1 vinces, among which 1,962 are newly reported
here.
2 diversity in fibroblast phenotypes observed
here.
3 Here,
34 untrained individuals performed contralateral r
4 Here,
a combination of hydrogen-deuterium exchange, elec
5 Here,
a novel and cost-effective strategy is proposed to
6 Here,
a novel method for targeted near-infrared (NIR) fl
7 Here,
a scalable method is shown for the fabrication of
8 Here,
a strategy which uses chemical bonds as electron r
9 Here,
Abi1 knockdown by shRNA reduced human airway smoot
10 Here an alternative approach to the existing selective r
11 Here,
an inexpensive cellulase-linked immunomagnetic met
12 Here,
as part of the Pan-Cancer Analysis of Whole Genome
13 The analysis presented
here can be applied to any peptide-MHC complex of intere
14 t the QTR-FRET detection technique presented
here can be readily applied to dual-parametric assays fo
15 tability of these interactions characterized
here comprehensively reveal the nature of SARAH domain-m
16 Here,
cysteine aminoethylation using 2-bromoethylamine w
17 Here,
for the first time, differential pulse voltammetry
18 Here,
for the first time, we present a method of transie
19 Here,
I discuss the similarities and differences between
20 for the presence of metaphosphates, reported
here in whole bacterial cells for the first time, opens
21 Here,
in vivo characterization of tumor-associated USP22
22 We observe
here increased responses to vasoconstrictors in arteries
23 though the computational framework presented
here is developed for RNA hairpin systems, the general m
24 Here,
it is reported on Ti(3) C(2) T(x) MXene microstrip
25 Here,
male rats were trained to exert effort for a high-
26 Here,
participants associated pairs of faces in two cond
27 d or coreceptor-unbound (free) forms, and we
here present evidence that the two pools of Lck have dif
28 s than any individual model, we consider the
here presented results to be the current best estimate o
29 The statistical model used
here provides a robust framework for making best use of
30 We report
here pseudoviruses carrying S(G614) enter ACE2-expressin
31 Here,
single-cell multi-omics analysis demonstrates a sh
32 iminish PCSK9's ability to bind LDL reported
here supports the notion that PCSK9-LDL association in t
33 Using a temporal order judgment task, we
here tested the hypothesis that alpha power reflects the
34 We show
here that at low doses these SCFAs directly impact B cel
35 ey and human electrophysiology data, we show
here that attractor dynamics that control neural spiking
36 We show
here that RAD50-deficient fibroblasts exhibit a marked d
37 We report
here that the bacterial sRNA SsrA plays an essential rol
38 We assessed
here the degree to which variation in magnitude of N bal
39 We explored
here the oligomerization of a structurally diverse set o
40 Here,
the effect of PKH labelling on the size of EVs was
41 Here,
the fundamental principles of MRI contrast agents
42 Here,
the response of tumour spheroids formed from two e
43 Here,
to further study the process of fusion, we incubat
44 Here,
using a helical-hairpin construct derived from CFT
45 Here,
using focal trans-synaptic anterograde tracing, we
46 Here,
using high spatial and temporal resolution live-ce
47 Here,
using mass cytometry, we characterise five main dI
48 Here,
using molecular dynamics simulation approaches, we
49 Here,
using our recently established mammary specific Te
50 Here,
using recombinantly expressed proteins, in vitro t
51 Here,
using single-channel electrical recording in plana
52 Here,
using the melanoma lineage survival oncogene MITF
53 Here,
using three long-term datasets on bird reproductio
54 Here,
various molecular organic semiconductors (OSCs), w
55 Here we address that question by trapping an early state
56 Here we apply pH gradient cation exchange chromatography
57 Here we approach this problem by adapting the random-dot
58 Here we build on recent achievements in the accuracy of
59 Here we characterized the virus diversity and abundance
60 Here we compared the electrophysiological effects of nat
61 Here we couple digital pathology and transcriptome analy
62 venomous agent X (VX)-inhibited human AChE,
here we created seven uncharged acetamido bis-oximes as
63 Here we demonstrate that autoSTOMP can efficiently label
64 Here we demonstrate that, in regions of high exchange en
65 Here we demonstrate the successful application of femtos
66 ll-described olfactory neuron in C. elegans,
here we derive a general and broadly useful model that m
67 Here we describe a platform for efficient Cas12a gene ed
68 Here we describe a platform for the detection of IgG ant
69 Here we describe an ex vivo cultured human skin explant
70 Here we describe an ultrasensitive form of polymerizatio
71 Here we describe the production of a range of mini-spidr
72 Here we describe the use of discarded wound dressings as
73 Here we design small peptidic inhibitors based on the at
74 Here we develop a mathematical model to show, that in hi
75 Here we employ a series of mouse mutants with constituti
76 Here we establish a linear relationship between the heat
77 However,
here we found that when expressed in human cells, two hi
78 Here we have developed monobodies, synthetic binding pro
79 Here we have systematically studied Zn(2+) inhibition of
80 Here we identify a novel and critical function of IKK2 a
81 Here we identify an adaptive circuit-based mechanism tha
82 Here we integrate species differences in susceptibility
83 Here we introduce a generalized GREML, named CORE GREML,
84 Here we investigated how excitatory and VIP inhibitory c
85 Here we investigated the interaction between vancomycin
86 Here we present an End-to-End deep learning framework, c
87 To address this challenge,
here we present an enzymatic method to clean up and reco
88 Here we present the first analysis of the N- and O- and
89 Here we present two cryo-electron microscopy structures
90 Here we provide evidence supporting the key predictions
91 Here we quantified Mediator-controlled Pol II kinetics b
92 Here we refine an enrichment culture that exhibits expon
93 ant to tumorigenesis and cancer cell growth,
here we report a chemoproteomic analysis of a kidney-der
94 Here we report a cryo-electron microscopy (cryoEM) struc
95 Here we report a mechanism regulated by the oncogenic SO
96 Here we report a multicenter "modern-era" validation stu
97 Here we report a single-cell transcriptomic analysis of
98 Here we report ac(4)C-seq, a chemical genomic method for
99 Here we report an analysis of resting-state FC using mag
100 scontinuous frost pattern on natural leaves,
here we report findings on the condensation frosting pro
101 Here we report switching of fibroblast subtypes from a n
102 Here we report that Fc engineering of anti-influenza IgG
103 Here we report that multiple MYO7A isoforms are expresse
104 Here we report that serotonin 2c receptor (Htr2c)-expres
105 Here we report the design, synthesis, and biological eva
106 Here we report the development of a tantalum oxide nanop
107 Here we review the current understanding of the molecula
108 Here we sequenced and assembled approximately 3.1 Mb of
109 Here we show a strong association between low circulatin
110 Here we show by in vivo fluorescence and MR imaging, tha
111 Here we show that beta-cells express abundant Kindlin-2
112 Here we show that beta4*nAChRs also are involved in non-
113 Here we show that dynamically growing somatosensory neur
114 Here we show that Dysf(-/-) mice develop adverse LV remo
115 Here we show that heterotypic multicomponent interaction
116 Here we show that keratin intermediate filaments directl
117 Here we show that primary mouse and human T cells engage
118 isms can affect RNA secondary structure, and
here we show that single nucleotide polymorphisms can af
119 Here we show that this problem can be circumvented by as
120 Here we show that this system exhibits physiology-depend
121 Here we show that transcription factor EB (TFEB), a mast
122 Here we show that using prior knowledge to facilitate le
123 Here we show that Wdp modulates the Hedgehog (Hh) pathwa
124 Here we study sulfuramidimidoyl fluorides, a class of we
125 Here we study the impact of confined and controlled swin
126 Here we study the neuronal circuitry that allows larval
127 Here we use ancestral protein reconstruction and biophys
128 Here we use behavioural modelling and functional magneti
129 Here we use inelastic neutron scattering to study magnet
130 Here we use infrared photothermal heterodyne imaging (IR
131 Here we use National Wetland Inventory data and 5-kilome
132 Here we used the method to date the exploitation of dair
133 Here we utilize osteoclast ablation by denosumab (DMAb)
134 Here,
we adapted the 3D-bioprinting technology to develo
135 Here,
we address this issue by predicting sensing and co
136 Here,
we addressed the role of lipids during morphogenes
137 Here,
we aimed to assess the effects of long-term doxycy
138 Here,
we aimed to detect anomalies caused by technical e
139 Here,
we analyse two Dirac fermion species in two spatia
140 Here,
we analyze gut metagenomic data from mother-infant
141 Here,
we applied neuroimaging in a longitudinal sample o
142 Here,
we apply a high-resolution, pressure-based approac
143 Here,
we apply DETBAL, a computer application, to system
144 Here,
we assess ribosomal integrity following oxidative
145 Here,
we assess the splicing activity of 34 inteins (bot
146 Here,
we build a simple model of sexual reproduction and
147 Here,
we combine induced neurons (iNeurons) derived from
148 Here,
we combined transcranial magnetic stimulation (TMS
149 Here,
we compare fixed-time to on-the-fly decisions, bas
150 Here,
we compared two splicing variants (V1, V2) of muri
151 Here,
we demonstrate that DCLK1-overexpressing primary h
152 Here,
we demonstrate that DXO also catalyzes the hydroly
153 Here,
we demonstrate that Parkin has functions in the nu
154 Here,
we demonstrate that the RarA protein makes a major
155 Here,
we demonstrate that the Ras->Raf->rho kinase (ROCK
156 ertical settling from surface accumulations;
here,
we demonstrate that the spatial distribution and u
157 Here,
we demonstrate the applicability of the integratio
158 Here,
we demonstrate the application of this method in a
159 Here,
we demonstrate translational read-through across t
160 Here,
we describe a function for NEK10 in the regulation
161 Here,
we describe a mechanism by which the innate immune
162 cylindrus and Pseudo-nitzschia multistriata
Here,
we describe how functional genomics and reverse ge
163 Here,
we describe the extent of resistance of E. dermati
164 Here,
we describe the UBPs developed by three research t
165 Here,
we described a new, comprehensive system of in sil
166 Here,
we develop 3D printed bionic corals capable of gro
167 Here,
we developed a CRISPR-based system for simultaneou
168 Here,
we developed a piecewise approach for all-atom ste
169 Here,
we developed a simple enzyme-linked immunosorbent
170 Here,
we devised an ethologically inspired behavioral pa
171 Here,
we devised novel analytical procedures enabling ex
172 Here,
we discovered a novel size law that connects cell
173 Here,
we discovered site-specific fragmentation of NOTCH
174 Here,
we discuss genetic models of mouse DC development
175 Here,
we discuss recent development, optimization, and a
176 Here,
we establish that partial time reversal transforms
177 Here,
we establish the Drosophila border cells as a mode
178 Here,
we evaluate the growth of genetically defined rena
179 Here,
we evaluate the phylogenetic relationships of the
180 Here,
we examine how the distinct motor programs of the
181 Here,
we examine the temperature sensitivity of phenolog
182 Here,
we explore speciation alongside development, empha
183 Here,
we explore the application of various dimensionali
184 Here,
we explore the transcriptional profile and DNA rep
185 Here,
we explored autophagy as a mechanism to reduce tau
186 Here,
we explored the function of this kinase in macroph
187 Here,
we explored the mechanisms underlying MHV68 activa
188 Here,
we fill this gap by incorporating the habitat sele
189 Here,
we find that involvement of the budding yeast Hsp7
190 Here,
we focus on how these 'cue-locked' neurons exhibit
191 Here,
we focus on loss of the histone demethylase UTX (a
192 Here,
we found an age-associated increase in stiffness i
193 Here,
we found that when phage infections occur on solid
194 Here,
we functionally characterized human TMEM165 by het
195 Here,
we further demonstrate that more than ten fundamen
196 Here,
we globally identify ZMAT3-regulated RNAs and thei
197 Here,
we have addressed these questions in a series of g
198 Here,
we have developed and extensively characterized a
199 Here,
we highlight how different microrobots, ranging fr
200 Here,
we highlight key studies testing intrinsic and ext
201 Here,
we highlight the developments in understanding TIM
202 Here,
we hypothesized that the u-opioid system-extensive
203 Here,
we identified a novel mTORC1-interacting protein c
204 Here,
we identified the E3 ubiquitin ligase Peli1 as an
205 Here,
we identify a neuronal circuit in the nematode Cae
206 Here,
we identify the conditions and substrates that dec
207 Here,
we illustrate a particular relationship between hu
208 Here,
we incorporate rather thick two-dimensional layere
209 Here,
we introduce a novel platform that allows IC-FPOP
210 Here,
we introduce the Bitome, a matrix composed of bina
211 Here,
we investigate how a benzene motif influences the
212 Here,
we investigate whether predispositions for uncerta
213 Here,
we investigated the ability of dysbiotic Pg-strain
214 Here,
we investigated the individual and combined contri
215 Here,
we investigated the mechanistic basis of this endo
216 Here,
we investigated the role of PAG1 in a preclinical
217 Here,
we investigated whether reduced HCV replication af
218 Here,
we investigated, in rat hippocampal neuronal cultu
219 Here,
we performed in vitro integration assays, finding
220 Here,
we present a combined analysis of 135 fungal genom
221 Here,
we present a framework to quantitatively infer com
222 Here,
we present a protein design algorithm called TopoB
223 Here,
we present a single-cell aggregation and integrati
224 Here,
we present an approach to modulate extruded inks a
225 Here,
we present global analyses of viral transcript lev
226 Here,
we present new tools to overcome these limitations
227 Here,
we present the near-atomic structures of the BBSom
228 Here,
we propose a multi-process causal mechanism for in
229 Here,
we quantitatively assessed the internal heating ex
230 Here,
we reconstituted the maturation of mitochondrial [
231 Here,
we report a chromosome-scale assembly of the T. si
232 Here,
we report a critical role for proline catabolism i
233 Here,
we report a crystal structure of the DNA-binding d
234 Here,
we report a time-calibrated phylogenomic analysis
235 Here,
we report an experimental investigation of BP memb
236 Here,
we report an update of the VDJdb database with a s
237 Here,
we report on acoustically detected presence of rig
238 Here,
we report that an active form of the ESCRT-associa
239 Here,
we report that beta1 subunits are phosphorylated b
240 Here,
we report that CD2 costimulation plays a critical
241 Here,
we report that mice lacking Pdcd1 (Pd1-/-) demonst
242 Here,
we report that Na(+) substantially accumulated in
243 Here,
we report that octopamine activity through the bet
244 Here,
we report that octopus arms use a family of cephal
245 Here,
we report that pharmacologic restoration of the bl
246 Here,
we report that the Arabidopsis calcium-dependent p
247 Here,
we report that the immobilization of TD-NTs in siz
248 Here,
we report that the pol mu insertion products of ri
249 Here,
we report that the soluble, nonfibrillizing Abeta
250 Here,
we report the directed differentiation of human iP
251 Here,
we report three Turing-inspired tests designed to
252 Here,
we review current understanding of the molecular m
253 Here,
we review progress and challenges in the use of AD
254 Here,
we sequenced the whole genomes of 24 individual pi
255 Here,
we set out to understand the heterogeneity of HbF
256 Here,
we show a molecular mechanism of how plants can se
257 Here,
we show an N. gonorrhoeae diagnostic workflow for
258 Here,
we show that adrenergic stimulation of BAT activat
259 Here,
we show that adult animals respond to ascarosides
260 Here,
we show that Agd3 deacetylates GAG in a metal-depe
261 Here,
we show that an AT-hook motif-containing nuclear l
262 Here,
we show that constrained 31-residue-peptides ('msR
263 Here,
we show that cytotoxic chemotherapies induce dynam
264 Here,
we show that efficiency of these processes is enha
265 Here,
we show that expression of a fusion protein combin
266 Here,
we show that GAGA factor (GAF), a Drosophila pione
267 Here,
we show that histone H4 lysine 16 acetylation (H4K
268 Here,
we show that LDs induced by the yeast triacylglyce
269 Here,
we show that macrophages not only fail to efficien
270 Here,
we show that phosphatidylethanolamine (PE) synergi
271 Here,
we show that resistance to glyphosate in the studi
272 Here,
we show that SOX11 confers distinct features to ER
273 Here,
we show that Syrian hamsters, in contrast to mice,
274 Here,
we show that the MA region is required for nuclear
275 Here,
we show that the microcephalin 1/BRCT-repeats inhi
276 Here,
we show that the three major classes of LCCBs acti
277 Here,
we show that this differentiation becomes possible
278 f intravacuolar pathogens such as Salmonella
Here,
we show that this mechanism requires aconitate dec
279 Here,
we show that this toughness design approach can be
280 Here,
we show that tree mortality concomitant with droug
281 Here,
we show that TRYPTOPHAN AMINOTRANSFERASE OF ARABID
282 Here,
we stabilize immature Zika virus via an antibody t
283 Here,
we study the roles of GABA and insulin signaling i
284 Here,
we summarize clinical and preclinical findings of
285 Here,
we test the hypothesis that vessel noise level is
286 Here,
we tested the hypothesis that gene expression prof
287 Here,
we tested the hypothesis that the S-OFF response i
288 Here,
we took advantage of a protozoan ciliate infestati
289 Here,
we traced the cellular development of a recently e
290 Here,
we use a combination of atom-resolved scanning pro
291 Here,
we use a general model based on biochemical kineti
292 Here,
we use a machine-vision-based single-particle anal
293 Here,
we use multiple mouse models to investigate in viv
294 Here,
we use population-based data from ~22,000 persons
295 Here,
we use quantum-logic techniques to prepare a trapp
296 Here,
we used genetic colocalization analysis to identif
297 Here,
we used integrated optical imaging in a rat self-a
298 Here,
we used psychoacoustics and electroencephalography
299 Here,
we used rER BOLD fMRI in macaque monkeys while vie
300 properties of such proteins, we investigate
here whether their ability to reversibly associate and d