ライフサイエンスコーパス: in response to

1 nute IPA at light transmittance aggregometry in response to 20 mumol/L adenosine diphosphate.

2 ial expression of many transcription factors in response to 5,8-diHODE.

3 concentration-time curve for C-peptide level in response to a 4-hour mixed-meal tolerance test (4-hou

4 (by visual analog scale appetite perceptions in response to a fixed test meal) were measured.

5 In response to a longstanding Federal mandate to minimiz

6 ular switch that triggers RNA-dependent LLPS in response to a rise in intracellular free RNA concentr

7 g in the nucleus accumbens core at baseline, in response to a single dose of cocaine, and in response

8 icted self-organised gene expression domains in response to a single gradient.

9 Conditioned freezing in response to a tone paired with a weak footshock was i

10 l plant taxonomic and phylogenetic diversity in response to a wide range of environmental variables.

11 ation of human neutrophils into the airspace in response to A. fumigatus Together, these data provide

12 nt role in non-canonical poly(A) site choice in response to abiotic stresses.

13 wer can be effectively adjusted at real-time in response to acceleration changes, i.e., P of 72.78-13

14 n cortex compression or dilation is possible in response to acting forces at sufficiently fast timesc

15 to inhibit inflammatory mediator expression in response to activators of the pattern recognition rec

16 sults highlight a pathway that involves BCL2 in response to adalimumab.

17 In response to altered multimodal input, reciprocal inhi

18 81 miRs screened in the perivascular tissues in response to Ang II (angiotensin II)-mediated hyperten

19 nses to environment, revealing heterogeneity in response to anthropogenic change.

20 ween the heat and carbon uptake of the ocean in response to anthropogenic emissions.

21 olf habitat selection and movement behaviour in response to anthropogenic habitat modification, thoug

22 he Ocn-Cre(+) dDG neurons were highly active in response to anxiogenic environment but had lower exci

23 er of a phosphate group onto another protein in response to appropriate regulatory cues.

24 regulators of replication checkpoint arrest in response to AZD1775 and defined PTEN as a promising b

25 ve feedback control of macrophage activation in response to bacterial infection.

26 Brain changes in response to binge EtOH treatment were more pronounced

27 The development of anti-drug Abs in response to biological products (BP) is a major drawb

28 at TARK1 functions in stomatal movement only in response to biotic elicitors and support a model in w

29 ch in turn modulates afferent nerve activity in response to bladder filling during the urination cycl

30 e rise to non-self-renewing cytotrophoblasts in response to BMP4.

31 n experiments and mast cell activation tests in response to both Ara h 2 and Ara h 6 were performed.

32 on were found in Th1, Th2, and Th17 immunity in response to both unspecific and pathogen-specific sti

33 ssigned to 18 FG) reveals regional variation in responses to both long-term (2006-2016) change and a

34 arized gas MRI was more sensitive to changes in response to bronchodilator inhalation (58%) than spir

35 Contractile forces of FDB fibers increase in response to caffeine and the troponin-calcium stabili

36 nsing proteins that trigger calcium dynamics in response to calcium fluctuations.

37 d that YAP/TAZ were activated in hepatocytes in response to carbon tetrachloride toxic injury.

38 the PINK1-Parkin signaling pathway is active in response to CCCP treatment, we observed no change in

39 We also see no increase in GSIS in response to CCK peptides.

40 ive protein whose expression is up-regulated in response to cell stress to protect against pathologic

41 le RB1-mutant cells fail to arrest at G(1)-S in response to cell-cycle restriction point signals, thi

42 ons and impaired outgrowth of thalamic axons in response to cell-extrinsic factors.

43 Inf-cDC2s matured in response to cell-intrinsic Toll-like receptor and typ

44 The ability to switch fuels for oxidation in response to changes in macronutrient composition of d

45 ssemble filamentous polymers in cells, often in response to changes in physiological conditions.

46 on factor LuxR directly regulates >100 genes in response to changes in population density.

47 ve only investigated life-history plasticity in response to changes in temperature, yet wild animals

48 -sensing regulators to alter gene expression in response to changes in the availability of zinc, an e

49 spreading processes, pathogens often evolve in response to changing environments and medical interve

50 nd the recent work examining animal movement in response to changing phenology from migratory birds a

51 The alterations in polyamine metabolism in response to chemotherapy, as well as DFMO-induced pre

52 ded through the ubiquitin-proteasome pathway in response to cholesterol and other sterol intermediate

53 atform to study miR signature in human lungs in response to CI/EVR.

54 variation across sites in community dynamics in response to climate change.

55 s around the world are shifting their ranges in response to climate change.

56 an astrocyte-mediated synaptogenic mechanism in response to cocaine experience and embed critical cue

57 in response to a single dose of cocaine, and in response to cocaine-paired cues.

58 urs in brown adipose tissue to generate heat in response to cold ambient temperatures.

59 icle stem cells to promote hair regeneration in response to cold.

60 ations at five levels of the auditory system in response to conspecific vocalizations masked by noise

61 Australian public and government authorities in response to COVID-19 were sufficiently early and assi

62 The velocity of actions made in response to cues prospectively triggered by STN beta

63 d national organization leaders was convened in response to current practice challenges and to develo

64 expression of the proapoptotic molecule Hrk in response to cytokine withdrawal.

65 In response to damage, Gal9 displaces USP9X from complex

66 s demonstrated robust remyelinating activity in response to demyelinating agents in both chronic cupr

67 It is known that in response to dietary nutrients and PI3-kinase activati

68 nt influenced richness and diversity, likely in response to differences in soil properties.

69 RG oscillatory potential (OP) implicit times in response to dim-flash stimuli (<-1.8 log cd . s/m(2))

70 the differential loss of these RGC subtypes in response to disease or injury.

71 of innate immune defence that are activated in response to diverse stimuli, including pathogen-assoc

72 nd lung MV (microvascular) endothelial cells in response to DNA damage and oxidant stress regulated i

73 er amnesiac is involved in cAMP/PKA dynamics in response to dopamine and acetylcholine co-stimulation

74 Here we report that, in response to DPC induction, the deubiquitinase VCPIP1/

75 Forest types varied in response to drought events: those dominated by drough

76 growing evidence that individual differences in responses to drug and nondrug reward are linked and t

77 s-segregation due to imperfect DDR signaling in response to dysfunctional telomeres creates a prepond

78 id production revealed differential patterns in response to each inhibitor.

79 Neuronal VAChT staining and airway narrowing in response to electrical field stimulation in precision

80 onstrate a functioning complex nerve network in response to electrical stimulation of the CN, which w

81 parabrachial neurons, which promote arousal in response to elevated blood carbon dioxide levels, as

82 Here, we find that cAMP synthesis in response to elevated glucose and the selective P2Y(11

83 Central activation in response to emotion and cognitive stress induces pert

84 (S1P) and site-2 protease (S2P) sequentially in response to endoplasmic reticulum (ER) stress.

85 mice rescued vascular permeability increase in response to endotoxin, indicating that targeting of D

86 usual phospholipidome that is highly dynamic in response to environmental changes.

87 laining how cambium-driven growth is altered in response to environmental changes.

88 echanisms to precisely control gene programs in response to environmental cues to regulate cell fate

89 regulate the composition of their membranes in response to environmental cues.

90 directly influences motor behavior, possibly in response to environmental cues.

91 nsive measures and developmental transitions in response to environmental cues.

92 otypes that can be differentially manifested in response to environmental cues.

93 ivity of E-cadherin expressed on tumor cells in response to environmental factors is an important det

94 exhibit volumetric and dielectric variations in response to environmental glucose concentrations-thes

95 In response to environmental or developmental cues, sigm

96 tes and function by altering gene expression in response to environmental stimuli.

97 af function, controlling water transpiration in response to environmental stresses and modulating the

98 heir expression profiles in plant organs and in response to environmental stresses, in their calcium

99 expression patterns in different tissues and in response to environmental stressors such as treatment

100 nary process by which phenotypic flexibility in response to environmental variation is reset by genet

101 In response to ER stress, FORCP depletion results in dec

102 n mediating Ca(2+)-induced insulin secretion in response to ER stress.

103 that leads to an inhibition of shoot growth in response to ethylene.

104 ell markers were downregulated in fat-1 mice in response to EtOH, while defense responses and PPAR si

105 yokines, skeletal muscle-specific cytokines, in response to exercise.

106 oped modest cardiac dysfunction and dilation in response to exercise.

107 to evaluate how microbial compositions shift in response to exposure of environmentally relevant conc

108 fied and inhibited by cysteine S-nitrosation in response to exposure to both free nitric oxide and ni

109 he folding dynamics of single talin proteins in response to external mechanical noise and cyclic forc

110 in the olfactory center of transgenic flies in response to external stimuli including odor and body

111 Cell size varies during the cell cycle and in response to external stimuli.

112 In response to extracellular DA, both the red and green

113 hat modulate physiology across human tissues in response to extracellular signals.

114 NF-kappaB- and interferon-mediated signaling in response to extracellular stimuli and pathogen infect

115 caspase-dependent apoptosis, or necroptosis in response to extracellular stimuli.

116 Spatial predictions demonstrated variation in responses to extreme weather across species' ranges,

117 lular acidification rate but consumed oxygen in response to FAs.

118 expression of transcription factor gene FIT in response to Fe deficiency via an indirect mechanism.

119 ngitudinal assessments of retinal blood flow in response to flicker stimulation and systemic hyperoxi

120 e longitudinal changes in retinal blood flow in response to flicker stimulation and systemic hyperoxi

121 tion of invading pathogens, cell-cell fusion in response to foreign bodies, and their self-sacrifice

122 on of the majority of inflammatory cytokines in response to G. vaginalis, isolates from women with no

123 within-hypha phenotypic variation for growth in response to gallic acid, a plant-produced antifungal

124 interact with and be activated by beta-Arr2 in response to GCPR activation.

125 ines accompanied by an increase of PGC1alpha in response to genetic (shRNA and CRISPR/Cas9) and pharm

126 tome size does not exhibit a simple doubling in response to genome doubling, and individual gene dosa

127 In response to genomic size differences, it appears that

128 In response to genotoxic stress, multiple kinase signali

129 covered that Cryptococcus cells polyploidize in response to genotoxic stresses that cause DNA double-

130 ch infection may lead to unexpected outcomes in response to global change.

131 g the "shrubification" of northern peatlands in response to global change.

132 ic alpha cells, express and secrete glucagon in response to glucose and some glucagon secretagogues,

133 Rs critical for restoration of normoglycemia in response to glucose deficit.

134 in rat islets blocks beta-cell proliferation in response to glucose ex vivo and in vivo in transplant

135 Expression of FLCN in response to glucose was greater in individuals with d

136 ranslational silencing of inflammatory genes in response to HFD as an endogenous defense against athe

137 bolite changes including low inositol levels in response to high blood alcohol levels support a mecha

138 In response to high fat diet (HFD) feeding for 6 or 18 w

139 We determined differential gene expression in response to high glucose in lymphoblastoid cell lines

140 reveals clonal dynamics and genome evolution in response to hormonal and chemotherapy.

141 Robust activation of Cds1 in response to hydroxyurea prevents the endonuclease Mus

142 Further, Parkin translocates to the nucleus in response to hypoxia which correlates with increased u

143 s (glomus cells), which release transmitters in response to hypoxia, hypercapnia, and acidemia to act

144 te the proteome shifts exhibited by OS cells in response to hypoxia.

145 Plants have developed various adaptations in response to hypoxic stress and these have been descri

146 onstrate that circulating Il-18bp is induced in response to Ifn-gamma during CpG-induced macrophage a

147 -18R1 and promoted donor-specific antibodies in response to IL-18 in vivo.

148 of the muscle boundary relative to the skin) in response to impact forces elicited by walking and run

149 ype 2 diabetes (T2D) fail to secrete insulin in response to increased glucose levels that occur with

150 AM-associated trees showed increased growth in response to increased inorganic nutrients, but ECM tr

151 t adjusts the balance of fusion and division in response to increased mitochondrial connectivity.

152 changes in terrestrial mammal movement rates in response to increasing temperature.

153 ture can allow organisms to maintain fitness in response to increasing temperatures, thereby "buying

154 otes, TcHTE protein and mRNA levels decrease in response to increments in heme concentration, confirm

155 ts are activated in a-nucleated erythrocytes in response to infection with malaria parasites, but the

156 ize published results on age-related changes in response to infection with the influenza virus and on

157 Overall, MSH3's shuttling in response to inflammation enables accumulation in the

158 velocity and inhibits neutrophil recruitment in response to inflammation in a zebrafish model.

159 In response to inflammation, MDS HSPCs switched from can

160 tric oxide, which is produced in hepatocytes in response to inflammation, triggers the ubiquitin-depe

161 of inflammation that activate sets of genes in response to inflammatory signals.

162 The ability to prevent blood loss in response to injury is a conserved function of all ver

163 Stem cells undergo dynamic changes in response to injury to regenerate lost cells.

164 ted in more severe and prolonged proteinuria in response to injury, as well as worse glomeruloscleros

165 ing the notion that RGC cell size is dynamic in response to injury.

166 ons may contribute to enhanced contractility in response to inotropic stimuli.

167 )-containing vesicles to the plasma membrane in response to insulin stimulation.

168 ng, PYHIN1 induced proinflammatory cytokines in response to interleukin-1 (IL-1) or tumor necrosis fa

169 1) is produced by tumor-associated microglia in response to interleukin-4 (IL-4) stimulation.

170 ut dysbiosis, miRNA profiling and SCFA level in response to intestinal inflammation.

171 Sex differences in responses to intestinal ischemia-reperfusion (IR) hav

172 stasis, and attenuated superoxide production in response to ischemia and excitotoxicity in vitro and

173 phenotype, and acquire a Th17-like phenotype in response to iTreg polarization.

174 sing desmin or vimentin generated less force in response to KCl and carbachol relative to the levels

175 of the ISCs niche, augment the ISCs function in response to L-arginine.

176 ited slightly worsened locomotor performance in response to L-DOPA and enhanced LID scores.

177 okine production by vaginal epithelial cells in response to lactobacilli in the presence and absence

178 n (PLIN2) that exhibits altered fluorescence in response to LD interactions with the lysosome.

179 , we found high inter-individual variability in response to lexico-semantic anomalies.

180 stronger advancements in reproductive timing in response to light exposure, potentially creating phen

181 olic gene induced in the liver via PPARalpha in response to lipids in mice (neonates- and food-restri

182 ever, endemics with small ranges did decline in response to logging.

183 zinc transporter in skeletal muscle of mice in response to LPS-induced inflammation.

184 facilitate protein secretion in macrophages in response to LPS.

185 tal gut microbiome undergoes dynamic changes in response to many nutritional and environmental variab

186 les to increase the numbers of dividing GSCs in response to mating.

187 In response to MCC cells with restored STING, cocultured

188 In response to measles and diphtheria cases, first docum

189 rated by the dynamic reorganization of cells in response to mechanical forces.

190 annels that exhibit a preference for calcium in response to mechanical stimuli.

191 injury in RVD patients, but does not change in response to medical or interventional therapy over 3

192 l 5' cap-binding protein eIF3d was activated in response to metabolic stress in human cells.

193 a attenuates hepatic inflammasome activation in response to metabolic stress through induction of lnc

194 densates of ribonucleoproteins that assemble in response to metabolic stresses.

195 This Matters Arising paper is in response to Micheletti et al. (2020), published in Th

196 kinetics and selectivity of gene activation in response to microbial ligands; however, these studies

197 resulting in different DOX release profiles in response to mild HT.

198 ntaneous intestinal adaptation, particularly in response to modifications of luminal content, includi

199 , and disturbance [currently disturbed]) and in response to multiple environmental change factors (wa

200 metabolites were differentially accumulated in response to N and S availability.

201 ntly to higher rates of litter decomposition in response to N deposition.

202 d accounts for the large Stokes shift of GFP in response to near UV excitation.

203 ated in acute kidney injury, which can arise in response to nephrotoxins, sepsis, and ischemia/reperf

204 -state trajectories at the single-cell level in response to neuronal activation.

205 iched in the mammalian brain and upregulated in response to neuronal differentiation and depolarizati

206 covery of drug leads with clinical potential in response to new infectious diseases for which no spec

207 in reproductive timing and hatching success in response to noise exposure were explained by vocaliza

208 n, FRO2 and AHA2 are not largely endocytosed in response to non-iron metal excess, unlike IRT1.

209 romoted apoptosis in colorectal cancer cells in response to Nutlin-3A, which otherwise predominantly

210 ess a sexual dimorphism, developmentally and in response to nutritional stress.

211 by the induction of synaptic plasticity and in response to object location learning.

212 show alterations in hormone levels and SWLS in response to OC.

213 on of the histone residues H4-S47 and H4-T30 in response to osmotic and heat stress, respectively.

214 ding is unable to activate the Hippo pathway in response to osmotic stress, as measured by LATS and Y

215 its function in activating the Hippo pathway in response to osmotic stress.

216 In response to P starvation, 40% of all protein-coding g

217 antimicrobial properties, is not upregulated in response to P. aeruginosa by cystic fibrosis airway e

218 eticulum (ER) and global cellular physiology in response to pathologic ER stress.

219 Further, in response to perturbations, subjects with an mTBI util

220 ry elements and might modulate transcription in response to pH stimuli.

221 CLM displayed a drug release pattern in response to pH/enzyme dual stimuli and was enzymatica

222 c transport of bacteria within a leaf tissue in response to photosynthesis occurring within plant mes

223 In response to Ras-activating cell signaling, SOS autoin

224 all-holder farmers, implies that they may be in response to reduced yields.

225 cells are mobilized from bone marrow niches in response to remote ischemic injury and migrate to the

226 and multi-unit activity (MUA) in the cortex in response to repeated brief optogenetic stimulation of

227 We first show that in response to repeated tones pyramidal (Pyr) neurons in

228 In response to replication stress, certain loci, such as

229 y paradoxical upregulation of RNA polymerase in response to rifampicin.

230 with increasing frequency as the globe warms in response to rising concentrations of greenhouse gases

231 hosphorylation (Ser73), and AP-1/DNA-binding in response to S. mansoni infection.

232 In response to secretion of inflammatory cytokines (e.g.

233 ls) restrict immune system activity, such as in response to self-antigens, and are switched on by tum

234 then reinitiate development inside the host in response to sensory cues, a process called activation

235 ination profiles to diversify circuit tuning in response to sensory experience.

236 %, and we investigated the cortical activity in response to sensory stimuli in these conditions.

237 xpression is induced in differentiated VSMCs in response to serum stimulation.

238 e phenotypic and functional changes in Tregs in response to SP in DED.

239 rfaces, structures, properties or even shape in response to specific stimuli (such as pressure, tempe

240 modelled, processed, protected and restarted in response to specific types of stress.

241 ed to a failure of the uterus to decidualise in response to steroid hormones.

242 -terminal tail of DHHC5 can be palmitoylated in response to stimulation and such modification is impo

243 ucible localized changes in tissue impedance in response to stimulation of individual fascicles (tibi

244 transcript levels can increase substantially in response to stress, but toxin is not liberated.

245 les (SGs) are condensates of mRNPs that form in response to stress.

246 transcriptional activation of various genes in response to stress.

247 een implicated in restricting rosette growth in response to stress.

248 triterpene-diversifying enzymes, presumably in response to strong environmental selection pressure.

249 switching, and memory B cell differentiation in response to T cell-independent type 2 Ags (TI-2 Ags)

250 ctivity (GEP) and ecosystem respiration (RE) in response to T(a) and EF anomalies were compared for d

251 at differential regulation of 12-OPDA and JA in response to T. virens colonization results in ISR ind

252 LANDD EPSPs show little depression in response to tetanic stimulation and, therefore, can b

253 ing the ability to activate SHH target genes in response to TGF-beta.

254 docytosis of TGFbeta receptor II (TbetaRII), in response to TGFbeta stimulation, is a prerequisite fo

255 d deficient ECM production in SA fibroblasts in response to TGFbeta.

256 family that initiates inflammatory signaling in response to the bacterial motif muramyl dipeptide.

257 sion of the tetraspanin family member, CD82, in response to the chemotherapeutic, daunorubicin.

258 proliferate upon activation of FAK-signaling in response to the cold and irisin.

259 Cancer services worldwide had to adapt in response to the COVID-19 pandemic to minimise risk to

260 In response to the COVID-19 pandemic, many governments h

261 ive scientists have ramped up online testing in response to the COVID-19 pandemic.

262 are seeded with cell-laden collagen, which, in response to the gradual slope of the circumferential

263 study confirms the plasticity of the retina in response to the natural photic conditions.

264 rater reliability of radiomics features vary in response to the number of raters were largely feature

265 anscripts whose translation was up-regulated in response to the stress in a Gcn2-dependent manner.

266 Although the difference in Trk-A behavior in response to the two ligands has been previously attri

267 kably consistent; both varied seasonally and in response to the warming treatment, tracking variation

268 s and the impact of reducing the variability in responses to the influenza vaccine across the populat

269 In response to these challenges, we provide two contribu

270 t their learning dynamics more appropriately in response to these factors.

271 In response to this immunity, many phages have anti-CRIS

272 In response to this need, an induced pluripotent stem ce

273 ible escape behavior exhibited by C. elegans in response to threats relies on a combination of feedba

274 sponse to TNFalpha and pro-survival activity in response to TLRs signaling.

275 in regulating its pro-death kinase activity in response to TNFalpha and pro-survival activity in res

276 is along with increased caspase 3 activation in response to TNFalpha.

277 ing quality was evaluated as vector strength in response to tones at best frequency, and by construct

278 rized limb coordination and walking behavior in response to transient activation of mechanosensitive

279 Dissociative experiences commonly occur in response to trauma, and while their presence strongly

280 ression and as a therapeutic outcome measure in response to treatment.

281 nts, all lesions on (68)Ga-PSMA PET resolved in response to treatment.

282 -1 and IL-34 secretion from GF was evaluated in response to tumor necrosis factor-alpha (TNF-alpha),

283 Trk-A is expressed in neurons and signals in response to two ligands, NGF and neurotrophin-3 (NT-3

284 increased expression of IFN-stimulated genes in response to type I IFN and leads to 1) promotion of c

285 s to the upregulation of antiviral effectors in response to type I interferons.IMPORTANCE Viral infec

286 pathway genes are conserved and upregulated in response to UV-B irradiation of the SAM.

287 vels of metabolic hormones (glucocorticoids) in response to variation in food and density are one mec

288 unconventional pathway that activates mTORC1 in response to variations in threonine (Thr) levels via

289 f1 affects ammonium and nitrate assimilation in response to various nitrogen sources.

290 g primrose flowers adaptively secrete nectar in response to vibrations from hovering bees lacks suppo

291 tem, which also generates cyclic nucleotides in response to viral infection.

292 (pDCs) produce abundant type I IFNs (IFN-I) in response to viral nucleic acids.

293 In response to virus infection, the acetylated Lys129 is

294 esults suggest that yield risk will increase in response to warmer temperatures, with a 1 degrees C i

295 ad to quantify the ecosystem C and N cycling in response to warming and advances our capacity to pred

296 utrophils, macrophages, and epithelial cells in response to wounding.

297 ic response that the typical mammal displays in response to wounding.

298 atabolic diversity during adaptive evolution in response to xenobiotics released into the environment

299 rs released heightened IL-1beta specifically in response to Y. pestis.

300 K), a master regulator of energy metabolism, in response to ZIKV challenge.