1 , and gemcitabine in biological matrices was
further demonstrated.
2 ing factor with a step-and-flash approach is
further demonstrated.
3 We
further demonstrate a novel and powerful approach to app
4 We
further demonstrate a room-temperature sodium-based plas
5 We
further demonstrated a direct preventive potential of Pr
6 We
further demonstrated a multiplex and scalable approach t
7 This research
further demonstrates a durable Li-Se/S pouch cell with h
8 It
further demonstrates a more complex evolutionary scenari
9 Reverse phase protein array
further demonstrated activation of noncanonical WNT sign
10 We
further demonstrate an unprecedented role for AP-1B at t
11 We
further demonstrate analogous relationships between exon
12 We
further demonstrate by both in vitro and in vivo tests t
13 Overlap with regulatory regions was
further demonstrated by comparisons to the 127-epigenome
14 The applicability of the method was
further demonstrated by conducting a limited survey on t
15 SMOLT's clinical utility is
further demonstrated by developing a multiplex assay for
16 The cell-like potential of this design was
further demonstrated by leveraging the outward pumped pr
17 The value of this assay was
further demonstrated by quantifying differences in TSDR
18 sion in Tet2- and Tet3-deficient B cells was
further demonstrated by the restriction, albeit not comp
19 The synthetic utility is
further demonstrated by the total syntheses of salinipyr
20 We
further demonstrate cotranscriptional self-assembly of t
21 We
further demonstrate electrokinetic separation of two ani
22 We
further demonstrate entanglement manipulation by using G
23 We
further demonstrate experimentally that CA decomposition
24 We
further demonstrate fast and streamlined fabrications of
25 nly associated with adolescent THC exposure,
further demonstrating functional and long-term neuroprot
26 or observed for defect-rich g-C(3)N(4), thus
further demonstrating g-C(3)N(4) can be both a photoanod
27 To
further demonstrate GCIM, a series of Monte Carlo simula
28 We
further demonstrate here the linked arrangement of 5S an
29 We
further demonstrate higher levels of intra-lesion hetero
30 and autobiographical memory as examples that
further demonstrate how cultural elements shape the proc
31 We
further demonstrate how fragmentation of THF-doped DOM i
32 We
further demonstrate how MAG-ganglioside interactions can
33 We
further demonstrate how our audience segmentation method
34 We
further demonstrate how the charge current can switch th
35 We
further demonstrate how the enzymatic cycle is detuned b
36 We
further demonstrate how the most common FC measures (cor
37 Solute transport modelling
further demonstrates how increases in the importance of
38 We
further demonstrated improved neutrophil function: norma
39 We
further demonstrate in vitro that proliferation, and in
40 N-MADD-4B interaction with NLG-1 in vitro We
further demonstrate in vivo that this Ig-like domain is
41 The pathophysiological relevance is
further demonstrated in a conditional and adipocyte-spec
42 The versatility of FERM was
further demonstrated in models of inflammatory bowel dis
43 or of extreme air pollution events, has been
further demonstrated in predicting the seasonal agricult
44 ility in biologically relevant detection was
further demonstrated in simulated urine using Ni(3)HHTP(
45 ed nanoparticles was shown in 2D culture and
further demonstrated in spheroids.
46 Its functional significance was
further demonstrated in vivo using Xenopus laevis embryo
47 We
further demonstrate its utility by pairing the method wi
48 We
further demonstrate its utility for understanding myobla
49 We
further demonstrated its applicability by analyzing glyc
50 ation mediated by the unconventional system,
further demonstrating its catalysis-independent nature.
51 We
further demonstrate multilocation decoupling and multimo
52 We
further demonstrate nanostructure morphology can be tune
53 We
further demonstrate novel applications of this model to
54 We
further demonstrate O(2) uptake behavior similar to that
55 Substantial improvement of ULM is
further demonstrated on a chicken embryo tumor xenograft
56 We
further demonstrate our assay by detecting SARS-CoV-2 vi
57 We
further demonstrate printed transistor devices and chemi
58 In situ localization studies
further demonstrated reduced expression of mutant UNC-45
59 asty of normal breast tissue (e.g. 184A1) to
further demonstrate similar traits in the frequency of a
60 Using chemogenetic manipulation, we
further demonstrate specific roles for this circuitry in
61 We
further demonstrate that a joint analysis of both common
62 By paired patch-clamp recordings, we
further demonstrate that acutely introducing an N-termin
63 We
further demonstrate that addition of epitope tags to the
64 We
further demonstrate that aerosolized fomites can be gene
65 We
further demonstrate that agency's impact on patience is
66 We
further demonstrate that another mutation, located in th
67 We
further demonstrate that ATM- and NBS1-dependent recruit
68 Using a conditional KO approach, we
further demonstrate that Bax acts via the bipolar cell p
69 In vitro studies
further demonstrate that BBR induces TRIB1 mRNA expressi
70 We
further demonstrate that bio-advection, rather than wate
71 We
further demonstrate that blocking the interaction of ApE
72 We
further demonstrate that CcfM promotes motility and magn
73 We
further demonstrate that CHK2-mediated autophagy has an
74 We
further demonstrate that claudin trafficking and half-li
75 We
further demonstrate that common variability at genes imp
76 We
further demonstrate that communities from similar ecosys
77 We
further demonstrate that concurrent disruption of the ac
78 o complement these structural attributes, we
further demonstrate that covalently tethering a supramol
79 We
further demonstrate that cross-linking impairs the chole
80 We
further demonstrate that DEMETER access to some of these
81 an in vivo biophotonic imaging platform, we
further demonstrate that dietary Mg(2+) supplementation
82 We
further demonstrate that distinct segments accumulate in
83 eptidase-4 (DPP4) in glucose homeostasis, we
further demonstrate that DMAb-treated participants have
84 We
further demonstrate that Dnmt3b is linked to a control o
85 We
further demonstrate that ELBA collaborates with other in
86 We
further demonstrate that enhanced n-type doping can be r
87 We
further demonstrate that Env trimers are confined to sub
88 cipitation and proximity ligation assays, we
further demonstrate that ETS1 and p300 physically intera
89 We
further demonstrate that FBP1-deficient hepatocytes prom
90 We
further demonstrate that full-length sequencing platform
91 We
further demonstrate that geosmin can be used as bait und
92 Our results
further demonstrate that GNL1 promotes cell growth and s
93 Ex vivo osteoclastogenesis assays
further demonstrate that Hdac3 deficiency limits osteocl
94 We
further demonstrate that Hec1 tail phosphorylation regul
95 We
further demonstrate that IL-4 limits neutrophil migratio
96 We
further demonstrate that improved retinal contrast trans
97 s self-organizing criticality properties, we
further demonstrate that in vitro brain-derived neuronal
98 Our data
further demonstrate that increase in intra-tumoural alph
99 We
further demonstrate that infection with MHV induces a se
100 We
further demonstrate that inhibition of mTOR was sufficie
101 We
further demonstrate that integrin alpha6beta4 regulates
102 We
further demonstrate that it performs remarkably well eve
103 We
further demonstrate that L-whirlin binds to PCDH15 and C
104 We
further demonstrate that late graft rejection in recipie
105 We
further demonstrate that ManN and two N-glycosylation in
106 We
further demonstrate that mannose supplementation can att
107 We
further demonstrate that mantle oxygen fugacity has an e
108 We
further demonstrate that MAOA is down-regulated as a res
109 Using a coimmunoprecipitation approach, we
further demonstrate that mMOR-1G physically associates w
110 asurements and first-principles calculations
further demonstrate that MnBi(4)Te(7) is a Z(2) antiferr
111 Here, we
further demonstrate that more than ten fundamental equat
112 We
further demonstrate that MsrB2 selectively reduces oxidi
113 We
further demonstrate that mucosal secretory IgA is not re
114 We
further demonstrate that n-apo AI binds to neutrophils a
115 4 to produce DHCR24* in vitro and in vivo We
further demonstrate that NS3-4A cleaves DHCR24 between r
116 equencing and high resolution 3D imaging, we
further demonstrate that organoid cultures derived from
117 We
further demonstrate that our genetically engineered tumo
118 We
further demonstrate that our non-local alternative model
119 We
further demonstrate that p21-activated kinase 4 (PAK4) c
120 We
further demonstrate that p53 influences expression of th
121 We
further demonstrate that potent and selective UCHL1 inhi
122 en the acquisition and extinction phases, we
further demonstrate that proximal threats impaired extin
123 We
further demonstrate that Psi strengthens U4/U6 RNA-RNA a
124 We
further demonstrate that Rad54 disrupts the donor templa
125 We
further demonstrate that radiation shielding reduces the
126 We
further demonstrate that RBOHD and RBOHF are both requir
127 Using a novel D-loop Mapping Assay, we
further demonstrate that Rdh54/Tid1 uniquely restricts t
128 We
further demonstrate that RecA filaments disrupt G4 struc
129 We
further demonstrate that repression of subtelomere silen
130 We
further demonstrate that revamp results in easily interp
131 ng cell lines and lymphoma primary cells, we
further demonstrate that S70pBcl2 reduces the interactio
132 We
further demonstrate that select analogs potently increas
133 Field experiments
further demonstrate that Sesarma-grazed creekheads, thro
134 We
further demonstrate that similar mechanisms are involved
135 We
further demonstrate that some of these interactions migh
136 We
further demonstrate that SPD confers liver protection by
137 We
further demonstrate that subtle disequilibria also affec
138 We
further demonstrate that SUMOylation regulates SG disass
139 We
further demonstrate that temporal integration of auxin c
140 We
further demonstrate that TFIIH restricts CDK7 kinase fun
141 We
further demonstrate that the affinities of eIF4GI and DA
142 We
further demonstrate that the conformational "readout" ca
143 designing different analyte aptamers, and we
further demonstrate that the constructed PIERS sensor ca
144 We
further demonstrate that the cytoprotective function of
145 ibit negative polarization degrees, and they
further demonstrate that the dependence of polarization
146 We
further demonstrate that the disconnection-mediated GB m
147 We
further demonstrate that the ectopic Olig2 accounts for
148 In the same theoretical framework, we
further demonstrate that the effects of noise correlatio
149 We
further demonstrate that the fatigue-resistant hydrogel
150 We
further demonstrate that the high (1)O(2) production eff
151 ciation constant (K(D) ) as low as 0.8 nm We
further demonstrate that the identified antibodies have
152 We
further demonstrate that the ion-conducting pore of TMEM
153 We
further demonstrate that the meshes generated by the Geo
154 We
further demonstrate that the model can be used to identi
155 We
further demonstrate that the Rpfs function as endo-actin
156 We
further demonstrate that the signaling function of OPDA,
157 We
further demonstrate that the SUMO protease activity is r
158 We
further demonstrate that these are the only binding prot
159 We
further demonstrate that this behavior depends on the me
160 We
further demonstrate that this effect of AMOT on BMP-SMAD
161 We
further demonstrate that this level of cross-linking den
162 We
further demonstrate that this macrophage recruitment req
163 We
further demonstrate that this particle motion can be des
164 We
further demonstrate that this reciprocal regulation serv
165 We
further demonstrate that this signaling pathway can be s
166 We
further demonstrate that this total marine dark extracel
167 We
further demonstrate that this virus is broadly distribut
168 We
further demonstrate that total internal reflection fluor
169 We
further demonstrate that transfer learning, the process
170 We
further demonstrate that treatment with radiation and po
171 Results
further demonstrate that TSWV titers in the vector were
172 We
further demonstrate that using an ensemble of neural net
173 amyl-tRNA reductase by immature tRNA(Glu) We
further demonstrate that whereas overexpression of tRNA(
174 We
further demonstrate that, in the presence of contaminati
175 The results
further demonstrated that 2-OH-NQ, similar to dUMP, bind
176 We
further demonstrated that a feedback control mechanism c
177 We
further demonstrated that abolishing Arl4D-EB1 interacti
178 We
further demonstrated that acute CMV infection-mediated t
179 We
further demonstrated that AKT1 protein deficiency caused
180 We
further demonstrated that APOA1 mimetic peptides: i) inh
181 Using logistic regression, our study
further demonstrated that asplenia, fever, and reduced O
182 We
further demonstrated that because of the force-dependent
183 We have
further demonstrated that BMPRII deficiency promotes exc
184 m where only pDCs had access to antigens, we
further demonstrated that cross-presenting pDCs were una
185 st adenosine receptors A(2A)R and A(2B)R, we
further demonstrated that ENT1/2 blockade protected agai
186 -reactive serology and a child with ASD, and
further demonstrated that exposure in utero to a monoclo
187 We
further demonstrated that FAK's kinase activity is requi
188 We
further demonstrated that FHR1 and FHR3 compete with CFH
189 They
further demonstrated that fumarate changes FrdA's confor
190 We
further demonstrated that Gal2-KO mice developed signifi
191 We
further demonstrated that gene therapy that combines AAV
192 We
further demonstrated that global differential DNA methyl
193 We
further demonstrated that GOC plants had significant adv
194 ibit IFN-gamma by binding to EIF2AK2, and we
further demonstrated that GRASLND exhibits a protective
195 We
further demonstrated that in vivo lung delivery of the m
196 We
further demonstrated that juvenile csf1r-deficient zebra
197 We
further demonstrated that MAP was more robust than the l
198 t-derived induced pluripotent stem cells, we
further demonstrated that MCM10 is required for NK cell
199 h different levels of mgrA transcription, we
further demonstrated that MgrA negatively impacted invas
200 Using CRBN-deficient mice, we
further demonstrated that microvessal formation can occu
201 We
further demonstrated that miRNAs contained in the ATI-EV
202 Thermoelectric transport studies
further demonstrated that MoS(2) films show p-type therm
203 We
further demonstrated that Msi1 overexpression affects IE
204 We
further demonstrated that NF-kappaB activation contribut
205 We
further demonstrated that NP1 directly interacts with CP
206 orrelative light and electron microscopy, we
further demonstrated that one of these membraneless orga
207 We
further demonstrated that our model could be transferred
208 We
further demonstrated that P2 excision greatly hinders gr
209 This study
further demonstrated that p36(CBX7) was localized to the
210 We
further demonstrated that palmitoyl coenzyme A is a liga
211 We
further demonstrated that rapid screening of mitochondri
212 We
further demonstrated that ROS suppressed the type I inte
213 We
further demonstrated that SOX9 knockdown increases cellu
214 We
further demonstrated that synchrotron-based X-ray imagin
215 We
further demonstrated that TFAM binds directly and select
216 We
further demonstrated that the anodization of GCE at high
217 We
further demonstrated that the anti-angiogenic variant, V
218 We
further demonstrated that the CAR synapse can be enginee
219 It was
further demonstrated that the cold-water intrusions may
220 onsortium for Neuropsychiatric Phenomics, we
further demonstrated that the connectivity of the identi
221 We
further demonstrated that the CRY2-CRY1 heterooligomeriz
222 ar, cellular and pharmacological experiments
further demonstrated that the expression of K-Cl co-tran
223 We
further demonstrated that the GAd capsid fiber shared th
224 We
further demonstrated that the increased triglyceride acc
225 We
further demonstrated that the metabolic fate of the guai
226 Multivariate pattern analysis
further demonstrated that the modulation patterns of ben
227 We
further demonstrated that the NAD-dependent protein deac
228 We
further demonstrated that the positively charged basic a
229 benchmark of other LRR protein complexes, we
further demonstrated that the present approach may be br
230 We
further demonstrated that the role of YAP signaling is c
231 The authors
further demonstrated that these imaging patterns could p
232 Computational modeling
further demonstrated that these trait-related performanc
233 We
further demonstrated that this could be explained by the
234 We
further demonstrated that treatment with the DNA-polymer
235 We
further demonstrated that tumor-cell expression of the a
236 We
further demonstrated that vHipp input photostimulation i
237 We
further demonstrated that we can control the binding fun
238 Our data
further demonstrates that CPK3 is required for resistanc
239 Our study
further demonstrates that G2019S LRRK2-induced dopaminer
240 on for induction of the silent CD40 gene and
further demonstrates that H1 eviction, seeded by activat
241 e charge properties of interfaces, this work
further demonstrates that SICM should generally become a
242 Structural modeling
further demonstrates that the binding epitope can only b
243 ion of a comprehensive climate model (CCSM4)
further demonstrates that the enhanced predictability af
244 Our dataset
further demonstrates that the most rapid erosion is achi
245 eletion of Ifngr1 gene in peripheral B cells
further demonstrates that TLR7-driven autoimmune AFC, GC
246 llular ATP level of the living muscle cells,
further demonstrating that membrane diffusion is strongl
247 tes airway inflammation during RSV infection
further demonstrating that versican's role in inflammato
248 ith previously defined integration sites and
further demonstrate the ability to measure lentiviral in
249 ying the metal filling ratio from 1 to 0, we
further demonstrate the abrupt change of a topological i
250 We
further demonstrate the acceleration-feedback-controlled
251 We
further demonstrate the application of this approach to
252 th (+/-)-hamacanthin B and (+/-)-quinagolide
further demonstrate the broad synthetic potential of thi
253 We
further demonstrate the bulk-boundary correspondence bet
254 We
further demonstrate the disulfide bonds in cbEGF domains
255 diseases, including cancers and non-cancers,
further demonstrate the effectiveness of our method in r
256 of the caridean shrimp Lebbeus groenlandicus
further demonstrate the existence of mushroom bodies in
257 We
further demonstrate the flexibility of the technique, by
258 We
further demonstrate the Men1 protein is stabilized in re
259 We
further demonstrate the model on two applications: first
260 We
further demonstrate the origination of MA-TAMs from peri
261 e system to diverse His-tag-labeled proteins
further demonstrate the potential applicability of such
262 We
further demonstrate the potential of narrowband 2D MS fo
263 Together, our results
further demonstrate the potential of targeting 20E signa
264 ed methyl groups, and tandem ring formation,
further demonstrate the potential of the direct decarbox
265 We
further demonstrate the prevalence of positive epistasis
266 We
further demonstrate the selective synthesis of geometric
267 The present results
further demonstrate the sensitivity of the triazapentale
268 ace modification techniques are presented to
further demonstrate the technique's ability to produce s
269 ly mapped sequences can be misleading, so we
further demonstrate the use of differential expression s
270 We
further demonstrate the utility of GBOs to test personal
271 We
further demonstrate the utility of Malibu-Glo assay for
272 To
further demonstrate the utility of this new viral expres
273 We
further demonstrate the utility of this strategy by synt
274 We
further demonstrate the value of exome sequencing by sur
275 Laboratory experiments
further demonstrated the ability of isoprene-derived SOA
276 We
further demonstrated the coupling of the enzyme urease w
277 Our results
further demonstrated the effectiveness of AFM-IR in diff
278 We
further demonstrated the MDSCs mediated stabilization of
279 ts conducted in a heterogeneous aquifer cell
further demonstrated the potential for stabilized-PAC to
280 ferent levels and types of deficiencies, and
further demonstrated the restoration of Ca(2+)-dependent
281 thetic peptides and a model protein, we have
further demonstrated the robustness and predictability o
282 We have
further demonstrated the use of cpRAPID to generate chem
283 ring antigen processing and presentation and
further demonstrates the potential of SWATH-MS for the q
284 e of substrates including glass and plastic,
further demonstrating the broad applicability of this ma
285 berrant cell migration in zebrafish embryos,
further demonstrating the function of the M-Ras/Shoc2/ER
286 controlling for climate and biogeochemistry,
further demonstrating the importance of plant species co
287 ressed CSC phenotypes and progression of GC,
further demonstrating the pivotal role of DOCK6 in GC pr
288 ory birds and ungulates to an apex predator,
further demonstrating the potential effects of changing
289 s the founding member of a new viral family,
further demonstrating the remarkable genetic diversity o
290 We
further demonstrate their topological nature through far
291 We
further demonstrate their utility by labeling and separa
292 Here, we
further demonstrate through in-depth cell wall structura
293 Enhanced living character was
further demonstrated through the preparation of block co
294 Finally, 1 is
further demonstrated to access similar capacities as a s
295 minute isothermal amplification step, and is
further demonstrated using a clinical plasma sample with
296 We
further demonstrated,
using biochemical assays and live
297 These analyses
further demonstrate variants driving MSMB expression dif
298 f the electronic correlations in LSCO/STO is
further demonstrated via temperature-dependent spectral-
299 idity of this new catalyst-design concept is
further demonstrated with the regioselective acetylation
300 he usefulness of these catalytic systems was
further demonstrated with the synthesis of several valua