1 We show that (
1) tandem-TIMS/MS retains native-like avid
2 Here
we show that 20E-triggered oviposition in these mosquito
3 We show that 21-plex DiLeu tags generate strong reporter
4 We show that a +4 stem cell (SC) in the gastric antrum,
5 We show that a 20% increase in the intake of fruit/veget
6 YAP and target gene transcription dynamics,
we show that a cycle of fast exodus of nuclear YAP to th
7 ient-derived induced pluripotent stem cells,
we show that a mutation at the C terminus of eIF2gamma i
8 Here
we show that a previously uncharacterized gene, ENLARGED
9 Here,
we show that a second-generation amino-acyl tRNA synthet
10 Here,
we showed that a green fluorescence protein (GFP) report
11 Here
we showed that ACE2, but not TMPRSS2 or Furin, has a hig
12 More specifically,
we show that acidic residues N-terminal to the substrate
13 Here
we show that activation of the non-canonical NF-kappaB s
14 We show that active enhancer units are precisely delinea
15 Previously,
we showed that active K-Ras4B dimerizes in silico and in
16 We show that activity-induced Kv4.2 phosphorylation trig
17 activated truncated forms of the receptors,
we show that ADGRE2/EMR2 and ADGRE5/CD97 are G protein-c
18 Here,
we show that adrenergic stimulation of BAT activates a P
19 Here,
we show that adult animals respond to ascarosides produc
20 Here
we show that aerobic exercise training up-regulates DICE
21 Here,
we show that Agd3 deacetylates GAG in a metal-dependent
22 Here,
we show that although structurally clustered mutations i
23 We show that,
although myosin motors throughout the fila
24 Here
we show that,
although the N-terminal region of RNF4 bea
25 the evolution of steroid hormone receptors,
we show that an ancient hydrophobic interface, conserved
26 Ultimately,
we show that an as-yet-unidentified nonsecreted cell wal
27 Using nascent RNA sequencing,
we show that an AS15 analogue triggers the unfolded prot
28 Here,
we show that an AT-hook motif-containing nuclear localiz
29 We show that AP-1B colocalized with beta1 integrin in fo
30 We show that apoptotic lymphocytes and macrophages relea
31 We show that aspartic acid inhibits aragonite precipitat
32 Previously,
we showed that ATP-DnaA, not ADP-DnaA, undergoes a confo
33 Finally,
we showed that B. miyamotoi-stimulated DCs induced proli
34 Here
we show that beta-cells express abundant Kindlin-2 and d
35 We show that beta-HPV E6 more broadly impairs cellular s
36 Here
we show that beta4*nAChRs also are involved in non-nicot
37 We show that bioluminescence evolved in the last common
38 Here,
we show that both IFN-gamma stimulation and murine norov
39 0% cofactor incorporation, and additionally,
we show that,
bound to UvrC, the [4Fe4S] cofactor is sus
40 Here
we show that branched actin filament networks, the main
41 Here,
we show that cancer cells can be selectively deprived of
42 In addition,
we show that cancer somatic mutations have different eff
43 efficient Cas12a gene editing in Drosophila
We show that Cas12a from Lachnospiraceae bacterium, but
44 We show that CEP85L is a centrosome protein localizing t
45 We show that chemometric analysis of peanut leaflet spec
46 ld chimpanzee (Pan troglodytes) communities,
we show that chimpanzees exhibit greater behavioural div
47 o identify novel transcriptional regulators,
we show that chromatin remodeler Hmga1 is highly express
48 Here,
we show that constrained 31-residue-peptides ('msR4Ms')
49 sing simulations with neural network models,
we show that contemporary statistical methods for functi
50 We show that copy numbers of triptolide biosynthetic pat
51 Using a novel GLD model,
we show that cross-correction does not occur efficiently
52 We show that CSB forms a stable complex with Pol II and
53 We show that CTP analogs are readily incorporated into a
54 Here,
we show that cytotoxic chemotherapies induce dynamic cha
55 Using a cultured keratinocyte model system,
we show that depletion of alpha-catenin perturbs adheren
56 sing genetic and pharmacological approaches,
we show that depletion of the hyaluronic acid precursor
57 Here
we show that depletion of transforming growth factor-bet
58 We show that differences in allele frequencies and linka
59 We show that distinct multimode patterns of light can be
60 We show that DM prevalence and clinical characteristics
61 Here,
we show that Drosophila mutants in the homolog of the hu
62 Here
we show that dynamically growing somatosensory neurons i
63 Here
we show that Dysf(-/-) mice develop adverse LV remodelin
64 Finally,
we show that eCLIP peak co-occurrences across RBPs enabl
65 Here,
we show that efficiency of these processes is enhanced,
66 Using several techniques,
we show that electron paramagnetic resonance (EPR) spect
67 enhancer-associated chromatin modifications,
we show that enCRISPRa and enCRISPRi modulate gene trans
68 We show that EPEC induces pyroptosis in IECs in a Tir-de
69 We show that epimutations arise spontaneously at a rate
70 nt predictions for cerebellar mechanism, and
we show that evidence appearing to contradict the origin
71 We show that exposure of leukemia cells to daunorubicin
72 Here,
we show that expression of a fusion protein combining wh
73 Here
we show that expression of m(6)A demethylase ALKBH5 is r
74 lung tissues from IPF and control subjects,
we showed that expression of TOLLIP gene in the lung par
75 protein overexpressed in most human cancers,
we show that FBXL16 stabilizes C-MYC by antagonizing FBW
76 enes are required using different Cre lines,
we show that Fgf8 and Fgf17 are required in the presomit
77 Here,
we show that fibroblasts counteract the cytotoxic effect
78 We showed that Flvcr2 was necessary for angiogenic sprou
79 Finally,
we showed that footedness is only marginally influenced
80 We show that force lengthens kinetochore-fibers by persi
81 We show that,
from birth to hearing onset, the auditory
82 Furthermore,
we show that GacB is inhibited directly by cyclic di-GMP
83 Here,
we show that GAGA factor (GAF), a Drosophila pioneer-lik
84 Finally,
we show that gene deletion has further shaped the SVMP c
85 We show that genetic ablation of IFT20 in vitro slows ke
86 Here,
we show that genotoxic agent-activated Wnt/beta-catenin
87 We show that GFP-tagged proteins can be localized in nan
88 We show that glycolysis is required to maintain the plas
89 We showed that H19X regulates DDIT4L gene expression, sp
90 In this review,
we show that having so many materials allows us to use b
91 Here
we show that heterotypic multicomponent interactions dom
92 We show that high-elevation aquatic insects may not be p
93 We show that high-fat diet attenuates the response of Ag
94 Here,
we show that histone H4 lysine 16 acetylation (H4K16ac)
95 We show that homologs of the identified protein-coding g
96 Here,
we show that human METTL2 forms a complex with DALR anti
97 We show that IDACombo predictions closely agree with mea
98 Here
we show that impact angle and direction can be diagnosed
99 We show that in 80% of ecoregions, protected areas offer
100 g high-content imaging and cluster analysis,
we show that in male rats SCI decreases opioid responsiv
101 Here
we show that in neurons with no history of activity what
102 We show that in oocytes TBPL2 does not assemble into a c
103 We show that in the absence of Dcc, some ganglion cell a
104 We show that in vitro development of tamoxifen-resistanc
105 g examples of breast and colorectal cancers,
we show that individual cells evolve into tumors or aspe
106 We show that individual heterogeneity provides a key int
107 Finally,
we show that inhibition of the insular cortex using GABA
108 We show that inhibitory phosphorylation of eIF2alpha (P-
109 isease bioassays and transcriptomic analysis
we show that intact SA-signalling is required for potato
110 Here,
we show that interleukin (IL)-22, induced by colonizatio
111 Finally,
we showed that interleukin-4 treatment was sufficient to
112 We show that intermediate-wavelength velocities are usef
113 Tribolium castaneum and Tribolium confusum,
we show that interspecific competition dramatically slow
114 Here,
we show that intestinal epithelial cells expressing IRE1
115 Moreover,
we show that intestinal flow and bacterial motility are
116 We show that isothiocyanate formation requires the actio
117 We show that it efficiently crosslinks noncovalent RNA c
118 As a result,
we show that it is possible to tune the O(2) affinity at
119 ngivalis-mediated periodontal disease model,
we show that JAK3 inhibition enhances infiltration of in
120 Here,
we show that JMJD1C is a specific histone demethylase fo
121 Here
we show that keratin intermediate filaments directly reg
122 We show that language can also shape our knowledge about
123 ent environmental and taxonomical structure,
we show that large scale patterns in the EMP can be repr
124 Here,
we show that LDs induced by the yeast triacylglycerol (T
125 We showed that lncRNAs are distinct from both protein-co
126 We show that local plant and animal diversity dropped ma
127 We show that loss of sympathetic innervation is ongoing
128 Moreover,
we show that low N-induced root elongation is associated
129 a lineage survival oncogene MITF as a model,
we show that low-affinity binding sites act as a competi
130 Finally,
we show that LukE targets murine Darc through DR1 in viv
131 Here,
we show that lung-specific loss of Kmt2d promotes lung t
132 Here,
we show that macrophages not only fail to efficiently ki
133 We show that male elephants increased their energetic al
134 We show that mantis shrimp rely on navigational strategi
135 In this study,
we show that MCV sT protein stimulates differential expr
136 We show that mechanochemically generated thiol-terminate
137 In this paper,
we show that megakaryocytes contain extranuclear histone
138 In conclusion,
we show that MEKi leads to CD8(+) T cell reprogramming i
139 Here,
we show that melanoma cells can adapt to targeted therap
140 In this paper,
we show that mice chronically infected with CL13 succumb
141 Here,
we show that mice in which alpha2-Na/K ATPase is conditi
142 Here
we show that mice with inducible conditional knockdown (
143 Further,
we show that microglia, not peripheral myeloid cells, re
144 We show that mismatch between the nature of the generati
145 We showed that mouse cholangiocytes in the channel of th
146 Here,
we show that multiple linked but recombining loci underl
147 We showed that multiple histological samples per patient
148 We show that mutant strains lacking gigC have impaired g
149 In this study,
we show that MVs isolated from the human lactic acid com
150 Here,
we show that MYCN-amplified neuroblastomas are character
151 Overall,
we show that NetPAS can take topological constraints of
152 We show that neutral evolution and nucleotide substituti
153 We show that newly introduced mtDNA is stably retained i
154 With the available immunodetection methods,
we show that Nf-L measurement based on DPS microsampling
155 Here
we show that North America warmed at the rate of 0.02 de
156 Here,
we show that NP-Ct is necessary for IB formation when NP
157 We show that NVP was readily taken up by dendritic cells
158 Here
we show that obstruction of vascular invasion during bon
159 Here
we show that only females and not males show a highly si
160 Using computational fluid dynamics,
we show that osteostracan headshield morphology is compa
161 We show that our assembly model reproduces many key feat
162 le approach to CNN parameter interpretation,
we show that our trained network ("AI-TAC") does so by r
163 We show that oxygen delivery through PMCs is dependent o
164 Using antibiotic-treated or germ-free mice,
we show that parathyroid hormone (PTH) only caused bone
165 Here,
we show that Pavarotti also functions during wound repai
166 We show that permissive epigenetic regulation of cldn5 e
167 ecular mechanisms of its antiviral activity,
we show that PG specifically inhibits NF-kappaB and Akt
168 Here,
we show that phosphatidylethanolamine (PE) synergizes wi
169 In addition,
we show that phosphorylation of Ser(3) may be an additio
170 In the present study,
we show that phosphorylation of the newly introduced Thr
171 In doing so,
we show that piecewise all-atom steered molecular dynami
172 In this study,
we show that PIFs positively regulate the ABA signaling
173 We show that Plasmodium berghei CDK-related kinase 5 (CR
174 Here
we show that polysynaptic inhibition between ChINs is a
175 We show that PP(i)-PFKs of Clostridium thermosuccinogene
176 Here
we show that primary mouse and human T cells engage in m
177 Overall,
we show that protecting Tie2 shedding might offer a new
178 Second,
we showed that PTP1B (13)C-methyl group side chain fast
179 ultiple sources of genetic and genomic data,
we show that putative G-quadruplex forming sequences (pG
180 mples and orthotopic PDAC biological models,
we showed that radiotherapy increased inducible nitric o
181 Previously,
we showed that rat kidney mesangial cells dividing durin
182 ef that modern culture evolves very quickly,
we show that rates of modern cultural evolution are comp
183 We show that repeated mating reduced the sperm pool and
184 Here
we show that resistance to 5FC in Cryptococcus deuteroga
185 Here,
we show that resistance to glyphosate in the studied pop
186 We show that Rho can prematurely terminate transcription
187 We show that RHT/AGIL, previously shown to interact with
188 Importantly,
we showed that ROS targeted by NAC was selectively requi
189 planation for the poor cell uptake of Ru360,
we show that Ru360 is deactivated by biological reductan
190 Mechanistically,
we show that RUNX1 is a component of the HDAC3 corepress
191 edia markets for 771 matched rural counties,
we show that rural residents are more likely to practice
192 g a temperature-sensitive allele (Sac1(ts)),
we show that Sac1 is required for structural integrity o
193 Here
we show that SARS-CoV-2 causes a respiratory disease in
194 We show that SARS-CoV-2 Spike-pseudotyped virus and genu
195 Here,
we show that serotonergic input has separable suppressiv
196 can affect RNA secondary structure, and here
we show that single nucleotide polymorphisms can affect
197 We showed that SnRK2.8 was required for AvrPtoB virulenc
198 n of electrode surfaces via cold-air plasma,
we show that soft biocompatible materials can be rapidly
199 Finally,
we show that,
somewhat unexpectedly, the autophagy machi
200 Here,
we show that SOX11 confers distinct features to ER-negat
201 We show that SST interneuron-selective overexpression of
202 Here,
we show that starved bacteria encountering new resources
203 Here
we show that STAT5 is the earliest factor binding and re
204 Here,
we show that Stattic exerts many STAT3-independent effec
205 We show that stimulus-driven and goal-directed influence
206 We show that strategically expanding the existing global
207 We show that such tracking can be achieved by canonical
208 We show that synapses can switch from glycolytic to oxid
209 Here,
we show that Syrian hamsters, in contrast to mice, are h
210 Here,
we show that TA transcript levels can increase substanti
211 We show that tatM2NX inhibits over 90% of TRPM2 channel
212 We show that termination is completely abolished by rapi
213 Here,
we show that TGFbeta promotes protein translation at lea
214 As compared with WT mice,
we show that the activity of IL-13 is dramatically augme
215 Here,
we show that the age-dependent downregulation of lamin B
216 Here,
we show that the chemical potentials of chalcogenide mat
217 In total,
we show that the conformationally orthogonal reactions o
218 We show that the degree to which cases of COVID-19 are c
219 In this way,
we show that the density scaling law for molecular dynam
220 We show that the distinct molybdenum isotopic compositio
221 Moreover,
we show that the distribution and stability of different
222 We show that the double tag does not interfere with the
223 We show that the effect of subduction on the deep nitrog
224 We show that the GLN method is a significantly faster te
225 Here, using satellite observations,
we show that the global extent of river ice is declining
226 separate parental and zygotic contributions,
we show that the H2A.B status of both the father and mot
227 Here,
we show that the human cysteine protease legumain exhibi
228 We show that the inclusion of noise leads to systematic
229 We show that the increased cytokinin signaling in ARR1 g
230 Here
we show that the larval zebrafish retina extracts a dive
231 Intriguingly,
we show that the ligand shell of Au(25) nanoclusters bec
232 Here
we show that the limitations imposed by fluid instabilit
233 Here,
we show that the MA region is required for nuclear impor
234 Here,
we show that the microcephalin 1/BRCT-repeats inhibitor
235 Moreover,
we show that the model accurately predicts participants'
236 ng focal trans-synaptic anterograde tracing,
we show that the motor-action-related topographical orga
237 We show that the non-canonical tubulin Tuba8, transientl
238 Here
we show that the observed part of Phaethon does not exhi
239 Using ChIP,
we show that the occurrence of G4 structures peaks at th
240 By doing so,
we show that the original elements of the codon theory c
241 We show that the phosphorylation of the RNA-DNA binding
242 l Ruddlesden-Popper perovskite and graphene,
we show that the plane-contacted perovskite and graphene
243 We show that the policies investing capital in local mar
244 We show that the proposed model surpasses the statistica
245 urements with population-scale genomic data,
we show that the response of a model replicative DNA pol
246 d survival, and chromatin landscape effects,
we show that the SE ensures robust Atoh7 transcriptional
247 We show that the speckle contrast in scattering from wat
248 In this study,
we show that the T2D heart is metabolically inflexible a
249 Here,
we show that the three major classes of LCCBs activate S
250 th luciferase and GFP plasmid transfections,
we show that the time delay between injury and polyplex
251 In this study, using a knockout mouse model,
we show that the transcription factor hypoxia-inducible
252 Using a Grp-Cre knock-in mouse line,
we show that the upper epidermis of the skin is exclusiv
253 s) and JPH-203 (a specific LAT-1 inhibitor),
we showed that the efflux agonist did not inhibit the up
254 We showed that the enzyme was active on Galalpha1-3Gal b
255 In this work,
we show that there exists a correlation which is not att
256 We show that these biosensors can be used to monitor equ
257 We show that these dendrites develop by retrograde exten
258 We show that these filaments are coated by a highly asym
259 We show that these puzzling properties arise from a dual
260 ts role in the synthesis of heparan sulfate,
we show that this activity is required for efficient inf
261 ly superior to traditional Fourier analysis,
we show that this algorithm also uncovers phase sensitiv
262 We show that this can be explained by genuine Neandertha
263 Here,
we show that this differentiation becomes possible by ad
264 We show that this is due to acid inhibition of monocarbo
265 Here
we show that this is possible using a surface plasmon re
266 avacuolar pathogens such as Salmonella Here,
we show that this mechanism requires aconitate decarboxy
267 ing plants, protists, and algae with grazers-
we show that this method predicts the results of unobser
268 We show that this plasticity in rats is robust at 1 and
269 Here
we show that this problem can be circumvented by assembl
270 species with cryo-electron tomography, here,
we show that this subcomplex persists after flagellum di
271 Here
we show that this system exhibits physiology-dependent t
272 As such,
we show that this system presents as a novel druggable t
273 Here,
we show that this toughness design approach can be appli
274 -depth analysis of its mechanisms of action,
we showed that this miRNA specifically inhibits Salmonel
275 Here
we show that topoisomerase 1-DNA covalent cleavage compl
276 Here
we show that transcription factor EB (TFEB), a master re
277 ual viral-mediated gene transfer of DREADDs,
we show that transient inactivation of dMSNs or activati
278 ical properties of the macroscopic matrices,
we show that transparency results from structural partia
279 We show that treatment with lysozyme-functionalized orig
280 Here,
we show that tree mortality concomitant with drought has
281 We show that Treg cells in food allergy (FA) had decreas
282 Moreover,
we show that TRPV3 and PAR2 were upregulated in skin bio
283 Here,
we show that TRYPTOPHAN AMINOTRANSFERASE OF ARABIDOPSIS
284 We show that UBA(Cez) binds Lys(11)-, Lys(48)-, Lys(63)-
285 For short-degron protein substrates,
we show that unfolding can occur directly from the initi
286 Herein,
we show that use of the singlet oxygen ene reaction, com
287 Here
we show that using prior knowledge to facilitate learnin
288 Here
we show that Wdp modulates the Hedgehog (Hh) pathway.
289 Here,
we show that we can decode natural sounds from activity
290 es based on the dynamics of the bulk liquid,
we show that we can predict the activation energy for cr
291 Using a community of beetle species,
we show that when dispersal ability and climate toleranc
292 We show that whereas spatial approaches are relatively c
293 ng an experimental setup and analysis tools,
we show that,
within the whole system (beyond the drople
294 Furthermore,
we show that WNK1 negatively regulates LFA1-mediated adh
295 We show that Wnt3a is expressed in the caudal embryo in
296 In the current study,
we show that Wnt5A, a non-canonical Wnt ligand that driv
297 We show that working memory performance depends on the s
298 internal reflection fluorescence microscopy
we show that Wsp1 synergizes with Dip1 to co-activate Ar
299 Consistent with this observation,
we show that ZBED2 can repress the pancreatic progenitor
300 Here,
we show that zebrafish embryonic tissue explants, prepar