ライフサイエンスコーパス: PBS

1 PBS can be used in the micromolar range, equivalent to a

2 PBS containing SDS and beta-ME, performed significantly

3 PBS elution of DBS offers a sensitive and specific metho

4 PBS, urine, and saliva samples were concentrated up to 2

5 than 100 pg/ml in diluted PBS buffer (0.01X PBS).

6 was performed using a mixed riboflavin 0.1% PBS solution followed by UVA irradiation.

7 s injection of either PBS (control, n = 10), PBS-primed ECFCs (ECFCPBS, n = 13), or erythropoietin-pr

8 were stable for 6 weeks when stored in 0.1M PBS, pH 7.4 at 4 degrees C.

9 al activity after 6 weeks of storage in 0.1M PBS, pH 7.4 at 4 degrees C.

10 Ab-bound MTPs, stored at 4 degrees C in 0.1M PBS, pH 7.4, retained its biological activity for 8 week

11 icromolar range, equivalent to about 0.1% 1x PBS (150 muM).

12 le binding and detection of PSA in pH 7.4 1x PBS solutions, whereas control experiments with proteins

13 mice injected with alpha-syn fibrils and 20 PBS-injected mice at three timepoints (10 males and 10 f

14 ingBlock phosphate buffer saline- Tween-20; (PBS-T20) blocking buffer was utilized to minimize nonspe

15 glucose in phosphate buffer solution (0.25M PBS, pH 7.0), with a linear range between 0 mM and 0.9mM

16 ve release of the encapsulated tPA in pH 7.4 PBS buffer was 10% after 6 h.

17 aline (PBS) containing 0.02% Tween 80; pH7.4 PBS containing 1.0% triethyl citrate (PBStc); and pH7.4

18 tt score >=2 had similar discrimination as a PBS >=4 in nonbacteremia infections.

19 ohort of 475 patients with CRE infections, a PBS >=4 was associated with mortality in patients with n

20 peptide LbL immunosensor was immersed into a PBS solution containing the non-specific Ab (anti-HCV fo

21 were assessed by intravital microscopy after PBS, IL-1beta, TNF-alpha, or recombinant Gal-3 treatment

22 hours than HBSS mice treated with PFCE-air, PBS-O2, or PBS-air (P < .05).

23 O/phosphate buffered saline (PBS) or albumin/PBS solutions in an in vitro M. tuberculosis-infected ma

24 However, Na(2)CO(3), pH 9.6 and PBS containing 1 M GuHCl recovered 65% +/- 4% and 77% +/

25 ps) or air only (hereafter, the PFCE-air and PBS-air groups) gas mixtures.

26 Succinate, fumarate, and PBS have no effect on cell viability, regardless of cell

27 e lidocaine were more cytotoxic than MMC and PBS (P < 0.01 for all).

28 0%; hereafter referred to as the PFCE-O2 and PBS-O2 groups) or air only (hereafter, the PFCE-air and

29 -linking using glutaraldehyde of the OCP and PBS followed by liquid chromatography coupled to tandem

30 with PPCN+SDF-1, SDF-1 only, PPCN only, and PBS, respectively.

31 product upon reaction by Cys-SeH in aqueous PBS buffer by exhibiting a approximately 210-fold fluore

32 ng its selectivity toward Cys-SeH in aqueous PBS buffer, in bovine serum, and on the silica gel surfa

33 No difference was observed between PBS and succinate on (18)F-fluorocholine uptake in the t

34 polyadenylation (PolyA), and primer binding (PBS) elements, do not participate in intermolecular base

35 ng alpha-l-fucosidase concentrations in both PBS and human blood serum.

36 generated by CAPs in a physiological buffer (PBS, pH 7.4).

37 PE dose was compared with change produced by PBS injection.

38 C) treated with platinum-based chemotherapy (PBS).

39 (Pt) during screening in "clean" conditions (PBS), and no degradation in performance during the opera

40 conformation and in the corresponding (-)/(+)PBS duplex.

41 ASO (66 mg/kg/wk), lisinopril (100 mg/kg/d), PBS (control), or scrambled ASO (66 mg/kg/wk) for 10 wk,

42 compared with the sensing cannula delivering PBS as determined by integrating the area-under-the-curv

43 tion limit is less than 100 pg/ml in diluted PBS buffer (0.01X PBS).

44 sing Ebola glycoprotein suspended in diluted PBS buffer, human serum, and plasma.

45 P2, HCP3) and another capable of dissipating PBS excitation (HCP4).

46 Log DMW,PBS values above 5.5 are only experimentally feasible wi

47 phosphate buffered saline (PBS) medium (DMW,PBS) for 19 cationic surfactants.

48 factant species account for the observed DMW,PBS.

49 received an intravenous injection of either PBS (control, n = 10), PBS-primed ECFCs (ECFCPBS, n = 13

50 G uptake by muscle when compared with either PBS or fumarate, highlighting the effect of succinate on

51 Mice were injected with either PBS, free rapamycin (5 mg/kg), or rapamycin-loaded leuko

52 sulin-treated group compared with the FIV(+)/PBS-treated group.

53 iva samples were concentrated up to 20-fold (PBS), 15-fold (urine), and 5-fold (saliva) in less than

54 kBq of (212)Pb-Daratumumab instead of 11 for PBS control groups.

55 iosensor was found to be 0.994 and 0.997 for PBS and milk respectively.

56 good linearity of the calibration curves for PBS and lysate solutions at low Sur concentrations confi

57 good linearity in the range 0.3-10 ng/mL for PBS and 0.3-50 ng/mL for milk.

58 s from MOG-psigma1-treated EAE or Bregs from PBS-treated EAE mice did not resolve disease, whereas th

59 h were fully protected by HA/MF59 but not HA/PBS immunization against intranasal challenge with the h

60 hook-shaped anterior ascending branches (ie, PBS).

61 igh electrical conductivity (~20 S cm(-1) in PBS, ~40 S cm(-1) in deionized water), high stretchabili

62 dimetric assays the RSD values were 9+/-5 in PBS and 12+/-6 in serum.

63 achieves classification accuracy of 98.9% in PBS, and 100% in undiluted human serum.

64 c determination of hemoglobin is achieved in PBS buffer as well as in the whole blood sample.

65 ng to the transport protein serum albumin in PBS buffer at ambient conditions.

66 2O2, malondialdehyde, and a lysine analog in PBS at a physiological temperature, which resulted in M2

67 f continuous monitoring of propofol, both in PBS and in undiluted human serum, to demonstrate that ML

68 es (H(2)O(2), NO(2)(-)) generated by CAPs in PBS and observed the mean dynamic of RONS chemistry duri

69 ic profile of the binding does not change in PBS solution.

70 le amino groups and more positive charges in PBS buffer, therefore few of the BPEI groups could induc

71 d the hydrodynamic size of the AgIONs-Chi in PBS remained below 200 nm.

72 ed glucose transport through the coatings in PBS media and this was considered to be a as a consequen

73 ion curves of %B/B0 vs. OTA concentration in PBS showed that half-inhibition occurred at 1.17 microg

74 ar with logarithmic BoNT/A concentrations in PBS, milk and human serum across a 0.27-268pgmL(-1) rang

75 atings: in agar gel at static conditions, in PBS solution with agitated conditions, extraction in PBS

76 essfully stabilize it against degradation in PBS (pH=7.4).

77 we investigate the effect of H2 dissolved in PBS in the concentration 0.5 ppm wt/vol, applied on rabb

78 omplement, and Ig regulation are enhanced in PBS-treated Nrf2 null gene profiles compared with those

79 posite coatings during prolonged exposure in PBS.

80 tion with agitated conditions, extraction in PBS solution in the presence of an HSA binding matrix, a

81 e electrode analytical response to fetuin in PBS samples, obtained by square wave voltammetry, exhibi

82 n reaction in the presence of CAO-NSs/GCE in PBS.

83 75 muW cm(-2) is obtained in 5 mM glucose in PBS, the highest to date under these conditions, providi

84 hermore, we show that prolonged hydration in PBS has a significant effect on the measured corneal pro

85 nhibitors on release of Dox from implants in PBS, in vivo Dox distribution and retention in a subcuta

86 tervals was 0.680 for solutions incubated in PBS, 0.642 for MMC, 0.612 for MMC + 1% preservative-free

87 Additionally, while incubation in PBS led to a significant decrease in the metabolic activ

88 ly the tunica media, following incubation in PBS, in contrast with incubation in the HypoRP solution

89 e) to deliver agents (methylene blue, MB, in PBS) into bovine AC.

90 ction limit is calculated to be 0.1 ng/mL in PBS buffer with a linear range of 0-9.0 ng/mL.

91 etection limit was approximately 30cfu/mL in PBS buffer.

92 % is obtained compared to result obtained in PBS (phosphate buffered saline).

93 n PBS, and show that the results obtained in PBS run buffer are much closer to previously reported va

94 D) of 3+/-1 and 7+/-4 (all in percentage) in PBS and serum, respectively, meanwhile for impedimetric

95 tammetric response to 2 muM physostigmine in PBS at a pH of 7.0.

96 along with a limit of detection of 90 pM in PBS.

97 sitivity, with detection limits (0.01 ppm in PBS and 0.3 ppm in milk) below the maximum allowed level

98 acid that can reversibly release a proton in PBS buffer (pH = 7.4) under visible light is reported.

99 Sunset Yellow, Tartrazine and Allura Red in PBS (pH 3).

100 n and its DNA aptamer, which was selected in PBS, and show that the results obtained in PBS run buffe

101 logP = 7.1) with no measurable solubility in PBS buffer.

102 and observed that this complex is stable in PBS and upon incubation with human lens-epithelial cell

103 creased over time for artery rings stored in PBS and UW solution but not for those stored in HypoRP s

104 molecule, biotinylated anti-streptavidin, in PBS.

105 Studies in PBS buffer solutions and in a model body liquid demonstr

106 dothelial cells (hESC-ECs) were suspended in PBS or Matrigel and kept at 4 degrees C.

107 laparotomy, induced delivery earlier than in PBS control groups (P < 0.01).

108 erum albumin was almost identical to that in PBS.

109 s of sub-10 pg/mL in 25% serum (by volume in PBS).

110 Long-term release was tested over 9 weeks in PBS + 0.02% Tween 80 + 0.02% sodium azide pH 7.4 (PBST)

111 s fluorescent nucleoside when included in (-)PBS or (-)/(+)PBS duplex fully preserves their stability

112 After immersing into PBS for 7 days, the transmittance of the optimal constru

113 the injection of their ethanol solution into PBS produced monodisperse nanometer size assemblies.

114 coronary artery followed by intramyocardial PBS injections (control group), and LAD ligation followe

115 ric acid (UA), and serotonin (5-HT) in 0.1 M PBS (pH = 7.4).

116 ium where the immunoassay takes place (0.1 M PBS pH 7.2), avoiding the use of additional and more haz

117 utomer is strongly favored in matched (-)/(+)PBS duplexes, while the relative emission of the H3 taut

118 was investigated in phosphate buffer medium (PBS) with various pH ranges and the electron transfer pr

119 66pg/mL to 666ng/mL in physiological medium (PBS).

120 aded substantially in 1:1 acetonitrile:10 mM PBS, pH 7.4, at 37 degrees C, generating primarily o(LA)

121 with S19, 16MDeltavjbR + Quil-A, or 100 mul PBS + Quil-A (as control).

122 AAV viruses (1 x 10(12 )GC/mouse in 200 mul PBS) were injected into Balb/cj mice via tail veins.

123 Median age of PBS was 55-59 years and median OS was 108 months.

124 showing the insufficient buffer capacity of PBS to maintain a stable pH at the given conditions.

125 rmine clinicopathological characteristics of PBS and estimate their associations with overall surviva

126 rated clinicopathological characteristics of PBS in the US population and supports performing BCS if

127 When the PBS composition of PBS/PLA blends was changed from 40 wt% to 50 wt%, the me

128 tions are far from the isotonic condition of PBS ( approximately 150 mM) that is normally used with b

129 and 0.93, respectively) for the detection of PBS.

130 Hydrolysis dynamics of PBS, poly(butylene adipate), poly(lactic acid), and poly

131 ae (RoL), we detected complete hydrolysis of PBS thin films at pH 5 and 40 degrees C that proceeded t

132 ection of thrombin but not with injection of PBS as a vehicle control, demonstrating the first aptame

133 ory mucus was washed out by the injection of PBS to mouse nasal cavity, the response of MOR161-2 to a

134 24 hours after intratracheal instillation of PBS or S. pneumoniae, and differentially expressed (DE)

135 KSHV) in a fingerprick volume (50 microL) of PBS, plasma, and artificial saliva samples for a broad r

136 Using offspring of PBS- or HDM-exposed mothers, the magnitude of HDM or Asp

137 Compared with offspring of PBS-exposed mothers, offspring of HDM-exposed mothers de

138 als could be controlled by the proportion of PBS and the degradation time.

139 increase of the enzymatic hydrolysis rate of PBS than of nonpolymeric dibutyl adipate.

140 aluated the microchip with spiked samples of PBS with bacteria concentration between 10(1) to 10(8) C

141 t volume (i.e., by adding the same volume of PBS to a sample).

142 When incorporated into the loop of (-)PBS, the (-)DNA copy of the HIV-1 primer binding site, b

143 ered saline (PBS) or the same volume of only PBS solution was injected into gingival tissue approxima

144 after intranasal challenges with allergen or PBS.

145 with 0.1% ethanol (control for RvD2) and/or PBS (control for LPS), and control microRNA mimics and i

146 nasally with Alternaria extract (Alt-Ext) or PBS for 4 consecutive days to evaluate innate airway all

147 lenged with house dust mite (HDM) extract or PBS five days per week for four weeks.

148 after intratumoral injection of fumarate or PBS.

149 njugated hydrogel (QHG213H), control gel, or PBS was injected into the peri-infarct/MI zone.

150 to receive daily atorvastatin 1.14 mg/kg or PBS (control) starting 7 days before end-to-side carotid

151 ected intraperitoneally with anti-IgE mAb or PBS 6 hours before challenge with AP or saline.

152 HBSS mice treated with PFCE-air, PBS-O2, or PBS-air (P < .05).

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

154 24 h after instillation of S. pneumoniae or PBS.

155 KI and wild-type mice received PPIs or PBS intraperitoneally and were analyzed for survival, in

156 potential of PSA in HSE by infecting PSA or PBS treated 129S6 mice with HSV1, followed by delayed Ac

157 nucleoside when included in (-)PBS or (-)/(+)PBS duplex fully preserves their stability and exhibits

158 ted OCP(r) interacts with the phycobilisome (PBS), the cyanobacterial antenna, and induces excitation

159 ssipation at the level of the phycobilisome (PBS), the cyanobacterial antenna, induced by the orange

160 rbed by the light-harvesting phycobilisomes (PBS) in cyanobacteria.

161 The pathogenesis of PI-PBS appears to involve changes in the intestinal microbi

162 Control animals received PBS injection.

163 fects of up to 6-day incubation in a saline (PBS), UW, or HypoRP solution on the structure, cell viab

164 omer 5S,12S-diHETE is produced after saline (PBS) administration.

165 tine (NIC) in 0.1 M phosphate buffer saline (PBS) at physiological pH of 7.

166 5 mM glucose using phosphate buffer saline (PBS), monitored for 1 min were selected as the ideal con

167 evel (~100%) when phosphate buffered saline (PBS containing 137 mM NaCl) was used as a protein suspen

168 f 5 mM glucose in phosphate-buffered saline (PBS) (50 mM phosphate buffer solution, pH 7.4, with 150

169 were incubated in phosphate-buffered saline (PBS) (control), MMC (0.2 mg/ml), a mixture of 0.2 mg/ml

170 of WTC-PM(53) or phosphate-buffered saline (PBS) (controls).

171 e toxin (LTB), or phosphate-buffered saline (PBS) alone and then challenged with 10(11) CFU of H10407

172 room temperature phosphate-buffered saline (PBS) also caused significant alteration of protein phosp

173 t 3 days by using phosphate-buffered saline (PBS) and cysteine/methionine-free Dulbecco's Modified Ea

174 ection of cTnT in phosphate buffered saline (PBS) and human serum (HS) buffers was achieved at low sa

175 d substances from phosphate-buffered saline (PBS) and human urine using Fe(2)O(3) magnetic nanopartic

176 10(7) CFUs/mL in phosphate buffered saline (PBS) and peritoneal dialysis (PD) fluid.

177 n G (IgG) in both phosphate buffered saline (PBS) and spiked in E. coli cell lysate.

178 usly with PFCE or phosphate-buffered saline (PBS) and then managed in either air/O2 (FiO2 proportion,

179 all compounds in phosphate-buffered saline (PBS) and urine samples owing to the large volume and cap

180 ine treatments or phosphate-buffered saline (PBS) as a control and challenged them with Pd upon trans

181 mast cells or 1x phosphate-buffered saline (PBS) before collecting serum, liver, and cholangiocytes.

182 nanotube yarn in phosphate-buffered saline (PBS) buffer.

183 wly degradable in phosphate buffered saline (PBS) but more rapidly degraded in the presence of a lipa

184 rrhea compared to phosphate-buffered saline (PBS) controls (PE = 84.1%; P < 0.02).

185 TFC and TCC than phosphate buffered saline (PBS) extracts for all the fruits parts.

186 te, fumarate, and phosphate-buffered saline (PBS) in different cell models.

187 rus elution using phosphate-buffered saline (PBS) may provide an alternative analyte for lower-cost q

188 yer membranes and phosphate buffered saline (PBS) medium (DMW,PBS) for 19 cationic surfactants.

189 ation of SDF-1 in phosphate buffered saline (PBS) on wound healing was evaluated in a diabetic murine

190 compared to DMSO/phosphate buffered saline (PBS) or albumin/PBS solutions in an in vitro M. tubercul

191 ere injected with phosphate-buffered saline (PBS) or GBV-B, respectively.

192 TSG-6 in 5-microL phosphate-buffered saline (PBS) or the same volume of only PBS solution was injecte

193 livered a control phosphate buffered saline (PBS) solution with no insulin.

194 rough dilution of phosphate-buffered saline (PBS) to tune Cdl to dominate the overall capacitance cha

195 with ~0.5 muL of phosphate-buffered saline (PBS) via pipet immediately after Raman spectral measurem

196 nged hydration in phosphate buffered saline (PBS) was found to significantly increase the elastic mod

197 When phosphate buffered saline (PBS) was present in the channel, the additional minimum

198 mmol/L in 100 mM phosphate-buffered saline (PBS) without significant interference: high-density lipo

199 concentration for phosphate buffered saline (PBS), a typical ionic medium for biological samples, and

200 h IgM, not IgG or phosphate-buffered saline (PBS), had decreased expression of chitin synthetase, CHS

201 ch as nonvolatile phosphate-buffered saline (PBS), should be replaced before analysis.

202 studied probes in phosphate-buffered saline (PBS), urine, and whole blood.

203 P. aeruginosa in phosphate-buffered saline (PBS), while sterile PBS was used for controls.

204 rol mice received phosphate-buffered saline (PBS).

205 h air and flowing phosphate buffered saline (PBS).

206 buffers, such as phosphate buffered saline (PBS).

207 d rate in aerated phosphate buffered saline (PBS).

208 n to be stable in phosphate buffered saline (PBS).

209 ccharide (LPS) or phosphate-buffered saline (PBS).

210 s DSP solution or phosphate buffered saline (PBS).

211 0 pM to 100 nM in phosphate-buffered saline (PBS); the limit of detection was 14.6 pM.

212 ed batch systems: phosphate-buffered saline (PBS, oligotrophic) and basal culture medium (BCM, eutrop

213 animals received phosphate-buffered saline (PBS; n = 5 to 7).

214 5.5, 6.5, and 7.4 phosphate buffered-saline (PBS) containing 0.02% Tween 80; pH7.4 PBS containing 1.0

215 nated with REG or phosphate-buffered saline [PBS]) after homologous or heterologous RSV challenge.

216 Primary breast sarcoma (PBS) is a rare and heterogeneous group of malignancies w

217 In SCI + PBS rat bladders, cystometry showed increased peak voidi

218 nd SCI plus phosphate-buffered saline (SCI + PBS), human embryonic kidney 293 (HEK293) cells, and hAF

219 ation caused no difference compared to SCI + PBS group.

220 The Pitt bacteremia score (PBS) is commonly used as a predictor of early mortality

221 ter, it has native support for the LSF, SGE, PBS Pro, and Slurm job schedulers and can scale up to th

222 NAs and target the tRNA primer binding site (PBS) essential for ERV reverse transcription.

223 -stranded region of the primer binding site (PBS)-segment of the 5'-UTR.

224 NA copy of the HIV-1 primer binding site, (-)PBS, both in its stem loop conformation and in the corre

225 et of features from potential binding sites (PBSs) in the mRNA and then train a classifier to disting

226 mination in 0.1 M phosphate buffer solution (PBS) at pH 7.0.

227 Fe(CN)6(4-)) in a phosphate buffer solution (PBS) containing AFB1, the magnitude of anodic current at

228 e (GSH) in pH 7.2 phosphate buffer solution (PBS) has been reported.

229 mA cm(-2) in 1 m phosphate buffer solution (PBS, pH 7.0).

230 accomplished in a phosphate buffer solution (PBS, pH=7) for ZnO/MWCNT/GCE samples.

231 bodies (Ab) in phosphate buffered solutions (PBS).

232 lative to in vivo from 64%, using a standard PBS dissolution method, to 92%.

233 combination of population branch statistics (PBS) and number of segregating sites by length (nSL) to

234 osphate-buffered saline (PBS), while sterile PBS was used for controls.

235 Poly(butylene succinate) (PBS) and poly(lactic acid) (PLA) were melt-blended and f

236 n experiments with poly(butylene succinate) (PBS) and the lipase of Rhizopus oryzae (RoL), we detecte

237 Prune Belly Syndrome (PBS) is a rare entity, usually found in male neonates.

238 ding was prevented using starting block T20 (PBS).

239 rs in cortex of TBI + Sp compared with TBI + PBS mice after both early and late infection, indicating

240 motor function recovery compared with TBI + PBS mice.

241 Four protocols were tested: PBS vehicle, DAC, ICI (anti-PD-1 or anti-VISTA), and DAC

242 sons showed that MMC was more cytotoxic than PBS (P < 0.001).

243 significantly lower EAE clinical scores than PBS control, while PLG-L and PDLA particles had modest o

244 Here we show that PBS-soluble phosphorylated high-molecular-weight (HMW) t

245 e interaction on photoabsorbance showed that PBS was least cytotoxic and an optimal control for this

246 The PBS offers a unique target to specifically inhibit LTR-r

247 The PBS was found in 23 (62%) of 37 total patients with FCD2

248 lize the interaction between the OCP and the PBS.

249 utable to structure-dependent binding at the PBS-segment of the HIV-1 5'-UTR during virus assembly.

250 e parameter as originally calculated for the PBS was not independently associated with mortality.

251 ecovery protein (FRP) detaches OCP1 from the PBS core, accelerating its back-conversion to OCP(O) ; b

252 This shift of the minimum from the PBS reference point reached saturation after 30 minutes

253 ction limit of approximately 4.8pg/ml in the PBS buffer.

254 ected by adding specific antibodies into the PBS buffer.

255 l domain of the OCP burrows tightly into the PBS while leaving the OCP C-terminal domain on the exter

256 photoactivated OCP bound to the core of the PBS affords almost total energy dissipation.

257 We analyzed each component of the PBS in the prediction of mortality, assessed the appropr

258 ios to analyze the predictive ability of the PBS overall and each of its components individually.

259 status, and cardiac arrest parameters of the PBS were independent risk factors for 14-day all-cause i

260 ve ability of the qPitt score to that of the PBS.

261 cellent reproducibility and specificity, the PBS, when present, could become a useful qualitative dia

262 Here, we validated that the PBS and qPitt score can be used as reliable predictors o

263 In vitro degradation suggests that the PBS-based porous materials have a good corrosion resista

264 ffect on their plasma levels compared to the PBS control.

265 rface areas on aortic arches compared to the PBS control.

266 When the PBS composition of PBS/PLA blends was changed from 40 wt

267 We determined whether the PBS predicts 14-day inpatient mortality in nonbacteremia

268 residues of the OCP that cross-link with the PBS are situated in the linker region, between the N- an

269 to 2-fold) animal survival compared with the PBS-treated control group.

270 (FRP), dislodges the active OCP(r) from the PBSs and accelerates its conversion to the inactive OCP.

271 However, they do not consider whether the PBSs are functional or not, and consequently result in h

272 ased NETosis and PAD4 expression compared to PBS-treated control.

273 sion (6.2-fold reduction in size compared to PBS-treated controls) and highest survival when treatmen

274 d within collagen gels over 72 h compared to PBS.

275 Pregnant female mice were exposed to PBS or HDM during pregnancy.

276 protease-inactivated D pteronyssinus, or to PBS during lactation.

277 n Linux-based clusters running SLURM, Torque/PBS, or SGE.

278 gle point and clustered mutations in the U5, PBS, and gag leader sequences (GLS), generating potentia

279 2 (mug/mL)(-1)] in comparison with undiluted PBS.

280 No previous KCE studies of DNA used PBS as the run buffer.

281 Here, we test the feasibility of using PBS as a KCE run buffer for analysis of DNA and show tha

282 o 4 weekly gavages with CpG/PN-NPs, vehicle (PBS), nanoparticles alone, peanut alone, CpG nanoparticl

283 following infusions of ANI, TTX, or vehicle (PBS).

284 received non-immunized colostrum or vehicle (PBS).

285 h injection repeated at week 3 (n=16) versus PBS control (n=16).

286 Human serum diluted 1:2 with PBS buffer was analyzed by LDL-MIP sensors to demonstrat

287 Allergen detection in 2D-Western blots with PBS resulted in greater sensitivity than with TBS or Tri

288 Balb/c mice were challenged with PBS or house dust mite (HDM) (Days 0, 7, 14-18) and expo

289 Adult mice were intranasally challenged with PBS or mixed allergen ( Alternaria alternata, Aspergillu

290 visually cued navigation, when compared with PBS-treated animals.

291 attenuated cardiac remodeling compared with PBS-treated control animals.

292 AR-gamma in glia was increased compared with PBS-treated FIV(+) control animals.

293 tivity in Ngb-H64Q-CCC-treated compared with PBS-treated, CO-poisoned mice.

294 ers exposed to D pteronyssinus compared with PBS.

295 female mice was similar (4.7 +/- 2.0 g with PBS treatment and 3.3 +/- 2.1 g with EPO treatment).

296 Male Sprague Dawley rats were injected with PBS or G-CSF during (1) extinction or (2) abstinence fro

297 and received weekly tail vein injection with PBS, EGCG, void nanoparticles (Vnano), Enano, ligand-coa

298 est that modifying the carrier solution with PBS, sucrose, and/or IPA would enable characterization a

299 reated with GCV, or tk-positive treated with PBS.

300 Control animals vaccinated with PBS had attack rates of 70 to 90% on challenge.