ライフサイエンスコーパス: determine

1 act target of the drug has been difficult to determine.

2 (>=50%), AF recurrence, and AF ablation were determined.

3 effects on I(to) in other species yet to be determined.

4 ary states, fatigue, and quantum yields were determined.

5 scaffold, and PSMA inhibition constants were determined.

6 e biological relevance largely remains to be determined.

7 T quenching, and a range of K(d) values were determined.

8 fruit fly contractile proteins have not been determined.

9 p1lc3b, Me2, Prkd2, and Scarb2) remain to be determined.

10 odrug (PEG-[SN22](4)) compared with SN38 was determined.

11 atio, and pulmonary arterial blood flow were determined.

12 n for culturing SARS-CoV-2 from surfaces was determined.

13 (xylose, glucose, sucrose) in pure water are determined.

14 maintenance of genome stability remain to be determined.

15 romolecule, its tertiary structure was never determined.

16 o the second protonation event as being rate-determining.

17 , and 20 alkyl and halobenzenes were used to determine 39 parameters to calibrate for 6 different RO

18 gain, residual pocket) mainly contributed to determine a treatment failure.

19 We thus determine a trend that the membrane diffusivity drops wi

20 xulub crater - offer a unique opportunity to determine an extinction process during the last 20 milli

21 inities for the A(2A) AR were experimentally determined and investigated through a cycle of ligand-FE

22 om which Threshold Time of sensor signal was determined and then TVC values (CFU/cm(2)) were calculat

23 aggregated, the location of cells is readily determined, and the morphology of the cells is maintaine

24 icantly dysregulated genes and pathways were determined, and those in common with type 2 diabetes wer

25 f antigen expression at the cell surface may determine antibody-mediated cell death.

26 rene Islands, southwestern Indian Ocean), to determine any potential unique characters.

27 (SM) Directive, standardizing the method of determining appropriate nurse staffing for VHA facilitie

28 of a 20 keV Ar(1800)(+) ion on ice has been determined as 1500 (+/-8%) water molecules per Ar(1800)(

29 imal concentration of both drugs for BAT was determined as 5 mg/mL.

30 We determined associations of MC1R genetic risk categories

31 We further determined associations with change in ADHD symptoms.

32 he primary outcome was ventilator-free days, determined at 28 days after admission.Measurements and M

33 The flow-gradient pattern was determined at baseline transthoracic echocardiography an

34 This is determined at population scales for students in Auckland

35 Warning signs were determined based on daily clinical assessments, laborato

36 combination with the anti-spike IgG assay to determine baseline status.

37 ell as a single residue, aspartate 348, that determines both cation selectivity and pH gating.

38 atures can serve as potential biomarkers for determining BRAF mutation status and as predictors of 5-

39 mic, with reduced interstitial sodium stores determined by (23)Na-magnetic resonance imaging.

40 Better and worse eye was determined by 10-2 VF mean deviations (MDs).

41 Many lysosome functions are determined by a lumenal pH of ~5.0, including the activi

42 ity and specificity of the PANDAA assay were determined by a proprietary application designed by Alda

43 nt efficacy for diabetes mellitus is largely determined by assessment of HbA1c (glycated hemoglobin A

44 assessed, and strength of evidence (SOE) was determined by consensus according to standard criteria.

45 report the structure of human SOAT1 (hSOAT1) determined by cryo-EM.

46 ions typical of age-related maculopathy were determined by grading stereoscopic color fundus photogra

47 and B strains in study 1, whereas the titers determined by HI were higher than those determined by MN

48 Cottonseed ethanol extracts were determined by HPLC-MS analysis to be essentially free of

49 to their relative abundances in solution, as determined by hydrophilic interaction-ultrahigh-performa

50 ters determined by HI were higher than those determined by MN against the A/H3N2 strain.

51 the solutions of these fluid inclusions was determined by optical and spectroscopic methods.

52 rt the structure of an unliganded human Fzd5 determined by single-particle cryo-EM at 3.7 angstrom re

53 hNM dynamics was determined by solid-state NMR and revealed that the lame

54 lics, curcumin and antioxidant capacity were determined by spectrophotometry.

55 tion polymerase chain reaction and genotypes determined by subgenomic sequencing.

56 re, the optimal network structure was mostly determined by the data nature (photographic, calligraphi

57 e triggering and magnitude of earthquakes is determined by the friction evolution along faults.

58 fic differences in T(reg) cells from VAT are determined by the tissue niche in a sex-hormone-dependen

59 f trees to withstand drought is likely to be determined by traits associated with their hydraulic sys

60 Total duration of therapy was determined by treating clinicians and the beta-lactam wa

61 tures associated with postoperative PVR were determined by univariate feature selection.

62 e reported, and statistical significance was determined by using the Wilcoxon signed-rank test.

63 poprotein particles co-isolated with EVs was determined by Western blot analysis of lipoprotein marke

64 omogenate) and FATP2, 4, and 6 (MVM, BM) was determined by Western blotting.

65 were crystallized, and their structures were determined by X-ray diffraction.

66 spects and have emerged as key components in determining cancer cell metabolism.

67 Advance in determining cardiac lineage diversification has often be

68 ving CsCLV3, CsWUS, CsFUL1(A) and CsARF14 in determining carpel number variation in an important vege

69 se (UPR)-a signaling network that ultimately determines cell fate.

70 with fluorescence microscopy allows users to determine cells or regions of interest for the targeted

71 This computational study determined changes in IQ [peak IQ, best focus and depth

72 peptidase inhibitor, clade A, member 1), in determining chronic obstructive pulmonary disease risk a

73 nto the RNA structure-function relationship, determining cis- and trans-acting lncRNAs in vivo, and g

74 Electronic patient records were reviewed to determine clinical response to vedolizumab.

75 flexible and pleomorphic assemblies, we have determined cryo-EM structures of apo-CA hexamers and in

76 icies identified significant variability and determined current policies are largely inadequate to en

77 xtracted for later comparison against EEG to determine degrees of accuracy.

78 e evolutionary relationship of subgroups was determined, delineating the divergence between enzymes b

79 entified this QTL plus a few other QTLs that determine developmental trajectories of leaf allometry,

80 e" consisting of several distinct genes that determine different traits of the syndrome and are held

81 Experimental methods to determine disease related miRNAs are time consuming and

82 the ultrasound diagnostic thresholds used to determine disease severity.

83 lt using Partial Least Squares regression to determine dry matter (DM), soluble solids (SS), flesh fi

84 edge of their existence region are not only determined during growth but also at room temperature by

85 Geographic variation in aridity determines environmental productivity patterns, includin

86 intervention, based on principles of CBT, to determine feasibility and preliminary efficacy for preve

87 The MICs of CFDC were determined for 610 Gram-negative bacilli, including 302

88 ee text] and [Formula: see text] states were determined for [Formula: see text]In.

89 Annual and aggregate 5-year incidences were determined for all cataract surgeries and specifically f

90 The apparent diffusion co-efficient was determined for each lesion, and then the mean of each gr

91 We determined frogs' current vulnerability across habitats,

92 onal hazards regression modeling was used to determine hazard ratios for coronary heart disease, CVD,

93 We applied the methods to determine HIV prevalence in men having sex with men in B

94 We also determine how 14-3-3 relieves the negative regulatory ef

95 er ways in which eye-tracking can be used to determine how animals work within attentional constraint

96 ucture and sulfation pattern, allowing us to determine how heparanase recognizes HS substrate and sel

97 We sought to determine how it could influence the gut environment in

98 ted distance while keeping angle constant to determine how path integration operated over both shorte

99 copy suite, as well as functional studies to determine how polyunsaturated phosphatidylglycerols cont

100 was identified, categorized, and analyzed to determine how supervisors affect autonomy of residents.

101 ere, we used a phylogenetic meta-analysis to determine how the mean and variability in antipredator r

102 f sister chromatids has made it difficult to determine how they topologically interact in replicated

103 Here, we determine how two extragenic CREs that are prominent in

104 files of brain region-specific GCN edges, we determined how well the brain region samples could be di

105 ased on longitudinal GPS data, allowed us to determine ideal habitat ratios (grassland:open woodland:

106 The aim was to determine if clinical course or characteristics of mecha

107 The primary objective was to determine if dietary nervonic acid content alters the me

108 Future studies should be designed to determine if our findings directly impact vaccine effect

109 To determine if Pou3f4 is normally required for SGN periphe

110 Purpose To determine if screening with DBT is associated with lower

111 To determine if structure informs function, we generated mi

112 To determine if terrestrial nutrients were incorporated int

113 Therefore, to determine if there is a genetic relationship in a C(4) p

114 However, further consideration is needed to determine if there is sufficient patient load to maintai

115 ed for patient selection in future trials to determine if tricuspid valve intervention improves outco

116 Average pO2 is important for determining if a transplant site and capsules with certa

117 estionnaires were compared to average values determined in healthy volunteers and in patients with es

118 digestibility (TID) of their amino acids was determined in minipigs, to calculate the digestible indi

119 MICs were determined in triplicate via reference broth microdiluti

120 We determined incident dementia including Alzheimer's disea

121 a suitable, rapid, nondestructive method to determine isoflavone composition in ground soybeans.

122 and workup of parathyroid carcinoma (PC) and determine its clinical prognostic parameters.

123 he method as a challenge to the community to determine its security.

124 the antenna relative to the excitation field determines its directional coupling into a six-way cross

125 f the genetic pathway of which it is a part, determining its role in the initial evolution of the Aqu

126 of monthly spectral-domain (SD) OCT scans to determine MA prevalence, incidence, and progression in H

127 Purpose To determine normal liver stiffness, and associated normal

128 While it is not feasible to experimentally determine optimal growth temperature (OGT) for every kno

129 te (D112) in extracellular loop 1 that helps determine Orai1 turnover.

130 Membrane tension pores determine organelle dynamics and functions, giving rise

131 comes reached a steady state and analyzed to determine pathological processes that were activated, in

132 to predict the natural course of disease, to determine pharmacotherapy and the extent of surgery, and

133 Hits can be profiled to determine potency and the site of crosslinking, and subs

134 noma in situ (DCIS) for ER is recommended to determine potential benefit of endocrine therapies to re

135 in CARD, identify trends in AMR mobility and determine previously undescribed and novel resistance va

136 ll single-molecule imaging in human cells to determine rate constants of the AGO2 cleavage cycle in v

137 ol BMP activation in the progenitor niche to determine regenerative outcome in fibrosis.

138 of large complexes and membrane proteins are determined regularly.

139 Based on a mixed effects model, we determined risks of transfer of allergen-specific IgE or

140 CEPR1 in the maternal reproductive tissue in determining seed size and yield, likely via the control

141 The principle QTL determining SET (SET1: dormancy cycling) is physically c

142 proach based on potentiometric titrations to determine solubility limits of various organic compounds

143 ctivity of the regio- and stereoisomers were determined spectroscopically and, in many cases, using s

144 nge in the turnover-limiting and selectivity-determining step induced by the optimal ligand.

145 U(VI) from the UO(2)(s) surface as the rate-determining step rather than electron transfer or ion di

146 residue 848 and cryo-electron microscopy, we determined structures that capture RAG engaged with tran

147 ccurate sub-compartment predictions when SCI-determined sub-compartments are used as labels for train

148 in the different regions in each subject to determine subject specific graph measures.

149 ral targets of cellular immunity and factors determining successful mounting of T cell responses are

150 Factors determining susceptibility to and severity of RSV diseas

151 gical, biochemical, and structural assays to determine that rigosertib, an anti-cancer agent in phase

152 FM) and kinetic modeling which allowed us to determine that septin filament assembly was a diffusion-

153 gas chromatography and mass spectrometry to determine that the majority (>85%) of non-polar extracta

154 n a supramolecular tetrahedral assembly, and determined that a dynamically distinct network of 9 +/-

155 It was determined that both the bromine atom and the phosphate

156 We also determined that breast cancer co-culture stimulated lymp

157 We additionally determined that in l-DOPA-naive rats striatal rAAV-Nurr1

158 this issue of the JCI, Sevillano and authors determined that parenchymal PrPSc plaques of the mouse b

159 Using viral tracing techniques, we determined that PVN -> NAc has origins in the parvocellu

160 a proxy for the neutron-capture reaction and determined that the compact two-dimensional (2D) LiInP(2

161 Using standard morphological assessments, we determined that the lissoirs were produced on ribs of me

162 Here, we determined that transplantation of BAT (+BAT) improves c

163 volume by using restricted cubic splines to determine the association between volume and short-term

164 ppocampal self-regulation abilities may help determine the clinical significance of hippocampal hyper

165 uld modulate microglial function and, if so, determine the consequences for the surrounding tissue.

166 Thus, this model can be used to determine the contribution of host and bacterial factors

167 erichia coli-induced acute pyelonephritis to determine the contribution of neutrophils and monocytes

168 Therefore, we determine the crystal structure of Sulfolobus acidocalda

169 We aimed to determine the diagnostic accuracy of three-dimensional m

170 From the lineshape broadening we determine the diffusion coefficient, the diffusion energ

171 ng the filament at 4-nm intervals and we can determine the domains that associate with features of th

172 um, lead, and arsenic in dried mushrooms, to determine the effect of cooking on the contents of these

173 Our aim was to determine the efficacy, safety, and tolerability of bero

174 activity-dependent tagging system in mice to determine the epigenetic state, 3D genome architecture a

175 ss all size categories and polymer groups to determine the fate and danger of plastic contamination.

176 We performed lineage tracing experiments to determine the fates of peribiliary mesenchymal cells (PM

177 The primary outcome of this study was to determine the frequency of venous thromboembolism and th

178 performed a random effects meta-analysis to determine the growth rates of GA.

179 ), Sr(II), Eu(III), and Ce(III) were used to determine the immobilization potential of carboxybenzotr

180 ion velocity, measure its normal values, and determine the intra- and interobserver variability of me

181 PDA tissue array and cell lines were used to determine the levels of MPC-1 and KDM5A expression, and

182 y and their sense of rotation hypothetically determine the locomotion characteristics of a species.

183 Accordingly, we aimed to prospectively determine the lowest dose of (64)Cu-DOTATATE that facili

184 Studies are needed to determine the mechanisms of mucosal dysregulation in pat

185 ility such as bisulfite Sanger sequencing to determine the methylation status of the Treg-specific de

186 s to combine two decision analytic models to determine the minimum diagnostic accuracy criteria for N

187 In our quest to determine the molecular mechanisms of its antiviral acti

188 yxin-resistant (PR) Klebsiella pneumoniae to determine the molecular mechanisms of PR and the role of

189 We suggest that the effort to determine the neural basis of adaptive behavior could be

190 d to a full-mouth periodontal examination to determine the occurrence of periodontitis and PISA.

191 nonperiodic DFT calculations are deployed to determine the origin of the selectivity for the syn dias

192 we adapt modern image analysis technology to determine the parcel-specific neurite lengths of every n

193 ction in full-length transcripts, helping to determine the pathogenicity of BRCA2 leaky splicing vari

194 rticle analysis (SPA) method to successfully determine the pH-solubility profile, intrinsic solubilit

195 Our aim was to determine the prevalence and associated impact of trypta

196 The main objective of the study was to determine the prevalence of venous thromboembolism event

197 The objective of this study was to determine the relationship between hysteresis, mechanica

198 DS content of the underlying communities, to determine the relative performance (sensitivity, positiv

199 The feedback time constant is shown to determine the relaxation above the critical point.

200 The purpose of this study was to determine the repeatability of (68)Ga-PSMA-HBED-CC in a

201 apabilities, we undertook ITC experiments to determine the respective CMCs of n-octyl beta-d-glucopyr

202 aracteristics of transferring hospitals, and determine the risk factors of transfer and mortality in

203 Thus, we sought to determine the role of dicarbonyl electrophiles in inflam

204 Here we determine the role of mammalian EIPR1 in insulinoma cell

205 To determine the roles of Akt isoforms in this model we cro

206 To determine the severity of damage within these connection

207 This was applied on WGS data to determine the source of human campylobacteriosis, the ge

208 hiral acylated hydroxamic acids were used to determine the stereochemistry of primary amines, as well

209 structure and function of chromatin, we must determine the structures of nucleosomes containing nativ

210 ngredients; additional studies are needed to determine the systemic absorption of additional active i

211 ion of temperature from 5 to 45 degrees C to determine the thermodynamics of the base pair opening fo

212 , we used quantitative kinetic approaches to determine the transient kinetics of recognition and repa

213 hat these electrodes can be used directly to determine the unbound acetaminophen fraction without the

214 Ecologically, the DIB method developed could determine the variation of TPCs within cultivars and was

215 nderstand which irregular corneal parameters determine the visual quality in keratoconus subjects.

216 nations of the individual type signatures to determine the volume ratios of the types.

217 Here, we determined the ability of a C. trachomatis recombinant m

218 sthma Research Program (SARP) III cohort, we determined the association between DHEA-sulfate and perc

219 We determined the crystal structure of the HA protein of th

220 a nucleosome and not just histones, we have determined the crystal structure of the LSD1/CoREST comp

221 standing of the levan synthesis reaction, we determined the crystallographic structure of Bacillus su

222 ionships among dystonia-associated genes, we determined the enrichment of these genes in co-expressio

223 This study determined the incidence and risk factors of obesity amo

224 vely suppressed (AMPKalpha1/alpha2 cKO), and determined the isoform-specific effects in mice of eithe

225 h a first ICH with follow-up to 10 years, we determined the long-term risks of recurrent stroke, disa

226 or 799 northern hemisphere woody species, we determined the number of dimensions needed to summarise

227 en the parental species and the hybrids, and determined the origin of the hybrids.

228 imensionality and chaotic dynamics, we first determined the physiological range of effective coupling

229 osecond X-ray crystallography (SFX), we have determined the pristine structures of the Fe(III) and Fe

230 is of the localization of MEN components, we determined the relative importance of MEN signaling from

231 f medium spiny neurons (MSNs) in the NAc and determined the role of GSK3beta in spike timing-dependen

232 nstability and crystallization kinetics that determines the achievable feature sizes.

233 than surface wettability or surface charge, determines the anti-wetting performance of the composite

234 icrosite concentrations of O(2) , which then determines the PDF of microsites that produce or consume

235 idative decomposition of soil organic matter determines the proportion of carbon that is either store

236 ate of true effects is the major factor that determines the replication rate of scientific results.

237 STing determines the sequence type of traditional 7-gene MLST

238 an alternative biological probe for further determining the clinical utility and safety of pharmacol

239 In conclusion, determining the cPRA per titer is a reliable approach to

240 of exposure to the plume from Mount Etna in determining the high rates of thyroid cancer.

241 We characterize the phase diagram determining the minimal volume of transactions that woul

242 d microbial biofilms play important roles in determining the settlement location of scleractinian cor

243 (NTA), which is a widely used technique for determining the size and concentration of nanoparticles.

244 e microbial cells remains the bottleneck for determining the specific turnover numbers of individual

245 the central role that light regimes play in determining the timing of biological activity.

246 of dark- and light-adapted states have been determined, the molecular mechanisms underlying photoact

247 erties of biological neurons is essential to determine their complement of ion channels and to unders

248 he subgroup of neighbors they 'listen to' to determine their own behavior.

249 identify the features of TOP sequences that determine their potency and quantify these as a metric t

250 ss how to achieve atomically precise NCs and determine their total structures.

251 pectroscopy (TEM-EDX) is a powerful tool for determining these particle characteristics, but it requi

252 ged the primary role assigned to culture, in determining this spatial numerical association (SNA).

253 extensive molecular dynamics simulations to determine three-dimensional (3D) structures of activated

254 ingle-time-point dose factors for tumor were determined to be 11.0, 12.1, 13.6, and 15.2 Gy per MBq/m

255 water columns that span the indentation were determined to be on-path transients that precede the nuc

256 While their structures are normally determined under solvent-free conditions, the structures

257 ar conditions or genetic context, the latter determined using a pairwise genetic interaction map that

258 Iron bioavailability was determined using an in vitro simulated peptic-pancreatic

259 oping alcohol-related cirrhosis and HCC were determined using logistic regression analysis.

260 VL was determined using quantitative PCR and log10 transformed

261 KCC2 and NKCC1 levels were determined using Western blot and quantitative polymeras

262 , we study how these multiple FLC paralogues determine vernalization requirement as a system.

263 um inhibitory concentrations (MIC) were then determined via simple colorimetric reactions in only 4.5

264 tment switches were not important factors in determining visual acuity outcomes.

265 al exercise test to volitional exhaustion to determine VO2 peak with lumbar intrathecal fentanyl or p

266 rs developed 4 sets of guidance: criteria to determine when risk-modeling approaches are likely to id

267 This study was undertaken to determine whether a low residual quantity of dystrophin

268 orescence microscopy, making it difficult to determine whether actin filaments are directly associate

269 d with establishing evidence-based policy to determine whether an RCT with hard outcomes is needed be

270 To determine whether ARL13B is required within cilia, we kn

271 related faces (attentional bias); and (b) to determine whether attentional control moderated this rel

272 To determine whether cell-cycle-dependent gene regulation o

273 enrichment (MPE) and concentration and (ii) determine whether glucose availability or workload regul

274 Purpose To determine whether imaging with the HER2-targeted PET tra

275 The purpose of this study was to determine whether IRMA may evolve directly into NV.

276 The purpose of this study was to determine whether patterns of resting-state connectivity

277 s soil organic C (SOC) must be considered to determine whether planting trees for climate change miti

278 The aim of this study was to determine whether recAP prevents the progression of acut

279 The purpose of the study was to determine whether returning CYP2C19 genotype results alo

280 as a distinct ARDS phenotype.Objectives: To determine whether such Crs-based phenotypes existed amon

281 This study aimed to determine whether the fraction and arrangement of parenc

282 To determine whether the in vitro susceptibility of multi-N

283 This prospective comparative study aimed to determine whether there are phenotypic differences in co

284 ) published during the past 2 decades and to determine whether there has been an improvement in their

285 individuals recovered from mild COVID-19 to determine whether they develop and sustain multifaceted

286 To determine whether this glycosylation site may be the bin

287 The aim of this study was to determine whether Tregs suppress effector T cell-mediate

288 We determined whether an audit on the adherence to guidelin

289 Here, we determined whether mTORC1 signaling is also a target for

290 on in infected lung regions, no studies have determined whether such extreme degrees of perfusion red

291 The presence or absence of PSB then determines whether the two states have fused or not, lea

292 The factors determining whether an individual naive B cell will prol

293 tes to identify any new evidence and to help determine which topics should be the highest priority fo

294 gions of cancer-biology related genes (gHFI) determines which and how many somatic mutations (sM) mus

295 Problematic with class modeling is determining which one-class classifier to use followed b

296 served nucleotide sequences (CNSs) were also determined, which are essential for the activity of the

297 To determine why individuals with MRS specifically lack pan

298 gnitive and affective deficits remains to be determined with a large cohort of participants.

299 n grade II/III) and 1p/19q codeletion status determined with FISH that were accrued from January 1, 2

300 tions, in which the photoproduct ratios were determined with maximum errors of 3%.