1 We demonstrate that a highly reactive CF3(-) adduct can
2 In this article,
we demonstrate that a human ornithine transcarbamylase g
3 We demonstrate that a monolayer of PtSe2 can be grown on
4 Here,
we demonstrate that a radio-frequency deflector in combi
5 Here
we demonstrate that a subset of GABAergic chandelier cel
6 We demonstrate that a subset of these SSPs can enter L.
7 Here
we demonstrate that a synthetic G4 ligand, Y2H2-6M(4)-ox
8 Here,
we demonstrate that A. marginale outer membrane protein
9 Furthermore,
we demonstrated that a bidirectional code with both odor
10 ein translation and neural network activity,
we demonstrated that a ubiquitin E3 ligase, murine doubl
11 We demonstrated that AEI of PEX6 is a common phenomenon
12 Here,
we demonstrated that AKG effectively attenuated corticos
13 ntation models using mouse and human islets,
we demonstrated that alpha-1 antitrypsin (AAT; Prolastin
14 ure cell model and clinical patient samples,
we demonstrated that although CAFs promoted prostate can
15 Using this translational platform,
we demonstrated that amyloid-beta pathology recapitulate
16 Thus,
we demonstrate that an approach of local, randomized tai
17 We demonstrate that an arcsin transformation of Laplace-
18 Taken together,
we demonstrate that apolipoprotein B mRNA-editing cataly
19 In this study,
we demonstrated that apolipoprotein B mRNA-editing catal
20 Most strikingly,
we demonstrated that AqJAG disproportionally controls th
21 Here,
we demonstrate that Arabidopsis (Arabidopsis thaliana) S
22 We demonstrate that B-lymphocytes activated by un-methyl
23 approximations and Monte-Carlo simulations,
we demonstrate that balanced polymorphism and recombinat
24 ing siRNA-induced in vivo knockdown approach
we demonstrated that beneficial effects of IVIG were med
25 In this study,
we demonstrate that binding domains from autolysins and
26 We demonstrate that both curing of [URE3] and enhancemen
27 We demonstrate that both TNF-R and nucleotide-binding ol
28 In summary,
we demonstrated that both colorectal adenoma and CRC are
29 Using specific inhibitors,
we demonstrated that both steps were critical in the del
30 We demonstrated that candidates not previously implicate
31 rbon networks and polymerized ionic liquids,
we demonstrate that carbon-based porous nanoarchitecture
32 Here,
we demonstrate that CCHFV nucleocapsid protein (CCHFV-NP
33 We demonstrated that CD25 expression is largely restrict
34 We demonstrate that CD34(+) Gp38(+) cells are the major
35 inactivation and replacement in human cells,
we demonstrate that CENP-A mutants that cannot be phosph
36 Here
we demonstrate that CFIm functions as an enhancer-depend
37 Finally,
we demonstrate that changes in the size of the D3-D4 cle
38 Nonetheless, here
we demonstrate that chimpanzee and gorilla A3C have appr
39 We demonstrate that chloride cannot act as a two-electro
40 ere, using human in vivo deuterium labeling,
we demonstrate that classical monocytes emerge first fro
41 We demonstrate that clemizole binds to serotonin recepto
42 Finally,
we demonstrate that co-targeting of ROS1 and EGFR could
43 Importantly,
we demonstrate that combined use of MEK1/2 and Src inhib
44 We demonstrate that,
compared to existing methods, our m
45 Here,
we demonstrate that comprehensive two-dimensional gas ch
46 We demonstrate that conditioning of mammalian cells by e
47 Here, however,
we demonstrate that contact frequency is distinct from a
48 Here
we demonstrate that cortical neurons directly innervate
49 We demonstrate that COX20 stabilizes COX2 during inserti
50 We demonstrate that CRISPR-Cas activity and acquisition
51 Here,
we demonstrate that CRISPR/Cas9 genome editing of promot
52 We demonstrate that crossovers reside in genomic regions
53 In this work,
we demonstrate that cryo-electron microscopy (cryo-EM) c
54 We demonstrate that cubic splines can capture the shape
55 Herein,
we demonstrate that cucurbit[7]uril (CB[7]) can catalyse
56 In this study,
we demonstrate that culturing cells in different physica
57 We demonstrate that currently existing experimental prot
58 Furthermore,
we demonstrate that CX-4945 treatment inhibits the matur
59 Here,
we demonstrate that Cx43 is dysregulated in the hearts o
60 We demonstrate that dengue-specific antibodies enhance t
61 Here,
we demonstrate that denitrifying polyphosphate-accumulat
62 Finally,
we demonstrate that depletion of the single Drosophila h
63 We demonstrate that deregulated necroptosis results in s
64 Using an ex vivo assay for HIV-1 mRNA,
we demonstrated that despite this immunomodulatory effec
65 Previously,
we demonstrated that development of fatty liver depends
66 We demonstrate that differently from LPS-mediated dimeri
67 We demonstrate that direct empirical comparisons between
68 We demonstrate that disease-associated variants from an
69 We demonstrate that dKDM4A demethylase activity is dispe
70 We demonstrated that DNMT1 and KIT form a positive regul
71 We demonstrate that double heterojunctions designed into
72 Using a glioma mouse model,
we demonstrate that doxorubicin-loaded (D)CDX-RBCNPs hav
73 We demonstrate that dressmakers' stereoscopic acuities a
74 Using multiple genetic strategies,
we demonstrated that E proteins E2A and HEB acted in syn
75 Furthermore,
we demonstrated that E2f3a overexpression substantially
76 In this study,
we demonstrate that ectopic expression of insulin epitop
77 Here
we demonstrate that eIF4E regulates HAV IRES-mediated tr
78 We demonstrate that elevated Ctnnd1 expression contribut
79 Recently,
we demonstrated that enhancing endogenous levels of kynu
80 Here,
we demonstrate that ENSO drives intrabasin variability o
81 We demonstrate that Env-specific HLA-B*14-restricted act
82 We demonstrate that even though the direction of force m
83 We demonstrate that expanded mFPPs have increased DA neu
84 We demonstrated that experimentally induced memory react
85 We demonstrate that expression levels largely determine
86 Furthermore,
we demonstrate that expression of Sema3a, Sema3d, and Se
87 We demonstrate that F-actin automata implement OR, AND,
88 xplore this family of molecules further, and
we demonstrate that flavonoids specifically inhibit quor
89 We demonstrate that for RBCs entering the capillary bed
90 We demonstrate that forced apical localization of Par3,
91 We demonstrate that four closely related Photoregulatory
92 We demonstrate that GdOA signal enhancement correlates w
93 Here,
we demonstrate that gene silencing of KIND1 decreased ke
94 We demonstrated that genome-scale fingerprints of an org
95 We demonstrated that glutamate acts through kainic acid
96 Using simulation of data,
we demonstrate that group sequential designs have the po
97 Here,
we demonstrate that gut microbes from the sand fly are e
98 Here,
we demonstrate that hamsters devoid of functional STAT2
99 In this study,
we demonstrate that HBoV1 induces a DDR that plays signi
100 Recently,
we demonstrated that HCV infection leads to monocyte dif
101 Mechanistically,
we demonstrated that HDAC6 maintains Ku70 in a hypoacety
102 Previously
we demonstrated that Hedgehog (Hh) morphogen is transpor
103 We demonstrate that hepatic inflammation, fibrosis stage
104 Here,
we demonstrated that HIGH EXPRESSION OF OSMOTICALLY RESP
105 of-function and loss-of-function approaches,
we demonstrate that HIPK2 can elicit a cytoprotective re
106 We demonstrate that honesty can be increased in humans w
107 We demonstrate that Hoxb8 mutants contain corticostriata
108 r4(-/-) mice, and human immune cell culture,
we demonstrate that hRetn binds the LPS receptor Toll-li
109 Here,
we demonstrated that human SS and mouse tumors arising f
110 eover, using liver-specific TRbeta1-KO mice,
we demonstrate that hypothyroidism-associated changes in
111 We demonstrate that imiquimod induces a monomorphic and
112 Using a malaria transmission model
we demonstrate that in such regions dominated by zoophil
113 We demonstrated that in addition to being secreted, TFPI
114 Finally,
we demonstrate that,
in addition to binding DNA, PRDM9's
115 We demonstrate that,
in the case of the three- and four-
116 Mechanistically,
we demonstrated that,
in FANCM-depleted ALT cells, BRCA1
117 We demonstrate that individual modulatory neurons can in
118 In summary,
we demonstrated that inducible lentiviral-mediated ChR2
119 Previously,
we demonstrated that infection with Turnip mosaic virus,
120 Using a genome-wide approach,
we demonstrate that inhibition of transcription is the p
121 Here,
we demonstrate that integration of long-lived Mn(2+) upc
122 Here,
we demonstrated that interferon regulatory factor 4 (IRF
123 Here,
we demonstrate that interplay of p300-HDAC2-Sin3A in the
124 We demonstrate that introduction of equivalent stop codo
125 We demonstrate that IpoC installs a cysteine-derived thi
126 We demonstrate that isolated nuclei regulate their volum
127 Moreover,
we demonstrate that it can also be used to postsynthetic
128 Here
we demonstrate that it is possible to predict the evolut
129 Finally,
we demonstrated that JAM-C controls Src family kinase (S
130 Here,
we demonstrate that KCa1.1 regulates RA-FLS adhesion thr
131 Here
we demonstrate that key RQC activities-Ltn1p-dependent u
132 We demonstrated that kisspeptin administration enhanced
133 nucleotides (nt) of the rabies virus genome,
we demonstrate that L alone initiates synthesis on naked
134 Here,
we demonstrate that largazole and its analogues are isof
135 We demonstrate that Lep-MAP3 obtains very good performan
136 We demonstrate that ligation of TLR3, TLR4, and TLR9 ind
137 We demonstrate, that like PABPN1, MATR3 is critical for
138 We demonstrate that linker labilization method can creat
139 We demonstrate that long-range electrostatic fields eman
140 We demonstrate that loss of STIM2 results in decreased S
141 We demonstrate that loss of Wnt5a results in cerebellar
142 steine in the protein was modified; instead,
we demonstrate that lysine-56 is the key nucleophilic re
143 rating mouse digit tip as a mammalian model,
we demonstrate that macrophages are essential for the re
144 Here,
we demonstrate that many endstage fibrotic diseases, inc
145 n of MAPK1 with open versus closed vinculin,
we demonstrate that MAPK1 exhibits preferential binding
146 Finally,
we demonstrate that MAPPIN outperforms CADD and Eigen in
147 Here
we demonstrate that mass cytometry by time-of-flight pro
148 Here
we demonstrate that mate choice in the fruit fly Drosoph
149 Using this material,
we demonstrate that matrix degradability switches three-
150 Using mouse models,
we demonstrate that melanoma growth is drastically reduc
151 Finally,
we demonstrate that mice with endothelial-specific delet
152 model of inferior vena cava (IVC) stenosis,
we demonstrate that mice with general inducible deletion
153 Here,
we demonstrate that microcalorimetry provides a sensitiv
154 Here
we demonstrate that microsomal triglyceride transfer pro
155 We demonstrate that miR-21-5p is released in the exosoma
156 -directed mutagenesis of histidine residues,
we demonstrated that MsrQ is able to bind two b-type hem
157 Overall,
we demonstrate that Mt/AFM-SECM enables high throughput
158 Here,
we demonstrate that mutant M41L/D67N/K70R/S215Y HIV-2 RT
159 Finally,
we demonstrate that Myo1-facilitated association of Mcp5
160 In addition,
we demonstrate that Nbeal2 is primarily localized in the
161 Here,
we demonstrate that NCC colonize the spleen during embry
162 Mechanistically,
we demonstrate that Nedd4-1 is required for efficient in
163 We demonstrate that neither loss of spatially coordinate
164 Using a mouse model of peritonitis,
we demonstrate that neutrophils elicited in the presence
165 Here
we demonstrate that nigrostriatal dopamine biases ongoin
166 Using 3 nm NiPd NPs as an example,
we demonstrate that NiPd-NG-Si (Si=silicon wafer) can fu
167 In this study,
we demonstrate that novel coordination chemistry accessi
168 We demonstrated that nucleosomes form compact domains wi
169 Finally,
we demonstrate that OA induces mature miR-7 production i
170 verse relaxation-optimized NMR spectroscopy,
we demonstrate that only three of the six domain orienta
171 We demonstrate that optical fibers with tapered tips can
172 We demonstrate that optical spatial solitons with non-re
173 We demonstrate that OsMTP11 functions in alleviating Mn
174 epileptic efficacy or lacking such evidence,
we demonstrated that our set of repurposable drugs is ap
175 We demonstrate that ovarian cancer exhibits a targetable
176 We demonstrate that PABPN1 and MATR3 are required for pa
177 Using in vivo infection assays,
we demonstrate that parasites undergoing coat replacemen
178 Using fiber-FISH,
we demonstrate that parents transmitting the de novo 3 M
179 We demonstrate that partial direct reprogramming of meso
180 We demonstrate that partial loss of p85alpha increases t
181 We demonstrate that particle morphology and evaporation
182 We demonstrate that patterns of species abundance and ri
183 Furthermore,
we demonstrate that performing 96-CBS extractions at the
184 f morphine in the rat.SIGNIFICANCE STATEMENT
We demonstrate that periaqueductal gray (PAG) microglia
185 Consequently,
we demonstrate that persister cells acquire a dependency
186 We demonstrate that perturbations of this assembly machi
187 We demonstrate that photoconductance at resonant illumin
188 d dual-color uncaging of glutamate and GABA,
we demonstrate that plateau potentials can broaden the s
189 cording single unit and population activity,
we demonstrate that PNN removal alters the balance betwe
190 ression of the luteinizing hormone gene, Lhb
We demonstrate that poorly differentiated gonadotropes e
191 Here
we demonstrate that Prdm16 is required for neural stem c
192 We demonstrate that PRMT5-MEP50 is essential for transcr
193 In this study,
we demonstrate that programmed cell death 1 ligand 2 (PD
194 Collectively,
we demonstrate that Raman-DIP can not only indicate meta
195 Mechanistically,
we demonstrated that RCN2 interacted with the epidermal
196 Second,
we demonstrate that reciprocal crosstalk does not occur
197 s and a highly pigmented melanoma cell line,
we demonstrate that reduced expression of either TSC1 or
198 Recently,
we demonstrated that reduced mucociliary clearance, a ch
199 We demonstrate that REEP6 is detected in a subset of Cla
200 Here,
we demonstrate that regulated expression of cytosolic po
201 Finally,
we demonstrate that regulated SRF expression, in turn, i
202 Here
we demonstrate that RPE degeneration in human-cell-cultu
203 Here,
we demonstrated that SERT (-/-) mice display abnormal fa
204 Lastly,
we demonstrate that SHF ventricular and OFT progenitors
205 We demonstrate that shoot meristematic activity can occu
206 We demonstrate that Si(OH)4 cycling through the Holocene
207 We demonstrate that similarity in the transcriptomic res
208 We demonstrate that single droplets with <100 pg of anal
209 We demonstrate that skin pigmentation is highly heritabl
210 Here,
we demonstrate that Ssp1 activates a second ARK, Ssp2/AM
211 the Philadelphia Neurodevelopmental Cohort,
we demonstrate that structural network modules become mo
212 Here
we demonstrate that sub-nanosecond spin-orbit torque pul
213 In this work
we demonstrate that such a photosensitiser, chlorin e6,
214 ta-driven factorizations of this likelihood,
we demonstrate that such approaches can achieve accuracy
215 Finally,
we demonstrated that systemic application of antibiotics
216 Here,
we demonstrated that T-cell intrinsic MyD88 signaling is
217 We demonstrate that TAF11/TAF13 competes for TBP binding
218 We demonstrate that targeted next-generation DNA sequenc
219 In summary,
we demonstrate that the ability of Lon to bind DNA is de
220 ycin class of meroterpenoid antibiotics, and
we demonstrate that the alpha-hydroxyketone rearrangemen
221 We demonstrate that the amplitude of beta activity in th
222 Here,
we demonstrate that the antidepressant-like efficacy of
223 Using a constitutively open mutant of ENaC,
we demonstrate that the augmentation of Na(+) transport
224 Here
we demonstrate that the autocorrelation of the sensor ou
225 Here,
we demonstrate that the clonal stability and number of c
226 We demonstrate that the Co(III)2(IV)2 cubane may be elec
227 Here,
we demonstrate that the co-repressor protein Sin3a is cr
228 We demonstrate that the common anti-malaria drug chloroq
229 Here,
we demonstrate that the compound PF-06446846 inhibits tr
230 ingle nucleotides within DNA macromolecules,
we demonstrate that the distance over which molecular ju
231 Here,
we demonstrate that the emergence of mature topography a
232 Finally,
we demonstrate that the EphB1-ephrin-B1 pathway is disru
233 Here, through limited proteolysis analysis,
we demonstrate that the evolutionarily conserved human C
234 Here,
we demonstrate that the evolutionary fates of the subgen
235 Here
we demonstrate that the expression of an endogenous Braf
236 Moreover,
we demonstrate that the framework allows performing anat
237 Using this approach
we demonstrate that the frequency of a small number of l
238 We demonstrate that the frequency of CXCR5(+)PD-1(+)ICOS
239 Here,
we demonstrate that the FX/SR-AI-complex comprises a thi
240 Through simulation
we demonstrate that the gene tree probabilities computed
241 n the wild-type Landsberg erecta background,
we demonstrate that the GFP-RGA protein is specifically
242 ments and electronic structure calculations,
we demonstrate that the intercalation is driven by the e
243 Gas Chromatography Mass Spectrometry (GCMS),
we demonstrate that the major sterol of Acanthamoeba cas
244 Here,
we demonstrate that the Mn4O5Ca complex poised in the S0
245 Finally,
we demonstrate that the model can be used to quantify si
246 Here
we demonstrate that the N terminus of E3 is necessary to
247 We demonstrate that the N(6)-adenosine methyltransferase
248 sylation and thus loss of effector function,
we demonstrate that the N297G variant has better stabili
249 We demonstrate that the polo-like kinase PLK-1 mediates
250 Finally,
we demonstrate that the regulation of EHD2 oligomerizati
251 ecies to ocean acidification is complex, but
we demonstrate that the response of assemblages to eleva
252 In the present study,
we demonstrate that the robust response observed in infa
253 We demonstrate that the sensor is selective and is able
254 Using a network model,
we demonstrate that the synchronous oscillations in thes
255 Furthermore,
we demonstrate that the transcriptional regulation by th
256 We demonstrate that the transcriptional regulator Runx1
257 erresolution cross-correlation spectroscopy,
we demonstrate that the two flows are correlated and, in
258 In the case of the IRIS system,
we demonstrate that the use of two standards of CO2 in a
259 Here,
we demonstrate that the Wnt/ss-catenin effector Lef1 is
260 Through scenario simulations,
we demonstrated that the estimation of biotransformation
261 We demonstrated that the glycosyl cross-coupling resulte
262 To validate this prediction,
we demonstrated that the modulation of heat-shock factor
263 We demonstrated that the presence of pentobarbital incre
264 Interestingly,
we demonstrated that the significance of ASS1 was not re
265 T9-T10 hemisection spinal cord injury (SCI),
we demonstrated that the tailored scaffolding maintained
266 We demonstrated that the transition from full potency to
267 Moreover, by implementing a novel technique,
we demonstrate that these gaps have opposite sign with r
268 We demonstrate that these, when added as an additive to
269 We demonstrated that these endothelial cells supply the
270 We demonstrated that these mutations reduce MRPS34 prote
271 a metastable mixed disulfide bond with TG2,
we demonstrated that these proteins specifically recogni
272 Here,
we demonstrated that these two miRNAs are prominently ex
273 scence in single cells in vivo in the liver,
we demonstrate that this activates tissue-specific expre
274 We demonstrate that this inability to activate mast cell
275 Furthermore,
we demonstrate that this mechanism is disrupted in conge
276 We demonstrate that this notion is not a general princip
277 r preferences before and after the invasion,
we demonstrate that this species experienced a significa
278 We demonstrate that this technique provides an effective
279 We demonstrate that this unusual cyclic behaviour is gov
280 In addition,
we demonstrated that this protease rapidly hydrolyzes St
281 Of five azoles tested,
we demonstrate that tioconazole and voriconazole have th
282 Here,
we demonstrate that tool-assisted foraging on shellfish
283 We demonstrate that transcranial static magnetic field s
284 Here,
we demonstrate that treatment of human MCF-7 breast canc
285 In this study,
we demonstrate that treatment with recombinant human IL-
286 In this study,
we demonstrated that treatment and distribution processe
287 In this report,
we demonstrate that two cardiotonic steroids already in
288 We demonstrate that two distinct chemical entities contr
289 In this study,
we demonstrated that two of the six GH12 proteins produc
290 Furthermore,
we demonstrated that,
under realistic scenarios, common
291 set of CPK28 autophosphorylation sites, and
we demonstrate that,
unexpectedly, autophosphorylated CP
292 aluation study including 11 sites worldwide,
we demonstrate that using SWATH-mass spectrometry data a
293 We demonstrate that variation in Fgf8 expression has a n
294 munities across a natural predation gradient
we demonstrate that variation in the identity of top pre
295 Here,
we demonstrate that we can reversibly control the hole c
296 We demonstrated that while ICH induced mast cell activat
297 We demonstrate that,
while free enzymes display weak act
298 We demonstrated that,
with the exception of Delta4 desat
299 We demonstrated that wrinkled surfaces can guide water s
300 We demonstrate that YonO is a bona fide RNAP of the SPbe