1 sponse relationship, specificity, and animal
experimental evidence).
2 ing only realistic parameters constrained by
experimental evidence.
3 t to interpret the available statistical and
experimental evidence.
4 erroelectric, which, however, requires clear
experimental evidence.
5 Cys106, which supports previous preliminary
experimental evidence.
6 tational study allowed us to rationalize the
experimental evidence.
7 rks are largely consistent with the existing
experimental evidence.
8 However, there is lack of
experimental evidence.
9 nd found to compare favorably with available
experimental evidence.
10 d from public resources of fusion genes with
experimental evidences.
11 omposite film due to lack of the convincible
experimental evidences.
12 Apart from
experimental evidence,
a numerical simulation is develop
13 In particular,
experimental evidence about IL-10/GAG binding sites is l
14 However, little
experimental evidence actually demonstrates a selective
15 However, there is little
experimental evidence addressing how many cell divisions
16 Observational studies and
experimental evidence agree that rising global temperatu
17 Experimental evidence and computational modeling suggest
18 Based on
experimental evidence and computational modeling, we sho
19 This perspective will present
experimental evidence and evolutionary theory to challen
20 on of loci that have limited annotations and
experimental evidence and for identifying candidate caus
21 Our results provide the first
experimental evidence and mechanistic support for the as
22 uclear egress in herpesviruses, examines the
experimental evidence and models, and outlines outstandi
23 Experimental evidence and preliminary clinical evidence
24 Experimental evidence and theoretical modeling suggest t
25 Although
experimental evidence as well as modeling suggest that f
26 Experimental evidence as well as molecular docking poses
27 Here, we detail recent computational and
experimental evidence associated with sequence-specific
28 lly - or collectively - explain the range of
experimental evidence available.
29 We provide direct
experimental evidence,
backed by theory, that this motio
30 The majority of the available
experimental evidence,
both in humans and other species,
31 We investigated whether the diverse
experimental evidence can be unified by creating a spati
32 er than wet conditions, although some recent
experimental evidence challenges this view.
33 Here we report on the
experimental evidence,
confirmed by ab initio calculatio
34 However,
experimental evidence correlating the function of X-chro
35 Experimental evidence,
corroborated by theory, reveals t
36 Our
experimental evidence demonstrates that P. galapageium l
37 Mounting
experimental evidence demonstrates that platelets suppor
38 Observational and
experimental evidence demonstrates that protein intake i
39 This
experimental evidence demonstrates that rapid evolution
40 The
experimental evidence demonstrates that there exists an
41 llations in isoprene emission provide direct
experimental evidence demonstrating that the response of
42 he distribution of it, thus providing direct
experimental evidences demonstrating that the long myste
43 In line with the
experimental evidence,
DFT studies reveal that initiatio
44 ion primarily through their migration, while
experimental evidence documenting large-scale sliding of
45 Experimental evidence ex vivo suggests that direct manip
46 ed to originate from primary sources, little
experimental evidence exists directly linking combustion
47 infection to cattle abortion, little direct
experimental evidence exists.
48 We provide the first
experimental evidence for a direct Au(III)-F/B transmeta
49 Here, we provide
experimental evidence for a functional communication bet
50 Here we present
experimental evidence for a phase of fluctuating nematic
51 rian metazoans, but there has been no direct
experimental evidence for a specific role for BMP signal
52 Overall, we found robust
experimental evidence for a total of only thirteen preny
53 tributions to stress susceptibility--and the
experimental evidence for and against the existence of s
54 Here we report
experimental evidence for cell-cell communication that s
55 Here we provide
experimental evidence for direct reactions occurring bet
56 We provide computational and
experimental evidence for diverse mechanisms of gene res
57 We provide
experimental evidence for electron transfer from As(III)
58 Here, we demonstrate
experimental evidence for electronic catalyst-support in
59 ened water hydrogen bonding, but there is no
experimental evidence for enhanced hydrogen bonding and/
60 Yet there is no
experimental evidence for how sidechain dynamics control
61 These results complement recent
experimental evidence for immiscible methane-rich fluids
62 This
experimental evidence for interfacial thin film and drop
63 ll relatively poorly understood, with little
experimental evidence for intermediates, although an org
64 These results provide the first
experimental evidence for ISR and suggest a functional r
65 n of an intermediate iron-peroxo complex but
experimental evidence for its existence is still missing
66 Taken together, this provides direct
experimental evidence for jamming by shear, rather than
67 ved nutrients on selection pressures provide
experimental evidence for key components of eco-evolutio
68 resonance techniques, we provide unambiguous
experimental evidence for long-wavelength helimagnetic o
69 Here, we report
experimental evidence for magnetic Weyl fermions in Mn3S
70 Both anion structures provide
experimental evidence for near-linear M-N-N coordination
71 eview assesses the mechanistic rationale and
experimental evidence for nutritional interventions comm
72 Experimental evidence for oxetanes as reactive intermedi
73 ges in protein function and thus can provide
experimental evidence for phylogenomic relationships.
74 Thus, we provide the first
experimental evidence for production-related vocal learn
75 Following previously published
experimental evidence for S-glutathionylation induced de
76 or less compact chromatin fibers but direct
experimental evidence for such models are lacking.
77 s study provides the first direct structural
experimental evidence for the binding of dextrin-colisti
78 is investigation firstly provides the direct
experimental evidence for the crystallized feature of th
79 Thus, our data provide the first
experimental evidence for the dynamic control of stereoc
80 Our results provide direct
experimental evidence for the existence of distinct bifu
81 pore diameters (3.2-29 nm), providing direct
experimental evidence for the formation of a molecular-l
82 In this work we provide strong
experimental evidence for the hydrodynamic nature of the
83 We summarize
experimental evidence for the importance of thrombus sta
84 Thus, we provide
experimental evidence for the important contribution of
85 We present
experimental evidence for the optically induced metastab
86 pectroscopy measurements that provide direct
experimental evidence for the ozonide and establish its
87 i-review, we summarize current knowledge and
experimental evidence for the potential of bacteria and
88 We provide
experimental evidence for the proposed mechanism and sho
89 These findings provide
experimental evidence for the role of behaviors directed
90 scattering techniques and provides the first
experimental evidence for the self-assembly of CESA into
91 g distribution in the intestine and provided
experimental evidence for the suggested absorption behav
92 Taken together, this study provides
experimental evidence for the therapeutic potential of 8
93 However, conclusive
experimental evidence for their functional relevance is
94 ively novel therapies for IF/TA and provided
experimental evidence for their therapeutic activities i
95 d mobilize gene fragments in eukaryotes, but
experimental evidence for their transposition is lacking
96 olesterol-binding sites in VDAC1, but direct
experimental evidence for these sites is lacking.
97 abilize each other as metastable dimers, yet
experimental evidence for these species and their mutual
98 of single neurons, here we provide the first
experimental evidence for this effect.
99 re and the walls of the container, clear-cut
experimental evidence for this prediction is lacking.
100 the literature reports provide little or no
experimental evidence for this.
101 Our results provide the first
experimental evidence for vocal elaboration as a male-sp
102 However, the
experimental evidences for such strain are scanty.
103 Focusing on vertebrate cells but drawing on
experimental evidence from a wide range of systems, we w
104 energy-related metabolites are in line with
experimental evidence from Escherichia coli.
105 We highlight
experimental evidence from mouse models and patient-base
106 tner violence, to date there has been little
experimental evidence from sub-Saharan Africa that can b
107 principles computational methods, along with
experimental evidence from the literature, were used to
108 The
experimental evidence from these studies is confirmed by
109 However,
experimental evidence,
from pre-erythrocytic vaccine can
110 In silico and
experimental evidence further revealed that miR-211 dire
111 Experimental evidence had shown that the first step invo
112 Recently
experimental evidence has been presented suggesting that
113 mes, such as toroviruses and roniviruses, no
experimental evidence has been reported thus far.
114 in thermoelectric performance, but no direct
experimental evidence has been reported.
115 l theoretical models have been proposed, but
experimental evidence has demonstrated that a rich class
116 Recent
experimental evidence has demonstrated that path lengths
117 A large body of
experimental evidence has provided support for a modulat
118 Experimental evidence has shown a close correlation betw
119 In this regard, recent
experimental evidence has shown that the genetic or phar
120 Experimental evidence has suggested that unresolvable DN
121 ignificantly enriched in cancer genomes, but
experimental evidence implicating condensin dysfunction
122 t this assumption is consistent with current
experimental evidence in chimeric motors, as well as wit
123 Accumulating
experimental evidence in mammalian, and recently plant,
124 Here, we provide theoretical arguments and
experimental evidence in support of an alternative appro
125 However, direct
experimental evidence in support of any of these models
126 There is no experimental or quasi-
experimental evidence in the United States that links ch
127 Experimental evidence,
including exaggerated ventilatory
128 Experimental evidence indicates a direct role of transac
129 Experimental evidence indicates that about 60% of miRNA-
130 Experimental evidence indicates that bivalent chromatin
131 Experimental evidence indicates that each tip link is a
132 Growing clinical and
experimental evidence indicates that improper involution
133 Experimental evidence indicates that intestinal microbio
134 Experimental evidence indicates that PFAS alter glucose
135 Experimental evidence indicates that the lobes integrate
136 c cancer cells, despite growing clinical and
experimental evidence indicating that intratumoral hypox
137 Thus, the overall
experimental evidence is consistent with a pattern of HI
138 mutations are tumor drivers, although direct
experimental evidence is lacking.
139 o-low-density transition are debated and new
experimental evidence is needed.
140 he hydroallylation reaction is proposed, and
experimental evidence is provided for the key steps of t
141 study, for the first time to our knowledge,
experimental evidence is provided on the link between mu
142 ity of the model in general, but more direct
experimental evidence is required to validate the model
143 Experimental evidence,
kinetic measurements, and correla
144 ersial primarily because of a lack of direct
experimental evidence linking magnetic field (MF) exposu
145 is still debated as a result of the lack of
experimental evidence obtained without drastic manipulat
146 Here we provide bioinformatic and
experimental evidence of a conserved mitochondrial stres
147 ifference in universality class, with recent
experimental evidence of a dynamic Mott transition in a
148 Here we show
experimental evidence of a hetero-site pump-probe signal
149 the TamA barrel domain, providing the first
experimental evidence of a lateral gate in TamA: a struc
150 Our findings provide
experimental evidence of a microbial strategy for transi
151 Based on
experimental evidence of activity-dependent tuning of co
152 Experimental evidence of cerebellar dysfunction in prete
153 d whole genome sequencing, we present unique
experimental evidence of chromosomal DNA transfer betwee
154 entific and practical importance, conclusive
experimental evidence of confined acoustic phonon polari
155 We report the first
experimental evidence of EOF hysteresis induced by a pH
156 Despite such interest in nano-optics, no
experimental evidence of Fano interference was reported
157 Here we show the
experimental evidence of giant enhancement of the absorp
158 For the first time, we provide
experimental evidence of growth rates of Ag nanoparticle
159 We present
experimental evidence of how competition introduces both
160 However, we lack direct
experimental evidence of how the net carbon uptake of ec
161 A:target interactions in myogenesis based on
experimental evidence of individual miRNAs which were ne
162 m phase transition and to present convincing
experimental evidence of its existence for a charged and
163 Detailed
experimental evidence of kink blocking validates classic
164 d subsequent sequence data analysis provided
experimental evidence of low-level detection of the targ
165 Based on
experimental evidence of metabolic oscillations, we show
166 2Te3 and the band insulator GeTe, we provide
experimental evidence of multiple topological modes in a
167 ccurring C9 proteoforms and the first direct
experimental evidence of O-linked glycans in the N-termi
168 Our findings provide
experimental evidence of recent predictions and open the
169 Here, we present direct
experimental evidence of sequence-specific inter-segment
170 Motivated by
experimental evidence of such flow asymmetry, here we ex
171 ctioning networks, and we end by summarizing
experimental evidence of such interactions.
172 Our study provides
experimental evidence of the basic carbohydrate metaboli
173 Our results provide the
experimental evidence of the close connection between KZ
174 We provide the first
experimental evidence of the deleterious effect of acute
175 Here, we report direct
experimental evidence of the J eff = 3/2 state in GaTa4S
176 These findings provide
experimental evidence of the resistance mechanism of the
177 Our results provide simple and direct
experimental evidence of the role of the defects in chem
178 Direct
experimental evidence of these states has been limited s
179 r pollution during gestation is in line with
experimental evidence on cigarette smoke and diesel exha
180 otein (CP) in encapsidating the RNA progeny,
experimental evidence on positive sense single-stranded
181 al sessions, and therefore, there is limited
experimental evidence on the adjustments in MU propertie
182 We provide the first
experimental evidence on the influence of the Al-induced
183 gle nanowires (nano-ARPES) to provide direct
experimental evidence on the nontrivial topological char
184 In fact, the existing
experimental evidence points to a graded rather than an
185 We review
experimental evidence pro et contra different theoretica
186 The combination of theoretical and
experimental evidence provided here offers a unified fra
187 Our theory is consistent with
experimental evidence regarding the influence of BG on s
188 This finding brings under scrutiny the
experimental evidence reporting that limiting (zero-torq
189 e high (10-100 mM), however, and there is no
experimental evidence ruling out a role for the lipid bi
190 Here, we present
experimental evidence showing how a stimulus can increas
191 Thus, we obtained direct
experimental evidence showing that a tight cavity can ge
192 Here, we present new
experimental evidence showing that fragility reflects th
193 the origins of this polymorphism and provide
experimental evidence showing that it is the result of a
194 However,
experimental evidence shows that some plant virus RdRPs
195 Quantum chemistry calculations, supported by
experimental evidence,
shows that the (CF3)2CFCN + OH re
196 Extensive
experimental evidence (
spectroscopic characterization, k
197 base our assessment of disorder strictly on
experimental evidence,
such as X-ray crystallography and
198 Several lines of
experimental evidence suggest that PIN-mediated polar au
199 In particular, computational modeling and
experimental evidence suggest that static crosslinking p
200 Various epidemiological and
experimental evidence suggest that uric acid has a role
201 Our findings, largely consistent with the
experimental evidence,
suggest higher serum calcium may
202 and fluorescence measurements, and obtained
experimental evidence suggesting a complex mechanism in
203 Here, we present
experimental evidence suggesting that the majority of kn
204 cryptic binding sites have been debated, but
experimental evidence suggests multiple domains may cont
205 Cumulative genetic and
experimental evidence suggests that alterations in vario
206 Experimental evidence suggests that boryl radical interm
207 Experimental evidence suggests that cyclosporine prevent
208 Epidemiologic and
experimental evidence suggests that individuals with dia
209 Experimental evidence suggests that physiological challe
210 Furthermore,
experimental evidence suggests that STDP is not the only
211 Experimental evidence suggests that the fusion is preced
212 Experimental evidence suggests that the retinal circadia
213 While
experimental evidence suggests that these changes may be
214 Experimental evidence suggests that when an artemisinin
215 d framework to evaluate relevant genetic and
experimental evidence supporting or contradicting a gene
216 We also describe strong
experimental evidence supporting our hypothesis through
217 have led to the enhanced virulence of ZIKV,
experimental evidence supporting the role of specific ge
218 ummarizes the often fragmentary clinical and
experimental evidence supporting the role of surgery and
219 Experimental evidence supporting their existence in vivo
220 ver half a century ago, there is a dearth of
experimental evidence supporting their existence.
221 With large amounts of
experimental evidence supporting theories of either gold
222 Experimental evidence supporting this hypothesis shows t
223 psychology (e.g., William James), definitive
experimental evidence supporting this idea is lacking de
224 However, there is little
experimental evidence supporting this mechanism in TRP c
225 ctivity is not required for cell growth, but
experimental evidence supporting this notion has been la
226 expression in B. burgdorferi However, direct
experimental evidence supporting this putative autoregul
227 Experimental evidence supports a protective role of 25-h
228 Computational and
experimental evidence supports an asymmetric atom-transf
229 Increasing
experimental evidence supports the idea that Mycobacteri
230 ght to underlie absence seizures, converging
experimental evidence supports the key involvement of th
231 Although
experimental evidence supports the role of sharp-wave ri
232 impairments in CSF reabsorption, but little
experimental evidence supports this concept.
233 Moreover, we provide conclusive
experimental evidence that 'ballistic' separation prevai
234 h as a model system, we successfully provide
experimental evidence that a large number of miRNAs can
235 This study provides
experimental evidence that a plant-type FA beta-oxidatio
236 These results provide
experimental evidence that a wild animal in a natural se
237 A new paper provides intriguing
experimental evidence that age may cause a breakdown in
238 o calls from unknown individuals - the first
experimental evidence that bonobos can identify individu
239 In the current studies, we provide
experimental evidence that caspase-3 directly and specif
240 In this study, we provide
experimental evidence that ComFA binds to single strande
241 together, these findings provide compelling
experimental evidence that DAT N and C termini synergist
242 Our results provide
experimental evidence that females can alter male behavi
243 This work provides additional
experimental evidence that highly oxygenated intermediat
244 We also provide
experimental evidence that is inconsistent with endocyto
245 We also provide the first
experimental evidence that it is the amounts and types o
246 These results provide the first
experimental evidence that ivacaftor is a potential ther
247 This review collects the diverse
experimental evidence that leads to these conclusions.
248 Our findings provide the first
experimental evidence that modulating activity in the DL
249 This study provides the first
experimental evidence that N-alkylation results in a dra
250 pid flippase, although there is currently no
experimental evidence that Neo1 catalyzes this activity
251 The present study provides
experimental evidence that neurogenic spots exhibit all
252 These data provide
experimental evidence that NOD2 recognizes naturally occ
253 This study provides the first
experimental evidence that oxidation of a K(+) channel c
254 We provide
experimental evidence that parasites influence host-medi
255 These data provide direct
experimental evidence that parasympathetic vagal drive g
256 Here, we present
experimental evidence that Paxillus involutus-a basidiom
257 In summary, our studies provide
experimental evidence that pericytes in the brain have t
258 for a central pattern generator, and recent
experimental evidence that proprioception drives locomot
259 We provide
experimental evidence that protonation of Glu37, a gluta
260 Taken together, we provide the first
experimental evidence that proximate risk of predation c
261 Hence, we provide
experimental evidence that Schwann cells gain antigen-pr
262 This study provides
experimental evidence that self-organization can be para
263 We present
experimental evidence that shows rapid clay formation un
264 Our results provide strong
experimental evidence that side-chain dynamics play a cr
265 e results are consistent with the collective
experimental evidence that species richness increases co
266 In this article, we provide
experimental evidence that subset #4 CLL cells show low
267 In this work, we provide
experimental evidence that such communication can be ach
268 This study provides the first
experimental evidence that synthetic ion transporters ca
269 We provide
experimental evidence that the human prefrontal cortex's
270 This provides the first
experimental evidence that the interleukin-like EMT indu
271 We provide
experimental evidence that the intrinsic level of combin
272 We provide
experimental evidence that the MLV CAH belongs to a grou
273 belling mass spectrometry, we provide direct
experimental evidence that the O2 generated during the O
274 Overall, we present
experimental evidence that the reactivity continuum with
275 We report
experimental evidence that the resistance of restricted
276 This report provides
experimental evidence that the spontaneous mutation T544
277 Our results provide
experimental evidence that this grape gene promoter is a
278 Collectively, we provide direct
experimental evidence that this novel avian-origin DTMUV
279 We further provide
experimental evidence that this salt-bridge lock exists
280 ular dynamic simulations and provides direct
experimental evidence that unordered off-pathway NFGAIL
281 We provide the first
experimental evidence that variable sequence arrangement
282 Our study shows
experimental evidence that within heterogeneous populati
283 iety of techniques, we were unable to obtain
experimental evidence that would support the formation o
284 In this study, we provide new
experimental evidence that, together with our previous f
285 ids/beta-CDs inclusion complexes and provide
experimental evidences that beta-CDs inclusion renders t
286 working hypothesis, based on theoretical and
experimental evidence,
that SM results from feedforward,
287 However, in absence of direct
experimental evidence,
the compensatory nature of the ch
288 This work provides direct
experimental evidence to conduct more realistic modellin
289 para-Z-substituted thioanisoles and utilize
experimental evidence to distinguish between the theoret
290 o coordination in a bonobo), and there is no
experimental evidence to indicate its biological functio
291 This study provides
experimental evidence to mechanistically understand some
292 We present the first
experimental evidence to our knowledge that ingroup rela
293 We have provided the first
experimental evidence to show that Li ions favor the pat
294 LPLAT thioesterase activity, and we provide
experimental evidence to support an ordered-binding and
295 tes of (bio)catalytic nitrogen fixation, yet
experimental evidence to support this hypothesis has bee
296 However,
experimental evidence to support this prediction still r
297 Here, we present
experimental evidence to the contrary.
298 Based on apparently contradictory
experimental evidence,
two distinct molecular mechanisms
299 we present a contrasting paradigm combining
experimental evidence (
using IgG antibodies and Matrigel
300 n the structural modeling of RepC and on our
experimental evidence,
we propose a model where RepC nic