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1 To quantify this rewiring of contacts at a certain position i
2 eletal metastases over standard imaging methods, being able to quantify biologic processes related to the bone microenvir
3 nsive optimization of experimental parameters, we were able to quantify down to ~10(9) vesicles/mL, using as little as 60
6 Here, we provide a global-scale meta-analysis to quantify how changes in the diversity of organic matter de
7 his line of research and used a preregistered meta-analysis to quantify the longitudinal associations between reward proc
8 containing eGFP-Wnt-3a to visualize its binding to FZD and to quantify Wnt-FZD interactions in real time in live cells,
9 S) and a broad range of childhood psychiatric symptoms, and to quantify the extent to which such associations can be attr
10 nt for this variability using a spatially explicit approach to quantify regional-scale diversity through the Phanerozoic.
11 reaction monitoring (MRM)-based targeted proteomic approach to quantify systemically the changes in expression of small G
12 address this problem, we describe a diversity of approaches to quantify intrinsic growth rates of plant populations, incl
13 Here we used a modified Ramsay assay to quantify the impact of Malpighamoeba infection on fluid se
14 grate SVs with RNA-sequencing from human post-mortem brains to quantify their dosage and regulatory effects.
17 vironments where growth substrate availability is difficult to quantify can have large downstream impacts on our ability
18 this analysis underlines the need for a coordinated effort to quantify the genetic and biochemical diversity of this spe
21 aviventer) living in two different elevational environments to quantify age-specific reproductive success of daughters bo
23 lear theranostic model by showing a requirement for imaging to quantify, in situ, the concentration of a metastable bioan
24 15.8 years) underwent optical coherence tomography imaging to quantify foveal point thickness and foveal pit diameter, d
26 Here, we use a general model based on biochemical kinetics to quantify the combined effects of water content, body size
27 curacy in lifetime measurements and provides powerful means to quantify biochemical dynamics in living cells.
29 Herein, we established a novel method to quantify SCFAs by coupling amidation derivatization of SCF
30 It successfully identified a methodology to quantify microcirculatory alterations associated with dise
31 eline using plus-end tip tracking and intravital microscopy to quantify MT dynamics in live xenograft tumor models.
32 tive range and applied spatially varying coefficient models to quantify region-specific trends in trait coordination and
33 generated semiautomated and flexible ImageJ2/Fiji pipelines to quantify kinetochore misalignment at metaphase plates as w
34 nnings of subjective perception, and offers the possibility to quantify or manipulate such priors in future studies.
35 entiation Genes' Interaction Enrichment (DGIE) is presented to quantify the interaction enrichment of genes related to di
36 c imaging (MRSI) 7 Tesla (7 T) provides enhanced resolution to quantify GABA and Glu levels in the thalamus of CHR indivi
39 otein and employ isotope-labeled peptide internal standards to quantify chosen surrogate peptides.
40 n one of the authors (K.J.H.) published an organized system to quantify the accuracy of intraocular lens (IOL) power calc
41 with radiolabeled exendin has proven to be a powerful tool to quantify beta-cell mass (BCM) in vivo.
42 our model is performed in a Bayesian framework, allowing us to quantify uncertainty in the allocation of proteins to new
43 Single-molecule spectroscopy allows us to quantify the effects of crowding on a comprehensive set of
45 Therefore, under these circumstances, the 2-FDG LC used to quantify in vivo glucose utilization should not be expecte
47 tio (VR) and coefficient of variation ratio (CVR) were used to quantify relative variability in symptom change.
49 Therefore, the objective of this study was to quantify the effect of maternal heat exposure during early