1 n the high affinity of DupA to PR-ubiquitinated substrates,
we exploited a catalytically inactive DupA mutant to trap and
2 We exploited a convolutional neural network to embed soundsca
3 We exploited a microbial phospholipase D (PLD), which produce
4 Using a structure-guided approach,
we exploited a newly discovered polar interaction to lock ago
5 Here,
we exploited a reverse genetic system for an enteric CoV, por
6 m the OX1R and OX2R crystal structures bound to suvorexant,
we exploited a single amino acid difference in the orthosteri
7 We exploited an in vitro phage therapy model for studying bac
8 Here,
we exploited antibody cooperativity to develop a therapeutic
9 Here,
we exploited CRISPR interference and programmable base editin
10 cardiac activity, vocal-fold vibrations and other sources,
we exploited frequency-domain analysis and machine learning t
11 Toward this end,
we exploited gramicidin channels as molecular force probes an
12 Here,
we exploited human haploid cells as a robust comparative scre
13 As a means to identify potentially new anti-HIV Abs,
we exploited humanized NOD-scid IL2rgamma(null) mice systemic
14 We exploited intrinsic substrate-recognition properties of el
15 To evaluate the role of MHC clustering,
we exploited nanoscale discoidal membrane mimetics (nanolipop
16 Therefore,
we exploited pharmacological inhibition of sphingolipid metab
17 We exploited putative hypomorphic and EOfAD-like mutations in
18 Here,
we exploited recent developments in virtual reality (VR) and
19 Herein,
we exploited spectral editing techniques to identify and quan
20 solution three-dimensional view of the investigated tissue,
we exploited synchrotron X-ray phase contrast tomography (XPC
21 We exploited the ability to increase the local tissue concent
22 We exploited the anomalous scattering of bromine and iodine t
23 We exploited the broad host range of Fusarium virguliforme to
24 Consequently, here
we exploited the capsule polymerase Cps1B of App1 as an in vi
25 Herein
we exploited the cell-cell communicative properties of exosom
26 echanistic basis of variation in seedling emergence timing,
we exploited the contrasting behaviour of two Arabidopsis tha
27 We exploited the distinctive nature of DURTs and gammadelta T
28 Here,
we exploited the fact that the temporal dynamics of thermal s
29 We exploited the high temporal and spatial resolution of neut
30 In this study
we exploited the hyaloid vascular network in murine eyes, whi
31 We exploited the independence of this PM domain to investigat
32 In this work
we exploited the lipoprotein transport pathway to engineer OM
33 dissect the mechanisms driving human NK cell proliferation,
we exploited the methodology used in cell therapy to numerica
34 We exploited the MinION, a portable nanopore device from Oxfo
35 To map the telomerase side of the interface,
we exploited the predicted structural similarities for human
36 Herein,
we exploited the presence of a unique structural motif of DDX
37 (MGE) associated with archaea of the phylum Thaumarchaeota,
we exploited the property of most MGE to integrate into the g
38 In this study,
we exploited the proximity-based biotinylation approach to id
39 To probe this poorly understood paradox,
we exploited the rapidly evolving Drosophila telomere-binding
40 rted so far; to introduce such an investigational approach,
we exploited the structural motifs of the benzodiazepinic sca
41 To resolve this,
we exploited the unique amenability to mitochondrial DNA muta
42 In this context,
we exploited the validated antitumor targets carbonic anhydra
43 investigate the role of IL-17F and IL-17AF in more detail,
we exploited this "experiment of nature" by creating a mouse
44 We exploited this draft genome sequence to reconstruct the ph
45 We exploited this link to explore the role of the secreted gr
46 We exploited this model through WaterLOGSY nuclear magnetic r
47 We exploited this paradigm to target pancreatic cancer, one o
48 We exploited this phenomenon to find candidate loci underlyin
49 table outside of the seed, especially D-2'-deoxyribose, and
we exploited this property to facilitate exploration of great
50 In detail,
we exploited Vivid(TM) Plasma Separation membrane to threat t