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1 ace was very low (<3 ng/cm (2) for undiluted blood plasma).
2 tive capture of MC-LR from aqueous media and blood plasma.
3 derived from both normal and cancer patient blood plasma.
4 ENV), and West Nile (WNV) virus infection in blood plasma.
5 ral therapy (ART) with suppressed HIV RNA in blood plasma.
6 assay biosensor, measuring cTnI in undiluted blood plasma.
7 e complex lipid species diversity present in blood plasma.
8 ontology term extracellular space as part of blood plasma.
9 s shed from the endothelial surface into the blood plasma.
10 ral therapy (ART) with suppressed HIV RNA in blood plasma.
11 V5 region of env from genital secretions and blood plasma.
12 s present in rat liver microsomes and bovine blood plasma.
13 alyses of Drosophila hemolymph and mammalian blood plasma.
14 tion of target analytes from undiluted human blood plasma.
15 mes and 24.0 (+/-1.5)% to 82.5 (+/-14.0)% in blood plasma.
16 n of a microRNA cancer biomarker (miR-16) in blood plasma.
17 ng, and levels of anti CMV immunoglobulin in blood plasma.
18 he cell free DNA (cfDNA) fraction of patient blood plasma.
19 its target in a complex media such as human blood plasma.
20 containing metabolites from cell lysates and blood plasma.
21 in vitro by stability-measurements in human blood plasma.
22 ll as in the cerebrospinal fluid, but not in blood plasma.
23 ation of IL-1beta, IL-6, and TNFalpha in the blood plasma.
24 ding specificity toward SOD-1 in presence of blood plasma.
25 ne falls below the minimal content of normal blood plasma.
26 y of binding toward SOD-1 in the presence of blood plasma.
27 ance upon exposure to CA 125 in spiked human blood plasma.
28 f antigen-antibody interactions in undiluted blood plasma.
29 complex proteolytic digests of, for example, blood plasma.
30 sitive and specific detection of proteins in blood plasma.
31 -chemical principles of aqueous solutions to blood plasma.
32 cal model system, and experiments with human blood plasma.
33 hat were validated experimentally with human blood plasma.
34 SBF) with ionic composition similar to human blood plasma.
35 and an aqueous buffer solution or undiluted blood plasma.
36 -cysteine (H-cys) with a DL of 43nM, even in blood plasma.
37 model mice intravenously injected with young blood plasma.
38 ties of individual fibrin fibers formed from blood plasma.
39 and specific fragmentation pattern in human blood plasma.
40 BRE capacity and resistance to fouling from blood plasma.
41 level of hemolysis by measuring the color of blood plasma.
42 s in human cerebrospinal fluid as well as in blood plasma.
43 e composition of biofluids such as urine and blood plasma.
44 in complex biological systems such as human blood plasma.
45 specific selectivity, in water and in human blood plasma.
46 f Hepatitis B virus antigen (HBsAg) in human blood plasma.
47 may be accompanied by a change in the RP of blood plasma.
48 of this protein has been described in human blood plasma.
49 rform direct isoelectric separation of human blood plasma.
50 nal grafts, in graft tissue and in recipient blood plasma.
51 secretions (4.96 log(10) copies/mL) than in blood plasma (4.24 log(10) copies/mL) or seminal plasma
52 n buffer as well as native proteins in human blood plasma additionally exhibit properties in keeping
53 ingivitis macaques could also be observed in blood plasma, although the effects at both compartments
56 s were performed on samples of monocytes and blood plasma and correlated with magnetic resonance imag
57 nal characterization of viral populations in blood plasma and CSF obtained at short time intervals ov
61 ly high adenosine concentrations in neonatal blood plasma and heightened sensitivity of neonatal mono
62 an serum albumin (HSA) binds 95% of Abeta in blood plasma and is thought to inhibit plaque formation
63 essentially prevented peptide degradation in blood plasma and liver homogenates versus an unstapled c
64 escribes microfluidic experiments with human blood plasma and numerical simulations to determine the
69 phosphorylated alpha-syn can be detected in blood plasma and shows more promise as a diagnostic mark
70 can increase the level of HDL cholesterol in blood plasma and suppress the risk of cardiovascular dis
71 e to capture dengue-specific IgM antibody in blood plasma and the reverse, a blood plasma functionali
72 spectrometry (HPLC-ICP-MS) analysis of mouse blood plasma and urine postadministration showed conside
73 NA during primary infection was cleared from blood plasma and urine within 10 d, viral RNA was detect
74 f low-density lipoprotein cholesterol in the blood plasma and, thereby, occurrence or resistance to a
76 body fluids (for example, saliva, sweat and blood plasma) and under extreme hypoxic and acidic condi
78 was designed to be hydrolytically stable in blood plasma, and an investigation of its hydrolysis in
79 oward the human GRPr, metabolic stability in blood plasma, and biodistribution in mice bearing GRPr-e
80 tide receptor (GRPr), metabolic stability in blood plasma, and biodistribution in mice bearing GRPr-e
81 lls (1.00+/-0.62 ng/g ww), whereas in liver, blood plasma, and brain all OPs were not detectable.
82 ts from fibrinogen, either in solution or in blood plasma, and could aggregate human platelets, eithe
85 n P (Sepp1) contains most of the selenium in blood plasma, and it is utilized by the kidney, brain, a
88 dose-response relationships between maternal blood, plasma, and breast milk to better understand lact
91 multiple biological specimens such as whole blood, plasma, and peritoneal dialysis effluent with cli
92 tick) whole-blood specimens and venous whole blood, plasma, and serum was tested for HIV-1 antibodies
93 inactivated ZEBOV at known titers and whole-blood, plasma, and urine clinical specimens collected fr
99 cross the day and that serotonin profiles in blood plasma are also rhythmic in LD, but were not rhyth
102 uspended in solutions much more viscous than blood plasma assume an almost steady-state orientation w
103 d cells, red blood cells, and platelets from blood plasma at flow velocities of 1,000 microm/sec and
104 -reactive protein (CRP) and D-dimer in human blood plasma based on a white light interference spectro
105 hly sensitive LC-MS/MS multimethod for human blood plasma based on derivatization with o-phenylenedia
106 man with Zostavax, we sorted his circulating blood plasma blasts and amplified expressed immunoglobul
108 1 (HIV-1) RNA was measured in paired SP and blood plasma (BP) at baseline and after 1, 2, 4, 6, 8, 1
109 RNA was measured in seminal plasma (SP) and blood plasma (BP) at baseline, on days 3, 7, and 14, and
110 ral RNA in paired vaginal secretion (VS) and blood plasma (BP) samples of 14 women followed for 1.5 t
111 s quantified in seminal plasma (spVL) and in blood plasma (bpVL) from 2 paired samples collected 4 we
113 t elevated levels of free cell hemoglobin in blood plasma can, as early as the first trimester, poten
116 ements of microliter sample volumes of human blood plasma coagulation (0.009 cP for viscosity range 0
117 env pyrosequencing data were generated from blood plasma collected from 7 individuals with evidence
119 on performance as a function of its measured blood plasma concentration: it reduced reflection impuls
126 , unless biofilm lysine exceeded the minimal blood plasma content, in which case PI was further incre
127 bral blood volume (CBV)-weighted fMRI with a blood plasma contrast agent (monocrystalline iron oxide
128 pes' and models for five biological systems: blood plasma, cytoplasm, synaptic vesicles, HIV and a my
133 een-blue to blue can be detected directly in blood plasma, even at picomolar concentrations of antibo
138 lar extravascular volume fraction, v(e); and blood plasma fraction, v(p)) were determined by fitting
141 jugate hydrolysis in maternal urine and cord blood plasma from a cohort of 181 expecting mother/infan
142 orms both the sample preparation (separating blood plasma from erythrocytes) and the assays; it also
143 HIV-1 and of 6 herpesviruses in seminal and blood plasma from HIV-1-infected and HIV-uninfected men.
144 In fetal and maternal lungs, and in maternal blood plasma from pregnant rats exposed to environmental
145 nd design, we demonstrated the separation of blood plasma from the blood cells (white, red, and plate
146 ation, thereby decreasing iron transfer into blood plasma from the duodenum, from macrophages involve
147 -1 variants that were shared with peripheral blood plasma from those that were compartmentalized in C
148 t sequencing of reverse-transcribed RNA from blood plasma from three of nine colobus monkeys yielded
149 array and qPCR, and incubation of VSMCs with blood plasma from zinc-deficient rats strongly changed t
150 antibody in blood plasma and the reverse, a blood plasma functionalized surface to capture DENV-2.
156 inhibitors of PCR reactions, including whole blood, plasma, hemoglobin, lactoferrin, serum IgG, soil
163 n aquatic environments and representative of blood plasma in living organisms, respectively, on bioav
164 eover, dimeric alpha2M is generated in whole-blood plasma in the presence of physiologically relevant
167 ability of blood vessels is that exposure to blood plasma increases bone marrow HSPC ROS levels, augm
168 al inflammatory cytokine gene expression and blood plasma interleukin-6 levels were not influenced.
170 tive level, systemic administration of young blood plasma into aged mice improved age-related cogniti
179 g intravascular hemolysis from the cell into blood plasma, it produces a state of NO depletion, oxida
181 amine the relationship between pericytes and blood plasma leakage during photothrombotic occlusion of
183 he most important in the periodic table with blood plasma levels of H(+), Na(+) and Ca(2+) being indi
187 thylphenidate and amphetamine at therapeutic blood/plasma levels during peri-adolescence in non-human
188 t sample preparation protocols for optimized blood plasma lipid extraction and measurement by UPLC-MS
189 cs the composition of interstitial fluid and blood plasma, LJM-3064 rapidly switches to a parallel-st
190 high stability in mouse liver microsomes and blood plasma, low intrinsic microsome clearance, and low
194 different lipid compositions and applying to blood plasma obtained from healthy individuals and from
195 istribution in cerebrospinal fluid (CSF) and blood plasma of 141 patients was measured with an immuno
196 ms in DIA data acquired from >200 samples of blood plasma of a human twin cohort and assessed the con
197 nthesis, reflecting the presence in neonatal blood plasma of a soluble, low molecular mass inhibitory
198 varies substantially, from picomolar in the blood plasma of healthy organisms to nanomolar in diseas
199 further found to be dramatically elevated in blood plasma of individuals with CCRC compared with heal
200 h transthyretin (TTR)-binding potency in the blood plasma of polar bear cubs were identified with eff
202 ccurate HIV incidence estimates using stored blood plasma or serum samples without a requirement for
205 xime ethers bind selectively to TTR in human blood plasma over the plethora of other plasma proteins,
207 parabiosis) or repeated injections of young blood plasma (plasma from 2- to 3-month-old mice) into o
210 stress in humans was quantified by measuring blood plasma protein carbonyls using the two commerciall
212 tionally, we quantified urinary excretion of blood plasma proteins alpha1-microglobulin, albumin, and
213 This includes a predominant contribution of blood plasma proteins that is conserved with human SF.
214 ns, metabolic enzymes, some myofibrillar and blood plasma proteins were identified, which were charac
215 =.144; P=.032), levels of cell-free virus in blood plasma (R=.365; P<.001), and the detection of prov
218 ite(s) in a complex biological fluid such as blood plasma, required for inhibition of amyloidogenesis
219 drolyzed by nonspecific esterases present in blood plasma, resulting in the formation of the inactive
221 oximately 10(6) based on analyses of a human blood plasma sample, for which 835 distinct proteins wer
222 rder to explore and seek differences between blood plasma samples acquired from NPC1 (untreated and m
223 Of 464 participants, 124 had insufficient blood plasma samples and 97 had no CMI grading (none, in
225 for exhaustive lipid fingerprinting of human blood plasma samples based on the employment of methyl t
227 1 env V4/V5 genetic populations in multiple blood plasma samples collected over an average of 7 mont
230 tivity of blood-accumulating contaminants in blood plasma samples of approximately 4-months-old polar
231 mployed to measure the NSE level in clinical blood plasma samples taken from deidentified TBI patient
232 n injury (TBI) protein biomarker, in diluted blood plasma samples, achieving a LOD of 0.86 ng/mL.
237 r the collection and transportation of dried-blood-plasma samples, SampleTanker (ST), was developed a
243 say performance in complex media (i.e. whole blood, plasma, serum) due to the non-specific adsorption
245 MR)-based metabolic phenotyping of urine and blood plasma/serum samples provides important prognostic
247 w abundance proteins (e.g., </= 100 pg/mL in blood plasma/serum) using targeted proteomics approaches
248 s effects of abundant proteins in the intact blood plasma/serum, which underscores the need for alter
249 a) tests were performed on fingerstick whole blood, plasma/serum, and CSF in 207 HIV-infected adults
251 da cheese) and biological samples (urine and blood plasma) signifying its potential as an alternative
252 on the exact metabolite compositions of the blood plasma, since the concept relies only on identifyi
253 on several data sets, including one of mouse blood plasma spiked with low concentrations of recombina
257 uble plasma Fn (pFn), an abundant protein in blood plasma that is normally soluble and nonadhesive.
258 adir of less than 10,000 viral copies per ml blood plasma that was not seen in Mamu-A*01-negative DNA
259 Thus, following analytical validation, in blood plasma, the technique was applied to a group of 59
260 o be metabolized by nonspecific esterases in blood plasma to biologically inactive carboxylic acid de
261 uling from complex biological fluids such as blood plasma to biorecognition element (BRE)-functionali
264 , suggesting that they are taken up from the blood plasma, together with yolk, during oocyte growth a
266 ain polyP can accelerate clotting of flowing blood plasma under flow at low to sub-physiological shea
267 tform was used to detect a target protein in blood plasma using a sensitive surface plasmon resonance
268 biomarker carcinoembryonic antigen (CEA) in blood plasma using antibody against CEA and a surface pl
269 rring dengue NS1 antigen in infected patient blood plasma using straight long-range surface plasmon w
270 Optical determination of protamine in human blood plasma using the exhaustive nanosensors was attemp
271 eriophage T7 in both salt solution and mouse blood plasma, using just ~1 x 10(-)(6) l of analyte.
272 eal-time and label-free manner in full human blood plasma, using ultra-high frequency acoustic wave s
273 icated that proteolytic hydrolysis of animal blood plasmas, using fungal protease preparations in par
275 pite similar baseline CD4(+) cell counts and blood plasma viral loads, women with subtype C had the h
278 of Na(+), K(+), and Ca(2+) in diluted sheep blood plasma was demonstrated for the first time, using
284 -free DNA (cfDNA), isolated from circulating blood plasma, we generated maps of genome-wide in vivo n
285 sity, density, and coagulation rate of human blood plasma were measured along with the standard coagu
287 ds in brain tissue, cerebrospinal fluid, and blood plasma were robustly correlated to immunoproteasom
288 effective at triggering clotting of flowing blood plasma when localized on a surface than when solub
289 ected against phagocytic killing, whereas in blood plasma where the concentration of IgG is high, the
291 termination of the coagulation time of human blood plasma, which both provided reliable results.
292 ence of ADAMTS13 activity we also observe in blood plasma, which is relevant to predict hemostatic dy
293 rotein was directly detected from 100% human blood plasma with extraordinary specificity and sensitiv
294 investigated bradykinin-forming pathways in blood plasma with newly developed nanobody-based analyti
295 n of whole blood components and isolation of blood plasma with no dilution by using a continuous-flow
298 ble of measuring vancomycin in buffer and in blood plasma within the range of 0.001-70 nM with a dete
300 n in humans and rodents has little effect on blood plasma zinc levels, and yet cellular consequences
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