ライフサイエンスコーパス: response of @2 to

1 The transcriptomic response of A. thaliana to 2,5-dichlorobiphenyl (2,5-DCB

2 Here we show the responses of ecosystem C to 8-12 years of experimental d

3 We also assessed the acute response of C. dubia to a binary mixture of microplastic

4 rently takes weeks to months to evaluate the response of cancer patients to a drug.

5 e stochastic dynamics and the time-dependent response of colloids subject to a small external perturb

6 To do this, we explicitly evaluate the response of electron density to a change in the system,

7 mir et al. (2017) reveal that the pathogenic response of mice to a Plasmodium berghei infection is do

8 hypertrophy response suggesting that the non-response of muscle to a hypertrophic stimulus could be m

9 Vascular reactivity, the response of the vessels to a vasoactive stimulus such as

10 tion of mechanisms of action of drugs or the responses of an organism to a specific impact (e.g. a di

11 demographic, life history, and morphological responses of large mammals to a very isolated and ecolog

12 the stimuli enabled characterization of the responses of neurons to a single quantum (pulse) of evid

13 We investigated the responses of odorant receptors to a large spectrum of se

14 The electrochemical responses of this device to a reversible redox pair were

15 We propose that the observed response of Kleaf to ABA may be part of the overall ABA

16 The responses of organisms to abrupt warming and associated

17 We understand far less about the response of SOM decomposition to accelerated RSLR.

18 injection of PBS to mouse nasal cavity, the response of MOR161-2 to acetophenone was reduced, while

19 We used quantitative measurements of the response of a cells to alpha-factor to produce a predict

20 The olfactory response of Drosophila to ammonia has been studied in so

21 is a phenomenon in which noise enhances the response of a system to an input signal.

22 toxicological assessments often focus on the response of an organism to an individual contaminant und

23 vide preliminary evidence of a sex-dependent response of IR to an n-3 PUFA intervention.

24 tices at age 10 y appeared to be primarily a response of mothers to an unhealthy weight of their chil

25 nd water as well as monitoring the metabolic responses of living organisms to an ever changing enviro

26 Time-dependent responses of materials to an ultrashort optical pulse ca

27 sea level rise have led to concern about the response of parasites to anthropogenic climate change.

28 nvestigate the potential role of DJ-1 in the responses of human MCs to antigen stimulation.

29 In recent years, the responses of various species to attractants have been do

30 pressed gene upregulated during the adaptive response of prostate tumors to ATTs and a prognostic bio

31 microwave conversion efficiency and temporal response of the MASER to be measured as a function of ex

32 gh mechanical strain can explain the plastic response of cells to bending(4) and quantitatively predi

33 ul molecular markers to predict the ultimate response of pituitary adenomas to BIM-23A760.

34 n is uniquely able to suppress the excessive response of macrophages to both M1 and M2 stimuli and th

35 investigate this phenomenon, we measured the response of microtubule assembly to both rapid and long-

36 associated with an APOE- and TREM2-dependent response of microglia to brain tissue damage that accumu

37 de channels; here, we investigate the direct response of CFTR to calmodulin-mediated calcium signalin

38 ression-based algorithm that can predict the response of tumors to cell-cycle-targeting miRNAs.

39 First, the response of ANPP to changes in precipitation and biodive

40 cytosolic metabolite availability alters the response of isoprene emission to changes in atmospheric

41 Quantifying the response of mobile consumers to changes in habitat avail

42 s thaliana to quantify the dependence of the response of NPQ to changes in light intensity on the pre

43 cing compounds is often part of a more broad response of the plant to changes in the environment.

44 ups on polymer chains determines the overall response of the system to changes in the external pH.

45 somes in the absence of C9orf72 and impaired responses of mTORC1 signaling to changes in amino acid a

46 rocesses, such as competition, physiological responses of plants to changes in atmospheric CO2 concen

47 argest user of PGMs) reflecting the rational response of firms to changing prices.

48 nces in fitness are explained in part by the response of photosynthesis to changing soil moisture.

49 interaction preferences in males as well as responses of MeA neurons to chemosensory cues.

50 of N-linked glycosylation in modulating the response of cancer cells to chemotherapeutic and biologi

51 r heterogeneity and monitor the pathological response of breast cancer to chemotherapy in a large coh

52 whereas expression of DnaJC15 regulates the response of cancer cells to chemotherapy.

53 deposited in the past) records evolutionary responses of populations to chronic pollutant exposure.

54 ABSTRACT: 'Adaptive' responses of the liver to chronic alcohol consumption ma

55 omparisons were employed to characterize the response of fruit to CI expression.

56 e for histone deacetylation and inflammatory responses of primary microglia to classic inflammatory s

57 The response of catotelm C to climate forcing is uncertain,

58 The response of hailstorm intensity to climate variability/c

59 rn spatial distribution pattern modulate the response of its yields to climate change at the state le

60 The response of marine plankton to climate change is of crit

61 e used the relationship between the observed response of species to climate change and a set of intri

62 The response of tropospheric oxidants to climate change is p

63 The responses of metabolic rates to climate warming may be g

64 rient supply and use efficiency in mediating responses of primary producers to climate warming.

65 ication and that habitat plays a role in the responses of species to climate change.

66 r results give insight into the geographical responses of tree species to climate change and demonstr

67 Each of the methods indicated a significant response of gm to CO2 .

68 , predicts the adaptation-induced changes in response of single neurons to complex stimulus configura

69 ill be to predict how these divergent future responses of marine microorganisms to complex multiple v

70 nvestigate the role of magnitude in adaptive response of osteoblasts exposed to compressive stress.

71 s and measured the aboveground morphological responses of each species to conspecific vs heterospecif

72 py, optical activity, and sub-millisecond EO response of BPIII to conventional nematic LCs.

73 provide a molecular-scale perspective on the response of plants to copper nanopesticides.

74 phenomenon, we exploit the nonlinear dynamic response of microelectromechanical oscillators to couple

75 If so, then phasic response of dopamine neurons to cues in this setting can

76 hesis that RUNX1 is directly involved in the response of hematopoietic cells to cytotoxic agents.

77 our patients (88.9%) had a complete clinical response of CV to DAA therapy at week 24, defined by imp

78 The function of p53 alters the response of cells to defects associated with decreased C

79 This study highlights the dynamic biologic response of multicellular organisms to deguelin perturba

80 ools must be developed to measure the immune responses of individuals exposed to DENV either via vira

81 likely mediator of the initial physiological response of intestinal enterocytes to dietary lipid.

82 ledge, this study is the first to assess the response of MBF to different levels of hypercapnia in he

83 work, we have studied the similarity in the response of the toxicity to different species and we hav

84 ese tools were then used to characterize the responses of MTB to different O2 concentrations and iron

85 (DCM) is best understood as the final common response of myocardium to diverse genetic and environmen

86 Loss of APE1 attenuates the response of melanoma cells to DNA damage induced by reac

87 However, the underlying mechanism of the response of cotton to drought stress remains elusive.

88 Some models show a response of k to drought in temperate forests as a resul

89 strate that similarity in the transcriptomic response of species to drought is a significantly better

90 The model predicts the response of the system to each of these experimental per

91 The response of electron systems to electrodynamic fields th

92 tion is complex, but we demonstrate that the response of assemblages to elevated CO2 are correlated w

93 ver, the molecular mechanisms underlying the response of macrophages to elevated fatty acids (FAs) an

94 S93-4118, but there was no difference in the response of photosynthetic traits to elevated [CO2 ] in

95 the hypothesis that Ms 9a-1 potentiates the response of TRPA1 to endogenous agonists followed by per

96 the coreceptor CD14 reduced the profibrotic responses of uremic leukocytes to endogenous components

97 The response of bacterial communities to environmental chang

98 ntal factors offers a new perspective on the response of global vegetation to environmental changes.

99 Consequently, it is very hard to predict the response of the ecosystem to environmental changes.

100 the two sides of a coin, linked by movement responses of individuals to environmental heterogeneity.

101 Here, we hypothesized that the responses of phylogenetic structure to environmental cha

102 tionary history of traits that influence the responses of species to environmental change can help to

103 rs can predict the magnitude of evolutionary responses of subsequent generations to environmental cha

104 ping enhanced NEE due to a stronger positive response of GPP compared to ER, indicating that clipping

105 indings imply an asymmetry in the geomorphic response of badlands to erosion such that in the early e

106 y by their input-output behaviors; (iii) the response of the system to every possible perturbation ba

107 The differing response of ER subtypes to exercise and ajmaline provoca

108 e cellular level, VHH6 was able to alter the response of endothelial cells to exogenous IL-6, promoti

109 Basin, YRB) were evaluated, determining the response of precipitation to external changes over typic

110 omic analysis by RNA-Seq to characterize the response of Pseudomonas aeruginosa to external 0.5 mm Cu

111 PON-2 did not alter the response of ENaC to extracellular Na(+), mechanical shea

112 Observed differences in the response of functional types to extreme postfire weather

113 Local mRNA translation mediates the adaptive responses of axons to extrinsic signals, but direct evid

114 to modulate the behavioral and physiological responses of male mice to females on a moment-to-moment

115 lternative stable states driven by threshold responses of recruitment to fire and moisture regimes.

116 describe a new strategy to characterize the response of bimolecular interactions to forces even in t

117 electivity likely contribute to the specific response of T cells to foreign antigens.

118 f the primary and anamnestic Ag-specific IgG responses of mice to four clinically relevant vaccine fo

119 r understanding of how hypoxia modulates the response of ATMs to free fatty acids within obese adipos

120 redictive capacity of the role of TGP in the response of organisms to future climate change.

121 have been conducted to explore the possible responses of forest landscapes to future climate change,

122 e major differences in both the quantitative response of these genes to galactose and in the position

123 systematically integrate the transcriptional response of B-ALL to GCs with a next-generation short ha

124 However, the response of soil stoichiometry to global changes in natu

125 essary to improve our ability to project the response of the Arctic to global environmental change.

126 tes of warming are central to understand the response of wetland soils to global climate change.

127 The differing responses of taxa to global warming will cause spatial r

128 bition of PERK did not change the short-term response of beta cells to glucose.

129 e reproduced in silico the different dynamic responses of Msn2 to glucose limitation and osmotic stre

130 chemotactic model, calibrated from observed responses of cells to gradients, thereby provides insigh

131 to elucidate the molecular mechanisms of the responses of maize to grey leaf spot (GLS) disease cause

132 NC-93B are dispensable for a potent cytokine response of blood monocytes to group B Streptococcus, al

133 The response of the skin to harmful environmental agents is

134 rentiation in mice led us to investigate the response of human monocytes to HCMV following LPS stimul

135 erved significant genetic variability in the response of wheat to heat stress needs to be considered

136 els depending on specific phenotypic plastic responses of a plant to herbivory.

137 To study the transcriptional response of stem cells to HH signaling, we searched for

138 The response of resistant cells to high concentrations of ci

139 To investigate the physiological responses of plants to high root-zone temperature (HT, 3

140 ity of HIF-1alpha and strengthening adaptive response of cells to hypoxia.

141 We show that the response of the skin to hypoxia feeds back on a wide ran

142 nd may serve to regulate the proinflammatory response of endometrium to IL1B2 during conceptus elonga

143 an immune suppressive microenvironment, and response of ovarian cancers to immune therapies has thus

144 which create neoantigens that influence the response of patients to immune checkpoint inhibitors.

145 the role of the Bcl-2 family proteins in the response of cancer cells to immunotoxin challenge.

146 tation that atmospheric haze was a transient response of the biosphere to increased nutrient availabi

147 The response of the brainstem to increased levels of carbon

148 Responses of forest ecosystems to increased atmospheric

149 e that, in contrast with previously observed responses of plants to increased snow depth at the same

150 Understanding responses of forests to increasing CO2 and temperature i

151 q and ribosome profiling to characterize the response of macrophages to infection with the intracellu

152 on by a bacterial pathogen, we evaluated the response of Sts(-/-) mice to infection by a Gram-negativ

153 Inflammation is part of the physiological response of the organism to infectious diseases caused b

154 t targeting apoptosis regulators can improve response of these tumors to inhibitors of the PI3K/mTOR

155 We model the responses of these sensors to intracellular-buffered con

156 Predicting the responses of biological systems to ionising radiation is

157 ocessing algorithms to simulate the cellular response of tumours exposed to ionizing radiation, model

158 The response of CR-39 to ions is studied based on the energy

159 nd susceptibility to oxidative stress in the response of diatoms to iron quota in the marine environm

160 e of gravel is important for forecasting the response of rivers to large influxes of sediment trigger

161 carriers are important to understanding the response of materials to laser pulses.

162 Recently, the response of cryptochromes to light was extended to nearl

163 Changes in the response of NPQ to light acclimation in WT and mutant pl

164 The model accurately predicted steady-state responses of gS to light, atmospheric CO2 and oxygen, so

165 Electrophysiological responses of SCN neurons to light steps are well establi

166 voked vasopressin release contributes to the responses of SCN neurons to light, and enhances expressi

167 ght-induced vasopressin release enhances the responses of SCN neurons to light.

168 Inhibition of Src decreased the inflammatory response of CF cholangiocytes to lipopolysaccharide, res

169 Acute responses of the OE to liquid nPM suspensions were studi

170 sus European ancestry on the transcriptional response of primary macrophages to live bacterial pathog

171 The response of Arabidopsis thaliana to low-oxygen stress (h

172 rhythmic cue we investigated transcriptomic response of maize seedlings to low temperature in the co

173 s to compare the differential transcriptomic response of human blood to LPS and MPLA.

174 Our findings implicate the response of innate macrophages to M. leprae PGL-1 in ini

175 Here, we map the response of topological states to magnetic impurities at

176 ased on arsM sequences and the physiological response of cultures to media conditions, we propose tha

177 ry that allows us to make predictions on the response of a protein to medically relevant stimuli such

178 Remarkably, the loss of SIRT2 blunted the response of AMPK to metformin treatment in mice infused

179 examined electrophysiological and behavioral responses of honey bees to microbial volatiles.

180 The response of aging skin to MNs has not been explored, and

181 However, the differential response of human leukocytes to MPLA and LPS has not bee

182 nylation in zebrafish to analyse the initial response of neutrophils to Mycobacterium marinum, a clos

183 This first line response of astrocytes to myelin injury may exert benefi

184 However, the general response of species richness to N deposition across diff

185 Our model results predict that the responses of GHG fluxes to N are highly nonlinear and th

186 Here we analyse responses of V2 neurons to natural stimuli and find thre

187 and subharmonic imaging can help predict the response of breast cancer to neoadjuvant chemotherapy.

188 of CCL3 in OM, we evaluated middle ear (ME) responses of ccl3(-/-)mice to nontypeable Haemophilus in

189 Responses of phytoplankton to OA may depend on the times

190 erm changes should be measured to understand responses of primary producers to OA, especially in wate

191 he objective of this study was to assess the response of plasma lysophospholipids to obesity, n-3 PUF

192 pearing, or quickly moving stimuli restricts responses of WF cells to objects that are small and movi

193 Predicting the responses of macroalgal species to ocean acidification i

194 AB is a key factor supporting the pathogenic response of astrocytes to oligodendrocyte injury.

195 le control, we demonstrate sequence-specific responses of RNA variants to oligonucleotide signals.

196 Studies on the long-term responses of marine phytoplankton to ongoing ocean acidi

197 These differences in the response of periodontal tissues to orthodontic force in

198 The response of lipid bilayers to osmotic stress is an impor

199 surgery rat model to gain insights into the response of human bone to osteotomy site preparation.

200 not yet sufficient to predict the molecular responses of PTPs to oxidative stress.

201 This unexpected response of human mDCs to P. falciparum exhibited a tran

202 Understanding response of solids to particle irradiation remains a maj

203 tivation of vM1 supra-linearly amplified the response of vS1 neurons to passive vibrissa stimulation

204 eron (IFN-beta) is essential for many of the responses of macrophages to pathogen-associated molecula

205 eotide given intratumorally may increase the response of cancer patients to PD-1 blockade, increasing

206 the human cortical surface to elucidate the response of cortical oscillations to periodic stimulatio

207 of systems biology is to predict the kinetic responses of living systems to perturbations starting fr

208 tulate the transcriptional and morphological responses of opaque cells to pheromone.

209 f root architecture is a major developmental response of plants to phosphate (Pi) deficiency and is t

210 Growth responses of pioneers to phosphorus addition revealed a

211 nced SK activity contributes to the adaptive responses of MNCs to physiological challenge, such as la

212 In this regard, although the long-term responses of plants to Pi stress are well documented, th

213 The nonlinear and asymmetric responses of soil respiration to precipitation changes s

214 in vitro system allowing to track migratory responses of DCs to precisely controlled immobilized gra

215 Our study revealed different responses of tree species to projected climate change.

216 t." Further support for a strongly nonlinear response of monsoons to radiative forcings is found in t

217 ition as a metabolic strategy to improve the response of GBM to radiotherapy.

218 ies link the spatial correlations and strain response of softness to rearrangement size and yield str

219 ia in order to investigate the physiological response of these trees to regional warming.

220 ce theory and with models based on nonlinear response of the brain to rhythmic stimuli.

221 A prevailing response of crops to rising [CO2 ] is an increase in lea

222 Uncertainties in the response of vegetation to rising atmospheric CO2 concent

223 We evaluated the damage responses of CAF to RT and investigated changes in color

224 We find that the differential response of DESE to Runt is due to an inhibitory effect

225 idopsis thaliana) and how Pi levels modulate responses of the root to salt stress.

226 underpinning the observation of an amplified response of summer LSWT to SAT variability using 20 year

227 re we present observational evidence for the response of precipitation to sea ice reduction and asses

228 be important for understanding the potential responses of coastal species to sea-level rise, especial

229 volutionary rescue compared with the plastic response of fitness to seasonal climate change.

230 stream of the auditory cortex, we found that responses of hippocampal neurons to self-generated sound

231 Here, we characterized the response of CaMPARI to several common types of neuronal

232 K-3 activation, we studied the concentration-response of TASK-3 to several anesthetics (isoflurane, d

233 ssion) of adult females, and the orientation responses of adult males to sex pheromone were also sign

234 The response of amorphous steels to shock wave compression h

235 o test this, we compared transcriptome-level responses of disparate Pooideae to short-/long-term cold

236 d DFT calculations, can reliably dissect the response of small GTPases to site-specific modifications

237 he population level was a consequence of the responses of individual cells to sodium chloride that we

238 At the same time, the response of different species to spatial and interannual

239 erties, which thereby determines the precise responses of synapses to spike patterns in a neuron and

240 Investigating the time-dependent response of the system to square pulses, oscillations in

241 ended culture ex vivo, correctly defines the response of nine patients to standard-of-care drugs acco

242 and NK T cells was measured, as well as the response of PBMCs to stimulation with TLR ligands.

243 transcriptomics, and genome scans to measure responses of lizard populations to storm-induced selecti

244 We investigated the in vivo responses of osteocytes to strains ranging from 250 to 3

245 The acute response of blubber to stress axis activation, measured

246 opathology, developmental differences in the response of this system to stress may contribute to incr

247 ndothelium might contribute to inappropriate responses of immature arteries to stress or injury.

248 hough this might contribute to inappropriate responses of immature arteries to stress or injury.

249 Karenina effects are a common and important response of animal microbiomes to stressors that reduce

250 Moreover, the direction and intensity of the response of forest trees to such perturbations are unkno

251 model also correctly predicts a plateau-like response of translation to super-physiological increases

252 nique to TAARs and can extend to an aversive response of potential importance to survival.

253 asia, thought to be responsible for the poor response of patients to systemic therapies.

254 Adequate and advance knowledge of the response of forest ecosystems to temperature-induced dro

255 nd microfluidics to investigate the adaptive response of budding yeast to temporally controlled H2O2

256 ic relationship that captured the functional response of CO2 flux to thaw, water table depth, and pla

257 More recently, it has been proposed that the response of aortic SMCs to the hemodynamic load on a str

258 ty and, consistent with that, potentiate the response of cells to the drug.

259 AP1 depletion, RanBP2 depletion impaired the response of cells to the microtubule poison Taxol.

260 ponent system plays an essential role in the response of enterobacteria to the environment of their m

261 iment, we cross-fostered eggs and tested the response of hatchlings to the scent of genetic vs. foste

262 ssis and acts by specifically inhibiting the response of myeloid leukocytes to the pathogen.

263 We further analyzed the response of NS to the GABA receptor antagonist bicuculli

264 te the similarities in their properties, the response of the bacteria to the two nanomaterials was fu

265 down or mutation of TAR2 also eliminated the response of tubules to the related amine octopamine (OA)

266 tools of network theory to shed light on the response of world trade to the financial crisis of 2007

267 We demonstrate that responses of CovRS to the stress signals Mg(2+) and a fr

268 iltering by variation and covariation in the responses of individual species to the characteristics o

269 Exploiting the behavioural responses of mosquitoes to the entire suite of host stim

270 d thus provides a unique model to assess the responses of separate clones to the same anti-multiple m

271 rst element of the pathways that control the response of cells to their environment.

272 scaling mechanism.SIGNIFICANCE STATEMENT The response of sensory neurons to their preferred stimulus

273 lesions and was effective in monitoring the response of these lesions to therapy.

274 rocess, as well as dictate the heterogeneous responses of cancer cells to therapy.

275 organization partly dictate the differential responses of roots to these two auxin analogues.

276 However, unexpected differences in the responses of societies to these factors in North America

277 ls to study the role of host genetics in the response of macrophages to this obligate human pathogen.

278 However, little is known regarding the response of soil nematodes to this degradation.

279 tainties in projected climate change and the response of the forest to this change (forest resiliency

280 ow that genetic knockout of Gsto1 alters the response of mice to three distinct inflammatory disease

281 In the brain, the postsynaptic response of a neuron to time-varying inputs is determine

282 The default response of most cells to TNF is survival and NF-kappaB-

283 We analyzed the responses of fetal SPNs to transient disturbances in fet

284 ffusion-weighted imaging (DWI) to assess the response of bone metastases to treatment in patients wit

285 t removal should be useful for assessing the response of MNV to treatment using OCTA imaging.

286 Response of the surrogates to treatment with paclitaxel

287 e of (99m)Tc-duramycin for imaging the early response of tumors to treatment.

288 is an important target for imaging the early response of tumors to treatment.

289 ns-on a microscopic level-the extremely fast response of this material to ultrafast optical excitatio

290 maB network that controls the general stress response of Bacillus subtilis to uncover widely relevant

291 n translation, respectively, we analyzed the responses of host cells to vaccinia virus infection at b

292 rospectroscopy was used to quantify freezing response of cells to various cooling rates and solution

293 resting membrane potential and regulate the response of excitable cells to various stimuli.

294 ion factors, accounting for the differential responses of promoters to various transcription factor m

295 Furthermore, we characterized the response of microglia to VSV infection and found that in

296 linked to photosynthetic physiology, but the response of GPP to warming over longer timescales could

297 an Earth system model to illustrate how the response of ocean circulation to warming does not suppor

298 The estimated responses of metabolic processes to warming were usually

299 Furthermore, we found that the CD8(+) T cell responses of pregnant mice to ZIKV infection were dimini

300 hts into molecular mechanisms underlying the responses of the diatom to ZnO-NPs and Zn(2+) under vari