1 suppression around the curved waveguide are
further demonstrated.
2 We
further demonstrate a concurrent increase in NF-kappaB s
3 degrees C) to recover the cell capacity, and
further demonstrate a flow battery system based on the r
4 ato reporter cell line with AHR deletion, we
further demonstrate a marked enhancement of hematopoieti
5 We
further demonstrate a multiplexing strategy to simultane
6 We
further demonstrate a room temperature thermomechanical-
7 Prenatal stress
further demonstrated a positive, dose-response relations
8 We
further demonstrated a similar increase in glutamate fol
9 ffectiveness of integrated RTC strategies is
further demonstrated against tightening environmental st
10 We
further demonstrate an important role for non-adrenergic
11 We
further demonstrate an improvement in directly acquiring
12 Under the same knockdown condition, we
further demonstrate an increase in fatty acid content, p
13 study and no change in healthy controls, and
further demonstrates an increase of free water in Parkin
14 The 3D CNTs-AMB1 nanocomposite scaffold is
further demonstrated as a potential substrate for electr
15 We
further demonstrate by an in vitro approach that this pr
16 Separation selectivity was
further demonstrated by application of the scheme to the
17 e synthetic utility of the reaction has been
further demonstrated by converting the intermediate orga
18 al-write and optical-erase memory element is
further demonstrated by coupling ion migration with elec
19 ous species accumulation in CO2 reduction is
further demonstrated by replacing Pd with Rh.
20 The power of CR-FS and SVM classification is
further demonstrated by segregating the crystal structur
21 the CNS and leptomeningeal infiltration was
further demonstrated by specific reduction of CNS leukem
22 The power of targeting APC was
further demonstrated by the complete normalization of bl
23 racticability and utility of our approach is
further demonstrated by the construction of a chemically
24 at position 11 for NTS1/NTS2 selectivity was
further demonstrated by the design of new NT analogues b
25 The necessity of S831 GluA1 was
further demonstrated by the lack of extinction in S831A
26 The orthogonality of the two stimuli is
further demonstrated by UV-vis, NMR, and density functio
27 We
further demonstrate capillary breakup of cylindrical por
28 We
further demonstrate cellular AMPK signaling independent
29 on most envelope proteins in all viruses and
further demonstrated conserved patterns of O-glycans on
30 DHC-treated stroke mice
further demonstrated decreased neuronal loss and astrogl
31 Our data
further demonstrated defects in autophagic flux and lyso
32 Novel living devices are
further demonstrated,
enabled by 3D printing of programe
33 This paper
further demonstrates enhanced electron transport by clos
34 We
further demonstrate enrichment of ZBTB24 at the CDCA7 pr
35 We
further demonstrate EptA orthologs from non-cholerae Vib
36 We
further demonstrate examples of how GLITTER can evaluate
37 Remarkably, we have
further demonstrated for the first time that engineered
38 Our simulations
further demonstrate how active scale selection controls
39 for ASO depend on chemical modifications and
further demonstrate how ASO-protein interactions influen
40 We
further demonstrate how combining data from multiple sen
41 We
further demonstrate how different regulatory sequences g
42 We
further demonstrate how the geometry of these pores can
43 We
further demonstrate how these nanomolecules grafted with
44 We
further demonstrate how this electronic behavior changes
45 We
further demonstrate how this novel synaptic arrangement
46 The model
further demonstrated how EF can be maintained in ventric
47 Our work
further demonstrates how rapidly A. baumannii can genera
48 tive deletion of Il4ra on Foxp3(+) cells, we
further demonstrate IL-4 is required for the development
49 We
further demonstrate in nasopharyngeal carcinoma CNE2 and
50 Such a pH-sensing mechanism is
further demonstrated in the EnvZ-OmpR two-component syst
51 The synthetic utility of the method is
further demonstrated in the oxidation of a sterically hi
52 RPA and decreased expression of HLA-DRB1 was
further demonstrated in this HPVOPC subject and an addit
53 We
further demonstrate increased expression of KATII and KM
54 We
further demonstrated MERFISH measurements of complex tis
55 We
further demonstrate near-100% position-controlled partic
56 We
further demonstrate non-contact, in situ measurement of
57 We
further demonstrated protein misfolding cyclic amplifica
58 In line with this, our functional results
further demonstrated region-selective roles of cortical
59 y temporarily inactivating Bop1 function, we
further demonstrate selective killing of p53-deficient c
60 troscopic photon localization microscopy, we
further demonstrated simultaneous multi-colour super-res
61 We
further demonstrate single-mRNA detection across the ent
62 Upon CAR T-cell termination, we
further demonstrated successful hematopoietic engraftmen
63 We
further demonstrate tHapMix utility by creating a simula
64 We
further demonstrate that a bispecific anti-CD70/SIRPalph
65 We
further demonstrate that a previously reported V-ATPase
66 We
further demonstrate that Abeta pathology and neuroinflam
67 We
further demonstrate that adrenergic modulation of Kv1.1
68 We
further demonstrate that AhR suppresses class switching
69 We
further demonstrate that AIPL1 significantly modulates t
70 We
further demonstrate that application of this conjugation
71 We
further demonstrate that atomic mass modifications influ
72 Our findings
further demonstrate that BD-induced C cycle impacts (i)
73 We
further demonstrate that both Chd7 and Top2b are necessa
74 We
further demonstrate that both Schottky (Ti/p-Si) and poo
75 We
further demonstrate that CD4+T cells from AD patients re
76 We
further demonstrate that cells with ALDH activity can co
77 We
further demonstrate that co-disruption of Apob, whose ge
78 We
further demonstrate that concurrent inhibition of MDM2 a
79 We
further demonstrate that conserved CREs bind master regu
80 We
further demonstrate that covalent coupling prevents rele
81 We
further demonstrate that Cu stress impairs the pathway f
82 Density functional theory calculations
further demonstrate that Cu11 Bi7 can be stabilized (rel
83 We
further demonstrate that DCA can differentiate between s
84 Here, we
further demonstrate that depletion of AUF1 abolishes the
85 Through simulations, we
further demonstrate that depth can be estimated reasonab
86 We
further demonstrate that differences in the aggregation
87 We
further demonstrate that downregulation of Cygb prevents
88 We
further demonstrate that Dpb11 can directly recruit DDK
89 We
further demonstrate that DTD positively selects the univ
90 We
further demonstrate that EGR1, a transcription factor pr
91 We
further demonstrate that either depleting SRSF1 or preve
92 e Vk*MYC mouse model of multiple myeloma, we
further demonstrate that exogenously administered CgA wa
93 We
further demonstrate that exposure of HAECs to oxidized p
94 We
further demonstrate that expression of a significant fra
95 We
further demonstrate that EZH2(Delta/Delta)FOXP3(+) T cel
96 We
further demonstrate that folate activates a metabolic re
97 Here, we
further demonstrate that Gab2 mediates hepatocarcinogene
98 We
further demonstrate that Gag-Pro is not the main driver
99 We
further demonstrate that GFP can be mechanically switche
100 We
further demonstrate that GIT2 inhibits the interaction o
101 We
further demonstrate that glucosylsphingosine specificall
102 Behavioral studies
further demonstrate that GLYX-13 does not influence 5-HT
103 We
further demonstrate that GP-specific IgG1 is by far the
104 We
further demonstrate that IEC Ifnlr1 expression is requir
105 We
further demonstrate that in the presence of membrane-ass
106 We
further demonstrate that inhibiting NETosis by blocking
107 interactions with its neuronal receptor, and
further demonstrate that inhibiting toxin binding to the
108 We
further demonstrate that inhibition of PDE2A, by enhanci
109 We
further demonstrate that inhibition of TLR4 signaling ab
110 We
further demonstrate that iPSC-derived OL disperse and my
111 We
further demonstrate that IQF substrates containing unnat
112 We
further demonstrate that knockdown of keratin 18 phenoco
113 We
further demonstrate that LFY has an inhibitory effect on
114 We
further demonstrate that lncRNAs overlapping expression
115 We
further demonstrate that loop 5 preceding these ten C-te
116 We
further demonstrate that loss of one allele of PTEN is s
117 We
further demonstrate that matriptase and APP directly int
118 We
further demonstrate that MEK/ERK and PI3K-C2beta are req
119 We
further demonstrate that mESCs must be released from Oct
120 We
further demonstrate that microglia regulate the activity
121 We
further demonstrate that miR-26a directly target Jagged1
122 We
further demonstrate that MMP expression and binding of t
123 We
further demonstrate that molecules structurally related
124 We
further demonstrate that mtl-1 is responsible for the bi
125 We
further demonstrate that murine SCLC tumors were highly
126 We
further demonstrate that MV-associated VEGF90K has a wea
127 aspects of GC-induced OHT in humans, and we
further demonstrate that myocilin does not play a major
128 We
further demonstrate that Nop9 inhibits Nob1 cleavage, th
129 We
further demonstrate that nucleosome occupancy around ori
130 We
further demonstrate that our deprivation did not impair
131 Additionally, we
further demonstrate that overexpression of VGLL4 reduces
132 We
further demonstrate that P2X5 is required for ATP-mediat
133 Our observations
further demonstrate that previously unknown virus-host r
134 We
further demonstrate that production can be enhanced up t
135 We
further demonstrate that prolonged inflammatory stress c
136 We
further demonstrate that Prosapip1 is required for alcoh
137 We
further demonstrate that pseudocobalamin is several orde
138 We
further demonstrate that receptor-interacting protein ki
139 We
further demonstrate that Shv is selectively released dur
140 We
further demonstrate that Sirt1 interacts and deacetylate
141 We
further demonstrate that SIRT2-mediated lysine defatty-a
142 We
further demonstrate that specific GAS clinical isolates
143 We
further demonstrate that such a widely tunable BP photod
144 Our data
further demonstrate that SWI/SNF-dependent distal enhanc
145 We
further demonstrate that targeting the CAR to the TRAC l
146 We
further demonstrate that the absence of IL-4Ralpha signa
147 We
further demonstrate that the ADF3-dependent defense mech
148 We
further demonstrate that the agile and transparent hydro
149 We
further demonstrate that the ALS-associated UBQLN4 varia
150 We
further demonstrate that the atypical chemokine receptor
151 We
further demonstrate that the binding involves an almost
152 The far field results
further demonstrate that the camera can capture quantita
153 We
further demonstrate that the charge transport anisotropy
154 We
further demonstrate that the chromatin modifier USP21 re
155 Our data
further demonstrate that the combination of TIE2 and cav
156 We
further demonstrate that the endosomal beta2-adrenergic
157 We
further demonstrate that the extra transmembrane domain
158 We
further demonstrate that the gene for guanosine monophos
159 transgenic multiple system atrophy mice and
further demonstrate that the glucagon-like peptide-1 ana
160 We
further demonstrate that the heme scavenger hemopexin pr
161 Using nylon 12 as an example matrix, we
further demonstrate that the inclusion of C-coated compo
162 We
further demonstrate that the inhibition of the CamKKB or
163 We
further demonstrate that the intersection between the Wn
164 We
further demonstrate that the master transcriptional regu
165 We
further demonstrate that the occurrence of bulges is not
166 We
further demonstrate that the production of PGE2 provides
167 We
further demonstrate that the proposed logic-device, whic
168 We
further demonstrate that the prototypical Ca(2+) sensor
169 We
further demonstrate that the Sm proteins and pICln, SMN
170 We
further demonstrate that the structural integrity of sel
171 We
further demonstrate that these interactions are also req
172 We
further demonstrate that these interneurons gate sensory
173 ructure-guided cell-based inhibition studies
further demonstrate that these loops could serve as exce
174 We
further demonstrate that these native silk micrococoons
175 cancer and precursor lung cancer lesions and
further demonstrate that these results can be derived us
176 We
further demonstrate that these substrates can be shed by
177 ic simulations of a CA1 pyramidal neuron, we
further demonstrate that theta-driving neurons possess t
178 We
further demonstrate that this Kirkendall cavitation proc
179 We
further demonstrate that this postsynthetic modification
180 We
further demonstrate that this process has evolved separa
181 We
further demonstrate that this protective complex preserv
182 We
further demonstrate that this proxy-CRISPR strategy is a
183 We
further demonstrate that this same population of CB1 rec
184 We
further demonstrate that this signal is initiated by ext
185 We
further demonstrate that this unique dimerization interf
186 We
further demonstrate that this unique FIN219-FIP1 structu
187 We
further demonstrate that translation of CD20 mRNA is sig
188 We
further demonstrate that TRC35 binding is critical not o
189 We
further demonstrate that treatment of myelin-specific T
190 Using cell lineage tracing, we
further demonstrate that trunk neural crest cells do, in
191 We
further demonstrate that turnover of damage-induced nucl
192 We
further demonstrate that type I and type II agonists hav
193 We
further demonstrate that viruses harboring either a W237
194 Through functional assays, we
further demonstrate that wild-type SCARB1 promotes cellu
195 We
further demonstrate that Wnt signaling regulates stem ce
196 We
further demonstrate that ZBP1 senses viral ribonucleopro
197 We
further demonstrate that, within these same fiber tracts
198 We
further demonstrated that 3 APOA5 SNPs with established
199 We
further demonstrated that a U-shaped relationship betwee
200 We
further demonstrated that actin filaments in the entotic
201 ytometry and confocal imaging with QD620-IRS
further demonstrated that binding specifically to HCC827
202 We
further demonstrated that both JNK1 and JNK2 regulated N
203 dy 2 (n = 3,064) replicated this finding and
further demonstrated that callers' prediction accuracy w
204 We
further demonstrated that CAMK2gamma suppressed growth f
205 We
further demonstrated that caspase-1 and caspase-11 diffe
206 We
further demonstrated that CB6 click can be used in conju
207 We
further demonstrated that CD137 was important for the ac
208 of RNA-seq data from The Cancer Genome Atlas
further demonstrated that concordant upregulation of the
209 We
further demonstrated that COUP-TFII also reduces the act
210 Studies with baculosomes
further demonstrated that CYP2D6 and CYP3A4 could transf
211 We
further demonstrated that deletion of ami1 leads to incr
212 It is
further demonstrated that deterministic, nonvolatile wri
213 We
further demonstrated that dilated vasculature, loss of v
214 NMR spectroscopy
further demonstrated that DREB2A underwent coupled foldi
215 We
further demonstrated that extracellular lumican physical
216 We
further demonstrated that following vaccination of a rep
217 We
further demonstrated that HDAC5 promoted the protein sta
218 We
further demonstrated that higher MARCKS expression promo
219 tial profiling of the iron-laden infiltrates
further demonstrated that higher numbers of infiltrating
220 We
further demonstrated that HOTAIR regulates DR5 expressio
221 assay, but not in vitro Sequencing analyses
further demonstrated that Hsp90 increased both A3G cytos
222 We
further demonstrated that IL-17 contributes to persisten
223 of JUN target genes, including DLL4 Our work
further demonstrated that JUN strongly stimulates endoth
224 we not only confirmed these results but also
further demonstrated that Kir2.1-52V is associated with
225 ated with no change in transcription, and we
further demonstrated that Klhl31 targets FlnC for ubiqui
226 Immunofluorescence analysis
further demonstrated that macrophages were a significant
227 Application of MB to this 3D skin model
further demonstrated that MB improved skin viability, pr
228 We
further demonstrated that MKL can influence cell migrati
229 Using the N-WASP inhibitor wiskostatin, we
further demonstrated that N-WASP is required for localiz
230 Our results
further demonstrated that nitrogen availability might pl
231 g genetically encoded calcium indicators, we
further demonstrated that NPS reliably induces a transie
232 We
further demonstrated that optogenetic activation of stri
233 This analysis
further demonstrated that patch-leaving decisions were n
234 Our study
further demonstrated that PDZK1 inhibited cell prolifera
235 We
further demonstrated that Rac1 activation is responsible
236 These data
further demonstrated that Raf kinases are required for p
237 We
further demonstrated that RNAi-mediated ABHD5 silencing
238 We
further demonstrated that SERS can be used as a broad de
239 Our studies
further demonstrated that SHP1 encoded by Ptpn6 binds an
240 We
further demonstrated that stress-induced release of sCD9
241 We
further demonstrated that Sty1-mediated Atf1 phosphoryla
242 hairpin and monomer and Monte Carlo modeling
further demonstrated that such nano-assemblies have elev
243 Quantitative imaging analysis
further demonstrated that the ability of Smy1 to directl
244 We
further demonstrated that the absence of Sirt1 or the ec
245 We
further demonstrated that the conformational cross-talk
246 We
further demonstrated that the hydrolysis activity of GIM
247 We
further demonstrated that the immune-enhancing effects o
248 We
further demonstrated that the increase in HP [1-(13)C]la
249 Protein-protein interaction studies
further demonstrated that yeast yUtp23 and human hUTP23
250 We
further demonstrated that ZEB1 is required for early car
251 We
further demonstrated that, in NSCs, MBD1 binds and repre
252 We
further demonstrated that, upon CREB activation, HDAC2 r
253 nalysis with Treg fate-mapping reporter mice
further demonstrates that IL-27 signaling in Tregs may c
254 ocal-enhancement/global-inhibition mechanism
further demonstrates that positioning of rear retraction
255 It
further demonstrates that this community is thermally re
256 Evolutionary analysis
further demonstrates that this haematopoietic programme
257 g, which included following Brainbow clones,
further demonstrates that this process is sustained by t
258 The identification of these four UBPs
further demonstrates that when optimized, hydrophobic an
259 We
further demonstrate,
that the suppression of alpha-syn a
260 We
further demonstrate the ability of the local concentrati
261 We
further demonstrate the ability to control extrusion hot
262 We
further demonstrate the ability to process the neural ac
263 We
further demonstrate the applicability of our method in a
264 We
further demonstrate the broad applicability of the platf
265 Our results
further demonstrate the computational power of synaptic
266 Our results
further demonstrate the dependence of local fitness land
267 We
further demonstrate the detection of a unique protein pr
268 We
further demonstrate the efficacy of the brain-permeant P
269 Experimental breakthrough curves
further demonstrate the excellent performance of these h
270 We
further demonstrate the existence of adiabatic pumping f
271 Our findings
further demonstrate the general importance of fine-tunin
272 We
further demonstrate the impact of these multiple vortice
273 Our results
further demonstrate the importance of dust in aerosol-cl
274 We
further demonstrate the importance of eliminating WT vir
275 These results
further demonstrate the importance of external factors,
276 Our data
further demonstrate the importance of Vascular Endotheli
277 These results
further demonstrate the interest in foldaxanes to design
278 Results of the study also
further demonstrate the potential of ultrasonication tec
279 These results
further demonstrate the prion-like characteristics of al
280 We
further demonstrate the rapid prototyping capability of
281 We
further demonstrate the system's compatibility with exis
282 We
further demonstrate the utility of CRISPR-Cas9 generated
283 These findings
further demonstrate the utility of noninvasive in vivo P
284 These data
further demonstrate the utility of PfMSP8 as a parasite-
285 We
further demonstrate the utility of this collection of sc
286 es identified by different statistical tests
further demonstrated the advantage of EBT.
287 We
further demonstrated the JMJD6 function in alternative s
288 We
further demonstrated the versatility of this copolymeriz
289 Our study
further demonstrates the use of a combined genomics and
290 a more traditional aluminosilicate catalyst,
further demonstrating the capacity of the MOF to contain
291 L2* partially rescued the defects of bri1-5,
further demonstrating the conserved function of GmBZL2 w
292 We
further demonstrate their effectiveness in identifying m
293 entire chromosomal locus encoding the T3SS,
further demonstrating their desirability and effectivene
294 of the pyrazole-5-aldehyde intermediates was
further demonstrated through a deprotection and double-r
295 of the products derived from this method is
further demonstrated through derivatization of the chira
296 Acoustic-transfection was
further demonstrated to deliver CRISPR-Cas9 systems to s
297 This specific Rab7(+) compartment was
further demonstrated to serve as a major site for active
298 The application of this protocol is
further demonstrated to the synthesis of azafluorenone r
299 ntial of these 2D ferroelectric materials is
further demonstrated using the examples of van der Waals
300 The advantages of the proposed framework are
further demonstrated with real datasets from two microbi