戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 relationships within Aculeata, including the phylogenetic affinities of ants and bees [5-7].
2                             Establishing the phylogenetic affinities of ants and bees helps us unders
3      The morphology and previously suggested phylogenetic affinities of Parvancorina are also re-eval
4 es long reads with sufficient depth for many phylogenetic analyses and can therefore provide insights
5 sing studies, bulk-segregant RNA sequencing, phylogenetic analyses and functional tests to identify t
6 ella The remaining six isolates are shown by phylogenetic analyses based on four loci to represent tw
7                                  Genomic and phylogenetic analyses can give insight into a patient's
8                       Additionally, Bayesian phylogenetic analyses corroborate several lineage-specif
9                                       Recent phylogenetic analyses have retrieved aglaspidids within
10 lowly than those from the United States, and phylogenetic analyses indicated that isolates from Europ
11 means of nucleotide sequencing and extensive phylogenetic analyses of a 400-nucleotide region of the
12                                          Our phylogenetic analyses of miRNAs in bryophytes, lycophyte
13                                              Phylogenetic analyses of the 11 available membracoid mit
14                                 Here we used phylogenetic analyses of the vision genes involved in th
15                                In silico and phylogenetic analyses of these protein families revealed
16                                              Phylogenetic analyses of three concatenated nucleotide d
17 d microRNA (miRNA) candidates, and performed phylogenetic analyses on small RNA pathways as well as m
18                                              Phylogenetic analyses placed this population from northe
19                                              Phylogenetic analyses resolve C. kroegeri as a stem-grou
20                                              Phylogenetic analyses reveal that the ISC and CIA pathwa
21                                              Phylogenetic analyses revealed several cryptic Hepatocys
22                                Comprehensive phylogenetic analyses revealed that ISE2 is a non-canoni
23                                          The phylogenetic analyses show the presence of several disti
24                                              Phylogenetic analyses suggest it diverged from a human S
25                                              Phylogenetic analyses suggest that the origin of rebound
26                                          Our phylogenetic analyses suggest that this major retroviral
27                                              Phylogenetic analyses suggest that titin, the largest kn
28                                              Phylogenetic analyses suggested that G-LSR2 was acquired
29                                              Phylogenetic analyses support co-speciation as having a
30 cialized characteristics, and the results of phylogenetic analyses that support the hypothesis that h
31                                              Phylogenetic analyses used maximum likelihood estimation
32  of protein characterization, expression and phylogenetic analyses we identified a novel class of Ara
33                                      WGS and phylogenetic analyses were performed on a sample of USA3
34 In this study, we have used a combination of phylogenetic analyses with syntenic alignment of mammali
35 mily classification, transcriptome analyses, phylogenetic analyses, and pathogenicity experiments wer
36                             A combination of phylogenetic analyses, gene silencing, and biochemical a
37                                           In phylogenetic analyses, partitioning strategies involve e
38  were identified as Sapajus apella, based on phylogenetic analyses, pelage pattern and geographic pro
39                  Using homology modeling and phylogenetic analyses, we present evidence that SDH6 and
40                              By sequence and phylogenetic analyses, we show that it is a betaherpesvi
41 ransmission dynamics were investigated using phylogenetic analyses.
42                                            A phylogenetic analysis based on protein sequences showed
43                                              Phylogenetic analysis based on whole-genome sequencing o
44                                            A phylogenetic analysis combined with an analysis of the s
45                                              Phylogenetic analysis demonstrated high similarity with
46                                              Phylogenetic analysis demonstrated that 58% (7 of 12) of
47                                              Phylogenetic analysis found close clustering of strains
48                                              Phylogenetic analysis identified a clade of MHC-B, defin
49                                              Phylogenetic analysis indicated that Rv2633c is a member
50                                              Phylogenetic analysis indicates that the outbreak was ca
51 novel approach to this problem, performing a phylogenetic analysis indicating that family living is a
52 leotide dataset, implying that probabilistic phylogenetic analysis methods are needed.
53            Here, we performed a whole-genome phylogenetic analysis of 368 IAV circulating in swine fr
54                                          Our phylogenetic analysis of 37 GET3 orthologs from 18 diffe
55                        Genome sequencing and phylogenetic analysis of 387 isolates, representing the
56                                              Phylogenetic analysis of all coding genes showed a close
57                                              Phylogenetic analysis of apple bHLH (MdbHLH) genes and t
58 cal contact tracing of patients and Bayesian phylogenetic analysis of bacterial WGS data were used to
59  angiosperms and gymnosperms were used for a phylogenetic analysis of end wall types, calculation of
60 nd CISD3, Miner2) as our guides to conduct a phylogenetic analysis of eukaryotic NEET proteins and th
61                                              Phylogenetic analysis of metagenome sequences indicated
62                                          The phylogenetic analysis of NucS indicates a complex evolut
63                                 Kingdom-wide phylogenetic analysis of over 400 CYP716s from over 200
64                                      HTS and phylogenetic analysis of paired specimens confirmed shed
65                                              Phylogenetic analysis of plastid and mitochondrial genes
66                                              Phylogenetic analysis of SNAP genes from 22 diverse plan
67                                              Phylogenetic analysis of the algal fermentative enzyme s
68                                     Temporal phylogenetic analysis of the emergence of ST69 and ST131
69                                              Phylogenetic analysis of the whole genome identified a c
70                                              Phylogenetic analysis of translation system components,
71                                              Phylogenetic analysis revealed that all NPC-EBV genomes
72                      Metagenomic binning and phylogenetic analysis revealed that two anammox populati
73                                              Phylogenetic analysis showed distinct GII.4 variants in
74                                              Phylogenetic analysis showed most of the HRSVA sequences
75                                              Phylogenetic analysis showed that disease flares were as
76                                              Phylogenetic analysis showed that in the structural regi
77                                              Phylogenetic analysis suggested that SbCYP82D2 might hav
78                                              Phylogenetic analysis supported close relationships amon
79  its relationships by designing an inclusive phylogenetic analysis that broadly incorporates definiti
80                                Then, using a phylogenetic analysis to examine actin evolution, we sho
81          We used whole-genome sequencing and phylogenetic analysis to investigate the patterns of glo
82  Here, Grabowski and Jungers use comparative phylogenetic analysis to reconstruct the likely size of
83                              The accuracy of phylogenetic analysis was 100%.
84               In support of RNA mutation and phylogenetic analysis, a web server (RNA-TVcurve) was de
85 were performed with hierarchical clustering, phylogenetic analysis, and principal component analysis.
86 ural and mechanistic insights, together with phylogenetic analysis, suggest convergent evolution of p
87  In this study, based on homology search and phylogenetic analysis, we identified three homologs of A
88                                              Phylogenetic and demographic analyses indicate that Chin
89              Finally, using a combination of phylogenetic and distance-based approaches, we showed th
90 ally variable RNA virus populations, but for phylogenetic and evolutionary analyses, longer sequences
91                                 We conducted phylogenetic and expression analysis for eight SEP-like
92 proteins from 4,650 samples, improving their phylogenetic and functional interpretation.
93                                              Phylogenetic and genetic evidence suggests that the comp
94                                        Their phylogenetic and genomic diversity suggests ecological n
95 ass of 69 notoungulate taxa, placed in their phylogenetic and geological contexts.
96 nd those isolated from humans, comprehensive phylogenetic and molecular analyses of viruses collected
97                                              Phylogenetic and motif analyses indicated that XND1 and
98                               Interestingly, phylogenetic and physiological studies suggest that homo
99 ee key dimensions of biodiversity-taxonomic, phylogenetic, and traits-and (ii) determine the overlap
100 doubled due to progress of the Gene Ontology Phylogenetic Annotation Project.
101                     Our multimodel inference phylogenetic approach showed that the barriers that need
102                   Currently, widely accepted phylogenetic approaches are based on multiple sequence a
103 d for continued synthesis between fossil and phylogenetic approaches to macroevolution.
104 tification of homologs between species using phylogenetic approaches, a consideration of the inter- a
105                 We assessed the temporal and phylogenetic associations between the serogroup W outbre
106 d the potential associations (functional and phylogenetic) between host plants and butterflies in 561
107                                     Genetic, phylogenetic, bioinformatics, structural, and biochemica
108  (N), syntenies, and tuning sites along each phylogenetic branch during evolution.
109 profiling of tumours depends on the earliest phylogenetic branching event during tumour growth.
110                                              Phylogenetic character analysis demonstrates that high A
111 gly, partial 'un-scoring' of the problematic phylogenetic characters was proposed.
112                               Based on their phylogenetic closeness and the similarity of their MTL (
113 ture) had lower alpha diversity and midrange phylogenetic clustering, characteristic of ecosystem dis
114               Candidate phyla (CP) are broad phylogenetic clusters of organisms that lack cultured re
115                                          Two phylogenetic clusters were suggestive of interclass MRSA
116 tives within Brassicaceae identified a clear phylogenetic co-occurrence between ER bodies and IGs, bu
117                                     Based on phylogenetic comparative analyses on 3,005 bird species,
118                Here we report results from a phylogenetic comparative analysis of over 1000 species o
119                           Here, we develop a phylogenetic comparative framework for testing if and ho
120                       Using state-of-the-art phylogenetic comparative methods, we show that successfu
121 zed karyotype evolution in Agrodiaetus using phylogenetic comparative methods.
122 tly between all three land use types, as did phylogenetic composition.
123                          The hypothesis of a phylogenetic connection between protorespect in primate
124                             When placed in a phylogenetic context, our new taxon indicates that filte
125                                              Phylogenetic, cytogenetic, and genomic analyses implied
126 cess combined with targeting rRNA to exploit phylogenetic differences for sensitive and unambiguous s
127                             Determination of phylogenetic dis(similarities) showed that the bacterial
128 argely comparable and generally unrelated to phylogenetic distance among hosts.
129                 Here, we show how the use of phylogenetic distance based redundancy analysis provides
130                        Consistent with their phylogenetic distance from described subgroups, the geno
131 during an immunological challenge, we used a phylogenetic distance metric to analyze Ig heavy-chain t
132 nsory ecology plays a stronger role than the phylogenetic distance of the three species in structurin
133 ose a hybrid approach that also incorporates phylogenetic distance to provide greater resolution.
134 ther potentially explanatory traits, such as phylogenetic distance, as well as female reproductive sc
135 yrmecoid clades are separated by substantial phylogenetic distances-as much as 105 million years.
136                                 Based on its phylogenetic distribution and sequence clustering, Anbu
137 e disparate biosynthetic origins and distant phylogenetic distribution implies these loops evolved in
138                                We review the phylogenetic distribution of plant feeding in the Crusta
139 ein family, and shed additional light on the phylogenetic distribution of selenoprotein containing ge
140 acid polymerase families, (b) the origin and phylogenetic distribution of TBP, TFB, and TFE transcrip
141 t microbiotas was independent of dietary and phylogenetic divergence among hosts.
142 tial mechanistic diversity, underscoring the phylogenetic divergence of related CRISPR-Cas systems.
143 es in microbial composition, alpha, beta and phylogenetic diversity associated with a higher radiativ
144  body sites; it also quantified species with phylogenetic diversity under-represented in isolate geno
145 mate change-mediated range shifts can reduce phylogenetic diversity within high latitude communities,
146 ent analyses targeting the genetic identity, phylogenetic diversity, and spatial distribution of Balt
147                   Bacterial diversity (Faith phylogenetic diversity, P = .003) and composition change
148 e in novel protein families as a function of phylogenetic diversity.
149 ition increased ecological stochasticity and phylogenetic diversity.
150 o account slope estimation error and examine phylogenetic, ecological and geographic predictors of in
151   Furthermore, we demonstrate that community phylogenetic ecology coupled with phylodynamic technique
152                      We then linked genomic, phylogenetic, epidemiologic, and clinical data in order
153 proaches often use static representations of phylogenetic, epidemiological, statistical and evolution
154                  This represents unambiguous phylogenetic evidence for a single origin of the group's
155 uction of protein ancestry in the absence of phylogenetic evidence.
156 ombination of factors such as anatomical and phylogenetic evolutionary constraints, and further empir
157   Here we test this hypothesis using a solid phylogenetic framework of Neotropical Catasetinae, the a
158   Some network parameters are similar within phylogenetic groups (e.g., non-primates, strepsirrhines,
159 mportance of incorporating biogeographic and phylogenetic history in predicting community and ecosyst
160 leles throughout the tumour we can infer the phylogenetic history of the tumour, identify epialleles
161                       The lasting imprint of phylogenetic history on current day ecological patterns
162                 To evaluate support for this phylogenetic hypothesis at the molecular level, we seque
163 cate reticulate evolution as a main cause of phylogenetic incongruence.
164               On the basis of three existing phylogenetic inference algorithms, we built an integrate
165 - and compute-intensive applications such as phylogenetic inference for large-scale sequences.
166                                              Phylogenetic inference is an attractive means to reconst
167                                      Because phylogenetic inference is an important basis for answeri
168                                              Phylogenetic inference typically invokes nocturnality as
169 tes for computationally intensive methods of phylogenetic inference using (for example) maximal likel
170 s and assess the effects of recombination on phylogenetic inference.
171  components analysis, incorporated modulated phylogenetic information and enhanced interpretation thr
172                                 Inclusion of phylogenetic information provides a powerful framework f
173 , knowing that there is unexplained residual phylogenetic information should spur the search for addi
174 es to selection arising from fluctuations in phylogenetic integration, thus influencing differential
175 ed the computational burden for even routine phylogenetic investigations.
176 uction method to visualize large multi-locus phylogenetic landscapes and demonstrate that 3D projecti
177 oaches to aid in the comparison of different phylogenetic landscapes are presented.
178 ical characterization of orthologs along the phylogenetic lineage from cassava to A. thaliana, sugges
179 tepping that are conserved among these three phylogenetic lineages of the Rad51/RecA family and also
180 d others unique to their specific species or phylogenetic lineages.
181 lative representation and abundance of grass phylogenetic lineages.
182                                Specifically, phylogenetic linear mixed models show that the formation
183 ection has been relatively under-employed in phylogenetics, mainly due to the cost of sequencing geno
184 ernal transcribed spacer (ITS) region as the phylogenetic marker for HRM, we observed complex melt cu
185  applied for taxonomic classification of any phylogenetic marker gene sequences.
186 ferent regions of the 16S rRNA gene or other phylogenetic marker genes.
187                               We conducted a phylogenetic meta-analysis of 342 host-parasite interact
188 build a viral tree of life using traditional phylogenetic methods based on conserved proteins.
189 ata from 20 historical outbreaks and applied phylogenetic methods to assess genetic relatedness and t
190                    In this review we discuss phylogenetic methods used to study the emergence of drug
191                      Using several different phylogenetic methods, we analyzed viral gp120 sequences
192                                          Our phylogenetic models indicate that Dinocephalosaurus dete
193 e we quantify faunal cosmopolitanism using a phylogenetic network approach for 891 terrestrial verteb
194                Here, Button et al. develop a phylogenetic network approach to test this hypothesis an
195 itionally, fimH subtyping was evaluated on a phylogenetic network of 122 sequence type 131 (ST131) E.
196 the patient sample titre was compared to the phylogenetics of RSV, emergent clades were identified th
197 nth has shown considerable potential for the phylogenetics of this and other groups.
198                          We use whole-genome phylogenetics on 182 strains from 17 countries to provid
199 han triple the protected range of species or phylogenetic or functional units.
200 ongly supported the hypothesis that ERA is a phylogenetic orthologue of Ls, although it plays a broad
201                                              Phylogenetic placement was concordant between direct and
202 DNA barcoding, as well as the morphology and phylogenetic position of each symbiont, all three repres
203    The characteristics of its symbionts, its phylogenetic position within Teredinidae, the reduction
204                                       Such a phylogenetic position would indicate the presence of a s
205                   Consistent with its unique phylogenetic position, small RNA sequencing revealed 29
206                       Depending on its exact phylogenetic position, the meiofaunal habit of Saccorhyt
207 e also tested alternative hypotheses for the phylogenetic positions of ants and bees.
208  Longidorus and Paralongidorus and different phylogenetic possibilities for the three Xiphinema speci
209                         Overall, species and phylogenetic priorities are more similar to each other t
210 m compatibility is a useful tool for certain phylogenetic problems, such as inferring the relationshi
211 anging this paradigm, particularly given the phylogenetic range and relatively unknown characteristic
212 loid populations spanning the geographic and phylogenetic range of the Campanula rotundifolia polyplo
213                                              Phylogenetic reconstruction indicates that these two vir
214                                              Phylogenetic reconstruction of the linker set was consis
215  sequence divergence from active copies, and phylogenetic reconstruction suggests that they represent
216         Maximum compatibility is a method of phylogenetic reconstruction that is seldom applied to mo
217 ombination of tools that include large-scale phylogenetic reconstruction to determine the sequence, s
218                            We apply Bayesian phylogenetic reconstruction to infer the time point at w
219                                 We performed phylogenetic reconstruction, resurrection and biophysica
220 he choice of loci can have a major impact on phylogenetic reconstruction.
221                     Comparative analyses and phylogenetic reconstructions revealed that fungal Fzo1 a
222 nd hence, random signals of relationships in phylogenetic reconstructions.
223 more often than retrotransposons, and unveil phylogenetic relatedness and geographical proximity as m
224  measures of functional trait similarity and phylogenetic relatedness and that transcriptomics has th
225 6S-based ecological datasets, accounting for phylogenetic relatedness of the taxa.
226                            We controlled for phylogenetic relatedness, body mass and the size of the
227                                        Using phylogenetic relatedness, climatic ranges, growth form a
228 lades within human body sites increases with phylogenetic relatedness.
229 stance-abundance slope and species traits or phylogenetic relatedness.
230 single fovea, controlling for the effects of phylogenetic relatedness.
231 ome sequence analysis was used to assess the phylogenetic relationship among LA-MRSA CC398 isolates f
232  kmer ID results were explained by the close phylogenetic relationship between the two species and we
233 ns in major tetraconate taxa suggest a close phylogenetic relationship of Remipedia, Cephalocarida, a
234                   However, given their close phylogenetic relationship, geographic proximity, and tem
235                            Despite the close phylogenetic relationship, Hepatocystis parasites lack t
236 t orders of birds did not strictly depend on phylogenetic relationship.
237                                              Phylogenetic relationships among Laverania species are c
238                                              Phylogenetic relationships among major lineages of the E
239                                          The phylogenetic relationships among these variants as well
240 tes; however, their evolutionary origins and phylogenetic relationships are obscure, thus hampering c
241 between TB&S and WGS data, revealed the true phylogenetic relationships between different species of
242 nocturnality has long been inferred from the phylogenetic relationships of crown Mammalia, which is p
243 dge on the identity, function, genomics, and phylogenetic relationships of insect-bacteria symbioses
244                                 However, the phylogenetic relationships of the genes that convert Ca(
245 o more accurately identify subclones, define phylogenetic relationships, and probe genotype-phenotype
246        Based on bioinformatic properties and phylogenetic relationships, we named the new families OC
247 otential contingencies on species traits and phylogenetic relationships.
248  clans, which attested its usefulness in the phylogenetic representation of the evolutionary relation
249             Examining the system with higher phylogenetic resolution revealed a moderate contribution
250 velopmental events in organisms spanning the phylogenetic scale.
251       Considering microbiomes at appropriate phylogenetic scales allows us to model their evolution a
252 f species, that their expression has varying phylogenetic signal among lineages, and that the crown s
253 nitrogen concentration showing the strongest phylogenetic signal and specific root length showing int
254                   Finally, we detect a clear phylogenetic signal from one ochrophyte subgroup, the li
255                             We find a strong phylogenetic signal in the non-autoregressive co-varianc
256               The present study analyzes the phylogenetic signal of genomic regions with different in
257             Traits were linked but showed no phylogenetic signal, suggesting that syndromes were envi
258 und that chromosome numbers possess a strong phylogenetic signal.
259 logists have increasingly sought to quantify phylogenetic signals in environmental niche preferences
260 ne data set, including traits eliminated all phylogenetic signals in the residual variation of both a
261  their stability in biological fluids, their phylogenetic similarities, and their tissue specificity.
262 wledge about the geographic distribution and phylogenetic structure of mitochondrial lineages that ha
263 hange can help to predict future patterns in phylogenetic structure.
264                                              Phylogenetic structuring accounts for most of the variat
265  to which these controls are confounded with phylogenetic structuring remains unclear.
266                                              Phylogenetic studies have shown that ZIKV has evolved in
267                                 Furthermore, phylogenetic studies indicated that it was evolutionaril
268                                              Phylogenetic studies revealed a patchy distribution of b
269                                              Phylogenetic studies, transport assays with the recombin
270 ing nuclear data for polyploids have impeded phylogenetic study of these groups.
271                                 A multilocus phylogenetic study was carried out to assess species ide
272 mpositions differ systematically between the phylogenetic subgroups, indicating high potential for ch
273                                              Phylogenetic survey suggests that reduced dependence on
274  Namely, that they are conserved across deep phylogenetic timescales, are associated with gene/genome
275                                        Using phylogenetic 'tip-dating' analysis with fossils, we show
276                     Structural alignment and phylogenetic tree analysis indicate that StnA represents
277 cture of individual genes; (ii) genes in the phylogenetic tree can now be also grouped according to K
278  This package aims to improve the quality of phylogenetic tree construction especially in instances o
279 community-onset and HO-USA300 strains on the phylogenetic tree indicates that these strains derive fr
280                                     When the phylogenetic tree is mis-specified or non-informative, o
281                                    Our dated phylogenetic tree places Macrauchenia as sister to Peris
282                            Maximum parsimony phylogenetic tree reconciliation is an important techniq
283 greedy alignment-free distance estimator for phylogenetic tree reconstruction based on the concept of
284 s somatic mutations into clones and infers a phylogenetic tree that describes the evolutionary histor
285 etermined because the branching order in the phylogenetic tree was inconsistent with the order of iso
286 orrelation of viral loads in cherries of the phylogenetic tree, showing that both models of character
287                                   A Bayesian phylogenetic tree, together with associated dating analy
288 s only when inconsistent with most taxa in a phylogenetic tree.
289 torial constraints defined by the underlying phylogenetic tree.
290 patients were more widely distributed in the phylogenetic tree.
291 ures: (i) a new viewer was developed to show phylogenetic trees displayed along with the structure of
292                               We constructed phylogenetic trees for 794 subtype A1 and 64 subtype B s
293                                  Analyses of phylogenetic trees generated by cgMLST displayed a high
294 t was associated with more unbalanced tumour phylogenetic trees, suggesting the need of denser sampli
295 the interpretation of the relationship among phylogenetic trees.
296 approaches from ancestor-descendant pairs to phylogenetic trees.
297  relationship among a large set of competing phylogenetic trees.
298 e DNA regions to reconstruct high-confidence phylogenetic trees.
299 press disturbance (long-term) influences the phylogenetic turnover of soil microbial communities resp
300                                           In phylogenetics, we often seek to reconcile gene trees wit

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top