ライフサイエンスコーパス: microliter

1 DA assay (1 contaminating molecule per assay microliter).

2 njections of either glutamate or saline (0.5 microliter).

3 ble for small volume samples (few to hundred microliter).

4 vant limit of detection of 500 parasites per microliter.

5 00 CD3(+) autologous circulating T cells per microliter.

6 mall area from applied volumes as low as one microliter.

7 uid containing 2.08 x 10(6) viral copies per microliter.

8 blood eosinophil count of less than 1000 per microliter.

9 spinal fluid contained at least 500 RBCs per microliter.

10 n absolute neutrophil count of 100 cells per microliter.

11 eripheral blood CD4(+) cell counts above 200/microliter.

12 nd decline of CD4(+) T cells to </=200 cells/microliter.

13 at less than 0.75 infected erythrocytes per microliter.

14 ed to be near 16 genome copy equivalents per microliter.

15 including 2 who had levels below 25,000 per microliter.

16 whole blood minuscule samples of only a few microliters.

17 ato leaves with the sample volume of several microliters.

18 nano-molar/L range and the volume of tens of microliters.

19 ventricular infusion of butorphanol (26 nmol microliter-1 h-1) via osmotic minipumps for 3 days.

20 ceptor agonist, SKF 82958 (2.0 microgram 0.5 microliter-1 side-1) on the acquisition and expression o

21 tor antagonist, SCH 23390 (2.0 microgram 0.5 microliter-1 side-1), on the acquisition and expression

22 a total leukocyte count of 14 000 cells per microliter (14 cells x 10(9)/L) (normal range, 4500-11 0

23 0(9)/L) (normal range, 4500-11 000 cells per microliter [4.5-11 cells x 10(9)/L]), a normal different

24 er, administration of LY288513 (17 nmol/0.25 microliter) 55 min prior to pentagastrin (1.0 nmol/0.25

25 en-20-yn-3-one; 3.0, 10.0, or 30.0 ng in 0.5 microliter) administered into the dorsal hippocampus of

26 patient had platelet counts below 50,000 per microliter after enhanced platelet-monitoring began.

27 CA3 area of the dorsal hippocampus) with 5.0 microliters aggregated A beta in suspension, and the rem

28 ophosphate (8-bromo-cAMP) (0.2-7 nmol in 0.2 microliter) alone or together with the alpha1-adrenocept

29 The SHPPSI MS requires only microliter amounts of analyte solutions, allows easy sam

30 We developed a simple pairing scheme using microliter amounts of E. coli osmotic shockates bearing

31 , it is possible to measure BCAT activity in microliter amounts of rat tissue homogenates.

32 system is generally useful for separation of microliter amounts of unreactive trace volatile compound

33 ained at least 10 red blood cells (RBCs) per microliter and bloody LP as one in which the cerebrospin

34 rum containing 6.10 x 10(2) viral copies per microliter and influenza A virus in lung lavage fluid co

35 ow that in contrast to techniques delivering microliter and nanoliter volumes, evaporation has a majo

36 gle-cell RNA amplification methods with both microliter and nanoliter volumes, using sequence from bu

37 rum containing 2.50 x 10(8) viral copies per microliter and porcine respiratory coronavirus (PRCV) in

38 ystem that performs rapid thermal cycling of microliter and smaller liquid volumes inside glass capil

39 ents with CD4(+) T cell counts >/= 350 cells/microliter and viral load below the limits of detection

40 covery of analyte can be achieved with a few microliters and conducted until steady-state is attained

41 umbers in children with malnutrition (28 per microliter) and a recovery in cell number (48 per microl

42 nia virus particles (down to 60 virions in a microliter) and distinguish them from nonviable viruses

43 ax infection (>100 to <100,000 parasites per microliter) and normal glucose-6-phosphate dehydrogenase

44 que requires a minimal protein amount (a few microliters) and allows monitoring the bound Cu(II) ions

45 Aliquots of normal saline (1 x NS, 100 microliters) and higher concentrations (3 x NS, 6 x NS,

46 amine (0.0, 2.0, 10.0, or 20.0 microgram/0.5 microliter), and lever pressing was tested in the absenc

47 w cost, flexibility, low volume samples (few microliters), and homogeneous format.

48 , eosinophil count of at least 150 cells per microliter, and autoimmune disease were associated with

49 , eosinophil count of at least 150 cells per microliter, and autoimmune disease, were evaluated for a

50 ; eosinophil count of at least 150 cells per microliter aOR = 1.54 [95% CI = 1.21-1.97]; and autoimmu

51 icroinjection of IL-1ra (50 microgram in 0.5 microliter at 0 + 1 h) into the anterior hypothalamus (A

52 , eosinophil count of at least 150 cells per microliter, autoimmune disease, and other allergic and i

53 3, 7 and 10 days after the injection of 100 microliter autologous blood in the right basal ganglia.

54 In the second study, 100 ng/microliter bicuculline administered unilaterally prior t

55 However, 250 ng/microliter bicuculline produced motor dyskinesias and/or

56 ared (NIR) fluorescence detection to analyze microliter biological samples with an amol limit of dete

57 ling is a promising method for collection of microliter blood samples.

58 asite density infections (<100 parasites per microliter blood) that work in resource-limited settings

59 capable of detection below two parasites per microliter blood, a limit of detection suggested by the

60 hours after injection of IL-1beta (1 ng in 1 microliter), cerebral blood volume was significantly inc

61 om milliliter aqueous samples and performing microliter chemical amplification, serial enzymatic reac

62 s can serve as well-mixed, easily controlled microliter chemical reactors for characterizing homogene

63 Day 14 M-MDSC >179.2 per microliter conferred 6.98 times (95% confidence interval

64 ssful in testing dose-response analysis, the microliter consumption of expensive reagents and hours o

65 tz capillary mixer with an approximately 0.5 microliter delivery volume to the midpoint of the EPR-ac

66 55 min prior to pentagastrin (1.0 nmol/0.25 microliter) delivery blocked the facilitatory effects of

67 A hanging microliter drop of 1-octanol is shown to be an excellent

68 robust device capable of detecting DNA on a microliter drop with a zepto-molar (10(-21)) concentrati

69 an infrared (IR) laser from the surface of a microliter droplet deposited on a stainless steel post.

70 temporal polymerase chain reaction (PCR) in microliter droplets.

71 mple system (RSS), a convection platform for microliter drops.

72 e Langmuir model and tensiometry results for microliter drops.

73 and concentration into small-volume (tens of microliters) eluates.

74 y active in minuscule water droplets (1 to 3 microliters) entrapped in oil.

75 blood eosinophil count of less than 600 per microliter for 8 or more consecutive weeks was achieved

76 0 mg/d, ANC was maintained at >500 cells per microliter for a median of 12.6 hours, and ALC was maint

77 s, and ALC was maintained at >1000 cells per microliter for up to 16.9 hours.

78 he concentrated total sample is collected in microliter fraction at the center.

79 ns from several milliliter sample volumes to microliter fractions.

80 rain transfer constant of AraC was 2.5+/-1.4 microliter g(-1) min(-1), compatible with high water sol

81 hetized rabbits at various time points via a microliter glass capillary tube, and the miniature senso

82 the levels of [3H]IP at 0.3 to 3 micromol/8 microliter i.c.v. with lower doses resulting in less eff

83 nt, pertussis toxin treatment (1 microgram/5 microliter, i.c.v.; 48 hr before the 8-OH-DPAT challenge

84 roliter, icv, n=8), prazosin (10 microgram/5 microliter, icv, n=12) or alpha-helical CRF(9-41) (10 mi

85 Yohimbine (3 microgram/5 microliter, icv, n=8) pretreatment did not alter hemodyn

86 etreatment with phentolamine (30 microgram/5 microliter, icv, n=8), prazosin (10 microgram/5 microlit

87 ) or alpha-helical CRF(9-41) (10 microgram/5 microliter, icv, n=9) prevented the decrease in cardiac

88 4(+) T-lymphocyte counts were <200 cells per microliter in 0/20, 2/20, and 6/20 donors, respectively

89 sensitivity to at least 1 viral RNA copy per microliter in a sample.

90 sitivity of at least 50 viral RNA copies per microliter in a sample.

91 itemia level of fewer than ten parasites per microliter in a volume below 10 mul of whole blood is de

92 ive intermediate monocytes to >100 cells per microliter in patients with sarcoidosis and a fivefold d

93 analytes from small sample volumes of a few microliters in an automated and high-throughput manner,

94 s only 2% of all Tregs (one to six Tregs per microliter) in peripheral blood but, when isolated, exhi

95 nnabinoid agonist CP55,940 (5 microgram/0.25 microliter) induced strong contralateral turning when mi

96 Two-microliter injections of succinylcholine chloride in a 5

97 microliter) or intracaudate (2 microgram/0.5 microliter) injections of either glutamate or saline (0.

98 ic antagonist atropine (0.5 microgram in 0.2 microliter) into either the ipsilateral or contralateral

99 following injection of MK-801 (2 microgram/3 microliter) into the fourth ventricle.

100 or antagonist atenolol (0.5 microgram in 0.2 microliter) into the ipsilateral, but not the contralate

101 d subcutaneous injections of 5% formalin (50 microliter) into the plantar surface of the right hind p

102 the CCK-A antagonist, PD140548 (34 nmol/0.25 microliter), into the PAG failed to alter response laten

103 agonist, LY288513 (1.05, 4.2, 17.0 nmol/0.25 microliter), into the PAG suppressed the hissing respons

104 Delta(9)-THC (15-30 microgram/microliter intracerebellar) resulted in a significant mo

105 bolished Delta(9)-THC (15 and 25 microgram/1 microliter intracerebellar)-induced motor impairment.

106 l min-1 cmH2O-1; post-enzyme, 3.11 +/- 0.45 microliter l min-1 cmH2O-1).

107 lining by 2.3 times (control, 1.34 +/- 0.22 microliter l min-1 cmH2O-1; post-enzyme, 3.11 +/- 0.45 m

108 vicurvature, and extremely low (0.0005-0.001 microliter L-1) ethylene concentrations can restore the

109 tive stress induced by clinical drugs at the microliter level.

110 tection limits down to the low femtomole per microliter levels were achieved for propafenone and vera

111 resonator were utilized to measure PP(*) in microliter microdialysis samples (LOD 0.36 pmol).

112 At a flow rate of 5 microliter min-1, arteries from the WKY dilated signific

113 ly with time, to the lowest value of 44+/-11 microliter/min at the end of the experiment.

114 /-S.D.) value for CSF production was 51+/-10 microliter/min initially and decreased significantly but

115 microdialysis probes (3 mm; flow rate of 2.1 microliter/min) implanted in the left hippocampus.

116 basolateral) reduced JWL-->B from 6.1 to 4.4 microliter/min/cm2 (p < 0.05, n = 5) and abolished the P

117 roM luminal) reduced JWL-->B from 5.7 to 3.7 microliter/min/cm2 (p < 0.05, n = 5) and reduced PD by 4

118 The JWL-->B (6.1 microliter/min/cm2) was larger than JWB-->L (4.5 microli

119 oliter/min/cm2) was larger than JWB-->L (4.5 microliter/min/cm2, p < 0.05, n = 30).

120 retation of molecules of microbial cfDNA per microliter (MPM) of plasma.

121 is (7,718 and 21,612 copies of viral RNA per microliter nasal wash, respectively; P = 0.48).

122 ytes, lymphocytes, or eosinophils (cells per microliter), nor was there any relationship between IL-1

123 study, unilateral administration of 10-50 ng/microliter of bicuculline did not alter behavior.

124 In the third study, 75 ng/microliter of bicuculline was administered unilaterally

125 h) monocytes rose from 64+/-5 to 108+/-9 per microliter of blood (P<0.05).

126 formed, as few as six bacteria spiked in 200 microliter of blood could be detected.

127 cells, with an average of 100 cells lost per microliter of blood per year.

128 the number of responding CD8(+) T cells per microliter of blood.

129 od cell count can be defined directly from a microliter of crude whole blood.

130 tection down to 50 femtogram of PFCs, in one microliter of human plasma.

131 quantifiable by Western blot in less than a microliter of plasma from lung cancer patients.

132 ) probing 12 independent areas with a single microliter of processing liquid and (ii) processing a 2

133 27 gauge cannula, which was used to infuse 1 microliter of saline over 5 min.

134 of parasitemia (no. of asexual parasites per microliter of whole blood), sensitivities were 83% (>0 t

135 n the multi-analyte formate are 44 fmol (100 microliters of 0.1 ng/ml TNT solution) and 224 fmol (100

136 of 0.1 ng/ml TNT solution) and 224 fmol (100 microliters of 0.5 ng/ml RDX solution), respectively.

137 rapid digestion of particulate metals using microliters of acid added directly to a punch taken from

138 kappa light chains that requires only a few microliters of biological material.

139 ic acid in human blood, where only dozens of microliters of blood (few drops) was required, demonstra

140 ot of conditioned medium in culture or a few microliters of blood in vivo at different time points.

141 globin and its tryptic digests directly from microliters of blood, achieving a detection limit of les

142 ated by detecting allergen-specific IgE from microliters of characterized human serum and unprocessed

143 One hundred microliters of dual-labeled liposomes (DLLs) containing

144 o a paper strip to evaporate off hundreds of microliters of liquid to concentrate the target analyte.

145 d to enable analysis of nucleobases in a few microliters of liquid.

146 d point extraction (CPE) in which only a few microliters of micellar extracting phase is sufficient f

147 Few microliters of milk samples have been digested with tryp

148 Mean QO2 rates (microliters of O2/cm2 per hour) were: whole cornea, QO2

149 licity of the experimental procedure, use of microliters of organic solvent, short analysis time, sel

150 in the low ppm range and requires only a few microliters of protein sample at micromolar concentratio

151 periments, it is very difficult to add a few microliters of reagent into the solution in an EPR tube

152 method is simple to operate, requires a few microliters of reagent volume, is portable, is reusable,

153 ders of magnitude and requiring only tens of microliters of reagents.

154 uantification take minutes and require a few microliters of sample using only basic laboratory equipm

155 With a few microliters of sample, it is possible to aliquot up to 4

156 s of hours/days, this approach requires only microliters of sample, provides results within minutes,

157 Some microliters of samples were directly dispensed into the

158 tion to handle many samples and requires few microliters of serum samples.

159 tibody specificities with as little as a few microliters of serum specimen.

160 ching a few hundreds nanomolar in only a few microliters of solution.

161 inant taxa found in only several hundreds of microliters of surface seawater is similar to that found

162 Twenty microliters of whole blood or 10 mul of packed RBCs was

163 ant levels of trypsin activity in only a few microliters of whole blood.

164 Fifteen microliters of Xe were encapsulated into each 1 mg of li

165 m specimens with low concentrations (<1 copy/microliter) of HPV DNA.

166 dialysis report comparing concentrations (pg/microliter) of norepinephrine (NE), serotonin (5-HT) and

167 e relatively large volumes (over one hundred microliters) of blood samples, and therefore, are not su

168 lyzing PFCs in small volumes (less than five microliters) of blood.

169 th morulae concentration of 282 +/- 48 cells/microliter on day 5 (P = 0.004) and 242 +/- 63 cells/mic

170 er on day 5 (P = 0.004) and 242 +/- 63 cells/microliter on day 8 (P = 0.005).

171 ng neutrophils in blood was 122 +/- 22 cells/microliter on day 8.

172 ntrolled as discrete droplets (picoliters to microliters) on an array of insulated electrodes.

173 d eosinophil count of at least 300 cells per microliter or a sputum eosinophil level of at least 3% w

174 systemic host factors, CD4+ cell counts <200/microliter (OR = 3.0, 95 percent CI 1.3, 6.9) and nucleo

175 ptor agonist clenbuterol (3-3000 pmol in 0.2 microliter) or 8-bromoadenosine 3':5'-cyclic monophospha

176 sttraining intrahippocampal (1 microgram/0.5 microliter) or intracaudate (2 microgram/0.5 microliter)

177 n approximate cell density of five cells per microliter (P < .01).

178 ter) than in 2003-2005 (44+/-169 genomes per microliter, P=0.02), as were parasite densities in place

179 liter) and a recovery in cell number (48 per microliter; p < 0.01) with standard treatment.

180 When a liquid flow rate in the low microliter per minute range was used, the reconstructed

181 connected to a flow restrictor enabling low microliter per minute water flow through a solid phase e

182 nes and Ag/AgCl electrodes was shown to pump microliter per minute-range flow through a 0.5-mm-diamet

183 nic receptor agonist oxotremorine (10 ng/0.2 microliter per side) or saline.

184 nactivation with lidocaine (10 microgram/0.2 microliter per side), and control rats received buffered

185 ospheric carbon dioxide was increased by 200 microliters per liter in a forest plantation, where comp

186 ) enrichment (ambient concentration plus 200 microliters per liter) in an intact forest.

187 grobacterium tumefaciens, 5% sucrose and 500 microliters per litre of surfactant Silwet L-77.

188 ing at flow rates greater than a few hundred microliters per minute, and providing analysis rates gre

189 e i.c.v. administration of FIVgp120 (5 ng/10 microliter) produces changes in the latency of both cort

190 to reduce sample volumes from milliliters to microliters provides increased clinical utility.

191 Hollow microneedles permitted flow of microliter quantities into skin in vivo, including micro

192 f UV-excited fluorescence from nanoliter and microliter quantities of material, mixed at microsecond

193 ction of both polar and nonpolar analytes in microliter quantities of samples under ambient condition

194 f rapid, automated, parallel immunoassays of microliter quantities of samples.

195 Since the reaction volumes are in the microliter range and upscaling of the measurement system

196 ven at low levels, very small samples in the microliter range become accessible for pH-stating: a red

197 ication of DNA at levels in the picogram per microliter range.

198 -free cloning of custom DNA libraries in sub-microliter reaction droplets using programmable digital

199 In the improved procedure, we combine sub-microliter reaction volumes, optimization of enzymatic m

200 e preparation, handling, and monitoring of 1-microliter reaction volumes.

201 sed thrombin assays, requiring only minimal (microliter) reagent use.

202 IV) and with CD4 cell counts below 100 cells/microliter received fluconazole daily (200 mg; five pati

203 hind paw, and 24 rats were injected with 50 microliter saline as a control.

204 asurements with high temporal resolution and microliter sample consumption is presented.

205 lar (nM) cortisol concentrations in a single microliter sample droplet within less than 25min.

206 and millimolar G concentrations in a single microliter sample droplet within less than 30 min, inclu

207 the information, allowing the use of minute microliter sample volumes and 100 muM sample concentrati

208 highly precise and sensitive measurements of microliter sample volumes of human blood plasma coagulat

209 ll experiments were carried out using minute microliter sample volumes of lipid vesicle solutions, us

210 Ten-microliter sample volumes reduce reagent consumption and

211 nation against nonhybridized DNA, the use of microliter sample volumes, and disposable transducers an

212 orm for multiplexed detection of analytes in microliter sample volumes.

213 y solid, reliable, and selective response on microliters sample volumes on the minutes time scale, th

214 veguide approach not only affords the use of microliter samples but also provides significant improve

215 Now, new technologies using microliter samples of whole blood and exploiting the spe

216 It operates on microliter samples of whole blood, provides positive, co

217 on and detection in a manner that allows for microliter samples to be screened for infectious pathoge

218 Five-microliter samples were injected onto a 4-cm-long by 50-

219 haride (LPS) associated with sepsis shock in microliter samples.

220 on of proteins at very low concentrations in microliter samples.

221 bsorbance spectroscopy of high absorptivity, microliter samples.

222 de substrates and is readily achievable on a microliter scale (2mul of total volume containing 2mug o

223 ectrodes for monitoring and concentration of microliter scale biofluid samples.

224 hese structures ranges from the nanoliter to microliter scale depending on the number of cycles and c

225 ce designed for electrochemical studies on a microliter scale has been utilized for the examination o

226 e also report PET-RAFT polymerization at the microliter scale in a mammalian cell culture medium.

227 ancer cells, and even whole blood on the low microliter scale is suitable for direct PCR amplificatio

228 the silk solutions to be tested rapidly with microliter scale sample sizes.

229 he resulting calcium flux is released into a microliter scale thin layer reservoir, and the resulting

230 pment of miniature MFCs at the milliliter to microliter scale.

231 otein profiles in mouse urine samples at the microliter scale.

232 n (HTE) for electroorganic synthesis at a 15-microliter scale.

233 ics for mediated anodic oxidations using the microliter-scale cyclic voltammetry.

234 retching and glass coverslip deposition from microliter-scale DNA samples.

235 When a microliter-scale droplet containing mitochondria is disp

236 Microliter-scale droplet generation, reactant introducti

237 ribes a method for local heating of discrete microliter-scale liquid droplets.

238 rcome the long-standing, stubborn barrier to microliter-scale peak volumes and achieved the highest r

239 Microliter-scale photosynthetic microbial fuel cells (mi

240 rises just four direct reagent additions, in microliter-scale volumes, over the course of a 6-h proce

241 ceiving the lowest dose (0.125 microgram/0.5 microliter/side) demonstrated a robust delayed threshold

242 f SCH 23390 into the NAcc (0.5 microgram/0.5 microliter/side) were significantly higher than those as

243 tricular (i.c.v.) IL-1ra (500 microgram in 5 microliter) significantly attenuated LPS fever (IL-1ra,

244 The ability to perform kinetics in microliter-size samples makes this methodology particula

245 R enables us to detect ca. 30 parasites in a microliter-sized blood sample, which is the same order o

246 ethods involved characterizing adsorption in microliter-sized droplets by drop tensiometry and in nan

247 olled vibration selectively propels multiple microliter-sized drops along microstructured tracks, lea

248 veraging electrodes with results obtained in microliter-sized hemispherical samples with a source in

249 up to at least 26 nM (800 mug L(-1)) in the microliter-sized samples of bodily fluids.

250 o support different analytical techniques in microliter-sized samples.

251 emaining six subjects were injected with 5.0 microliters sterile water.

252 pores could be detected when seeded in a 100-microliter stool sample and 10 to 30 C. cayetanensis ooc

253 ter which nearly all the medium (hundreds of microliters) surrounding the docked and tagged cells was

254 ometric mean [+/-SD], 409+/-1569 genomes per microliter) than in 2003-2005 (44+/-169 genomes per micr

255 liquid-liquid extractions generally require microliter to milliliter volumes of solvents and sample,

256 ers of magnitude in analyte concentration in microliter to submicroliter volumes of analyte fluid.

257 priate volumes of both samples and reagents (microliters to hundreds of nanoliters) through the syste

258 and precision deteriorate considerably from microliters to nanoliters.

259 ers of magnitude in analyte concentration in microliter-to-submicroliter volumes of analyte fluid.

260 GDNF (10 microgram in 2 microliter vehicle) or vehicle was injected into the rig

261 dling aqueous and organic solutions at a low microliter volume and acts as a front-end to online liqu

262 Microliter-volume ( approximately 2.5 muL) aqueous dropl

263 which ions are extracted from the surface of microliter-volume droplets.

264 stem allows size exclusion chromatography of microliter volumes (termed muL-SEC) to be performed with

265 TH assay and IL-5 assays were carried out on microliter volumes and demonstrated physiologically rele

266 nding in its native serum environment within microliter volumes and without any surface attachments.

267 DNA fragments dissolved in microliter volumes are captured in a nanoliter-sized ban

268 emperature control to accurately thermocycle microliter volumes in microchips fabricated from polyimi

269 The design of our device requires only microliter volumes of affinity chromatography resin-a co

270 counting and can measure levels of (14)C in microliter volumes of biological samples with negligible

271 l without cross-contamination and using only microliter volumes of blood.

272 been used for colorimetric determination on microliter volumes of extract.

273 y ring-down spectroscopy can be performed on microliter volumes of liquids.

274 e acoustic levitation and inherent mixing of microliter volumes of reactants (3 muL droplets), yieldi

275 extract and analyze organic matter (OM) from microliter volumes of salt containing soil solution samp

276 s developed for reliable application of (sub)microliter volumes of sample without the need of commerc

277 per-based devices wick fluids and distribute microliter volumes of samples from single inlet points i

278 ecovery of model proteins from approximately microliter volumes of serum in a sample-to-answer run ti

279 better than millisecond resolution using sub-microliter volumes of solutions.

280 ation associated with collection of discrete microliter volumes of sweat.

281 tical plates/m while generating single digit microliter volumes of waste for a complete chromatograph

282 Samples were deposited in microliter volumes on thin silicon nitride windows and d

283 lation of voltage to volume extending to the microliter volumes that can be handled by digital microf

284 ment took just a few seconds and was done in microliter volumes with nanomolar concentrations of labe

285 peline combines automated sample handling of microliter volumes, temperature and anaerobic control, r

286 Carrying out reactions in very small (microliter) volumes in capillaries has many advantages i

287 a starting concentration of 37.5 copies per microliter was successfully purified from a 10% serum sa

288 Forty microliters was taken for LC/ESI-MS analysis using elect

289 f eNO > 10 ppb and eosinophilia (> 200 cells/microliter) was 90% in predicting airway obstruction (FE

290 ection; a rapid decline in CD4(+) PBMC (<350/microliter) was seen in five of six animals 21 days and

291 e adult skeletal muscle Na+ channel isoform (microliter), we compared the effects on both TTX and STX

292 uding patients with CD4(+) cell counts < 200/microliter weakened this correlation, possibly because o

293 ction volumes ranging from 250 pL to several microliters were made without electrophoretic flow.

294 group had platelet counts below 100,000 per microliter, whereas 15 of 33 patients in the volanesorse

295 consumption of drugs was reduced to tens of microliters, which is thousands of times less than tradi

296 ophilia, defined as more than 1500 cells per microliter with end-organ involvement and no recognized

297 lex pool of over 10(10) unique sequences per microliter with no evidence that we have begun to approa

298 10(2) EID(50)/mL (50% egg infective dose per microliter), with a virus specificity of 90%.

299 me and can detect as low as 200 exosomes per microliter, with a linear range spanning almost 4 orders

300 cal reaction in a microdrop of a few tens of microliters, with a kinetic time resolution of ca. 1 s.