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1 or screening of 18, 22, 24, 26, and 30 years were chosen for 2 of the strategies (conventional cytolo
2 uately characterized by measured covariates, are chosen for a specific therapy.
3 egular basis, and requiring that new strains be chosen for a new vaccine.
4  and low in vivo acute toxicity in mice, 36c was chosen for a more complete preclinical evaluation.
5 b vedotin, first in class and gold standard, was chosen for a proof of principle.
6                             Activation times were chosen for a 2-s epoch for each fibrillation episod
7 gh level of expression of the exogenous gene were chosen for a detailed analysis.
8                                     J20 mice were chosen for a highly stringent investigation of mito
9 pliance, and randomly 40% of nurses each day were chosen for accuracy spot-checks by reference raters
10              Understanding how a single gene is chosen for activation is critical for understanding m
11 e highest levels of ChAT, and that cell line was chosen for additional studies of ACh release and cel
12                                  Seven genes were chosen for additional analysis based on the availab
13  numbers of receptors as wild-type receptors were chosen for additional ligand binding and cAMP accum
14 alphaF46, alphaF49, alphaF114, and alphaF117 were chosen for additional mutations to Asp, Ser, and Ty
15    A total of 16 GABPbeta interface residues were chosen for alanine scanning mutagenesis.
16 re, an inert human IgG2/IgG4 hybrid C region was chosen for an rMil2.
17 nomolar activity in the cell-based assay and were chosen for analyses with isolated tubulin.
18             The relatively stable NS5 region was chosen for analysis because it allowed for dependabl
19                                   p19(INK4d) was chosen for analysis because it usually acts to block
20 ane immediately superior to the caudate head was chosen for analysis.
21 line derivatives doxorubicin and aclarubicin were chosen for analysis because they have been shown to
22 llected at both study entry and end of study were chosen for analysis.
23 graft surgery, Q wave myocardial infarction) were chosen for analysis.
24 wed overexpression in hippocampus and cortex were chosen for analysis.
25                           Compounds 6 and 21 were chosen for analyzing the underlying action mechanis
26 s by which the flow rate and the voltage can be chosen for any nanosuspension to precisely operate in
27 on has a major impact on which method should be chosen for AS analysis.
28             One such compound, ferulic acid, was chosen for biochemical analysis.
29 hermococcus sp. 9 degrees N-7 DNA polymerase was chosen for biochemical characterization.
30 ese and other considerations, three pathways were chosen for biologic validation of the metabolomic d
31 ot be totally avoided when panel members are being chosen for certain guidelines or in certain settin
32 6E10 and 4G8) used for immunohistochemistry, were chosen for characterization of their kinetics of bi
33  and orally active factor Xa inhibitor which was chosen for clinical development.
34  5-HT(4) partial agonist candidates 2d and 3 were chosen for clinical development.
35                                   265 papers were chosen for closer screening of the abstracts and 93
36                                      UniGene is chosen for comparison because of its high quality and
37 isease, and a highly virulent isolate, PSE9, was chosen for comparison by subtractive hybridization t
38                                     High fat was chosen for comparison to determine whether palatabil
39 complex (Coregonus artedi and C. zenithicus) were chosen for comparison.
40 gions of interest (ROIs) within each patella were chosen for correlation between ultrashort-TE bicomp
41                                     CA_C2195 was chosen for crystal structure determination for struc
42 d-type protease ranging from 58 nM to 0.8 pM was chosen for crystallographic analysis.
43           The liguleless locus (liguleless1) was chosen for demonstration of targeted mutagenesis in
44 heart SMPs, with high natural CoQ10 content, were chosen for depletion/reconstitution experiments.
45 eria by which specific regions of the genome are chosen for deposition of distinguishing chromatin ma
46                   One clone from each family was chosen for detailed analysis by Southern blot hybrid
47  highly conserved region of the PR promoter, was chosen for detailed analysis.
48 entified in Pseudomonas stutzeri WM88, which was chosen for detailed studies from a group of organism
49 hages were identified, and two of each group were chosen for detailed analysis.
50              One clone, designated ACAM1000, was chosen for development based on its comparability to
51 O121 specific, so regions in these two genes were chosen for development of PCR assays.
52 , allowing the most appropriate functions to be chosen for displaying the most meaningful positions i
53 ars, when cut-off values of 40 and 0.5 ng/ml were chosen for DJ-1 and alpha-synuclein, respectively,
54                            Nivolumab 3 mg/kg was chosen for dose expansion.
55 nd therefore the most suitable PCI-IS has to be chosen for each analyte.
56 st defect and changes in one marker compound was chosen for each defect type, that is, indole for lig
57                               Three controls were chosen for each case, adjusted for sex, age, CD4 co
58 and third identifying the therapy that would be chosen for either themselves or a family member.
59 TNP peptides, two octamers, and two nonamers were chosen for eliciting anti-TNP CTL responses.
60                                          ATM was chosen for evaluation because of the increased radio
61 nnective tissues to allow tissue dissolution were chosen for evaluation, employing well-known antidep
62 plaque in a proximal coronary artery segment were chosen for evaluation.
63 es out of 50 subjected to the SA simulations were chosen for evaluation; these 14 structures have a f
64  well as the potent inhibitor sulfaphenazole was chosen for examination in further detail.
65                               Two RNAi lines were chosen for examining global protein and metabolite
66 e special pair bacteriochlorophyll dimer, P, was chosen for excitation.
67 llion compounds were screened from which 192 were chosen for experimental evaluation.
68 LVE, Ac-YYD, Ac-LLE, Ac-YLD, Ac-MYD, Ac-VIE) were chosen for experimental validation in order to illu
69       In one model, once an odorant receptor is chosen for expression, other receptor genes are suppr
70        A total of 62 nondiabetic individuals were chosen for extremes of insulin sensitivity (31 insu
71 spectra of membrane phosphatidylcholine, has been chosen for fluorescence and TOF-SIMS imaging of mem
72 dent tumor models, the C18 analogue, NM-404, was chosen for follow-up evaluation in human lung cancer
73 neous nuclear ribonucleoprotein A1 (HNRNPA1) was chosen for follow-up since rs3846662, an HMGCR SNP t
74 eturned 4997 citations, of which 84 articles were chosen for full-text review.
75 ographic data, a subset of these mutants can be chosen for functional studies to test their importanc
76                A high-ranking candidate STK4 was chosen for functional validation and identified to p
77                            These regions may be chosen for further experimental studies.
78 g such a genome scan, individual regions may be chosen for further sequencing and a more detailed ana
79 excellent imaging properties in mice and has been chosen for further evaluation as a potential PET ra
80 satile synthesis of 3, and this compound has been chosen for further preclinical and clinical develop
81 R-repressed two-component system (TCS) trxSR was chosen for further analysis based on its homology to
82                                         CD58 was chosen for further analysis because of its abundant
83 uciferase activity specifically in petioles, was chosen for further analysis.
84 ne domain (TM6) of the E. coli protein YjiO, was chosen for further analysis.
85 nsverse sinuses, a venous ROI input function was chosen for further analysis.
86 e strain Lactobacillus plantarum ATCC 14917, was chosen for further analysis.
87                                   One mutant was chosen for further analyzes; rme1 (for resistance to
88                                Derivative 4d was chosen for further cell cycle and apoptosis studies
89                                       tcvSOD was chosen for further characterization because it was e
90 on (ATF2d), encodes a novel ATF2 isoform and was chosen for further characterization in this study.
91    One of the highest affinity aptamers, D8, was chosen for further characterization.
92             One mutant from the second class was chosen for further characterization.
93 and had cross-reactivity with macaque CTLA-4 was chosen for further development.
94                                           It was chosen for further development.
95 he basis of its superior overall profile, 39 was chosen for further evaluation and has progressed int
96  these studies, one of these lines (clone 5) was chosen for further evaluation.
97           Guar gum (1.5 wt %) with 4 wt % KF was chosen for further evaluation.
98 ing 143+/-5.5mg sunitinib in the inner layer was chosen for further pharmacokinetic assessment in viv
99           For these reasons, compound 13-(S) was chosen for further preclinical evaluation.
100 ated the best anti-inflammatory activity and was chosen for further research.
101                                         SmaI was chosen for further studies because it produced 11 to
102 ne subunit of glutamate dehydrogenase (GDH), was chosen for further studies for its role in tricarbox
103        A daniplestim dose of 2.5 microg/kg/d was chosen for further study because it was hematopoieti
104                                     TSHR-261 was chosen for further study because it was secreted ver
105 inst a lethal intranasal Y. pestis challenge was chosen for further study.
106 n5, a component of the spliceosomal complex, was chosen for further study.
107 n the anthranilate dioxygenase (AntDO) genes was chosen for further study.
108 d in this screen, the SEPALLATA3 (SEP3) gene was chosen for further study.
109 r visible abnormalities, and one mutant, V5, was chosen for further study.
110                    Consequently, this mutant was chosen for further study.
111 f the particularly mucoid transposon mutants was chosen for further study.
112  these clones contained a 3.1-kbp insert and was chosen for further study.
113 d the murine pathogen Mycoplasma arthritidis was chosen for further study.
114                            P. gingivalis 381 was chosen for further testing in a mouse abscess model
115                   miRNAs miR-100 and miR-101 were chosen for further analyses based on their reproduc
116             Five interesting candidate genes were chosen for further analysis from a larger set of ca
117  (RIL) population derived from these parents were chosen for further analysis of Cd and Zn tolerance
118  in response to either mild or severe stress were chosen for further analysis using real-time polymer
119                                   Two clones were chosen for further analysis which displayed appropr
120       Viruses from two different time points were chosen for further analysis, an early culture-adapt
121 DD45B, HO-1, PTGS2, RGS2, TIEG, and ID3) and were chosen for further analysis.
122 ate plants with a range of expression levels were chosen for further analysis.
123           Five of the newly identified genes were chosen for further characterization, and clean, unm
124  extraordinary hypersensitivity to mAMSA and were chosen for further characterization.
125 8, a control positive for both cat and BAG1, were chosen for further characterization.
126 active CpG-specific methyltransferase M.MpeI were chosen for further characterization.
127                                 Five regions were chosen for further characterization: three correspo
128 these in vitro assays, four compounds (7c-f) were chosen for further evaluation.
129 g epitopes on the EpCAM extracellular domain were chosen for further evaluation.
130         Based on this analysis, three models were chosen for further examination and comparison.
131          CUCU and UCGA fit both criteria and were chosen for further studies.
132 es, caveolin-1, caveolin-2, and GDF10/BMP3b, were chosen for further study on the basis of their loca
133 ed from the qHTS, 6 distinct chemical series were chosen for further study.
134 s, showing comparable toxicity and efficacy, were chosen for further study.
135 e scFv-phage clones of which two, 5B and 7E, were chosen for further study.
136           Two differentially displayed bands were chosen for further study.
137 Sorting Complex Required for Transport-III), were chosen for further study.
138  based on their DNA restriction patterns and were chosen for further subcloning into a pBluescript ve
139 al genetics and functional genomics, and has been chosen for genome sequencing.
140 om the Age-Related Eye Disease Study (AREDS) were chosen for genotyping.
141 ds and specific polyphenols, some selections were chosen for growing and could also be recommended fo
142 ng in which one of the three central symbols was chosen for identification starting with the 1.0- or
143                Altogether, 228 protein spots were chosen for identification, yielding 77 different pr
144              As proof of principle, one drug was chosen for in depth evaluation in vitro and a transg
145 -fluoro-N-pyrrolidylamido)benzothiazole (57) was chosen for in vivo efficacy studies based upon in vi
146 mutant that is hypersensitive to cold stress was chosen for in-depth characterization.
147  The protected form of dihydroxyacetone that was chosen for in-depth study was 2,2-dimethyl-1,3-dioxa
148 stewater microorganisms like Pseudomonas sp. were chosen for in-silico screening toward polyester hyd
149  with the inactivated X of the somatic donor being chosen for inactivation.
150 wo sites within each variable loop of SIV239 were chosen for individual epitope tag insertions.
151                           How incoming cells are chosen for integration or elimination remains unclea
152  sites conserved in all four subtypes of HBV were chosen for intracellular inhibition experiments.
153                       The 12 kDa PEG carrier was chosen for investigating the third parameter, the Ma
154                            The Q67H mutation was chosen for investigation as it was previously found
155                            Pyrene nucleotide was chosen for investigation because it has been previou
156 -mm2 region of the sublingual tongue surface was chosen for investigation.
157                               This index has been chosen for its simplicity and flexibility in handli
158                       The acridine component was chosen for its ability to delivery an appendage to t
159 ve of DNA, and the silyl-protected component was chosen for its ability to generate two quinone methi
160                            The IL-4 cytokine was chosen for its ability to induce a strong host antit
161  this study was poly(ethylene glycol), which was chosen for its ability to reduce nonspecific interac
162 .8 nM for mouse and human MMR, respectively, was chosen for its favorable in vivo biodistribution pro
163 imide derivative carrying a BODIPY dye which was chosen for its fluorescence to be out of the range o
164                                         ApoE was chosen for its potential as a biomarker for Alzheime
165 oid scaffold derived from 4-oxo-4H -chromene was chosen for its radical capture and beta-secretase 1
166  with cerebellar gray matter as a reference, was chosen for kinetic analysis of the (11)C-DED data.
167                      The alpha210GPI protein was chosen for large scale expression in transfected Chi
168 EQ (EhILWEQ) and E. histolytica BAR (EhBAR), were chosen for localization via SNAP tag labeling and l
169 re unique or displayed different intensities were chosen for MALDI-TOF MS analysis.
170 orphisms (SNPs) (referred as "tag SNPs") can be chosen for mapping genes responsible for human comple
171  this group, a random sample of 200 patients was chosen for medical record review.
172                       The central ectodomain was chosen for modification because a peptide spanning a
173 The 8-position of the FAD isoalloxazine ring was chosen for modification because in PHBH it has minim
174 on with the i-motif DNA, and His24 and Arg26 were chosen for modification based on their potential ab
175 The 8-position of the FAD isoalloxazine ring was chosen for modifications, because in PHBH it has min
176 igma = 3.4 x 10(-19) cm(2) molecule(-1)) has been chosen for monitoring trace acetone in exhaled brea
177                                        FGF-2 was chosen for more extensive study in view of its impor
178                   One of these mutants, hr2, was chosen for more in-depth study based on a more hepat
179   Five structurally distinct GalNAc clusters were chosen for more extensive evaluation using ASOs tar
180 tal and the proximal surface of the molecule were chosen for mutagenesis.
181                               Forty residues were chosen for mutation to alanine using the criteria t
182                           One of the methods was chosen for optimisation of the duration of incubatio
183              The most acid-sensitive (Fur)dG was chosen for optimization of solid-phase DNA synthesis
184                  Compound 18 (IC90 = 8.7 nM) was chosen for oral bioavailability studies based on its
185  33-mer (LQLQPFPQPQLPYPQPQLPYPQPQLPYPQPQPF), was chosen for our study.
186 which targets the DNA sequence 5'-WGWWCW-3', was chosen for our synthesis studies as this oligomer ex
187 these data, a fluconazole dose of 200 mg/day was chosen for patient 2 and a dose of 400 mg/day was ch
188 hosen for patient 2 and a dose of 400 mg/day was chosen for patient 3, with clinical resolution in bo
189 iotic with anti-enterococcal activity should be chosen for PD prophylaxis.
190 cle (AMMP) detection, two pathway biomarkers were chosen for pharmacodynamic analysis and compared wi
191                                Of these, two were chosen for pharmacokinetic evaluation, 14 and 17.
192 and thrombocytopenia, and 200 mg twice daily was chosen for phase 2 testing.
193                          Several wavelengths were chosen for photoexcitation, ranging from the S(0)-S
194                                          Two were chosen for physical characterization and were found
195 DLC-1), and nonmetastatic clone 23 (NM23-H2) were chosen for post hoc functional studies based on the
196                             Maximum settings were chosen for power and lavage.
197 nt and highly selective inhibitor of TF/VIIa was chosen for preclinical, intravenous proof-of-concept
198                       An alpha-level of .025 was chosen for primary and secondary comparisons.
199 assays met prespecified criteria, of which 6 were chosen for primary analysis to determine the roles
200  many more dye pairs than that of FRET could be chosen for probe design.
201                      A DEN-2 virus candidate was chosen for production of a monotypic, purified, inac
202                                    If benzyl was chosen for protection of the 3-hydroxyls, all protec
203 explored whether substrates themselves could be chosen for proteolysis via ICD modification.
204    Only the most appropriate patients should be chosen for PTA.
205 respectively from the light and heavy chain, were chosen for quantification of each mAb.
206              Mineral water and energy drinks were chosen for removal of lead since the latter is seve
207 , a beef cattle feedlot, and a sheep feedlot were chosen for repeated diurnal and seasonal measuremen
208     The mechanisms that govern how nucleoids are chosen for replication and distribution are not unde
209     For the shift update rule, an individual is chosen for reproduction proportional to fecundity; th
210 r a mean period of 38.54 mo between studies, were chosen for retrospective analysis.
211             Three important material systems are chosen for review here, all of which are under inves
212  in Slovakia and Pinus sylvestris in Norway) were chosen for sampling in ski resorts.
213           A single acid hydrolysis condition is chosen for screening a large collection of bacterial
214 tails of the distribution, where individuals are chosen for selection.
215                      One aptamer (CELAPT 14) was chosen for sequence minimization and more detailed b
216               Escherichia coli strain MG1655 was chosen for sequencing because the few mutations it c
217 nd archaeal genomes available, most of which were chosen for sequencing on the basis of their physiol
218                                     Residues were chosen for site-specific alanine substitution based
219 ere individuals are in strong competition to be chosen for social interactions.
220 having high intracellular antioxidant levels was chosen for stable overexpression of HABP1.
221                                Five subjects were chosen for stable clinical status and CD4 counts (s
222 ifferent bulk size and electronic properties were chosen for structural analyses by MALDI-TOF, MALDI-
223 classes of flavonoids, at least 12 compounds were chosen for studies.
224                              This TPR domain was chosen for study because its three-dimensional struc
225                                 This antigen was chosen for study because passive immunoprophylaxis,
226 ity for the platelet receptor GPIIb-IIIa and was chosen for study by 1H NMR techniques.
227 nduction in the leaves of treated plants and was chosen for study by in situ hybridisation.
228 of the 120-kDa envelope glycoprotein (gp120) was chosen for study.
229                         CD4(+) T lymphocytes were chosen for study because of the particularly dense
230                                These neurons were chosen for study because they are amongst the first
231 la in order of decreasing side-chain volume) were chosen for study in vitro and in mammalian cell cul
232 opic, and four that were dual- or polytropic were chosen for study of their sensitivity to neutraliza
233                                    Compounds were chosen for study that differed from the parent comp
234 whom the mother's infection status was known were chosen for study.
235 cture, two main areas of subunit interaction were chosen for study: (1) the hydrophobic ball and sock
236              Thus, the SC 5-HT(2C)R antibody was chosen for subsequent studies.
237                         Of 15 compounds, two were chosen for subsequent functional studies, namely ur
238                     How should global models be chosen for such studies, and what effect do such choi
239 fection date estimates between 1996 and 2009 were chosen for surveillance of TDR in HIV-1 subtype B (
240                            A number of these were chosen for synthesis and assessment of their abilit
241 situation where independent Bernoulli priors are chosen for the individual predictors.
242 this case, weakly predicted splice sites may be chosen for the optimal scoring spliced alignment on t
243 d long-term palliation of dysphagia needs to be chosen for the patient.
244 nother one in the blue spectral region, have been chosen for the present study.
245 logies is studied and the optimal morphology is chosen for the BAEC adhesion.
246                                        OccK1 was chosen for the analysis of these transitions, becaus
247  in the control of G1 to S phase transition, was chosen for the analysis.
248 of the MATalpha strain B-4500 (JEC21), which was chosen for the C. neoformans genome project.
249                   A single transfected clone was chosen for the drug screen based on basal luciferase
250                                        PaAPR was chosen for the experiment because it is a highly sta
251         The mixture of methanol/acetonitrile was chosen for the extraction of the compounds and chlor
252           Solid-phase microextraction (SPME) was chosen for the extraction of the compounds from the
253 mplex with the amide analogue of chymostatin was chosen for the initial coordinates for the MD simula
254                         Coulometry detection was chosen for the interrogation of the thin layer, empl
255                           The NL scan method was chosen for the open detection of glucuronoconjugated
256                  The calibration line method was chosen for the quantification of a five-component mo
257                     In this fashion, the C-4 was chosen for the substitution of the second aminoalkyl
258 linked tightly and flanking the TIMP3 locus, were chosen for the analysis.
259 igh and low levels of plasma protein binding were chosen for the development and application of the a
260 ing two Arg's, scattered through the peptide were chosen for the distance measurements.
261 l C(71) butyric acid methyl ester (PC(71)BM) were chosen for the photoactive layer.
262 ion, precipitation, and ion-exchange methods were chosen for the separation of the long-lived beta-em
263 d 2a-c and five types of alkenyl iodides A-E were chosen for the study, thereby demonstrating that th
264                       The MZO nanostructures are chosen for their multifunctionality, biocompatibilit
265  of predefined chemical species, which might be chosen for their metabolic significance, and could be
266                  Therefore, oak chips should be chosen for their potential to release ellagitannins r
267 NPs that are within the MHC and that had not been chosen for their ability to predict HLA alleles, su
268                                  These genes were chosen for their ability to positively or negativel
269 ed because the precursors of the B-CLL cells were chosen for their antigen-binding capabilities by an
270 cillus cereus sensu lato (s.l.) species that were chosen for their genetic diversity within the speci
271 ic style, and Barbary (M. sylvanus) macaques were chosen for their lower level of despotism.
272                        These metal complexes were chosen for their metal open-coordination site and l
273                                These systems were chosen for their structural differences, simplicity
274 measurements of >200 reference probes, which were chosen for their tissue-selectivity, dynamic range
275 inant adeno-associated virus (scAAV) vectors were chosen for therapeutic delivery of the miRNA cluste
276 The SKOV3ip.1 human ovarian cancer cell line was chosen for these studies because it lacks endogenous
277 ues that surround the surface of the protein were chosen for these studies and mutated to cysteine re
278                                 "Older" mice were chosen for these studies to more closely resemble t
279 reforming of biomass derived molecules, have been chosen for this review.
280  graph made of five vertexes and eight edges was chosen for this experiment.
281                       The m-pyridinium group was chosen for this purpose.
282 the rRNA spacer in the large inverted repeat was chosen for this study because it contains both direc
283                                      Cry2Aa2 was chosen for this study because of its toxicity to man
284                                      alpha16 was chosen for this study instead of alpha17, because al
285 at is defective in fliC mRNA translation and was chosen for this study.
286      A retrospective, two-stage panel design was chosen for this study.
287           A Simon's optimal two-stage design was chosen for this trial: an additional 19 patients cou
288                   (89)Zr-labeled trastuzumab was chosen for this validation because it is currently b
289 EDTA, Pb/EDTA, Cd/EDTA, Fe/EDTA, and Cu/EDTA were chosen for this study.
290             Three different SAM-terminations were chosen for this study: (a) carboxylic acid, (b) alc
291                            Five Tm mutations were chosen for this study: the hypertrophic cardiomyopa
292 , rs8129776, rs7354779, and rs2276248, which were chosen for thoroughly covering the locus of interes
293                      The best-fitting models were chosen for three diagnostic groups: acute lymphobla
294 r TRI volume increases, higher-risk patients are chosen for TRI.
295  identification numbers (ID) 1 and 55, which were chosen for vaccine development.
296 asolateral-to-apical transport of K+ and Cl- was chosen for validation by immunofluorescence and conf
297                      Of these, 86 candidates were chosen for validation in adipose from an independen
298 e secretion and morphological abnormalities, was chosen for virulence studies.
299 ragments from a single rectal adenocarcinoma were chosen for whole-exome sequencing followed by mutat
300                       Appropriate parameters were chosen for working hamster cheek-pouch retractor mu

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