ライフサイエンスコーパス: be activated in

1 e provide evidence that the hedgehog pathway is activated in 20% of T-ALL samples.

2 The same PF3D7_1255200 var gene was activated in 4 different experimental infections.

3 we show that Shh and Bmp4 signaling pathways are activated in a complementary pattern along the oral-

4 Here, we show that although caspases are activated in a well-studied neoplastic tumor model i

5 s emerging that signal transduction elements are activated in a-nucleated erythrocytes in response to

6 This system can be activated in a convertase-independent manner from int

7 and involves approximately 10% of the genome being activated in a highly dynamic pattern.

8 vation has been proposed, in which PKGIalpha is activated in a cGMP-independent fashion via oxidation

9 The innate immune system is activated in a number of degenerative and inflammator

10 Moreover, Notch1 is activated in a small subset of SCC cells at the invas

11 in addition to canonical Hh signaling, GLI1 is activated in a Smoothened-independent manner.

12 chemically-induced injury, Ascl3 expression is activated in a subset of horizontal basal cells (HBCs

13 This cell subset is activated in a TCR-dependent and MHC-unrestricted fas

14 em2)(-/-) Tg-AD reveals that the DAM program is activated in a two-step process.

15 address this question, where the SHH pathway is activated in a very specific subset of cells lying ne

16 lones expressing an array of Vbeta receptors were activated in a dose-, time-, and processing-depende

17 Jag1 are expressed in, and Notch2 signaling is activated in, a subset of human HCC samples.

18 Inflammatory signaling is activated in ACM and drives key features of the disea

19 eroceptive insular cortex (a region known to be activated in acute MWD) also prevented the establishm

20 both vascular pathology and inflammation and is activated in AD patients and AD mice.

21 Here we report that p38 signaling is activated in adult Drosophila midgut enterocytes in r

22 A third IL17 subfamily is activated in adult immune cells indicating that expre

23 This AMPK-PDHc axis is activated in advanced breast cancer and predicts poor

24 quadripolar biventricular single-site pacing was activated in all patients (n=506).

25 After this visit, both leads were activated in all patients for an additional 3 month

26 ment groups for 6 months, after which alarms were activated in all subjects (Alarms ON).

27 tment group for 6 months, after which alarms were activated in all subjects.

28 The complement pathway is activated in Alzheimer's disease.

29 er spinal cord injury (SCI), meningeal ILC2s are activated in an IL-33-dependent manner, producing ty

30 us-infected patients, the host immune system is activated in an uncontrolled manner and is unable to

31 The WNT signaling pathway is activated in APAs.

32 they have restricted mobility but reside and are activated in apposition to CX3CR1(+) macrophages.

33 The PI3K pathway is activated in approximately 70% of breast cancers.

34 post infection, indicating that ET signaling was activated in Arabidopsis early by SCN infection.

35 trast, no new cohesion is detected when Rec8 is activated in arrested oocytes by tamoxifen despite co

36 over PI3K/AKT2 as a direct PDGFA target that is activated in ASCs during WAT hyperplasia and is funct

37 We conclude that HIF1alpha is activated in ATII cells after lung injury and promote

38 , a cytosolic sensor of double-stranded DNA, is activated in autoinflammatory disorders and by DNA da

39 We show that this network is activated in Barrett's esophagus, the putative precur

40 We establish that beta-catenin signaling is activated in basal cells during early pregnancy, and

41 gene encoding the nuclear receptor PPARgamma is activated in bladder cancer, either directly by gene

42 In the infarcted heart, Smad3 signaling is activated in both cardiomyocytes and interstitial cel

43 Intriguingly, although NFAT is activated in both DLBCL subtypes, long-term calcineur

44 ike endoplasmic reticulum (ER) kinase (PERK) was activated in both intact and Gcn2(-/-) mice.

45 The autophagy and proteasome pathways were activated in both muscles at varying intensities ov

46 Several inflammatory pathways were activated in both subtypes.

47 rvation suggests that dopamine receptors may be activated in breast cancers, and is the first time to

48 Its expression is activated in breast cancers, where high tumor levels

49 y contrast, the Notch, Wnt and EGFR pathways were activated in BSCs and their progeny after LC ablati

50 Intriguingly, meiosis-specific genes are activated in C. neoformans and contribute to ploidy

51 iopsies showing chronic rejection, caspase-1 is activated in C4d(+) ECs of interstitial microvessels,

52 We report here a mechanism by which they are activated in cancer cells, involving release of the

53 these stress response factors, many of which are activated in cancer.

54 These results show that PP2A can be activated in cancer cells to inhibit proliferation.

55 Furthermore, this pathway is activated in cancer cells, and correlates with pro-in

56 We show that the MRTF-SRF pathway is activated in cancer-associated fibroblasts (CAFs).

57 c-MET receptors are activated in cancers through genomic events like tyr

58 NF2 was activated in cardiomyocytes subjected to H2O2 and in

59 expression demonstrated that the Hh pathway is activated in CD34(+) CP-CML stem/progenitor cells.

60 edia, whereas transcription of MDH1 and MDH2 is activated in cells cultured in YNB + Glu but not in Y

61 Although nuclear factor-kappaB is activated in cells from patients with inflammatory di

62 how that the aryl hydrocarbon receptor (AhR) is activated in cells infected with a prototypic coronav

63 Here, we show that AhR is activated in cells infected with mouse hepatitis viru

64 tiapoptotic, prometastatic JAK-STAT3 pathway was activated in chemoresistant tumors, and treatment wi

65 Many enzymes are activated in chemotransduction to hydrolyze ATP.

66 Here we show that both pathways are activated in chondrocytes after treatment with TGF-b

67 In addition, this pathway is activated in chondrocytes by FGF signaling, a critica

68 We demonstrate that PRC2 is activated in cis by the unmodified side chain of H3K3

69 , we evaluate whether the kynurenine pathway is activated in clinical HAT and associated with CNS inf

70 The Trp-Kyn-NAD+ pathway is activated in CNS infections and provides highly accur

71 o1-CIN tissues upregulated pathways known to be activated in colon cancer, including lipid metabolism

72 ian olfactory system have long been known to be activated in combinatorial fashion by odorants.

73 rget of rapamycin complex 1 (mTORC1) pathway was activated in Cpt2M(-/-) hearts; however, daily rapam

74 HSCs were activated in culture and used in array analyses of

75 Subsequently, Wnt/beta-catenin signaling is activated in cushion mesenchymal cells where it suppo

76 of home-cage mice to a novel stimulus, SINEs are activated in dentate granule neurons in a time cours

77 Both lipid metabolism and lipid synthesis are activated in DENV-infected cells, so we used lipid s

78 Villin-CreER(T2) was activated in developed tumors by administration of t

79 While retrotransposons must be activated in developing germ cells in order to surviv

80 e time, the BMP signal transducers SMAD1/5/8 were activated in developing coronary arteries.

81 and why the integrated stress response (ISR) is activated in different forms of neurodegeneration rem

82 Differential genetic programs are activated in each cell type to construct functionall

83 DDK, despite being activated in early S phase, does not phosphorylate

84 levels are increased in ECs, stress pathways are activated in ECs, and ISCs overproliferate.

85 Both Pdgfrb and Igf1r were activated in ex vivo T-ALL cells, and coculture wit

86 otein kinase kinase kinase kinase-4 (MAP4K4) is activated in failing human hearts and relevant rodent

87 mapping suggested dorsal horn laminae II-IV was activated in females but showed net inhibition in ma

88 We show that JUN is activated in fibrotic fibroblasts that expressed incr

89 Both AMPK and mTORC1 were activated in Fnip1-deficient B cell progenitors.

90 As complement is activated in food-induced anaphylaxis, we aimed to as

91 ducer and activator of transcription pathway is activated in GA, likely in part through the activity

92 numerous genes that control inflammation and is activated in glomerular cells in glomerulonephritis (

93 the present study, we showed that ER stress was activated in granulosa cells of PCOS patients as wel

94 The renin-angiotensin system (RAS) is activated in heart failure (HF) and inhibition of RAS

95 amplified in many types of cancer cells and is activated in hepatocellular carcinomas (HCCs) from pa

96 We found that YAP/TAZ were activated in hepatocytes in response to carbon tetr

97 silent in the genome, this group of viruses is activated in HIV-1-infected and cancer cells.

98 Importantly, BCAT1 expression not only is activated in human blast crisis CML and de novo acute

99 -MAP kinase pathway and because this pathway is activated in human cancers, we asked whether phosphor

100 n patients with AAV indicated that NF-kappaB is activated in human NCGN also.

101 Here, we report that STAT3 is activated in infiltrating monocytic cells near active

102 scle cells of the human intestinal tract and is activated in inflamed and fibrotic tissue.

103 Here, we show ATP citrate lyase (Acly) to be activated in inflammatory macrophages and human ather

104 We found that Ikkepsilon was activated in intestinal tumors forming upon loss of

105 In this study, we found that caspase-3 is activated in L88 bone marrow stroma cell-derived exos

106 nuclease inositol-requiring enzyme 1 (IRE1), is activated in lipid-laden macrophages that infiltrate

107 A bidirectional response is activated in <5 min of training, in which phosphoryla

108 rate that the canonical Hh signaling pathway is activated in lung stroma by Hh ligands secreted from

109 rd reduces expression in vitro of genes that are activated in M2-biased macrophages; however, the mut

110 arkinson's disease (PD)-related kinase LRRK2 is activated in macrophages by pathogen- or sterile-indu

111 Hippo pathway is activated in major cellular components of the blood-b

112 SCF E3 ligases are activated in many cancers and inhibitors could have

113 mponents of the MAPK signaling pathway which is activated in many cancer types.

114 The Hedgehog (Hh) signaling pathway is activated in many cancers and is a promising target f

115 Although the UPR is activated in many cancers, its effects on tumor growt

116 er organisms, one Notch-responsive gene that is activated in many different cell types encodes the No

117 Further, MEILB2-BRME1 is activated in many human cancers, and somatically expr

118 sis of epithelial barrier tissues; how MASPs are activated in mature epithelia is unknown.

119 Here, we show that, when ERK1/2 are activated in mature quiescent oligodendrocytes durin

120 Abl kinases (Abl/Arg) are activated in melanomas and drive progression; howeve

121 cell migration as a key molecular event that is activated in mesenchymal progenitors in response to e

122 cal adhesion formation and FAK/SRC signaling is activated in mesenchymal tumor cells by crosslinked c

123 noma metastases and delineates pathways that are activated in metastases that could be targeted in co

124 We previously showed that beta1 integrins are activated in metastatic prostate cancer (PCa) cells,

125 We show that CGRP(PBN) neurons are activated in mice implanted with Lewis lung carcinom

126 In both ICH models, STAT6 was activated in microglia/macrophages (i.e., enhanced e

127 , and calmodulin-dependent protein kinase II-were activated in MO fetuses.

128 egulation of critical cellular processes and is activated in more than 30% of human cancers.

129 Oncogenic NOTCH signaling, which is activated in more than 65% of T-ALL patients by activ

130 In these studies, we show that RA signaling is activated in mouse and zebrafish models of AKI, and t

131 We found that Jak/Stat-signaling is activated in Muller glia in response to NMDA-induced

132 1 knockouts, indicating that the endocardium is activated in multiple cases where sinus venosus angio

133 data demonstrate that the NOD2-RIP2 pathway is activated in murine and human VL and plays a role in

134 ived growth factor (PDGF) signalling pathway is activated in mutant iPSC-CMs compared to isogenic con

135 activated kinase (AMPK), a metabolic sensor, was activated in myotubes exposed to high CO2, and loss-

136 quires intact TLR9, but how the TLR9 pathway is activated in NASH is not clear.

137 These findings suggest that Edn signalling was activated in NCCs before duplication of the vertebra

138 c family kinase (SFK) signaling pathway that is activated in neighbor cells when the apoptotic cell r

139 We found that these channels can be activated in neurons of the medial nucleus of the tra

140 We found that Cdc25A is activated in neurons undergoing ischemic stress media

141 ow mechanistic target of rapamycin complex 1 is activated in neuropathic pain pointing to a key role

142 oot cap regulators SOMBRERO and BEARSKIN1/2, are activated in nlp7-1 seedlings.

143 m of the large, membrane fission GTPase, can be activated in nonneuronal cells downstream of cancer-r

144 nscriptional activity and a stemness program-were activated in nonresponders.

145 To identify whether striatal brain regions are activated in Npas2 mutant females, we measured cocai

146 lays a vital role in cell cycle progression, is activated in numerous human malignancies, and is link

147 STATEMENT Nuclear factor kappaB (NF-kappaB) is activated in oligodendrocytes in multiple sclerosis (

148 KRAS GTPases are activated in one-third of cancers, and KRAS(G12C) is

149 The AKT pathway was activated in one subtype while MAP kinase pathway wa

150 Lgmn was activated in OSCC patient tumors, compared with matc

151 Hedgehog signaling is activated in osteoarthritis, where it promotes chondr

152 kinase Src promotes osteoclast activity and is activated in osteoclasts by the receptor-type tyrosin

153 In addition, proapoptotic pathways are activated in P1 knock-in premegakaryocyte/erythroid

154 SPHK1/Akt/NF-kappaB signaling pathway, which is activated in pancreatic cancer.

155 We also reveal that ATM is activated in pancreatic precancerous lesions in the c

156 ormal adult lymphatic endothelial cells, but is activated in pathological situations such as inflamma

157 sion programs that promote cancer initiation are activated in patients with lung cancer depending on

158 We found here that although MSKs are activated in peritoneal B cells in response to TLR4

159 In nature, this strategy may be activated in phytochrome-disabling, vegetation-dense

160 gen-specific B lymphocytes and T lymphocytes are activated in piperacillin-hypersensitive patients.

161 Our studies revealed that SPT known to be activated in planta to SPT-enol acts as a development

162 The unfolded protein response (UPR) is activated in plants in response to endoplasmic reticu

163 We found that necroptosis was activated in postmortem human AD brains, positively

164 memories, nerve cells in the cerebral cortex are activated in precisely timed sequences.

165 NR1D1 was activated in primary mouse and human macrophages by

166 thermore, we confirm that BMP/SMAD signaling is activated in protocol pancreas allograft biopsies fro

167 roblastoma RAS viral oncogene homolog (NRAS) is activated in PSC cholangiocytes.

168 istence of enhancer regulatory elements that are activated in regenerating tissue.

169 murine leukemia virus envelope protein (Env) are activated in relation to each other, sequentially or

170 of recent interest to understand how AGPCRs are activated in relation to their two-fragment topologi

171 The NLRP3 inflammasome can indeed be activated in resident macrophage/monocyte-like cells

172 These kinases are activated in response to cellular stress signals, bu

173 tant sentinels of innate immune defence that are activated in response to diverse stimuli, including

174 We report here that mTORC1 and mTORC2 are activated in response to exogenously supplied fatty

175 em cell population in adult skeletal muscle, are activated in response to hypertrophic stimuli and gi

176 8(MAPK) molecules and 36.5% of MK2 molecules are activated in response to IL-1beta.

177 In the CNS, microglia are activated in response to injury or infection and in

178 ctivated kinase (PAK) isoforms PAK1 and PAK2 are activated in response to insulin in skeletal muscle

179 lammatory caspases (caspases 1, 4, 5 and 11) are activated in response to microbial infection and dan

180 and the associated ribosome-quality control are activated in response to nucleobase alkylation and o

181 These promoters are activated in response to unique signals.

182 HSCs) are dormant in the bone marrow and can be activated in response to diverse stresses to replenis

183 alateral prefrontal cortex are also shown to be activated in response to INMS.

184 omponent of the innate immune system and can be activated in response to microbial and endogenous dan

185 diated proteasome degradation mechanism that is activated in response to abnormal Ca(2+) homeostasis.

186 Chaperone-mediated autophagy (CMA) is activated in response to cellular stressors to preven

187 The p38/MK2 pathway is activated in response to cellular stressors, includin

188 However, the mechanism by which p53 is activated in response to centrosome loss remains unkn

189 The allelochemical DIMBOA gene cluster is activated in response to co-cultivation with rice, wh

190 The integrated stress response (ISR) is activated in response to diverse stress stimuli to ma

191 The non-receptor tyrosine kinase c-Abl is activated in response to DNA damage and induces p73-d

192 f human ataxia telangiectasia-mutated (ATM), is activated in response to DNA double-strand breaks.

193 The DNA damage checkpoint pathway is activated in response to DNA lesions and replication

194 The RNF168 E3 ubiquitin ligase is activated in response to double stranded DNA breaks (

195 trast, the lipogenic transcriptional program is activated in response to fructose in a manner that is

196 l (HOG) stress-activated protein kinase Hog1 is activated in response to hyperosmotic stress, inducin

197 sive Polycomb complexes in growing cells but is activated in response to oncogenic stress.

198 Autophagy is activated in response to stress, but its regulation i

199 Alkaloid accumulation in plants is activated in response to stress, is limited in distri

200 p38 MAPK signaling is activated in response to stretch, and inhibition of p

201 cell line and animal models showed that Pak1 is activated in response to UV-B radiation, and this act

202 es unfolded protein response genes(2,3)-that was activated in response to IL-15 in human NK cells.

203 Here, we found that ROCK2 was activated in response to key T cell signals like CD4

204 he noncanonical 5' cap-binding protein eIF3d was activated in response to metabolic stress in human c

205 This biosensor was activated in response to various inflammatory stimul

206 RNase L was activated in response to ZIKV infection, which degra

207 n-activated protein kinase kinase-1 (MEKK-1) were activated in response to TNF-alpha.

208 l phenotype and DNA damage response pathways are activated in RPV-stratified tumors.

209 Yap and Taz are activated in Schwann cells by mechanical stimuli and

210 onstrates that oncogenic ErbB2 signaling can be activated in SCs but not impede transdifferentiation

211 filtrated by inflammatory macrophages, which are activated in situ by RBC transfusions via a Toll-lik

212 Here we show that complement is activated in skeletal muscle injury and plays a key r

213 nfiguration and proximal or distal geometry, were activated in solution by ultrasound-generated elong

214 particular NADPH oxidase (NOX) isoforms that are activated in specific cardiovascular diseases.

215 used to create SPECS for gene therapies that are activated in specific cell states, as well as to stu

216 he host epigenetic surveillance, this family is activated in specific meristematic areas fundamental

217 Both ER and mitochondrial stress responses are activated in sqrd-1 mutant animals exposed to H2S, b

218 In a mouse model in which both pathways are activated in stem and progenitor cells, LSCs expande

219 gellar synthesis showed that flagellar genes are activated in stochastic pulses without the means of

220 ulation of the right and left phrenic nerves were activated in synchrony with mechanically ventilated

221 The mechanism by which mast cells (MCs) are activated in T cell-mediated inflammatory processes

222 NF-kappaB was activated in T cells by inducing the expression of a

223 pathways linked to epigenetic reprogramming were activated in TBDM above levels observed with DM alo

224 Human and mouse CD4 T cells were activated in Th1, Th2, Th17, or regulatory T cell (

225 fied a group of CTNNB1/TCF target genes that are activated in the absence of TCF7L1, including EPHB3,

226 ests that serine-aspartyl proteases-caspases are activated in the AD brain.

227 tes are pivotal in this process because they are activated in the attempt to digest Abeta which start

228 farnesoid X receptor (FXR, encoded by NR1H4) are activated in the liver in the fasted and fed state,

229 ase- and oxidative stress-dependent pathways are activated in the lung tissue of C57/BL6J-betaENaC-Tg

230 al nervous system tumors and found that MNKs are activated in the majority of tumors tested.

231 mmune encephalitis (EAE), autoimmune T cells are activated in the periphery before they home to the C

232 ation and cytokine production when basophils are activated in the presence of CD300c cross-linking co

233 effectors downstream of Rho, MRTF and YAP1, are activated in the Rho(High) BRAFi-resistant cell line

234 ory can be induced when alloreactive T cells are activated in the setting of tolerance.

235 We examined whether macrophages are activated in the skin of imiquimod (IMQ)-treated mic

236 Intriguingly, TEs are activated in the sperm companion cell - vegetative c

237 Furthermore, it can be activated in the cytosol by mitochondrial oxidative s

238 first time that this prominent catalyst can be activated in the dark even when electrically insulate

239 and this downstream axis were also found to be activated in the human ex vivo vein graft pathologica

240 low and it is unclear how Ca(2+) release can be activated in the interior of atrial cells.

241 ising subpopulations that have been found to be activated in the stromal microenvironment that regula

242 dings suggest that the CgA-angiogenic switch is activated in the BM of multiple myeloma patients and

243 Our studies demonstrate that p53 is activated in the brain following reovirus infection a

244 Here we show that IIS is activated in the cells surrounding an epidermal wound

245 nistic study reveals that each N(2) molecule is activated in the confined region between cluster and

246 In wild-type cells, GSR transcription is activated in the dark and nearly off in the light, an

247 Our results indicate that endogenous YAP is activated in the heart during acute PO.

248 WT1 is activated in the hippocampus following induction of l

249 cess, whereas APOBEC signature targeting C>G is activated in the intermediate phase of disease progre

250 ke; inflammatory and growth factor signaling is activated in the later stage of limited OPC different

251 The MAPK pathway is activated in the majority of melanomas and is the tar

252 system, the human sex-determining gene hSRY is activated in the single-cell embryos of the mouse.

253 Tryptophanase is activated in the stationary phase by the stationary-p

254 EGFR is activated in the ventral midline and neurogenic ectod

255 ignaling network that maintains proteostasis-was activated in the brains of DS mice and individuals w

256 GUS fusion assays we established that miR827 was activated in the initial feeding cells and this acti

257 LBOW was activated in the intestinal epithelium, and a year-l

258 ated in one subtype while MAP kinase pathway was activated in the other.

259 Here, we found that the mTOR pathway was activated in the parathyroid of rats with secondary

260 (RGD)-binding alphaPAT-2/betaPAT-3 integrin was activated in the pharynx and recruited high levels o

261 that highly relevant immunological pathways were activated in the animal which experienced late graf

262 sical complement pathway associated proteins were activated in the glaucoma samples suggesting an inn

263 orated the finding that immune-related genes were activated in the LV but not in the RV during storag

264 However, WFV cells were activated in the most uniform manner; 85% of these

265 IL1RAP CAR T cells were activated in the presence of IL1RAP(+) cell lines o

266 When naive Th cells were activated in the presence of various cytokines, we

267 ytokine production is regulated, ILC subsets were activated in the presence or absence of the immunor

268 entially expressed and 94 signaling pathways were activated in the topical MSCs transplanted onto the

269 in the hearing condition at those sites that were activated in the two conditions.

270 le a generally lower number of brain regions were activated in the zebra finch.

271 egulated in daughters of overweight fathers, was activated in their mammary tissues and tumors.

272 oints, and that different metabolic pathways were activated in their transcriptomes.

273 gation in megakaryocytes, an endomitotic SAC is activated in these cells upon Plk1 inhibition.

274 However, the immune receptors that are activated in this context remain elusive.

275 at the level of activation, but how TGF-beta is activated in this disease is unknown.

276 It is not clear how ARL-8 is activated in this process.

277 How the inflammasome is activated in this untreatable disease is largely unkn

278 uring cisplatin therapy, antitumour immunity was activated in this poorly immunogenic breast cancer m

279 anaerobe nanovesicle mimic that can not only be activated in THRs but also induce hypoxia in tumors b

280 (ER) stress-induced ATF4-CHOP-GADD34 pathway is activated in TM of human and mouse glaucoma.

281 mTORC2 is activated in TMEM127-deficient hepatocytes suggesting

282 nd other Treg cell signature genes, began to be activated in Treg precursor cells.

283 We found that GLI1 is activated in triple-negative breast cancer cells in r

284 use and contains multiple MYC enhancers that are activated in tumor cells.

285 RhoA is activated in tumors from neuroblastoma patients, and

286 cytidine deaminase-induced mutagenesis might be activated in tumourigenesis and limited therapeutical

287 In vivo, we demonstrate NLRP3 is activated in urothelia from a genetic type 1 diabetic

288 iety of DNA repair mechanisms, many of which are activated in vascular disease.

289 e we show that about 100 heterochromatic TEs are activated in VCs, mostly by DEMETER-catalyzed DNA de

290 L is an IFN-regulated endoribonuclease that is activated in virus-infected cells and cleaves single-

291 al assays show that the sweet taste receptor is activated in vitro by a new scaffold of natural compo

292 Thus, we found that when donor cells were activated in vitro and injected intraperitoneally,

293 Macrophages were activated in vitro by the venom, becoming more phag

294 Human CD19(+) B cells were activated in vitro in the presence or absence of 9c

295 In the current study, human neutrophils were activated in vitro with immobilized extracellular m

296 Artemisinin (ART)-class drugs are activated in vivo by newly released heme, which crea

297 n complex theories as to how these receptors are activated in vivo, complicating pharmacological adva

298 rial diseases, we show that the ATF4 pathway is activated in vivo upon mitochondrial stress.

299 in vitro and injected intraperitoneally, or were activated in vivo, they migrated simultaneously to

300 Previously we demonstrated that FOXO1 was activated in wound healing but to higher levels in d