1 lts with respect to the definition of forest
we employed.
2 We employ a Bayesian approach to estimate the posterior
3 We employ a bulky methylcyclopropylacetoxymethyl ether t
4 Here
we employ a combination of NMR, fluorescence spectroscop
5 Here
we employ a combined approach of ab initio protein model
6 Furthermore,
we employ a custom image-based method for measuring hypo
7 We employ a flexible graph encoding to preserve multiple
8 In this paper,
we employ a joint analysis scheme of experimental data a
9 We employ a kinetic model for cell morphological sicklin
10 We employ a method of quasi-static compression elastogra
11 We employ a modular 2-D strategy wherein the central mod
12 Here
we employ a new technique, reflection enhanced two-dimen
13 Here
we employ a novel analytical approach that incorporates
14 Here
we employ a quantum-mechanical Hamiltonian model for van
15 Here,
we employ a recently developed concatenated tandem array
16 In this work,
we employ a recently developed multifunctional trityl pa
17 Here,
we employ a self-accelerating optical pump wave-packet t
18 Here
we employ a set of RNA Polymerase II (Pol II) activity m
19 Herein,
we employ a single-molecule fluorescence method to asses
20 We employ a statistical method, TROM, to identify both p
21 We employed a Bayesian phylogeography approach to charac
22 In study 2,
we employed a big data approach to explore the time cour
23 To address this question,
we employed a cell type-specific viral expression approa
24 To address this challenge,
we employed a cell-based, high-throughput method using a
25 We employed a central composite design to study three va
26 Here,
we employed a combination of behavioral, molecular and c
27 We employed a combination of both (15)N{(13)C} rotationa
28 ective role of TBK1 in cancer cell survival,
we employed a combination of broad-scale chemogenomic an
29 We employed a combination of genomics, computational bio
30 In this study,
we employed a combination of MALDI imaging mass spectrom
31 Here,
we employed a combination of ultra-performance liquid ch
32 To explore this possibility,
we employed a computational model for supragingival plaq
33 We employed a difference-of-Gaussian model to capture th
34 In this work,
we employed a DNA methyltransferase Dnmt3a-Dnmt3L constr
35 As scaffold,
we employed a double-stranded DNA rotaxane for its abili
36 hout substantially altering cell phenotypes,
we employed a fluorescence activated cell sorting method
37 We employed a functional-morphological approach, combini
38 In this study,
we employed a gene-centered approach utilizing the yeast
39 We employed a genome-resolved metagenomic approach to re
40 Here,
we employed a glycosylphosphatidylinositol (GPI)-scFv X5
41 In this study,
we employed a helper virus-based reverse genetics system
42 ks that control this differentiation switch,
we employed a high-throughput microfluidic imaging syste
43 elineate the underlying molecular mechanism,
we employed a high-throughput strategy to characterize t
44 In this study,
we employed a hybrid diffuse optical system consisting o
45 We employed a hybrid simulation and experimental approac
46 For this study,
we employed a library preparation method in which sequen
47 We employed a mathematical model to reveal the penetrati
48 Also,
we employed a mice model to study the inflammation and p
49 We employed a modified genotyping-by-sequencing approach
50 We employed a monozygotic (MZ) twin difference design to
51 brils within the pregnancy microenvironment,
we employed a mouse bioassay and RT-QuIC.
52 To test this,
we employed a mouse model for conditional ablation of Sm
53 In this Technical Note,
we employed a multimodal imaging approach, using matrix
54 We employed a murine model of influenza infection to ide
55 To address these points,
we employed a novel cationic bolaamphiphile that binds T
56 We employed a novel procedure designed to capture spectr
57 We employed a novel statistical approach, Bayesian kerne
58 Here
we employed a novel weight-transportation task, in which
59 ide strands correlating with gene knockdown,
we employed a peptide-nucleic acid (PNA) hybridization a
60 We employed a phage-displayed ubiquitin variant (UbV) li
61 in initiating PIWI-directed gene silencing,
we employed a Piwi-interacting RNA (piRNA)-targeted repo
62 To unravel this puzzle,
we employed a poly(A) tag sequencing protocol and uncove
63 We employed a portable emissions measurement (PEMS) to m
64 Here
we employed a quantitative mass spectrometry approach to
65 Here,
we employed a quantitative mass spectrometry-based appro
66 We employed a recently developed computational approach,
67 We employed a retrospective cohort approach using longit
68 We employed a RNAi screen simultaneously monitoring diff
69 We employed a SEFL paradigm in inbred male and female C5
70 Here,
we employed a series of techniques, including size-exclu
71 Here,
we employed a social exclusion paradigm, namely the Cybe
72 We employed a split-colony design where one half of a co
73 First,
we employed a strain lacking fliL.
74 te the role of macrophages during infection,
we employed a system with a shifted proinflammatory macr
75 We employed a tiered approach that first examined proces
76 To assess the paracrine contributions,
we employed a Transwell system in which HE-iPSCs were se
77 We employed a tryptophan scan to the protein surface one
78 We employed a two-component strategy, allowing peptide a
79 We employed a unified synthetic strategy for constructio
80 We employed a unique combination of long-term (1980-2010
81 Here,
we employed a unique molecular ecological approach and c
82 We employed a whole-genome segmented amplification appro
83 We employed a within-session behavioral-economic (BE) pr
84 We employ ab initio and density functional methods to in
85 We employed affinity purification and immunoblotting to
86 First,
we employ an Earth system model to illustrate how the re
87 Here
we employ an optogenetic approach to explore the effect
88 Here,
we employ an ultrasensitive three-dimensional (3D) chemi
89 ics of early events in trypanosome division,
we employed an "AEE788 block and release" protocol to st
90 In this study,
we employed an adapted change detection paradigm to inve
91 We employed an anti-Brownian electrokinetic (ABEL) trap
92 We employed an anti-transducin antibody (Galphat-S), in
93 We employed an approach that involves the searching of m
94 We employed an established observe/imitate task of emoti
95 We employed an Illumina iSelect 90K single nucleotide po
96 ns that might contribute to cardiac disease,
we employed an in silico screen for cardiac-enriched cDN
97 Here,
we employed an in vitro technique called single-molecule
98 le markers of corneal epithelial stem cells,
we employed an inducible transgenic "pulse-chase" murine
99 Here
we employed an innovative progressive black top hat tran
100 In this study,
we employed an integrated approach that combines computa
101 We employed an integrated strategy combining pharmacokin
102 Here,
we employed an integrative strategy for the repositionin
103 Here,
we employed an integrative systems immunology approach t
104 To test this hypothesis,
we employed an isolated perfused rat kidney model.
105 the fundamental mechanisms in these systems,
we employed an operando multimodal x-ray characterizatio
106 Here,
we employ and validate an RNA-sequencing-based method to
107 To illustrate this strategy,
we employed aryl fluorosulfates, an underexplored class
108 In this work,
we employ atomic-scale simulations to uncover the interf
109 occur when an optic nerve glioma is present,
we employed atomic force microscopy to measure the stiff
110 Herein,
we employed attenuated total reflection Fourier transfor
111 Here
we employed backscattering interferometry (BSI), a free-
112 We employed BCL11A overexpression with recombination sub
113 We employed behavioral, MRI, and biochemical techniques
114 We employ bi-phase emulsion droplets fabricated from imm
115 Here,
we employed bioinformatic analysis and immunofluorescenc
116 Here,
we employed bioinformatics and molecular genetics to ide
117 Here,
we employed both chemical treatment and cells that were
118 Finally,
we employed CaMPARI and optogenetics for functional circ
119 e heart tissue from HIV-1/SIV-infected cells
we employed cell and molecular biology approaches to inv
120 Here
we employed cell signaling pathway signatures to predict
121 We employed ChIP-seq and 4sU-RNA-seq to identify aberran
122 We employed ChIP-sequencing for H3K4me3 to examine effec
123 We employed coarse-grained Langevin dynamics simulations
124 and abp1-TD1, and the TILLING mutant abp1-5
We employed Coimbra, an accession that exhibits an amino
125 We employed complementary biophysical methods, including
126 functional magnetic resonance imaging study,
we employed computational modeling to elucidate the neur
127 We employed Cox proportional hazards regression analysis
128 Here,
we employ CRISPR/Cas9 technology to build a cloning-free
129 Here
we employ CRISPR/Cas9 to facilitate use of the dimerisab
130 We employed data from a sucrose injection experiment in
131 In this study,
we employed data from ChEMBL20 to examine the evolution
132 Here,
we employed de novo complementarity determining region (
133 Third,
we employ deep convolutional neural networks (CNNs) to r
134 We employ deformable image registration methods to segme
135 Here
we employ detailed quantum transport modeling of photocu
136 We employ DFT(M06-2X) computations to understand the mec
137 We employ diabetes as an exemplar and discuss its comorb
138 To address this,
we employed diffusion tensor magnetic resonance imaging
139 Here
we employ direct, real-time, biochemical and physiology-
140 Here,
we employ diverse CRISPR/Cas9 genome editing tools to ge
141 in VP1 outside the SA11-tsC genetic context,
we employed ectopic expression systems.
142 The functional trait perspective
we employed enabled capturing community processes in ana
143 into a vein, which, for the rat animal model
we employ,
entails devices less than 200 mum in diameter
144 We employ EPA's CMAQ model to the continental U.S. durin
145 Here
we employed equilibrium hydrogen/deuterium fractionation
146 In this study,
we employed explorative mass spectrometry to profile pro
147 We employed facility-demand models (active travel) and l
148 Here
we employ first-principles calculations to discover a br
149 At the lowest water contents,
we employed fixed relative humidities to control water f
150 We employed fluorescence imaging and GCaMP6 reporter mic
151 Here,
we employed fluorescence resonance energy transfer (FRET
152 We employed fluorescence-activated cell sorting (FACS) t
153 Herein,
we employed fluorescently labeled alpha-syn preformed fi
154 To prove the concept,
we employed free energy perturbation (FEP) coupled with
155 Here,
we employed fundus photography, spectral domain optical
156 self was essential for Leishmania viability,
we employed "
genetic metabolite complementation." First,
157 We employ genetics, cell lineage tracing, and single mol
158 cing revealed several of the KDSR mutations,
we employed genome sequencing to discover a pathogenic 3
159 Here,
we employed genomic DNA sequencing of multiple variable
160 uctural family on ligand-gated ion channels,
we employed HEK cells transfected with cDNAs encoding th
161 transfer process linked to the Q reduction,
we employ here multiscale quantum and classical molecula
162 Here
we employ heterologously expressed seleno-fragments to o
163 Here
we employ high-resolution transmission electron microsco
164 Here
we employed high-resolution (1)H nuclear magnetic resona
165 Here,
we employed high-resolution confocal microscopy to analy
166 Therefore, in this study
we employed human islets isolated from donors with and w
167 Here,
we employed hydrogen-deuterium exchange mass spectrometr
168 Herein,
we employed hydrogen-deuterium exchange MS (HDXMS) to sp
169 Here,
we employed hydrogen/deuterium exchange coupled with mas
170 In the present study,
we employed immunofluorescence staining and Western blot
171 Here,
we employ in situ liquid-cell transmission electron micr
172 We employ in-situ transmission electron microscopy and o
173 of the SWI/SNF chromatin remodeling complex,
we employed in vitro models of melanocyte differentiatio
174 ze the gross dimensions of full-length NEMO,
we employed in-line size exclusion chromatography-small-
175 We employed infrared spectro-electrochemistry and site-s
176 Here,
we employed integrated population models to demonstrate
177 tance of microRNAs (miRNAs) in neurogenesis,
we employed isogenic human RTT patient-derived induced p
178 Here,
we employ isothermal titration calorimetry and NMR spect
179 Here
we employ isotopic labeling combined with hyperspectral,
180 Here
we employed iterative deletion mapping to elucidate how
181 Here,
we employed laboratory experiments to measure the influe
182 Here,
we employed LAESI-MS to explore the well characterized s
183 Here,
we employ large-scale, all-atom molecular simulations an
184 We employed live-cell imaging, gene silencing and coimmu
185 We employ LMJ-SS in the ex vivo analysis of mouse brain
186 In this study,
we employed LPMO9C from Neurospora crassa, which is acti
187 We employed lymphocyte-laden microwell technologies to m
188 We employed machine learning in an unsupervised, unbiase
189 We employ measurements throughout an entire winter from
190 We employed metabolic (15)N labeling and shotgun ultra-h
191 Here
we employ metal triflates, which are water-tolerant Lewi
192 As SCNP system
we employed methyl methacrylate (MMA) statistically copo
193 Here,
we employed MHC class II tetramers designed to immunodom
194 We employ micropipette aspiration to show that anisotrop
195 We employed microwave conductivity, X-ray photoelectron
196 In parallel experiments,
we employed mito-TALENs to induce breaks in distinct loc
197 Here
we employ molecular dynamics simulations to determine wh
198 To establish this relation,
we employ molecular dynamics simulations to generate kno
199 We employed molecular cloning to examine how PTEN's stab
200 Here,
we employed molecular modeling, mutagenesis, and patch c
201 Here
we employ mouse models to define the role of MCSCs as me
202 on and loss of brain mass in the cKO cortex,
we employed mRNA sequencing (mRNA-Seq), immunohistochemi
203 We employ multi-muscle spatial sampling and deconvolutio
204 Here,
we employed multi-scale models to determine how intersti
205 We employed multiple genetic mouse models for stringentl
206 In this study,
we employed multiple surface-sensitive techniques to cha
207 Here,
we employed multiscale analyses to identify and characte
208 We employed multivariable linear regression to evaluate
209 We employed nanoString nCounter system for miRNA profili
210 Here
we employed native mass spectrometry (MS) to determine h
211 Here
we employed neuroanatomical tracers to map projections f
212 Here,
we employ newly developed quantitative imaging methods t
213 To determine the potential role of lncRNAs,
we employed next generation sequencing to examine the tr
214 Here,
we employed nuclear magnetic resonance (NMR) and biochem
215 We employ OH* chemiluminescence to visualize the evoluti
216 e the efficiency of combinatorial screening,
we employ orthogonal Cas9 enzymes from Staphylococcus au
217 We employ our modelling concept to analyse calcium spike
218 We employed our approach to capture a panel of 5000 STRs
219 In this study,
we employ Overhauser dynamic nuclear polarization (ODNP)
220 ules governing binding to the AR of zDHHC17,
we employed peptide arrays based on zDHHC AR-binding mot
221 Taking advantage of this dependence,
we employed pharmacological inducers of autophagy to inc
222 Here
we employed physically separated neuron-astrocyte cocult
223 To this end,
we employed physiologically relevant HBV infection model
224 In task 2,
we employed pictures of partially exposed snakes, lizard
225 In Task 1,
we employed pictures with close-ups of snake skins, liza
226 In this study,
we employed planar pore-spanning membranes (PSMs) prepar
227 Here,
we employ potato spindle tuber viroid (PSTVd) infecting
228 We employed probe 2 and label-free mass spectrometry to
229 To address this knowledge gap,
we employed proteomics approaches to analyze blood sampl
230 In this study,
we employed proteomics to identify mechanisms of posttra
231 Here,
we employ PSCs to identify the key minimal signaling pat
232 Here
we employ purified, intact and active VanSA membrane pro
233 We employed quantitative proteomics to characterize Hat1
234 Here,
we employed quantitative proteomics to profile protein e
235 We employed radioactive isotopes to quantify occluded ca
236 We employ rational design and a toxin/antitoxin titering
237 We employed restriction-site-associated DNA sequencing a
238 We employed RNA sequencing analysis to reveal dysregulat
239 We employ RNAseq analyses to assess allele-specific expr
240 We employed shotgun liquid chromatography-mass spectrome
241 We employ simultaneous exposure of Cot molecules and Eu
242 Here
we employed single molecule FRET, single molecule pull-d
243 tone H4-V21C and histone H2A-E64C mutations,
we employed single-molecule force spectroscopy to measur
244 w it interacted with charged lipid bilayers,
we employed Small Angle Neutron Scattering to probe lipi
245 lution structures of individual VSG domains,
we employed small-angle X-ray scattering to elucidate th
246 Here
we employed sodium cyanide to probe the metal-ligand exc
247 Here
we employ spatially-explicit individual-based evolutiona
248 We employ standard quantum chemistry techniques to descr
249 We employ such device to measure the impedance change as
250 As a proof of concept,
we employed sUHR to determine the lipidome composition a
251 Specifically,
we employ surface-plasmon-polariton thermal emitters and
252 Here
we employ synchrotron-based X-ray fluorescence microscop
253 Specifically,
we employ tandem ubiquitin binding entities (TUBEs) and
254 To test this hypothesis,
we employed targeted mass-spectrometry proteomic analysi
255 Here
we employ the 75 ka Toba super-eruption as a case study
256 odel non-equilibrium, heterogeneous plasmas,
we employ the DDFT-QHD framework to generate a model for
257 We employ the device to analyse the OAM spectrum of elec
258 tal antimicrobial susceptibility assessment,
we employ the dropFAST platform to evaluate the antibact
259 We employ the high-speed synchrotron hard X-ray imaging
260 We employed the 21-day Caco-2/BBe cell model to replicat
261 We employed the assay for transposase-accessible chromat
262 As our first proof-of-principle
we employed the bacterial chemotaxis protein CheY as our
263 We employed the crystal structure of the KOR-JDTic compl
264 in a future outbreak of Ebola virus disease,
we employed the Grading of Recommendations Assessment, D
265 To address this hypothesis,
we employed the growing pollen tube, a well-established
266 We employed the Hazard Index (HI) method by using BDE co
267 Here,
we employed the high-throughput Expression of Soluble Pr
268 To prove this hypothesis
we employed the ICH collagenase mouse model.
269 We employed the integrated exposure-response model devel
270 In this study,
we employed the next generation high-throughput deep seq
271 We employed the purified DII S1-S4 protein to create a s
272 To reconstitute C-methylation,
we employed the rarely used heterologous host Rhizobium
273 ce activating and non-activating conditions,
we employed the ScanLag methodology.
274 To clarify these discrepancies,
we employed the technology of direct electron counting t
275 We employed the thermodynamic parameterization to estima
276 We employed the three-spined stickleback and three ecolo
277 To detect rare tissue-specific expression,
we employed the transcript-enrichment method CaptureSeq
278 In both contests,
we employed the tyrosine-protein kinase Yes as an exampl
279 We employed these data to devise and test a mathematical
280 Therefore,
we employed these four radiolabeled liposome types as pl
281 We employed these mice to investigate the contribution o
282 We employed these models in conjunction with transcripto
283 Second,
we employ this assay system to show that a dualsteric de
284 We employ this method to assess the brainstem's activity
285 Indeed,
we employ this random walk model to estimate the seeding
286 We employed TPEF to study the metabolism of primary rat
287 We employ trans-ethnic meta-regression to model allelic
288 vestigate the role of NO in drought response
we employed transgenic barley plants (UHb) overexpressin
289 c variants in vascular overgrowth syndromes,
we employed tumor genetic profiling via high-depth next-
290 We employ two local gates to fully tune the thermoelectr
291 In this work,
we employ two-photon fluorescence lifetime imaging micro
292 In this study,
we employ Ubiquitin Chain Enrichment Middle-down Mass Sp
293 Here
we employed uptake and release assays in rat brain synap
294 First,
we employed vesicles to show that in intact membrane-emb
295 We employed viral-genetic approaches to reduce corticotr
296 ot confounded by mass transport limitations,
we employed Weisz's modulus (Phi), which compares observ
297 duction in U. botrytis, under the conditions
we employed,
while the reciprocal heterologous complemen
298 Here,
we employed whole-exome sequencing in two unrelated cons
299 We employed whole-genome RNA-sequencing to profile mRNAs
300 Here,
we employ zebrafish as a model system to explore the phy