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1 thin-layer chromatography (HPTLC-UV/Vis/FLD-bioassay).
2 vity and specificity of our proposed stacked bioassay.
3 luorophore photobleaching in a solid surface bioassay.
4 ctivity of truncated TSLP using a PBMC-based bioassay.
5 and in vitro ADCC potency with a cell based bioassay.
6 er-linked databases, Substance, Compound and BioAssay.
7 ng assay and ex vivo using a rat aortic ring bioassay.
8 using the embryonic zebrafish (Danio rerio) bioassay.
9 in a multigenerational reproductive toxicity bioassay.
10 of hUII and URP ex vivo in a rat aortic ring bioassay.
11 ssay, and antibiotic levels were measured by bioassay.
12 d a commercially available hydrogen peroxide bioassay.
13 road applications in protein diagnostics and bioassay.
14 vestigated by use of a Myriophyllum spicatum bioassay.
15 ein (PrP(Sc)) and prion infectivity by mouse bioassay.
16 ia a complement dependent cytotoxicity (CDC) bioassay.
17 t activity toward UT receptor in a rat aorta bioassay.
18 entified and quantified using a colorimetric bioassay.
19 drug, and (v) neutralizing bioactivity using bioassay.
20 soconstriction in an ex vivo rat aortic ring bioassay.
21 the first time, a GMR-based time-domain MRX bioassay.
22 y to neutralize BoNT/H in the standard mouse bioassay.
23 ts revolutionized the development of digital bioassays.
24 All were antagonists in bioassays.
25 h decreased larval survival and/or growth in bioassays.
26 abolition, of a clearing zone on plate-based bioassays.
27 seen as prerequisites for improved DNA-based bioassays.
28 iplexed electrochemical detection of magneto bioassays.
29 e magnetic bead-based readout of homogeneous bioassays.
30 stently analyze the data produced by in vivo bioassays.
31 inked to relative potencies in pathway-based bioassays.
32 are improving the accuracy and efficiency of bioassays.
33 ve that is commonly employed in quantitative bioassays.
34 ncorporating metabolic enzymes into in vitro bioassays.
35 tional roles by providing pure compounds for bioassays.
36 showed antioxidant activity in DNA and lipid bioassays.
37 tive strategy for developing FRET probes for bioassays.
38 over time, in agreement with reported algae bioassays.
39 onic toxicity of Cl to Daphnia in soft-water bioassays.
40 be found in the literature for the different bioassays.
41 the engineering of paper-based microfluidic bioassays.
42 to practice for the specific application of bioassays.
43 h is competitive with existing contact-based bioassays.
44 MARCKS activity and subjected to functional bioassays.
45 e little or no cytotoxic activity in several bioassays.
46 use of paper as a platform for microfluidic bioassays.
47 ine sediments during 10-day laboratory-based bioassays.
48 f OSPW in mammals using a series of in vitro bioassays.
49 uman in vitro liver microsomal and cytosolic bioassays.
50 studied using conjugation and transformation bioassays.
51 c systems that incorporate these widely used bioassays.
52 for cytokinin activity in several cytokinin bioassays.
53 th Aliivibrio fischeri and Bacillus subtilis bioassays.
54 concentrations (EC50) obtained after 10 min bioassay, 2.9, 1.0, 0.7 and 18.3 mg L(-1) for copper, zi
55 y(HEMA-co-AEMA) hydrogel and an amperometric bioassay (50s) we obtained maximum inhibition at 10 mug
56 not enhance their acute toxicity in E. coli bioassays above that observed for as-received powders.
61 a critical adjustable parameter for certain bioassay analyses where magnetic nanoparticles are used
63 notoxicity using the DT40 chicken lymphocyte bioassay and developmental toxicity using the embryonic
64 re used as probe compounds to search PubChem Bioassay and generate a response profile, which containe
69 d dLPG, in low RI region (1.333-1.347) where bioassays and biological events were usually carried out
71 ological based analytical methods, including bioassays and biosensors, as well as MFCs design and ope
73 ADs enable simple, rapid, and cost-effective bioassays and environmental monitoring, which provide pr
74 microfluidic devices is vital for efficient bioassays and fabrication of complex microstructures.
78 was assessed using three in vitro short-term bioassays and their migrations were carried out using a
79 Antibiotic exposure was ascertained by serum bioassay, and for cases, by a record of antibiotic treat
80 ng nonspecific signals in wash-free magnetic bioassays, and enhancing signal to noise ratios by sever
81 strengths of digital microfluidics, digital bioassays, and optical tweezers, resulting in a powerful
82 nalyses, short-duration in vivo and in vitro bioassays, and quantitative structure activity relations
84 icant potential for translation into broader bioassay applications or development as a POC diagnostic
86 compounds with regard to the five assays or bioassays applied were detected in the samples, meaning
92 d cell product was tested using cell culture bioassays as surrogates for in vivo engraftment quality.
94 is work, fast and sensitive optical toxicity bioassay based on dual wavelength analysis of bacterial
95 ll-based in vitro and low-complexity in vivo bioassays based on algae, daphnids or fish embryos are a
96 additivity for carcinogenic PAHs and (ii) a bioassay-based approach that employs the in vitro mutage
98 10) greater than those calculated using the bioassay-based approach; most are less than 5-fold great
99 iological-based analytical methods including bioassays, biosensors, MFCs design, operating principles
100 toxicity of water samples can be tested with bioassays, but a metabolomic approach has the advantage
101 n transmission have been studied with animal bioassays, but the influence of prion protein structure
103 g predictive genotyping methods and targeted bioassays can focus toxicity assessments on ecologically
105 h data, redesigned BioAssay record page, new BioAssay classification browser and new features in the
106 lower in the overlying waters of most field bioassays compared to the laboratory, causing difference
107 ncidence in liver tumors in mice in a 2-year bioassay conducted by the National Toxicology Program.
108 Therefore, it is necessary to establish a bioassay correlating with the drug's known mechanism of
113 ew structured vocabulary designed to capture bioassay data in a formalized manner, with particular em
114 spectrometry (GC x GC-TOFMS) data set to the bioassay data obtained from normal-phase LC fractions is
116 Aside from its vector control potential, our bioassay data, in contrast to numerous other reports, pr
117 s work, we provide an update for the PubChem BioAssay database describing several recent development
121 odified somatropin to hGHBp; and (iv) a hGHR bioassay demonstrated initiation of the signal transduct
124 es to manage thrips in China, and laboratory bioassays demonstrated that F. occidentalis is significa
126 udy of SpinDx versus the gold-standard mouse bioassay demonstrates 100-fold improvement in sensitivit
127 ns were compared to those determined using a bioassay-derived method (BDM) (i.e., an additivity-indep
128 estimates are less than their corresponding bioassay-derived values; differences are less than 10%.
129 phase liquid chromatography in parallel with bioassay detection via nanofractionation and with online
132 implifying detection schemes of colorimetric bioassays, e.g. enzyme, gene, immuno and aptamer assays
133 tor-mediated potency by use of the H4IIE-luc bioassay, effects on production of steroid hormones by u
136 attempted copulation ( approximately 70%) in bioassays, equivalent to rates observed at orchid flower
137 plate can have broad applications in various bioassays, especially in resource-limited settings.
141 iveness of the overall procedure, analytical bioassays exploiting the enzyme-containing beads have be
142 paper we describe the development of a fast bioassay for determining IFX concentration in serum usin
143 e a simple and robust drug-assisted dot blot bioassay for endotoxin detection that can be used right
144 was comparable to the approved in vivo mouse bioassay for human iPSC-derived neurons and neural stem
147 ate the development of a rapid and effective bioassay for oral delivery of dsRNA to screen additional
148 of the applicability of the newly developed bioassay for screening urine for CB receptor activity ex
149 lized on the catalytic porous platform and a bioassay for the colorimetric determination of glucose w
152 (limit of detection of 0.5 nM) and specific bioassay for thiamine and its phosphorylated derivatives
153 ) of the colorimetric and fluorescence based bioassays for GFAP was decreased by ~1000 times using th
154 as found to be inactive in vivo in microbial bioassays for methionine synthase and acted as an in vit
156 e sampling in blubber to a range of in vitro bioassays for screening mixtures of bioaccumulative chem
157 d evaluated methods that are compatible with bioassays, for extracting nonvolatile and volatile DBPs
158 eral flow tests (LFTs), the current standard bioassay format used in low-resource point-of-care (POC)
161 , traditional NP discovery, largely based on bioassay-guided approaches, is biased toward abundant co
164 of live/dead screening followed by iterative bioassay-guided fractionation affords no information abo
173 tions as they have been determined either in bioassay-guided purification approaches or in bioassays
182 e present an alternative platform to perform bioassays in a microplate format that exploits evaporati
185 We used guinea pig primary cells, tissue bioassay, in vivo electrophysiology, and a guinea pig co
187 atography (HPTLC) coupled with six bacterial bioassays including two plant pathogens, a radical scave
188 ids may enable key hallmarks of tissue-based bioassays, including drug screening, tumor dissemination
196 ork for the incorporation of next-generation bioassays into biomaterials design to effectively optimi
197 lopment (OECD)-validated rodent uterotrophic bioassay is considered the "gold standard" for identifyi
199 ecosystem-level effects from single-species bioassays is a major challenge in environmental risk ass
203 work, we employed the microwave-accelerated bioassay (MAB) technique, which is based on the combined
209 th cell wall digesting enzymes, coupled with bioassay of guard cell function) plus modeling lead us t
210 ty measurements obtained from single-species bioassays of various species that can be used to estimat
213 ere detected by effect-directed assays, like bioassays or an enzymatic assay, directly linked with ch
214 y not feasible in the absence of appropriate bioassays or predictive markers for characterization of
215 technology, an all-fiber optofluidics-based bioassay platform (AFOB) was developed for the rapid imm
216 ich is based on the combined use of circular bioassay platforms and microwave heating, for rapid and
217 mes using the MAB technique and our circular bioassay platforms as compared to the commercially avail
218 e use of the MAB technique with the circular bioassay platforms for the rapid detection of GFAP in bu
222 usefulness of performing counter-screens for bioassay promiscuity and assay interference, and raise c
223 This is especially important in wash-free bioassay protocols, which do not require removal of part
224 red with chromatographic fingerprinting, the bioassay provided better discrimination ability for some
225 ivity in orally inoculated pigs with a mouse bioassay raises the possibility that naturally exposed p
226 A, respectively, was transferred to isolated bioassay rat hearts subjected to 30/120 minutes global i
227 g added sources of research data, redesigned BioAssay record page, new BioAssay classification browse
228 dical research, and the vast majority of the bioassays rely on thermocycling that uses time-consuming
233 ivo correlations (IVIVCs), the most relevant bioassay(s) related to hepatotoxicity were identified.
234 o appropriately select bioreceptors for this bioassay, seven commercial antibodies against influenza
235 se findings support the notion that toxicity bioassays should account for the cells' complex dynamic
242 riants differed strikingly among the various bioassays, suggesting that the NCR peptide-based languag
244 ility was measured for protective effect and bioassay test was performed on the formulations of Bt.
245 ng an in silico approach in combination with bioassay testing and highlighted the importance of metab
246 one receptors in Arabidopsis, we developed a bioassay that can be used to identify chemicals and crop
247 ve designed a simple yet rapid and sensitive bioassay that detects Mtb DNA electrochemically using co
248 an be used to create an autologous coculture bioassay that responds by releasing a plethora of cytoki
250 thod for determining limits of detection for bioassays that is statistically robust and reduced to pr
252 enabling high-resolution and high-throughput bioassays that, if incorporated into a biomaterial desig
259 multiple PCP-B mutant lines were utilized in bioassays to assess effects on pollen hydration, adhesio
260 nmental risk assessment relies on the use of bioassays to assess the environmental impact of chemical
261 Fluorescent labels are commonly used in bioassays to enhance sensitivity, but autoluminescence o
262 ere is an urgent unmet need for human tissue bioassays to predict cytokine storm responses to biologi
264 experiments have also demonstrated that the bioassay used in the experiments has excellent specifici
268 for the DeltaBbpacC strain in topical insect bioassays using larvae from the greater waxmoth, Galleri
270 pe, and showed decreased virulence in insect bioassays using the greater wax moth, Galleria mellonell
271 es including water, sediment, and biota into bioassays using total extraction or polymer-based passiv
272 The established point-of-care (POC) FO-SPR bioassay was also used to measure IFX in 100-fold dilute
273 n quality of red and green lentils, a rodent bioassay was conducted and compared to an in vitro metho
275 gG) covalent immobilization, an IgG/anti-IgG bioassay was implemented along the grating region and th
280 ccurring between laboratory- and field-based bioassays, we investigated changes in metal fluxes to DG
283 phytoplankton production, nutrient addition bioassays were conducted in the N-limited Neuse River Es
287 relevance of using in vitro zebrafish-based bioassays when screening for endocrine disrupting chemic
290 s an alternative to the qualitative duckling bioassay which is the "gold-standard" assay currently be
291 lent agreement with the Dex-EQ obtained from bioassay, which demonstrated that the detected glucocort
292 nsfer the mixtures from the environment into bioassays, while conserving (or re-establishing) their c
293 ntibody conjugate to obtain a sandwich-based bioassay with the capability to increase the SPR signal
295 s-based molecular simulations and label-free bioassays with a unique photonic crystal biosensor.
296 t reveals new complexities arising in Hg(II) bioassays with cysteine and emphasizes the need for cons
298 ioassay-guided purification approaches or in bioassays with plants in which the expression of specifi
300 in different pH conditions using behavioural bioassays with shore crabs (Carcinus maenas) as a model
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