ライフサイエンスコーパス: interspecies

1 cation, pathogenicity, transmissibility, and interspecies adaptation of influenza A viruses.

2 The ability to efficiently achieve interspecies allele introgression in one generation open

3 The intra- and interspecies analysis underlined how some mitochondrial

4 ed within the OA neural circuitry to inhibit interspecies and conspecific male-male courtship and ind

5 We estimate that overall, interspecies and inter-tissue differences in gene expres

6 nist, termed SR-717, that demonstrates broad interspecies and interallelic specificity.

7 Indole, as an interspecies and interkingdom signaling molecule, plays

8 Interspecies and intraspecies interaction approaches wit

9 In conclusion, interspecies and N supply interactively altered the cont

10 ponents regression (TransComp-R) to overcome interspecies and trans-omic discrepancies between mouse

11 city in E. bieneusi and its implications for interspecies and zoonotic transmission.

12 terial species and involved in intraspecies, interspecies, and interkingdom signalling.

13 ne autoinducer, AI-2, is proposed to promote interspecies bacterial communication, including in the m

14 ortantly, the ability of SIVcpz to cross the interspecies barrier to infect humanized mice correlates

15 Here, we developed a system to visualize interspecies behaviors at initial encounters.

16 Interspecies biochemical analyses show that COQ8A and ye

17 Interspecies blastocyst complementation enables organ-sp

18 evolution, embryogenesis, and human disease, interspecies blastocyst complementation might allow huma

19 ecellularization, 3-dimensional printing and interspecies blastocyst complementation, promise organoi

20 luripotent stem cells (PSCs) in mice through interspecies blastocyst complementation.

21 shift in the population structure and closer interspecies cell-to-cell interactions.

22 Identifying interspecies changes in gene regulation, one of the two

23 ened the repertoire and utility of mammalian interspecies chimaeras and carved out new paths towards

24 f human rsPSCs to generate post-implantation interspecies chimaeric embryos may facilitate our unders

25 discusses the different factors that affect interspecies chimera generation, such as evolutionary di

26 d comparisons, catalytic-site changes and an interspecies chimera indicate that pneumococcal MltG is

27 human and baboon APOL1 orthologs, along with interspecies chimeras and individual amino acid substitu

28 A refined approach to generating interspecies chimeras could contribute not only to a bet

29 yos and rat, monkey and human PSCs to create interspecies chimeras cultured in vitro to the early egg

30 to mouse embryonic chimeras, thereby forming interspecies chimeras that could survive to adulthood.

31 tudy this process is through construction of interspecies chimeras that preserve or disrupt particula

32 hiPSCs and hESCs form interspecies chimeras with high efficiency, colonize the

33 ds of experimental chimeras, including human-interspecies chimeras, they are a provocative resource f

34 sters of mouse NCC-derived cells expanded in interspecies chimeras, whereas adjacent human donor NCC-

35 pluripotent stem cell differentiation in pig interspecies chimeras.

36 Interspecies chimeric assays are a valuable tool for inv

37 Furthermore, human EPS cells exhibit interspecies chimeric competency in mouse conceptuses.

38 ty of generating human organs in animals via interspecies chimeric complementation.

39 o-barriers will facilitate the generation of interspecies chimeric embryos from distant species, incl

40 n tetraploid complementation and human-mouse interspecies chimerism assays.

41 remaining population that confers fitness in interspecies co-culture.

42 ing gene in F. nucleatum that is involved in interspecies coadherence.

43 e several highly potent signals in intra and interspecies communication as well as cross-kingdom inte

44 However, general principles of interspecies communication have not been discovered.

45 ibiotics in modulating biofilm formation and interspecies communication in bacteria.

46 al observation studies we explored potential interspecies communication signalling mechanisms underpi

47 olecules to sense and orchestrate intra- and interspecies communication.

48 ntibiotic activity and is likely involved in interspecies communication.

49 ensing (QS) molecule utilized by bacteria in interspecies communication.

50 ide variety of bacteria and thus facilitates interspecies communication.

51 However, interspecies comparative analyses of the genomic landsca

52 Here, we use an interspecies comparative approach to investigate differe

53 By performing interspecies comparative RNA sequencing analyses and fun

54 In this study, we perform an interspecies comparison showing that the selective perme

55 ver, using BOLD fMRI in NHP is desirable for interspecies comparison, and the BOLD signal's faster re

56 which subjects both epigenome and genome to interspecies comparison, has become a powerful approach

57 eneity within hPSC cultures complicates this interspecies comparison.

58 ) a strong theoretical foundation for making interspecies comparisons of rs-fcMRI, and (3) a unique l

59 showcase its biological applications on (1) interspecies comparisons of syntenic regions in human an

60 putida lysis was less critical in mitigating interspecies competition and PEf1 eliminated E. coli fas

61 isms in fostering a pathogenic habitat where interspecies competition and synergies occur to drive th

62 d under planktonic conditions to discern how interspecies competition contributes to E. coli suppress

63 mposition is thought to be largely shaped by interspecies competition for the available resources, bu

64 ost range) affects bacterial suppression and interspecies competition in environments harboring enter

65 . pertussis growth in vitro, indicating that interspecies competition may limit B. pertussis coloniza

66 P. putida lysis, which decreased stress from interspecies competition relative to incubations with T4

67 study the impact of resource fluctuations on interspecies competition.

68 res using a mathematical model of intra- and interspecies competition.

69 Previous studies have demonstrated that interspecies complementation of rodent blastocysts lacki

70 We suggest that interspecies connectivity may be an important source of

71 Given the interspecies conservation of miRNAs and preliminary data

72 Interspecies conservation of this inhibitory activity wa

73 = 432), including: genomic data, intra-, and interspecies conservation, gene expression, protein-prot

74 ion from population genetics and traditional interspecies conservation.

75 into viral transmission in a setting of high interspecies contact.

76 ealed a correlation between intraspecies and interspecies convergence and several altered immune resp

77 Interspecies correlation analysis links PinT to host cel

78 s Internet application Web-ICE is a suite of Interspecies Correlation Estimation (ICE) models that ca

79 Interspecies correlation estimation (ICE) models were de

80 evelopment of SSDs, which may be filled with Interspecies Correlation Estimation (ICE) models.

81 were also measured, and there were positive interspecies correlations between CFC-11 and CHCl(3), CC

82 With increasing evolutionary distance the interspecies correlations in gene expression decreases.

83 Within this trend, the interspecies correlations of developmental control genes

84 k, we derive the probability distribution of interspecies covariance under Brownian motion and Ornste

85 an make acapsular pneumococcus virulent, and interspecies cps transfer should be considered a potenti

86 Interspecies cross-feeding is a fundamental factor in an

87 The general infertility in the interspecies crossings suggests that genetically unrelat

88 ) neurons exhibit courtship toward divergent interspecies D. virilis and D. yakuba females and a decr

89 amination and validation for a surface-based interspecies deformation process, (2) a strong theoretic

90 hPSCs and provides evidence that human-mouse interspecies developmental competency can occur.

91 This interspecies difference of telomere homeostasis poses a

92 With our approach, we measure major interspecies difference regarding astrocytes, whereas de

93 nd DNA methylation, are also responsible for interspecies differences as well as differences between

94 in healthy men, which may reflect important interspecies differences between rodents and humans with

95 e B. pertussis bvgAS genes revealed that the interspecies differences in bfrD modulation are partly d

96 fferences in protein turnover play a role in interspecies differences in developmental tempo.

97 Interspecies differences in drug sensitivity and mechani

98 ins show marked quantitative and qualitative interspecies differences in interactions with strains of

99 Surprisingly, we discovered substantial interspecies differences in methylation features associa

100 a powerful tool for the characterization of interspecies differences in mycotoxin toxicity for a ran

101 g of regulatory gene expression may underlie interspecies differences in neuronal projection fate spe

102 o after Irma's impact, thus underscoring the interspecies differences in nutrient uptake.

103 The interspecies differences in PAH concentrations cannot be

104 capabilities and spatial movements, can mask interspecies differences in PFASs, especially PFCAs, exp

105 In addition, despite interspecies differences in rumen bacterial composition,

106 is new frontier highlights the potential for interspecies differences in the biophysics of dendritic

107 hat they are homologous, although there were interspecies differences in the numbers of neurons in th

108 This could reflect well-known interspecies differences in the organization of sensorim

109 leavage by all three RNAPs and eliminate the interspecies differences in the reaction rates.

110 human and zebrafish PR and highlights major interspecies differences in their activity, which may re

111 d less prevalent than in rodents, suggesting interspecies differences in theta's function.

112 Our results show that interspecies differences in translation contribute subst

113 e production by mammalian dynein have called interspecies differences into question.

114 In particular, our results suggest interspecies differences regarding the integration of th

115 Some interspecies differences stem from the diversity of geno

116 nserved form of programmed cell death, shows interspecies differences that may reflect evolutionary d

117 ectra revealed intraspecies similarities and interspecies differences that were the basis of species

118 didates failed due to poor pharmacokinetics, interspecies differences, and adverse effects.

119 To identify possible interspecies differences, we assessed in vitro the abili

120 inhibit ABCG2 may be an explanation of these interspecies differences.

121 h plasma protein binding of lead structures, interspecies discrepancies, nuisance inhibition, sophist

122 compared to 16S rDNA amplicons with enhanced interspecies discrimination.

123 on, which suggests that careful attention to interspecies divergence is needed when modeling human se

124 ment remains relatively unexplained owing to interspecies divergence(2,3) and limited accessibility t

125 global genetic and molecular bases for these interspecies divergences were unknown.

126 ity of the mapA-ceuE assay was the result of interspecies diversity and intraspecies conservation of

127 In addition, we propose that interspecies diversity of PCP-Bs may contribute to repro

128 Collectively, we unveil the interspecies diversity of the ability of ISG15/USP18 axi

129 enting both mouse intraspecies and mouse/rat interspecies donor chimerism that continuously increases

130 populations, which is important for tracking interspecies dynamics needed for successful site remedia

131 DIET is the primary mode of interspecies electron exchange in some anaerobic digeste

132 Direct interspecies electron transfer (DIET) between Geobacter

133 Direct interspecies electron transfer (DIET) has biogeochemical

134 resulted from the establishment of a direct interspecies electron transfer (DIET), based on magnetit

135 By accepting these electrons through direct interspecies electron transfer (DIET), M. concilii was c

136 corrosion (EMIC), from other living cells by interspecies electron transfer (IET), or from an electro

137 ht interactions via both mediated and direct interspecies electron transfer (MIET and DIET), induced

138 matic analyses to determine the mechanism of interspecies electron transfer by two model syntrophic m

139 id electrode or acetate oxidation via direct interspecies electron transfer from a heterotrophic part

140 cS-deficient strain unable to participate in interspecies electron transfer or Fe(III) oxide reductio

141 cteria for disproportionation and (3) direct interspecies electron transfer.

142 ransport to insoluble electron acceptors and interspecies electron transfer.

143 recent recommendations to use BSA to derive interspecies equivalents for therapeutic dosages of drug

144 Here, we showed interspecies events of recombination of an endemic drome

145 dant, lending support to the hypothesis that interspecies extracellular electron transfer is the synt

146 Interspecies fertilization is rare, partly due to specie

147 s the evasion of early developmental arrest, interspecies fetuses with high levels of organ chimerism

148 signature similarities on the one hand, and interspecies fingerprint differences on the other, can b

149 Interspecies fitness enhancements were also identified,

150 Our data show that intra- and interspecies gene expression models can successfully pre

151 gene coexpression network analysis to create interspecies gene networks and assess the capacity of ea

152 Interspecies gene swaps result in phenotypically normal

153 that contribute substantially to intra- and interspecies gene transfer, host adaptation, and virulen

154 ally an altered murM, presumably products of interspecies gene transfer.

155 cryptic plasmid, suggesting a mechanism for interspecies genetic exchange that promotes antimicrobia

156 signaling pathways is indeed a predictor of interspecies genetic rewiring due to unbalanced TATA box

157 bstantially higher than those attainable via interspecies H2 transfer.

158 d disease, we assessed the circRNAome of the interspecies homologue rhesus macaque lymphocryptovirus

159 Interspecies hybridization between southern platyfish an

160 types, one of which is derived from a recent interspecies hybridization with O. longistminata.

161 view imprinted gene expression in intra- and interspecies hybrids and examine the evolutionary scenar

162 t and divergent evolutionary trajectories of interspecies hybrids and their impact on innovation in l

163 heterosis in yeasts, but the full breadth of interspecies hybrids associated with human fermentations

164 rmented beverage, lager beer, is produced by interspecies hybrids of the brewing yeast Saccharomyces

165 e used allele-specific ribosome profiling in interspecies hybrids to compare the relative contributio

166 ontrast, the undomesticated parents of these interspecies hybrids were all from wild Holarctic or Eur

167 sa of Drosophila mauritiana in the testes of interspecies hybrids.

168 nd Methanosaeta species is an alternative to interspecies hydrogen transfer (IHT) in anaerobic digest

169 ey role in the development of the concept of interspecies hydrogen transfer.

170 umtS in 23 eukaryotic species using an intra/interspecies in silico approach based on a cross-species

171 These data suggest that the mouse-human interspecies in vitro chimera assay does not accurately

172 c blastocyst injection and in vitro culture (interspecies in vitro chimera assay) that enables the de

173 e survival of all organisms, but its role in interspecies interaction is unknown.

174 Currently, the impact of interspecies interaction on S. aureus antibiotic suscept

175 e limited accuracy with which we can predict interspecies interactions and environmental dependencies

176 egions of the CF lung is likely to influence interspecies interactions and in turn, potentially influ

177 in a degenerate Fermi gas of lithium atoms, interspecies interactions can give rise to an effective

178 Interspecies interactions can impact antibiotic activity

179 on the contextual microbiome, we assess how interspecies interactions can shape genetic diversity an

180 l processes may have selected convergence in interspecies interactions in other animal clades.

181 ction and analysis of metabolites present in interspecies interactions of microorganisms on surfaces.

182 ether cocolonization patterns represent true interspecies interactions or whether they result from co

183 energy conservation mechanisms that dictate interspecies interactions salient to methanogenic alkane

184 Not all interspecies interactions studied were antagonistic, as

185 ulations, we identified the multidimensional interspecies interactions that define composition and dy

186 of virulence in polymicrobial infections and interspecies interactions within animal models.

187 hanistic understanding of the coupling among interspecies interactions, environmental pH, and antibio

188 , the srtA-deficient mutant fails to mediate interspecies interactions, or coaggregation, even though

189 egions suggested that FapA may contribute to interspecies interactions, that FapA and FapB may contri

190 influenced by their environment, intra- and interspecies interactions.

191 mon in animals, generating the potential for interspecies interactions.

192 owth, virulence, biofilm formation and intra/interspecies interactions.

193 y age and season supports the idea of active interspecies interactions.

194 iota form and stabilize communities based on interspecies interactions.

195 on of protein homeostasis is a mechanism for interspecies interactions.

196 dominant animals, raising safety concerns in interspecies interactions.

197 aining genomic information and examining the interspecies interactions.

198 l bacteria, including the discovery of novel interspecies interactions.

199 h less is known about the molecular basis of interspecies interplay.

200 conserved geometrical features and striking interspecies invariance within certain animal classes.

201 bcellular, cellular, tissue, interorgan, and interspecies levels, which will have important implicati

202 xpression based models built in an intra- or interspecies manner to predict chemosensitivity and trea

203 Interspecies meta-analysis suggested interactions betwee

204 With substantial interspecies metabolic similarity in post-resuscitation

205 ifferences can be explained by corresponding interspecies methylation changes more often.

206 s protection and highlight the importance of interspecies microbial antagonism for the outcome of ani

207 tions for exploring the molecular origins of interspecies morphological variation.

208 Here we report a literature-curated interspecies network of the human gut microbiota, called

209 microbials further reinforces this intricate interspecies network.

210 rations in digester microbiome and intricate interspecies networks during substrate variation, symbio

211 derstanding of the fundamental properties of interspecies networks will lead to the development of ef

212 Interspecies organ generation via blastocyst complementa

213 roduction of gene-edited sheep as a host for interspecies organ generation.

214 on strain properties triggered by intra- and interspecies passage.

215 lines in native pollinators may be caused by interspecies pathogen transmission originating from mana

216 Here, we describe an interspecies pathway for gut bacterial l-dopa metabolism

217 protein (PrP(C)) into new infectious PrP(Sc) Interspecies prion transmissibility studies performed by

218 provide insights into mechanisms regulating interspecies prion transmission and a framework to recon

219 anding the biology of competitive exclusion, interspecies protection, and gene flow of adaptive funct

220 Finally, real-world interspecies proximity was observed and found to be best

221 d by two residues, which helps to understand interspecies PrP propagation on a molecular level.

222 ging evidence suggests that intraspecies and interspecies QS plays an important role in antimicrobial

223 extreme atomic-physics phenomena-firstly, an interspecies radiative transition; and, secondly, the br

224 les among different compartments, and define interspecies reactions with selected kinetic constants,

225 infection with HSV-1 and HSV-2 yields viable interspecies recombinants in the natural human host.

226 However, it is unknown whether interspecies recombination can affect other loci and whe

227 rose in its current host, demonstrating that interspecies recombination continues to occur today.

228 At least 4 small, ancient HSV-1 x HSV-2 interspecies recombination events have affected the HSV-

229 indings show that the sizes and locations of interspecies recombination events in HSV-2 are significa

230 In addition, two further interspecies recombination events involving the S gene w

231 enome sequences, we comprehensively assessed interspecies recombination in HSV.

232 Interspecies recombination is even rarer for rhinoviruse

233 Interspecies recombination is even rarer in this virus g

234 These results suggest that interspecies recombination may play an important role in

235 To further assess the rhinovirus intra- and interspecies recombination potential, we used artificial

236 tic classification methods is complicated by interspecies recombination.

237 ies with explicit representation of inferred interspecies recombination.

238 Indeed, many interspecies relationships are multidimensional, and the

239 at the cycloalternan pathway plays a role in interspecies resource competition-potentially within the

240 able viruses with high frequency, whereas no interspecies rhinovirus recombinants could be recovered.

241 ally engineered 5' untranslated region (UTR) interspecies rhinovirus/rhinovirus or rhinovirus/non-rhi

242 nd anatomical traits; trait synergisms; and (interspecies) root competition.

243 drug development, future recommendations for interspecies scaling must be scientifically justified us

244 These results identify an interspecies signaling cascade allowing ticks to detect

245 It provides a foundation for interspecies signaling in environmental and clinical bio

246 ll-cell associations known as coaggregation, interspecies signaling, secretion and turnover of antimi

247 Indole is well known as an interspecies signalling molecule to modulate bacterial p

248 ue that enteric pathogens respond to DSFs as interspecies signals to identify appropriate niches in t

249 re, we report that these "toxins" can act as interspecies signals, affecting filamentous fungal devel

250 In contrast to this interspecies similarity, the intraspecies comparison of

251 Here we examined the influence of interspecies spatial positioning as it relates to biosyn

252 ry networks, metabolic network modeling, and interspecies studies utilizing Caenorhabditis elegans an

253 acteria, and methanogenic archaea, and their interspecies symbioses allow complex metabolisms for the

254 Here, we used an interspecies systems biology approach with Caenorhabditi

255 ns and its bacterial diet provide a powerful interspecies systems biology model that facilitates the

256 robing coupled with nanoSIMS, we demonstrate interspecies transfer of reduced sulfur metabolites from

257 We used a paradigm with interspecies translation validity (the four-choice seria

258 icate relationship between prion strains and interspecies transmissibility barriers.

259 tinental viral spread, numerous instances of interspecies transmission and emergence in hosts represe

260 To identify cellular determinants of interspecies transmission and establish a novel immunoco

261 transmissibility and could be a barrier for interspecies transmission between humans and swine for i

262 HTLVs arose from interspecies transmission between nonhuman primates and

263 The factors that allow interspecies transmission but limit human-to-human trans

264 emiological studies in children suggest that interspecies transmission contributes to rotavirus strai

265 The efficient interspecies transmission demonstrated for the H3.2010.1

266 ong heterologous hosts providing evidence of interspecies transmission events.

267 The likelihood of GBS interspecies transmission is largely unknown.

268 strain in both host species, suggesting that interspecies transmission may be possible.

269 ver, the molecular properties accounting for interspecies transmission of influenza viruses remain un

270 PORTANCE Swine play an important role in the interspecies transmission of influenza viruses.

271 ter connectivity to other bird species, with interspecies transmission of reassortant viruses peaking

272 ors for HTLV-1 acquisition in humans via the interspecies transmission of STLV-1 (its simian counterp

273 ile we were not able to demonstrate frequent interspecies transmission of TPE in Tanzanian monkeys, o

274 important in assessing the relative risk of interspecies transmission of viruses from one host popul

275 important in assessing the relative risk of interspecies transmission of viruses.

276 Interspecies transmission via the airborne route was obs

277 These aspects, their interspecies transmission, and certain factors that impa

278 important implications in the natural hosts, interspecies transmission, animal models, and molecular

279 ence and structural variations on intra- and interspecies transmission, we integrated studies in deer

280 Vs), and some of them have the potential for interspecies transmission.

281 g the possibility of bats as a reservoir for interspecies transmission.

282 AVs of 1 market customer and swine indicated interspecies transmission.

283 routes of occupational exposure and risk for interspecies transmission.

284 ew opportunities for zoonotic infections and interspecies transmission.

285 es host range and is the major constraint to interspecies transmission.

286 ecificity of the virus and may also regulate interspecies transmission.

287 rs bypass this requirement during particular interspecies transmissions.

288 yploid (Mimulus peregrinus), a resynthesized interspecies triploid hybrid (M. robertsii), a resynthes

289 nalysis on seabirds and investigated whether interspecies variation in maternal investment contribute

290 Interspecies variation in maternal pollutant transfer ma

291 nts, of these eggshells display a remarkable interspecies variation in number and shape, and the epit

292 Interspecies variation in sensitivity to synthetic chemi

293 multidimensional framework for understanding interspecies variation in states of consciousness.

294 This approach revealed considerable interspecies variation in the cell shape changes and nei

295 same strain are robustly identified, despite interspecies variation in the pairwise distance distribu

296 In aquatic risk assessment, this interspecies variation is often quantified via species s

297 y system harbor a disproportionate amount of interspecies variation.

298 show quantitative and qualitative intra- and interspecies variations in expression patterns on leukoc

299 portions while accommodating both intra- and interspecies variations in size.

300 Interspecies virus transmission involving economically i