ライフサイエンスコーパス: in response to

1 In response to 1-desamino-8-D-arginine vasopressin (DDAV

2 ort, the range of global warming projections in response to a doubling of CO2-from 1.5 degrees C to 4

3 gated, the sensitivity of a motor's velocity in response to a force is not well-understood.

4 e must determine the deformation of a tissue in response to a known force with cellular resolution.

5 In response to a need for better sepsis diagnostics, sev

6 statistics of the central node, which fires in response to a noisy input at peripheral nodes.

7 ime the physiological changes of algal cells in response to a novel form of mechanical stimulation, o

8 al phenotypes of breast cancer cells adopted in response to a nutrient-deficient microenvironment.

9 ow or high changes in cardiac repolarization in response to a pharmacological challenge with sotalol.

10 Expansion of adipose tissue in response to a positive energy balance underlies obesi

11 y genes exhibit altered levels of expression in response to abiotic stress, which requires concerted

12 to carbohydrate fermentation or inflammation in response to accumulated plaque select for a cariogeni

13 ons exhibited increased locomotor activation in response to acute cocaine administration and an alter

14 to transgenerational epigenetic modification in response to acute periods of starvation.

15 binding domain and substrate-binding domain) in response to adenine nucleotides and substrates.

16 Platelets displayed reduced aggregation in response to adenosine 5'-diphosphate and epinephrine,

17 e protein complexes regulate the Rag GTPases in response to amino acids, including GATOR1, a GTPase a

18 ion to neddylation, inhibiting EGFR dynamics in response to an acute ligand stimulus.

19 measured from changes in diaphragm thickness in response to an applied force provided by an indenter.

20 in between any two target nodes in a network in response to an applied source strain on any other pai

21 subject to audience effects and/ or changes in response to an arousing stimulus (e.g. food) alone.

22 eurospheres, can be triggered to migrate out in response to an exogenous signal but then regroup into

23 ia-inducible factor (HIF)-1alpha and -2alpha in response to angiotensin II and hypoxia, respectively,

24 re controlled by pituitary hormones released in response to annual environmental changes.

25 justed its use of habitat and energy sources in response to annual variations in lake temperatures du

26 mum extractable AO activities were decreased in response to aphids in all genotypes.

27 platelet deposition on immobilized collagen in response to arterial shear.

28 lts showed that the JAZ1 stability decreased in response to ATP addition in a proteasome-dependent ma

29 unction in translation reinitiation pathways in response to auxin.

30 can undergo subtype differentiation in vitro in response to bacterial pathogen infection.

31 fficiently than their wild-type counterparts in response to BCR cross-linking.

32 cture that changes its architecture and size in response to biochemical and physical cues.

33 ied a set of host genes that are upregulated in response to biofilm formation by B. subtilis.

34 Significant quantitative changes in response to blue light percentage were obtained for b

35 er Hamp at 8 weeks and failed to induce Hamp in response to Bmp6 in primary hepatocyte cultures.

36 he age distribution of measles cases changes in response to both demographic and vaccination processe

37 er survival rate than wild-type control mice in response to Candida albicans infection, and the expre

38 reased proliferation and cytokine production in response to CD200(+) leukemia cells, supporting clini

39 enhanced proliferation and effector function in response to CD200(+) leukemic cells in vitro.

40 ases co-operate and/or complement each other in response to cellular stress.

41 echanism by which humans adapt eye movements in response to central vision loss is still not well und

42 e of biomaterials is their ability to deform in response to certain external bio-stimuli.

43 ite-specific mTOR phosphorylation (on S2159) in response to certain growth factor receptors (i.e., EG

44 cient animals developed increased metastases in response to challenge with B16 melanoma cells.

45 ved suggests vascular redistribution efforts in response to challenges in the perinatal period may pe

46 e to predict the change in species abundance in response to changes in diets with minimal additional

47 cificity in the learning of oculomotor plans in response to changes in front-end sensory processing a

48 ntly (P < 0.05) different amounts of insulin in response to changes in glucose concentration (2 vs. 2

49 n channel, receptor, or transporter function in response to changes in membrane potential.

50 cteria by opening a large, water-filled pore in response to changes in membrane tension.

51 e functionally programmed to release insulin in response to changes in plasma glucose concentration.

52 espiratory O2 fixation, and starch synthesis in response to changes in the environment.

53 ut has also varied on millennial time-scales in response to changes in the seasonal distribution of i

54 ter, adjusting the double sigmoidal behavior in response to changes in the time.

55 w PFC ensembles represent shifts in behavior in response to changes in these contingencies remains un

56 emographic analyses of migratory populations in response to changing climatic conditions.

57 okadaic acid, restores lymphocyte migration in response to chemokines, both in vitro and in vivo.

58 ient cancer cell line exacerbated DNA damage in response to chemotherapeutics.

59 Also, the significance of this regulation in response to chromosome detachment has not been fully

60 nhance their excitability and oxidative load in response to chronic mutant alpha-synuclein overexpres

61 lls and the expression was further increased in response to cisplatin.

62 read may be an important adaptation strategy in response to climate change.

63 ommunities have not reorganized successfully in response to climate change.

64 In response to climate warming, subalpine treelines are

65 ted protection from death in Nlrp3(-/-) mice in response to CLP.

66 ibution among excitatory SNc afferent nuclei in response to cocaine, and suggest a compelling archite

67 ides a direct measure of cerebral blood flow in response to cognitive activity.

68 t be thermogenic lipokines that activate BAT in response to cold.

69 ter phosphoproteomic profile modification(s) in response to combined MEK/mTOR inhibition in PTEN-loss

70 t remapping of their spatial representations in response to contextual manipulation.

71 m (GIRK) channels and hyperpolarization, but in response to continued signaling MORs undergo acute de

72 ed GnRH neurons fired more action potentials in response to current injection during positive feedbac

73 ric oxide (NO) produced by endothelial cells in response to cytokines displays anti-inflammatory acti

74 ndergoing development, maturation and repair in response to damage.

75 The opal5 mutant does not close in response to darkness but exhibits wild-type (WT) beha

76 ed the morphological transformation of HESCs in response to deciduogenic cues.

77 lease and that sensory neurons released GABA in response to depolarization.

78 d in mitochondrial oxidative phosphorylation in response to Dex.

79 In response to dextran sodium sulfate, colonic infiltrat

80 domains that undergo different shape changes in response to different DNA sequences.

81 rous oxide emission by denitrifying bacteria in response to different environmental signals.

82 ssential to accurately modeling yeast growth in response to different environments.

83 O mice, impaired glucagon secretion occurred in response to different secretagogues and was mediated

84 d in sensing amino acid levels) was assessed in response to different stimuli modulating amino acid c

85 tch controlling an RbohD-dependent mechanism in response to different stresses, subsequently maintain

86 First, distinct patterns of activation occur in response to different task demands.

87 It is also observed in response to disease.

88 Here, the authors uncover functions, in response to DNA damage, for the bromodomain of the IS

89 d that PARP3 regulates G quadruplex (G4) DNA in response to DNA damage, which suppresses repair by no

90 oters and regulate target gene transcription in response to DNA damage.

91 icrotubule dynamics, can mobilize the genome in response to DNA damage.

92 Dictyostelium histones are modified in response to DNA double strand breaks (DSBs) in vivo b

93 ls in cells ectopically overexpressing KDM5B in response to dosing with TCA cycle metabolite pro-drug

94 experienced larger increases in CH4 emission in response to drawdown (R(2) = 0.84, p < 0.01), suggest

95 and carbon dioxide uptake occur, are closed in response to drought by the phytohormone abscisic acid

96 Plant mortality rates and biomass declines in response to drought depend on stomatal and xylem flow

97 and activation of ROS eliminating processes in response to drought tolerance were mechanisms exclusi

98 time, significantly elevated proline levels in response to drought were demonstrated for the grapevi

99 X1 seems to play a particular role in shoots in response to drought.

100 en improves the stratification of cell lines in response to drug treatment.

101 olonocytes showed increased metabolic stress in response to DSS with higher levels of phospho-AMPK an

102 However, yield prediction in response to E-[CO2] varied significantly among the ri

103 n be rapidly and safely implemented at scale in response to Ebola virus disease outbreaks in rural se

104 rizing granule cells, which likely discharge in response to either concerted activity among a large p

105 mong 16 crop models in predicting rice yield in response to elevated [CO2] (E-[CO2]) by comparison to

106 integral part of the hypothalamic engagement in response to elevated circulating E2 Collectively, we

107 cts siesta onset, but not night sleep onset, in response to elevated temperatures.

108 ngs together efforts to understand evolution in response to environmental change while developing new

109 GNIFICANCE STATEMENT Animals adjust behavior in response to environmental changes, such as fluctuatio

110 The particles are fully degradable in response to esterases due to an embedded ester cross-

111 kocytes to release proinflammatory cytokines in response to ex vivo stimulation.

112 rt here that mTORC1 and mTORC2 are activated in response to exogenously supplied fatty acids via the

113 implant sites during native inflammation and in response to experimental plaque accumulation.

114 Conventional fluids only flow in response to external pressure.

115 Structures that change their shape in response to external stimuli unfold possibilities for

116 In response to extracellular matrix signalling, these ce

117 and precise regulation of protein expression in response to extrinsic stimuli.

118 The induction of SMARCA2 in response to EZH2 inhibition is required for apoptosis

119 nd the master transcription factor NF-kappaB in response to FGF and IL-1/TNF, respectively.

120 iboside efficiently rescues NAD(+) synthesis in response to FK866-mediated inhibition of nicotinamide

121 ead RNA motifs that regulate gene expression in response to fluctuating metabolite concentrations.

122 earrangement of the macromolecular structure in response to force.

123 ive immune responses and antibody production in response to foreign antigens.

124 athogens, and guiding the host immune system in response to foreign invasions.

125 s up-regulated within the BM HSC compartment in response to G-CSF treatment.

126 eaf transcripts and metabolites were changed in response to genotype, and cell wall composition was l

127 ranscription factors to control plant growth in response to gibberellin (1) .

128 ting in ubiquitylation and degradation of GS in response to glutamine.

129 significantly and selectively overexpressed in response to GNAQ/11 mutation in UM.

130 posterior glycolytic gradient is established in response to graded transcription of glycolytic enzyme

131 In response to gradual changes in oxygen influx, this mo

132 nment is supported by the production of PTX3 in response to GroEL, which thus has therapeutic potenti

133 d that Lon may help regulate DNA replication in response to growth conditions.

134 (ECs) coordinate migration and proliferation in response to growth factor activation to form new vess

135 itment is sufficient for Akt phosphorylation in response to growth factors.

136 of the cell cycle and improves cell survival in response to growth-induced pressure.

137 hanges in the methylome of Arabidopsis roots in response to H. schachtii infection.

138 vation of the elastin monomer, tropoelastin, in response to heat and salt is a critical step in the a

139 hS) surfaces that transform their morphology in response to heat are developed.

140 ically unwinged but produce winged offspring in response to high population densities and deteriorati

141 h NAL and SAL displayed physiological stress in response to high temperature, but neither showed sign

142 , resulting in greater interaction with eNOS in response to histamine.

143 tein synthesis, and increased autophagy flux in response to hyperammonemia, which were partially reve

144 ly determine the changes of pHi and [Cl(-)]i in response to hypercapnia and seizure activity.

145 Here we found that in response to hyperglycemia, neutrophil-derived S100 ca

146 iated gene conversion both spontaneously and in response to I-SceI-induced DSBs.

147 that both cell types increased PGE2 release in response to IH.

148 of the miRISC in primary human chondrocytes in response to IL-1beta treatment.

149 d isoforms of miRNAs (isomiRs) to the miRISC in response to IL-1beta, including miR-146a-5p, miR-155-

150 ic T cells that produce high levels of IL-17 in response to IL-23.

151 oles for inducible degradation of Socs mRNAs in response to IL-7 signalling in order to reprogram nai

152 s failed to up-regulate PPARgamma expression in response to IL4 treatment resulting in 4-fold lower P

153 Ps) produce monocytes during homeostasis and in response to increased demand during infection.

154 likely a result of interspecific variability in response to increased pCO2 and changes in species int

155 As a result, we expect fecundity to rise in response to increases in elephant prices.

156 In response to increases in pertussis morbidity and mort

157 ts of carbon dioxide (CO2) to the atmosphere in response to increasing temperatures, representing a p

158 and are able to resolve conductivity changes in response to induced back-gate voltages.

159 the efflux of ATP and AMP from cancer cells in response to induction of extrinsic apoptosis by death

160 hylesterification status is strongly altered in response to infection.

161 Secretion of interleukin 1beta (IL-1beta), in response to inflammasome activation, is ablated in FA

162 2-AG levels were increased in response to inflammation and hypoxia in Caco-2 cells.

163 allenging because SF concentrations increase in response to inflammation or infection.

164 OEA and PEA (P < 0.001-0.001) were increased in response to inflammatory mediators.

165 IDO-1 is induced in response to inflammatory stimuli and promotes immune

166 of iMGLs reveals that they secrete cytokines in response to inflammatory stimuli, migrate and undergo

167 Activation of hepatic stellate cells (HSCs) in response to injury is a key step in hepatic fibrosis,

168 o study its dynamics at multiple time scales in response to inputs approximating real spatiotemporal

169 d deposition of STAT5 at the promoter of Id2 in response to interleukin (IL)-15.

170 metabolism, immune defense, and reproduction in response to internal and external stimuli.

171 d that Sirt2 deletion reduced cell viability in response to iron deficiency.

172 s to suppression of CHK1 and CHK2 activation in response to irradiation, impaired G2 checkpoint profi

173 ng was reduced but not completely inhibited, in response to JAG1(Ndr) compared with JAG1.

174 ure vibration in excised whiskers in a flume in response to laminar flow and disturbed flow.

175 nd is activated through proteolytic cleavage in response to ligand engagement.

176 lso synthesize reactive oxygen species (ROS) in response to light, suggesting the possibility of an a

177 05) and reduced leukocyte cytokine secretion in response to lipopolysaccharide stimulation.

178 and reinstatement of extinguished preference in response to low-dose cocaine administration did not d

179 AND We analyzed ECP and histamine production in response to LPS by ELISA.

180 TII) are instrumental in early wound healing in response to lung injury, restoring epithelial integri

181 RNF145 expression is induced in response to LXR activation and high-cholesterol diet

182 ls from HIV-infected ART-treated individuals in response to M. tuberculosis antigen stimulation.

183 xhibit an inherent force orienting mechanism in response to mechanical constraints.

184 e dynamic structures that adapt their growth in response to mechanical force.

185 In response to mechanical stimulation, these IS cells di

186 ions is their ability to change conformation in response to mechanical stimuli.

187 Recovery of cardiac function in response to mechanical unloading was assessed by echo

188 ncreased myeloid invading injured myocardium in response to MI.

189 y transducing signals in innate immune cells in response to microbial products.

190 ealed that insulin signaling is up-regulated in response to miR-277 depletion.

191 s necessary for PI3K/AKT signaling induction in response to MPhi activation.

192 ional reprogramming that supports metastasis in response to mTOR inhibition.

193 greater capacity for altering network states in response to multiple and diverse external demands.

194 es in humans, Elongin controls transcription in response to multiple stimuli, such as DNA damage, oxi

195 8 as a genetic driver of IFNgamma production in response to mycobacterial antigens provides new insig

196 rom studies measuring free-living N fixation in response to N, P and Mo fertilizers.

197 time is central to the evolution of genomes in response to natural selection.

198 ral prefrontal cortex and anterior cingulate in response to negative affective cues, as well as durin

199 ge transitions of the beta8-beta9 loop occur in response to neurotransmitter binding.

200 t photothermal effect and quick drug release in response to NIR irradiation.

201 upstream of NRT1.1 and independently of NLP7 in response to nitrate.

202 Rodents sniff in response to novel odors, reward expectation, and as p

203 Yet reefs are degrading rapidly in response to numerous anthropogenic drivers.

204 ple feedback controls to regulate metabolism in response to nutrient and signaling inputs.

205 lator that becomes activated at the lysosome in response to nutrient cues.

206 nd the accumulation of triacylglycerol (TAG) in response to nutrient starvation.

207 ned by phosphorylation and dephosphorylation in response to oscillations in cytosolic calcium.

208 ied by consortium members or self-identified in response to our protocol (published prior to the star

209 blunted platelet activation and aggregation in response to oxLDL and targeted genetic deletion of ER

210 lance between muscle growth and regeneration in response to oxygen fluctuations, and hypoxia-inducibl

211 In conclusion, TSG-6 is necessary for AHR in response to ozone or sHA, in part because it facilita

212 ges from CalpTG mice produced less IL-1alpha in response to particulate activators of inflammasome.

213 We show that R-motif regulates translation in response to pattern-triggered immunity induction thro

214 teus medius muscle activities, respectively, in response to perturbations.

215 re, we report a reduction in atherosclerosis in response to pharmacological stimulation of thermogene

216 In response to photoreceptor-EGF, glia produce insulin-l

217 m an actin cap to resist nuclear deformation in response to physiological mechanical stresses.

218 regulated nucleocytoplasmic exchange of C3G in response to physiological stimuli and provide insight

219 that LSK(-) cells produce the cytokine IL-17 in response to Plasmodium infection.

220 In response to poly(I:C) addition, the metastatic IECs a

221 ng of how these soil communities will change in response to predicted increases in global temperature

222 Remodeling of the left ventricle (LV) in response to pressure overload leads to the re-express

223 of inherited variation that change over time in response to processes such as selection, migration, a

224 of the inhibitory scaffold protein gephyrin in response to protocols inducing LTP of inhibitory syna

225 und that many plant species flowered earlier in response to reductions in diversity, with peak flower

226 to activate the S-phase checkpoint in yeast in response to replicative stress, but whether this mech

227 ges in neuronal activity were then evaluated in response to right ventricular outflow tract PVCs with

228 be expected from a substance to be released in response to RIPC and to protect the myocardium during

229 ampling in time, which maximises information in responses to salient light changes while antialiasing

230 clear whether C. hirsuta petal number varies in response to seasonal changes in environment.

231 -moving sports, we must be ready to act fast in response to sensory events and, in our preparation, p

232 ng host innate and adaptive immune responses in response to sepsis, transplantation, and autoimmunity

233 d the expression of cytokines and chemokines in response to sequential challenges with LPS and Poly I

234 enhanced limbic brain activity specifically in response to sexual and couple-bonding stimuli.

235 uman chronic myeloid leukemia cell line K562 in response to shRNA knockdown of the RNA editing enzyme

236 nteractions are subject to rapid modulations in response to signals is unknown.

237 her levels of separation anxiety and arousal in response to social separation, but infants carrying t

238 eceptor genes revealed a different induction in response to soil flooding (CsPYL5) or drought (CsPYL8

239 d by essential and non-essential isoprenoids in response to soil water availability and solar radiati

240 en level dependent (BOLD) signal differences in response to SS and neutral stimuli (NS) were compared

241 strate large inter-individual variation even in response to standardized exercise training programmes

242 observe the pH conditions inside glycosomes in response to starvation conditions.

243 ho-effluxing T cells proliferated vigorously in response to stimulation with anti-CD3/CD28 beads and

244 A and repressing or activating transcription in response to stimuli.

245 iently inserted serine, alanine and cysteine in response to stop and sense codons, depending on the i

246 le pro-survival mechanisms and overexpressed in response to stress in cancer cells.

247 the cell surface and boost the IKs amplitude in response to stress.

248 anscriptional repression of cell cycle genes in response to stress.

249 molecule Annexin A2 (AnxA2) at Y23 and Y333 in response to stromal signals HGF and IGF-1, respective

250 did not change from wk 0 to 9, and also not in response to submaximal exercise training.

251 e cytokines, chemokines, and lipid mediators in response to subsequent TLR stimulation.

252 g mechanisms in the elongation of hypocotyls in response to Suc.

253 1-7 and med12 aux1 single and double mutants in response to sucrose and/or N-1-naphthylphthalamic aci

254 rast, females do not show activation of ERK1 in response to sucrose, but notably hemideletion females

255 recent finding of sustained weight reduction in response to systemic administration of a long-acting

256 , CD4 T cells produced less interferon-gamma in response to T-cell stimulation.

257 cantly reduced IL-1beta cleavage and release in response to T. gondii infection, without affecting th

258 No OVA-specific antibodies were induced in response to TAC in cMy-mOVA-OT-II mice, yet more CD3(

259 ansition to a slow-cycling, persistent state in response to targeted kinase inhibitors.

260 transcriptional up-regulation of miR-34c-5p in response to TCR stimulation in naive CD4 T cells.

261 tivate gene expression rapidly and precisely in response to temperature, while preventing leaky trans

262 hway that mediates induction of angiogenesis in response to TGF-beta1.

263 nd Kyn production controlled by cancer cells in response to the activated T-lymphocytes.

264 ed a comparative analysis of cytokinin genes in response to the beet cyst nematode (BCN), Heterodera

265 In response to the commentaries, we have refined our sug

266 uth China Sea (SCS) increased by 2 degrees C in response to the developing Pacific El Nino.

267 hard pericarp determines germination timing in response to the environment are currently unknown.

268 n the brain undergoes substantial remodeling in response to the environment.

269 sease, modulates its gene expression profile in response to the environments encountered throughout i

270 may reflect prolonged mGluR5 internalization in response to the glutamate surge.

271 rophage infiltration of the DRG was observed in response to the HFD, absent any pain model.

272 ral selection typically generates adaptation in response to the immediate selection pressures that a

273 rocess to regulate miRNA activity in neurons in response to the induction of long-term depression.

274 resses a range of pro-inflammatory cytokines in response to the infectious challenge.

275 can arise from cone photoreceptor precursors in response to the loss of pRB function.

276 periment, chicks begged significantly longer in response to the odour of their genetic mother or fath

277 between its "liquid" and "solid" properties in response to the rate of lithium growth to provide uni

278 deficit in mitochondrial oxygen consumption in response to the respiratory complex II substrate succ

279 subtherapeutic concentrations is increasing in response to the rising demand for food animal product

280 An average of 8.5% of murres flew off in response to the UAV, but >99% of those birds were non

281 ish species dramatically and rapidly changed in response to the warming conditions occurring in 2014-

282 al stem cells (MSCs) and their nuclei spread in response to thickness-corrected matrix microelasticit

283 qual numbers of monocytes are also recruited in response to this lectin.

284 In response to this rising threat, a highly efficient, e

285 eated astrocytes containing factors produced in response to this treatment, but not rPrP(c) by itself

286 Stopping or pausing in response to threats, conflicting information, or surp

287 ith eIF4E, eIF4G1 and eIF4G2 change globally in response to three defined stresses that each cause a

288 d can sustainably regulate blood coagulation in response to thrombin.

289 and human intestinal organoids, died rapidly in response to TNF.

290 USP5 mRNA expression increased in adipocytes in response to TNFalpha, parallel with ERK1/2 dephosphor

291 the feedback inhibition of ERK1/2 signaling in response to TNFalpha, which resulted in increased inf

292 cs of cough frequency throughout the day and in response to tuberculosis therapy.

293 apid and compartment-specific reorganization in response to unilateral changes in auditory input.

294 in genetically susceptible individuals who, in response to unknown environmental factors, develop an

295 ermine the propensity of acquiring mutations in response to vaccine or treatment with one or a cockta

296 Phosphorylation of the eIF2alpha subunit in response to various cellular stresses converts eIF2 i

297 odifiers regulate proper cellular activities in response to various environmental stress by modulatin

298 ed hypothetical proteins and may be involved in responses to various signals and crosstalk among sign

299 BST2 is a host protein with dual functions in response to viral infections: it traps newly assemble

300 NAT expression, and the significance of NATs in response to WS.