ライフサイエンスコーパス: -sensitized

1 s identified were then fed orally to Met e 1-sensitized Balb/c mice twice a week for four weeks.

2 sponses of splenocytes isolated from Met e 1-sensitized Balb/c mice upon stimulation by 18 synthetic

3 by means of ELISA with sera from 48 Ara h 2-sensitized patients with peanut allergy.

4 ine can prevent allergic symptoms in For t 2-sensitized mice.

5 From Bet v 2-sensitized patients, 40 were also sensitized to Phl p 12

6 A novel Nd(3+) -sensitized upconversion nanoparticle (UCNP) that can be

7 gh olive pollen exposure, where many Ole e 7-sensitized patients exhibit a co-sensitization to the pe

8 3) SERCA2a 971-990-sensitized T cells produce both Th1 and Th17 cytokines.

9 5) Finally, SERCA2a 971-990-sensitized T cells were able to transfer disease to naiv

10 genetic marks by the ACK1 inhibitor (R)-9bMS-sensitized naive and enzalutamide-resistant prostate can

11 eems to identify more than 80% of A. aegypti-sensitized individuals, indicating that these allergens

12 blood and the nasal mucosa from aeroallergen-sensitized subjects before and during the first year of

13 eosinophils acquire Ag from the lumen of Ag-sensitized but not naive mice in vivo.

14 d, double-blind crossover study, 14 allergen-sensitized participants (9 with airway hyperresponsivene

15 In a randomized crossover study, 16 allergen-sensitized participants were exposed to control air or D

16 and induces airway eosinophilia in allergen-sensitized and -challenged mice by a platelet- and type

17 airway remodeling were analyzed in allergen-sensitized and airway-challenged mice.

18 ilia, and goblet cell metaplasia in allergen-sensitized mice.

19 ntibody responses were decreased in allergen-sensitized, M pneumoniae-infected animals compared with

20 er of eosinophils from the lungs of allergen-sensitized and challenged mice into influenza virus-infe

21 ells were transferred adoptively to allergen-sensitized animals before allergen challenge.

22 gulatory T cells (Tregs) control alloantigen-sensitized inflammation of GVHD, sustain GVT, and preven

23 sistant bacteria while protecting antibiotic-sensitized bacteria.

24 ducing predominantly IL-17A, and the antigen-sensitized T cells could transfer the disease to naive r

25 In AP-sensitized and challenged mice, anti-IgE mAb treatment a

26 xis, and inhibits airway tryptase in Ascaris-sensitized cynomolgus monkeys with favorable pharmacokin

27 Birch-sensitized individuals are frequently cosensitized to ha

28 atches containing cashew allergens to cashew-sensitized mice.

29 n to the cat lipocalin Fel d 7 among 140 cat-sensitized Swedish patients and elucidated its allergeni

30 el d 7 is a common allergen in a Swedish cat-sensitized population that cross-reacts with Can f 1, an

31 triplet dissolved organic matter to the CDOM-sensitized photochemical oxidation of Cys.

32 her unknown pathway was dominant in the CDOM-sensitized photodegradation of Cys, which will require f

33 light-protected TiO2 |MnP cathode with a CdS-sensitized photoanode to enable solar-light-driven CO2 r

34 preventing alloantibody production in T cell-sensitized recipients.

35 ipheral CGRP action, we used transgenic CGRP-sensitized mice that have elevated levels of the CGRP re

36 We used the CNT-sensitized photoisomerization of sorbic acid ((2E,4E)-he

37 Asthmatic and nonasthmatic cockroach-sensitized individuals exhibit similar TH 2-polarized re

38 ens were determined in 2 groups of cockroach-sensitized 10-year-old children with (n = 19) or without

39 known organic dyes, carbon nitride, and COF-sensitized photocatalytic H(2)O reduction systems.

40 aive and cortical spreading depression (CSD)-sensitized trigeminovascular neurons in the spinal trige

41 Here, twenty cat dander-sensitized patients were randomized to receive three inj

42 ar energy applications in dye or quantum dot-sensitized solar cells, polymer-fullerene polymer solar

43 This work reports a PbS-quantum-dot-sensitized solar cell (QDSC) with power conversion effic

44 of rApi m 5 was more than doubled in double-sensitized patients, while there was no difference for r

45 haracterize the proteins complexed to a drug-sensitized variant of the multidomain kinase Src.

46 These results suggest that DSA-sensitized patients with high MFI levels can receive tra

47 Dye-sensitized conductive oxides also promote long-lived cha

48 Dye-sensitized photoelectrochemical cells (DS-PECs) for wate

49 Dye-sensitized photoelectrosynthesis cells (DSPECs) provide

50 Dye-sensitized solar cells (DSCs) are a next-generation phot

51 Dye-sensitized solar cells (DSSCs) are emerging as one of th

52 Dye-sensitized solar cells (DSSCs) have motivated many resea

53 Dye-sensitized TiO2 can be used as the active layer of solar

54 pment of a tandem system consisting of a dye-sensitized photoelectrochemical cell (DSPEC) wired in se

55 r splitting is exploited here based on a dye-sensitized photoelectrosynthesis cell (DSPEC) with a mes

56 ubstrates are applied as photoanode in a dye-sensitized solar cell (DSC).

57 ical cell (DSPEC) wired in series with a dye-sensitized solar cell (DSC).

58 charges into a SnO(2)/FTO electrode in a dye-sensitized solar cell (DSSC) architecture.

59 ight (lambda > 590 nm) illumination in a dye-sensitized TiO2 solar cell.

60 Here we demonstrate that a dye-sensitized TiO2 surface can selectively change the wetta

61 s such as dye-sensitized solar cells and dye-sensitized photoelectrosynthesis cells.

62 sh-pull systems for nonlinear optics and dye-sensitized solar cells, DTT polymers in light-emitting d

63 e it promising as a catalyst in fuel and dye-sensitized solar cells.

64 solar energy conversion devices such as dye-sensitized solar cells and dye-sensitized photoelectrosy

65 ns and pave the way toward better chiral dye-sensitized photoelectrochemical cells.

66 d overall solar spectrum utilization for dye-sensitized photoelectrosynthesis cells.

67 here an enhancement in photovoltage for dye-sensitized solar cells (DSSCs) where halogen-bonding int

68 s a cost-effective counter electrode for dye-sensitized solar cells (DSSCs); where M denotes monoclin

69 Here we describe a novel strategy for dye-sensitized solar energy applications in which redox-sepa

70 lts point to a new chemical strategy for dye-sensitized solar energy conversion based on molecular ex

71 stigated architecture comprises a Ru(II) dye-sensitized TiO2 substrate tethered to an IrO2 nanopartic

72 ning to interfacial electron transfer in dye-sensitized metal oxides and the design and mechanism of

73 ectrocatalyst ratios are also desired in dye-sensitized photoelectrochemical cells.

74 perties of water-splitting assemblies in dye-sensitized photoelectrosynthesis cells is a key to the e

75 films were tested as photoelectrodes in dye-sensitized photoelectrosynthesis cells.

76 ntegral role of the I(-)/I3(-) couple in dye-sensitized solar cell technology.

77 lock allows for NIR photon absorption in dye-sensitized solar cells (DSCs) when used as a pi-bridge.

78 the photocurrent and the photovoltage in dye-sensitized solar cells (DSCs).

79 (4)) are synthesized for application in dye-sensitized solar cells (DSSC) based on a donor-pi-bridge

80 igned and synthesized for application in dye-sensitized solar cells (DSSC).

81 odes, in imaging and sensing systems, in dye-sensitized solar cells and as photocatalysts are present

82 nt for replacement of precious metals in dye-sensitized solar cells and in luminescent devices by ear

83 wastewater as well as for photoanodes in dye-sensitized solar cells and light absorbers in perovskite

84 esign of new generations of materials in dye-sensitized solar cells, in nonlinear optical application

85 teries, the iodine reduction reaction in dye-sensitized solar cells, the hydrogen evolution reaction

86 nterest as earth-abundant sensitizers in dye-sensitized solar cells.

87 pplications, including bioimaging and in dye-sensitized solar cells.

88 ery (SFB) by incorporation of a built-in dye-sensitized TiO2 photoelectrode in a Li-I redox flow batt

89 rein, we present the concept of internal dye-sensitized hybrid perovskite compounds involving five no

90 s and catalysts with semiconductors into dye-sensitized solar fuel devices (DSSFDs) requires control

91 Nowadays, dye-sensitized solar cells (DSSCs) are the most extensively

92 nces in our mechanistic understanding of dye-sensitized electron transfer reactions occurring at meta

93 ition, the open circuit voltage (Voc) of dye-sensitized solar cells was also increased to 0.769 and 0

94 Adsorption of FDH on dye-sensitized TiO(2) allows for visible-light-driven CO(2)

95 tizers (for singlet oxygen generation or dye-sensitized solar cells), and hence, it is important to d

96 odetector array that contains an organic-dye-sensitized graphene hybrid composite is reported to serv

97 via coalescence of brine droplets on our dye-sensitized TiO2 surface upon visible light illumination.

98 ayers and fabricate a proof-of-principle dye-sensitized photosensing device.

99 conductive counter-electrode of the rear dye-sensitized solar cell.

100 ng a LED and a cathode in a fiber-shaped dye-sensitized solar cell (DSSC) with one of the highest ene

101 the counter electrode for a fiber-shaped dye-sensitized solar cell to fabricate a self-powered fiber-

102 pment of photoanodes for water-splitting dye-sensitized photoelectrochemical cells' by John R.

103 Solid-state dye-sensitized solar cells (sDSCs) are devoid of such issues

104 thium-sulfur batteries, supercapacitors, dye-sensitized solar cells, electrocatalysis, and photoelect

105 deposit this insoluble polymer into the dye-sensitized mesoporous working electrode is in situ photo

106 The dye-sensitized photoelectrosynthesis cell (DSPEC) integrates

107 redox-active electrolyte species in the dye-sensitized solar cell has a significant impact on the ra

108 improved conversion efficiencies of the dye-sensitized TiO2 solar cells were 6.79 and 6.08 respectiv

109 rials for solar fuels production through dye-sensitized photoelectrochemical cells.

110 a better performance of NiO-based p-type dye-sensitized solar cells (p-DSCs), the function of the sur

111 -efficiency C-H/C-H green catalysis with dye-sensitized solar cell applications.

112 f food challenge-proven egg allergic and egg-sensitized and egg-tolerant, age-matched 12-month infant

113 fering RNA-mediated knockdown (k/d) of eIF4E-sensitized CRPC cells to RAD001+bicalutamide, whereas eI

114 l death and features of pancreatitis in EtOH-sensitized acinar cells by suppressing the adaptive unfo

115 Almost a quarter of ever-sensitized children did not have any disease.

116 methylation was increased in peanut extract-sensitized and challenged mice, whereas in tolerized mic

117 nt of new chromophores for efficient fission-sensitized solar cells.

118 A gyrase cleavage core and a fluoroquinolone-sensitized mutant were determined in complex with DNA an

119 Food-sensitized-tolerance in infancy appears to be associated

120 allenge-proven food allergic cases, 199 food-sensitized tolerant cases and 156 non-food allergic cont

121 b) in n=722 (n=367 food-allergic, n=199 food-sensitized-tolerant and n=156 non-food-allergic controls

122 Fifty-eight food-sensitized patients (aged 11-15 months) were assessed, h

123 allenging because approximately half of food-sensitized patients are asymptomatic.

124 ABPA when compared with those in A fumigatus-sensitized and nonsensitized patients with CF without AB

125 function and body mass index in A fumigatus-sensitized but not nonsensitized patients with CF.

126 The BAT discriminates A fumigatus-sensitized from nonsensitized patients with CF.

127 not IgG, levels are increased in A fumigatus-sensitized patients with CF and ABPA when compared with

128 CF into 3 groups: nonsensitized, A fumigatus-sensitized, and ABPA.

129 ized TH responses in a cohort of adult Bla-g-sensitized subjects, either with (n = 55) or without (n

130 n individual allergy diagnosis for alpha-Gal-sensitized patients.

131 tients with alpha-gal syndrome, 12 alpha-gal-sensitized subjects, and 18 control subjects.

132 of a PKD inhibitor protects d-galactosamine-sensitized mice from shock-mediated death caused by anti

133 Administration of ATIs to gluten-sensitized mice expressing HLA-DQ8 increased intestinal

134 Ad5-hACE2-sensitized mice developed pneumonia characterized by wei

135 Of the 161 hazelnut-sensitized subjects, 109 (68%) were also sensitized to p

136 n and cross-reactivity to peanut in hazelnut-sensitized individuals, children (n = 81) and adults (n

137 HDM-sensitized mice and controls were infected with influenz

138 HDM-sensitized mice were treated with JNJ-26481585 to demons

139 However, among HDM-sensitized children, one-third showed no PBMC response t

140 B cells were depleted in HDM-sensitized animals to investigate the importance of B ce

141 B-cell depletion before HDM challenge in HDM-sensitized mice resulted in a dramatic reduction of alle

142 parenchyma, and draining lymph nodes in HDM-sensitized mice.

143 onatal and adult but reduced in juvenile HDM-sensitized mice.

144 oduced higher levels of IL-5 whereas non-HDM-sensitized individuals mounted higher levels of IFN-gamm

145 IgE reactivity of HDM-allergic and non-HDM-sensitized individuals to 15 HDM allergens was establish

146 BMC response to HDM, and the majority of HDM-sensitized children did not have asthma or wheeze.

147 s of total sphingolipids in the lungs of HDM-sensitized mice compared with those in control mice.

148 Neurons, heat-sensitized by expressing TRPV1 are activated with magnet

149 while facilitating transplantation of highly-sensitized patients and preserving pediatric access to h

150 5 years follow-up were compared between HLA-sensitized (HS) and non-HLA sensitized (non-HS) recipien

151 and reducing anti-HLA Abs in chronically HLA-sensitized patients; however, Ab rebound was observed ov

152 ombined with alemtuzumab induction gives HLA-sensitized patients an opportunity for successful kidney

153 Highly HLA-sensitized (HS) patients have an increased risk for the

154 We administered IdeS to 25 highly HLA-sensitized patients (11 patients in Uppsala or Stockholm

155 mited and ineffective in the most highly HLA-sensitized patients.

156 nd be very carefully discussed in highly HLA-sensitized patients.

157 ted from calcineurin inhibitors (CNI) in HLA-sensitized (HS) kidney transplant recipients has not bee

158 cilizumab (TCZ) for treatment of cAMR in HLA-sensitized kidney transplant patients.

159 ted from calcineurin inhibitors (CNI) in HLA-sensitized kidney transplant recipients has not been est

160 A (Cw/DP DSA group) with (i) 104 matched HLA-sensitized kidney transplant recipients with No DSA at D

161 llow-up were compared between HS and non-HLA-sensitized (non-HS) recipients using the Kaplan-Meier pr

162 echanism that is further amplified by a hole-sensitized or photosensitized mechanism in the device.

163 Cs from 26 Spanish grass-allergic donors IgE-sensitized to profilin.

164 ildren were lower at age 2 years than in IgE-sensitized children, and they were extremely heterogeneo

165 ks to interrupt the development of FA in IgE-sensitized children; and tertiary prevention, which seek

166 population has become significantly less IgE-sensitized and clinically more tolerant to NMBAs.

167 Rapid desensitization of naive, IgE-sensitized huFcepsilonRIalpha mice and huFcepsilonRIalph

168 at free Fel d 1 induces degranulation of IgE-sensitized mast cells whereas Fel d 1 displayed on VLPs

169 lly administrated to mice that were then IgE-sensitized to milk proteins.

170 s mainly to foodborne allergens, whereas IgE-sensitized children also produce strong IgG responses to

171 also evident in prior exercised and insulin-sensitized human skeletal muscle.

172 tly and reliably terminate AT in atria light-sensitized via gene delivery.

173 if the human atria can be successfully light-sensitized via gene delivery of ChR2.

174 scan FT-IR spectroscopy of the visible-light-sensitized catalysis, using Ir(ppy)3 in wet acetonitrile

175 t oxygen, (1)O2) in dissolved organic matter-sensitized photoreactions, and identification of oxidati

176 was induced by methylated BSA (mBSA) in mBSA-sensitized wild-type (WT), Ido1(-/-), or Ifnar(-/-) mice

177 We developed a methylation-sensitized interaction screen which revealed that TRIM28

178 reactivity was assessed using sera from milk-sensitized donors in direct binding and inhibition ELISA

179 Among mite-sensitized children across all populations and at differ

180 cells and dendritic cells of house dust mite-sensitized mice to dampen IFN-beta expression and preven

181 d in Der f 1-stimulated PBMCs from dust mite-sensitized patients (adjusted P < .04).

182 In mite-sensitized subjects, GDF was associated with physician-d

183 In non-mite-sensitized subjects, the corresponding ORs were 1.1 (0.5

184 are effective in reducing the number of mite-sensitized children with asthma attending the hospital w

185 We randomized mite-sensitized children with asthma (ages 3-17 yr) after an

186 ector cells, which was only detected in Mono-sensitized patients.

187 higher inflammation at inclusion, while Mono-sensitized patients presented a reduced activity of mast

188 her they reduce asthma morbidity among mouse-sensitized and exposed children and adolescents is unkno

189 intervention on asthma morbidity among mouse-sensitized and exposed children and adolescents with ast

190 Among mouse-sensitized and exposed children and adolescents with ast

191 Three hundred fifty mouse-sensitized/exposed asthmatic children (5-17 years old) w

192 ssociated with lung function growth in mouse-sensitized/exposed asthmatic children.

193 Participants were mouse-sensitized and exposed children and adolescents (aged 5-

194 a specific excitonic transition in both N719-sensitized anatase TiO2 and wurtzite ZnO nanoparticles.

195 A nitrate-sensitized and targeted functional genomic screen identi

196 pal wastewater effluent, nitrate and nitrite-sensitized photolysis pathways resulted in production of

197 We analyzed 28 non-sensitized kidney transplant patients with ABMR associat

198 n two cohorts of allergen sensitized and non-sensitized 3- to 11-year-old children (conducted at Univ

199 r provided as an aerosolized exposure in non-sensitized mice, induced multiple asthma-associated phen

200 Compared to non-sensitized subjects, subjects with specific IgE to cat >

201 had higher F(E) NO levels compared with non-sensitized subjects 26% and 29%, P < 0.001 for both.

202 nodominant, while, in contrast, nonasthmatic-sensitized subjects responded mostly to Bla-g 5 and 4 an

203 NsLTP-sensitized individuals were stratified according to clin

204 hil activation test (BAT) and sIgG4 in nsLTP-sensitized patients from Antwerp (ANT, Belgium) and Barc

205 g children (<5 years) were most commonly nut-sensitized (8-40%); and this prevalence decreased in ado

206 status to peanut and tree nuts in multi-nut-sensitized children and may reduce the need for high-ris

207 The majority of nut-sensitized patients (71% hazelnut, 83% almond, 73% peanu

208 nt molecules can be used to identify oleosin-sensitized patients by BAT.

209 Naive and ovalbumin (OVA)-sensitized and challenged C57BL/6 wild-type and TLR2(-/-

210 s) on airway inflammation in ovalbumin (OVA)-sensitized asthmatic mice.

211 Ovalbumin (OVA)-sensitized C57BL/6 mice were exposed to a first set of i

212 Ovalbumin (OVA)-sensitized mice were desensitized to OVA by means of rep

213 h nodes of tape-stripped and ovalbumin (OVA)-sensitized skin were examined for their ability to polar

214 OVA-sensitized BRP-39(-/-) mice showed decreased epidermal t

215 OVA-sensitized mice were challenged with OVA or PBS for 4 wk

216 OVA-sensitized mice with SD had more severe airway inflammat

217 report that mice with severe asthma and OVA-sensitized/challenged mice had increased PTX3 levels in

218 Breastfeeding by OVA-sensitized mothers or maternal supplementation with IgG-

219 transfer of splenic CD8(+) T cells from OVA-sensitized WT mice suppressed the enhancement of eosinop

220 nflammatory cytokine levels in BALF from OVA-sensitized, M pneumoniae-infected or S pneumoniae-infect

221 pneumoniae antibody levels were found in OVA-sensitized animals.

222 ransfer-induced immunogenic tolerance in OVA-sensitized mice might not be due to SOCS3 gene depletion

223 els, more IL-4, IL-13 mRNA expression in OVA-sensitized skin, and lower Th1 immune response, includin

224 A challenge were significantly higher in OVA-sensitized wild-type mice than in control challenged wil

225 pression levels of BRP-39 were higher in OVA-sensitized WT mice than in control mice.

226 tially ablated in M pneumoniae-infected, OVA-sensitized animals.

227 Moreover, OVA-sensitized mice treated intranasally with 20 ng/kg of IR

228 and IgG1 concentrations in the blood of OVA-sensitized Cyp27b1-KO mice compared with wild-type litte

229 Groups of OVA-sensitized PHIL mice received bone marrow from WT or IL-

230 cted on DCs from draining lymph nodes of OVA-sensitized skin to selectively suppress their ability to

231 RSV infection of OVA-sensitized/challenged BALB/c mice resulted in significan

232 inophilic inflammation in mice receiving OVA-sensitized splenocytes from AQP3(-/-) mice compared with

233 CD4(+) effector T cell populations than OVA-sensitized WT mice.

234 ole lung was significantly higher in the OVA-sensitized and -challenged mice which was associated wit

235 Intranasal administration of LTC4 to OVA-sensitized C57BL/6 mice markedly increased the numbers o

236 DClps migrated to OVA-sensitized lungs with higher efficiency than immature DC

237 educed compared with those in uninfected OVA-sensitized control animals.

238 d eosinophil infiltration, in uninfected OVA-sensitized/challenged mice.

239 atology and immune responses in an ovalbumin-sensitized mouse model of food allergy.

240 skin of cathelicidin knockout and ovalbumin-sensitized filaggrin mutant mice.

241 muscle from asthmatic patients and ovalbumin-sensitized mice.

242 from prenatally stressed, non-BMC, ovalbumin-sensitized females unveiled a deregulated expression of

243 blocks cellular ADAM8 activity in ovalbumin-sensitized and challenged Balb/c mice.

244 way epithelial barrier function in ovalbumin-sensitized control and prenatally stressed offspring was

245 were intratracheally injected into ovalbumin-sensitized and ovalbumin aerosol-challenged leukotriene

246 asthmatic patients and in lungs of ovalbumin-sensitized mice.

247 Transfer of Tregs from oxazolone-sensitized wild-type mice, but not Dock8(-/-) mice, redu

248 ss the proliferation of adjacent Ras pathway-sensitized epithelial cells.

249 Challenges were undertaken in all peanut-sensitized children at 1 and 4 years of age, irrespectiv

250 era from peanut-allergic (n = 25) and peanut-sensitized but asymptomatic (n = 25) patients from Swede

251 children with peanut allergy (PA) and peanut-sensitized but tolerant (PS) children and (2) the presen

252 te the efficacy of this novel EPIT in peanut-sensitized mice.

253 pitopes did not induce anaphylaxis in peanut-sensitized mice.

254 ed a model of gastric eosinophilia in peanut-sensitized piglets to evaluate the efficacy of epicutane

255 animal model of gastric eosinophil in peanut-sensitized piglets.

256 r can potentially lower plasma IgE of peanut-sensitized C3H/HeJ mice.

257 Another set of peanut-sensitized mice treated by EPIT or OIT were sacrificed f

258 Natural pigment-sensitized TiO2 sensor was prepared by immersing porous

259 ature gas sensor was fabricated with pigment-sensitized TiO2 thin film as the sensing layer.

260 ctional recovery in wild-type and plasticity-sensitized mice lacking Nogo receptor 1.

261 man, 37 Dutch, and 24 Spanish) and 29 pollen-sensitized control subjects with wheat-specific IgE but

262 binding assays using sera of cypress pollen-sensitized patients.

263 ted to increase awareness among grass pollen-sensitized individuals.

264 t (APE) using sera from short ragweed pollen-sensitized patients.

265 Poly-sensitized patients presented a higher inflammation at i

266 22 patients were allocated in Mono- or Poly-sensitized groups, excluding patients allergic to epithe

267 tient sensitization phenotype (Mono- or Poly-sensitized).

268 The method is demonstrated for a pressure-sensitized ubiquitin variant that contains two Val to Al

269 the T-cell response to Phl p 12 in profilin-sensitized patients, by measuring the prevalence, streng

270 rts the fabrication of CdSe quantum dot (QD)-sensitized photocathodes on NiO-coated indium tin oxide

271 ading to the construction of various CdSe QD-sensitized photocathodes.

272 Interestingly, ragweed-sensitized patients also displayed an IgG response to Am

273 ut pH-dependent kinetics were observed in RB-sensitized solutions, suggesting EBS reaction with activ

274 contributing to ERalpha reactivation and re-sensitized chemotherapeutic efficacy of anti-hormone the

275 Similarly, amastigotes are re-sensitized to azoles following addition of metabolites u

276 cteria that develop resistance to DNM are re-sensitized to fluoroquinolones, suggesting that resistan

277 o conventional chemotherapy, yet could be re-sensitized to PLX-4032 by BCL-2 family inhibition in viv

278 JB5 in CCA cells that overexpressed MIR21 re-sensitized them to HSP90 inhibitors.

279 gically inactivating Skp2 synergistically re-sensitized CRPC cells toward chemotherapies such as pacl

280 showed that this combinatorial treatment re-sensitized ERalpha-dependent cellular inhibitory respons

281 Riboflavin-sensitized porcine and human tarsus samples were irradia

282 here was robust microglial reactivity in RSD-sensitized mice associated with prolonged sickness behav

283 ented the re-establishment of anxiety in RSD-sensitized mice.

284 accumulation in the brain and anxiety in RSD-sensitized mice.

285 immune reactivity ex vivo and in vivo in RSD-sensitized mice.

286 Moreover, elimination of RSD-sensitized microglia prevented monocyte accumulation in

287 only the immune reactivity component of RSD-sensitized microglia was prevented by elimination/repopu

288 SE-sensitized participants had higher median specific IgE t

289 4 kUA /L, IQR 10.1-118.4) compared to non-SE-sensitized participants (18.0 kUA /L, IQR 5.5-48.6, P=.0

290 ls that readily form endoperoxides in a self-sensitized manner and then thermally release singlet oxy

291 This domino self-sensitized photooxygenation cascade of conjugated carbon

292 ttern also has a dramatic effect on the self-sensitized reactivity of the acenes toward O(2) and the

293 revented the recurrence of anxiety in stress-sensitized mice.

294 osition as well as increased life span in TE-sensitized Dicer-2 mutants.

295 t under inert atmosphere and acetone triplet-sensitized conditions indicating that the triplet excite

296 Crucially, such "triplet-sensitized CO-release" occurred in solid-state materials

297 In this work, we investigate the triplet-sensitized photodegradation of cysteine sulfinic acid, a

298 ad-to-tail), or exclusively 5 in the triplet-sensitized photoreaction, in the presence of benzophenon

299 isomerization occurs efficiently via triplet-sensitized energy transfer, whereas trans-to-cis isomeri

300 evidence of a similar time course, while un-sensitized cells showed no response to stimulation.