1 Several cycles of repetitive
exposure of cells to 0.1 g/L nZVI induced a persistent p
2 density gradient centrifugation showed that
exposure of roots to 0.5 mM H2O2 induces significant dep
3 ADT thin films were increased and subsequent
exposure of the films to 1,2-dichloroethane vapor led to
4 eractions were investigated after 10 days of
exposure of Arabidopsis thaliana to 10 mg.L(-1) of negat
5 Acute (minutes)
exposure of cultured neurons to 10 nM clothianidin, but
6 Exposure of the nanoparticles to 2-propanol at 30 degree
7 We show that three-week
exposures of periphyton to 20.6 +/- 0.4 muM PbT (330 nM
8 Exposure of cells to 25mM glucose (diabetic-type conditi
9 is neither bactericidal nor bacteriostatic,
exposure of V. cholerae to 2D6 IgA (or Fab fragments) re
10 Exposure of YAMC cells to 4-HNE induced Gsta4 expression
11 d bisretinoid formation were studied and pre-
exposure of mice to 430 nm light enriched for dicarbonyl
12 locus is methylated in differentiated cells,
exposure of DAOY cells to 5-aza-2'-deoxycytidine or thei
13 Exposure of cells to (
56)iron or (28)silicon promotes Bc
14 pure phosphatidylcholine (PC) bilayers upon
exposure of both to 70 muM Cu(2+) and 10 mM hydrogen per
15 Headspace
exposure of Arabidopsis thaliana to a mixture of the bic
16 to the extracellular space immediately after
exposure of astrocytes to a physiological rise in extrac
17 These results indicate that 2 h of
exposure of beta cells to a low but not a high concentra
18 Combined
exposure of cells to a small-molecule inhibitor of NMD,
19 Exposure of G. pallida to a diurnal temperature stress f
20 We demonstrate that sequential
exposure of human astrocytes to a cocktail of nine small
21 nt susceptibility to hypoxia, as revealed by
exposure of naive animals to a hypoxic environment.
22 Exposure of PEL cells to a chemical inducer of XBP-1s ca
23 s circulating in the blood following aerosol
exposure of rhesus macaques to a lethal dose of Marburg
24 Our data suggest the environmental
exposure of ruminants to a broad range of strains and ye
25 substrate binding channel of COX-1 in vitro,
exposure of volunteers to a single therapeutic dose of e
26 In Alzheimer's disease (AD) brain,
exposure of axons to Abeta causes pathogenic changes tha
27 Exposure of Xenopus embryos to AChE-inhibiting chemicals
28 s study, we focused on a genotoxic aspect of
exposure of esophageal cells to acidic bile reflux (BA/A
29 Mechanistically, our data showed that
exposure of esophageal cells to acidic bile salts induce
30 Notably,
exposure of histones to acrolein prior to histone acetyl
31 at suggests Au-CO complex formation upon the
exposure of CO to active sites (step edges and threading
32 Interestingly,
exposure of YAP(-/-) hESCs to Activin induces cardiac me
33 In vitro
exposure of blood DCs to acute IM plasma resulted in los
34 Prolonged
exposure of trypanosomes to AEE788 inhibited transferrin
35 s to distinct nuclear foci specifically upon
exposure of cells to alkylating agents.
36 These data demonstrate that the
exposure of neutrophils to allergens leads to generation
37 clinical facilities allowing for controlled
exposure of subjects to allergens in an enclosed environ
38 Exposure of these cells to allergens induces the release
39 fluidic device was used to precisely control
exposure of cells to alternating stimulatory and non-sti
40 Continuous
exposure of soil to AMD induced progressively greater ra
41 e, even when assays were preceded by chronic
exposure of cells to an established chaperone, nicotine.
42 Here we report on the
exposure of pregnant ewes to an environmental mixture of
43 Exposure of young HSCs to an OPN knockout niche results
44 life and are PG targets, we investigated if
exposure of pregnant rats to analgesics (indomethacin or
45 ding to irreversible inactivation; and (iii)
exposure of cryptic epitopes to antibodies, allowing vir
46 Prolonged
exposure of hippocampal neurons to antibodies from patie
47 f this regimen makes this one of the largest
exposures of humans to antimicrobials, yet the effects o
48 Patients had a median
exposure of 1 day to antipsychotic medication prior to b
49 Exposure of NHBE to any eCig liquid resulted in the indu
50 f the first research to demonstrate that the
exposure of plants to APIs is likely to cause impacts on
51 Exposure of these people to arsenic was assessed using s
52 gated the processes governing U release upon
exposure of reduced sediments to artificial groundwater
53 the conditions of oxidative gold catalysis,
exposure of ethylene to aryl silanes and alcohols genera
54 a4 and alpha4beta2 nAChRs are upregulated by
exposure of cells to AT-1001 for 3 days.
55 ed patterns of cytokine expression after the
exposure of iHOs to bacteria.
56 Daily
exposure of differentiated adipocytes to blue light resu
57 owever the effects of antibiotic loading and
exposure of beads to body fluids on release kinetics are
58 Exposure of HTEpC cells to both CSE and IL-17A increased
59 The protein corona that forms upon
exposure of nanoparticles to bovine serum albumin was ut
60 Concerns have been raised over
exposure of humans to BP-3, owing to the estrogenic pote
61 eceipt paper; however, little is known about
exposure of cashiers to BPA and alternative compounds in
62 r significant cognitive disruption following
exposure of humans to BPA.
63 Colocalization studies revealed that
exposure of HK cells to brain homogenate resulted in inc
64 anied by macrophage infiltration after brief
exposure of the retina to bright light.
65 n structural rearrangements resulting in the
exposure of positive charges to bulk solvent rather than
66 ough time, and provide the first evidence of
exposure of polar bears to C. burnetii, N. caninum, and
67 n this article, we demonstrate that in vitro
exposure of human neutrophils to C5a significantly incre
68 Exposure of laboratory mice to carbon nanotubes mimics e
69 Acute
exposure of GSCs to CBL0137 increased asymmetric cell di
70 Mucosal
exposure of macaques to cell-associated SIV by using inf
71 This pathway is triggered upon
exposure of plasma to certain anionic polymers and artif
72 Importantly,
exposure of P. aeruginosa to CF-ALF drives the activatio
73 d labor-intensive purification operations or
exposure of the operator to CH2N2.
74 Exposure of DNA to chemicals can result in the formation
75 Exposure of immune cells to cigarette smoke extract in v
76 However, we also demonstrate that the
exposure of marine ecosystems to climate change-induced
77 Exposure of young animals to commonly used anesthetics c
78 ry mechanisms and gene expression changes on
exposure of cells to completely novel environments.
79 wa River water) and after 12 h of continuous
exposure of MWCNTs to concentrated ozone solutions.
80 Exposure of mice to constant light disrupted the clock i
81 Exposure of the samples to copper sulfate solution induc
82 hronic anxiety and pain induced by prolonged
exposure of the CeA to CORT.
83 In contrast,
exposure of Fh simultaneously to Cr(VI) and As(III) led
84 EMVs amplified their own biological signals:
exposure of "inert" fibroblasts to CSp-EMVs rendered the
85 Exposure of HeLa cells to Cu(PyBD).SO4 (IC50 = 10 muM) r
86 tress response was also evident upon in vivo
exposure of mouse uteri to culture medium conditioned by
87 Exposure of hPGCLCs to CXCL12/SDF1 induced cell migratio
88 Prolonged
exposure of beta-cells to cytokines or thapsigargin lead
89 n of a drug gradient concentration, allowing
exposure of cancer cells to different doses, and the imm
90 Moreover,
exposure of V. cholerae to different environmental cues
91 We found that in utero
exposure of rats to DINCH from gestational day 14 until
92 produced bovine embryos, we demonstrate that
exposure of embryos to DKK1 during the period of morula
93 Exposure of neurons to DNA damaging agents or the excito
94 ystems framework for assessing the financial
exposure of utilities to drought, with further considera
95 Exposure of cells to DTT immediately before CO exposure
96 ations, including separations, which require
exposure of the polymer to dynamic flow conditions.
97 Collectively, our results suggest that acute
exposure of neurons to E2 leads to destabilization of GA
98 Exposure of tissue to EcN cells, but not MG1655 cells, w
99 Exposure of pregnant ewes to ECs over 80 day periods dur
100 Exposure of mCCDC11 cells to ECVs isolated from cells ov
101 d albumin filtration, resulting in increased
exposure of the PTs to endogenous albumin.
102 In cell culture studies,
exposure of macrophages to endothelial NO similarly redu
103 We show that the early
exposure of rat pups to enriching environmental conditio
104 Moreover, we report that the
exposure of adult animals to environmental enrichment en
105 eased resource development, which will alter
exposure of biota to environmental agents of disease.
106 The
exposure of fish to environmental free-living microbes a
107 Transient
exposure of healthy females to environmental stresses su
108 ity, and was directly cytotoxic, whereas the
exposure of cells to equivalent doses of the OSPW-OF had
109 Additionally, the
exposure of 2 to ethylene or molecular hydrogen gave sil
110 In these methods, continuous
exposure of bran to external forces causes bran to retai
111 In contrast,
exposure of the biosensor to extracts from MSSA-infected
112 Exposure of Africans to fatal pathogens, such as Plasmod
113 Exposure of cultured neurons to fetal plasma or to secre
114 ese observations show that early and limited
exposure of pulp cells to FGF2 alone promotes odontoblas
115 Our results showed that early and limited
exposure of pulp cells to FGF2 did not have significant
116 Continuous
exposure of pulp cells to FGF2 inhibited odontoblast dif
117 t differentiation, whereas early and limited
exposure of pulp cells to FGF2 resulted in marked increa
118 Exposure of AMs to fluorescein isothiocyanate-labeled IA
119 Exposure of AmelX(-/-) mice to fluoride enhanced the min
120 and voluntary folic acid fortification, the
exposure of children to folic acid has been a focus of c
121 We conducted a 91-day chronic laboratory
exposure of Cyprinodon variegatus to four concentrations
122 nge scenarios, specifically by assessing the
exposure of coffee farming to future climatic shifts.
123 In brain slices,
exposure of LC neurons to GABAAR agonists increased toni
124 Exclusive
exposure of rat oligodendrocytes to GD1a, but not other
125 However,
exposure of eosinophils to GM-CSF, IL-4, and IL-33 prior
126 We show that
exposure of neurons to growth-limiting molecules--such a
127 However,
exposure of CaMKIIdelta to GSNO prior to Ca(2+)/CaM expo
128 a C(sp(3) )-H bond and can be reversed upon
exposure of 4 to H2 .
129 Although the
exposure of 2a to H2O afforded a stable silicon analogue
130 Exposure of H9c2 cardiomyocytes to H2O2 or pharmacologic
131 irions changes in the same way following the
exposure of virus to heat or to soluble integrins.
132 We demonstrate that
exposure of cultured macrophages to hemolytic aged red b
133 Exposure of 13-HODE to Hepa-1c1c7 cells induced oxidativ
134 Prolonged
exposure of islets to high concentrations of IL-1beta (>
135 P15 inhibits anthocyanin accumulation during
exposure of plants to high light intensity by modulating
136 H2O2 that reaches the viable epidermis after
exposure of skin to high concentrations of peroxide (0.5
137 In vitro
exposure of CMs to histones caused loss of homeostasis o
138 Exposure of sympathetic neurons to HNE resulted in neuri
139 Exposure of hydrated cysts to host plant root exudates r
140 Indeed, direct
exposure of PCCL3 cells to human serum from two patients
141 Calculations revealed that the
exposures of the NPs to human lung due to the abrasion o
142 ercury (Hg) into the atmosphere to lower the
exposure of Hg to humans.
143 zed that ingestion of microplastic increases
exposure of aquatic organisms to hydrophobic contaminant
144 oxia may explain elevated CA in vivo because
exposure of cultured cells to hypoxia or mimicking hypox
145 s the ability of Mre11 to bind DNA following
exposure of cells to HZE particles.
146 Exposure of cells to IFN-gamma has been shown to trigger
147 Chronic
exposure of mice to IFN-alpha alone was sufficient to st
148 Moreover, we show that
exposure of tumours to IFN-gamma-producing antigen-speci
149 f Rc3h1 restricts Il17a expression, and that
exposure of T cells to IL-10, a cytokine with immunosupp
150 s a field-based technique for monitoring the
exposure of fish to impacted surface waters.
151 ort studies are often enriched for a primary
exposure of interest to improve cost-effectiveness, whic
152 While denaturation curves obtained after
exposure of PrP(Sc) to increasing GdnHCl concentrations
153 These findings suggest that
exposure of aquatic ecosystems to individual pesticides
154 as(V12) specifically in the liver by a brief
exposure of mifepristone to induce permanent genomic rec
155 cally in the zebrafish liver only by a brief
exposure of mifepristone to induce permanent genomic rec
156 n challenge studies-involving the deliberate
exposure of participants to infectious substances-have h
157 s such as ZO-1, claudin, and JAM-A; however,
exposure of SCs to inflammatory mediators derived from Z
158 ase activity and genetic haplotype and after
exposure of epithelial cells to interleukin (IL)-13, and
159 Exposure of the epithelium to interleukin-13 (IL-13) rec
160 enhancement of antiproliferative effect upon
exposure of cells to irradiation by visible light, proba
161 erase in a stepwise manner, providing higher
exposure of 1 compared to its direct administration, esp
162 However,
exposure of S940A mice to kainate induced lethality with
163 Exposure of urothelium to ketamine resulted in apoptosis
164 Upon
exposure of TiO2 -N3 to light, the N3 injected electrons
165 In vivo
exposure of a mouse to low environmental oxygen causes G
166 rt to the nucleus and requires the transient
exposure of AdV5 hexon to low pH, presumably mimicking p
167 otion received support from the finding that
exposure of I-MPhis to low pH or treatment with 2-(1-ada
168 However, long-term
exposure of tissue to low levels of dexamethasone result
169 Using the inflammasome protocol,
exposure of cardiomyocytes (CMs) to LPS followed by ATP
170 We found that a first
exposure of mice to LPS activated the ligand-operated tr
171 oted ROS in acutely inflamed lungs following
exposure of mice to LPS.
172 We analyzed the direct
exposure of T cells to LTA in vitro.
173 Prolonged
exposure of NRVMs to LUF7244 or LUF7244 plus astemizole
174 h 2007-January 2009) from Plynlimon (UK) and
exposure of air masses to marine chlorophyll a and to ot
175 humans, epidemiological studies suggest that
exposure of fetuses to maternal inflammation increases t
176 Early-life
exposure of the PVH to maternal obesity through postnata
177 could occur without mating and required only
exposure of hermaphrodites to medium in which males were
178 The ongoing
exposure of humans to MERS-CoV from the reservoir is of
179 cination and immunity by selective microbial
exposure of laboratory animals to mimic that of humans.
180 Moreover,
exposure of cells to mitotane, cisplatin, or radiation r
181 hine treatment (in vivo) but not upon direct
exposure of glia to morphine (in vitro).
182 Exposure of P1 ECs to MPs shed from senescent P3 cells o
183 ization is more cost-effective but increases
exposure of noncarriers to mupirocin and the risk of res
184 The
exposure of European population to mycotoxins through be
185 g active photosynthetic complexes even after
exposure of cells to N deprivation for 3 d.
186 Exposure of the dihydrodiols to N-bromoacetamide in THF-
187 Furthermore,
exposure of endothelial cells to nanomolar concentration
188 Exposure of myofibroblasts to nanomolar concentrations o
189 RCP4.5) while simultaneously maintaining the
exposure of corals to natural variations in their enviro
190 Exposure of C. bombi to naturally occurring levels of ph
191 Following
exposure of cells to NCS-C, DNA was isolated, and labile
192 superficial nanoshells from skin surface and
exposure of skin to near-infrared laser, nanoshells loca
193 Exposure of bacteria to NO results in the nitrosylation
194 It is modelled by
exposure of the protein to non-physiological low pH in v
195 astrin expression is rapidly eliminated upon
exposure of beta-cells to normal glucose levels.
196 Moreover,
exposure of a fly to novel odors evokes an alerting resp
197 anwhile, population growth is increasing the
exposure of human beings to novel pathogens, particularl
198 Short
exposures of Bacillus spores to nutrient germinants can
199 he Puma gene and induces its expression upon
exposure of neurons to oligomeric Abeta(1-42).
200 on content, and pore saturation, control the
exposure of U(IV) to oxidants, moderating its oxidative
201 Exposure of cells to oxidative stress conditions caused
202 We further demonstrate that
exposure of HAECs to oxidized phospholipids or pro-infla
203 Exposure of macrophages to oxidized low-density lipoprot
204 Exposure of monocytes to oxidized low-density lipoprotei
205 0.8 parts per million), we demonstrated that
exposure of rats to ozone induced whole-body insulin res
206 ption of HSP90 tertiary structure, promoting
exposure of R502/R510 to PAD modification and subsequent
207 robabilistic model for estimating cumulative
exposure of humans to PAHs.
208 High-fat feeding in mice and chronic
exposure of human islets to palmitate decreases endogeno
209 Exposure of C. jejuni to pancreatic amylase promotes bio
210 Upon
exposure of TAS to pancreatic cancer cell-conditioned me
211 The widespread
exposure of humans to parabens present in personal care
212 time to our knowledge on a global scale, the
exposure of surface waters to particularly toxic agricul
213 alysis of integration data demonstrated that
exposure of radish to Pb stress resulted in profound bio
214 Thus,
exposure of neonatal mice to PC-bearing pneumococci sign
215 Exposure of bis-amides to Pd(II) catalyst triggered the
216 edgehog and TGFbeta signalling pathways, and
exposure of the cells to pertinent growth factors led to
217 icides in agriculture may lead to downstream
exposure of farmers' families to pesticide residues inad
218 east as difficult as assessing the potential
exposure of foraging bees to pesticide.
219 In this study, we found that the
exposure of mature biofilms to physiologic levels of the
220 In vivo assessment of the
exposure of AHLs to plasma was examined using a standard
221 PMN were shown to generate C1q and C3a;
exposure of hNSC to PMN-synthesized concentrations of th
222 passive samplers to assess cumulative 5-day
exposure of 30 individuals to polar PRs.
223 We aimed to assess whether direct
exposure of B cells to pollen constituents affects aller
224 e observed low-level productive infection on
exposure of these cells to primary cell-free HIV-1 super
225 After an eight-day
exposure of zebrafish larvae to probiotic Lactobacillus
226 Exposure of experimental animals to purified recombinant
227 is study confirms the importance of reducing
exposure of the heart to radiation to avoid excess risk
228 We investigated whether
exposure of pancreatic tissues to radiocontrast agents d
229 Exposure of cells to reactive oxygen species (ROS) cause
230 e model of multiple infections, we show that
exposure of mice to repeated doses (4x) of Schistosoma m
231 Exposure of PT cells to RFS-kappaLCs resulted in kappaLC
232 Exposure of cysteine residues to ROS in the presence of
233 We found that growth rate was not altered by
exposure of P. gingivalis to SAPP, while monospecies and
234 Overall, our findings suggest that previous
exposure of humans to seasonal influenza can poise them
235 The
exposure of mantle rocks to seawater during the breakup
236 We show that
exposure of mouse embryos to short-term gestational hypo
237 ce, and information on current trends in the
exposure of nonsmokers to SHS across various occupationa
238 rian pharynx is selectively induced by brief
exposure of animals to sodium azide.
239 In this study, we demonstrate that acute
exposure of cultured neurons to soluble Abeta oligomers
240 into bioactive conformations that determine
exposure of polar atoms to solvation by water and lipids
241 that temperature activation is driven by the
exposure of hydrophobic residues to solvent.
242 Sustained
exposure of colonocytes to SP activates NF-kappaB and st
243 Exposure of PLC-PDXs to standards of care or therapeutic
244 Exposure of R. oryzae to statins at concentrations below
245 had MICs of >64 microg/mL against R. oryzae
Exposure of R. oryzae to statins decreased germling form
246 We found that
exposure of mice to sterilized cecal contents also resul
247 Here, we demonstrate that
exposure of S. aureus to sublethal concentrations of H2O
248 We show that
exposure of AT to Th2 cytokines, such as IL-4, IL-13, an
249 l activation during inflammatory conditions,
exposure of APCs to the Toll-like receptor 7/8 agonist R
250 It has been suggested that excessive
exposure of children to the dynamic and highly salient a
251 Exposure of DCs to the new class of triterpenoid CDDO-DF
252 Exposure of Drosophila melanogaster to the IMI NAPs at a
253 Here we show that
exposure of F0 mice to the obesogen tributyltin (TBT) th
254 Exposure of hypertrophied myocytes to the Orai channel b
255 Through directed
exposure of individual cells to the pore-forming agent a
256 During host cell infection, VipD reduces
exposure of L. pneumophila to the endosomal compartment
257 The low cytotoxicity allows a long time
exposure of live cells to the dyes without the necessity
258 Exposure of newborns to the maternal vaginal microbiota
259 The
exposure of PS to the outer membrane and to extracellula
260 In contrast, the
exposure of smooth muscle to the microtubule depolymeriz
261 The
exposure of spirits to the soapstone exhibits a linear r
262 t respond to eculizumab will avoid prolonged
exposure of such individuals to the infectious complicat
263 Our results revealed that after the
exposure of synthesized aerosol to the insect antenna, A
264 individual pixel results in continuous long
exposure of the cell to the laser and eventual bleaching
265 ross generations without the need for direct
exposure of the child to the index environmental insult
266 the effect of the chemical and the nature of
exposure of the environment to the chemical.
267 Exposure of the films to the enzyme resulted in the degr
268 ly decreased off-target effects with a pulse
exposure of the genome to the Cas9/sgRNA complex.
269 tential safety of inadvertent or intentional
exposure of these agents to the developing fetus.
270 Furthermore, we find that
exposure of Treg to the mechanistic target of rapamycin
271 a cell-specific antiviral response following
exposure of viral DNA to the intracellular compartment.
272 This suggests that
exposure of virions to the cell culture medium is obliga
273 enzootic cycle as well as for the increasing
exposure of humans to them.
274 pathways whose modulation could improve the
exposure of tumors to therapeutic agents.
275 the data presented here indicate a long-term
exposure of Homo to these elements, via fires, fumes and
276 Nevertheless, the
exposure of infants to these chemicals through the use o
277 contaminants, but little is known about the
exposure of wildlife to these contaminants, particularly
278 d increased cresol levels in these mice, and
exposure of cultured oligodendrocytes to this metabolite
279 and profiles of BP-3 in PCPs and sources of
exposure of humans to this estrogenic compound are not w
280 ruent responses can be explained by the long
exposure of the monkeys to this condition.
281 The long-term
exposure of vegetation to this arid environment has favo
282 Exposure of aged HSCs to thrombin-cleaved OPN attenuates
283 a and colleagues demonstrated that prolonged
exposure of cancer cells to TKIs give rise to small popu
284 Exposure of bdMphi to TLR agonists and/or bdIFNgamma res
285 Direct
exposure of platelets to TMAO enhanced sub-maximal stimu
286 Our data show that
exposure of cells to TNF-alpha altered cellular redox, i
287 Exposure of cultured MECs to TNFalpha redistributed ZnT2
288 ts by plants is an important process for the
exposure of humans to toxic chemicals.
289 ggest that bacterial infections likely alter
exposure of the conceptus to toxins and drugs during ear
290 We estimated
exposure of children to TPP using a screening-level indo
291 st that dust ingestion is the major route of
exposure of children to TPP.
292 Exposure of cultured fibroblasts to uniaxial cyclic stre
293 tive system as a surrogate for environmental
exposure of parents to unmeasured developmental risk fac
294 (iii) PAGE of each single-cell lysate; (iv)
exposure of the gel to UV light to blot (immobilize) pro
295 Exposure of thrombocytopenic mice to UVB light provokes
296 For experimental
exposure of astrocytes to variant CJD (vCJD), the kineti
297 Exposure of cells to various oxygen levels alters their
298 Here we show that
exposure of tumor cells to various stress situations led
299 Exposure of plants to white light (WL) induces a rapid (
300 and merocyanine (a ring-open) states, simple
exposure of the hydrogels to white light can reverse col