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1 gnment data in metagenomics, which are often interspecies alignments.
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                                Indole, as an interspecies and interkingdom signaling molecule, plays
6                                              Interspecies and intraspecies interaction approaches wit
7                      To investigate possible interspecies and intraspecies transmission of picornavir
8 taphylococcus aureus colonization and reveal interspecies and species-host interactions.
9  metabolic exchange factors of intraspecies, interspecies, and polymicrobial interactions.
10 a Prevotella and Actinomyces showed the most interspecies associations, suggesting a central role for
11 ne autoinducer, AI-2, is proposed to promote interspecies bacterial communication, including in the m
12 or and its secretory machinery in intra- and interspecies bacterial interactions.
13 ne expression in response to cell density or interspecies bacterial interactions.
14 ortantly, the ability of SIVcpz to cross the interspecies barrier to infect humanized mice correlates
15 a new Genome Browser with RNAseq expression, interspecies Basic Local Alignment Search Tool alignment
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 luripotent stem cells (PSCs) in mice through interspecies blastocyst complementation.
20 shift in the population structure and closer interspecies cell-to-cell interactions.
21                                  Identifying interspecies changes in gene regulation, one of the two
22 we show that differences can be explained by interspecies changes in the regulation of the cortical G
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             A refined approach to generating interspecies chimeras could contribute not only to a bet
28 yos and rat, monkey and human PSCs to create interspecies chimeras cultured in vitro to the early egg
29 to mouse embryonic chimeras, thereby forming interspecies chimeras that could survive to adulthood.
30 tudy this process is through construction of interspecies chimeras that preserve or disrupt particula
31                        hiPSCs and hESCs form interspecies chimeras with high efficiency, colonize the
32 ds of experimental chimeras, including human-interspecies chimeras, they are a provocative resource f
33                                              Interspecies chimeric assays are a valuable tool for inv
34         Furthermore, human EPS cells exhibit interspecies chimeric competency in mouse conceptuses.
35 ty of generating human organs in animals via interspecies chimeric complementation.
36 o-barriers will facilitate the generation of interspecies chimeric embryos from distant species, incl
37 enetic diversity of EVs and the existence of interspecies chimerism that characterizes the novel vari
38 remaining population that confers fitness in interspecies co-culture.
39 ing gene in F. nucleatum that is involved in interspecies coadherence.
40 e several highly potent signals in intra and interspecies communication as well as cross-kingdom inte
41  is a QS signaling molecule that is used for interspecies communication by both Gram-positive and Gra
42 ibiotics in modulating biofilm formation and interspecies communication in bacteria.
43 ueneberg ganglion in intraspecies as well as interspecies communication of danger.
44 ensing (QS) molecule utilized by bacteria in interspecies communication.
45 olecules to sense and orchestrate intra- and interspecies communication.
46 biology, signal transduction mechanisms, and interspecies communication.
47  and, as such, represents a new paradigm for interspecies communication.
48 ntibiotic activity and is likely involved in interspecies communication.
49                                     However, interspecies comparative analyses of the genomic landsca
50                              Here, we use an interspecies comparative approach to investigate differe
51 al anatomical similarities to other insects, interspecies comparison also revealed several features t
52 Here, we introduce "comparative epigenomics"-interspecies comparison of DNA and histone modifications
53                                          The interspecies comparison of eggs sampled in 2008 found th
54                 In this study, we perform an interspecies comparison showing that the selective perme
55                          These are the first interspecies comparisons for PFASs in seabirds from the
56 ) a strong theoretical foundation for making interspecies comparisons of rs-fcMRI, and (3) a unique l
57 putida lysis was less critical in mitigating interspecies competition and PEf1 eliminated E. coli fas
58 isms in fostering a pathogenic habitat where interspecies competition and synergies occur to drive th
59 d under planktonic conditions to discern how interspecies competition contributes to E. coli suppress
60 mposition is thought to be largely shaped by interspecies competition for the available resources, bu
61 ost range) affects bacterial suppression and interspecies competition in environments harboring enter
62                Pneumocins mediate intra- and interspecies competition in vitro and have been shown to
63 . pertussis growth in vitro, indicating that interspecies competition may limit B. pertussis coloniza
64 P. putida lysis, which decreased stress from interspecies competition relative to incubations with T4
65 o track natural product modifications during interspecies competition.
66 study the impact of resource fluctuations on interspecies competition.
67 based silencing machinery, as defined by two interspecies complementation groups (SIR2 and SIR3).
68                  In the Saccharomyces genus, interspecies complementation tests can be used to evalua
69                                        Thus, interspecies complementation tests can be used to identi
70 ions, which in the MHV genome act in a fully interspecies-compliant manner.
71          These findings point to significant interspecies conservation in thymocyte-stroma interactio
72                                    Given the interspecies conservation of miRNAs and preliminary data
73                                              Interspecies conservation of this inhibitory activity wa
74  evidence and analysis of mRNA structure and interspecies conservation suggest that there is an evolu
75                               LILR show more interspecies conservation than the closely related Kille
76 = 432), including: genomic data, intra-, and interspecies conservation, gene expression, protein-prot
77 ion from population genetics and traditional interspecies conservation.
78              We report that Cubn is a novel, interspecies-conserved Fgf receptor.
79 into viral transmission in a setting of high interspecies contact.
80 ealed a correlation between intraspecies and interspecies convergence and several altered immune resp
81                                              Interspecies correlation analysis links PinT to host cel
82 s Internet application Web-ICE is a suite of Interspecies Correlation Estimation (ICE) models that ca
83                                              Interspecies correlation estimation (ICE) models were de
84 evelopment of SSDs, which may be filled with Interspecies Correlation Estimation (ICE) models.
85                              The patterns of interspecies correspondences are not, however, always th
86 k, we derive the probability distribution of interspecies covariance under Brownian motion and Ornste
87 must be carefully selected in order to avoid interspecies cross-reactivity, and is therefore restrict
88 same species but are most easily detected in interspecies crosses, leading to dramatically lowered fi
89               The general infertility in the interspecies crossings suggests that genetically unrelat
90                                         This interspecies curli assembly enhanced bacterial attachmen
91 ) neurons exhibit courtship toward divergent interspecies D. virilis and D. yakuba females and a decr
92 rganizing maps are a useful means to analyze interspecies data, as orthologs can be assigned to indep
93                                   From these interspecies data, we have established key components of
94 amination and validation for a surface-based interspecies deformation process, (2) a strong theoretic
95 hPSCs and provides evidence that human-mouse interspecies developmental competency can occur.
96                         The reasons for this interspecies difference in regenerative capacity remain
97          With our approach, we measure major interspecies difference regarding astrocytes, whereas de
98         The aim of this study was to unravel interspecies differences and commonalities between the r
99  in healthy men, which may reflect important interspecies differences between rodents and humans with
100                               We discuss how interspecies differences highlight the necessity for hum
101 e B. pertussis bvgAS genes revealed that the interspecies differences in bfrD modulation are partly d
102                              Given potential interspecies differences in biodistribution, the purpose
103                                              Interspecies differences in drug sensitivity and mechani
104 tion of the SR within the cell is related to interspecies differences in excitation-contraction coupl
105  Interestingly, we observed an enrichment of interspecies differences in H3K4me3 at the TSS of genes
106                                 These marked interspecies differences in IgG binding between human an
107 ins show marked quantitative and qualitative interspecies differences in interactions with strains of
108      Surprisingly, we discovered substantial interspecies differences in methylation features associa
109 mparing translation regulatory divergence to interspecies differences in mRNA sequence features, we s
110                                          The interspecies differences in PAH concentrations cannot be
111 hat they are homologous, although there were interspecies differences in the numbers of neurons in th
112                This could reflect well-known interspecies differences in the organization of sensorim
113 leavage by all three RNAPs and eliminate the interspecies differences in the reaction rates.
114 d innate immune diversification by analyzing interspecies differences in the transcriptional response
115                        Our results show that interspecies differences in translation contribute subst
116 e production by mammalian dynein have called interspecies differences into question.
117 and it is still not clear if they are due to interspecies differences or depend on photosynthetic typ
118 ectra revealed intraspecies similarities and interspecies differences that were the basis of species
119 inhibit ABCG2 may be an explanation of these interspecies differences.
120 h plasma protein binding of lead structures, interspecies discrepancies, nuisance inhibition, sophist
121 compared to 16S rDNA amplicons with enhanced interspecies discrimination.
122                                   Intra- and interspecies distributions of body sizes are thus major
123                                              Interspecies divergence in regulatory pathways may resul
124 ity of the mapA-ceuE assay was the result of interspecies diversity and intraspecies conservation of
125                 In addition, we propose that interspecies diversity of PCP-Bs may contribute to repro
126                                      We used interspecies domain swapping to identify motifs for rece
127 populations, which is important for tracking interspecies dynamics needed for successful site remedia
128  on the electron transfer systems, ratios of interspecies electron carriers, energy generating system
129                  DIET is the primary mode of interspecies electron exchange in some anaerobic digeste
130                                       Direct interspecies electron transfer (DIET) between Geobacter
131                                       Direct interspecies electron transfer (DIET) has biogeochemical
132 ossibility that biochar could promote direct interspecies electron transfer (DIET) in a manner simila
133  resulted from the establishment of a direct interspecies electron transfer (DIET), based on magnetit
134 corrosion (EMIC), from other living cells by interspecies electron transfer (IET), or from an electro
135 matic analyses to determine the mechanism of interspecies electron transfer by two model syntrophic m
136 id electrode or acetate oxidation via direct interspecies electron transfer from a heterotrophic part
137 f hydrogen producers and consumers linked by interspecies electron transfer in syntrophic consortia t
138                                              Interspecies electron transfer mechanisms between Bacter
139 cS-deficient strain unable to participate in interspecies electron transfer or Fe(III) oxide reductio
140             Genome-scale modelling of direct interspecies electron transfer reveals insights into the
141 ransport to insoluble electron acceptors and interspecies electron transfer.
142 were developed to maximize the efficiency of interspecies epigenomic comparisons.
143  recent recommendations to use BSA to derive interspecies equivalents for therapeutic dosages of drug
144 dant, lending support to the hypothesis that interspecies extracellular electron transfer is the synt
145 er than those derived from toxicology-based, interspecies extrapolations.
146                                              Interspecies fertilization is rare, partly due to specie
147  signature similarities on the one hand, and interspecies fingerprint differences on the other, can b
148                                              Interspecies fitness enhancements were also identified,
149                Our data show that intra- and interspecies gene expression models can successfully pre
150                                              Interspecies gene swaps result in phenotypically normal
151  is needed to understand the contribution of interspecies gene transfer to resistance emergence.
152  that contribute substantially to intra- and interspecies gene transfer, host adaptation, and virulen
153 ally an altered murM, presumably products of interspecies gene transfer.
154  signaling pathways is indeed a predictor of interspecies genetic rewiring due to unbalanced TATA box
155 bstantially higher than those attainable via interspecies H2 transfer.
156 types, one of which is derived from a recent interspecies hybridization with O. longistminata.
157 generates selection for traits that decrease interspecies hybridization.
158 view imprinted gene expression in intra- and interspecies hybrids and examine the evolutionary scenar
159 nally, a hemizygosity modifier screen in the interspecies hybrids identified additional genes involve
160                     Complementation tests in interspecies hybrids identified an evolutionarily conser
161 ibute to the aberrant phenotypes observed in interspecies hybrids in mammals and flowering plants, wh
162 e used allele-specific ribosome profiling in interspecies hybrids to compare the relative contributio
163 nd Methanosaeta species is an alternative to interspecies hydrogen transfer (IHT) in anaerobic digest
164 ey role in the development of the concept of interspecies hydrogen transfer.
165 umtS in 23 eukaryotic species using an intra/interspecies in silico approach based on a cross-species
166      These data suggest that the mouse-human interspecies in vitro chimera assay does not accurately
167 c blastocyst injection and in vitro culture (interspecies in vitro chimera assay) that enables the de
168                 Our results demonstrate that interspecies interaction can also be mediated by interfe
169                     Currently, the impact of interspecies interaction on S. aureus antibiotic suscept
170 -dimensional, structured genotype space with interspecies interaction.
171                             Intraspecies and interspecies interactions influence pneumococcal carriag
172                                        These interspecies interactions may prove critical to some inf
173                                              Interspecies interactions of the nasopharyngeal microbio
174  environment, even in the absence of complex interspecies interactions or spatial structuring.
175 ether cocolonization patterns represent true interspecies interactions or whether they result from co
176  energy conservation mechanisms that dictate interspecies interactions salient to methanogenic alkane
177 ulations, we identified the multidimensional interspecies interactions that define composition and dy
178 of virulence in polymicrobial infections and interspecies interactions within animal models.
179 role in many population-based phenotypes and interspecies interactions, including those in host envir
180                              To explore such interspecies interactions, we focused on Bacillus subtil
181          This material is obtained by tuning interspecies interactions.
182  influenced by their environment, intra- and interspecies interactions.
183 mon in animals, generating the potential for interspecies interactions.
184 owth, virulence, biofilm formation and intra/interspecies interactions.
185 y age and season supports the idea of active interspecies interactions.
186 iota form and stabilize communities based on interspecies interactions.
187  conserved geometrical features and striking interspecies invariance within certain animal classes.
188 ying the Xenopus system, whereby homogametic interspecies males are always sterile, thus violating Ha
189 xpression based models built in an intra- or interspecies manner to predict chemosensitivity and trea
190          In this issue, Fan et al. show that interspecies mating is inhibited by the taste receptor G
191                                              Interspecies meta-analysis suggested interactions betwee
192 he ratio shift in electron carriers used for interspecies metabolite exchange (hydrogen/formate).
193 producers and consumers obligately linked by interspecies metabolite exchange in syntrophic consortia
194 s protection and highlight the importance of interspecies microbial antagonism for the outcome of ani
195 as a mechanism underlying such observations, interspecies microbial antagonism might represent an alt
196 to serve a variety of purposes in intra- and interspecies microbial extracellular activities.
197 r the migration, stopover time, fitness, and interspecies mixing of migratory birds, and consequently
198 tions for exploring the molecular origins of interspecies morphological variation.
199          Here we report a literature-curated interspecies network of the human gut microbiota, called
200 microbials further reinforces this intricate interspecies network.
201                                              Interspecies nucleolar dominance is thought to result fr
202  receptors have the capacity for recognizing interspecies odors.
203 roduction of gene-edited sheep as a host for interspecies organ generation.
204 es host proteins onto which intraspecies and interspecies pathogen effectors converge.
205 lines in native pollinators may be caused by interspecies pathogen transmission originating from mana
206                   Climate change may disrupt interspecies phenological synchrony, with adverse conseq
207 ron carriers, energy generating systems, and interspecies physical associations.
208  findings support a model in which efficient interspecies prion conversion is determined by small str
209 protein (PrP(C)) into new infectious PrP(Sc) Interspecies prion transmissibility studies performed by
210  provide insights into mechanisms regulating interspecies prion transmission and a framework to recon
211                                              Interspecies prion transmission often leads to stable ch
212 the beta2-alpha2 loop structure can modulate interspecies prion transmission.
213 divergence was also associated with enhanced interspecies promoter conservation.
214 anding the biology of competitive exclusion, interspecies protection, and gene flow of adaptive funct
215 d by two residues, which helps to understand interspecies PrP propagation on a molecular level.
216                 In our model, we incorporate interspecies rabies infection in addition to rabid popul
217 les among different compartments, and define interspecies reactions with selected kinetic constants,
218  propagated using the same approach and that interspecies recombinant DNA molecules can produce a bio
219 infection with HSV-1 and HSV-2 yields viable interspecies recombinants in the natural human host.
220                     In addition, two further interspecies recombination events involving the S gene w
221                                              Interspecies recombination is even rarer for rhinoviruse
222                                              Interspecies recombination is even rarer in this virus g
223                   These results suggest that interspecies recombination may play an important role in
224  To further assess the rhinovirus intra- and interspecies recombination potential, we used artificial
225 obtained N. gonorrhoeae-specific DNA through interspecies recombination.
226 ecosystems and are the product of intra- and interspecies regulation of the relative abundance of org
227 infections, very little is known about their interspecies relationship.
228 specificity of the phenotype was verified by interspecies rescue experiments and further mutant analy
229 at the cycloalternan pathway plays a role in interspecies resource competition-potentially within the
230 able viruses with high frequency, whereas no interspecies rhinovirus recombinants could be recovered.
231 ally engineered 5' untranslated region (UTR) interspecies rhinovirus/rhinovirus or rhinovirus/non-rhi
232  order of host phylogeny is incongruent with interspecies root microbiota diversity, indicating that
233 nd anatomical traits; trait synergisms; and (interspecies) root competition.
234 drug development, future recommendations for interspecies scaling must be scientifically justified us
235 nces that are pathogen specific with minimum interspecies sequence homology for the design of Flavivi
236              Our work provides an example of interspecies signaling by a small molecule and illustrat
237                    These results identify an interspecies signaling cascade allowing ticks to detect
238                 It provides a foundation for interspecies signaling in environmental and clinical bio
239 ll-cell associations known as coaggregation, interspecies signaling, secretion and turnover of antimi
240 n with community members through a number of interspecies signalling systems including AI-2 and conta
241 re, we report that these "toxins" can act as interspecies signals, affecting filamentous fungal devel
242 both rabbit and human tissue, underlying the interspecies similarities of the recognized epitopes.
243            Here we examined the influence of interspecies spatial positioning as it relates to biosyn
244 ry networks, metabolic network modeling, and interspecies studies utilizing Caenorhabditis elegans an
245                                          Our interspecies systems biology approach provides a paradig
246                             Here, we used an interspecies systems biology approach with Caenorhabditi
247 ns and its bacterial diet provide a powerful interspecies systems biology model that facilitates the
248 robing coupled with nanoSIMS, we demonstrate interspecies transfer of reduced sulfur metabolites from
249 f the HSV-1 gD receptor nectin-1 may explain interspecies transfer of the viruses, and altered recept
250  of them, suggesting the occurrence of their interspecies transfer.
251                                     Using an interspecies transgenesis approach, we find functional c
252 icate relationship between prion strains and interspecies transmissibility barriers.
253 tinental viral spread, numerous instances of interspecies transmission and emergence in hosts represe
254         To identify cellular determinants of interspecies transmission and establish a novel immunoco
255  transmissibility and could be a barrier for interspecies transmission between humans and swine for i
256                             HTLVs arose from interspecies transmission between nonhuman primates and
257                       The factors that allow interspecies transmission but limit human-to-human trans
258 emiological studies in children suggest that interspecies transmission contributes to rotavirus strai
259 ong heterologous hosts providing evidence of interspecies transmission events.
260 PORTANCE Swine play an important role in the interspecies transmission of influenza viruses.
261 l features that make them ideal vehicles for interspecies transmission of influenza viruses; however,
262 ter connectivity to other bird species, with interspecies transmission of reassortant viruses peaking
263 ring of resistance outbreaks consistent with interspecies transmission of resistance elements.
264 ring of resistance outbreaks consistent with interspecies transmission of resistance elements.
265 ors for HTLV-1 acquisition in humans via the interspecies transmission of STLV-1 (its simian counterp
266 ection of pigs by strain HS206 suggests that interspecies transmission of this strain is possible und
267  important in assessing the relative risk of interspecies transmission of viruses from one host popul
268  important in assessing the relative risk of interspecies transmission of viruses.
269                  The precise determinants of interspecies transmission remain unclear, although struc
270                                              Interspecies transmission requires adaptation of the vir
271                                              Interspecies transmission via the airborne route was obs
272 vital roles in replication, host adaptation, interspecies transmission, and pathogenicity.
273 ence and structural variations on intra- and interspecies transmission, we integrated studies in deer
274 routes of occupational exposure and risk for interspecies transmission.
275 ew opportunities for zoonotic infections and interspecies transmission.
276  raising public health concerns of potential interspecies transmission.
277 ng the importance of the nuclear envelope in interspecies transmission.
278 Vs), and some of them have the potential for interspecies transmission.
279 g the possibility of bats as a reservoir for interspecies transmission.
280 AVs of 1 market customer and swine indicated interspecies transmission.
281                                   Lentiviral interspecies transmissions are partly driven by the evol
282 rs bypass this requirement during particular interspecies transmissions.
283 yploid (Mimulus peregrinus), a resynthesized interspecies triploid hybrid (M. robertsii), a resynthes
284                            While the 10-fold interspecies uncertainty factor does provide a reasonabl
285   We quantitatively examined the validity of interspecies uncertainty factors by comparing the respon
286                                              Interspecies uncertainty factors in ecological risk asse
287 nly weak differences, which are dominated by interspecies variability and may reflect neutral drift a
288  sequences shared with other flaviviruses as interspecies variants highlights the possible hazard of
289 into the relationship between individual and interspecies variation and show evidence for the functio
290  other antiretroviral proteins, CNP displays interspecies variation in antiviral activity.
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          This approach revealed considerable interspecies variation in the cell shape changes and nei
294             In aquatic risk assessment, this interspecies variation is often quantified via species s
295 therefore, are well suited for investigating interspecies variation, and potential links between endo
296 y system harbor a disproportionate amount of interspecies variation.
297 show quantitative and qualitative intra- and interspecies variations in expression patterns on leukoc
298 portions while accommodating both intra- and interspecies variations in size.
299               This correlation suggests that interspecies' variations of tkv expression are responsib
300 n the FCs are dynamic and exhibit a range of interspecies' variations.

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