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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                                      Bet v 1-sensitized birch pollen-allergic patients (n = 35) were
4          IgE binding of 64 sera from Bet v 1-sensitized subjects with birch pollen allergy was determ
5 sic force components and the onset of Ca(2+)-sensitized force.
6 ine can prevent allergic symptoms in For t 2-sensitized mice.
7                                 From Bet v 2-sensitized patients, 40 were also sensitized to Phl p 12
8                              A novel Nd(3+) -sensitized upconversion nanoparticle (UCNP) that can be
9                           3) SERCA2a 971-990-sensitized T cells produce both Th1 and Th17 cytokines.
10                  5) Finally, SERCA2a 971-990-sensitized T cells were able to transfer disease to naiv
11 genetic marks by the ACK1 inhibitor (R)-9bMS-sensitized naive and enzalutamide-resistant prostate can
12 eems to identify more than 80% of A. aegypti-sensitized individuals, indicating that these allergens
13 blood and the nasal mucosa from aeroallergen-sensitized subjects before and during the first year of
14  eosinophils acquire Ag from the lumen of Ag-sensitized but not naive mice in vivo.
15  and induces airway eosinophilia in allergen-sensitized and -challenged mice by a platelet- and type
16  airway remodeling were analyzed in allergen-sensitized and airway-challenged mice.
17 ucus hypersecretion in the lungs of allergen-sensitized and allergen-challenged mice compared with WT
18 er of eosinophils from the lungs of allergen-sensitized and challenged mice into influenza virus-infe
19 e further supported by treatment of allergen-sensitized mice with LiCl during challenge.
20 ells were transferred adoptively to allergen-sensitized animals before allergen challenge.
21 gulatory T cells (Tregs) control alloantigen-sensitized inflammation of GVHD, sustain GVT, and preven
22 sistant bacteria while protecting antibiotic-sensitized bacteria.
23 ducing predominantly IL-17A, and the antigen-sensitized T cells could transfer the disease to naive r
24                                        In AP-sensitized and challenged mice, anti-IgE mAb treatment a
25        ROC analyses between eight atracurium-sensitized patients and seven nonexposed controls allowe
26 toimmune encephalomyelitis, that autoantigen-sensitized XX lymph node cells, compared with XY, are mo
27                                        Birch-sensitized individuals are frequently cosensitized to ha
28 n to the cat lipocalin Fel d 7 among 140 cat-sensitized Swedish patients and elucidated its allergeni
29 el d 7 is a common allergen in a Swedish cat-sensitized population that cross-reacts with Can f 1, an
30 triplet dissolved organic matter to the CDOM-sensitized photochemical oxidation of Cys.
31 her unknown pathway was dominant in the CDOM-sensitized photodegradation of Cys, which will require f
32 light-protected TiO2 |MnP cathode with a CdS-sensitized photoanode to enable solar-light-driven CO2 r
33 preventing alloantibody production in T cell-sensitized recipients.
34 ipheral CGRP action, we used transgenic CGRP-sensitized mice that have elevated levels of the CGRP re
35 atracurium was positive in one cisatracurium-sensitized patient and negative in all cisatracurium-exp
36 me-linked immunospot assays may identify CMV-sensitized individuals more accurately, regardless of se
37                              We used the CNT-sensitized photoisomerization of sorbic acid ((2E,4E)-he
38           Withdrawal from cocaine in cocaine-sensitized rats induced an apparent time-dependent rebou
39         Asthmatic and nonasthmatic cockroach-sensitized individuals exhibit similar TH 2-polarized re
40         Lung cells and sera of nDer p 2-Conj-sensitized C57Bl/6 mice were studied by means of cytolog
41 aive and cortical spreading depression (CSD)-sensitized trigeminovascular neurons in the spinal trige
42                      Here, twenty cat dander-sensitized patients were randomized to receive three inj
43 ar energy applications in dye or quantum dot-sensitized solar cells, polymer-fullerene polymer solar
44          This work reports a PbS-quantum-dot-sensitized solar cell (QDSC) with power conversion effic
45  of rApi m 5 was more than doubled in double-sensitized patients, while there was no difference for r
46               These results suggest that DSA-sensitized patients with high MFI levels can receive tra
47                                          Dye-sensitized photoelectrochemical cells (DS-PECs) for wate
48                                          Dye-sensitized photoelectrosynthesis cells (DSPECs) provide
49                                          Dye-sensitized solar cells (DSSCs) are emerging as one of th
50                                          Dye-sensitized solar cells (DSSCs) have motivated many resea
51                                          Dye-sensitized solar cells with an energy storage function a
52                                          Dye-sensitized TiO2 can be used as the active layer of solar
53 pment of a tandem system consisting of a dye-sensitized photoelectrochemical cell (DSPEC) wired in se
54 icle TiO2 films provides the basis for a dye-sensitized photoelectrosynthesis cell (DSPEC) for sustai
55 r splitting is exploited here based on a dye-sensitized photoelectrosynthesis cell (DSPEC) with a mes
56 nd hydrogen has been shown to occur in a dye-sensitized photoelectrosynthesis cell (DSPEC).
57 ical cell (DSPEC) wired in series with a dye-sensitized solar cell (DSC).
58 ubstrates are applied as photoanode in a dye-sensitized solar cell (DSC).
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 rove the performance of quantum dot- and dye-sensitized solar cells, respectively.
62 e it promising as a catalyst in fuel and dye-sensitized solar cells.
63 ensitizers in nanocrystalline TiO2-based dye-sensitized solar cells (DSSCs).
64 l of the conductivity of the HTM in both dye-sensitized and perovskite-absorber solar cells in an ine
65 SSSC, making it actually overshadowed by dye-sensitized solar cell (DSSC).
66 ns and pave the way toward better chiral dye-sensitized photoelectrochemical cells.
67 d overall solar spectrum utilization for dye-sensitized photoelectrosynthesis cells.
68 recently have become good candidates for dye-sensitized solar cells (DSCs).
69  here an enhancement in photovoltage for dye-sensitized solar cells (DSSCs) where halogen-bonding int
70 t electron transfer under conditions for dye-sensitized solar cells and a slower electron transfer un
71    Here we describe a novel strategy for dye-sensitized solar energy applications in which redox-sepa
72 lts point to a new chemical strategy for dye-sensitized solar energy conversion based on molecular ex
73 s in photoelectrochemical systems (e.g., dye-sensitized solar cells) by showing more efficient charge
74 stigated architecture comprises a Ru(II) dye-sensitized TiO2 substrate tethered to an IrO2 nanopartic
75 ectrocatalyst ratios are also desired in dye-sensitized photoelectrochemical cells.
76 tal oxide electrodes for applications in dye-sensitized photoelectrosynthesis cells (DSPECs).
77  films were tested as photoelectrodes in dye-sensitized photoelectrosynthesis cells.
78 ntegral role of the I(-)/I3(-) couple in dye-sensitized solar cell technology.
79 lock allows for NIR photon absorption in dye-sensitized solar cells (DSCs) when used as a pi-bridge.
80 the photocurrent and the photovoltage in dye-sensitized solar cells (DSCs).
81  (4)) are synthesized for application in dye-sensitized solar cells (DSSC) based on a donor-pi-bridge
82 igned and synthesized for application in dye-sensitized solar cells (DSSC).
83 he samples were tested as photoanodes in dye-sensitized solar cells (DSSCs) using N719 as dye and a n
84 rt, and electrolyte pore-infiltration in dye-sensitized solar cells (DSSCs).
85 ocyanate (GdmSCN) improves efficiency in dye-sensitized solar cells (DSSCs).
86 nt for replacement of precious metals in dye-sensitized solar cells and in luminescent devices by ear
87 wastewater as well as for photoanodes in dye-sensitized solar cells and light absorbers in perovskite
88 esign of new generations of materials in dye-sensitized solar cells, in nonlinear optical application
89 can be successfully applied as anodes in dye-sensitized solar cells.
90 nterest as earth-abundant sensitizers in dye-sensitized solar cells.
91 pplications, including bioimaging and in dye-sensitized solar cells.
92 ery (SFB) by incorporation of a built-in dye-sensitized TiO2 photoelectrode in a Li-I redox flow batt
93 odide redox shuttle to couple a built-in dye-sensitized titanium dioxide photoelectrode with the oxyg
94 vious work incorporating these dyes into dye-sensitized solar cells (DSSCs), where the oxygen- and se
95 s and catalysts with semiconductors into dye-sensitized solar fuel devices (DSSFDs) requires control
96                                Nowadays, dye-sensitized solar cells (DSSCs) are the most extensively
97 ition, the open circuit voltage (Voc) of dye-sensitized solar cells was also increased to 0.769 and 0
98 mitations for the long-term operation of dye-sensitized solar cells.
99                      When immobilized on dye-sensitized TiO2 nanoparticles, fcc3 catalyzes visible-li
100 via coalescence of brine droplets on our dye-sensitized TiO2 surface upon visible light illumination.
101 ayers and fabricate a proof-of-principle dye-sensitized photosensing device.
102 alyst heterointerfaces in a prototypical dye-sensitized photoanode for water oxidation.
103 conductive counter-electrode of the rear dye-sensitized solar cell.
104 ng a LED and a cathode in a fiber-shaped dye-sensitized solar cell (DSSC) with one of the highest ene
105                          Water-splitting dye-sensitized photoelectrochemical (WS-DSPECs) cells employ
106 pment of photoanodes for water-splitting dye-sensitized photoelectrochemical cells' by John R.
107 cessfully fabricate in air a solid-state dye-sensitized solar cell (DSSC) with a mesoporous TiO2 film
108                              Solid-state dye-sensitized solar cells (sDSCs) are devoid of such issues
109 e transport material used in solid-state dye-sensitized solar cells and perovskite-absorber solar cel
110 s the first demonstration of solid-state dye-sensitized solar cells fabricated and operated with the
111  deposit this insoluble polymer into the dye-sensitized mesoporous working electrode is in situ photo
112                                      The dye-sensitized photoelectrosynthesis cell (DSPEC) integrates
113                                      The dye-sensitized solar cell (DSSC) is representative of next g
114  redox-active electrolyte species in the dye-sensitized solar cell has a significant impact on the ra
115  improved conversion efficiencies of the dye-sensitized TiO2 solar cells were 6.79 and 6.08 respectiv
116 rials for solar fuels production through dye-sensitized photoelectrochemical cells.
117                         This approach to dye-sensitized semiconducting materials offers a means to sp
118 -efficiency C-H/C-H green catalysis with dye-sensitized solar cell applications.
119                                          Egg-sensitized infants who have never eaten egg may react at
120                                       In egg-sensitized infants with EW SPT >/=8 mm and/or EW sIgE >/
121 fering RNA-mediated knockdown (k/d) of eIF4E-sensitized CRPC cells to RAD001+bicalutamide, whereas eI
122 l death and features of pancreatitis in EtOH-sensitized acinar cells by suppressing the adaptive unfo
123                     Almost a quarter of ever-sensitized children did not have any disease.
124  methylation was increased in peanut extract-sensitized and challenged mice, whereas in tolerized mic
125 nt of new chromophores for efficient fission-sensitized solar cells.
126 A gyrase cleavage core and a fluoroquinolone-sensitized mutant were determined in complex with DNA an
127 allenge-proven food allergic cases, 199 food-sensitized tolerant cases and 156 non-food allergic cont
128 b) in n=722 (n=367 food-allergic, n=199 food-sensitized-tolerant and n=156 non-food-allergic controls
129                             Fifty-eight food-sensitized patients (aged 11-15 months) were assessed, h
130 ntified: no allergic disease (70%), non-food-sensitized eczema (16%), single egg allergy (9%), multip
131 allenging because approximately half of food-sensitized patients are asymptomatic.
132  immobilized gQDs was responsible for a FRET-sensitized emission from the acceptor dye, which served
133 ABPA when compared with those in A fumigatus-sensitized and nonsensitized patients with CF without AB
134  function and body mass index in A fumigatus-sensitized but not nonsensitized patients with CF.
135            The BAT discriminates A fumigatus-sensitized from nonsensitized patients with CF.
136 not IgG, levels are increased in A fumigatus-sensitized patients with CF and ABPA when compared with
137 CF into 3 groups: nonsensitized, A fumigatus-sensitized, and ABPA.
138 ized TH responses in a cohort of adult Bla-g-sensitized subjects, either with (n = 55) or without (n
139 n individual allergy diagnosis for alpha-Gal-sensitized patients.
140 ortality in a mouse model of d-galactosamine-sensitized endotoxin shock.
141  of a PKD inhibitor protects d-galactosamine-sensitized mice from shock-mediated death caused by anti
142                          Of the 161 hazelnut-sensitized subjects, 109 (68%) were also sensitized to p
143 n and cross-reactivity to peanut in hazelnut-sensitized individuals, children (n = 81) and adults (n
144                                          HDM-sensitized mice and controls were infected with influenz
145                                          HDM-sensitized Pglyrp1(-/-) mice, compared with WT mice, had
146                           However, among HDM-sensitized children, one-third showed no PBMC response t
147                 B cells were depleted in HDM-sensitized animals to investigate the importance of B ce
148 B-cell depletion before HDM challenge in HDM-sensitized mice resulted in a dramatic reduction of alle
149  parenchyma, and draining lymph nodes in HDM-sensitized mice.
150              In vivo depletion of pDC in HDM-sensitized Pglyrp1(-/-) mice reversed the low responsive
151 onatal and adult but reduced in juvenile HDM-sensitized mice.
152 BMC response to HDM, and the majority of HDM-sensitized children did not have asthma or wheeze.
153                                Neurons, heat-sensitized by expressing TRPV1 are activated with magnet
154  Nephrotic syndrome was reported in a highly-sensitized patient receiving enzyme replacement therapy
155 while facilitating transplantation of highly-sensitized patients and preserving pediatric access to h
156                              Sera of 323 HLA-sensitized kidney transplant candidates positive with a
157 ombined with alemtuzumab induction gives HLA-sensitized patients an opportunity for successful kidney
158                                   Highly HLA-sensitized (HS) patients have difficulty accessing compa
159        We administered IdeS to 25 highly HLA-sensitized patients (11 patients in Uppsala or Stockholm
160 mited and ineffective in the most highly HLA-sensitized patients.
161                     Here, BKV viremia in HLA-sensitized patients after desensitization with IVIG and
162 A (Cw/DP DSA group) with (i) 104 matched HLA-sensitized kidney transplant recipients with No DSA at D
163 ferred in vivo to OVA and aluminum hydroxide-sensitized mice also maintained IL-17 secretion and did
164 mpared with controls; (ii) some activate IgE-sensitized basophils; and (iii) some inhibit allergen-in
165 e examined for their ability to activate IgE-sensitized human blood basophils in the presence and abs
166 Cs from 26 Spanish grass-allergic donors IgE-sensitized to profilin.
167 ildren were lower at age 2 years than in IgE-sensitized children, and they were extremely heterogeneo
168 ks to interrupt the development of FA in IgE-sensitized children; and tertiary prevention, which seek
169 r accuracy to predict offending foods in IgE-sensitized patients (sensitivity 87.5%, specificity 68%
170 entified cow's milk as a food trigger in IgE-sensitized patients.
171 population has become significantly less IgE-sensitized and clinically more tolerant to NMBAs.
172 , followed a 6-week sIgE-ED, whereas non-IgE-sensitized patients underwent a 6-week SFED.
173 at free Fel d 1 induces degranulation of IgE-sensitized mast cells whereas Fel d 1 displayed on VLPs
174                   Nineteen patients were IgE-sensitized to penicillin.
175 s mainly to foodborne allergens, whereas IgE-sensitized children also produce strong IgG responses to
176 ng its unique mechanism against inflammation-sensitized HI injury.
177  also evident in prior exercised and insulin-sensitized human skeletal muscle.
178 tly and reliably terminate AT in atria light-sensitized via gene delivery.
179 if the human atria can be successfully light-sensitized via gene delivery of ChR2.
180 scan FT-IR spectroscopy of the visible-light-sensitized catalysis, using Ir(ppy)3 in wet acetonitrile
181 matory responses in lipopolysaccharide (LPS)-sensitized HI injury in neonates.
182 tion enabled the proximity required for LRET-sensitized emission from Cy3, which was used as the dete
183 t oxygen, (1)O2) in dissolved organic matter-sensitized photoreactions, and identification of oxidati
184 was induced by methylated BSA (mBSA) in mBSA-sensitized wild-type (WT), Ido1(-/-), or Ifnar(-/-) mice
185                                      In milk-sensitized mice specific EPIT prevented further sensitiz
186                                   Among mite-sensitized children across all populations and at differ
187 d in Der f 1-stimulated PBMCs from dust mite-sensitized patients (adjusted P < .04).
188                                      In mite-sensitized subjects, GDF was associated with physician-d
189                                  In non-mite-sensitized subjects, the corresponding ORs were 1.1 (0.5
190 are effective in reducing the number of mite-sensitized children with asthma attending the hospital w
191                           We randomized mite-sensitized children with asthma (ages 3-17 yr) after an
192 ilitate sensitization to mites and that mite-sensitized individuals may be especially susceptible to
193 her they reduce asthma morbidity among mouse-sensitized and exposed children and adolescents is unkno
194 intervention on asthma morbidity among mouse-sensitized and exposed children and adolescents with ast
195                                  Among mouse-sensitized and exposed children and adolescents with ast
196                      Participants were mouse-sensitized and exposed children and adolescents (aged 5-
197 a specific excitonic transition in both N719-sensitized anatase TiO2 and wurtzite ZnO nanoparticles.
198                                    A nitrate-sensitized and targeted functional genomic screen identi
199                           We analyzed 28 non-sensitized kidney transplant patients with ABMR associat
200 n two cohorts of allergen sensitized and non-sensitized 3- to 11-year-old children (conducted at Univ
201 r provided as an aerosolized exposure in non-sensitized mice, induced multiple asthma-associated phen
202                              Compared to non-sensitized subjects, subjects with specific IgE to cat >
203 nodominant, while, in contrast, nonasthmatic-sensitized subjects responded mostly to Bla-g 5 and 4 an
204 g children (<5 years) were most commonly nut-sensitized (8-40%); and this prevalence decreased in ado
205                          The majority of nut-sensitized patients (71% hazelnut, 83% almond, 73% peanu
206 nt molecules can be used to identify oleosin-sensitized patients by BAT.
207                    Naive and ovalbumin (OVA)-sensitized and challenged C57BL/6 wild-type and TLR2(-/-
208 e purified from the lungs of ovalbumin (OVA)-sensitized and OVA-challenged (OVA-immunized) mice or hu
209                  Control and ovalbumin (OVA)-sensitized BALB/cJ mice were exposed via oropharyngeal (
210                              Ovalbumin (OVA)-sensitized C57BL/6 mice were exposed to a first set of i
211               Mice were then ovalbumin (OVA)-sensitized during the acute infection (3-days post inocu
212                              Ovalbumin (OVA)-sensitized mice were desensitized to OVA by means of rep
213                                          OVA-sensitized mice treated with an NO donor developed more
214                                          OVA-sensitized mice were challenged with OVA or PBS for 4 wk
215                                          OVA-sensitized mice with SD had more severe airway inflammat
216                                 Although OVA-sensitized and challenged wild type mice displayed a str
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 ciency was associated with higher AHR in OVA-sensitized and challenged mice than those in vitamin D-s
221 A challenge were significantly higher in OVA-sensitized wild-type mice than in control challenged wil
222 ls of P were also detected in the BAL of OVA-sensitized and challenged but not naive mice.
223 significantly in the airway epithelia of OVA-sensitized and OVA-challenged (OVA/OVA) mice compared wi
224  and IgG1 concentrations in the blood of OVA-sensitized Cyp27b1-KO mice compared with wild-type litte
225                                Groups of OVA-sensitized PHIL mice received bone marrow from WT or IL-
226                         RSV infection of OVA-sensitized/challenged BALB/c mice resulted in significan
227 inophilic inflammation in mice receiving OVA-sensitized splenocytes from AQP3(-/-) mice compared with
228 ole lung was significantly higher in the OVA-sensitized and -challenged mice which was associated wit
229 tion of SA-IVIg, but not non-SA-IVIg, to OVA-sensitized and OVA-challenged mice induced Treg cells an
230     Intranasal administration of LTC4 to OVA-sensitized C57BL/6 mice markedly increased the numbers o
231        Adoptive transfer of basophils to OVA-sensitized hosts enhanced lung IL-4 and IL-13 release wh
232 d eosinophil infiltration, in uninfected OVA-sensitized/challenged mice.
233 phils decreased in 6-week mice that were OVA-sensitized during an acute influenza infection.
234 ction in the 18-month old mice that were OVA-sensitized, there was little effect on the AHR and BALF
235 -challenged (OVA/OVA) mice compared with OVA-sensitized but PBS-challenged (OVA/PBS) control mice.
236 ness, and OVA-specific IgE compared with OVA-sensitized/challenged wild-type (WT) mice.
237 atology and immune responses in an ovalbumin-sensitized mouse model of food allergy.
238  skin of cathelicidin knockout and ovalbumin-sensitized filaggrin mutant mice.
239 muscle from asthmatic patients and ovalbumin-sensitized mice.
240  blocks cellular ADAM8 activity in ovalbumin-sensitized and challenged Balb/c mice.
241 were intratracheally injected into ovalbumin-sensitized and ovalbumin aerosol-challenged leukotriene
242                       Treatment of ovalbumin-sensitized mice with pLR during allergen challenge reduc
243 asthmatic patients and in lungs of ovalbumin-sensitized mice.
244 n asthmatic-like attacks using the ovalbumin-sensitized murine model of the disease, and identified a
245 ss the proliferation of adjacent Ras pathway-sensitized epithelial cells.
246  hypodermal-fated daughters in a Wnt pathway-sensitized background.
247             Peanut-allergic (n = 43), peanut-sensitized but tolerant (n = 36) and non-peanut-sensitiz
248     Challenges were undertaken in all peanut-sensitized children at 1 and 4 years of age, irrespectiv
249 era from peanut-allergic (n = 25) and peanut-sensitized but asymptomatic (n = 25) patients from Swede
250 frica compared to peanut-allergic and peanut-sensitized but asymptomatic patients from Sweden.
251 children with peanut allergy (PA) and peanut-sensitized but tolerant (PS) children and (2) the presen
252 ns of clinical tolerance to peanut in peanut-sensitized but asymptomatic patients from central Africa
253  no significant response to peanut in peanut-sensitized but tolerant (P < .001) and non-peanut-sensit
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 sitized but tolerant (n = 36) and non-peanut-sensitized nonallergic (n = 25) children underwent skin
257 tized but tolerant (P < .001) and non-peanut-sensitized nonallergic children (P < .001).
258                           Most of the peanut-sensitized children do not have clinical peanut allergy.
259                              Natural pigment-sensitized TiO2 sensor was prepared by immersing porous
260 ature gas sensor was fabricated with pigment-sensitized TiO2 thin film as the sensing layer.
261 ctional recovery in wild-type and plasticity-sensitized mice lacking Nogo receptor 1.
262                     We found that plasticity-sensitized mice recovered 50% of normal skilled locomoto
263 man, 37 Dutch, and 24 Spanish) and 29 pollen-sensitized control subjects with wheat-specific IgE but
264  binding assays using sera of cypress pollen-sensitized patients.
265 ted to increase awareness among grass pollen-sensitized individuals.
266 t (APE) using sera from short ragweed pollen-sensitized patients.
267    The method is demonstrated for a pressure-sensitized ubiquitin variant that contains two Val to Al
268  the T-cell response to Phl p 12 in profilin-sensitized patients, by measuring the prevalence, streng
269               We used an engineered protease-sensitized SARM1 to demonstrate that SARM1 activity is r
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 t states cannot be ignored when designing QD-sensitized solar cells.
273                       Interestingly, ragweed-sensitized patients also displayed an IgG response to Am
274 h the chemical inhibitors PP242 or rapamycin-sensitized DOV13, an ovarian cancer cell line incapable
275  contributing to ERalpha reactivation and re-sensitized chemotherapeutic efficacy of anti-hormone the
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 ulation of the CPEB2B isoform using siRNA re-sensitized the AnR cell lines to detachment-induced cell
280 gically inactivating Skp2 synergistically re-sensitized CRPC cells toward chemotherapies such as pacl
281  showed that this combinatorial treatment re-sensitized ERalpha-dependent cellular inhibitory respons
282 Inhibition of CDK5 activity with roscovitine-sensitized cells to heat induced apoptosis indicating a
283 ial defeat increased social avoidance in RSD-sensitized mice compared with naive mice.
284            Subthreshold social defeat in RSD-sensitized mice increased peripheral macrophage traffick
285 ented the re-establishment of anxiety in RSD-sensitized mice.
286 n and prevented anxiety-like behavior in RSD-sensitized mice.
287                                           SE-sensitized participants had higher median specific IgE t
288 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
289 d via cleavage on the ketone moiety and self-sensitized photolysis.
290 revented the recurrence of anxiety in stress-sensitized mice.
291 ibutes re-establishment of anxiety in stress-sensitized mice.
292            All rocuronium- and suxamethonium-sensitized patients displayed a negative BAT with atracu
293 osition as well as increased life span in TE-sensitized Dicer-2 mutants.
294 t under inert atmosphere and acetone triplet-sensitized conditions indicating that the triplet excite
295 s observed under direct irradiation, triplet-sensitized UV irradiation, and non-metal catalyzed visib
296                     Crucially, such "triplet-sensitized CO-release" occurred in solid-state materials
297 isomerization occurs efficiently via triplet-sensitized energy transfer, whereas trans-to-cis isomeri
298  evidence of a similar time course, while un-sensitized cells showed no response to stimulation.
299         Splenocytes of control-diet-fed whey-sensitized donors transferred immunologic memory.
300 ey-specific IgG1 levels were reduced in whey-sensitized donor mice fed the fish oil diet as compared

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