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 Two model analytes
were chosen for aggregating AgNPs, potassium phosphate f
16 A total of 16 GABPbeta interface residues
were chosen for alanine scanning mutagenesis.
17 re, an inert human IgG2/IgG4 hybrid C region
was chosen for an rMil2.
18 nomolar activity in the cell-based assay and
were chosen for analyses with isolated tubulin.
19 The relatively stable NS5 region
was chosen for analysis because it allowed for dependabl
20 p19(INK4d)
was chosen for analysis because it usually acts to block
21 e symptomatic knee with higher pain severity
was chosen for analysis.
22 ane immediately superior to the caudate head
was chosen for analysis.
23 line derivatives doxorubicin and aclarubicin
were chosen for analysis because they have been shown to
24 d in midguts and up-regulated by blood meals
were chosen for analysis.
25 llected at both study entry and end of study
were chosen for analysis.
26 graft surgery, Q wave myocardial infarction)
were chosen for analysis.
27 wed overexpression in hippocampus and cortex
were chosen for analysis.
28 rd addition protocol with internal standards
was chosen for analyte quantitation.
29 Compounds 6 and 21
were chosen for analyzing the underlying action mechanis
30 s by which the flow rate and the voltage can
be chosen for any nanosuspension to precisely operate in
31 on has a major impact on which method should
be chosen for AS analysis.
32 Genes
were chosen for assay (32 for bladder; 48 for colon) bas
33 One such compound, ferulic acid,
was chosen for biochemical analysis.
34 ese and other considerations, three pathways
were chosen for biologic validation of the metabolomic d
35 ot be totally avoided when panel members are
being chosen for certain guidelines or in certain settin
36 6E10 and 4G8) used for immunohistochemistry,
were chosen for characterization of their kinetics of bi
37 and orally active factor Xa inhibitor which
was chosen for clinical development.
38 5-HT(4) partial agonist candidates 2d and 3
were chosen for clinical development.
39 265 papers
were chosen for closer screening of the abstracts and 93
40 validity index Classification Accuracy (CA)
are chosen for comparative study.
41 UniGene
is chosen for comparison because of its high quality and
42 isease, and a highly virulent isolate, PSE9,
was chosen for comparison by subtractive hybridization t
43 High fat
was chosen for comparison to determine whether palatabil
44 gions of interest (ROIs) within each patella
were chosen for correlation between ultrashort-TE bicomp
45 CA_C2195
was chosen for crystal structure determination for struc
46 d-type protease ranging from 58 nM to 0.8 pM
was chosen for crystallographic analysis.
47 The liguleless locus (liguleless1)
was chosen for demonstration of targeted mutagenesis in
48 eria by which specific regions of the genome
are chosen for deposition of distinguishing chromatin ma
49 highly conserved region of the PR promoter,
was chosen for detailed analysis.
50 hages were identified, and two of each group
were chosen for detailed analysis.
51 One clone, designated ACAM1000,
was chosen for development based on its comparability to
52 O121 specific, so regions in these two genes
were chosen for development of PCR assays.
53 , allowing the most appropriate functions to
be chosen for displaying the most meaningful positions i
54 ars, when cut-off values of 40 and 0.5 ng/ml
were chosen for DJ-1 and alpha-synuclein, respectively,
55 Nivolumab 3 mg/kg
was chosen for dose expansion.
56 nd therefore the most suitable PCI-IS has to
be chosen for each analyte.
57 a basis for the space of internal fluxes can
be chosen for each microbe in a community and this basis
58 st defect and changes in one marker compound
was chosen for each defect type, that is, indole for lig
59 Three controls
were chosen for each case, adjusted for sex, age, CD4 co
60 The biodegradable thioether-hybridized HMONs
are chosen for efficient co-delivery of tert-butyl hydro
61 and third identifying the therapy that would
be chosen for either themselves or a family member.
62 TNP peptides, two octamers, and two nonamers
were chosen for eliciting anti-TNP CTL responses.
63 ssion and comparison of the results, MgCl(2)
was chosen for evaluating long-term assay performance.
64 ATM
was chosen for evaluation because of the increased radio
65 nnective tissues to allow tissue dissolution
were chosen for evaluation, employing well-known antidep
66 plaque in a proximal coronary artery segment
were chosen for evaluation.
67 es out of 50 subjected to the SA simulations
were chosen for evaluation; these 14 structures have a f
68 well as the potent inhibitor sulfaphenazole
was chosen for examination in further detail.
69 Two RNAi lines
were chosen for examining global protein and metabolite
70 e special pair bacteriochlorophyll dimer, P,
was chosen for excitation.
71 toxicity, a dose of 2.5 x 10(6) cells per kg
was chosen for expansion.
72 Schedule B and a 400-mg dose of venetoclax
were chosen for expansion.
73 and Saccharomyces cerevisiae, respectively)
are chosen for experimental purposes.
74 llion compounds were screened from which 192
were chosen for experimental evaluation.
75 Three
were chosen for experimental testing, based on their low
76 LVE, Ac-YYD, Ac-LLE, Ac-YLD, Ac-MYD, Ac-VIE)
were chosen for experimental validation in order to illu
77 In one model, once an odorant receptor
is chosen for expression, other receptor genes are suppr
78 A total of 62 nondiabetic individuals
were chosen for extremes of insulin sensitivity (31 insu
79 spectra of membrane phosphatidylcholine, has
been chosen for fluorescence and TOF-SIMS imaging of mem
80 dent tumor models, the C18 analogue, NM-404,
was chosen for follow-up evaluation in human lung cancer
81 neous nuclear ribonucleoprotein A1 (HNRNPA1)
was chosen for follow-up since rs3846662, an HMGCR SNP t
82 eturned 4997 citations, of which 84 articles
were chosen for full-text review.
83 ographic data, a subset of these mutants can
be chosen for functional studies to test their importanc
84 A high-ranking candidate STK4
was chosen for functional validation and identified to p
85 These regions may
be chosen for further experimental studies.
86 g such a genome scan, individual regions may
be chosen for further sequencing and a more detailed ana
87 excellent imaging properties in mice and has
been chosen for further evaluation as a potential PET ra
88 R-repressed two-component system (TCS) trxSR
was chosen for further analysis based on its homology to
89 CD58
was chosen for further analysis because of its abundant
90 uciferase activity specifically in petioles,
was chosen for further analysis.
91 ne domain (TM6) of the E. coli protein YjiO,
was chosen for further analysis.
92 nsverse sinuses, a venous ROI input function
was chosen for further analysis.
93 e strain Lactobacillus plantarum ATCC 14917,
was chosen for further analysis.
94 One mutant
was chosen for further analyzes; rme1 (for resistance to
95 Derivative 4d
was chosen for further cell cycle and apoptosis studies
96 tcvSOD
was chosen for further characterization because it was e
97 on (ATF2d), encodes a novel ATF2 isoform and
was chosen for further characterization in this study.
98 One of the highest affinity aptamers, D8,
was chosen for further characterization.
99 One mutant from the second class
was chosen for further characterization.
100 and had cross-reactivity with macaque CTLA-4
was chosen for further development.
101 It
was chosen for further development.
102 he basis of its superior overall profile, 39
was chosen for further evaluation and has progressed int
103 these studies, one of these lines (clone 5)
was chosen for further evaluation.
104 Guar gum (1.5 wt %) with 4 wt % KF
was chosen for further evaluation.
105 ing 143+/-5.5mg sunitinib in the inner layer
was chosen for further pharmacokinetic assessment in viv
106 For these reasons, compound 13-(S)
was chosen for further preclinical evaluation.
107 ated the best anti-inflammatory activity and
was chosen for further research.
108 SmaI
was chosen for further studies because it produced 11 to
109 ne subunit of glutamate dehydrogenase (GDH),
was chosen for further studies for its role in tricarbox
110 A daniplestim dose of 2.5 microg/kg/d
was chosen for further study because it was hematopoieti
111 d the murine pathogen Mycoplasma arthritidis
was chosen for further study.
112 inst a lethal intranasal Y. pestis challenge
was chosen for further study.
113 n5, a component of the spliceosomal complex,
was chosen for further study.
114 n the anthranilate dioxygenase (AntDO) genes
was chosen for further study.
115 d in this screen, the SEPALLATA3 (SEP3) gene
was chosen for further study.
116 r visible abnormalities, and one mutant, V5,
was chosen for further study.
117 Consequently, this mutant
was chosen for further study.
118 miRNAs miR-100 and miR-101
were chosen for further analyses based on their reproduc
119 Five interesting candidate genes
were chosen for further analysis from a larger set of ca
120 (RIL) population derived from these parents
were chosen for further analysis of Cd and Zn tolerance
121 in response to either mild or severe stress
were chosen for further analysis using real-time polymer
122 Two clones
were chosen for further analysis which displayed appropr
123 Viruses from two different time points
were chosen for further analysis, an early culture-adapt
124 DD45B, HO-1, PTGS2, RGS2, TIEG, and ID3) and
were chosen for further analysis.
125 ate plants with a range of expression levels
were chosen for further analysis.
126 The 388 strongest CodY-binding regions
were chosen for further analysis.
127 Five of the newly identified genes
were chosen for further characterization, and clean, unm
128 extraordinary hypersensitivity to mAMSA and
were chosen for further characterization.
129 8, a control positive for both cat and BAG1,
were chosen for further characterization.
130 active CpG-specific methyltransferase M.MpeI
were chosen for further characterization.
131 Five regions
were chosen for further characterization: three correspo
132 g epitopes on the EpCAM extracellular domain
were chosen for further evaluation.
133 these in vitro assays, four compounds (7c-f)
were chosen for further evaluation.
134 Based on this analysis, three models
were chosen for further examination and comparison.
135 es, caveolin-1, caveolin-2, and GDF10/BMP3b,
were chosen for further study on the basis of their loca
136 Sorting Complex Required for Transport-III),
were chosen for further study.
137 ed from the qHTS, 6 distinct chemical series
were chosen for further study.
138 e scFv-phage clones of which two, 5B and 7E,
were chosen for further study.
139 s, showing comparable toxicity and efficacy,
were chosen for further study.
140 ongest reduction in surface HLA-E expression
were chosen for further testing.
141 al genetics and functional genomics, and has
been chosen for genome sequencing.
142 om the Age-Related Eye Disease Study (AREDS)
were chosen for genotyping.
143 ds and specific polyphenols, some selections
were chosen for growing and could also be recommended fo
144 ng in which one of the three central symbols
was chosen for identification starting with the 1.0- or
145 Altogether, 228 protein spots
were chosen for identification, yielding 77 different pr
146 As proof of principle, one drug
was chosen for in depth evaluation in vitro and a transg
147 -fluoro-N-pyrrolidylamido)benzothiazole (57)
was chosen for in vivo efficacy studies based upon in vi
148 The baculoviral vector
was chosen for in vivo gene delivery because of its larg
149 mutant that is hypersensitive to cold stress
was chosen for in-depth characterization.
150 The protected form of dihydroxyacetone that
was chosen for in-depth study was 2,2-dimethyl-1,3-dioxa
151 stewater microorganisms like Pseudomonas sp.
were chosen for in-silico screening toward polyester hyd
152 with the inactivated X of the somatic donor
being chosen for inactivation.
153 Articles
were chosen for inclusion based on their relevance to se
154 wo sites within each variable loop of SIV239
were chosen for individual epitope tag insertions.
155 How incoming cells
are chosen for integration or elimination remains unclea
156 sites conserved in all four subtypes of HBV
were chosen for intracellular inhibition experiments.
157 The 12 kDa PEG carrier
was chosen for investigating the third parameter, the Ma
158 The Q67H mutation
was chosen for investigation as it was previously found
159 Pyrene nucleotide
was chosen for investigation because it has been previou
160 -mm2 region of the sublingual tongue surface
was chosen for investigation.
161 This index has
been chosen for its simplicity and flexibility in handli
162 The acridine component
was chosen for its ability to delivery an appendage to t
163 ve of DNA, and the silyl-protected component
was chosen for its ability to generate two quinone methi
164 The IL-4 cytokine
was chosen for its ability to induce a strong host antit
165 this study was poly(ethylene glycol), which
was chosen for its ability to reduce nonspecific interac
166 .8 nM for mouse and human MMR, respectively,
was chosen for its favorable in vivo biodistribution pro
167 imide derivative carrying a BODIPY dye which
was chosen for its fluorescence to be out of the range o
168 ApoE
was chosen for its potential as a biomarker for Alzheime
169 oid scaffold derived from 4-oxo-4H -chromene
was chosen for its radical capture and beta-secretase 1
170 Guanidinium
was chosen for its specific binding properties toward ox
171 with cerebellar gray matter as a reference,
was chosen for kinetic analysis of the (11)C-DED data.
172 The most selective (SI > 32) compound
was chosen for lethal action and immunomodulatory studie
173 EQ (EhILWEQ) and E. histolytica BAR (EhBAR),
were chosen for localization via SNAP tag labeling and l
174 re unique or displayed different intensities
were chosen for MALDI-TOF MS analysis.
175 orphisms (SNPs) (referred as "tag SNPs") can
be chosen for mapping genes responsible for human comple
176 Herein, 46 tetrapeptides
were chosen for MC3R agonist screening selectivity profi
177 this group, a random sample of 200 patients
was chosen for medical record review.
178 The central ectodomain
was chosen for modification because a peptide spanning a
179 The 8-position of the FAD isoalloxazine ring
was chosen for modification because in PHBH it has minim
180 on with the i-motif DNA, and His24 and Arg26
were chosen for modification based on their potential ab
181 The 8-position of the FAD isoalloxazine ring
was chosen for modifications, because in PHBH it has min
182 igma = 3.4 x 10(-19) cm(2) molecule(-1)) has
been chosen for monitoring trace acetone in exhaled brea
183 FGF-2
was chosen for more extensive study in view of its impor
184 One of these mutants, hr2,
was chosen for more in-depth study based on a more hepat
185 Five structurally distinct GalNAc clusters
were chosen for more extensive evaluation using ASOs tar
186 tal and the proximal surface of the molecule
were chosen for mutagenesis.
187 One of the methods
was chosen for optimisation of the duration of incubatio
188 The most acid-sensitive (Fur)dG
was chosen for optimization of solid-phase DNA synthesis
189 33-mer (LQLQPFPQPQLPYPQPQLPYPQPQLPYPQPQPF),
was chosen for our study.
190 which targets the DNA sequence 5'-WGWWCW-3',
was chosen for our synthesis studies as this oligomer ex
191 these data, a fluconazole dose of 200 mg/day
was chosen for patient 2 and a dose of 400 mg/day was ch
192 hosen for patient 2 and a dose of 400 mg/day
was chosen for patient 3, with clinical resolution in bo
193 iotic with anti-enterococcal activity should
be chosen for PD prophylaxis.
194 cle (AMMP) detection, two pathway biomarkers
were chosen for pharmacodynamic analysis and compared wi
195 Of these, two
were chosen for pharmacokinetic evaluation, 14 and 17.
196 and thrombocytopenia, and 200 mg twice daily
was chosen for phase 2 testing.
197 embrolizumab 200 mg and bevacizumab 15 mg/kg
were chosen for phase II.
198 Several wavelengths
were chosen for photoexcitation, ranging from the S(0)-S
199 Two
were chosen for physical characterization and were found
200 DLC-1), and nonmetastatic clone 23 (NM23-H2)
were chosen for post hoc functional studies based on the
201 Maximum settings
were chosen for power and lavage.
202 nt and highly selective inhibitor of TF/VIIa
was chosen for preclinical, intravenous proof-of-concept
203 An alpha-level of .025
was chosen for primary and secondary comparisons.
204 assays met prespecified criteria, of which 6
were chosen for primary analysis to determine the roles
205 many more dye pairs than that of FRET could
be chosen for probe design.
206 If benzyl
was chosen for protection of the 3-hydroxyls, all protec
207 explored whether substrates themselves could
be chosen for proteolysis via ICD modification.
208 Only the most appropriate patients should
be chosen for PTA.
209 respectively from the light and heavy chain,
were chosen for quantification of each mAb.
210 Mineral water and energy drinks
were chosen for removal of lead since the latter is seve
211 , a beef cattle feedlot, and a sheep feedlot
were chosen for repeated diurnal and seasonal measuremen
212 The mechanisms that govern how nucleoids
are chosen for replication and distribution are not unde
213 For the shift update rule, an individual
is chosen for reproduction proportional to fecundity; th
214 r a mean period of 38.54 mo between studies,
were chosen for retrospective analysis.
215 Three important material systems
are chosen for review here, all of which are under inves
216 in Slovakia and Pinus sylvestris in Norway)
were chosen for sampling in ski resorts.
217 tails of the distribution, where individuals
are chosen for selection.
218 One aptamer (CELAPT 14)
was chosen for sequence minimization and more detailed b
219 Escherichia coli strain MG1655
was chosen for sequencing because the few mutations it c
220 nd archaeal genomes available, most of which
were chosen for sequencing on the basis of their physiol
221 ere individuals are in strong competition to
be chosen for social interactions.
222 having high intracellular antioxidant levels
was chosen for stable overexpression of HABP1.
223 ifferent bulk size and electronic properties
were chosen for structural analyses by MALDI-TOF, MALDI-
224 classes of flavonoids, at least 12 compounds
were chosen for studies.
225 This TPR domain
was chosen for study because its three-dimensional struc
226 This antigen
was chosen for study because passive immunoprophylaxis,
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 la in order of decreasing side-chain volume)
were chosen for study in vitro and in mammalian cell cul
231 cture, two main areas of subunit interaction
were chosen for study: (1) the hydrophobic ball and sock
232 Thus, the SC 5-HT(2C)R antibody
was chosen for subsequent studies.
233 Of 15 compounds, two
were chosen for subsequent functional studies, namely ur
234 lute rate of cervical cancer incidence could
be chosen for such a threshold.
235 How should global models
be chosen for such studies, and what effect do such choi
236 fection date estimates between 1996 and 2009
were chosen for surveillance of TDR in HIV-1 subtype B (
237 A number of these
were chosen for synthesis and assessment of their abilit
238 situation where independent Bernoulli priors
are chosen for the individual predictors.
239 this case, weakly predicted splice sites may
be chosen for the optimal scoring spliced alignment on t
240 d long-term palliation of dysphagia needs to
be chosen for the patient.
241 nother one in the blue spectral region, have
been chosen for the present study.
242 logies is studied and the optimal morphology
is chosen for the BAEC adhesion.
243 OccK1
was chosen for the analysis of these transitions, becaus
244 in the control of G1 to S phase transition,
was chosen for the analysis.
245 of the MATalpha strain B-4500 (JEC21), which
was chosen for the C. neoformans genome project.
246 A single transfected clone
was chosen for the drug screen based on basal luciferase
247 PaAPR
was chosen for the experiment because it is a highly sta
248 The mixture of methanol/acetonitrile
was chosen for the extraction of the compounds and chlor
249 Solid-phase microextraction (SPME)
was chosen for the extraction of the compounds from the
250 th their Bostrychus sinensis photograph that
was chosen for the front cover of the January 2018 issue
251 mplex with the amide analogue of chymostatin
was chosen for the initial coordinates for the MD simula
252 Coulometry detection
was chosen for the interrogation of the thin layer, empl
253 The NL scan method
was chosen for the open detection of glucuronoconjugated
254 The calibration line method
was chosen for the quantification of a five-component mo
255 The content area
was chosen for the robust clinical trial activity in the
256 In this fashion, the C-4
was chosen for the substitution of the second aminoalkyl
257 igh and low levels of plasma protein binding
were chosen for the development and application of the a
258 ing two Arg's, scattered through the peptide
were chosen for the distance measurements.
259 MoSe(2) and WS(2)
were chosen for the near-degeneracy of their conduction-
260 l C(71) butyric acid methyl ester (PC(71)BM)
were chosen for the photoactive layer.
261 ion, precipitation, and ion-exchange methods
were chosen for the separation of the long-lived beta-em
262 d 2a-c and five types of alkenyl iodides A-E
were chosen for the study, thereby demonstrating that th
263 The MZO nanostructures
are chosen for their multifunctionality, biocompatibilit
264 of predefined chemical species, which might
be chosen for their metabolic significance, and could be
265 Therefore, oak chips should
be chosen for their potential to release ellagitannins r
266 NPs that are within the MHC and that had not
been chosen for their ability to predict HLA alleles, su
267 ed because the precursors of the B-CLL cells
were chosen for their antigen-binding capabilities by an
268 cillus cereus sensu lato (s.l.) species that
were chosen for their genetic diversity within the speci
269 These metal complexes
were chosen for their metal open-coordination site and l
270 hia coli, and Clostridium sporogenes species
were chosen for their redox enzyme systems and evaluated
271 These systems
were chosen for their structural differences, simplicity
272 measurements of >200 reference probes, which
were chosen for their tissue-selectivity, dynamic range
273 inant adeno-associated virus (scAAV) vectors
were chosen for therapeutic delivery of the miRNA cluste
274 The SKOV3ip.1 human ovarian cancer cell line
was chosen for these studies because it lacks endogenous
275 ues that surround the surface of the protein
were chosen for these studies and mutated to cysteine re
276 reforming of biomass derived molecules, have
been chosen for this review.
277 graph made of five vertexes and eight edges
was chosen for this experiment.
278 The m-pyridinium group
was chosen for this purpose.
279 Cry2Aa2
was chosen for this study because of its toxicity to man
280 A retrospective, two-stage panel design
was chosen for this study.
281 at is defective in fliC mRNA translation and
was chosen for this study.
282 A Simon's optimal two-stage design
was chosen for this trial: an additional 19 patients cou
283 (89)Zr-labeled trastuzumab
was chosen for this validation because it is currently b
284 Two grades of chalcopyrite
were chosen for this study (moderate and high purity), a
285 EDTA, Pb/EDTA, Cd/EDTA, Fe/EDTA, and Cu/EDTA
were chosen for this study.
286 Three different SAM-terminations
were chosen for this study: (a) carboxylic acid, (b) alc
287 Five Tm mutations
were chosen for this study: the hypertrophic cardiomyopa
288 , rs8129776, rs7354779, and rs2276248, which
were chosen for thoroughly covering the locus of interes
289 The best-fitting models
were chosen for three diagnostic groups: acute lymphobla
290 licated morphology, a pCONus stent and coils
were chosen for treatment.
291 r TRI volume increases, higher-risk patients
are chosen for TRI.
292 Each of these blocks
was chosen for two reasons: to drive the self-assembly i
293 identification numbers (ID) 1 and 55, which
were chosen for vaccine development.
294 asolateral-to-apical transport of K+ and Cl-
was chosen for validation by immunofluorescence and conf
295 atients homozygous for the minor allele) and
was chosen for validation through a CXCL12 protein enzym
296 Of these, 86 candidates
were chosen for validation in adipose from an independen
297 e secretion and morphological abnormalities,
was chosen for virulence studies.
298 ragments from a single rectal adenocarcinoma
were chosen for whole-exome sequencing followed by mutat
299 re collected at the same wards within 7 days
were chosen for whole-genome sequencing (WGS) and a phyl
300 Appropriate parameters
were chosen for working hamster cheek-pouch retractor mu