ライフサイエンスコーパス: mitogenic

1 ambiguous whether the signal is exclusively mitogenic.

2 lagen-activated NPY-rich platelets were more mitogenic (~2-fold vs. ~1.6-fold increase) for human mic

3 Both PDGF mitogenic action and calcium signaling are cPLA(2)alpha-

4 ia converts the myogenic action of IGFs into mitogenic action by differentially regulating multiple s

5 rb14 as a physiological repressor of insulin mitogenic action in the liver and further supports that

6 retinoic acid, correlated with sustained pro-mitogenic action of PACAP beyond the developmental switc

7 distinct pathways that produce pro- or anti-mitogenic actions.

8 ch mimicked the glucoregulatory, but not the mitogenic, actions of insulin.

9 or tyrosine kinases (RTKs) and/or downstream mitogenic activation is almost ubiquitous; thus tailored

10 phatidic acid (PA) is a critical mediator of mitogenic activation of mammalian target of rapamycin co

11 acid, have been established as mediators of mitogenic activation of mTORC1.

12 poR that cannot be ubiquitinated has reduced mitogenic activities and ability to stimulate the STAT5,

13 activity of FGF1 can be dissociated from its mitogenic activity and is mediated predominantly via FGF

14 ying EGF mutants with significantly enhanced mitogenic activity at low concentrations compared to tha

15 secretory activity in the lacrimal gland and mitogenic activity at the corneal epithelium.

16 the increase in tumor engraftment and serum mitogenic activity in mice pretreated with a chemotherap

17 val of mice after partial hepatectomy, FGF19 mitogenic activity is associated with liver carcinoma.

18 and protein assays, we further show that the mitogenic activity of TWEAK on primary astrocytes requir

19 However, its mitogenic activity was delayed compared with that of EGF

20 endent of its protease activity, FXII exerts mitogenic activity with implications for angiogenesis.

21 ations as well as macrophage recruitment and mitogenic activity, and a decrease in UVB-induced apopto

22 stigating factors that limit YAP's postnatal mitogenic activity, we found that the CM-enriched TEAD1

23 However, the molecular basis of its mitogenic activity, which is currently unknown, must be

24 s with the capacity to withstand an aberrant mitogenic activity, with a profound impact on the geneti

25 m of microorganisms and also had the highest mitogenic activity.

26 ve-like signaling properties with negligible mitogenic activity.

27 o-terminal microheterogeneity does not alter mitogenic activity.

28 proliferation, corresponding to their higher mitogenic activity.

29 ination of IRS-2 enhances IGF signalling and mitogenic activity.

30 yses revealed that a variety of antioxidant, mitogenic, acute phase genes were up-regulated in the li

31 ncers in which steroid hormones are powerful mitogenic agents.

32 We further demonstrated that the mitogenic and adipogenic effect of ghrelin were mainly d

33 member of the IGFBP family, which regulates mitogenic and antiapoptotic effects of IGFs.

34 ression of proinflammatory genes but is also mitogenic and antiapoptotic in hepatocytes.

35 receptor substrates 1 and 2 (IRS1/2) mediate mitogenic and antiapoptotic signaling from insulin-like

36 y as a C-terminal fragment homologous to the mitogenic and bactericidal region in human lacritin, sug

37 syndecan-1 binding is necessary for lacritin mitogenic and cytoprotective activities, TGM2 cross-link

38 sic 1-10 nM dose optimum, the same domain is mitogenic and cytoprotective for epithelia via a syndeca

39 ERalpha-mediated gene expression involved in mitogenic and developmental processes in MCF7 breast can

40 scaffold proteins that interact with various mitogenic and developmental signals, the genetic role of

41 We show that Gas6 is mitogenic and increases schwannoma cell-matrix adhesion

42 meostasis and critical to the integration of mitogenic and metabolic signaling pathways.

43 hedgehog (HH) pathway is well known for its mitogenic and morphogenic functions during development,

44 The surprising magnitude and the mitogenic and mutagenic nature of the effect exerted by

45 eta-catenin pathways effectively blocked the mitogenic and neurogenic effects of ETH.

46 ayers and growth factors alone, we sustained mitogenic and osteogenic signals with these growth facto

47 oxygenase-2 (COX-2) expression is induced by mitogenic and proinflammatory factors.

48 The interplay between mitogenic and proinflammatory signaling pathways plays k

49 Activation of the mitogenic and prosurvival transcription factor, STAT5b,

50 The mitogenic and second-messenger signals that promote cell

51 ine-threonine kinase, has been implicated in mitogenic and survival control, and it is markedly overe

52 s studies, we find that E-peptide signaling, mitogenic, and motogenic effects are dependent upon IGF-

53 renal ischemia-reperfusion injury, mainly by mitogenic, angiogenic, and anti-inflammatory mechanisms.

54 ture of murine CD3epsilon complexed with the mitogenic anti-CD3epsilon antibody 2C11 enabled the firs

55 role in this relationship, due to insulin's mitogenic/antiapoptotic activity.

56 Mitogenic assays in cultured cells showed an age-depende

57 ased upregulation of the CSF1R-dependent pro-mitogenic cascade, correlating with disease severity.

58 hibited C-RAF BxB-mediated activation of the mitogenic cascade.

59 rs (GEFs) of the Dbl family are activated by mitogenic cell surface receptors and activate the Rho fa

60 whose activity results in proliferative and mitogenic changes in the cell.

61 e function as a new class of human beta cell mitogenic compounds.

62 these data suggest mTOR signaling-dependent, mitogenic conditioning of AECII is a determinant of host

63 venting cell proliferation under unfavorable mitogenic conditions.

64 rexpression of Dsg2 increased EV release and mitogenic content including epidermal growth factor rece

65 assumption that metastatic cells are in the mitogenic cycle.

66 This mitogenic effect can be neutralized by RNA interference,

67 between in vivo and in vitro studies on the mitogenic effect of estrogen and raises questions regard

68 We show that the mitogenic effect of Ex-4 requires calcineurin/nuclear fa

69 endent of keratinocyte proliferation and the mitogenic effect of FGF signalling, which are only requi

70 f toll-like receptor 4, was essential to the mitogenic effect of NE on HMECs.

71 which abrogates STAT3 signaling, reduces the mitogenic effect of supernatants in CRC cells.

72 The mitogenic effect of tPA was independent of its protease

73 the WNT signaling pathway is known to have a mitogenic effect on cells, but relatively little is know

74 l properties against 11 human pathogens, and mitogenic effect on hamster spleen lymphocytes were also

75 Active neurons exert a mitogenic effect on normal neural precursor and oligoden

76 tumors and cell lines, leading to a similar mitogenic effect through activation of the MAP kinase pa

77 This mitogenic effect was abrogated by pharmacological inhibi

78 y smooth muscle cell proliferation, and this mitogenic effect was greatly pronounced in PAH-pulmonary

79 ion of KLF4, which mediates estrogen-induced mitogenic effect.

80 Both forms of IGFBP-3 are also without mitogenic effects alone or in combination with IGFs.

81 ese findings provide evidence that insulin's mitogenic effects are mediated by a subpopulation of IRs

82 Interestingly, BRAFV600E mitogenic effects in astrocytes were restricted, in part

83 three members of the MAPK family mediate the mitogenic effects of catecholoestradiols in the endothel

84 Moreover, we show that the mitogenic effects of estradiol require the presence of i

85 age dependent and critical for promoting the mitogenic effects of estradiol via ERalpha.

86 e endometrial epithelial cells to direct the mitogenic effects of estradiol.

87 rs (FGFs) that act as paracrine mediators of mitogenic effects of estrogen on the epithelium.

88 etic progestins were found to antagonize the mitogenic effects of estrogens.

89 n of direct from indirect and motogenic from mitogenic effects of genes and molecules affecting wound

90 ration, and clinical trials that exploit the mitogenic effects of IL-7 have achieved success in treat

91 only IRA transmits the growth-promoting and mitogenic effects of insulin-like growth factor 2.

92 that elafin is a counterbalance against the mitogenic effects of NE in G0 HMECs.

93 We tested mAbs neutralize mitogenic effects of SEB in vitro and in vivo with T-cel

94 But while the mitogenic effects of Shh signaling have been confirmed i

95 PRD1-BF1 does not contribute to the mitogenic effects of VEGF, but directly represses genes

96 se BPA exerted c-Myc-dependent genotoxic and mitogenic effects on ERalpha-negative mammary cells.

97 producing IL-22 and IL-17, which have direct mitogenic effects on hepatocytes and promote a regenerat

98 Neuregulin1 (Nrg1), previously shown to have mitogenic effects on mammalian cardiomyocytes, is sharpl

99 PcRH had mitogenic effects on rat splenic lymphocytes.

100 iferation, we investigated whether insulin's mitogenic effects result from activation of Ca(2+)-signa

101 olypeptide hormones with potent anabolic and mitogenic effects that regulate cell growth and differen

102 ration, linking EGFR recycling to downstream mitogenic effects.

103 ons, specifically attributable to its potent mitogenic effects.

104 ough E-cadherin, which prevents secretion of mitogenic epidermal growth factors (EGFs) by repressing

105 resses ER-alpha36, retains responsiveness to mitogenic estrogen signaling.

106 Hypoxia-induced mitogenic factor (HIMF), also known as found in inflamma

107 s strains have genes encoding IgA proteases, mitogenic factor deoxyribonucleases, nickel/cobalt uptak

108 Activation of Akt by mitogenic factor depends on phosphatidylinositol 3-kinas

109 wth factor (EGF) is a potent chemotactic and mitogenic factor for epidermal keratinocytes, and these

110 This study demonstrates that GDNF is a mitogenic factor promoting self-renewal that is conserve

111 Although FGF1 is known as a mitogenic factor, FGF1 knockout mice develop insulin res

112 moattractant protein-1 and hypoxia-inducible mitogenic factor, in the murine model of hypoxic pulmona

113 ng inducer of the myelinating phenotype, and mitogenic factors activating receptor tyrosine kinases (

114 ascades lead to the downstream production of mitogenic factors and the proliferation of neighboring s

115 In parallel, the levels of several ASM mitogenic factors, including the PAR-2 ligands, mast cel

116 f fenestrations and expression of growth and mitogenic factors, leading to proliferative changes and

117 We conclude that although insulin is mitogenic for intestinal tumour cells in vitro, impaired

118 Serotonin (5-hydroxytryptamine, 5-HT) is mitogenic for several cell types including pulmonary art

119 indicate that NANOG has a lineage-restricted mitogenic function in stratified epithelia.

120 sults show FOXM1 to be a key mediator of the mitogenic functions of ERalpha and estrogen in breast ca

121 Quiescent beta-cells exposed to a mitogenic glucose stimulation require 8 h to enter the G

122 Contact inhibition is often antagonized by mitogenic growth factor signaling.

123 sm, inhibition of Hippo pathway signaling by mitogenic growth factors.

124 e expression program, and estrogen-dependent mitogenic growth.

125 lation of which is stimulated in response to mitogenic, growth, and nutritional stimuli, and proteins

126 We demonstrate in this study that this is a mitogenic human B cell response that occurs independentl

127 insulin-sensitizing action for exogenous non-mitogenic human FGF1 with therapeutic potential for the

128 subthreshold TCR signaling in the context of mitogenic IL-2 signals, thereby rendering CD8 T cells ex

129 lls, suggesting that integration of multiple mitogenic inputs may alter the minimal requirement for T

130 stringently between the insulin receptor and mitogenic insulin-like growth factor receptor.

131 mechanism responsible for the generation of mitogenic IR-A and provides a novel interplay between IR

132 ntrol of ENaC activity and the activation of mitogenic kinase pathways; (b) provide evidence for a Cy

133 s a proximal target for EET-activated ERK1/2 mitogenic kinases, (c) characterize a mechanistic common

134 ed by activation of Sestrin2, which impaired mitogenic mammalian target of rapamycin (mTOR) signaling

135 FR through early endosomes, thereby limiting mitogenic MAPK signals.

136 tor through early endosomes are accelerated, mitogenic MAPK-ERK1/2 signals are rapidly terminated, an

137 motes maturation of endosomes and shuts down mitogenic MAPK-ERK1/2 signals from endosomes.

138 ur data demonstrate that IL-1 functions as a mitogenic mediator of encephalitogenic Th17 cells rather

139 Moreover, the IGF-1-mediated mitogenic microglia response was reduced by N-glycosylat

140 tant roles of the TNF-alpha ligand Eiger and mitogenic molecules in mediating these interactions duri

141 atocyte growth factor, Met signaling confers mitogenic, morphogenic, and motogenic activity to variou

142 ges in expression of the proinflammatory and mitogenic neurokinin-1 receptor (NK-1R).

143 ) SCLC cells, an increased expression of the mitogenic neuropeptide receptors for gastrin-releasing p

144 nt kinase (CDK) complexes to be activated by mitogenic/oncogenic pathways.

145 of a bivalent signaling node that is either mitogenic or proapoptotic.

146 axon guidance; 2) some very highly expressed mitogenic pathway genes (e.g., Map2k1, Igf1r, Rara, Runx

147 rectly link a well-established developmental mitogenic pathway with a key tumor suppressor and contri

148 eraction with monocytes to activate distinct mitogenic pathways in T(reg) but not effector T cells.

149 Loss of these critical mitogenic pathways induces cell cycle arrest and cell de

150 by converting a transcriptional repressor of mitogenic pathways into a transcriptional activator.

151 tion 5a (Stat5a), factors that influence key mitogenic pathways that regulate normal mammary gland de

152 n intestinal epithelial cells and stimulates mitogenic pathways upon activation.

153 of adrenomedullin (Adm, gene; AM, protein)-a mitogenic peptide hormone required for normal cardiovasc

154 for producing active endothelin-1 (ET-1), a mitogenic peptide implicated in the aetiology of a numbe

155 In contrast, DLX3 loss promotes a mitogenic phenotype associated with constitutive activat

156 cardiomyocyte (CM) proliferation, but YAP's mitogenic potency declines postnatally.

157 Herein, we further characterize the mitogenic potential of TWEAK on central nervous system c

158 tion of furin reduces IRA maturation and its mitogenic potential without altering the insulin effects

159 exhibiting autocrine/paracrine activity and mitogenic potential.

160 al mediator of FGF19 action on metabolic and mitogenic programs; thus, the involvement of mTORC1 in F

161 However, the detailed mechanism behind mitogenic properties of PMT is unknown.

162 hat controls endocytosis, down-regulation of mitogenic receptors and cell migration.

163 is a common mechanism of down-regulation of mitogenic receptors.

164 reased hepatocyte proliferation; however, no mitogenic response in hepatocytes to T3 was evident in t

165 demonstrate that neuronal activity elicits a mitogenic response of neural progenitor cells and OPCs,

166 ily of Ca(2+)-regulated PDEs, also induced a mitogenic response to AVP in NHK cells, similar to the e

167 We have identified T3-induced hepatocyte mitogenic response to be mediated by PKA-dependent beta-

168 V3 by RNA interference markedly impaired the mitogenic response to CD3/CD28 stimulation.

169 y reflect the requirement for an exceptional mitogenic response to growth factor signalling in the af

170 re rapid VEGFR2 clustering and a more potent mitogenic response triggered by VEGF-A in respect to gre

171 ation of PDGF-beta receptor, and an enhanced mitogenic response, after PDGF-BB stimulation.

172 teractions of RNase L and TTP to attenuate a mitogenic response.

173 strating its functional role in limiting the mitogenic response.

174 weakly acting phytoestrogen that mimics the mitogenic responses produced by E2 in an ERalpha-depende

175 A mitogenic role for Shh in cvg progenitor proliferation w

176 cholinergic neurons, revealing an important mitogenic role for the planarian hh signaling molecule i

177 e transcriptional mechanisms underlying this mitogenic role remain to be defined.

178 rn of events given the pathway's established mitogenic role, and they show that Hedgehog pathway atte

179 prominent prosecretory, cytoprotective, and mitogenic role.

180 inases and transcription factors with myriad mitogenic roles in diverse cell types.

181 phingolipids ceramide and sphingosine to the mitogenic S1P, thereby determining the susceptibility of

182 port that the ER-transiting and functionally mitogenic secreted proenzyme (pCatD) form of cathepsin D

183 their activity is specifically uncoupled by mitogenic Shh signaling.

184 regulated in CF SMGs and that this sustained mitogenic signal alters properties of the SMG progenitor

185 Previously, we found that PACAP was an anti-mitogenic signal from embryonic day 13.5 (E13.5) onward

186 ator, mediates this differential response to mitogenic signal gradients.

187 Although insulin is a mitogenic signal in proliferative cells, whether compone

188 However, although the mitogenic signal resulted in a more sustained mRNA respo

189 r activation, and hydrogen peroxide-mediated mitogenic signal transduction.

190 kinase impaired ERBB3 (HER3) create a potent mitogenic signal, but the phosphorylation of ERBB2 in th

191 gulated and extended the transduction of the mitogenic signal, whereas silencing of LNK produced the

192 haplotype, thus leading to a higher ERalpha mitogenic signal.

193 broblasts function cooperatively to activate mitogenic signaling activities and to induce their trans

194 , we propose that cilia decapitation induces mitogenic signaling and constitutes a molecular link bet

195 Cav-1 may provide a mechanism for regulating mitogenic signaling and modulating the cell-surface pres

196 Because a connection between mitogenic signaling and myelin loss has been suggested,

197 feedback potently suppress ligand-dependent mitogenic signaling and Ras function.

198 These SMAPs attenuated mitogenic signaling and triggered apoptosis in KRAS-muta

199 c transcription factor, blocked Ras-mediated mitogenic signaling at the level of MEK through the dire

200 cell proliferation by induction of paracrine mitogenic signaling between heterogeneous malignant cell

201 control cells, which suggests modulation of mitogenic signaling by TIMP3 and the miRs.

202 ng membrane potential to control the gain in mitogenic signaling circuits.

203 /PDGF/FGF receptors is sufficient to inhibit mitogenic signaling in EC but not in fibroblasts.

204 nockdown or small-molecule targeting reduced mitogenic signaling in non-small cell lung cancer cell l

205 oviding novel insight into how cells inhibit mitogenic signaling in response to cell contact.

206 ation, but how membrane potential influences mitogenic signaling is uncertain.

207 Because aberrant mitogenic signaling may be associated with elevated canc

208 expression activates PI3K, a key node in the mitogenic signaling network known to promote malignancie

209 hinery is a major recipient of the principal mitogenic signaling networks involving Raf-ERK1/2 and ph

210 wever, understanding the compound effects of mitogenic signaling on the translation apparatus and on

211 ry of knowledge for beta-cell researchers on mitogenic signaling pathways and to emphasize how little

212 findings show that an important activity of mitogenic signaling pathways is to inactivate the growth

213 increased hHSC proliferation through several mitogenic signaling pathways such as EGFR, PI3K and p38.

214 d translocation but also from alterations in mitogenic signaling pathways that affect Myc levels thro

215 nduces hHSC fibrogenic activity via multiple mitogenic signaling pathways, and is upregulated in muri

216 Moreover, multiple mitogenic signaling pathways, including ERK MAPK, Wnt an

217 pressor proteins act to blunt the effects of mitogenic signaling pathways.

218 cell proliferation, tissue growth, and many mitogenic signaling pathways; we investigated its role i

219 Taken together, these results indicate that mitogenic signaling regulates the miRNA effector machine

220 ogenitors that are driven to proliferate via mitogenic signaling that affects translation.

221 cellular desmosomal adhesion, Dsg2 regulates mitogenic signaling that may promote cancer development

222 ling, contraction, intracellular Ca(2+), and mitogenic signaling were determined in vivo and in vitro

223 uce the maturation of IRA and its associated mitogenic signaling without altering the signals emanati

224 Reduced tumor growth, proliferation, mitogenic signaling, and apoptosis induction were observ

225 pletion reduces smooth muscle proliferation, mitogenic signaling, and extracellular matrix deposition

226 nic demonstrated RTK blockade, inhibition of mitogenic signaling, and proapoptotic signal induction i

227 in receptor, allowing aberrant activation of mitogenic signaling, promotes aberrant splicing and expr

228 ermal growth factor receptor (EGFR)-mediated mitogenic signaling, promoting tumor cell survival throu

229 hophysiologies associated with dysfunctional mitogenic signaling.

230 C complexes that lack GW182 are regulated by mitogenic signaling.

231 d in liver regeneration and their downstream mitogenic signaling.

232 ctors induces apoptosis passively by lack of mitogenic signaling.

233 lls are more responsive to Pten null-induced mitogenic signaling.

234 ipase D2 (PLD2) plays a key role in mTOR/S6K mitogenic signaling.

235 iency as a potential inhibitor of overactive mitogenic signaling.

236 R activity prevented angiotensin II-mediated mitogenic signalling and profibrogenic gene expression.

237 r's association with endosomes is prolonged, mitogenic signals (ERK 1/2, Src, and STAT5) are amplifie

238 mTORC1, regulates cell growth in response to mitogenic signals and amino acid availability.

239 Well-characterized germinal zones, mitogenic signals and cell types make the cerebellum an

240 hai or Galphas, Akt signaling is suppressed, mitogenic signals are enhanced due to delayed transit ti

241 and implicate tumor-associated DCs and their mitogenic signals as auspicious therapeutic targets.

242 77-eGFP, c-Myc protein expression integrates mitogenic signals downstream of both IL-2 and the TCR, y

243 pathway plays a critical role in transducing mitogenic signals from receptor tyrosine kinases.

244 vels allows effective integration of diverse mitogenic signals in ISCs to adapt their proliferative a

245 ral progenitor groups to broadly distributed mitogenic signals in the embryonic environment.

246 alpha(q) and its coupled receptors transduce mitogenic signals is still unclear because of the comple

247 The ultimate receptor of these mitogenic signals is the retinoblastoma (Rb) family of p

248 The mitogenic signals of IGF-1 are predominantly transduced

249 the connection between oxidative stress and mitogenic signals remains obscure.

250 to permeate neurofibroma tissue, mediate key mitogenic signals that contribute to vascular ingrowth,

251 r cells, as well as to normal cells, sending mitogenic signals that greatly enhance tumor growth.

252 plex) is poised to be activated by extrinsic mitogenic signals that impinge upon p27 at the earliest

253 tal for oncogenic signaling as it integrates mitogenic signals to amplify production of pro-growth an

254 mature myometrial or leiomyoma cells to send mitogenic signals to neighboring tissue stem cells in re

255 clin D-dependent kinases sense a plethora of mitogenic signals to orchestrate specific transcriptiona

256 MEKK2 integrates stress and mitogenic signals to the activation of NF-kappaB, JNK1/2

257 We show that Activin directly inhibits the mitogenic sonic hedgehog pathway in a Gli3-dependent man

258 by regulating splicing to suppress fibrosis, mitogenic splicing, and EMT.

259 rs can contribute to the proinflammatory and mitogenic status of resident mural cells.

260 ptor using short-hairpin RNA abolished PACAP mitogenic stimulation at E10.5.

261 Furthermore, in vitro mitogenic stimulation demonstrated that defective blasti

262 In vitro mitogenic stimulation of PBMCs resulted in upregulation

263 -associated HIV-1 RNA was detected following mitogenic stimulation of peripheral blood CD4(+) T cells

264 During mitogenic stimulation of primary lymphocytes, MYC promot

265 an invariant minimal threshold of cumulative mitogenic stimulation required for cell division.

266 e protein complexes that can be activated by mitogenic stimulation to repress mitogen-stimulated targ

267 Mitogenic stimulation triggers the binding of Tiam1 to t

268 We found that mitogenic stimulation with keratinocyte growth factor (K

269 ents were isolated and subjected to in vitro mitogenic stimulation with PMA and ionomycin.

270 The effects of mitogenic stimulation with teduglutide in patients with

271 These cells respond to antigenic and mitogenic stimulation, but are distinct from IL-9(+) Th2

272 and temporarily dissociated from mTORC1 upon mitogenic stimulation, suggesting a mechanism underlying

273 Indeed, following mitogenic stimulation, T cells lacking casp8 or its adap

274 sence of exogenous stimuli and in the T cell mitogenic stimulation.

275 recruited into RISC complexes subsequent to mitogenic stimulation.

276 BRE site in the Skp2 promoter in response to mitogenic stimulation.

277 als with the mTOR inhibitor rapamycin before mitogenic stimulation.

278 ls were capable of producing cytokines after mitogenic stimulation.

279 is required for cell division in response to mitogenic stimulation.

280 vels that permit rapid cell cycle entry upon mitogenic stimulation.

281 ted EAE monkeys were also less responsive to mitogenic stimulation.

282 IL-2, IFN-gamma, and TNF-alpha) responses to mitogenic stimulations prior to infection.

283 s protein degradation that is antagonized by mitogenic stimulations.

284 f cord blood mononuclear cells to innate and mitogenic stimuli (P = .0009), with an average 1.7- to 2

285 nt phosphorylation of Ser-247 was induced by mitogenic stimuli and required prior phosphorylation of

286 lar B lymphocytes were expanded by providing mitogenic stimuli and then challenged with KSHV-specific

287 A failure in the ability to respond to mitogenic stimuli can cause embryonic growth restriction

288 lucose oxidation and an enhanced response to mitogenic stimuli in comparison to hAFSCs.

289 The concentration of Ag or mitogenic stimuli is known to play an important role in

290 itutes a central node in the transmission of mitogenic stimuli to the cell cycle machinery.

291 proliferation depends on the integration of mitogenic stimuli with environmental conditions.

292 hese conditions, hPSC-CMs were refractory to mitogenic stimuli, and we found that key proliferation p

293 In response to mitogenic stimuli, rpS6 undergoes ordered C-terminal pho

294 he mTOR-S6K signaling pathway in response to mitogenic stimuli.

295 ulation thereby evoking sustained and robust mitogenic stimuli.

296 irus 8 (HHV-8) is believed to contribute via mitogenic, survival, and angiogenic activities to HHV-8-

297 nd cytokine secretion after stimulation with mitogenic, TLR, and T-cell stimuli by cytometric bead ar

298 ing growth factor-beta1 (TGF-beta1), LRG1 is mitogenic to endothelial cells and promotes angiogenesis

299 owing that old beta cells can respond to the mitogenic trigger of enhanced glycolysis.

300 regenerative potential and cannot respond to mitogenic triggers.