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