ライフサイエンスコーパス: incubation

1 m RCs was possible after 5 min of Calcein AM incubation.

2 mbers, which are then returned to nature for incubation.

3 and that DMS neuronal ensembles mediate this incubation.

4 nches were not visible after 2h of enzymatic incubation.

5 g kg(-1) day(-1) ) from day 13 of the 21-day incubation.

6 17 times more toxic than curcumin after 48 h incubation.

7 in content decreased on myeloperoxidase/H2O2 incubation.

8 (DLS) and dorsomedial striatum (DMS) in this incubation.

9 similar following CuDox and free doxorubicin incubation.

10 se method with procedures using 37 degrees C incubation.

11 F-kB) translocation, were attributable to LC incubation.

12 ty, especially during the key step of sample incubation.

13 ts for some isolates after only 10 to 30 min incubation.

14 rs were decreased for all species in 10% CO2 incubation.

15 al testing techniques, which require days of incubation.

16 % at 10times or higher dilution after 24h of incubation.

17 pproximately 28 h along with three overnight incubations.

18 donor myocardium, both prior to and after OM incubations.

19 approaches and microsensors in flow-through incubations.

20 OM incubation (0.5 and 1.0 mumol/L) enhanced force generati

21 Our results show unexpectedly slow incubation (2.8 and 5.8 mo) like those of outgroup repti

22 Hypoxic incubation (3 kPa) caused (i) stabilization of HIF-2alph

23 After 24h incubation, 37.73+/-9.34% of TCMPs crossed the epitheliu

24 After 60 min of incubation, 5 potential metabolites of TBECH were identi

25 Furthermore, one-week bottle incubations amended with inorganic nutrients and carbon

26 itor cells into neonatal rat hearts, in vivo incubation and analysis.

27 Using native-like incubation and electrospray conditions together with an

28 This association was attenuated upon RNaseH incubation and entirely lost upon RNaseA digestion of na

29 The assay is fast (<1h for incubation and measurement) and very sensitive.

30 Traditional systems for ELISA incubation and reading are expensive and bulky, thus can

31 o complete all steps of the assay, including incubation and reading.

32 ructures gradually increase in number during incubation and show morphologies reminiscent of cells un

33 ours of methyl aminolevulinate hydrochloride incubation and subsequent red light illumination.

34 Reduced room temperature incubation and the addition of antifungal agents decreas

35 r WD60) selected to span the rising phase of incubation and the transition from low to high CP-AMPAR

36 ii) the presence of Ca(2+) and Mg(2+) in all incubation and washing buffers.

37 whether palatability differentially affected incubation and/or plasticity.

38 d with time consuming procedures (e.g., long incubations and multiple washings), indicates that the r

39 major errors (VMEs) were observed at 24 h of incubation, and 17.2% VMEs were observed at 48 h.

40 Full integration of droplet generation, incubation, and detection into a single, uninterrupted s

41 rapidly occurred within the first 120min of incubation, and there was higher DH in HG than in HB.

42 For the 10-minute incubation arm AK clearance for the microneedle pretreat

43 For the 20-minute incubation arm, average AK clearance was 76% vs 58% on t

44 zed to either the 20-minute or the 10-minute incubation arm.

45 Participants were randomized into 2 incubations arms, either 10-minute or 20-minute aminolev

46 Incubation at 0 degrees C, which globally weakens hydrop

47 After 3 days of incubation at 14 degrees C, the microbial communities fr

48 The formation of insoluble oxalate after incubation at 25 degrees C for 30min is a simple practic

49 After incubation at 37 (o)C for 24 h, the shape and organizati

50 Invariably, this has required enzymatic incubation at 37 degrees C, which can be expected to res

51 s (Fe, Cu, Mn, and Zn) were exchanged during incubation at 37 degrees C.

52 determined stability of monomeric insulin by incubation at a very low concentration to isolate protei

53 ained unicellular and viable after prolonged incubation at high temperature (50 degrees C).

54 FPW up to 80% of the overall content over 2h incubation at the slightly alkaline pHs simulating the s

55 We assayed SOC decomposition from these incubations by combining inverse modeling and microbial

56 However, alpha-amylase and cellulase incubation caused significant increases in the total fre

57 ing from surface provide fluidic channel and incubation chamber.

58 ted with fluidic system for reagent flow and incubation chamber.

59 ulation, collection year, after-ripening and incubation conditions on seed dormancy and germination o

60 After 0, 1, 3, 6, and 12 months of soil incubation, earthworms (Eisenia andrei) were introduced

61 detect signal from growing bacteria after 1h incubation, equivalent to 2-3 bacterial replications.

62 verted to N2O via extracellular NH2OH during incubation, estimated on the basis of NH2OH abiotic conv

63 endent decay of cells and body fluids during incubation ex vivo.

64 In a soil incubation experiment with (15)NH4NO3, NH4(15)NO3, or Na

65 rth America included in a 100-day laboratory incubation experiment, we identified a core group of abu

66 PP) in stable isotope-assisted ex vivo blood incubation experiments and through in vivo conversion of

67 Furthermore, incubation experiments conducted with naturally methane-

68 Copper incubation experiments suggest that Clade IV populations

69 ectrometry in combination with sediment core incubation experiments under manipulated redox condition

70 a sample preparation method, including cell incubation, extraction and signal enhancement, to obtain

71 xycholate versus a blank control tube, after incubation for 10 minutes at 36 degrees C using a spectr

72 ver, at the single-channel level, chronic co-incubation greatly increased F508del-CFTR channel activi

73 However, incubation in 1% O2 in the presence of SU1498 significan

74 enes generally declined with time during the incubation in all treatments, suggesting shifts of micro

75 n plaque biofilm formation after 72 hours of incubation in an experimental anaerobic flow chamber mod

76 Further, incubation in cholesterol-rich mouse serum resulted in t

77 ved in neurons from slices that had been pre-incubation in gabapentin.

78 als, an effect that was also reversed by pre-incubation in gabapentin.

79 ized at a single-microcolony level following incubation in neutral-pH buffer.

80 Following incubation in normal mouse serum, label-free quantitativ

81 r responses were monitored with postexposure incubation in submerged conditions, revealing CuO dissol

82 stem cells (iPSCs) after a 72-hour transient incubation in the four chemical inhibitors (4i)-naive re

83 Bacterial survival was measured after 3-hour incubation in the presence of eculizumab or control comp

84 (TA, the shell) was self-assembled by simple incubation in water.

85 Hypoxic incubation increased oxidative stress (4-hydroxynonenal,

86 Finally, we discovered that low-temperature incubation increased the steady-state levels of a Bartte

87 ints would have rendered tooth formation and incubation inherently slow in other dinosaur lineages an

88 ased significantly during dark and anaerobic incubation matching three components previously consider

89 , a consequence of a dislocation-based crack incubation mechanism.

90 NH2OH was measurable in the incubation media of Nitrosomonas europaea, Nitrosospira

91 BAG and BAG-F alkalinized the incubation media.

92 nsient and reversible as removal of NTZ from incubation medium restored the mitochondrial respiration

93 and processing-dependent manner; analysis of incubation medium revealed that 2.6% of Lys(541) in HSA

94 Our data showed that after 30 min of incubation, neutrophils failed to engulf P. stomatis eff

95 em equilibrium isotope exchange experiments, incubation of [2-(2)H]-(2R,3S)-2-methyl-3-hydroxypentano

96 Consistent with this, anoxic incubation of a sediment core resulted in an accumulatio

97 f adenylate cyclase A (ACA) with SQ22536 and incubation of a temperature-sensitive ACA mutant at the

98 Incubation of AR42J or primary mouse or human acinar cel

99 Pre-incubation of ATM protein with active DNA-PKcs also sign

100 Similarly, ex vivo incubation of baboon serum with thrombin, plasmin, or FX

101 Following incubation of blood CD4+ T cells with TFV or TAF, Medrox

102 stimulation compared to cells from controls; incubation of CD4(+) T cells from patients with ALF with

103 Cholesterol efflux was quantified by incubation of cholesterol-loaded THP-1 cells with the pa

104 striatum, a region that is not implicated in incubation of cocaine craving and does not undergo CP-AM

105 d the previously demonstrated time course of incubation of cocaine craving.

106 calcium-permeable (CP) AMPARs contributes to incubation of cocaine craving.

107 chow 45 mg pellets and were then tested for incubation of craving either 1 or 30 days after training

108 Rats showed robust incubation of craving for both food rewards, although re

109 Finally, incubation of craving for chow and high fat was accompan

110 t increased with 21 days of abstinence (ie, 'incubation of craving').

111 h time-dependent increases in food craving ('incubation of craving').

112 Injection of mice with TNF or incubation of crypt-derived enteroids with TNF reduced t

113 EndMT can be reproduced in vitro by incubation of cultured endothelial progenitor cells or s

114 Moreover, the incubation of differentiated Caco-2 cells with a non-tox

115 Co-incubation of differentiating myoblasts with rIL-15 and

116 stration, reinstatement of drug seeking, and incubation of drug craving.

117 iatum neuronal ensembles in this new form of incubation of drug craving.

118 Incubation of E. faecalis with heme increased growth and

119 Incubation of EAC cells with trastuzumab and pertuzumab

120 Incubation of EAC cells with trastuzumab, followed by 10

121 Incubation of embryoid bodies with the vital dye, Dil, r

122 Chronic (prolonged) co-incubation of F508del-CFTR-expressing cells with lumacaf

123 Our results suggest that incubation of food craving alters brain reward circuitry

124 Although incubation of FosDH2 with (3S)-3-hydroxybutyryl-FosACP2

125 history of heroin self-administration showed incubation of heroin craving after forced but not volunt

126 untary abstinence prevented the emergence of incubation of heroin craving in both sexes.

127 However, incubation of HMW oAbeta in mildly alkaline buffer led t

128 ry-competent cells can be produced following incubation of HOS cells lacking mitochondrial DNA (mtDNA

129 Incubation of human monocyte-derived macrophages with th

130 Cross-incubation of HV plasma with PV neutrophils resulted in

131 Incubation of IECs with TNF reduced expression of DRA.

132 Incubation of IL-1beta stimulated healthy tendon cells w

133 sus control cells was eliminated by in vitro incubation of infected cell RNAs with yeast or human DBR

134 Incubation of macrophage with the NR1D1 activator SR9009

135 We recently introduced an animal model of incubation of methamphetamine craving after choice-based

136 We recently developed a rat model of incubation of methamphetamine craving after choice-based

137 e of DMS dopamine D1 and D2 receptors in the incubation of methamphetamine craving after voluntary ab

138 Our results show that incubation of methamphetamine craving after voluntary ab

139 ntary or forced abstinence than after 1 day (incubation of methamphetamine craving).

140 21 d of voluntary abstinence than after 1 d (incubation of methamphetamine craving).

141 a long withdrawal interval when animals show incubation of methamphetamine craving.

142 of these products matched those observed on incubation of MtTPS5 with natural (2E,6E)-FDP.

143 In vivo reactivity was evaluated through incubation of N(2) -4-ethynylbenzyl-dG with wild-type an

144 In vitro incubation of nanomaterials with plasma offer insights o

145 In addition, we showed that incubation of normal RBCs and SS-RBCs with epinephrine,

146 In vitro, increased room temperature incubation of optisol-GS increased growth of Candida spe

147 Co-incubation of ovarian cancer cells with ascites fluid si

148 Incubation of plasma electronegative low-density lipopro

149 yptic soy broth (TSB) to incubate disks, and incubation of plates for 6 h versus 18 to 20 h.

150 PSE was induced by incubation of post-mortem chicken carcasses at 37 degree

151 Co- and pre-incubation of PPAA with 5-CQA significantly reduced PPAA

152 Incubation of primary or immortalized human keratinocyte

153 Finally, incubation of PrP(Sc) with recombinant GRP78 led to the

154 compartment is mediated by hemozoin, because incubation of purified malaria pigment with DNase abroga

155 ulation through osmotic minipumps, and after incubation of rat neonatal cardiomyocytes with isoprenal

156 Extended incubation of RGM medium for 28 days facilitates the iso

157 Incubation of RIN-m5F cells with 80 muM carbidopa did no

158 Incubation of S1P with airway smooth muscle cells signif

159 ponse to the stimuli was also reduced by pre-incubation of sensory neurons from untreated BALB/c mice

160 A 36-day incubation of soil samples was conducted under different

161 Incubation of steam-pretreated poplar (SPP) with sLac en

162 In contrast, incubation of stretched macrophages with sodium hydrosul

163 Incubation of the cells with albumin (40 mug/ml) for 72

164 ctable fluorescent signal was obtained after incubation of the cells with the MB alone (fluorescent s

165 hich takes approximately 6 min), followed by incubation of the CTC clusters for 48 h before analysis.

166 t bond formation to Cys-154 was confirmed by incubation of the inhibitors with wild-type JNK3 and JNK

167 Incubation of the L-selectin tail with cell extracts fro

168 denaturation followed by sequential on-chip incubation of the nucleic acids and MNPs, produces a sig

169 ere detected in methanol extracts, after 12h incubation of the samples assisted by ultrasound, at the

170 Based on the incubation of the thiolated aptamer with CT26 cells, the

171 After the incubation of tropomyosin with TROP aptamer probe, the p

172 Model 1: incubation of untreated or hTNFalpha-treated PAEC with 1

173 ompetence could not be generated in vitro by incubation of UreG with nickel, bicarbonate, and GTP.

174 tion of neuronal differentiation, similar to incubation of Zeb2(+/+) EPCs with EDN3.

175 Incubation of Zeb2(Delta/+) EPCs with EDN3, on the other

176 bling versus nibbling mechanisms, media from incubations of HDL with CHO-SR-B1 cells were analyzed by

177 ism of GalNAc-conjugated oligonucleotides in incubations of primary rat hepatocytes; the elucidation

178 reviously, a time-dependent intensification (incubation) of cue-induced cocaine craving has been demo

179 spores of several other Bacillus species by incubation on bSi wafers with and without nanopillars.

180 of kynurenine is increased 100-1000-fold by incubation or long-term storage and relies on the hydrop

181 Clinical illness follows a short incubation period and presentation ranges from asymptoma

182 disease closely in terms of host physiology, incubation period before onset of disease, clinical sign

183 The incubation period for NGU caused by Mycoplasma genitaliu

184 The incubation period for typhoid, polio, measles, leukemia

185 tential for rapid transmission and the short incubation period in the respiratory ward setting.

186 s of diffusion during static incubation, the incubation period is reproducibly achieved by varying th

187 ating JD is a difficult task due to the long incubation period of MAP, inefficient diagnostic tests,

188 The incubation period of sheep scrapie is strongly influence

189 ission potential and have a longer extrinsic incubation period than their wild-type counterparts.

190 The median incubation period was 1 day, and the median time from il

191 ome components of host resistance, including incubation period, lesion size, and lesion number.

192 tive bacillus Mycobacterium leprae: the long incubation period, limited knowledge about its mode of t

193 re measured over a five weeks anaerobic dark incubation period.

194 s to unmodified cellulose within a 30-second incubation period.

195 l was able to inhibit mould growth after the incubation period.

196 small numbers of large eggs with very short incubation periods (average 11-85 d).

197 Typical turnaround times vary, due to assay incubation periods and a lack of clinical laboratories p

198 able diseases typically associated with long incubation periods and characteristic spongiform changes

199 cells, we show that skewed distributions of incubation periods emerge for a wide range of assumption

200 Here, nonavian dinosaurian incubation periods in both small and large ornithischian

201 The capacity to determine incubation periods in extinct egg-laying amniotes has im

202 The presence of a D or S residue prolonged incubation periods significantly, and prions were detect

203 t and mosquito mortality rates and extrinsic incubation periods to be smallest in 2015.

204 Selective fungal culture media and longer incubation periods yielded higher rates of detection for

205 We estimated the incubation periods, and time delays from illness onset t

206 ion to contact-exposed birds, alongside long incubation periods, may enable unrecognized disseminatio

207 Mortality from infection, pathogen incubation rate, and host recovery rate were set to a ra

208 nd subjected to 2 different room temperature incubation regimens reflective of current corneal tissue

209 raceae and Hyphomonadaceae) in weeklong dark incubations relative to controls.

210 After in situ incubation, retrieval of the ichip and processing of its

211 Metagenomic sequencing of incubation samples revealed that LREE-containing MDHs we

212 Results of these incubations shed new light on nitrogen cycling complexit

213 Furthermore, keratinocyte-monocyte co-incubation studies across a 4 microM semipermeable membr

214 ise-conditioned serum for breast cancer cell incubation studies and murine exercise interventions, we

215 which was chosen as a substrate for in-situ incubation studies in shallow waters of Catalina Island,

216 elationships between hatchling mortality and incubation temperature and hence the broad applicability

217 We show that incubation temperature influences motility and limb bone

218 ch the sex of an embryo is determined by the incubation temperature of the egg during a critical peri

219 cal period during which sex is determined by incubation temperature.

220 However, as incubation temperatures near lethal levels, the natural

221 Verde Islands-we show the effects of warming incubation temperatures on the survival of hatchlings in

222 pment time among species with colder natural incubation temperatures.

223 At the end of the incubation, the changes in the total alkane and PAH cont

224 t the limitations of diffusion during static incubation, the incubation period is reproducibly achiev

225 2 were added in the detection cell after the incubation, the yield of resorufin formed from the react

226 After incubation, they were exposed to blue light (Blu-U, Dusa

227 red wines), temperature (85 degrees C), pre-incubation time (15min) were optimized for identificatio

228 he interactive effect of enzymatic units and incubation time (p-value <0.015), while CER was found to

229 wever, expedited exposure of a 10-minute ALA incubation time did not reach significantly different AK

230 Creamed emulsion assay incubation time dispersion was 1.7%, 3-fold less than ot

231 odilution method that requires a 16- to 20-h incubation time for B. anthracis Advances in high-resolu

232 A reduction of incubation time from 10min to 2min increased the method

233 ng low detection limit of 10 cellsmL(-1) and incubation time of 10min.

234 /40microL (i.e., 19-6250ng/mL), both with an incubation time of 10min.

235 trode detection limit was 28cellsml(-1) with incubation time of 10min.

236 had a detection limit of 2.6pgmL(-1) with an incubation time of 15min.

237 vourzyme(R), temperature 50 degrees C and an incubation time of 1h.

238 l(-1), detection limit of 20cellsml(-1) with incubation time of 20min for FA based electrode, and for

239 microneedle pretreatment at a 20-minute ALA incubation time significantly improved AK clearance with

240 receptor concentration, temperature, pH, and incubation time were optimized to obtain the high sensit

241 n could be influenced by drug concentration, incubation time, and surface coating, as well as the typ

242 Variations in media, temperature, incubation time, CO2 level, and inoculum concentration w

243 pH 7.0, temperature 25 degrees C and 6min of incubation time.

244 similar to that of a conventional 1-hour ALA incubation time.

245 spholipid among HDL species as a function of incubation time.

246 pore water, which increased with longer soil incubation times and decreasing soil pH.

247 However, prolonged incubation times and pain associated with treatment are

248 teins, varying pH, enzyme concentrations and incubation times to simulate infant and young child gast

249 inute or 20-minute aminolevulinic acid (ALA) incubation times, after pretreatment with a microneedle

250 analysis with a processing time from sample incubation to signal analysis of 20 min.

251 y, the use of the CIM (TSB and 18 to 20 h of incubation) to confirm screen-positive isolates resulted

252 Nitrospira inopinata) during incubation under standard cultivation conditions.

253 ) returning the ichip to the environment for incubation; (v) retrieving the ichip and harvesting grow

254 o each type of disk, which after 72 hours of incubation was assessed using an anaerobic flow chamber

255 In contrast, incubation was associated with an increase in NAc spine

256 the inactivation step and the length of this incubation was extended.

257 of the UHPLC-HRMS dataset obtained after 4h incubation was reduced with petroleomics-inspired strate

258 tion of marine oil snow (MOS) in oil-amended incubations was consistent with its formation during the

259 tion values measured after 24h of antibiotic incubation were similar to those calculated using Etest(

260 te-models and mouse organoids by basolateral incubation with a high concentration (1 mM) of conjugate

261 ve any impact on stomatal aperture following incubation with abscisic acid, malate, or citrate.

262 by ELISA and completely abolished after pre-incubation with alpha-gal.

263 atelet count; this phenomenon was blunted by incubation with an inhibitor of Toll-like receptor 4.

264 After incubation with beta-glycosidase, percentage of aglycone

265 chemically induced blue-fluorescent state by incubation with beta-mercaptoethanol (betaME).

266 Similarly, short incubation with Cp results in a strain-dependent macroph

267 the antibody-coated sensor was reduced after incubation with E. coli K-12 cultures, with the reductio

268 , showed significant (13)C-enrichments after incubation with either (13)C-labeled carbohydrates or am

269 Incubation with either exogenous PGE2 or selective EP2 a

270 ntibiotics for one hour followed by 24 hours incubation with fresh nutrients in MWP or continuous flo

271 escued the anemia phenotype in vivo, whereas incubation with HNF1A(-/-) plasma increased the osmotic

272 helial cells or Neisseria meningitidis after incubation with human serum was completely C3-dependent,

273 nnan was associated with T cells after their incubation with infected macrophages in vitro and when T

274 Their incubation with lactose plus the monosaccharides Gal or

275 Co-incubation with LC managed to prevent these alterations

276 Effects of Nlrp3 activation induced by incubation with lipopolysaccharide and ATP was studied i

277 y (M2) to proinflammatory (M1) subtype after incubation with MfP.

278 In mouse islets, incubation with ML351 improved glucose-stimulated insuli

279 After 6 hours of incubation with nanoceria at pH 9, P. aeruginosa showed

280 asured for the MWCNT/MIP-sensors after their incubation with non-diluted plasma.

281 EC incubation with OxPAPC also induced EP4 mRNA expression

282 Interestingly, incubation with PQS significantly reduced HO-1 and NrF2

283 ntrations in a DBS before and after a 30 min incubation with pyridoxine 5'-phosphate (PNP).

284 ochemical methods, we demonstrated that upon incubation with RBCs EhRab35 is recruited to the site of

285 Furthermore, we demonstrated that incubation with specific anti-CD73 serum significantly r

286 ed in primary mouse and human macrophages by incubation with SR9009; some of the cells were also incu

287 Proteins were glycated by incubation with sugars (glucose, methylglyoxal or ribose

288 oxidative modifications of amino acids after incubation with tert-butyl hydroperoxide and hypochlorou

289 ergic receptor in HEK293T cells, followed by incubation with the optimal thiosemicarbazide-functional

290 oteins were initially low and increased upon incubation with the proteases.

291 lls with trastuzumab, followed by 10 days of incubation with the TGFbeta receptor inhibitor in the pr

292 epG2, or pancreatic cancer cells, as well as incubation with thiostrepton (an inhibitor of forkhead b

293 s increased in control macrophages following incubation with TNF-alpha.

294 Laboratory incubations with (36)Cl as a Cl tracer were performed to

295 jor differences were confirmed in short-term incubations with bromodeoxyuridine followed by CARD-FISH

296 Laboratory static sediment-water incubations with different DO and temperature treatments

297 Here we show that during incubations with elevated nitrate, increased N2O fluxes

298 les of 5-LOX and COX-2, using inhibitors and incubations with exogenous substrates.

299 By conducting anoxic slurry incubations with lake sediments amended with (13)C-label

300 ss from interspecies competition relative to incubations with T4.