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

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

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

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

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

214 ACs - HDAC4, -5, -7, and -9 - are subject to signal-dependent phosphorylation by members of the Ca2+/

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

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

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

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

219 type one myosin, Myo1, is modulated by TORC2-signalling-dependent phosphorylation.

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

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

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

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

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

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

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

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

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

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

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

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

232 eceptor abundance is regulated by background signal-dependent receptor endocytosis and down-regulatio

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

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

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

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

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

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

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

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

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

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

243 n particular, TUB-1 is essential for sensory signaling-dependent reshaping of olfactory cilia morphol

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

245 Mirroring signal-dependent retrieval, signal-dependent ectocytosis

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

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

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

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

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

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

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

253 Signal-dependent sorting of proteins in the early secret

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

255 Signal-dependent splicing is a novel function of platele

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

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

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

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

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

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

262 Our work identifies a Nodal signalling-dependent switch in peri-gastrulation versus

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

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

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

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

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

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

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

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

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

272 The signal-dependent transcription factor activator protein

273 and eRNA production mediated by PU.1 and the signal-dependent transcription factor NF-kappaB.

274 tive binding, providing molecular beacons to signal-dependent transcription factors (SDTFs).

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

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

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

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

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

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

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

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

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

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

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

286 scaded activation by lineage-determining and signal-dependent transcription factors.

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

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

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

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

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

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

293 Signal-dependent translation in activated neutrophils ma

294 ion of KPNA4 attenuated nuclear localization signal-dependent transport activity and suppressed malig

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

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

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

298 Signal-dependent ubiquitylation of DREDD is required for

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

300 and flexibility to switch conformations in a signal-dependent way.