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1 asive, and for the first time, greatly enhances our ability to measure neonate turtle sex ratios at population levels acr
4 We used multivariate pattern analyses to measure reactivation of initial pair memories (A items) du
5 ity numerically along their own continuum of normality, and to measure any surgical changes against such a personalized b
6 pment, optimization, and applications of optical approaches to measure the spatial and temporal profiles of NT and NM rel
7 We used an enzyme-linked immunosorbent assay to measure levels of spontaneous release of molecules from ma
9 innovative single-molecule imaging approach in yeast cells to measure chromatin association of individual replisome subu
10 ecies; however, these reproductive barriers are challenging to measure within natural populations.
11 ded in the Tox21 portfolio are assays specifically designed to measure interference in the form of luciferase inhibition
12 Instruments were eligible if they were originally developed to measure the concepts of interest or developed in non-mealt
13 electrical resistivity measurement systems, it is now easy to measure the weighted mobility (electron mobility weighted
14 s the temperature-dependent loss of conformational epitopes to measure thermostability of GP embedded in viral membranes.
15 lifetime and blood flow imaging were performed in both eyes to measure retinal oxygen contents and total retinal blood fl
16 Here, we develop a quantitative framework to measure absolute abundances of individual bacterial taxa b
19 of their impact has been hampered by a lack of methodology to measure the amount of, and variability in, their intracell
20 d lethal factor (LF), we use sensitive quantitative methods to measure their enzymatic activities in mice intranasally ch
21 to various subcellular regions via sequence specific motifs to measure spatiotemporal changes in ERK activity.
22 Dams were allowed to deliver normally to measure pregnancy and neonatal outcomes, with a subset sac
23 We then used dLight fiber photometry to measure dopamine binding across the ventral striatum (medi
24 Our research demonstrates the potential to measure and characterise different steel thicknesses by de
25 leads to systematic errors in the ability of these programs to measure expression, including systematic underestimates of
27 measured after anti-CD3 or vaccinia virus (VV) stimulation to measure T cells elicited after childhood smallpox vaccinat
28 Coordinators Group, has implemented an assessment strategy to measure quality and impact of its entire training portfoli
29 RNFL may indicate that GCL thickness could be better suited to measure progression of structural glaucomatous loss.
30 ess feasibility and acceptability of using the NOTSS system to measure surgical team performance.
31 enotype-phenotype maps; however, it can be a herculean task to measure every phenotype in a combinatorial map.
34 Our method combines computational geometry and graph theory to measure the degree of order of any packed tissue.
35 rene-labeled actin has become the most widely employed tool to measure the kinetics of actin polymerization and the inter
36 ose oxidase (GOD) enzyme onto an ultramicro electrode (UME) to measure the local glucose consumption of Streptococcus mut
37 e electromyography of the suprahyoid muscles was undertaken to measure the swallowing muscle excitation, which then confi
38 sement membrane extract hydrogels (Matrigel) that allows us to measure contractile force from the shape of the relaxed an
39 ged with high-resolution X-ray computed tomography are used to measure aggregate structure and describe their morphology
40 Spontaneous blink rate (SBR) has previously been used to measure stress responses in humans and may provide a non-i
41 th osmotically induced changes in droplet volume being used to measure cell metabolism, while simultaneously imaging the
42 then apply reduced-form econometric methods, commonly used to measure the effect of policies on economic growth(5,6), to
43 terial spin labeling (ASL) is a neuroimaging technique used to measure cerebral blood flow (CBF; perfusion) to understand
45 In this work, X-ray fluorescence microscopy was used to measure diffusion constants of K(+), Cu(2+), and Cl(-) dif
47 Furthermore, flow cytometry was used to measure the frequency of EBV-specific T-cell responses bet
48 conditions, a high-throughput phenotyping facility was used to measure WUE(plant) in a recombinant inbred line (RIL) popu
50 We employ HIOs generated in this way to measure CFTR function using cystic fibrosis patient-derive