ライフサイエンスコーパス: induction

1 and increased beta-sheet formation upon heat induction.

2 upport optimal inclusion development and EMT induction.

3 ression signatures associated with tolerance induction.

4 lic acid (TCA) cycle function and metabolite induction.

5 cotyledonous plants through de novo meristem induction.

6 nse to T. virens colonization results in ISR induction.

7 real ligands inverts the sense of asymmetric induction.

8 binutuzumab- or rituximab-based chemotherapy induction.

9 6V mutation is responsible for defective SHM induction.

10 ntified a new pathway regulating tendon cell induction.

11 ped lung adenocarcinomas following transgene induction.

12 c-Fos proteins, without affecting their mRNA induction.

13 e cross-over point for majority via external induction.

14 ming Growth Factor beta (TGF-beta1)-mediated induction.

15 ular transformation through autophagic death induction.

16 nhibited cAMP and GH and reversed DNA damage induction.

17 talysts capable of high levels of asymmetric induction.

18 e marrow transplantation (BMT) for tolerance induction.

19 tem (FS) cells respond directly to germ cell induction.

20 fat1Delta mutant, likely accounting for UPR induction.

21 UPR) signaling and cell death upon ER stress induction.

22 comitant increase in MED12 enrichment during induction.

23 es of different signalling mechanisms in LTP induction.

24 still on study treatment) were high at post-induction (431 [84%] of 513 vs 405 [80%] of 509) and pos

25 ing donors (26% vs 20%), and lymphodepleting induction (64% vs 46%) compared to the SC group.

26 ted hypertension, miR-214 showed the highest induction (8-fold, P=0.0001).

27 At end-induction, 98.8% of evaluable participants had at least

28 erimental autoimmune encephalomyelitis (EAE) induction, a model that is frequently used to study infl

29 n all H2B-FP transgenes independent of label induction, accumulated with age in HSCs with high repopu

30 , was significantly more active in apoptosis induction, activation of caspase 3/7, and formation of D

31 between tonsillar TFH-cell and systemic IgG induction after LAIV.

32 work has uncovered a role for B cells in the induction and activation of Tregs during FV infection.

33 her decipher the role of phytohormones in BS induction and BS symptom development.

34 c strain combinations and analyzed for FoxP3 induction and functionality.

35 issue explants, prepared prior to germ layer induction and lacking extraembryonic tissues, can specif

36 rative efficacy of different medications for induction and maintenance of remission in patients with

37 mprovement in disease activity at the end of induction and maintenance studies.

38 ificant cause of immune suppression via HO-1 induction and may underlie the susceptibility of these i

39 let cell grafts under antithymocyte globulin induction and mycophenolate mofetil-tacrolimus maintenan

40 ze that phytohormones are key players for BS induction and suppress the expression of switch genes at

41 AR-alpha as a critical control point for the induction and the resolution of inflammation and to NAAA

42 The more reliable PTB induction and uniform uterine exposure provided by this

43 ted TGF-beta family signaling relying on the induction and utilization of activin A signaling.

44 (177)Lu-DOTATATE uptake and gammaH2AX focus induction between different regions of CA20948 xenograft

45 uced phospho-ERK activation and Egr-1/Zif268 induction, but without effect on the cocaine-induced beh

46 cellular manganese efflux and that Slc30a10 induction by BA pools is driven primarily by lithocholic

47 se technologies collectively as Dynamic Cyan Induction by Functional Integrated Receptors, or DCyFIR.

48 We then tested the prediction that NQO1 induction by pharmacological activation of the transcrip

49 s Socs1 m(6)A methylation and sustains SOCS1 induction by promoting Fto mRNA degradation, and forced

50 imination of xenobiotics, and it is prone to induction by xenobiotics, including phenobarbital via co

51 tive (ND) virus genomes and activate the IFN-induction cascade before ND PIV5 can block the productio

52 lock the ability of DVGs to activate the IFN-induction cascade.

53 baseline until neutrophil recovery following induction chemotherapy (IC) in 97 AML patients.

54 ntrol consisted of surgical resection during induction chemotherapy and radiotherapy after last SCT.

55 nt and concordant response assessments after induction chemotherapy were evaluated with the Wilcoxon

56 ced mTORC1 inhibition was not related to ROS induction, copper chelation, or PP2A activation.

57 ignificant factors for response after 1 or 2 induction cycles were ELN risk group and white blood cel

58 st in isochorismate synthase1/salicylic acid induction deficient2 and nonexpressor of pathogenesis-re

59 Photosynthetic induction describes the transient increase in leaf CO(2)

60 However, competence induction during host infection has not been examined.

61 During induction, efficiency is lower than at steady state.

62 innovative wireless system based on magnetic induction for human activity recognition to tackle these

63 they describe with only three parameters the induction-force-distance relationship, enabling accurate

64 hnologies could use in vivo paternal haploid induction (HI), which occurs when double fertilization p

65 There is scant data on the use of induction immunosuppression for simultaneous liver/kidne

66 hesized to serve as the basis for asymmetric induction in a subsequent C-N bond forming step, achievi

67 The mode of asymmetric induction in an enantioselective intramolecular allylic

68 MG53 inhibits IFNbeta induction in an RyR-dependent manner.

69 equently, this inhibits STAT1-mediated IL-12 induction in macrophages & STAT4-mediated IFN-gamma synt

70 ICH induction in male mice caused profound HN loss in the af

71 pressed on maturation, concomitant with Mxd1 induction in mature cDC1s.

72 cting cell proliferation, cell death, or UPR induction in murine myeloblast 32D and human promyelocyt

73 rescued gonad development but not germ cell induction in Tfap2 mutants.

74 a formation and inducible NO synthase (iNOS) induction, increased dissemination of bacteria throughou

75 RNA editing activity leads to innate immune induction, indicating that Drosophila Adar, despite bein

76 Sputum induction is a non-invasive method to evaluate the airwa

77 Egr2 induction is evolutionarily conserved during alternative

78 nclude that m(6)A methylation-mediated SOCS1 induction is required to maintain the negative feedback

79 chieve chirality-selective synthesis (chiral induction) is of great importance in stereochemistry, mo

80 This study analyzed transcriptional induction kinetics, chromosome looping, and enhancer RNA

81 BMP-2 induction leads to the expression of inhibitory Smad 6/7

82 ntiviral responses.IMPORTANCE IFN-alpha/beta induction limits CNS viral spread by establishing an ant

83 parameters are drastically altered with ATG induction, long-term clinical benefits remain unclear in

84 This was associated with an induction of a 48-kDa active beta-catenin with a preserv

85 e gammaherpesvirus MHV68 leads to a dramatic induction of a class of noncoding retrotransposons calle

86 hnique that destroys malignant cells through induction of a locoregional pH change.

87 Across all subjects, early induction of a minimal set of nasal cytokines that discr

88 legans activates RNAi-directed silencing via induction of a pathway homologous to the mammalian RIG-I

89 on, chemotaxis, and cell adhesion as well as induction of a proinflammatory and proadipogenic signatu

90 AF1/CIP1, which are findings consistent with induction of a response to DNA damage.

91 After induction of a specific context, I measured peri-saccadi

92 Tregs require Foxp3 expression and induction of a specific DNA hypomethylation signature du

93 T cell expansion, surprisingly causes robust induction of a suite of inflammatory factors.

94 Dynamic induction of ABCB1 by diverse stressors, including chemo

95 Genetic induction of active IL1beta or pharmacologic inflammasom

96 The induction of actomyosin relaxation by t-ASPP2 was depend

97 CD11c-expressing IMs are sufficient for the induction of acute T(H)2-cell responses in the lungs tha

98 ll (DC) maturation is a prerequisite for the induction of adaptive immune responses against pathogens

99 recent years as potential adjuvants for the induction of adaptive immune responses.

100 Furthermore, effects of coffee on induction of AHR- and Nrf2-pathway genes in Caco-2 cells

101 t and stem-like phenotypes via transcription induction of AKT co-activator TCL1A by NANOG.

102 l death is often closely associated with the induction of an immune response.

103 equently GM2/GD2, enhanced tumorigenesis via induction of angiogenesis, AIG, and cell motility.

104 Ms) that promote disease progression through induction of angiogenesis, tissue remodeling, and suppre

105 The induction of anti-CSP antibodies is important for protec

106 , as evidenced by detection of viral RNA and induction of anti-nucleoprotein antibodies after SARS-Co

107 l-like receptor 7 (TLR7) is essential in the induction of anti-RABV antibodies via the facilitation o

108 unable to bind to p53 thereby preventing the induction of antiangiogenic factors.

109 vity, both likely compromised because of the induction of antibodies that did not bind FCGR3A.

110 Env gp140 protein vaccines and assessed the induction of antibody responses and a putative protectiv

111 dies describe a platform for the therapeutic induction of antigen-specific tolerance in autoimmune di

112 esulting in inhibition of FAK/Src signaling, induction of apoptosis and re-sensitization to chemother

113 silencing a gene (caspase-3) responsible for induction of apoptosis.

114 bation of cell cycle progression rather than induction of apoptosis.

115 e signatures associated with redox dependent induction of ASK1 and activation of stress kinases p38 a

116 33/ST2 pathway play an important role in the induction of asthma-like phenotype.

117 Comparing the time course of induction of ATF6 and XBP1 targets suggested that the tw

118 Inhibition of Xbp1 splicing did not decrease induction of ATF6alpha targets.

119 Hypoxia-mediated induction of ATG9A was lost in cells lacking HIF-1.

120 cteristic neuroendocrine features of MCC via induction of ATOH1; thus, ATOH1 can be regarded as a lin

121 ethionine depletion, global hypomethylation, induction of autophagy, and robust poly(ADP-ribose) poly

122 l for class switching and contributes to the induction of B effector 2 (Be2) cells.

123 resistant to venetoclax due to CD40-mediated induction of Bcl-XL, Mcl-1, and Bfl-1.

124 ntal pulp stem cells via STAT3 signaling and induction of Bmi-1.

125 The induction of broadly neutralizing antibodies (bNAbs) is

126 Thus, by controlling the induction of C/EBPbeta and C/EBPdelta, PAGR1 plays a cri

127 ssion enhances beta-cell replication without induction of cell death or loss of insulin secretion, su

128 ion during both fetal and adult life without induction of cell death or proplatelet formation.

129 rough a variety of mechanisms, including the induction of cell death.

130 how that de novo formation of acini involves induction of cellular plasticity in multiple non-acinar

131 e to SARS-CoV-2 infection, and showed robust induction of chemokines following SARS-CoV-2 infection,

132 found that PRMT5 promoted SREBP1 SDM and the induction of cholesterol biosynthetic pathway enzymes th

133 Induction of cholesterol secretion was not a consequence

134 n facilitate disease progression whereas the induction of cortical gamma oscillations can reduce amyl

135 In contrast, induction of cydDC sensitizes cells to oxidative stress

136 Here, we report that age-dependent induction of cytokine unpaired 3 (upd3) in Drosophila oe

137 tive IL-22 signal transduction, indicated by induction of cytokine-dependent cellular proliferation,

138 This divergent expression and induction of cytokines appears to result from cell type-

139 d calcium influx and concentration-dependent induction of degranulation.

140 neuronal or astrocytic injury/activation or induction of dementia-related brain pathologies by the i

141 serving modest and statistically significant induction of desensitization, highest in children ages 4

142 We studied GLS2 expression after induction of differentiation with phorbol ester (PMA) an

143 urthermore, proteomics analyses revealed the induction of distinct proteins in dexamethasone-treated

144 urce of drug-drug interactions (DDIs) due to induction of drug metabolizing enzymes (DMEs).

145 elivered to the immune system for maximizing induction of dynamic immune responses.

146 al complex with NRPs, which is enhanced upon induction of EMT.

147 These data demonstrate the induction of epithelial-mesenchymal transition (EMT), wh

148 We propose that the induction of ER constrictions contributes to the BMB2-de

149 With these mutants, we show that induction of ERK5 transcriptional activity requires dire

150 Upon modest induction of FadR, cell size increases, but at the cost

151 ate seminiferous cord development, including induction of focal dysgenesis, as described in TDS.

152 s demonstrated in mice with potent and broad induction of FSP-specific CD8 and CD4 T-cell responses.

153 ted as immunogens in mice to demonstrate the induction of functionally active polyclonal antibody res

154 ol the magnitude of this process through the induction of genes involved in proliferation and glycoly

155 espond to environmental signals by eliciting induction of genes that preserve skin's integrity.

156 In this study we show that hyperosmotic induction of glutamine synthetase represents a prominent

157 s focused on the E or prM-E proteins and the induction of high levels of neutralizing antibodies.

158 Induction of high mannose is dependent upon the unfolded

159 signalling pathway by AZD5582 results in the induction of HIV and SIV RNA expression in the blood and

160 ceived by two sensory neurons to control the induction of hydrogen peroxide defenses in the organism.

161 e: To determine if vascular aging before the induction of hyperlipidemia enhances atherogenesis.

162 2016-17 outbreak may be related to the lower induction of IFN-beta.

163 inistration of GSK2656157 abrogated neuronal induction of IFNbeta, switched microglial polarization t

164 Subsequently, active STAT3 resulted in the induction of IkappaBzeta, which is a key proinflammatory

165 dded to OPCs, anacardic acid resulted in the induction of IL-33.

166 nvolved in psychostimulant addiction, blocks induction of immediate early genes by DRD1 stimulation,

167 tion is important or redundant for effective induction of immunity is, however, still unclear.

168 c, chemically modified gRNAs and demonstrate induction of indels and large genomic deletions in combi

169 and transcription factors to coordinate the induction of inflammatory genes(1-3).

170 tly inactivates OTUD3 and thus allows timely induction of innate antiviral immunity.

171 occurring polysaccharide, contributes to the induction of innate immune memory, which is associated w

172 Focused transcriptomic analysis revealed induction of innate immunity and phagocytotic pathways i

173 protein STING translocates to endosomes for induction of interferon production, while an alternate t

174 ed IRF members and the major factors for the induction of interferons, a key component in vertebrate

175 Prior work has described induction of intrauterine inflammation in mice with a si

176 cyclic lipopeptide vaccine showed successful induction of J8-specific systemic immunoglobulin G (IgG)

177 ed controlled trials (RCTs) have assessed if induction of labour (IOL) in uncomplicated pregnancies a

178 CLC cell lines demonstrated a dose-dependent induction of linc-SPRY3-2/3/4 following irradiation, whi

179 Last, we demonstrated that genetic induction of lipid cacostasis in the CNS of normal mice

180 tion in response to metabolic stress through induction of lncRNA Gm15441.

181 t inhibitory synaptic strength is malleable, induction of long-term plasticity at distinct inhibitory

182 We have previously demonstrated that the induction of macrophage death is dependent on the host's

183 Although induction of many mRNAs by budesonide plus formoterol wa

184 Ca(2+) uptake, collectively suggesting that induction of MCUb protein in the heart is protective.

185 Despite convincing evidence on the induction of MDSCs by pathogen-derived molecules and inf

186 utants display mitochondrial stress, and the induction of mitochondrial stress results in at least so

187 ategy of human cytomegalovirus (HCMV) is the induction of monocyte survival, where monocytes are norm

188 presenting low initial MT2A levels, a strong induction of MT2A expression could be observed during ci

189 wever, recent studies indicate that "gentle" induction of Myc expression enhances beta-cell replicati

190 n increase in dlPFC global connectivity, (2) induction of negative dlPFC-amygdala connectivity, and (

191 AIV using reverse genetics and evaluated the induction of neutralizing antibodies and protection by r

192 that involved activation of ATR and ATM and induction of NF-kB recruitment to the HEXIM1 promoter.

193 IL-10.CONCLUSIONThis study demonstrates the induction of NK cell effector functions early after Ad26

194 nfiltration of neutrophils and T cells after induction of NTS.

195 As a result, efficient induction of optical activity in the chromophoric system

196 -dependent IFN response was critical for the induction of optimal antifungal neutrophil killing of A.

197 he male germline to oxidative stress and the induction of oxidative DNA damage in spermatozoa.

198 Reactive oxygen species are linked to the induction of oxidative stress and inflammation in the li

199 eptin- and resistin-mediated transcriptional induction of PCSK9.

200 parison of ILC and IDC cell lines identified induction of PI3K/Akt and p90-RSK pathways specifically

201 n mitochondrial polarization, and blocks the induction of PINK-1-mediated mitophagy.

202 owed downregulation of adaptive immunity and induction of programs related to innate immunity and res

203 LT1 is also required for NF-kappaB-dependent induction of proinflammatory cytokines after FcepsilonR1

204 ment, resulting in robust ligand-independent induction of proinflammatory genes and oncogenes.

205 reased maturation of dendritic cells and the induction of protective CD8(+) T cell responses.

206 indicated that IL-25 signaling subverts the induction of protective immunity and amplifies the type

207 at infection of the GIT is not necessary for induction of protective immunity in the FRT, a finding t

208 ygenase (5-LOX) pathways, participate in the induction of protective innate immune responses during i

209 the mature cytokines IL-1beta and IL-18 and induction of pyroptosis.

210 iol (E2) is neuroprotective and critical for induction of reactive astrocytes and their ability to pr

211 We demonstrated the early induction of remodeling during infection by using isotop

212 thways controlling muscle growth and greater induction of ribosome synthesis.

213 ted by smaller IPSCs, which may underlie the induction of seizures.

214 We found that beta-actin depletion affects induction of several adipogenic genes during transcripti

215 ers the autophagic pathway that requires the induction of several Autophagy (ATG) genes.

216 vonoid fraction of clementine juice provoked induction of several genes and inhibition of both CYP3A4

217 , the Gli1 knockout abrogated SULF2-mediated induction of several STAT3 target genes, including suppr

218 logical role of the (6-4) photoadduct in the induction of skin cancer by sunlight, crucial mechanisti

219 the strains, suggesting stronger and faster induction of social motivation in SD rats.

220 in the cellular immune system in addition to induction of specific antibody responses.

221 significant reduction of pristane-dependent induction of splenocyte number and weight.

222 wth hormone and insulin signaling, including induction of suppressor of cytokine signaling.

223 The induction of sustained sensitivity and nociception witho

224 rlying molecular pathway is triggered by the induction of synaptic plasticity and in response to obje

225 des waning of antibody responses, suboptimal induction of T-cell responses may reduce protection.

226 et cell hyperplasia, elevated serum Igs, and induction of Th2 cytokines.

227 tabolic switch in Th17 cells that led to the induction of the amino acid starvation response and alte

228 icate that 12/15-LOX is a critical player in induction of the earliest aspects of the innate immune r

229 t roots associated with a reduced Nod factor induction of the Early Nodulin 11 (MtENOD11) infection m

230 lation of key flowering genes, including the induction of the florigen gene FTa1 and repression of th

231 migration were consistent with those of the induction of the glucocorticoid-responsive chemokine rec

232 ry for the suppression of BAX activation and induction of the intrinsic cell death program.

233 activating transcription factor 4 (Atf4) and induction of the ISR transcriptional program, increased

234 at astrocyte-derived E2 was critical for the induction of the JAK-STAT3 signaling pathway, as well as

235 rate that IL18 signaling is critical for the induction of the key thymus-homing chemokine receptor -

236 and/or carbon monoxide correlated with early induction of the long-chain acyl-CoA synthetase 1 (ACSL1

237 ytoplasmic sequestration of TFEB, preventing induction of the lysosomal genes required for lysosome f

238 omplex driving melanoma invasion through the induction of the sialyltransferase ST3GAL1.

239 OV10-defective mutant is associated with the induction of the unfolded protein response (UPR), a comm

240 ed cellular factors that are critical in the induction of the VS.

241 Understanding the features underlying induction of these elements following MHV68 infection sh

242 We established an in vitro model for the induction of these structures in mouse macrophages under

243 Although research into the induction of tissue-specific immunity by vaccines and wi

244 tion and nuclease sensitivity and coordinate induction of TNF, LTA, and hHS-8 enhancer RNA transcript

245 Alternatively, before induction of TnI-AM or after establishment of autoimmune

246 into immune response to foreign antigens vs. induction of tolerance to self-antigens.

247 tokine production was measured to assess the induction of trained immunity and adaptive responses, re

248 onally, the influence of vaccination time on induction of trained immunity was studied in an independ

249 the effect of BCG administration time on the induction of trained immunity.METHODSEighteen volunteers

250 in nonhuman primates and humans through the induction of transient donor chimerism.

251 ing both stages of hibernation that suggests induction of translation during interbout arousals.

252 n of mice with PM plus alum inhibits in vivo induction of Treg cells promoted by PM without altering

253 NKL immunoregulatory feedback, involving the induction of Tregs and a host response outcome with immu

254 Interestingly, induction of type I IFNs after A. fumigatus challenge wa

255 for protection against body weight gain and induction of UCP1 in adipose tissues associated with die

256 r to a partial agonist given BPTPE's delayed induction of UPR and apoptosis, with a higher probabilit

257 plicing dynamics or intensity, it did reduce induction of XBP1 targets.

258 Glucocorticoids are indispensable for PD-1 induction on human NK cells, in cooperation with a combi

259 phytoalexin sakuranetin after jasmonic acid induction, only very low amounts accumulated in the Kasa

260 ally powered bioelectronic implants based on induction or magnetothermal effects.

261 this phenotype was not caused by cell death induction or senescence.

262 y cleaved the key components of the hepcidin-induction pathway, including Hjv, Alk3, ActRIIA, and Hfe

263 overcoming a persistent cytochrome P450 3A4 induction problem.

264 tection achieved by a second bolus after the induction procedure.

265 ibility scores and responsiveness to symptom induction protocols were used to calculate standardised

266 At 14 days post-AAA induction, radiotracer uptake by either group did not si

267 ow-up and demonstrates the ability of 3-drug induction regimens in patients with newly diagnosed mult

268 71%) participants at diagnosis and at end of induction, respectively.

269 Greater induction resulted in further growth rate decreases and

270 acid, linked to systemic acquired resistance induction, seems to play a large role in protecting tole

271 stingly, in several combinations of genotype/induction strength, bioderivatization had a positive eff

272 We employ a heterologous media-independent induction system to express the yeast HO endonuclease or

273 a specially developed CRISPR/Cas9 DNA damage induction system, capable of inducing small clusters or

274 Here we report that, in response to DPC induction, the deubiquitinase VCPIP1/VCIP135 is phosphor

275 At the end of dasatinib induction therapy (day 85), 29% of the patients had a mo

276 subjects received amphotericin + fluconazole induction therapy and had serial quantitative CSF cultur

277 nt of histo-endoscopic mucosal healing after induction therapy is associated with lower disease activ

278 MRD at the end of induction therapy was high (>=10(-2) cells) in 61 (66%)

279 Patients who completed induction therapy were then randomly assigned (1:1) a se

280 ad increased minimal residual disease during induction therapy, and all these mutations were cleared

281 th low immunological risk according to their induction therapy.

282 pha expression, which culminated in IL-1beta induction thereby simulating pseudohypoxia.

283 nd 3D molecular localization reveal that LTP induction thus prompts spatial retreat of astroglial glu

284 Oxidation induction time (OIT) using differential scanning calorim

285 mune homeostasis and prevents oral tolerance induction to bystander food antigen through their protea

286 omyelocytic leukemia patients with intensive induction treatment and a minimum 12 months of follow-up

287 based on the transplant date and the type of induction treatment.

288 was to determine the prognostic influence of induction type: rabbit antithymocyte globulin (rATG; 2 m

289 -L1 expression with NFKB2 expression and its induction under hypoxic conditions.

290 Timing of undetectable MRD (after induction v intensification) had no impact on patient su

291 More intensive induction was associated with a significant lowering of

292 In adjusted and unadjusted models, ATG induction was associated with increased early event-free

293 le for MERS-CoV-triggered cytokine/chemokine induction was established based on the results of antibo

294 MiR-214 induction was pronounced in perivascular and circulating

295 Chaperone gene induction was reduced in such cells, which were prone to

296 ression mirrored the RGT, except basiliximab induction was substituted with CBMPs and mycophenolate m

297 c-Myc inhibition and apoptosis induction were additionally shown in hematologic maligna

298 eat AML sub-studies and those receiving SOC (induction with cytarabine + daunorubicin (7 + 3 or equiv

299 cephalomyelitis (EAE) is largely confined to induction with either the myelin oligodendrocyte glycopr

300 Catastrophe induction with vinblastine prevented microtubule overgro