1 Here,
we use 180 pairs of transcranial magnetic stimulation for app
2 Here,
we use a chromatin signature to infer MAE for genes in lympho
3 Here,
we use a different approach: we propose a model for language
4 In this paper,
we use a high-throughput microfluidic platform as a quantitat
5 Here
we use a library of Xenopus tropicalis genomic sequences in b
6 We use a multi-echo sequence with independent components anal
7 In the present work,
we use a nonlinear mathematical model representing the course
8 e of tactile defensiveness in autism.SIGNIFICANCE STATEMENT
We use a novel paradigm of repetitive whisker stimulation and
9 We use a numerical landscape evolution model to demonstrate t
10 Here
we use an engineered organotypic model of perfused microvesse
11 Here
we use an integrated photonic chip with a circuit-based appro
12 Here,
we use bacteria engineered with a strong Allee effect to inve
13 Here
we use biochemical and structural methods to show that two mo
14 Here,
we use ChAP-MS (chromatin affinity purification with mass spe
15 We use classical molecular dynamics and hybrid quantum mechan
16 Here,
we use computational methods to investigate small numbers of
17 Here,
we use CRISPR base editors to knock out genes by changing sin
18 Here
we use data from 3,035 sampling plots worldwide, to quantify
19 Here
we use extreme value theory to combine sea-level projections
20 Here
we use fMRI to relate changes in single voxel receptive field
21 Here
we use four-dimensional confocal microscopy of live animals t
22 Here,
we use genetic association of molecular, cellular, and human
23 Here,
we use genotypic data to study range-wide patterns of genetic
24 Here
we use geometric morphometrics and phenotypic matrix statisti
25 In this study,
we use glycoconjugates of type 3 Streptococcus pneumoniae CPS
26 Here,
we use in vivo functional imaging to identify a class of cuta
27 In this study,
we use Intergovernmental Panel on Climate Change (IPCC) Tier
28 Here
we use magnetic fields approaching 100 Tesla to reveal the ex
29 Here,
we use mobile phone data to quantify seasonal travel and dire
30 We use molecular dynamics simulations to resolve the molecula
31 To advance their utility,
we use noncovalent interactions to incorporate the biological
32 Here,
we use optical tissue clearing and a TAM-targeting injectable
33 Here
we use overexpression studies, mutagenesis, and flow cytometr
34 Here
we use ozone-activated silver-gold alloys in the form of nano
35 Here
we use precise data on over 50,000 Drosophilid fly wings to d
36 Here
we use resting-state fMRI data from 176 subjects to show that
37 Here,
we use stable isotopes and NanoSIMS to show that the cyanobac
38 Here,
we use superresolution structured illumination microscopy wit
39 We use the correlations of CO2 with trace elements to define
40 We use the experimentally constrained model to evaluate the c
41 Here
we use the nematode, Caenorhabditis elegans, to explore these
42 enriched in drugs (druggable CATH functional families) and
we use the network properties of these druggable protein fami
43 Here
we use the rapid turnover of venom genes in parasitoid wasps
44 To generalize to multistable stochastic system,
we use the stochastic least-action principle to derive the en
45 country, we estimate a common dose-response function, which
we use to compute national electricity loads for temperatures
46 elevated or suppressed oligomerization respectively, which
we use to tune the levels of Raf/MEK/ERK signaling.
47 We use two dimensionality reduction methods as well, robust P
48 Here
we use two independent systems to impair hepatocyte prolifera
49 Here
we use whole-genome sequences to examine the origin and adapt
50 Here
we use zebrafish larvae with pan-neuronal expression of GCaMP