ライフサイエンスコーパス: growth arrest

1 while nevi harboring the same mutations have growth arrest.

2 ession, leading to persistent DNA damage and growth arrest.

3 ial cells, thus promoting cell apoptosis and growth arrest.

4 eads to elevated levels of p53, resulting in growth arrest.

5 d NF-kappaB signaling, ultimately leading to growth arrest.

6 armacological inhibitors of PKDs resulted in growth arrest.

7 ependent cytostatic Smad signaling to induce growth arrest.

8 ine acetylation during growth transition and growth arrest.

9 prenylation, without affecting the senescent growth arrest.

10 or alpha (TNF-alpha) that induced tumor cell growth arrest.

11 l conditions applied simultaneously led to a growth arrest.

12 ls internalized enough RG7787 to only induce growth arrest.

13 stress, triggering thylakoid senescence and growth arrest.

14 curs despite relatively uniform induction of growth arrest.

15 r signaling to the MAP kinase p38 to mediate growth arrest.

16 hosphorylation and suppressed DspA/E-induced growth arrest.

17 n containing WT mazEF resulted in reversible growth arrest.

18 ring their activity over several days during growth arrest.

19 e cellular states acquired after the initial growth arrest.

20 remature senescence, a state of irreversible growth arrest.

21 growth and proliferation and premature leaf growth arrest.

22 n of auxin accumulation and concomitant root growth arrest.

23 rary for mutants resistant to DspA/E-induced growth arrest.

24 promoter rescued cells from (+)-JQ1-induced growth arrest.

25 an early inflammatory response, followed by growth arrest.

26 sion of cyclin D1 promoter activity and cell growth arrest.

27 and allowed BRCA1-deficient cells to bypass growth arrest.

28 expression induced a p53-dependent senescent growth arrest.

29 nistic underpinnings of panobinostat-induced growth arrest.

30 egulation of root meristematic zone-targeted growth arrest.

31 cessions recapitulated the DFPM-induced root growth arrest.

32 mal levels led to immediate, but reversible, growth arrest.

33 moting fungicide-dependent cell swelling and growth arrest.

34 s, whereas cells with functional p53 undergo growth arrest.

35 thway to regulate genes involved in cellular growth arrest.

36 induce membrane permeabilization and fungal growth arrest.

37 significantly exceed those required for cell growth arrest.

38 tized cells to proteasome inhibitor-mediated growth arrest.

39 t deletion of floxed CRK3, resulting in G2/M growth arrest.

40 of the DNA damage response and a G1/S-phase growth arrest.

41 ifesting as apoptosis highly correlated with growth arrest.

42 rring on a single day, the simultaneous silk growth arrest.

43 FKBP12, specifically inhibits TORC1, causing growth arrest.

44 e in Huh7.5 cells during HCV (JFH-1)-induced growth arrest.

45 d in the loss of HER3 and AKT activation and growth arrest.

46 f PKA targets upon sulfate-induced exit from growth arrest after sulfur starvation.

47 damage response, apoptosis and p53-mediated growth-arrest, all of which are under the control of the

48 atrol (10 microM, 48 hr) induces both a cell growth arrest and a metabolic reprogramming in colon can

49 r, Atg7-deficient MCs entered into premature growth arrest and accumulated reactive oxygen species (R

50 ermore, immune dormancy promotes cancer cell growth arrest and angiogenic control.

51 P) K13 in the modulation of anti-IgM-induced growth arrest and apoptosis in B cells.

52 clusion, we report consistent Notch-mediated growth arrest and apoptosis in human AML, and propose th

53 Sabutoclax induced growth arrest and apoptosis in pancreatic cancer cells a

54 ates expression of these targets and induces growth arrest and apoptosis in persister cells, at doses

55 dulator of the decision between p53-mediated growth arrest and apoptosis in vitro and in vivo.

56 s but not normal cells to chemotherapy, with growth arrest and apoptosis induced in vivo in part thro

57 Notch activation even promoted growth arrest and apoptosis of colorectal carcinoma cell

58 y RNA interference has been shown to promote growth arrest and apoptosis of tumor cells.

59 MCs showed enhanced DSB repair and decreased growth arrest and apoptosis, whereas SM22alpha-(DeltaC)N

60 ablished mechanism of action is induction of growth arrest and apoptosis.

61 may be pivotal to sensitizing CTCL cells to growth arrest and apoptosis.

62 SMCs showed reduced DSB repair and increased growth arrest and apoptosis.

63 egrin beta7 expression and function prior to growth arrest and apoptosis.

64 steroid-mediated transcriptional regulation, growth arrest and apoptosis.

65 However, excess ceramide is toxic, causing growth arrest and apoptosis.

66 xperience oncogene-induced senescence (OIS), growth arrest and apoptosis.

67 mature B-cell line, against anti-IgM-induced growth arrest and apoptosis.

68 more resistant to BET-inhibitor-induced cell growth arrest and apoptosis.

69 death, correct establishment of polarity and growth arrest and autophagy, respectively.

70 of Split 1 (HES1), consistently leads to AML growth arrest and caspase-dependent apoptosis, which are

71 in trophoblast cell line HTR8/SVneo induced growth arrest and cellular senescence via activation of

72 pollen-expressed EXO70 isoforms resulted in growth arrest and characteristic phenotypic deviations o

73 aurin/PKC412 are sensitive to GO-203-induced growth arrest and death.

74 can also exhibit a potent ability to induce growth arrest and death.

75 K-eEF2K axis) causes tumour cells to undergo growth arrest and differentiation.

76 oss of p44/wdr77 gene expression led to cell growth arrest and differentiation.

77 r long term physiological responses, such as growth arrest and differentiation.

78 p53-induced transcription of p21(cip1) and growth arrest and DNA damage 45 and resulted in the inac

79 the endoplasmic reticulum stress marker, the growth arrest and DNA damage induced gene-153 (gadd153,

80 APK, leading to transcription of a family of growth arrest and DNA damage inducible (GADD) genes, cul

81 in in vivo We also demonstrate that Gadd45g (growth arrest and DNA damage inducible gamma) is a direc

82 al TNF-related weak inducer of apoptosis and growth arrest and DNA damage-associated gene 45, two mol

83 Growth arrest and DNA damage-inducible beta (GADD45b) pl

84 Following relief of the stress, the growth arrest and DNA damage-inducible protein GADD34 as

85 ertain FOXO targets--e.g., FAS, GADD45alpha (growth arrest and DNA damage-inducible, alpha), and GADD

86 e mRNA coding for the stress response factor growth arrest and DNA-damage inducible 45 (GADD45) can a

87 ut genome-wide cDNA screen, we identify here growth arrest and DNA-damage-inducible protein 45 gamma

88 rain-derived neurotrophic factor (Bdnf), and growth arrest and DNA-damage-inducible, beta (Gadd45b)]

89 Ras-transformed cells override a131-induced growth arrest and enter mitosis where a131's ability to

90 ene expression and controls TGF-beta-induced growth arrest and epithelial-to-mesenchymal transition (

91 Whereas a high pheromone dose induces growth arrest and formation of a shmoo-like morphology i

92 f mating pheromone, the yeast cell undergoes growth arrest and forms a shmoo-like morphology; however

93 splay an accelerated senescence sustained by growth arrest and increased senescence-associated beta-g

94 reversed LIF-mediated effects, resulting in growth arrest and increased sensitivity to gamma irradia

95 hat VICTR is necessary for DFPM-induced root growth arrest and inhibition of abscisic acid-induced st

96 suppressors of MDM33 overexpression-induced growth arrest and isolated binding partners by immunopre

97 encoding genes resulted in late liver-stage growth arrest and lack of merozoite differentiation.

98 (INK4a) and p19(ARF), which are required for growth arrest and myeloid differentiation following Hhex

99 at RA resistance can occur in steps, wherein growth arrest and other differentiation events may be re

100 cellular response characterized by a stable growth arrest and other phenotypic alterations that incl

101 uce expression of genes associated with OIS, growth arrest and p53-dependent apoptosis.

102 reduced ER stress or Xbp1 splicing promotes growth arrest and premature senescence through hyperacti

103 of the MYC -428 and -525 ESE eRNA caused LCL growth arrest and reduced cell growth.

104 ition of TOR by inducible RNAi, led to plant growth arrest and reduced expression of BR-responsive ge

105 kers characteristic of HGPS cells, including growth arrest and senescence-associated beta-gal (SA-bet

106 istant cells, an effect associated with both growth arrest and senescence.

107 Cells committed to growth arrest and shmoo formation exhibited sustained Fu

108 d H3K9 methylation levels in cells and cause growth arrest and substantial apoptosis in LNCaP prostat

109 hypothesis of oncogene-induced senescence in growth arrest and tumor suppression in melanocytic nevi

110 he HIV protease inhibitor ritonavir elicited growth arrest and/or apoptosis in multiple myeloma.

111 that mutagenic NHEJ repair is suppressed in growth-arrested and serum-deprived cells, suggesting tha

112 sses such as differentiation, proliferation, growth arrest, and apoptosis.

113 n fail to redifferentiate, undergo premature growth arrest, and become atrophic.

114 8 in PC3, DU145 and LNCaP cells induced cell growth arrest, and decreased tumour volumes and mortalit

115 n increase in iron content of the parasites, growth arrest, and differentiation of wild-type (WT) pro

116 in translation, massive protein aggregation, growth arrest, and lethality.

117 al flg22 responses including gene induction, growth arrest, and plasma membrane depolarization.

118 teins increased AML cell maturation, induced growth arrest, and prolonged survival in an AML mouse mo

119 in was refractory to myristic acid-dependent growth arrest, and unlike the wild-type strain, was susc

120 expression of both transformability and the growth arrest are bet-hedging adaptations that improve f

121 duced differentiation, neurite extension and growth arrest, are dissociable at the level of the senso

122 ogression to melanoma, but only after stable growth arrest as nevi.

123 est progenitor cells (hNCPCs) did not induce growth arrest as seen in human melanocytes, but instead,

124 growth in LNCaP by rescuing LNCaP cells from growth arrest at G1 phase due to the lack of androgen.

125 and not feTHTR2, this blockade resulted in a growth arrest at physiological concentrations of extrace

126 tivation of CCN5 in TNBC cells promotes cell growth arrest at the G0/G1 phase, reduces cell prolifera

127 P1 to trigger DNA damage response and induce growth arrest at the G2/M phase, to induce senescence, a

128 27 and Wee1 to trigger DNA damage and induce growth arrest at the G2/M phase.

129 However, the mechanism for growth arrest at this stage is unknown.

130 fibers, bi-directional growth, with lateral growth arrested at a post-seeding stage.

131 We found that, even while growth-arrested, bacteria continued to produce proteins

132 lomerular epithelial cells that are normally growth-arrested because of the expression of cyclin-depe

133 ls to mediate p53-dependent transcription or growth arrest but can be rescued by substitution with as

134 ORP4M) in HEK293 and HeLa cells resulted in growth arrest but not cell death.

135 lone and propranolol shortened the period of growth arrest by 84 days (P = 0.0125 vs control) and inc

136 ein kinase HipA in Escherichia coli triggers growth arrest by activating synthesis of the alarmone gu

137 provide novel insights into the mechanism of growth arrest by WA in breast cancer cells.

138 ate distinct cellular outputs: p38-dependent growth arrest, cAMP response element-binding protein-dep

139 Means by which growth arrest can be overcome and how melanocytic nevi r

140 The growth arrest caused by TOR inactivation was partially r

141 eased fitness can result from a catastrophic growth arrest caused by unexpected darkness in a small s

142 and 4t) potently inhibited cell survival and growth, arrested cell cycle, and blocked angiogenesis an

143 At the plasma membranes of growth-arrested cells, AJUBA LIM proteins do not inhibit

144 motility, decreases adhesion, and induces a growth arrest, changes associated with a complete EMT th

145 C4 transport was similarly elevated in short growth-arrested cilia and remained high even when the am

146 Whereas knockdown of miRNAs causes growth arrest, concomitant knockdown of Tsc1 restores mT

147 broblasts with proliferating and transiently growth arrested controls using a combination of differen

148 riments show that HBI1 inhibits PAMP-induced growth arrest, defense gene expression, reactive oxygen

149 die secondary to p53-mediated apoptosis and growth arrest, demonstrating the absolute requirement of

150 Mechanistically, the PP2A-mediated growth arrest depends on GSK3beta and is ultimately medi

151 tion in primary endothelial cells with KSHV, growth arrest DNA damage-inducible gene 45 beta (GADD45B

152 Restoration of NOTCH signaling caused growth arrest due to activation of the NOTCH effector HE

153 ss of breast cancer cells is associated with growth arrest due to p21CIP1 upregulation.

154 abA5e displayed delayed seed germination and growth arrest during oxidative stress.

155 L-1 inhibited cell proliferation by inducing growth arrest during the G1/S phase transition, promoted

156 contributes to global protein acetylation in growth-arrested E. coli.

157 Furthermore, growth arrested elo3 mutants suffer a partial loss of sh

158 en embryos reaching the blastocyst stage and growth-arrested embryos (degenerates) using quantitative

159 ance in exponentially growing and stationary growth-arrested epimastigote parasites.

160 yl-tRNA hydrolase counteracts TacT-dependent growth arrest, explaining how bacterial persisters can r

161 bules recovering from AKI undergo pathologic growth arrest, fail to redifferentiate, and become atrop

162 Loss of C/EBPbeta expression prevents growth arrest following androgen deprivation or anti-and

163 testosterone, and reduced strength alongside growth arrest for up to 2 years after injury.

164 Although apoptotic and growth arrest functions of p53 remain as important mecha

165 Our previous studies showed: (i) that growth-arrested G0/G1 rat mesangial cells stimulated to

166 Cells cultured in HS undergo rapid growth arrest, have a hepatocyte-like morphology, and in

167 TR-CD4) potently induced IFN-gamma-dependent growth arrest in cancer cells.

168 Cellular senescence is a permanent growth arrest in cells with damage or stress that could

169 unteracts in vitro imatinib mesylate-induced growth arrest in CML CD34(+) progenitors via reactivatio

170 Arabidopsis thaliana accession-specific root growth arrest in Columbia-0 (Col-0) plants.

171 rescue experiments reversed miR-203-induced growth arrest in cSCC, which highlights the importance o

172 Indeed, the growth arrest in early infected cells could be rescued b

173 ate transforming growth factor-beta-mediated growth arrest in epithelial cells.

174 lls represses CDK2 expression and results in growth arrest in G1 phase.

175 lating the balance between proliferation and growth arrest in hematopoietic progenitors, myeloid line

176 p53-mediated fibrotic gene reprogramming and growth arrest in HK-2 cells.

177 hat tubulin is a novel target of WA-mediated growth arrest in human breast cancer cells.

178 dition, both compounds induced shrinkage and growth arrest in KD, associated with the inhibition of a

179 ts depletion robustly induces cell death and growth arrest in MTC cell lines in culture and in mouse

180 PIP4Ks inhibition by a131 causes reversible growth arrest in normal cells by transcriptionally upreg

181 lone and propranolol attenuates burn-induced growth arrest in pediatric burn patients.

182 After bud growth arrest in phyB-1, expression of dormancy-associat

183 TP53BP1 and USP28, but not TRIM37, prevented growth arrest in response to prolonged mitotic duration.

184 ioception mechanism is a key step leading to growth arrest in the whole sepal in response to its own

185 Here we show that BTIC growth arrest in vitro and in vivo is accomplished via c

186 amount equivalent to the amount that induced growth arrest in vitro.

187 ating Jag-1-induced p27(kip1) expression and growth arrest in VSMCs.

188 loss of nucleostemin triggers DNA damage and growth arrest independently of the p53 status or rRNA sy

189 The growth arrest induced by loss of p44/wdr77 expression wa

190 ; therefore, signaling can occur even during growth arrest induced by starvation or antibiotic treatm

191 -14-mediated Sp1 protein stabilization, G2/M growth arrest induction, and anchorage-independent growt

192 ne of the earliest key events in FGF-induced growth arrest is dephosphorylation of the retinoblastoma

193 by the addition of pyruvate suggesting that growth arrest is due to a pH-dependent checkpoint on met

194 ticular, we focus on the mechanisms by which growth arrest is established after BRAF(V600E) mutation.

195 Instead, a reversible growth arrest is induced that can be overcome by reoxyge

196 a wild-type shoot; however, the mechanism of growth arrest is not understood.

197 suggest that IR-induced p16(INK4a) dependent growth arrest is reversible in mice and that sustained p

198 ntal effects on plant development, including growth arrest, leaf necrosis, and reduced seed productio

199 of this repression system leads to a strong growth arrest, likely due to overly rapid galactose cata

200 ing stationary phase and in conjunction with growth arrest linked to carbon starvation.

201 Cellular senescence is a process of cellular growth arrest linked with aging and inflammation.

202 Braf(V600E) induces benign, growth-arrested melanocytic nevus development, but also

203 etal ciliopathies suffer from premature bone growth arrest, mirroring skeletal features associated wi

204 ociated with a dose- and time-dependent cell growth arrest, mitochondrial damage, and apoptosis induc

205 Growth-arrested Mtb is resuscitated by the addition of p

206 Here we show that growth arrest of AREG-silenced keratinocytes occurs in G

207 tivation through Stk11 (Lkb1) loss abrogates growth arrest of Braf(V600E) melanocytic nevi, but is in

208 latory machineries for the proliferation and growth arrest of cardiomyocytes is imperative.

209 Fibroblast growth factor (FGF)-induced growth arrest of chondrocytes is a unique cell type-spec

210 Our data indicate that growth arrest of endoreplicating cells is primarily attr

211 ew conceptual paradigm for understanding the growth arrest of melanocytic nevi in vivo termed stable

212 Previously, we found that cAMP-induced growth arrest of PC12 and NS-1 cells requires Epac2-depe

213 c effects of aristolochic acid are linked to growth arrest of proximal tubular epithelial cells; howe

214 ented p107 dephosphorylation and FGF-induced growth arrest of RCS (rat chondrosarcoma) chondrocytes.

215 lar environments, some of which may favour a growth arrest of Salmonella facilitating immune evasion

216 239 was not decreased by aphidicolin-induced growth arrest of the target cells.

217 Unexpectedly, the rapamycin hypersensitive growth arrest of vip1-1 cells was dependent on the prese

218 ar senescence, a stress-induced irreversible growth arrest often characterized by expression of p16(I

219 ization and activation of p53 and subsequent growth arrest or apoptosis.

220 daptive gene expression programme leading to growth arrest or cell death.

221 with CW remodeling and biosynthesis to avoid growth arrest or integrity loss.

222 When NR2F1 is blocked in vivo, growth arrest or survival of dormant DTCs is interrupted

223 an enhanced Cu-dependent phenotype involving growth arrest, oxidative stress, floral bud abortion, an

224 ent kinase inhibitors essential for myogenic growth arrest (p21(cip1) and p57(kip2)), the Notch pathw

225 Intriguingly, mortalin depletion induced growth arrest partly via the MEK/ERK pathway, whereas it

226 racterized by reduced cell division rates or growth arrest, persistence, or lysis, concomitant with I

227 Overexpression of CNGC18 produced a growth arrest phenotype coupled with accumulation of cal

228 pc2, was constructed that exhibited a severe growth-arrest phenotype.

229 kout strain fails to exhibit the long-lived, growth-arrested phenotype, suggesting that altered regul

230 Analysis of the compounds cellular growth arrest phenotypes and microtubule dynamics sugges

231 ) that triggers cell wall alkalinization and growth arrest, possibly through the inhibition of plasma

232 This growth arrest prevents long-term outgrowth of the majori

233 l rat ECFCs isolated from hyperoxic alveolar growth-arrested rat lungs mimicking bronchopulmonary dys

234 Growth-arrested rat mesangial cells (RMCs) at a G0/G1 in

235 Taken together, the data suggest that growth arrest reflected a changed interaction between th

236 ys (l-ascorbate utilization and metabolism), growth arrest response, heat shock response, DNA recombi

237 MazF-mediated growth arrest resulted in an increase in survival of bac

238 mes of cellular growth, including a phase of growth arrest resulting from toxicity of the metabolic p

239 of YjhX (85 amino acid residues) causes cell-growth arrest resulting in cell death, while YjhQ (181 r

240 Here, we studied the role of growth arrest specific 6 (GAS6), a ligand of the TYRO3-A

241 xl, one of the tyrosine kinase receptors for growth arrest specific 6 (Gas6).

242 The TAM receptor ligand, growth arrest specific 6, re-establishes the normal FM r

243 enib-resistant Huh-7 cells, inhibiting TYRO3/growth arrest specific 6-mediated cancer cell migration

244 jections by Shh requires its binding partner growth arrest specific gene 1 (Gas1) and its signaling c

245 was originally identified in fibroblasts as growth arrest specific gene 3 (gas3) and is expressed br

246 Growth arrest specific gene two (GAS2) is a highly conse

247 proteins related to hepatogenic lineage like growth arrest specific protein 6, oncostatin M, hepatocy

248 The down-regulation of lncRNA growth arrest specific transcript 5 (GAS5) has been repo

249 Gas6 (growth-arrest specific gene 6) plays a role in thrombus

250 GF signaling by activating the expression of growth arrest-specific 1 (Gas1), a novel WT1 target gene

251 ding Fas-associated phosphatase 1 (Fap1) and growth arrest-specific 2 (Gas2) and activates genes enco

252 Here, we demonstrate that the lncRNA growth arrest-specific 5 (GAS5) suppresses TGF-beta/Smad

253 on of steroid receptors (SRs) by the lincRNA growth arrest-specific 5 (Gas5), which regulates steroid

254 Based on recent evidence that (1) growth arrest-specific 6 (Gas6) regulates the expression

255 of wound healing cytokines, e.g., IL-10 and growth arrest-specific 6 (GAS6), and enhanced expression

256 The AXL receptor and its activating ligand, growth arrest-specific 6 (GAS6), are important drivers o

257 E2 stimulated LCs to produce growth arrest-specific 6 (GAS6), which mediates phagocyt

258 In contrast, MerTK and its known ligands, growth arrest-specific 6 and Protein S, were downregulat

259 Of these variants, two protein S/growth arrest-specific 6 chimeras, with either the whole

260 ernative model for SRC and MET activation by growth arrest-specific 6 in ccRCC and identify AXL as a

261 with lapatinib, a splicing mutation in GAS6 (growth arrest-specific 6) in the same patient; and a res

262 , substituted by the corresponding domain in growth arrest-specific 6, were unable to enhance TFPI.

263 verexpression of TAMs and their major ligand Growth arrest-specific factor 6 (Gas6) is associated wit

264 e expression and secretion of the Axl ligand growth arrest-specific gene 6 (Gas6) by bone marrow-deri

265 by endogenous ligands, protein S (PROS1) and growth arrest-specific gene 6 (GAS6).

266 Growth arrest-specific protein 6 (GAS6) is a soluble ago

267 egulation of larval diapause, the long-lived growth arrest state called dauer arrest, in Caenorhabdit

268 ells promoted the formation of organized and growth-arrested structures with basal polarity, and supp

269 One of these, the differentiation of growth-arrested stumpy forms in the mammalian blood into

270 port also ruled out trivial explanations for growth arrest, such as high-level induction.

271 amphiregulin (AREG), results in keratinocyte growth arrest that cannot be rescued by soluble extracel

272 Cellular senescence is a stable cell growth arrest that is characterized by the silencing of

273 d SMAD3-mediated fibrotic gene induction and growth arrest that were reversed by ectopic PPM1A expres

274 lgae is a stress response tightly coupled to growth arrest, thereby imposing a major limitation on pr

275 or, and GEF substrate of, Epac2 in mediating growth arrest through p38 activation in NS-1 cells.

276 nd effective strategy for inducing cancerous growth arrest through the direct epigenetic regulation o

277 ition is required for apoptosis, but not for growth arrest, through a mechanism involving the derepre

278 s absence switches response to TGF-beta from growth arrest to EMT.

279 Because numerous studies have linked such growth arrest to fibrosis after proximal tubular epithel

280 uring the early stage, cells transition from growth-arrested to growing.

281 Cellular senescence, an irreversible growth arrest triggered by a variety of stressors, plays

282 Here macrophages, growth-arrested tubular epithelial cells, the endotheliu

283 splanted RAS mutant organoids confirmed this growth arrest upon pan-HER/MEK combination therapy.

284 nti-MM activity of b-AP15 is associated with growth arrest via downregulation of CDC25C, CDC2, and cy

285 dominant for iron transport, indicating that growth arrest was an intrinsic property of the Delta10 v

286 iated Bax activation and that increased cell growth arrest was associated with elevated expression of

287 Growth arrest was attributed to inhibition of G1-phase c

288 The growth arrest was reversed at high extracellular concent

289 wn-regulation using shRNA, which caused cell growth arrest, was accompanied by increased H3K27me3 at

290 All Delta10 proteins that caused growth arrest were dominant for that phenotype.

291 ion of the Kras(ex3op) allele, which induced growth arrest when oncogenic and exhibited tumor-suppres

292 Inhibiting PGE2 production led to growth arrest, whereas addition of MSC-derived PGE2 rest

293 ectopic CELF1 overexpression caused G1-phase growth arrest, whereas CELF1 silencing promoted cell pro

294 p38 MAPK activation results in hepatocyte growth arrest, whereas increased proliferation has been

295 -catenin in the liver induces senescence and growth arrest, which is overcome by combined CAR activat

296 nal cells induces basal genes expression and growth arrest, which is rescued by TGFbeta pathway inhib

297 Noise can drive entry of single cells into growth arrest while a fast-growing majority sustains the

298 lular signal-regulated kinase inhibition and growth arrest, while miR-9-3p had little effect on growt

299 t of cultured human PA-SMCs resulted in cell growth arrest with the induction of senescence but not a

300 , total inhibition of protein synthesis, and growth arrest within 24 h.