ライフサイエンスコーパス: evidence for the existence of

1 We provide the first direct evidence for the existence of 2 distinct subpopulations

2 nom of Conus imperialis, providing the first evidence for the existence of a "non-native" peptide iso

3 Here, we obtain additional evidence for the existence of a Brownian ratchet during

4 We have obtained evidence for the existence of a Ca(2+)-binding site in t

5 The structure also provides evidence for the existence of a carbamate formed on the

6 In summary, our data provide strong evidence for the existence of a CD44+ ARP in the develop

7 The results provide evidence for the existence of a cellular entry receptor

8 Finally, we provide evidence for the existence of a cellular execution thres

9 ppear during apnoea, and thus cannot provide evidence for the existence of a central respiratory osci

10 These results provide strong evidence for the existence of a CO channel between clust

11 eletor represents the first direct molecular evidence for the existence of a complete spindle matrix

12 d with worse disability and provides in vivo evidence for the existence of a cortical pathological pr

13 Thus, the results provide direct evidence for the existence of a cryptic high-affinity fi

14 um castaneum, we provide the first molecular evidence for the existence of a cryptic subcoxal segment

15 In addition, we present evidence for the existence of a D" triplication (a putat

16 Furthermore, we observed evidence for the existence of a diabetes-related locus o

17 This work provides evidence for the existence of a diamond-bc8-liquid tripl

18 interface, the findings did not provide any evidence for the existence of a distinctive acellular pr

19 and theoretical IR spectra does not provide evidence for the existence of a double linkage isomer of

20 This is the first direct evidence for the existence of a functional SIN-MEN pathw

21 Together, these findings provide strong evidence for the existence of a gene antisense to HTT, w

22 This familiality is generally taken as evidence for the existence of a genetic etiologic mechan

23 Here, we present genetic evidence for the existence of a glacial refuge in Alaska

24 P expression in humans and provide the first evidence for the existence of a GLTP pseudogene, while d

25 Taken together, the data provides new evidence for the existence of a GPBC in nAChRs serving t

26 These data provide empirical evidence for the existence of a grassy corridor through

27 on and immunoprecipitation analyses provided evidence for the existence of a high molecular weight TR

28 Here, we present evidence for the existence of a higher-order organizatio

29 Here, we provide evidence for the existence of a highly conserved, contin

30 The present study provides evidence for the existence of a lamprey NF-L homolog (L-

31 We provide evidence for the existence of a light-mediated IR pathwa

32 ression of FLOWERING LOCUS T (FT), providing evidence for the existence of a light-quality pathway th

33 riability of visual information, and provide evidence for the existence of a low-level mechanism by w

34 al experiments have produced a large body of evidence for the existence of a magnetic sense in a wide

35 to be derived from mantle plumes is taken as evidence for the existence of a mantle reservoir that ha

36 on of protein synthesis; however, we present evidence for the existence of a mechanism of onconase-in

37 In particular, we find evidence for the existence of a much larger pocket of he

38 The results provide evidence for the existence of a MurA.UNAG collision comp

39 This study provides compelling evidence for the existence of a natural enzyme evolved t

40 Our data provide evidence for the existence of a negative regulator of th

41 We present evidence for the existence of a novel chromosome 2q32 lo

42 Here, we present numerical evidence for the existence of a novel first-order dynami

43 The data presented here provide evidence for the existence of a novel intracellular path

44 These results provide evidence for the existence of a novel mode of cytokine-i

45 These data provide the first direct evidence for the existence of a novel pathway activated

46 Altogether, these findings provide evidence for the existence of a novel RA-activated cellu

47 We now provide evidence for the existence of a novel regulatory mechani

48 These data provide evidence for the existence of a novel signalling pathway

49 This study provides evidence for the existence of a novel xenobiotic substra

50 among cynomolgus macaques provides the first evidence for the existence of a novel, small simian mode

51 These results provide evidence for the existence of a palmitoylation-dependent

52 We also report evidence for the existence of a parity-violating electro

53 e has been previously no strong experimental evidence for the existence of a plasma during single- or

54 Additionally, they emphasize strong evidence for the existence of a plastid-to-nucleus retro

55 We found no evidence for the existence of a pool of intracellular re

56 tomography, thus providing direct structural evidence for the existence of a portal complex in a gamm

57 prokaryotes, there has been no experimental evidence for the existence of a prokaryotic D-glucuronyl

58 In summary, these results provide evidence for the existence of a prostate cancer-suscepti

59 Our report provides the first evidence for the existence of a protein S/Mer/SHP2 axis,

60 ions of thrombosis in cancer and discuss the evidence for the existence of a prothrombotic or hyperco

61 We report evidence for the existence of a putative ABC transporter

62 and this report provides direct experimental evidence for the existence of a QQI between two contiguo

63 ts provide the first substantial statistical evidence for the existence of a regional variation in th

64 cean-ridge basalts (MORBs) have been used as evidence for the existence of a relatively undegassed pr

65 Through an experiment, we present evidence for the existence of a relevant behavioral dime

66 It represents evidence for the existence of a reservoir of antibiotic-

67 py, providing the first direct spectroscopic evidence for the existence of a second metal site in RCs

68 We also present evidence for the existence of a second quorum-sensing sy

69 s novel model of prostate neoplasia provides evidence for the existence of a selenoprotein or selenop

70 Our results provide evidence for the existence of a self-organized and nonpe

71 e q arm of chromosome 12 and provides strong evidence for the existence of a sex-specific predisposit

72 In summary, we provide evidence for the existence of a sortable population of m

73 We found no evidence for the existence of a stable folding intermedi

74 Here, we provide evidence for the existence of a stiffness estimator in t

75 Altogether, our findings provide compelling evidence for the existence of a syntaxin-1A/T-type Ca(2+

76 We found compelling evidence for the existence of a thermodynamic intermedia

77 tonic foraminifera, and find both compelling evidence for the existence of a third cryptic species du

78 Our results provide evidence for the existence of a tightly coordinated heat

79 Here I will describe experimental evidence for the existence of a Treg population specific

80 We show evidence for the existence of a trypanosome lipoprotein

81 In summary, our data provide further evidence for the existence of a type 2 diabetes locus on

82 In the present study we provide evidence for the existence of a Type I IFN-dependent sig

83 We present experimental evidence for the existence of a unique molecular-level o

84 Surprisingly, we find no evidence for the existence of a vagally derived enteric

85 d with the isotope partition data is a clear evidence for the existence of a viable [E-ATP] complex i

86 in how early the brain starts to accumulate evidence for the existence of a visual target.

87 These results also provide genetic evidence for the existence of additional critical substr

88 d protein (Hap40) and ubiquitin, and provide evidence for the existence of additional INR subtypes sh

89 lished susceptibility genes; there is strong evidence for the existence of additional risk loci.

90 I), while X-ray diffraction studies provide evidence for the existence of adducts of composition [H(

91 The NMR analysis provides direct evidence for the existence of Al in the precipitates and

92 The results of this study failed to provide evidence for the existence of altered or unusual vaginal

93 This is evidence for the existence of an "analysis-by-synthesis"

94 We also have found direct evidence for the existence of an additional G-protein bi

95 Our results also provide strong evidence for the existence of an Ag-presenting molecule

96 Our data provide evidence for the existence of an alternative RFC complex

97 hese results comprise the first experimental evidence for the existence of an amphipathic transmembra

98 These findings provide evidence for the existence of an apparatus for ATP relea

99 This provides evidence for the existence of an area of relative ecolog

100 It has provided the first direct evidence for the existence of an error-free lesion repli

101 yed comparative genome analysis and obtained evidence for the existence of an expanded human OPRM1 ge

102 and mechanistic studies of UGM have provided evidence for the existence of an FAD-Galf/p adduct as an

103 This study provides strong evidence for the existence of an HO-1-adiponectin regula

104 Importantly, we provide evidence for the existence of an Hsp70-Tomm34-Hsp90 trip

105 We provide evidence for the existence of an IFN-regulated cellular

106 Additionally, we provide evidence for the existence of an inhibitory action of Gi

107 These data provide evidence for the existence of an inhibitory descending p

108 We found no evidence for the existence of an inhibitory factor for a

109 Here, we present analytical and numerical evidence for the existence of an inverse energy cascade

110 We find evidence for the existence of an inverted (spinon) shado

111 Here we provide evidence for the existence of an ionic lock that constra

112 We report direct evidence for the existence of an iron(IV)-hydroxide.

113 variance over time and provides the clearest evidence for the existence of an object-selective percep

114 s found in ocean island basalts are the main evidence for the existence of an undegassed mantle reser

115 Our results provide evidence for the existence of an unrecognized tumor immu

116 -dihydro-2-benzofuran-1-yl)thiourea provided evidence for the existence of an unusual double displace

117 There is, however, no direct evidence for the existence of annexin 5 Ca(2+) channels

118 Furthermore, we provide evidence for the existence of another positive activity

119 We provide compelling evidence for the existence of areas V3, DM, and DL in ma

120 Quantitative evidence for the existence of aromaticity involving the

121 ervals for BBS2, BBS3, and BBS5; and present evidence for the existence of at least one more BBS locu

122 mains elusive, our study provides compelling evidence for the existence of at least one previously un

123 the same pathway as hy1 or, more likely, as evidence for the existence of at least one separate, non

124 compounds appearing in the reaction provide evidence for the existence of beta-hydride elimination a

125 These data provide in vivo evidence for the existence of bipotential hepatopancreat

126 We found evidence for the existence of both Hebbian and anti-Hebb

127 We give evidence for the existence of both repulsive and attract

128 and theoretical efforts have provided strong evidence for the existence of both two- and three-dimens

129 To date, evidence for the existence of caveolae in hematopoietic

130 Data from these patients provide evidence for the existence of CDH-related genes on chrom

131 presented here provide the first biochemical evidence for the existence of chemokine heterodimers und

132 We did not observe credible evidence for the existence of chimeric RNAs generated by

133 hese results provide biochemical and genetic evidence for the existence of chromosomal replicators in

134 lial marker antibody QH1 provides definitive evidence for the existence of circulating endothelial ce

135 However, there is no direct evidence for the existence of cis-trans protein isomers

136 Here, we provide evidence for the existence of citrate-mediated inhibitio

137 Electron microscopy has provided direct evidence for the existence of collagen VII dimers, but t

138 These data provide the first evidence for the existence of common, low-penetrance sus

139 HMM for cellular imaging and provided direct evidence for the existence of complex spatial-temporal r

140 The growing body of experimental evidence for the existence of complex textures of charge

141 ing models of cognitive control by providing evidence for the existence of conflict-specific control

142 of the juvenile songbird and provide further evidence for the existence of conserved cell types in th

143 tment of HIV-1-infected individuals, provide evidence for the existence of conserved receptor-inducib

144 r these defining characteristics, we provide evidence for the existence of CSCs in a transgenic mouse

145 Although definitive evidence for the existence of CSCs in prostate cancer is

146 The evidence for the existence of dark matter through its gr

147 We present tomographic evidence for the existence of deep-mantle thermal convec

148 gues between two chironomid species provides evidence for the existence of desiccation-specific gene

149 Results provide evidence for the existence of desorbed OH(*) near the an

150 SlGRL1 in the Gr mutant background provides evidence for the existence of different ethylene signali

151 Evidence for the existence of different populations of g

152 This study provides evidence for the existence of different respiratory/alle

153 This study provides evidence for the existence of different transitional B-c

154 euron, Lin and colleagues provide compelling evidence for the existence of direct synaptic contacts b

155 Our results provide direct experimental evidence for the existence of distinct bifurcations asso

156 udies in our laboratory have provided direct evidence for the existence of distinct cholesterol domai

157 While there is accumulating evidence for the existence of distinct neural systems su

158 Our findings provide further evidence for the existence of distinct regulatory progra

159 We interpret this as evidence for the existence of distributed neural populat

160 We conclude that there is no evidence for the existence of Drosophila courtship song

161 These data represent the first structural evidence for the existence of ECA(LPS) in the half-centu

162 ell-fate mapping strategies, we show in vivo evidence for the existence of EMT in breast cancer and s

163 e we present for the first time experimental evidence for the existence of endogenous non-CRAC STIM2-

164 f these theories, until recently integrative evidence for the existence of engram cells and circuits

165 context of previously reported experimental evidence for the existence of equilibria involving beta-

166 ripheral lymphoid tissues has been viewed as evidence for the existence of extrathymic T cell generat

167 This review summarizes the physiologic evidence for the existence of facilitated and active ure

168 unoreactivities in the midbrain raphe cells, evidence for the existence of FGFR1-5-HT1A receptor hete

169 byssal hill and plain, nor did we detect any evidence for the existence of fish aggregations at any s

170 ng concept, we have not had any experimental evidence for the existence of flux sensors and also we h

171 In this study, we provide evidence for the existence of four NK-lysin genes in a r

172 These results provide evidence for the existence of functional adenosine A(1)

173 This study provides evidence for the existence of functional glycinergic syn

174 Our results provide evidence for the existence of functional machinery requi

175 These results provide the first molecular evidence for the existence of fungal exosomes and associ

176 egate level (G); however, there is ambiguous evidence for the existence of g when analyzing data usin

177 and colleagues in this issue of Neuron, new evidence for the existence of gap junctions between pyra

178 This provides further evidence for the existence of gating-induced changes in

179 Evidence for the existence of genes that modify the expr

180 There is still no evidence for the existence of GlnRS in the Archaea.

181 Here, we present the evidence for the existence of graphene SPs on a tapered

182 s of DNA sequence variability; there is also evidence for the existence of heritable epigenetic varia

183 These studies provide direct evidence for the existence of high-Ca(2+) microdomains b

184 hermore, we provide direct mass spectrometry evidence for the existence of histone H3 K56 acetylation

185 udy provides morphological and physiological evidence for the existence of ICC-like cells in the gall

186 These data provide evidence for the existence of IESs in phyllopharyngean c

187 These data provide some preliminary evidence for the existence of immune correlates of prote

188 e absence of treatment as well as suggestive evidence for the existence of immunologically distinct s

189 of these theories, there is no direct neural evidence for the existence of inequality-averse preferen

190 These findings provide evidence for the existence of intercellular cytoprotecti

191 The data do not show compelling evidence for the existence of intrinsically different po

192 Here we provide evidence for the existence of its homolog in plants and

193 C(4) pathway and recent genomic data provide evidence for the existence of key enzymes involved in C(

194 Here the first direct evidence for the existence of large-scale two-dimensiona

195 There is also some evidence for the existence of localized excitations in a

196 Our results provide evidence for the existence of low-permeability barriers

197 e same genetic pathway, providing additional evidence for the existence of mammalian complexes that a

198 periments provide biological and biochemical evidence for the existence of MDA-induced DNA interstran

199 These results provide strong evidence for the existence of memory B-cell-independent,

200 We find experimental evidence for the existence of metastable bulk liquid wat

201 Lastly, we note that there is compelling evidence for the existence of metastable olivine (which,

202 These results bring strong evidence for the existence of mGlu2-4 heterodimers in na

203 Here we provide evidence for the existence of microbial communities in ~

204 We find theoretical evidence for the existence of minima in the Soret coeffi

205 an enhanced diffusion regime provides novel evidence for the existence of mixing in ciliated systems

206 Such detections offer direct evidence for the existence of molecular gas in these gal

207 otocol to the problem and come up with novel evidence for the existence of movement-selective mirror

208 Collectively, this study provides evidence for the existence of multicomponent animal viru

209 tus genome assembly and have gathered strong evidence for the existence of multiple gene families enc

210 Although this work with peptides provides evidence for the existence of multiple ligand binding si

211 by leptin administration provide compelling evidence for the existence of multiple physiological fun

212 We present evidence for the existence of multiple proximal t comple

213 These studies 1) provide further evidence for the existence of multiple subforms of alpha

214 Here, we present first evidence for the existence of multiple Widom lines in bi

215 ed in category-related subregions, providing evidence for the existence of multiple, category-specifi

216 vature of the proton inventory data provides evidence for the existence of multiple, proton-donation

217 We found no evidence for the existence of multipotent progenitors.

218 In addition, evidence for the existence of myeloid and lymphoid DC li

219 ling in a single beat and provide additional evidence for the existence of Na fuzzy space, where [Na+

220 cted their ground state structures and found evidence for the existence of new structural motifs.

221 ge of NEDD8 conjugates; this provides direct evidence for the existence of non-cullin NEDD8 conjugate

222 to the entire trimeric FMO complex and find evidence for the existence of nonlinear discrete breathe

223 These results provide strong evidence for the existence of NusA-binding sites in diff

224 vincing biochemical and electrophysiological evidence for the existence of P2X4/P2X7 heteromeric rece

225 This study provides evidence for the existence of parallel processing circui

226 ring particle size measurements did not show evidence for the existence of particles in the 3-800 nm

227 Evidence for the existence of persistent tetrahedral int

228 uring peroxisome content remodeling, provide evidence for the existence of pexophagy in plants, and i

229 ily (Pfam PF08000), which provide compelling evidence for the existence of PH-like domains in bacteri

230 n previously synthesized, there was no prior evidence for the existence of pincer cofactors in enzyme

231 We find strong evidence for the existence of PM-class and CW-class GPI

232 Here we sought definitive evidence for the existence of polyclonal seeding in huma

233 But there has hitherto been no conclusive evidence for the existence of polyols in meteorites, lea

234 IIalpha, the present data provide compelling evidence for the existence of protein kinase-PP2A signal

235 ology for proteogenomic mapping by providing evidence for the existence of proteins predicted at the

236 of antibiotic resistance genes, and provided evidence for the existence of putative 'viral-enterotype

237 We present experimental and theoretical evidence for the existence of quantum droplets in an ele

238 Our findings provide evidence for the existence of regulated heteromeric asse

239 Here, we provide strong evidence for the existence of repair centers.

240 This study provides a first evidence for the existence of ricinosomes in Arabidopsis

241 s suggest a mechanism of release and provide evidence for the existence of several forms of monomeric

242 molecular, and protein studies have provided evidence for the existence of several types of variant A

243 Structural equation modeling revealed no evidence for the existence of sex-specific genetic influ

244 However, empirical evidence for the existence of sexually antagonistic alle

245 These genome-wide maps provide evidence for the existence of silent epialleles in plant

246 pathways and provide first-hand biochemical evidence for the existence of Smad-independent TGF-beta

247 These results offer evidence for the existence of somatosensory responses in

248 kali-metal silicate solutions, but reveal no evidence for the existence of specialized zeolite buildi

249 complementary cathepsin probes and provides evidence for the existence of specific localization of c

250 our knowledge, this study provides the first evidence for the existence of SPW-R subtypes with differ

251 formation in the brain and there is emerging evidence for the existence of STDP at inhibitory synapse

252 Our data provide direct evidence for the existence of stem cells contributing to

253 The study also provides evidence for the existence of stem cells dispersed throu

254 ge in risk among migrants provide compelling evidence for the existence of strong environmental deter

255 d in the euphotic zone, as in the absence of evidence for the existence of strong Mn(III) ligands, Mn

256 Direct empirical evidence for the existence of study publication bias and

257 of motor features in SCA6, we provide novel evidence for the existence of subclinical motor dysfunct

258 RsbS complex from cellular extracts provides evidence for the existence of such a complex in vivo.

259 Here we provide direct evidence for the existence of such a model in the cerebe

260 Here, we summarize recent molecular evidence for the existence of such units, now known as "

261 We provide definitive evidence for the existence of 'suction pressure' in coll

262 We also showed evidence for the existence of supercoiling activity in A

263 Evidence for the existence of sympathetic vasodilator ne

264 These results provide strong functional evidence for the existence of the 3' flavivirus-conserve

265 al restrictive silencing factor), we find no evidence for the existence of the eight-zinc finger REST

266 In the present study, we further provide evidence for the existence of the G-quadruplex structure

267 llow C74-D3h cage and the first experimental evidence for the existence of the hollow fullerenes C76-

268 A significant portion of the evidence for the existence of the LHB comes from histogr

269 Here we present evidence for the existence of the putative acryloyl addu

270 the repair endonuclease provides additional evidence for the existence of the repair endonuclease in

271 This paper reviews evidence for the existence of the various types of agoni

272 Results provide functional evidence for the existence of the water-metal ion bridge

273 lymphocyte populations, review the available evidence for the existence of these populations in the k

274 The present study provides definitive evidence for the existence of these supraspinal presympa

275 Here we re-evaluate the evidence for the existence of this mitoKATP by measuring

276 Experimental evidence for the existence of this network comes from pr

277 Our findings provide strong evidence for the existence of this relation.

278 quotient along the gradient provide further evidence for the existence of this threshold.

279 In this study, we provide evidence for the existence of this type of synesthesia a

280 In this review, we present evidence for the existence of three highly conserved reg

281 There is evidence for the existence of three independent secretio

282 and some other animals exhibited sufficient evidence for the existence of three-dimensional and/or f

283 These findings provide evidence for the existence of Tor signaling complexes th

284 Additionally, we provided evidence for the existence of transcripts that contain s

285 We now present evidence for the existence of two actin-binding sites th

286 There is evidence for the existence of two AQP4 transcripts (M1 a

287 eotide binding at one or both sites provided evidence for the existence of two ATP-binding sites with

288 These observations provide physical evidence for the existence of two binding sites in SERT

289 oscopic and catalytic results provide strong evidence for the existence of two competing enantioselec

290 We present evidence for the existence of two different reaction pat

291 results not only provide the first explicit evidence for the existence of two distinct functional re

292 We find evidence for the existence of two folding pathways, whic

293 n contrast, quenching data for Y87W provides evidence for the existence of two lipid binding sites on

294 s important signaling mechanism by providing evidence for the existence of two phases of IKK activati

295 We present evidence for the existence of two phases of retinoic aci

296 We also gained evidence for the existence of two possible routes for NA

297 (5) GC-skew analysis showed evidence for the existence of two replication origins in

298 iminary single nucleotide polymorphism-based evidence for the existence of two subgroups of H. capsul

299 This review discusses the current body of evidence for the existence of vascular wall progenitor c

300 We also present firm evidence for the existence of very long-term variations