1 Here,
we have used (
31)P NMR with poliovirus RdRp to show that the
2 oundaries, including Fab-7 and Mcp To study Pita functions,
we have used a boundary replacement strategy by substituting
3 In this study,
we have used a combination of phylogenetic analyses with synt
4 Here,
we have used a fluorescence-based anisotropy assay to quantit
5 Here,
we have used a genetic approach to demonstrate that activatio
6 We have used a knock-out/knock-in strategy in Drosophila to g
7 rstanding of the molecular mechanisms of filament assembly,
we have used a synthetic biology approach to reconstitute, in
8 ion, which is known to be highly induced under salt stress,
we have used a Y1H system to screen a salt induced rice cDNA
9 We have used Caenorhabditis elegans as an invertebrate model
10 Therefore,
we have used cellular expression profiling tools to define th
11 We have used chronic electrophysiological recordings to inves
12 We have used co-immunoprecipitation and mass spectrometry to
13 Specifically,
we have used E-AB sensors to perform the multihour, real-time
14 We have used fluorescence correlation spectroscopy and cross-
15 Here,
we have used focused ion beam-scanning electron microscopy to
16 stent with the hypothesis of an apoptotic ceramide channel,
we have used here assays of calcein release from liposomes.
17 We have used high-speed pressure clamp and elastomeric pillar
18 Here
we have used human primary CD56(Pos) satellite cell-derived m
19 We have used Intracellular Antibody Capture technology to iso
20 We have used isotope labeling and two-dimensional infrared sp
21 We have used isoxazolo[3,4-b]pyridin-3(1H)-one and isoxazolo[
22 We have used mass spectrometry with (13)C tracers to systemat
23 In this study,
we have used molecular and genetic approaches to investigate
24 Here,
we have used mouse liver CRMs involved in regulatory activiti
25 Here, in a complementary study,
we have used our structure of Cdc42 bound to ACK via an intri
26 We have used pharmacological tools to explore the chemical sp
27 We have used RNA-sequencing analysis and linear mixed models
28 Here,
we have used single-molecule florescence resonance energy tra
29 Here,
we have used single-molecule fluorescence resonance energy tr
30 In this study
we have used single-molecule localization microscopy (SMLM) t
31 We have used structure-guided SCHEMA recombination to create
32 We have used targeted locus amplification (TLA) to efficientl
33 We have used the aldolase enzyme as a model protein to conduc
34 olecular modulators of synaptic stability and degeneration,
we have used the Cln3 (-/-) mouse model of a juvenile form of
35 In this study
we have used the cut-open oocyte voltage-clamp technique to i
36 Here,
we have used the epidermis as a model system to elucidate the
37 Toward this end
we have used the specially adapted version of H/D exchange ex
38 We have used the spectral clustering algorithm to cluster the
39 We have used thermodynamic insights to predict and demonstrat
40 We have used these reporters to measure differences in BER ca
41 We have used this stabilized background to study the effects
42 We have used this system to show that the nucleosome dramatic
43 Considering that the methodologies
we have used to delete Oxtr do not rule out targeting the nei
44 We have used transient absorption spectroscopy to compare the
45 Here,
we have used two-photon Ca(2+) imaging to monitor the activit
46 We have used umbrella sampling and multimicrosecond molecular
47 In this study
we have used Unlocked Nucleic Acids (UNAs) to discriminate a
48 Here,
we have used unnatural amino acid photo-cross-linking to inve
49 To this end,
we have used well-tempered bias exchange metadynamics simulat
50 To gain insight into how this occurs, here
we have used X-ray crystallography to describe the structures