ライフサイエンスコーパス: plasma

1 d on DPS microsampling is similar to that in plasma.

2 during pharmacokinetic evaluation in rabbit plasma.

3 FXI-deficient plasma, but not FIX-deficient plasma.

4 ion of inflammatory markers in monocytes and plasma.

5 apacity in the familial hypercholesterolemia plasma.

6 ruction and Hyp release into both saliva and plasma.

7 omatic patients was 100% in CSF and 81.3% in plasma.

8 rstanding global thermodynamics of multi-GeV plasma accelerators, which underlie their viability for

9 ic failure (>=1000 copies/mL) using leftover plasma after viral load testing during September 2017-Ja

10 DL-cholesterol, and the atherogenic index of plasma (AIP) suggesting its hypolipidemic action.

11 igher GRS was associated with an increase in plasma alanine aminotransferase (ALT) level of 26% in th

12 owed that dialysate electrolyte composition, plasma albumin, and plasma total CO2 accurately predict

13 Second trimester maternal plasma alpha-T concentration was 3-fold higher than in t

14 T amounts in virtual mice directly to target plasma ALT values in individual mice.

15 lung and pancreas by inflammatory cells, and plasma amylase activity compared with control mice given

16 crevicular fluid consisting of 70% of blood plasma, an abundance of T. forsythia in the bacterial bi

17 Using approximately 150 plasma analytes tracked across three time points, we ide

18 in, we compared the global metabolome of 231 plasma and 97 fecal samples from a large cohort of child

19 y, as well as the strong correlation between plasma and average brain [Li] ([Li](B) ~ 0.40 x [Li](P),

20 vant cytokine levels were assessed in serum, plasma and BAL.

21 enes, affording efficient drug liberation in plasma and cell culture.

22 ellularly in body fluids such as human blood plasma and cerebrospinal fluid (CSF).

23 ture cleavage and instability of the drug in plasma and enabled higher drug accumulation in tumors co

24 , these Slc7a7Lbu/Lbu mice exhibited reduced plasma and increased urinary concentrations of the catio

25 es, exposing the depth and complexity of the plasma and serum proteomes.

26 diagnosis of CRCs and adenomatous polyps in plasma and stool samples in an Iranian population.

27 for quantitation of ASOs and metabolites in plasma and tissue samples, showing a great potential to

28 Correlation between TFV plasma and urine concentrations was strong (rho = 0.78;

29 mmunoglobulin (IgG) antibodies, neutralizing plasma, and memory B and memory T cells that persisted f

30 We collected tonsils, plasma, and saliva samples from children and adults rece

31 lite-corrected radioactivity in whole blood, plasma, and urine.

32 hypothesis of a positive association between plasma ANGPTL5, and obesity, high sensitivity C-reactive

33 t a strong positive correlation between both plasma anti-RBD and anti-ECD IgG titers and in vitro VN

34 We compared plasma antibody binding to HIV antigens between 51 nontr

35 infected subjects, and a wide range of serum/plasma antibody levels was delineated in infected subjec

36 y and elevated NFL concentrations in CSF and plasma are associated in AD-vulnerable regions in the pr

37 cells (PWBCs), and circulating micro RNAs in plasma, are associated with female fertility, measured b

38 volved tri-enzyme extraction including human plasma as a deconjugase.

39 It circulates in plasma as a tetramer of two A-subunits and two B-subunit

40 nd enabled the selective detection in spiked plasma as well as in whole blood samples.

41 in buffer and initiated TG in normal pooled plasma, as well as FXII- or FXI-deficient plasma, but no

42 and physical systems, from DNA to turbulent plasmas, as well as in climbing, weaving, sailing, and s

43 entified 134 metabolites in maternal fasting plasma at 26-28 weeks of gestation.

44 nous administration showed that the liver-to-plasma AUC ratios could be significantly improved, compa

45 CHO cells during the production phase, or in plasma B cells.

46 However, no significant plasma-based Raman amplification of a laser pulse beyond

47 h an inverse relationship between AT pO2 and plasma BCAA concentrations.

48 egree of perturbation (MDP) score adapted to plasma biomarkers in two distinct databanks from studies

49 Using a multiplex system, we assayed plasma biomarkers related to tubular injury, inflammatio

50 Plasma bone turnover markers and bone mineral density (B

51 ed plasma, as well as FXII- or FXI-deficient plasma, but not FIX-deficient plasma.

52 r by oxPLs generated during HDL oxidation in plasma by the physiologically relevant MPO-H(2)O(2)-NO(2

53 HET mice receiving CAF (plasma CAF 893 ng/ml) have significantly shorter times t

54 , these data suggest that the miRNA cargo of plasma CD31(+) EVs is largely affected by T2DM and relat

55 isystem disease resulting from an underlying plasma cell (PC) dyscrasia.

56 Prospective studies targeting plasma cell clones and/or fibrotic pathways are warrante

57 type, whereas EBV-infected B cells expressed plasma cell differentiation markers.

58 1 expression, CSR, somatic hypermutation and plasma cell differentiation.

59 e generation of memory B cell and long-lived plasma cell responses.

60 ry cells, consisting of lymphocytes (n = 9), plasma cells (n = 6), and histiocytes (n = 6).

61 The dominant model holds that nascent plasma cells adapt to increased antibody synthesis by ac

62 antigen drives the generation of long-lived plasma cells and memory B cells and highlight the challe

63 ness of specific therapy when B cells and/or plasma cells are found.

64 and relapsed/refractory patients, including plasma cells bearing the t(4;14) translocation obtained

65 Tumours often contain B cells and plasma cells but the antigen specificity of these intrat

66 In the present study, we examined plasma cells from MM using a multi-epigenomics approach

67 IgA(+)CD138(+) plasma cells from Peyer's patches and lamina propria wer

68 nter (GC) B cells into memory B cells versus plasma cells is a major quest of adaptive immunity.

69 , when compared to normal B cells, malignant plasma cells showed an extensive activation of regulator

70 turation antigen (BCMA) is expressed only on plasma cells, a small subset of B cells and MM cells, wh

71 nal B cells, extrafollicular IgG2c-producing plasma cells, and activation of CD4 and CD8 T cells.

72 ighly active in vitro and in vivo against MM plasma cells, memory B cells, and MM-propagating cells.

73 cells by inhibiting their differentiation to plasma cells.

74 Plasma circulating tumor human papillomavirus DNA (ctHPV

75 Slower plasma clearance and increased drug exposure over time o

76 ate that SPM levels were broadly elevated in plasma collected from NOD/ShiLtJ female mice after disea

77 ts of CMV DNA terminase, were sequenced from plasma collected from subjects with clinically significa

78 Analyses of plasma collected pre- and postadministration of intraven

79 Biomarkers were measured in plasma collected preoperatively (PREOP), and 2 days (POD

80 19% of cases had antiretrovirals detected in plasma, compared with 87% of controls who were suppresse

81 al fitness and drives viral evolution in the plasma compartment in humanized mice.

82 nse axis independently aligns with the major plasma composition changes, with clinical metrics of blo

83 , multimeric recombinant VWF, and normal VWF plasma concentrates.

84 ND)) and binding potential relative to total plasma concentration (BP(P)) were derived using an arter

85 Plasma concentrations of BDNF were significantly affecte

86 Increased plasma concentrations of lipoprotein(a) (Lp(a)) are asso

87 Plasma concentrations of sRAGE (soluble receptor for adv

88 Plasma concentrations of TMAO and its precursors were me

89 s cerebral distribution and association with plasma concentrations, we used (7)Li magnetic resonance

90 Melanoma patients' plasma contains exosomes produced by malignant and norma

91 lase (Th)], glucocorticoid receptor (GR) and plasma corticosterone, as well as brain-derived neurotro

92 cortisol cut-off values were 0.015mug/dL for plasma cortisol levels below 3mug/dL (sensitivity 83%, s

93 We retrospectively performed nationwide plasma CrAg testing among ART-experienced Ugandan adults

94 slightly attenuated after adjusting for cord plasma creatinine (P = 0.05).

95 drofolate reductase (DHFR) genotype and cord plasma creatinine.

96 Urinary and plasma d3- and d6-alpha-CEHC concentrations varied diffe

97 including Kerr self-focusing, ionization and plasma defocusing, and dynamic spatial replenishment are

98 the EM of U87 glioblastoma cell-derived and plasma-derived sEVs and medium size EVs (mEVs, commonly

99 ed associated with a lower hazard for HHV-6B plasma detection (hazard ratio, 0.40; 95% confidence int

100 evelopment and the selection of convalescent plasma donors.

101 w experiments have successfully demonstrated plasma-driven undulator radiation.

102 due to significant impact of ion caging and plasma electron screening.

103 Plasma eotaxin-3 levels strongly associated with gastric

104 Plasma EVTF activity was transiently increased during HF

105 immune globulin + rituximab with or without plasma exchange were tested for total IgG and IgG1-4 by

106 provides an example of a weakly collisional plasma expanding from a thermal source in the presence o

107 ith a low anticipated clinically efficacious plasma exposure for migraine also suggests a reduced pot

108 nd C5a, which activate mast cells leading to plasma extravasation, pain, and itching.

109 ) and relate the ratio to albuminuria, renal plasma flow (RPF), fat mass, and insulin sensitivity (M/

110 edominantly via elevating red blood cell and plasma flux in already flowing capillaries.

111 tes, the efficacy and safety of convalescent plasma for treating coronavirus disease 2019 (COVID-19)

112 This led to elevated plasma free fatty acids (FFAs), which were transported t

113 ycolipids activate basophils sensitized with plasma from alpha-gal allergic subjects in an IgE-depend

114 NT1 tau and NfL were measured in plasma from prospectively followed patients with SCD or

115 determination of l-tyrosine (l-Tyr) in human plasma from tyrosinemia-diagnosed patients.

116 was used to investigate the relationship of plasma GFAP to clinical and imaging measures.

117 as associated with a significant increase in plasma glucagon and a decrease in the plasma insulin con

118 ion in WAT inversely correlated with fasting plasma glucose in both obese mice and humans.

119 microbiota increased adiposity but decreased plasma glucose.

120 3,2-c]pyridine-4,6(5H,7H)-dione), has a long plasma half-life (~ 24 hours) in mice, suggesting possib

121 ociated eruption, particle acceleration, and plasma heating.

122 In adults, oral iron doses increase plasma hepcidin (PHep) for 24 h, but not for 48 h, and t

123 Plasma histidine (measured in subjects who completed all

124 Plasma hsa_circ_0001445 was measured in a study populati

125 microbial clearance, we found that increased plasma IFN-gamma in early clinical sepsis was associated

126 Circulating plasma IFN-gamma levels were also assayed in 400 patient

127 IRF7 and NF-kappaB inversely correlated with plasma IFNalpha2 levels, implying that pDCs were refract

128 In contrast, IFN-gamma response via TCR and plasma IgG specific for Bp were still intact.

129 c immune responses and a concomitant rise in plasma inflammatory markers.

130 Arterial sampling was used to measure plasma input function.

131 ase in plasma glucagon and a decrease in the plasma insulin concentration compared with placebo.

132 IR), there is a compensatory increase in the plasma insulin response to offset the defect in insulin

133 ceptor binding domain IgG titer convalescent plasma is efficacious in early-disease patients.

134 Plasma islatravir pharmacokinetics and intracellular isl

135 was achieved using calibration standards in plasma, largely improving efficiency and consistency.

136 Cabotegravir plasma levels in macaques dropped below detectable level

137 We tested the association of rs72613567 with plasma levels of alanine transaminase (ALT) and clinical

138 two cohorts and tested the effects of OC on plasma levels of oxytocin, adrenocorticotropic hormone (

139 eatic ductal adenocarcinoma (PDAC) have high plasma levels of PRL.

140 ID was found to be associated with increased plasma levels of the B-cell-attracting chemokine CXCL13.

141 Tissue expression of miR-181a-5p reflected plasma levels.

142 Alcohol intake influences plasma lipid levels, and such effects may be moderated b

143 re used to construct genetic instruments for plasma lipid traits.

144 J proteins, mucosal inulin permeability, and plasma lipopolysaccharide (LPS) levels.

145 mined the association of the risk score with plasma markers of liver disease and with cirrhosis and H

146 the results obtained by inductively coupled plasma mass spectrometric method and no significant diff

147 further analysis by bulk inductively coupled plasma mass spectrometry (ICP-MS) and single-particle IC

148 able by highly sensitive inductively coupled plasma mass spectrometry (ICP-MS) operated in single par

149 Inductively coupled plasma mass spectrometry (ICP-MS) showed titanium presen

150 clusion chromatography - inductively coupled plasma mass spectrometry (ICPMS), and hydrophilic intera

151 oncentration analysis by inductively-coupled plasma mass spectrometry (ICPMS).

152 rescence, laser ablation inductively coupled plasma mass spectrometry of polished flat ore surfaces r

153 tals were measured using inductively coupled plasma mass spectrometry.

154 esolution laser ablation-inductively coupled plasma-mass spectrometry elemental mapping.

155 K-Ras must interact primarily with the plasma membrane (PM) for its biological activity.

156 ate and transitory protein engagement at the plasma membrane (PM) is crucial to a broad range of cell

157 are regulated through crosstalk between the plasma membrane (PM), where most cellular cholesterol re

158 ereby promotes rapid permeabilization of the plasma membrane and bacterial cell death.

159 sts of specific proteins present both at the plasma membrane and on insulin SGs.

160 ne, nonreceptor tyrosine kinase (SRC) to the plasma membrane and promotes activation of an SRC-depend

161 s nuclear transit before accumulating at the plasma membrane and recruiting nucleocapsids to the budd

162 ediates binding to phospholipids in both the plasma membrane and synthetic membranes, and is sufficie

163 ven crystal-like structures in the bacterial plasma membrane and thereby promotes rapid permeabilizat

164 by the presence of amphipathic components of plasma membrane because they may serve as interaction, c

165 ntain the plasma membrane potential and that plasma membrane depolarization blocks cellular uptake of

166 lighting the importance of these specialized plasma membrane domains in cellular feedback via the Hip

167 densities are in general lower at the basal plasma membrane due to partial limited accessibility for

168 Internally tagged Rho3 is restricted to the plasma membrane in a gradient corresponding to cell pola

169 er type 4 (GLUT4)-containing vesicles to the plasma membrane in response to insulin stimulation.

170 ns confer a steady-state organization of the plasma membrane in resting cells that is poised to orche

171 ular domain of TrkB in the cytosol or on the plasma membrane is able to induce the activation of down

172 Laurdan, which is redistributed within both plasma membrane leaflets and intracellular membranes.

173 an cell membranes, constituting up to 50% of plasma membrane lipids.

174 (Kir) Kir2.2 has multiple interactions with plasma membrane lipids: Phosphatidylinositol (4, 5)-bisp

175 both exercise-induced activation of AMPK and plasma membrane localization of the GLUT4 glucose transp

176 The plasma membrane of a cell is characterized by an asymmet

177 , PKA and Ca(V)1.2 into nanocomplexes at the plasma membrane of human and mouse arterial myocytes.

178 ly reconstitute the PC-1/PC-2 complex in the plasma membrane of mammalian cells and show that it func

179 actin meshwork that uniformly underlies the plasma membrane of the entire cell.

180 ally sequestered to the inner leaflet of the plasma membrane of the healthy eukaryotic cells.

181 eased transcription and translocation to the plasma membrane of TLR4 in donor TRAMs.

182 hat relies on the physical disruption of the plasma membrane once the peptide targets specific phosph

183 Therefore, we tested how the yeast plasma membrane P4-ATPase, Dnf2, responds to changes in

184 causing increased binding to an alternative plasma membrane partner, ITSN1.

185 that glycolysis is required to maintain the plasma membrane potential and that plasma membrane depol

186 The Na(+)/I(-) symporter (NIS), the plasma membrane protein that actively transports I(-) (s

187 Stimulation of plasma membrane receptor tyrosine kinases (RTKs), such a

188 by activating Galphaq to localize it to the plasma membrane returns differentiated PC12 and SK-N-SH

189 of magnitude more elastic than the classical plasma membrane suggesting a physical explanation for th

190 e mechanistic differences of the MA-mediated plasma membrane targeting of the B-type mouse mammary tu

191 osphoinositides 1 (Grp1) is recruited to the plasma membrane through its pleckstrin homology (PH) dom

192 e initiated by BDNF and its receptors at the plasma membrane to modulate BDNF-dependent gene expressi

193 cells rely on linker proteins to connect the plasma membrane to the actin network.

194 n of the C2AB domain of granuphilin from the plasma membrane to the cytosol.

195 Giant plasma membrane vesicles (GPMVs) are a widely used exper

196 Starting from the plasma membrane with the recognition of microbe-associat

197 ing the endoplasmic reticulum (ER) membrane, plasma membrane, and nanodomains induced by cholera toxi

198 may have limited mobility in the endothelial plasma membrane, but no biophysical investigation of the

199 L1/RFA family interact with ABA receptors at plasma membrane, cytosol, and nucleus, targeting them fo

200 nslocation of MT1-MMP-laden endosomes to the plasma membrane, enabling both invadopodia outgrowth and

201 to the recycling endosome rather than to the plasma membrane, our findings reveal the complexity of r

202 , which assemble in the cytoplasm and at the plasma membrane, respectively.

203 pressed suicides, and depressed nonsuicides, plasma membrane-associated tubulin showed significant de

204 A receptors are rapidly recycled back to the plasma membrane.

205 YP121(DeltaC), which blocks secretion at the plasma membrane.

206 olgi apparatus, prevacuolar compartment, and plasma membrane.

207 mide, which was located predominantly at the plasma membrane.

208 pholipids found on the cytosolic side of the plasma membrane.

209 s a cytotoxic cation channel in the parasite plasma membrane.

210 f Ca(2+)-activated potassium channels to the plasma membrane.

211 by lowering the expression of VDAC-1 in the plasma membrane.

212 d biophysical analysis of isolated mammalian plasma membranes (PMs).

213 and shifts the localization of ClVST1(97) to plasma membranes in sweet watermelons.

214 release of nascent virus particles from the plasma membranes of infected cells.

215 Children's plasma metabolome, especially lipidome, reflects gene re

216 Plasma miR-181a-5p was significantly downregulated in no

217 a-3 (n-6) PUFAs measured in second-trimester plasma; n-6/n-3 ratios were calculated.

218 Conversely, a log2 higher baseline plasma NfL level was associated with a higher risk of al

219 ermis endothelial NO synthase expression and plasma NO levels of diabetic mice.

220 Archived plasma obtained pre- and post-TCZ treatment (8 mg/kg, 6x

221 ties across the USA, we tested the remainder plasma of 28 503 randomly selected adult patients receiv

222 overing the entire sequence of ovomucoid, in plasma of 38 egg-allergic and 6 atopic children.

223 ting levels of individual fatty acids in the plasma of Hi-Myc mice and human subjects when compared t

224 0.01) concentrations of interferon-gamma in plasma of low responders compared to high responders pri

225 ce liquid chromatography-inductively coupled plasma-optical emission spectrometry (HPLC-ICP-OES) in a

226 se) hydrolyze ATP to pump protons across the plasma or intracellular membrane, secreting acids to the

227 o the growing body of evidence in the use of plasma p-tau181 as a non-invasive diagnostic and prognos

228 Our finding that plasma p-tau181 concentration is increased in symptomati

229 ive Abeta PET scans show little increase but plasma p-tau181 is increased if CSF Abeta has already ch

230 In summary, plasma p-tau217 increases during early Alzheimer's disea

231 ns in protein secondary structure induced by plasma, particularly contents of beta-sheet and beta-tur

232 High levels of IL-8 in plasma, peripheral blood mononuclear cells and tumors we

233 %ViableSperm of bulls was related to seminal plasma peroxiredoxin-5, spermadhesin-1 and the spermadhe

234 This phosphaturic effect lowered plasma phosphate levels in WT mice and in rats with CKD

235 We measured maternal plasma phospholipid FA concentration at preconception (o

236 Plasma phosphorylated-tau181 (p-tau181) is a promising b

237 e acceleration, attosecond pulse generation, plasma photonics, high-field physics and laboratory astr

238 alibration, MagLev showed that the levitated plasma proteins have a measured density in solution of 1

239 markers for MPV and PLT among 71 CVD-related plasma proteins measured in FHS (Framingham Heart Study)

240 We then correlated plasma proteins with left ventricular ejection fraction

241 Whole blood (WB) and platelet-rich plasma (PRP) were perfused at high shear rates (> 3,000

242 th one compound (5i) displaying better brain/plasma ratio than donepezil.

243 Survival also improved in plasma recipients (adjusted hazard ratio (HR), 0.34; 95%

244 king: the mean starting and ending values of plasma renin activity and serum aldosterone were 6.8 vs.

245 gated the effects of platinum-based drugs on plasma S1P levels in human cancer patients.

246 miRNAs were detected in two of 72 plasma samples (2.8%) and two of 47 samples (4.3%) with

247 Four plasma samples from blood donors with acute HIV-1 infect

248 magnetic resonance spectra were acquired in plasma samples from critically ill children.

249 assay for the detection of autoantibodies in plasma samples from immune-mediated thrombotic thrombocy

250 linositols (PI) were also detected in the BM plasma samples from MM compared to MGUS patients.

251 Cortisol levels were measured from plasma samples pre- and post-vaccination.

252 al sequencing of 12 patients with 2-5 serial plasma samples reveals clonal dynamics and genome evolut

253 eviations (RSD) between the cycles for human plasma samples were 0.84-6.6%.

254 spective study, a total of 226 stool and 178 plasma samples were received from patients referred to c

255 75 compounds previously identified in human plasma samples with annotations generated by three simil

256 determination in serum and preterm neonatal plasma samples with sepsis suspicion.

257 boratories to quantify proteins in serum and plasma samples.

258 Recently, plasma separation cards (PSCs) have become available and

259 operated centrifuge devices (high volume) or plasma separation membranes (PSM) coupled with lateral f

260 F were significantly affected by the type of plasma separator tube, storage-time, and number of freez

261 Therefore, the anticoagulant used in plasma separator tubes, storage-time, storage-temperatur

262 a strong association between low circulating plasma serine peptidase inhibitor Kunitz type-1 (SPINT1)

263 thin the 95% confidence interval of observed plasma silver concentrations in healthy human adults.

264 aper, the crystallization mechanism in spark plasma sintered Fe(48)Cr(15)Mo(14)Y(2)C(15)B(6) metallic

265 e mechanism of crystallization in this spark plasma sintered iron based metallic glass was establishe

266 ursors in nitrogen and consolidated by spark plasma sintering.

267 Laser-driven solid-density plasma-sources deliver both kinds of radiation, but most

268 homeostasis and define the sperm and seminal plasma specific programming effects on cardiovascular he

269 -three (39%) people in quartiles 3 and 4 for plasma sTNFR1 died over 4-year follow-up.

270 as attested by the reduction of mMCP-1/7 in plasma, suggesting that EPIT specifically decrease IgE-m

271 initial investigations on the time-dependent plasma-supported oxidation of benzyl alcohol, benzaldehy

272 A broad range of anti-HAV Ig plasma titers was observed among these centers, with som

273 Median (IQR) concentration of plasma TMAO was 3.05 mumol/L (2.10-4.60 mumol/L).

274 Clustering of patients based on plasma TNF and KYN/TRP yielded subgroups of high (N = 17

275 , a significant reduction of L-Kyn levels in plasma, together with a potent effect on abrogating immu

276 electrolyte composition, plasma albumin, and plasma total CO2 accurately predict the measured pH of b

277 The concentration of NETs was augmented in plasma, tracheal aspirate, and lung autopsies tissues fr

278 e demonstrated excitation and confinement of plasma tracks in the wakes of laser field.

279 bexarotene significantly (p < 0.01) elevated plasma triglycerides and cholesterol, treatment with MSU

280 g was well tolerated, without an increase in plasma triglycerides.

281 noglobulin G levels were correlated in donor plasma units (rho = 0.938; P < .001) and in the cumulati

282 myalgia) through the analysis of their blood plasma using attenuated total reflection Fourier-transfo

283 viruses could also be enriched from post-ATI plasma using macrophage-specific (CD14) but not CD4+ T c

284 blation of the miR-144/451 cluster increased plasma vimentin, while vimentin levels were decreased in

285 (P < 0.001); DBS samples with corresponding plasma viral load >250 copies/ml had a success rate of 8

286 Plasma viral load was significantly correlated with geno

287 zing antibodies that protect from detectable plasma viremia following rechallenge and persist for at

288 SARS-CoV-2 viral loads, especially plasma viremia, are associated with increased risk of mo

289 Overall, lower plasma viremia, reduced cell-associated SIV-DNA, and pre

290 irus rebound and a lower maximum decrease in plasma viremia, respectively, after treatment with a V3

291 cator of viral replication before detectable plasma viremia.

292 Plasma virus matched replication-competent virus culture

293 vestigate the correlation between fractional plasma volume (V(p)), a parameter derived from DCE perfu

294 Volume transfer constant and plasma volume from dynamic contrast-enhanced MRI as well

295 enhanced perfusion MRI parameter, fractional plasma volume, was able to differentiate between nonneop

296 Both stimuli elevated plasma VWF levels in a manner representative of thrombot

297 ctivation of electrode surfaces via cold-air plasma, we show that soft biocompatible materials can be

298 Overall sensitivity and specificity on plasma were respectively 98.0% (95% CI 96.7 - 98.9) and

299 ate (PFOS) and PFOA in P. major feathers and plasma were significantly and positively correlated when

300 e of trace level of SN-38G and free SN-38 in plasma, which suggests an improved therapeutic index of