ライフサイエンスコーパス: comparative analyses

1 to indicate statistical significance in the comparative analyses.

2 racy of detection and reliable for real-time comparative analyses.

3 canonical exon junction counts to facilitate comparative analyses.

4 published studies, in particular large-scale comparative analyses.

5 s for vegetation change using correlation or comparative analyses.

6 tations in non-model organisms has precluded comparative analyses.

7 a set of 'reference species' to anchor their comparative analyses.

8 r tests and were therefore excluded from the comparative analyses.

9 iction for the first time using phylogenetic comparative analyses.

10 e with this scale, to allow for combined and comparative analyses.

11 samples underwent histologic processing and comparative analyses.

12 ion factors in a gene or transcript list for comparative analyses.

13 gning chromatographic data for comprehensive comparative analyses.

14 s evolutionary origins cannot be traced with comparative analyses.

15 a comprehensive collection of organisms for comparative analyses.

16 lution but are seldom considered together in comparative analyses.

17 s to account for phylogenetic uncertainty in comparative analyses.

18 rom public mappings and integrated tools for comparative analyses.

19 For our comparative analyses, 621 patients were matched with con

20 works and sophisticated tools for on-the-fly comparative analyses across 14 species.

21 re of invertebrate brains, and exemplify how comparative analyses across ecologically divergent speci

22 ENCODE projects, we provide novel group-wise comparative analyses across sex, tissue type, state and

23 ts but are extraordinarily diverse, allowing comparative analyses aimed at identifying specific genot

24 paternity, and song information and perform comparative analyses alongside songbird genetic phylogen

25 Such comparative analyses also inform dietary reconstruction

26 current tool includes quick yet informative comparative analyses and a first pass visualization of b

27 s on evolutionary processes in cross-species comparative analyses and assist in efforts to conserve s

28 nnotation, enabling data sharing, reporting, comparative analyses and benchmarking, while promoting t

29 We used field experiments, phylogenetic-comparative analyses and computed-tomography scanning to

30 Comparative analyses and phylogenetic reconstructions re

31 nconsistent gene assignments that complicate comparative analyses and prevent efficient construction

32 be system described here can be employed for comparative analyses and subsequent structural character

33 tegrated using ontology-based annotation and comparative analyses, and accessed through both visual a

34 enomes from single-cell eukaryotes to human, comparative analyses are still relatively few and comput

35 vides a valuable resource for deep mammalian comparative analyses, as well as for monotreme biology a

36 We conducted a sequence-level comparative analyses, at the scale of complete bacterial

37 All comparative analyses between CBSV and UCBSV presented he

38 roposed here lays the groundwork for further comparative analyses between humans and NHPs and opens n

39 Comparative analyses between insertion- and non-insertio

40 These comparative analyses between lakes in two very different

41 Comparative analyses between pathologies and correlation

42 egion of the genome of B. rapa and conducted comparative analyses between the Brassica sequences and

43 Comparative analyses between these structures and publis

44 Comparative analyses between tomato and potato at the ge

45 ples exposed to RT for less than 2 hours for comparative analyses between various medical conditions.

46 Such inconsistencies hinder comparative analyses by non-uniformly extending or trunc

47 Comparative analyses can contribute to this effort by le

48 bed bugs, we present the genome sequence and comparative analyses centered on the milkweed bug Oncope

49 Comparative analyses classified 74 peptides that were co

50 Comparative analyses confirmed that significantly more i

51 current approaches suggests that systematic comparative analyses could identify best organizational

52 Taken together, these parallel comparative analyses demonstrate for the first time the

53 Comparative analyses demonstrate that similar molecular

54 spersed throughout the literature, rendering comparative analyses difficult.

55 Comparative analyses extend this scheme to explain how d

56 Results from our comparative analyses favor a model of divergence post ve

57 Kinannote produces a draft kinome and comparative analyses for a predicted proteome using a si

58 Phylogenetic comparative analyses further indicated that after their

59 Comparative analyses further revealed that human CXCR3(+

60 study, we sought to investigate-in parallel comparative analyses-Gag cellular distribution, VLP size

61 iraffe and okapi were sequenced, and through comparative analyses genes and pathways were identified

62 reatly expands the possibility of conducting comparative analyses giving tremendous insight into netw

63 However, comparative analyses have been unable to resolve the roo

64 In this study, parallel comparative analyses have been used to study Gag express

65 While comparative analyses have consistently failed to find st

66 ons of intraspecific diversification because comparative analyses have focused on species inhabiting

67 Comparative analyses have identified genomic regions pot

68 While multiple comparative analyses have investigated variation in brai

69 Comparative analyses have revealed that the Fusarium gen

70 human economic structures can be informed by comparative analyses; however, we do not agree with seve

71 In addition, comparative analyses identified three noncoding evolutio

72 Our comparative analyses identify signatures of convergence

73 blish their calibration data, and this makes comparative analyses impossible.

74 osporogenesis was studied using phylogenetic comparative analyses in 83 species dispersed throughout

75 Here, we performed comparative analyses in cultured mouse neurons of all ma

76 Comparative analyses in neurons and astrocytes further h

77 eration found in human hunter-gatherers [4], comparative analyses in the genus Pan have been limited

78 The sample for the comparative analyses included 897,232 records and 114,26

79 Phylogenetic comparative analyses indicate that for small-bodied mamm

80 Comparative analyses indicate that ORC encircles DNA, us

81 Comparative analyses indicated high wheat-specific inter

82 Recent phylogenomic comparative analyses indicated that the nodulation trait

83 44% and is broadly available for streamlined comparative analyses, interactive exploration, metabolic

84 ng, well-accepted measures are ill-suited to comparative analyses involving different entities (i.e.

85 uitable for use as a reference phylogeny for comparative analyses, is to perform a maximum likelihood

86 for transgenic studies or for multi-species comparative analyses, it is paramount that the CNEs are

87 ylogenetic diversity metrics, performs trait comparative analyses, manipulates phenotypic and phyloge

88 timately allow the more rapid integration of comparative analyses, metabolite identification, and dat

89 Further, comparative analyses of 17 genes involved in CPT biosynt

90 Comparative analyses of 31 fungal genomes (12 generated

91 We conducted phylogenetically informed comparative analyses of 81 taxa of Dalechampia (Euphorbi

92 Comparative analyses of a dataset of 93 Californian crop

93 In this study, comparative analyses of all available genomic sequences

94 Comparative analyses of all loci, including beta-tubulin

95 of dedicated online databases to facilitate comparative analyses of Borrelia genomes.

96 Comparative analyses of caffeine NMTs demonstrate that t

97 euechinoids, the cidaroids, suggesting that comparative analyses of cidaroid GRN architecture may co

98 Comparative analyses of consensus dominant quasispecies

99 Together with comparative analyses of data for the free-living nematod

100 r more Linked Experiments - which allows for comparative analyses of data from multiple experiments b

101 Additionally, it facilitates comparative analyses of datasets across multiple indepen

102 Phylogenetic comparative analyses of diploids revealed significant ne

103 ymes like the I-AniI nickase will facilitate comparative analyses of DNA repair and mutagenesis induc

104 a freely available web resource that enables comparative analyses of drug-disposition genes.

105 Comparative analyses of E. lenta CRISPR-Cas systems acro

106 this holds for all sea urchins necessitates comparative analyses of echinoid taxa that diverged deep

107 previously published method exists to enable comparative analyses of enrichment levels derived from d

108 a comprehensive reliable scaffold for future comparative analyses of evolutionary innovations among i

109 parison with parasitic genomes necessary for comparative analyses of existing and future trypanosomat

110 Here, we consider recent comparative analyses of extant species that are uncoveri

111 e brains and behaviors of feral animals, and comparative analyses of feral populations and taxa.

112 We used phylogenetic and comparative analyses of fruit and seed anatomy, biomecha

113 Comparative analyses of genome and transcriptome protein

114 osa isolates and pooled populations and used comparative analyses of genome sequences including phylo

115 plications of the D2 family of statistics in comparative analyses of genomic sequences, we developed

116 tetrapod genomes, making it a good model for comparative analyses of gnathostome genomes.

117 maps of growth open the way for standardized comparative analyses of growth patterns.

118 Using pigs as an animal model, we conducted comparative analyses of gut microbiota and short-chain f

119 Comparative analyses of Hubbard's sportive lemur were co

120 Comparative analyses of human erythropoiesis identify de

121 miR2GO is a web-based platform for comparative analyses of human miRNA functions.

122 69), and the method was also verified by the comparative analyses of human urine samples collected fr

123 fication of Hymenoptera and allow for future comparative analyses of Hymenoptera, including their gen

124 Despite its vital role in health, comparative analyses of IIS/TOR have been limited to inv

125 ing noncardiac surgery, and should allow for comparative analyses of in-hospital mortality.

126 ysis of somite-stage embryos, we carried out comparative analyses of key genes and found that the ano

127 However, few worldwide comparative analyses of long-term trends of body-mass in

128 Finally, through comparative analyses of mAb binding and neutralizing cap

129 ave begun to address these questions through comparative analyses of Medicago truncatula and Medicago

130 Here, we present comparative analyses of mitochondrial proteomes, cellula

131 Our species-level comparative analyses of morphotype and head size evoluti

132 In this study, we performed genome-wide comparative analyses of mRNAs encoding orthologous prote

133 analysis and underlying data environment for comparative analyses of multiple gene lists.

134 lude: a wide variety of sequence alignments, comparative analyses of multiple genome assemblies, and

135 Parallel, comparative analyses of multiple thiol oxidoreductases r

136 Comparative analyses of neuronal phenotypes in closely r

137 Through comparative analyses of normal cells from the same patie

138 Comparative analyses of nuclear transcriptome data sugge

139 ve states in room-temperature X-ray data and comparative analyses of other dimeric herpesvirus protea

140 Comparative analyses of other previous screening approac

141 Comparative analyses of P. trifoliata and nine Citrus ge

142 Comparative analyses of parental and infected A20 cells

143 Comparative analyses of patients with HFmrEF with improv

144 iants between the Fat and Lean mice and with comparative analyses of polymorphisms across 17 mouse st

145 Phylogenetic comparative analyses of portions of S and medium segment

146 CDD also supports comparative analyses of protein families via conserved d

147 For many decades comparative analyses of protein sequences and structures

148 information flows using pairwise phenotypic comparative analyses of protein-protein interactions.

149 nd analysis and visualization tool to enable comparative analyses of ribosome-profiling datasets.

150 Comparative analyses of S-locus sequences of these three

151 Our study highlights that comparative analyses of single-cell and bulk gene expres

152 Comparative analyses of six cucurbit genomes reveal that

153 Comparative analyses of sizes, relative ratios, and oxyg

154 rphology, and our results are beneficial for comparative analyses of spider respiration.

155 Comparative analyses of structures and enzyme kinetics r

156 Comparative analyses of survival and funding statistics

157 genome provides a valuable resource for deep comparative analyses of tetrapods, as well as for tuatar

158 the gadid phylogeny and performed fine-scale comparative analyses of the AFGP genomic loci and homolo

159 However, comparative analyses of the amounts of BV genomic DNA an

160 We conducted comparative analyses of the biophysical and ecophysiolog

161 sex-specific traits in D. melanogaster with comparative analyses of the condition dependence of male

162 Comparative analyses of the control of mammalian microbi

163 these surveys were similar enough to enable comparative analyses of the data across the 7 countries.

164 The comparative analyses of the data require appropriate sta

165 Comparative analyses of the deduced amino acid sequences

166 Comparative analyses of the distributions of various his

167 ms, and lays the phylogenetic groundwork for comparative analyses of the drivers and correlates of su

168 In the absence of comprehensive direct comparative analyses of the evolutionary processes at di

169 Comparative analyses of the flagellar toolkit showed a p

170 Comparative analyses of the genome of Apostasia odorata,

171 By comparative analyses of the genomes of cucumber, melon a

172 However, interspecies comparative analyses of the genomic landscapes demonstra

173 view seeks to address how the functional and comparative analyses of the gut microbiome from 'large'

174 Comparative analyses of the human and chimpanzee genomes

175 Comparative analyses of the human microbiome have identi

176 Comparative analyses of the human microbiome have reveal

177 Taken together, comparative analyses of the influenza-host protein inter

178 Comparative analyses of the interaction and of the abili

179 Comparative analyses of the interactomes identified comm

180 ired for nucleosomal destabilization, and by comparative analyses of the intercalator and salt induce

181 In this study, comparative analyses of the LOS structures and correspon

182 Comparative analyses of the LPS from the wild-type and w

183 Comparative analyses of the molecular processes that und

184 l predictions for uncharacterized genes from comparative analyses of the rapidly growing genomic data

185 elopment and following injury, which enables comparative analyses of the regenerative (neonatal) vers

186 n microbiome, providing a key foundation for comparative analyses of the role of the microbiome in hu

187 Comparative analyses of the sequences showed, as expecte

188 ts to any metabolic reaction or pathway; and comparative analyses of the transport capabilities of di

189 In psychiatry, comparative analyses of therapeutic options and the aggr

190 en identified that can be used for effective comparative analyses of these proteins.

191 As such, comparative analyses of these structures, especially the

192 Phenotypic comparative analyses of this double mutant, together wit

193 Here, we perform comparative analyses of three Pseudomonas aeruginosa str

194 Integrative comparative analyses of transcript and metabolite levels

195 Comparative analyses of transcription profiles in NSPCs

196 In particular, several genome-wide comparative analyses of transcriptional circuits across

197 Comparative analyses of transcriptional profiles from hu

198 Our framework provides an ideal tool for comparative analyses of transcriptional signatures contr

199 In this study, integrative comparative analyses of transcriptomics and metabolomics

200 Comparative analyses of transcripts expression based on

201 Comparative analyses of transfection efficiency and cell

202 Comparative analyses of V. cholerae mutants suggest that

203 Quantitative comparative analyses of various features of the brain, s

204 throughput and large-scale, quantitative and comparative analyses of various models.

205 human influenza virus NP and illustrates how comparative analyses of viral lineages from different ho

206 actin incorporation into HIV-1, we performed comparative analyses of virus-like particles (VLPs) obta

207 and quantifiable ways, enabling high-powered comparative analyses of vocal acoustics.

208 e light and transmission electron microscopy comparative analyses of wild type versus lavender corn s

209 Comparative analyses of wild-type (WT) and symbiotic mut

210 lation and its molecular basis, we performed comparative analyses of WSC components and the expressio

211 Here we perform phylogenetic comparative analyses on 106 unique host-bacterial symbio

212 se two closely related species, we performed comparative analyses on 14 new S. gordonii and 5 S. sang

213 Based on phylogenetic comparative analyses on 3,005 bird species, we demonstra

214 Comparative analyses on experimentally validated dataset

215 Finally, we performed comparative analyses on the pathological changes in the

216 Comparative analyses point to accelerated pollen tube gr

217 uerin vaccine demonstrated the importance of comparative analyses, potential difficulties in generali

218 Comparative analyses proved that the nanoCT can depict t

219 Large-scale comparative analyses provide an alternative and suggest

220 Comparative analyses provide data on the conservation an

221 teins and in combination with other existing comparative analyses provided assurance that food derive

222 , empirical support for this hypothesis from comparative analyses remains lacking.

223 Comparative analyses reveal a high level of diversity be

224 Comparative analyses reveal fundamental differences in h

225 Comparative analyses reveal how the helicase loading mec

226 tif has unusual direct-repeat structure, and comparative analyses reveal sequence and structural simi

227 Comparative analyses reveal that bovid horns and cervid

228 Comparative analyses reveal that each decoding factor ex

229 Comparative analyses revealed (1) up to 3-fold higher ex

230 Comparative analyses revealed that dipterans follow simi

231 Whole-genome comparative analyses revealed that species-specific alte

232 Subsequent phylogenetically controlled comparative analyses revealed that vibrato-like F0 modul

233 Comparative analyses revealed that WRKY33 possesses dual

234 Comparative analyses revealed unique large-scale genomic

235 Comparative analyses show faster rates of gene gain and

236 Comparative analyses show that the turkey vulture has ol

237 The comparative analyses show that the two data files yield

238 Comparative analyses showed that Asian colobines have an

239 Comparative analyses showed that each seashore paspalum

240 Comparative analyses showed that genes targeted by conse

241 Comparative analyses showed that KPS was a statistically

242 ights the importance of including fossils in comparative analyses, showing that freshwaters have play

243 he warming over a set time horizon, for most comparative analyses, static values provide reasonable b

244 e levels in standard and low salt media, and comparative analyses suggest that DacA-1 is V. cholerae'

245 Comparative analyses suggest that intramitochondrial rec

246 Furthermore, comparative analyses suggest that many Gammaproteobacter

247 Comparative analyses suggested that levels of leptin, in

248 In comparative analyses, T cells sensitized with AAPCs expr

249 es of seven organs across seven species, and comparative analyses that characterize the development a

250 to the feasibility of detailed cross-species comparative analyses that may allow strong testing of hy

251 Researchers are also making plans to use comparative analyses that will help to turn the data int

252 both label-free proteomics and metabolomics comparative analyses, the software can be operated in se

253 ork that integrates taxonomic and functional comparative analyses to accurately quantify taxon-level

254 is repeatability and allowing 'through time' comparative analyses to be performed.

255 We ran our algorithm on several large comparative analyses to evaluate its effectiveness; one

256 rganisms, trace their evolution, and perform comparative analyses to find structural features that ca

257 oducing Pseudomonas spp., paving the way for comparative analyses to identify new genetic determinant

258 l performance for these compounds and expand comparative analyses to include physicochemical properti

259 s question, we used psychoacoustic tests and comparative analyses to investigate whether this distinc

260 ed and continually updated, thereby enabling comparative analyses to reveal the basis for differences

261 l genome sequences has enabled us to perform comparative analyses to shed light on the distribution o

262 We used comparative analyses to show that infanticide primarily

263 Here we use phylogenetic comparative analyses to test whether ASR is related to t

264 ches together with phylogenetically informed comparative analyses to test whether changes in fine-roo

265 cation of peptides and proteins extends from comparative analyses to the determination of actual amou

266 Comparative analyses using SNPs equivalently identified

267 Comparative analyses using the opossum genome have alrea

268 However, comparative analyses using these types of events as pred

269 Here, based on whole-genome comparative analyses, we comprehensively investigated pr

270 For comparative analyses, we derived one-to-one paired cohor

271 , climatic data, and a range of phylogenetic-comparative analyses, we detected significant shifts in

272 demonstrate the utility of this gene set for comparative analyses, we further analysed the expression

273 For this study, comparative analyses were conducted on lichen-associated

274 Comparative analyses were done with the deletions and th

275 ding number of recurrences and CDI severity, comparative analyses were limited to the matched cohort.

276 Descriptive statistics for outcomes and comparative analyses were made.

277 Comparative analyses were performed between the early tr

278 Comparative analyses were performed between the SRTR mod

279 d phylogenetic information was extracted and comparative analyses were performed for various subsets

280 In parallel, comparative analyses were performed on monolayer tumor c

281 Further comparative analyses were performed to determine site-sp

282 Comparative analyses were undertaken to determine the sy

283 Comparative analyses were used to test for significant d

284 ing the composition of the microbiome and on comparative analyses, whereas significantly less effort

285 d to provide analysis tools particularly for comparative analyses, which are required to provide impr

286 Comparative analyses with 40 other sheep breeds showed t

287 or and a domesticated variety of cassava and comparative analyses with a partial inbred line.

288 caste populations of South India and perform comparative analyses with caste populations from the nei

289 Unfortunately, good quality comparative analyses with ER are scarce.

290 Comparative analyses with fresh camu-camu berries indica

291 Through comparative analyses with human and rhesus macaque, we c

292 ations in potential cancer drivers for cross-comparative analyses with ongoing sequencing efforts in

293 invadopodia in PC3 cells, we performed a few comparative analyses with osteoclasts, which utilize pod

294 Comparative analyses with other amniotes provide new ins

295 ive-pacer viper, Deinagkistrodon acutus, and comparative analyses with other representative snake and

296 Comparative analyses with previously available finished

297 Direct comparative analyses with regression coefficient were ca

298 Comparative analyses with two other distantly related in

299 These resources allow for detailed comparative analyses within and across populations as we

300 riables potentially reduces effect sizes for comparative analyses, yet test statistics require more o