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1 ertaken to confirm the role of interleukin-1 blockage.
2  provide a clear visual warning of impending blockage.
3 ons or provide warning of impending catheter blockage.
4  proliferation and erythroid differentiation blockage.
5 y 1-10 MPa) that likely stemmed from conduit blockage.
6 ha (GPIbalpha) receptor, thereby causing its blockage.
7 hindering effect on Hg(0) uptake due to pore blockage.
8  more resilient cake layer and membrane pore blockage.
9 administered mice and was reduced upon PAR-2 blockage.
10 d version of para-coumarate, can bypass this blockage.
11 mogeneous solution in order to preclude pore blockage.
12 o small experimental effects and a precolumn blockage.
13 x pump inhibitors (EPIs) to control catheter blockage.
14 he G-rich stretch dramatically increased the blockage.
15 mposition and single-stranded breaks on this blockage.
16 n, which accounts for the high efficiency of blockage.
17 d forecasts a danger over one month ahead of blockage.
18 in mouse lungs, which was reduced upon PAR-2 blockage.
19 nocytosine (epsilonC) causes transcriptional blockage.
20 s well as apoptotic cells in the lungs after blockage.
21 esence of species that do not cause catheter blockage.
22 f Proteus mirabilis infection and subsequent blockage.
23 s are essentially hollow with practically no blockages.
24 ctivation of Chk1 in response to replication blockages.
25 ome species have the ability to remove these blockages.
26 ence VAS -10 mm (95% CI -18 to -2) P = 0.02, blockage -0.7 (95% CI -1.3 to -0.1) P = 0.02, with recov
27 st doses: VAS 15 mm (95% CI 4-25) P = 0.009, blockage 1.1 (95% CI 0.5-1.6) P = 0.001.
28                                       IL-10R blockage abolished PPAR-gamma-mediated inhibition of MyD
29 m the 3' or 5' end produced distinct current blockages, allowing directional effects on unzipping kin
30                                          The blockage also becomes less pronounced upon reduced RNA p
31 cule, since the event residence times and/or blockage amplitudes for these metal chelates are signifi
32 dual inhibitors along with their ion channel blockage and antiviral activities.
33 xazole compound with potent AM2-S31N channel blockage and antiviral activity, in this study we report
34                              Pharmacological blockage and genetic deletion of D2R in DA neurons preve
35 ed codons instead of stops for translational blockage and have relaxed matching rules for takeoff/lan
36 case Rep, resulting in increased replication blockage and thus increased reinitiation away from oriC,
37 II)-catalyzed transformation by surface-site blockage and/or organic Fe(II) complexation.
38 e of alphaHL, resulting in decreased current blockages and slower unzipping.
39 atings provide up to 12h advanced warning of blockage, and are stable both in the absence of infectio
40 luding spontaneous ruptured membranes, shunt blockage, and dislodgement.
41 influenced by cannabinoid or opioid receptor blockage, and euphoria cannot be studied in mouse models
42 symptoms (rhinorrhea, mucus in throat, nasal blockage, and sense of smell), patient-reported outcomes
43 ligonucleotide effective charges and current blockages, and between their diffusion constants and DNA
44 us researchers also observed bacteria in the blockages, and this study demonstrated the same findings
45  determined not to cause cardiac ion channel blockage are more likely to pass successfully through cl
46             Bypassing requires translational blockage at a "takeoff codon" immediately upstream of a
47 hin approximately 10 min of replication fork blockage at a site-specific barrier in fission yeast, le
48 d data support the notion that transcription blockage at homopurine-homopyrimidine sequences is cause
49 ell as inappropriate replication stalling or blockage at Ter sites outside of the terminus trap regio
50 nd they suggest that the Gac system senses a blockage at the aconitase step of the tricarboxylic acid
51                         We found that VEGFR2 blockage attenuates steatosis and inflammation in a diet
52 queduct are critical for preventing physical blockage between the third and fourth ventricles and the
53 n factor IIS, which is in contrast to pol II blockage by a nucleosome barrier.
54 , the CPP modified drug is released from the blockage by a second triggering agent, while remaining i
55 ocess was dependent on integrin alpha(V), as blockage by antagonist echistatin (RGD peptide) or alpha
56                                  Replication blockage by DPC did not produce damaged forks or detecta
57       The channel activity is susceptible to blockage by known drugs and structurally diverse compoun
58 bited new protein synthesis, indicating that blockage by NPPB enhances the degradation of ABCB transp
59 duce the dangers associated with replication blockage by protein-DNA complexes, aiding clearance of b
60 nsing mechanism was based on the nanochannel blockage caused by MS2 binding to immobilized capture an
61 er in the channels, whereas the time between blockages characterizing the binding reaction on-rate st
62  of landing locations, the extent of current blockage, collision frequency, motion of beads on the el
63                                    Capillary blockages colocalised strongly with pericytes, where cap
64       The autophagic cascade triggered by AR blockage, correlated with the increased light chain 3-II
65                          Pharmacological xCT blockage counteracts NAC prophylactic effects.
66                The noise associated with the blockage current also depends on the stability of the du
67 il identified significant differences in the blockage current and the unzipping duration between the
68                We investigated variations in blockage current as a function of temperature (12-35 deg
69 ture), where a greater noise in the measured blockage current is observed for less stable duplexes.
70 centrations, where the noise in the measured blockage current is significantly lower.
71 urrent fluctuations that reflects a discrete blockage current level structure.
72  complex inducing a 3 fold increase in ionic blockage current relative to unmethylated DNA.
73 ion of guanine by any other base reduced the blockage, cytosine and thymine reduced the blockage more
74               The phenotypic results of this blockage define patterns of communication among distant
75 stis biofilm formation that is important for blockage-dependent plague transmission from fleas to mam
76            Surprisingly, the effect of ACAT1 blockage does not alter mTOR signaling or endoplasmic re
77 ation of the nanochannels (20 nm pore sized) blockage due to the immunocomplex formation.
78 of both electrostatic/steric effects in this blockage due to the subsequent formation of the aptamer-
79 e found to be the determining factor for the blockage efficiency of M3 receptor signaling under durat
80                                GCGR antibody blockage expanded alpha-cell mass 5.7-fold, and S961 had
81 ents who had bladder cancer, bladder stones, blockage, false passage, gross hematuria, accidental rem
82  diffusion constants and DNA-induced current blockage fluctuations.
83  m(-1) to 15.1+/-2.6 bar m(-1) due to spacer blockage from the developing biofilm.
84                               Amount of UV-A blockage from windshields and side windows.
85 cations to prevent methane clathrate hydrate blockages from forming in oil and gas pipelines.
86                             We confirmed the blockage function of Tbf1 using synthetic promoters.
87 y tuft input and (simulated) calcium-channel blockage functionally acts as a composite sigmoidal func
88             A high level of side-window UV-A blockage (>90%) was found in 4 of 29 automobiles (13.8%)
89 al enhancement in comparison to the membrane blockage has been observed.
90 ased pumping energy requirements from spacer blockage highlight the serious challenges of using high
91 active cancer vaccination, immune checkpoint blockage (ICB) and chimeric antigen receptor (CAR) for T
92                 Further analysis indicates a blockage in autophagic flux associated with lysosomal dy
93                            Furthermore, this blockage in cell surface expression was correlated with
94 onstruct markedly reduced APP-induced axonal blockage in Drosophila.
95  antiviral activity based on percent channel blockage in electrophysiological assays.
96  leading edge, the latter is consistent with blockage in membrane trafficking.
97                         The extensive vessel blockage in PD-susceptible grapevines was correlated to
98 t cells and antagonized tubulin-induced VDAC blockage in planar bilayers.
99 ed conditional reduced growth, near complete blockage in PSII supercomplex formation, and concomitant
100                            Chronic autophagy blockage in several conditions, including DRPLA and Vici
101 ilm formation in vitro and biofilm-dependent blockage in the oriental rat flea Xenopsylla cheopis res
102 xidation of [Fe(CN)(6)](4-), is based on the blockage in the pores which affects the diffusion of [Fe
103                              betaIII-Tubulin blockage in vivo reduced tumor incidence and growth.
104 bidopsis (Arabidopsis thaliana) mutants with blockages in the pathway simply redirect carbon flux to
105 at losses in pedicel kh were associated with blockages in vessel elements, whereas air embolisms were
106  correlated with direct competition and pore blockage indicators.
107 nfocal microscopy to show that the secretion blockage is due to the stabilization of open fusion pore
108 during recovery from arterial restriction or blockage is essential for health, but mechanisms are poo
109                                Notably, this blockage is exacerbated in Cockayne Syndrome and xeroder
110                           This transcription blockage is much less pronounced for a C-rich sequence,
111                              Remarkably, the blockage is not pronounced if transcription is performed
112 om control experiments, we conclude that the blockage is primarily due to the formation of stable RNA
113 ts prevent ion currents indicating that pore blockage is primarily responsible.
114 ticularly from ovulation disorders and tubal blockage, is associated with an increased GDM risk.
115                     Detailed analysis of the blockage kinetics of VDAC reconstituted into planar lipi
116                         Interestingly, IL-17 blockage led to an increase in the expression of IL-27 s
117                        Comparison of current-blockage levels of each protein yields volumetric inform
118       We further presented evidence that the blockage mechanism is widely used among genome-wide DGPs
119 biosynthesis pathway by chemical and genetic blockage mimicked these transcriptional responses, indic
120 e blockage, cytosine and thymine reduced the blockage more significantly than adenine substitutions,
121 nfer identical defects, including late onset blockage near the terminal cell-stalk cell junction and
122                    In vitro assays indicated blockage of (11)C-sarcosine uptake into PC-3 and LNCaP t
123 tion of RvD1 and RvD5, an action reversed by blockage of a key SPM biosynthesis enzyme 15-lipoxygenas
124 tudies suggest that this crisis is caused by blockage of a single elongated cell, recent experiments
125 her 4R-Me-Pro or 3S-OH-4S-Me-Pro, indicating blockage of a step upstream of Me-Pro formation.
126  that induces cell loss in NM and persistent blockage of afferent excitatory action potentials, revea
127                                              Blockage of angiotensin II receptor type 1 with 0.1 mg/k
128 s in attenuation of caspase 3 activation and blockage of apoptosis.
129 features were phenocopied by pharmacological blockage of Arf6 activation.
130 c deregulates the autophagic pathway through blockage of autophagic flux, resulting in accumulation o
131 f ciliogenesis partially inhibits autophagy, blockage of autophagy enhances primary cilia growth and
132                                              Blockage of Axl gene expression by small interfering RNA
133                                              Blockage of B cell-specific PD-L1 restored Th1 responses
134                                    Moreover, blockage of B1R inhibited neuroinflammation, as evidence
135 o signaling inactive central clusters, and a blockage of BCR internalization.
136  and the potential benefits arising from the blockage of both inflammation-related enzymes were thoro
137 estigate whether the enhancement of ADCML by blockage of CD59 function is mediated by nAbs, non-nAbs,
138                                        After blockage of CD59 function, the reactive Abs, regardless
139  have led to different models, including (i) blockage of cell wall synthesis, (ii) membrane pore form
140                                 Furthermore, blockage of CMA leads to hyperphosphorylation and destab
141 ent its massive aggregation, and we show how blockage of conserved protective features by endogenous
142                   Lack of Cx43 expression or blockage of Cx43 channels resulted in increased ROS-indu
143                                     Specific blockage of Cx43 HC function by TAT-Gap19, a Cx43 mimeti
144                                              Blockage of Cx43 hemichannels incompletely inhibited H2O
145                                              Blockage of Cx43-GJIC inhibited NK cell activation, thou
146                                 Induction or blockage of CYP3A1 by a miR-23b inhibitor or mimic could
147 m the ER, a process that correlates with LFG blockage of cytochrome c release to the cytosol and casp
148                                              Blockage of Delta-like 4 (DLL4)-directed Notch signaling
149 ive strain that fails to remove Pxr-mediated blockage of development and reintroduced variably trunca
150 ting in uncontrolled cell proliferation, and blockage of differentiation and chondrodysplasia in mice
151 tional twin-boundary (TB) strengthening from blockage of dislocations impinging on TBs, coupled with
152                                              Blockage of DNA recognition by the innate immune system
153 analysis studies support the mode-of-action, blockage of DNA synthesis by dual target topoisomerase i
154 yl-DL-tyrosine methyl ester hydrochloride or blockage of DOP1 receptor with antagonist SCH23390 impai
155 lerotic action in vivo via the AMPK-mediated blockage of Drp1-mediated mitochondrial fission.
156 tical for PTHrP action in chondrogenesis, as blockage of ECM1 nearly abolishes PTHrP regulation of ch
157  of both enzymes appears more promising than blockage of either protein alone.
158                                              Blockage of endogenous TGF-beta with either a TGF-beta-b
159 DAMB-231 and MDAMB-468 cells and resulted in blockage of ER stress-mediated GRP78 up-regulation.
160                                              Blockage of ETAE distinguishes Fe(III) reduction of laye
161  absence of other viral proteins resulted in blockage of exogenous IFN-mediated STAT1 phosphorylation
162   Deletion of ilp had no effect on bacterial blockage of flea blood feeding or colonization.
163                                          The blockage of FP with AL8810, a selective antagonist, hamp
164                              Pharmacological blockage of fructose uptake ameliorates leukemic phenoty
165 ea pig auditory cortex, we show that partial blockage of GABAA receptors by gabazine (GBZ) applicatio
166 binding to lagging strand ssDNA relieves the blockage of Gp43 polymerase activity by Gp59, whereas th
167 ding to ectopic Dpp signaling and consequent blockage of GSC differentiation.
168                                              Blockage of H. ducreyi uptake by cytochalasin D signific
169                                          The blockage of H4R could be a new therapeutic modality for
170 naptic connectivity; chronic pharmacological blockage of Ih channels reproduced these phenotypes, sug
171 The results of this small study suggest that blockage of IL-1beta using gevokizumab may be beneficial
172                                     However, blockage of IL-1R signaling did not abolish the deleteri
173 ioprotective effects against DCM through the blockage of inflammation, oxidative stress, and apoptosi
174                                              Blockage of K33-chain formation, Crn7 ubiquitination, or
175 erol accumulation, we propose that AnxA6 and blockage of LE cholesterol transport are critical for en
176 wth sharply declines with increasing sea-ice blockage of light from the benthic algal habitat.
177                  Pharmacological and genetic blockage of LPA receptor 1 (LPAR1) or autotoxin (ATX), a
178 cytosis was attributable to a combination of blockage of lymphocyte homing and the release of thymocy
179                                          The blockage of m(6)A inhibited splicing of the pre-mRNA enc
180            Using pharmacological and genetic blockage of macroautophagy both in vitro and in vivo, we
181            Coprecipitation led to a complete blockage of mineral surface sites and pores with >/=177
182                                    Moreover, blockage of miR-30b or 378 by locked nucleic acid inhibi
183 ntribution to peroxide metabolism during the blockage of mitochondrial electron transport.
184                                              Blockage of more than one oncoprotein or pathway is now
185      Improving potencies through concomitant blockage of multiple epitopes and avid binding by fusing
186                                              Blockage of NOS activity with the inhibitor L-NG-nitroar
187 ling that was more potent than pharmacologic blockage of Notch activation via gamma-secretase inhibit
188                                   Therefore, blockage of one of these molecules might represent a nov
189 ese cases, inhibition was shown to be due to blockage of passive H(+) translocation through F0 as ass
190 enhanced in Itk(-/-)Btk(-/-) mast cells, and blockage of phosphatidylinositol-4,5-bisphosphate 3-kina
191 nally, we find that neuronal death is due to blockage of plasma membrane recycling processes that uti
192                                              Blockage of PLCgamma2 function by inhibitors or knockdow
193 static synaptic plasticity elicited by acute blockage of postsynaptic receptors.
194 R4 internalization and it was related to the blockage of preformed TNF secretion.
195 meliorated the inflammatory response through blockage of proliferation of activated B cells, inhibiti
196                                        Thus, blockage of RCA function represents a novel approach to
197  mediated by mechanisms distinct from steric blockage of receptor binding.
198 olution resulting in complete and incomplete blockage of reproductive tract in infertile and fertile
199                        Abscisic acid-induced blockage of seed germination and cotyledon greening is r
200 moval of mature microRNAs or pharmacological blockage of signalling pathways drives PSCs into a low-n
201                                              Blockage of some ion channels and in particular, the hER
202 l to vitamin A-deficient (VAD) mice; (2) the blockage of spermatogonial differentiation by impaired r
203 and germ cells in juvenile mice results in a blockage of spermatogonial differentiation, similar to t
204                                          For blockage of spontaneous proton back-leak, the water chan
205  the observations by Sulzberger et al on the blockage of sweat ducts in AD.
206  findings by earlier investigators about the blockage of sweat ducts in miliaria, showing eosinophili
207 -pool is gradually silenced, leading to full blockage of synaptic transmission.
208  high levels of Dio3 provides double-pronged blockage of T3 action during glial lineage commitment.
209                                              Blockage of tetrapyrrole biosynthesis in the AtHEMN1 mut
210                          To permit selective blockage of the accessory site, alpha4 threonine 126 loc
211 ly used in the clinics, and most of them use blockage of the active site for their mode of inhibition
212 hibition that until now has mainly relied on blockage of the active site or occupation of a regulator
213 iers inactivating the proviral promoter, and blockage of the assembly of the host elongation factor P
214 iting phosphoinositide production leads to a blockage of the autophagy flux in LSD chondrocytes.
215 sidue 132 with phenylalanine caused a steric blockage of the B-type channel and no other material str
216  data, for the first time, demonstrated that blockage of the biological function of RCA members rende
217                                              Blockage of the biological function of RCA members, part
218 f circumventing the physical and biochemical blockage of the blood-brain barrier, could be a precious
219                                              Blockage of the c-met/hepatocyte growth factor axis atte
220 evated oxidative stress, cellular death, and blockage of the cell cycle.
221 occlusion (RVO) can cause vision loss due to blockage of the central retinal vein (CRVO) or a branch
222                              Transient, ~95% blockage of the channel current by alpha-syn was observe
223                                              Blockage of the cholecystokinin-1 receptor or the nicoti
224 hibitor of gamma-secretase (DAPT) led to the blockage of the expressions of reprogramming factors and
225 inhibiting apoptosis and necrosis, including blockage of the Fas receptor, neuroprotective peptides a
226 s a pivotal role in cell cycle regulation by blockage of the G1-to-S-phase transition.
227 iated interruption of the GABA signaling and blockage of the GABAA receptor by the specific inhibitor
228 lication of reverse voltages or irreversible blockage of the macroscopic conductance of lysenin chann
229                                              Blockage of the mGluRs alone only modestly reduced the m
230                                              Blockage of the mTORC2 signal pathway prevented cytokine
231                           Here, we show that blockage of the N-methyl-D-aspartate receptor impairs th
232                                     Complete blockage of the nanopore with Pt metal forms a closed bi
233 our previous studies showing that concurrent blockage of the NF-kappaB and Akt signaling pathways sen
234 ses chemoresistance, which is accompanied by blockage of the PD-L1 immune checkpoint.
235 tion for a substrate analogous inhibitor and blockage of the predicted ubiquinone binding site provid
236  the hematopoietic compartment resulted in a blockage of the progenitor B-cell-to-precursor B-cell de
237  in the bone can be effectively inhibited by blockage of the STAT3 signaling.
238                                 In addition, blockage of the STIM1-Orai pathway effectively abolishes
239  Inhibition of TLR4 resulted in differential blockage of the targets.
240 d repression is not due to the simple steric blockage of the transcriptional machinery.
241  of other IDTS, consistent with it causing a blockage of the translocation channel.
242  of dendritic beading during pharmacological blockage of these cotransporters.
243                          We hypothesize that blockage of these interactions through SAM contacts cont
244                                              Blockage of these pathways may improve muscle quality an
245 flux pumps were required for fuel tolerance; blockage of these pumps precluded growth in fuel.
246                                Pharmacologic blockage of these target pathways reduced CSLCs, and thi
247 bryos in vitro and in vivo demonstrated that blockage of this pathway accelerated myogenic differenti
248 transmission of TCR signals, a developmental blockage of thymocytes at the transition from double-neg
249  due to (124)I-BTT-1023 was 0.55 mSv/MBq, if blockage of thyroid uptake is assumed.
250 cted against anaphylaxis and was superior to blockage of tissue mast cell degranulation.
251                                              Blockage of TLR2-mediated endocytosis inhibited IL-10 pr
252 e-homopyrimidine sequences cause significant blockage of transcription in vitro in a strictly orienta
253                                              Blockage of TREM-1 signaling caused a more severe proinf
254 s as a dual-targeting agent that invokes the blockage of two signal transduction pathways that are ce
255                                              Blockage of ubiquitination at Lys124 was proposed to abr
256  activate the NRF2 signaling pathway through blockage of ubiquitylation and degradation of NRF2 in a
257           Mutants identified as defective in blockage of urethral catheters had disruptions in genes
258 ET activation also mainly contributes to the blockage of vascular invasion and metastasis of HCC.
259           Our results suggest, in fact, that blockage of VEGF through the use of an anti-VEGFA antibo
260           Results demonstrated a significant blockage of VEGF-VEGFR binding by bevacizumab.
261   Chal-24 robustly activated JNK and ERK and blockage of which effectively suppressed Chal-24-induced
262 ns must occur without fault to prevent fatal blockages of the airway.
263 lyses with lifetimes limited by irreversible blockages of the microchannels.
264 NA-PKcs is necessary to relieve the physical blockage on end-ligation imposed by the DNA-PKcs protein
265 pped on the paper leads to the ion diffusion blockage on microelectrodes, therefore cell concentratio
266                                              Blockage or activation of TREM-1 signaling lowered or ra
267                    Corroborating these data, blockage or knockdown of P2 x 7 only slightly reduced AT
268                              Pharmacological blockage or knockdown of STIM1 or ORAI1 reduced ENO-1-de
269  be a promising approach to control catheter blockage, or biofilm formation on other medical devices.
270 that voltage sensitivity of the tubulin-VDAC blockage practically does not depend on the lipid charge
271 dinated apical constriction nor its complete blockage prevent internalization and tube formation, alt
272 region, can be detected based on the current blockage prior to duplex unzipping.
273 mbination of antiretroviral therapy with RCA blockage, provirus activators, and therapeutic vaccines
274 of accessible focusing parameters, including blockage ratio, volumetric flow rate, cell concentration
275 activation pharmacological protein synthesis blockage results in mnemonic failure in hippocampus-depe
276 52, 95% CI: 1.23, 1.87; P < 0.001) and tubal blockage (RR = 1.83, 95% CI: 1.20, 2.77; P = 0.005).
277 ence between doxazosin and placebo for nasal blockage score and heart rate after single but not chron
278        Nasal visual analogue scale (VAS) and blockage scores were worse between baseline vs. first do
279 he non-template strand result in much weaker blockage signals extending downstream from the break eve
280 citive device is able to detect and forecast blockages, similar to early detection procedures in canc
281              We found multiple transcription blockage sites adjacent to and within sequences engaged
282 by at least two nasal symptoms: rhinorrhoea, blockage, sneezing or itching.
283 (starvation or mammalian target of rapamycin blockage) stimulated RACK1-ATG5 interaction.
284      Analysis of the detailed pattern of the blockage suggests that RNA polymerase is sterically hind
285 low inhibitory activity in hERG K(+) channel blockage testing, negativity in the Ames test, and 5/5 c
286 port into alpha-cells link glucagon receptor blockage to alpha-cell hyperplasia.
287                To correlate the AT1 receptor blockage to anticancer effects, VEGF levels and microves
288     However, the beneficial actions of ACAT1 blockage to treat Alzheimer's disease remained not well
289  inhibition of JNK was, similar to NF-kappaB blockage, toxic to autonomously proliferating CARD11(L22
290               Triplex-mediated transcription blockage varied significantly with changes in ambient co
291  average percentage of front-windshield UV-A blockage was 96% (range, 95%-98% [95% CI, 95.7%-96.3%])
292                                         This blockage was not observed in DM1 fibroblasts, demonstrat
293                                         This blockage was quantified by measuring the oxidation curre
294  by FFSS was blocked by PGE2 and CM and this blockage was reversed by U0126 and the CM depleted of PG
295 r than the average percentage of side-window blockage, which was 71% (range, 44%-96% [95% CI, 66.4%-7
296 perturbed axonal transport by causing axonal blockages, which were enhanced by reduction of kinesin-1
297                           Furthermore, PAPPA blockage with antibody inhibited embryo implantation in
298                   Androgen deprivation or AR blockage with inhibitor MDV3100 (Enzalutamide) leads to
299 erated that display a reduced sensitivity to blockage with quinidine.
300 ring ischemia of various severity or channel blockage with realistic timescales.

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