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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
54       Objectives: To determine whether young blood plasma ameliorates pathology and cognition in a mo
55 ance on the basis of known proteins in human blood plasma analyses.
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
58         Complex viral genetic populations in blood plasma and CSF were characterized using a heterodu
59 ine OSCs in cooked garlic samples as well as blood plasma and digestive fluids.
60 m several types of undiluted media including blood plasma and food media.
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
65                                 Longitudinal blood plasma and resting CD4(+) T cells were obtained fr
66 creen in human subjects of the metabolome of blood plasma and saliva at different times of day.
67                             The proteomes of blood plasma and serum represent a potential gold mine o
68  use in qualitatively distinguishing between blood plasma and serum samples.
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
75  to retain sodium and water despite expanded blood, plasma and extracellular fluid volumes.
76  body fluids (for example, saliva, sweat and blood plasma) and under extreme hypoxic and acidic condi
77 the extravascular extracellular space to the blood plasma), and volume of distribution (v(e)).
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
83 man blood samples (whole blood, blood serum, blood plasma, and formed elements) was realized.
84 n is present in human body fluids, including blood plasma, and is a potential biomarker for PD.
85 n P (Sepp1) contains most of the selenium in blood plasma, and it is utilized by the kidney, brain, a
86 ood sample, EBV load was quantified in whole blood, plasma, and B cells using qPCR.
87              We measured lead in 81 maternal blood, plasma, and breast milk samples at 1 month postpa
88 dose-response relationships between maternal blood, plasma, and breast milk to better understand lact
89 turated FAs from various biological samples (blood, plasma, and cell lines).
90  examine dose-response relationships between blood, plasma, and milk lead levels.
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
94                                 Serial whole-blood, plasma, and urine samples were collected for radi
95                                 Serial whole blood, plasma, and urine samples were collected for radi
96             Activity was determined in whole blood, plasma, and urine.
97 is without any sample preparation from dried blood, plasma, and urine.
98                       Metabolic profiling of blood plasma appears to be a promising approach for the
99 cross the day and that serotonin profiles in blood plasma are also rhythmic in LD, but were not rhyth
100             Urine provides an alternative to blood plasma as a potential source of disease biomarkers
101 viral inoculation, viral RNA was detected in blood plasma as early as 1 d after infection.
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
107                  Seven time-matched pairs of blood plasma (BP) and saliva samples were collected over
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
112                        Proteomic analysis of blood plasma can potentially identify biomarkers that ar
113 t elevated levels of free cell hemoglobin in blood plasma can, as early as the first trimester, poten
114 plasma (M2) as well as infant umbilical cord blood plasma (CB).
115           Monoclonal antibodies derived from blood plasma cells of acute HIV-1-infected individuals a
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
118  high affinity and minimal interference from blood plasma components.
119 on performance as a function of its measured blood plasma concentration: it reduced reflection impuls
120 s attributed to the higher tumour uptake and blood plasma concentrations.
121                          Remarkably, newborn blood plasma confers substantially reduced BLP-induced m
122 ensitivity and limit of detection (LOD) in a blood plasma-containing sample matrix.
123                                          The blood plasma contains four biologically important proteo
124                               Although human blood plasma contains molecules that inhibit the activit
125          When biofilm lysine exceeds minimal blood plasma content after OHR, less GCF appeared despit
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
129                   When matched against human blood plasma database, the detected IMS-TOF features wer
130                                      Newborn blood plasma demonstrates substantially higher adenosine
131 itric oxide (NO) by hemoglobin released into blood plasma during intravascular hemolysis.
132 relevant to biological fluids (urine, blood, blood plasma, etc.).
133 een-blue to blue can be detected directly in blood plasma, even at picomolar concentrations of antibo
134           The titer of infectious scrapie in blood plasma exceeded 10(7) 50% infectious doses per mil
135          Here we use immunoassays to examine blood plasma expression patterns of Keratin 9 and its re
136                                     LC/MS of blood plasma extracts from rats that were administered a
137          The protein was purified from human blood plasma, first by a cold ethanol precipitation proc
138 lar extravascular volume fraction, v(e); and blood plasma fraction, v(p)) were determined by fitting
139           Between 2006 and 2011 we collected blood plasma from 261 bald eagle nestlings in six study
140                                  We compared blood plasma from 72 healthy controls with that from 88
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.
151 acids such as siRNA while providing enhanced blood plasma half-life and tumor targeting.
152                Detection of PrP(C) in spiked blood plasma has been achieved and demonstrated a recove
153                Detection of PrP(C) in spiked blood plasma has been achieved in the same range of conc
154  SERS detection of Microcystin-LR (MC-LR) in blood plasma has been developed.
155            The level of protein carbonyls in blood plasma has been used as a measure of overall oxida
156 inhibitors of PCR reactions, including whole blood, plasma, hemoglobin, lactoferrin, serum IgG, soil
157        In a subanalysis of 100 subjects with blood plasma HIV <50 copies/mL, high levels of CMV in se
158 hort, and on the subset of 100 subjects with blood plasma HIV <50 copies/mL.
159 ve sex with men, who were receiving ART with blood plasma HIV <500 copies/mL.
160 t Dx assay (Aptima assay) is FDA cleared for blood plasma HIV-1 RNA quantitation.
161                                          The blood plasma ibuprofen sodium concentrations achieved in
162  to profile the time course of 263 lipids in blood plasma in 20 healthy individuals.
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
165 he siRNA nanoparticles do not disassemble in blood plasma in vitro and in vivo.
166 cture of hydrated fibrin clots made of human blood plasma in vitro.
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.
169 l inflammatory cytokine gene expression, and blood plasma interleukin-6 values were assessed.
170 tive level, systemic administration of young blood plasma into aged mice improved age-related cogniti
171                          Lipidomics of human blood plasma is an emerging biomarker discovery approach
172         Relaxivity of [Mn(PyC3A)(H2O)](-) in blood plasma is comparable to commercial Gd contrast age
173       The tracer enrichment determination in blood plasma is demonstrated for several triple combinat
174 e for the detection of homocysteine (Hcy) in blood plasma is described.
175            Although most circulating iron in blood plasma is destined for erythropoiesis, the mechani
176                Proteomic characterization of blood plasma is of central importance to clinical proteo
177                                 Serotonin in blood plasma is primarily synthesized in the duodenum, a
178                                              Blood plasma is the most popularly used sample matrix fo
179 g intravascular hemolysis from the cell into blood plasma, it produces a state of NO depletion, oxida
180        Intravitreal injections of autologous blood, plasma kallikrein (PK), bradykinin, and collagena
181 amine the relationship between pericytes and blood plasma leakage during photothrombotic occlusion of
182                    At the same consultations blood plasma levels of estradiol (E2) and thyroid hormon
183 he most important in the periodic table with blood plasma levels of H(+), Na(+) and Ca(2+) being indi
184                                          HPC blood plasma levels were also compared to known in vitro
185 lin in the brain are severalfold higher than blood plasma levels.
186                 Doses were titrated to reach blood/plasma levels comparable to therapeutic levels in
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
191 stable species without affecting other blood/blood plasma metabolites.
192       Superoxide dismutase activity in human blood plasma mirrored these reductions between prospecti
193            However, both soluble mannose and blood plasma more strongly inhibited antibody recognitio
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
201 ty of the former two for FU determination in blood plasma or serum (~500 nM).
202 ccurate HIV incidence estimates using stored blood plasma or serum samples without a requirement for
203 dant proteins, which is usually performed on blood plasma or serum samples.
204 rption from real-world complex media such as blood plasma or serum.
205 xime ethers bind selectively to TTR in human blood plasma over the plethora of other plasma proteins,
206 ly reduced in CSF with respect to autologous blood plasma (P < 0.042, Student's t-test).
207  parabiosis) or repeated injections of young blood plasma (plasma from 2- to 3-month-old mice) into o
208         A differentiation between the use of blood plasma powder and PPFG using the ratios of fibrino
209       Protein and proteome analysis of human blood plasma presents a challenge to current analytical
210 stress in humans was quantified by measuring blood plasma protein carbonyls using the two commerciall
211  and suppress irreversible interactions with blood-plasma protein cocktails.
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
216  in the plasma relative to cells (mean whole blood-plasma ratio, 0.799 +/- 0.096).
217              Initiation of clotting of human blood plasma required addition of a critical concentrati
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
220                                              Blood plasma, saliva, and urine were obtained from four
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
224             We detect CEA in three different blood plasma samples and demonstrate that this novel ref
225 for exhaustive lipid fingerprinting of human blood plasma samples based on the employment of methyl t
226                                              Blood plasma samples collected from patients with the sy
227  1 env V4/V5 genetic populations in multiple blood plasma samples collected over an average of 7 mont
228  chemometric techniques were used to analyze blood plasma samples from our cohort.
229               Deep sequencing was applied to blood plasma samples from the cohort to detect cases of
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.
233 d we demonstrate detection in actual patient blood plasma samples.
234 the evaluation of the lipid profile of human blood plasma samples.
235 sor has been developed to detect MG in human blood plasma samples.
236 onstrated using an artificially spiked human blood plasma samples.
237 r the collection and transportation of dried-blood-plasma samples, SampleTanker (ST), was developed a
238                               HIV-1 RNA from blood plasma, seminal plasma, or cervical wicks was quan
239                         The simple, portable blood plasma separation design is hand-driven and can ea
240                     A portable, microfluidic blood plasma separation device is presented featuring a
241                            We then simulated blood-plasma separation in arteriolar bifurcations with
242  exploited for analysis of AFP in real human blood plasma, serum and urine sample.
243 say performance in complex media (i.e. whole blood, plasma, serum) due to the non-specific adsorption
244            The method can assay GSH in whole blood, plasma, serum, lung lavage fluid, cerebrospinal f
245 MR)-based metabolic phenotyping of urine and blood plasma/serum samples provides important prognostic
246 lliliter level proteins in nondepleted human blood plasma/serum without affinity enrichment.
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
250                 Analysis of the duodenum and blood plasma showed that the amount of serotonin in the
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
254  inhibits PSD-95 and shows improved in vitro blood plasma stability.
255           Based on the diffusivity of LDL in blood plasma, such a Peclet number is found to be far le
256            We found 18 signaling proteins in blood plasma that can be used to classify blinded sample
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
262 res, addition of other drugs and addition of blood plasma to the colloidal suspensions.
263 investigated adsorption from undiluted human blood plasma to three different polymer brushes.
264 , suggesting that they are taken up from the blood plasma, together with yolk, during oocyte growth a
265                                        Here, blood plasma 'total alpha-synuclein' and 'Ser-129 phosph
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
274                                              Blood plasma viral loads and the time to progress to AID
275 pite similar baseline CD4(+) cell counts and blood plasma viral loads, women with subtype C had the h
276                                              Blood plasma volume was highly variable and the only par
277 d to quantify the BBB leakage rate and local blood plasma volume.
278  of Na(+), K(+), and Ca(2+) in diluted sheep blood plasma was demonstrated for the first time, using
279                                              Blood plasma was obtained, and organs were isolated typi
280 ensors, total calcium concentration in human blood plasma was successfully determined.
281                       Metabolic profiling of blood plasma was undertaken using proton nuclear magneti
282                                    Undiluted blood plasma was used to test the nonfouling properties
283                  Unexpectedly, in the native blood plasma we discover a large background of naturally
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
286                     Samples of monocytes and blood plasma were prospectively collected from healthy c
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
290                                           In blood plasma, where the concentration of SCN(-) is relat
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
296  limit of 0.13 unit/mL was obtained in sheep blood plasma with the stripping method.
297  format in buffer and complex media (milk or blood plasma) with sub-nM detection ability.
298 ble of measuring vancomycin in buffer and in blood plasma within the range of 0.001-70 nM with a dete
299                                         Most blood plasma zinc is bound to albumin, but the structure
300 n in humans and rodents has little effect on blood plasma zinc levels, and yet cellular consequences

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