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1 1-10 pg/mL PSA was also achieved in diluted human plasma.
2 ction of prostate cancer (PCa) biomarkers in human plasma.
3 their ability to neutralize FVIII in normal human plasma.
4 l provided excellent stability in monkey and human plasma.
5 he target DNA in the hybridization buffer or human plasma.
6 de metabolite, BMS-801576, concentrations in human plasma.
7 as good chemical and enzymatic stability in human plasma.
8 sease-relevant platelet aggregation assay in human plasma.
9 -induced complement activation in autologous human plasma.
10 /MS) bioanalytical assay of dapagliflozin in human plasma.
11 key soluble complement-regulating protein in human plasma.
12 o 50 femtogram of PFCs, in one microliter of human plasma.
13 on of insulin-like growth factor 1 (IGF1) in human plasma.
14 ied for selective extraction of quinine from human plasma.
15 to generate different coagulation times for human plasma.
16 This approach was further investigated from human plasma.
17 were within quantification range in control human plasma.
18 on product phloroglucinol aldehyde (PGAL) in human plasma.
19 of unconjugated fatty acids (FA) in fish and human plasma.
20 ct human insulin and five insulin analogs in human plasma.
21 ococcal agglutination with fibrin fibrils in human plasma.
22 successfully applied to real samples such as human plasma.
23 ffectively diagnoses protein C deficiency in human plasma.
24 presence had not been previously observed in human plasma.
25 ndard Reference Material 1950 Metabolites in Human Plasma.
26 .6 muIU/mL) for each insulin from 250 muL of human plasma.
27 f its low solubility and fast clearance from human plasma.
28 TRX80 showed an age-dependent increase in human plasma.
29 200 ng mL(-1) and high accuracy for diluted human plasma.
30 rch for loci contributing to DBH activity in human plasma.
31 s successfully applied to detect thrombin in human plasma.
32 al concentrations in cell culture medium and human plasma.
33 sin, trypsin, and chymotrypsin and stable in human plasma.
34 andwich assay was 7.3 pM in BSA and 15 pM in human plasma.
35 her with an increased enzymatic stability in human plasma.
36 minant thiol/disulfide redox couple found in human plasma.
37 inically relevant sensitivities in undiluted human plasma.
38 t are representative of those found in adult human plasma.
39 el-free detection of an analyte in undiluted human plasma.
40 The stability of (44)Sc-cm09 was tested in human plasma.
41 inds ~70% of amyloid beta-peptide (Abeta) in human plasma.
42 polymease chain reaction (RT-PCR) on HCV(+) human plasma.
43 vels of TF that clotted factor VII-deficient human plasma.
44 y the ligands for these virulence factors in human plasma.
45 f different glycoisoforms of intact ApoC3 in human plasma.
46 e plasma mimic the metabolite composition of human plasma.
47 ELISA to measure intact BPDE-HSA directly in human plasma.
48 ut oil unlike to moderate sn-3 preference in human plasma.
49 0.34 pg mL(-1) in PBS and 0.88 pg mL(-1) in human plasma.
50 factor IXa and prolongs the clotting time of human plasma.
51 t of rare proteins from buffer solutions and human plasma.
52 response of phenol conjugate metabolites in human plasma.
53 e differences in protein abundance levels in human plasma.
54 n molecules, and complement factors on CC in human plasma.
55 patterns within complex lipidomes including human plasma.
56 iological thiols such as glutathione) and in human plasma.
57 sa than the naturally-occurring AMP LL-37 in human plasma.
58 r genetic or iatrogenic iron overload and in human plasma.
59 ystem for the detection of EVs isolated from human plasma.
60 lity was evaluated on PLGA nanoparticles and human plasma.
61 ndogenous alpha-1-acid glycoprotein (AGP) in human plasma.
62 tein phosphorylation when compared to normal human plasma.
63 MS/MS bioanalysis of pasireotide (SOM230) in human plasma.
64 ed partial thromboplastin time of baboon and human plasmas.
65 fibrinogen from FXIII-A-deficient mouse and human plasmas.
66 dC concentrations present in murine, but not human, plasma.
68 Material (SRM) 1950, "Metabolites in Frozen Human Plasma", against benchmark consensus mean concentr
69 stable in vitro in FBS, BALB/c-nu plasma and human plasma, although release of the drug at HT was inc
72 otent activator of the complement cascade in human plasma and caused deposition of C5b-9 on the plate
73 all analogs were calculated in 6 sources of human plasma and CVs of the matrix factors were <15% in
75 tests, we find SSTNIGF1R is highly stable in human plasma and displays a half-life of 27 hours in mic
76 ACE2) on peptide metabolism was evaluated in human plasma and explanted heart tissue from patients wi
77 n quantification in buffer, human serum, and human plasma and for assaying hormone secretions from en
79 a high-molecular-weight leptin complex from human plasma and identified clusterin as a major compone
80 aintained higher levels of stability both in human plasma and in mice than the corresponding maleimid
81 onalization on protein arrays from undiluted human plasma and indicates the great potential of the pC
83 cells were treated with Lp(a) purified from human plasma and Lp(a) uptake studied using Western blot
84 cells were treated with Lp(a) purified from human plasma and Lp(a) uptake studied using Western blot
85 ss with biological samples both postprandial human plasma and lung samples from ferrets were analysed
86 /59 fragment was identified post-MI, both in human plasma and mouse LV, at levels that inversely corr
89 mino acids and amino-containing compounds in human plasma and serum using precolumn derivatization wi
91 all-trans geometric isomer in foods, whereas human plasma and tissues show greater proportions of cis
94 IgG4) directly in unfractionated samples of human plasma and we detect traces of previously unreport
95 rapidly hydrolyzed in rat plasma but not in human plasma and were stable in simulated gastrointestin
97 tion of the thrombin inhibitor dabigatran in human plasma and whole blood samples, highlighting its p
98 f the integrative approach, bacterial cells, human plasma, and cancer cells were analyzed by combined
99 of naturally occurring anti-influenza Abs in human plasma, and did not differ between HCMV(+) and HCM
100 trovafloxacin at drug concentrations seen in human plasma, and its inhibition led to dysregulated fra
101 e drug from the proteins that are present in human plasma, and some of the peptides are capable of di
105 rest because high levels of this molecule in human plasma are associated with an increasing risk of c
107 engineered library is structurally stable in human plasma as well as being hemocompatible (non-hemoly
108 zymatic release of payload from ADC-depleted human plasma at 144 h was able to account for almost 100
109 d in the liver hepatocytes and is present in human plasma at trace levels (picomolar or nanograms per
110 centrations routinely achieved clinically in human plasma, atovaquone inhibits STAT3 phosphorylation,
111 mbers of diverse RNA virus families within a human plasma background, some present at very low levels
112 drug (levothyroxine) and its metabolites in human plasma, based on precolumn derivatization followed
113 ino)hexanoate (13d), was stable in swine and human plasma but liberated 14 in swine brain homogenate.
115 In conclusion, lunasin can be isolated from human plasma by a simple DEAE microspin column technique
116 proach to investigate the entire spectrum of human plasma cell neoplasia and illustrate the utility o
117 recapitulates the systemic manifestations of human plasma cell neoplasms, and implicates cooperativit
121 ight-chain production and cause apoptosis in human plasma cells making intact IgGlambda antibodies.
122 mbda-light-chain production and secretion by human plasma cells regardless of sequence diversity.
127 ncer and the repertoire of autoantibodies in human plasmas collected at a preclinical time point and
129 s purified from either conditioned medium or human plasma could partially rescue the defects of HSCs
130 nity pull-down mass spectrometry analysis in human plasma demonstrated that the protein interacts wit
131 we demonstrate the detection of TNFalpha in human-plasma derived samples as an example for point-of-
133 plores critical issues in the development of human plasma-derived Hp and hemopexin as therapeutics fo
136 lated N-glycan fraction from haptoglobin and human plasma, enriched using weak anion exchange chromat
137 47 Da over the native albumin extracted from human plasma, exactly matching the mass of the linker-pa
139 olar activity toward HIV-1 and are stable in human plasma for more than 24 h with a therapeutic index
140 uality control samples, reference plasma and human plasma from a real nutrimetabolomic study were use
142 oring of the glucose and L-lactate levels in human plasma from patients with diabetes is demonstrated
144 ins from nonpregnant rats (n=6-7/group) with human plasma from women with EPE, LPE, or NP and measuri
145 ious concentrations of HFA spiked in diluted human plasma further demonstrates the potential utility
147 he mass of the major protein in ADC-depleted human plasma had an additional 1347 Da over the native a
148 high plasma protein binding abilities and a human plasma half-life of 160 min, resulting in formatio
152 xylated polystyrene (PS-COOH) NPs cloaked by human plasma HC were titrated with 3-[(3-Cholamidopropyl
153 ze and composition, isolated subfractions of human plasma HDL, cell lines stably expressing ABCA1 or
154 econd most abundant protein after apo A-I of human plasma high-density lipoproteins (HDL), is the mos
159 at canagliflozin concentrations measured in human plasma in clinical trials and was caused by inhibi
160 determination of a model peptide spiked into human plasma in the range of 0.45-9.0 mug/mL is demonstr
161 potassium were also determined in undiluted human plasma in the therapeutic concentration range.
162 Several splice variants of IgE exist in human plasma, including a variant called IgE-tailpiece (
163 ted peptides quantified in in vitro glycated human plasma increased more than 3-fold using this platf
164 to 4000 IU/L, phosphocreatine 5 mM) added to human plasma induced a dose-dependent reduction to compl
165 untreated or hTNFalpha-treated PAEC with 10% human plasma induced complement C3b/c and C5b-9 depositi
166 C with CHC (100 microg/ml) protected against human plasma-induced endothelial activation and damage.
167 und no evidence that progranulin in mouse or human plasma is a component of HDL either by ultracentri
168 whether polymeric IgA (pIgA) recovered from human plasma is able to associate with secretory compone
170 ccurate quantification of 36 NEFA species in human plasma is described, the highest numbers ever repo
172 ed reduction of these chemicals over time in human plasma is presumably related to the phase-out of P
176 is the first study to characterize sTim-3 in human plasma, its source, and mechanism of production.
177 on study of serum scuPAR levels identified a human plasma kallikrein gene (KLKB1) promoter polymorphi
179 haptoglobin (Hp)-hemoglobin (Hb) complex in human plasma leads to a high affinity recognition by the
182 te concentrations within even 2-fold diluted human plasma may be determined reliably using as few as
183 ospholipids from biological samples, such as human plasma, MDA-modified LDL and Cu(2+)-oxidized LDL.
184 ratio of metabolites in animal plasma versus human plasma measured over approximately 1 year apart we
186 dopamine in human cell lines expressing the human plasma membrane dopamine transporter (DAT) and hum
189 g the glycosylation of a cancer biomarker in human plasma, MUC5AC, using only 20 muL of the plasma.
192 The capacity to isolate immunochemically human plasma neuron-derived exosomes (NDEs), containing
193 onversely, when strain PC574 was cultured in human plasma, no similar increase in hemolytic activity
194 nonspecific protein adsorption to undiluted human plasma on both the antibody immobilized pCB spots
202 coccus pyogenes (GAS) interacts tightly with human plasma plasminogen (hPg) and plasmin (hPm) via the
205 ry program increased the fraction unbound to human plasma protein from below minimum detection levels
206 tification of genetic variants affecting the human plasma protein profile by combining high-throughpu
207 exploited to improve the fraction unbound to human plasma protein while retaining biochemical potency
212 mple-processing pipeline for analysis of the human plasma proteome that provides greatly increased de
216 xidized low-density lipoproteins (OxLDL) and human plasma, respectively, their analysis as risk bioma
217 AHHAHHAAD spiked in a protein digest and in human plasma, respectively, were used as the samples to
218 tical performance, four drugs were spiked to human plasma, resulting in highly acceptable precision (
219 that better recapitulates the composition of human plasma reveals unforeseen metabolic wiring and reg
220 on of cholesteryl esters from TG fraction of human plasma sample using our chiral HPLC/APCI-MS method
221 m gel electrophoresis of an albumin-depleted human plasma sample were excised for in-gel MAAH LC-MS a
230 cation of the proposed method to measure 124 human plasma samples from orchard workers and cotton far
234 urface (MAPS), for measuring MPO activity in human plasma samples using the bioluminescent substrate
236 values determined for the two analytes in 35 human plasma samples were in excellent agreement with th
237 roach can remove 95% of the total albumin in human plasma samples while retaining close to 100% for t
238 bled the selective Se speciation analysis of human plasma samples without the need of extensive clean
244 ics data set derived from approximately 3000 human plasma samples, we find that application of our al
245 c/hydrophilic LC-MS/MS analysis of mouse and human plasma samples, which enables the untargeted ("sho
255 icrospin column to isolate spiked lunasin in human plasma showed that most lunasin (37.8-46.5%) bound
256 hysema, infusion of purified AAT from pooled human plasma-so-called "augmentation therapy"-represents
260 lity in terms of biological sample analysis (human plasma), temporal stability, and reusability was a
262 cific modification of endogenous fetuin A in human plasma, the synthesis of tandem fluorophore-protei
264 y achieves the required sensitivity range in human plasma to allow reliable differentiation between h
265 ty of vinyl sulfonamide 4 are good enough in human plasma to serve as a starting point for medicinal
267 lbumin-AalphaC adducts were characterized in human plasma treated with N-oxidized metabolites of Aalp
268 /= 24 hours on biomaterials conditioned with human plasma under venous shear in iron-free cell cultur
269 alpha1-Antitrypsin (A1AT) purified from human plasma upregulates expression and release of angio
270 es and internal standard were extracted from human plasma using a simple protein precipitation proced
271 o develop a method of isolating lunasin from human plasma using an ion-exchange microspin column and
272 ation of empagliflozin (25-600 ng mL(-1)) in human plasma using dapagliflozin as an internal standard
274 First, we generated high purity apoA-I from human plasma, using thiophilic interaction chromatograph
275 es PKal activity in vitro in both murine and human plasma, via a factor XII (FXII)-dependent mechanis
277 orted tissue factor-dependent coagulation in human plasma, vs. APL with longer or shorter fatty acyl
281 for quantitative analysis of pasireotide in human plasma was evaluated and compared to those obtaine
284 cells in FBS, and a higher concentration of human plasma was necessary to reduce the cytotoxicity of
290 thods for the profiling of micronutrients in human plasma, we introduce a novel, validated workflow f
291 nding and radiometabolism of [(11)C]PBR28 in human plasma were achieved for up to 50 min after radiol
292 n, and human IgG) and a complex mixture from human plasma were fully deglycosylated in 20 min, withou
295 port on reagentless cholesterol detection in human plasma with a novel single-enzyme, membrane-free,
296 ion (mean bias <10%) of polar metabolites in human plasma with good reproducibility (CV approximately
297 ive analysis of the drug enalapril in pooled human plasma with ramipril as an internal standard, a gr
298 the measurement of thrombin added to healthy human plasma with same high sensitivity and a limit of d
299 nonhuman primates that repeated exposure to human plasma with trace amounts of HCV induced HCV-speci
300 eous detection of both antibiotics in spiked human plasma within a sample-to-result time of less than
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