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 s that were highly related, as determined by phylogenetic analyses.
2 ssessed using multilocus sequence typing and phylogenetic analyses.
3 d the isolated pathogen by morphological and phylogenetic analyses.
4 fied products were sequenced and analyzed by phylogenetic analyses.
5 ARC domain sequence can directly be used for phylogenetic analyses.
6 ransmission dynamics were investigated using phylogenetic analyses.
7  OTUs by combining local BLAST searches with phylogenetic analyses.
8 al distributions and performed comprehensive phylogenetic analyses.
9 genome sequences and conducted comprehensive phylogenetic analyses.
10 ools, as well as metagenomic and large-scale phylogenetic analyses.
11 idization assay, full-genome sequencing, and phylogenetic analyses.
12 an increase in the performance of downstream phylogenetic analyses.
13 bia to be coded for additional characters in phylogenetic analyses.
14 atterns, transposable element insertions and phylogenetic analyses.
15 tion and transmission were investigated with phylogenetic analyses.
16 ously suggested to be very young by standard phylogenetic analyses.
17 gain of an intron has only been suggested by phylogenetic analyses.
18  in simultaneously conducting behavioral and phylogenetic analyses across an entire group.
19                              Structure-based phylogenetic analyses also provide insight into the orig
20                                              Phylogenetic analyses also showed that the multiple inse
21 st in the study of using gene-order data for phylogenetic analyses and ancestral reconstruction.
22      In this study, we used a combination of phylogenetic analyses and bioinformatics to investigate
23 es long reads with sufficient depth for many phylogenetic analyses and can therefore provide insights
24 unction was modified as land plants evolved, phylogenetic analyses and cross-species complementation
25 sing studies, bulk-segregant RNA sequencing, phylogenetic analyses and functional tests to identify t
26 atures such as multiple sequence alignments, phylogenetic analyses and integration with the KEGG path
27 ch was located within Poales on the basis of phylogenetic analyses and its association with the 'sigm
28                      Comparative genomic and phylogenetic analyses and mRNA editing experiments revea
29 opod fossils, however, impedes comprehensive phylogenetic analyses and species descriptions according
30 fossil record, by the results of comparative phylogenetic analyses and through insights from evolutio
31 ial function in rice (Oryza sativa) based on phylogenetic analyses and transgenic experiments, respec
32  when combined with sequence data that allow phylogenetic analyses, and estimates of when these regio
33 mily classification, transcriptome analyses, phylogenetic analyses, and pathogenicity experiments wer
34                                     However, phylogenetic analyses, and rare emergent drug resistance
35 is study combined biochemical, molecular and phylogenetic analyses, and uncovered coordinated evoluti
36                                              Phylogenetic analyses are one useful method for assignin
37           Here, detailed Bayesian coalescent phylogenetic analyses are performed on 97 whole-genome s
38 d interactions of proteins, such comparative phylogenetic analyses are rarely performed, because they
39                             Morphology-based phylogenetic analyses are the only option for reconstruc
40 ware, in which the results of 24 single-gene phylogenetic analyses are used to generate a "primary co
41                                              Phylogenetic analyses, as well as Approximate Bayesian C
42                                              Phylogenetic analyses assigned the vap multigene family
43                                 We performed phylogenetic analyses based on five loci on 31 isolates
44 ella The remaining six isolates are shown by phylogenetic analyses based on four loci to represent tw
45                                              Phylogenetic analyses based on homologs of these two dom
46                                              Phylogenetic analyses based on models of molecular seque
47                                              Phylogenetic analyses based on morphology reconstruct Se
48                                          Our phylogenetic analyses, based on 11 novel xenacoelomorph
49                                     Detailed phylogenetic analyses, based on partial and full-length
50 bicans and C. dubliniensis, although further phylogenetic analyses better support its status as an un
51                                 We performed phylogenetic analyses, calculated viral diversity and di
52                                  Genomic and phylogenetic analyses can give insight into a patient's
53                                              Phylogenetic analyses classified the isolates in the P.
54                                              Phylogenetic analyses clearly distinguish historical iso
55                                              Phylogenetic analyses confirmed close relationships amon
56                                              Phylogenetic analyses confirmed that distinct from BioH,
57                  Unique genomic features and phylogenetic analyses confirmed that the tentatively nam
58                                              Phylogenetic analyses confirmed WSHBV as distinct from p
59                       Additionally, Bayesian phylogenetic analyses corroborate several lineage-specif
60               In-depth sequence searches and phylogenetic analyses demonstrate convergent evolution b
61                                          Our phylogenetic analyses demonstrate that these calcisponge
62                                              Phylogenetic analyses demonstrated geographic clustering
63                                              Phylogenetic analyses demonstrated that 44 of these GPCR
64                                              Phylogenetic analyses demonstrated that the virus repres
65 ontogenetic information from Limusaurus into phylogenetic analyses demonstrates surprisingly little e
66                       Population genetic and phylogenetic analyses determined that T. vaginalis popul
67                                           In phylogenetic analyses, eDNA-derived sequence tags often
68 ynechococcus isolates and correlate previous phylogenetic analyses encompassing a range of markers.
69                                     Bayesian phylogenetic analyses estimate the jump to the US at aro
70                                              Phylogenetic analyses estimated that the isolates shared
71                                              Phylogenetic analyses exposed cryptic host and symbiont
72                                              Phylogenetic analyses firmly place the palmophyllalean V
73                                              Phylogenetic analyses further identify groups (New World
74                             A combination of phylogenetic analyses, gene silencing, and biochemical a
75             Based on domain architecture and phylogenetic analyses grape homeobox genes can be classi
76                              Second, several phylogenetic analyses have identified animal-derived tri
77                                      Indeed, phylogenetic analyses have indicated their acquisition b
78                                 Furthermore, phylogenetic analyses have led to the inference that fel
79 20% sequence identity with eukaryotic actin, phylogenetic analyses have placed it much closer to euka
80                                              Phylogenetic analyses have placed the pangolins, order P
81                                       Recent phylogenetic analyses have retrieved aglaspidids within
82                        Previous whole-family phylogenetic analyses have suggested that the closest re
83 ecially given that most previous comparative phylogenetic analyses have tended to use both limited ta
84 r challenge in the early 21(st) century, and phylogenetic analyses have uncovered the dramatic effect
85  function between dicots and monocots, while phylogenetic analyses highlight distinct evolutionary pa
86 leles within multiple tumour regions enables phylogenetic analyses, identification of differentially
87                                              Phylogenetic analyses identified 32 independent incursio
88                                              Phylogenetic analyses identified a genetically related c
89                                              Phylogenetic analyses identified multiple introductions
90                                          Our phylogenetic analyses identified stabilizing selection a
91                                              Phylogenetic analyses identified transmission clusters.
92                          Genome sequence and phylogenetic analyses identify a derived point mutation
93         For example, genome-wide studies and phylogenetic analyses identify genes related in sequence
94                                              Phylogenetic analyses including symbionts of other Auche
95                                              Phylogenetic analyses indicate a highly dynamic evolutio
96                                  Extant-only phylogenetic analyses indicate freshwater ancestry, but
97                           BLAST searches and phylogenetic analyses indicate pXF-RIV5 and pXFAS01 shar
98                                          Our phylogenetic analyses indicate strong cranial support fo
99                                              Phylogenetic analyses indicate that AMF may influence ba
100                                              Phylogenetic analyses indicate that domesticated potato
101                                          Our phylogenetic analyses indicate that environmental isolat
102                                 Finally, our phylogenetic analyses indicate that premeiotic functions
103                                              Phylogenetic analyses indicate that PSFVaye is divergent
104                                       Recent phylogenetic analyses indicate that RNA virus population
105                                              Phylogenetic analyses indicate that THBs of eukaryotic S
106                                              Phylogenetic analyses indicate that the CaM-binding site
107             However, comparative genomic and phylogenetic analyses indicate that the mat chromosomes
108                                              Phylogenetic analyses indicate that they are paralogous
109                                              Phylogenetic analyses indicate that YacG is frequently a
110              In addition, genome content and phylogenetic analyses indicate that YSLV5 and YSLV7 are
111 ene and morphological analyses, genome-scale phylogenetic analyses indicate the sister taxon of land
112                                              Phylogenetic analyses indicated that all of the Japanese
113                                              Phylogenetic analyses indicated that four of these core
114 lowly than those from the United States, and phylogenetic analyses indicated that isolates from Europ
115                                              Phylogenetic analyses indicated that PnSERK1 and PnSERK2
116 hree sea lamprey UNC5 (UNC5L) receptors, and phylogenetic analyses indicated that the first two dupli
117                                              Phylogenetic analyses indicated that the sampled metasta
118                         This is in line with phylogenetic analyses indicating that JMJ24 (with the mu
119  approach to account for deep coalescence in phylogenetic analyses is the deep coalescence problem, w
120                       A surprising result of phylogenetic analyses is the relatively small proportion
121                      Such rigorous molecular phylogenetic analyses may prove a fruitful means for fur
122                                              Phylogenetic analyses of 125 regulators from the ArsR, C
123                                              Phylogenetic analyses of 16S rRNA, recA, nodA, nodC and
124 means of nucleotide sequencing and extensive phylogenetic analyses of a 400-nucleotide region of the
125                                              Phylogenetic analyses of arcC-containing loci, including
126 e 1a for location and genotype, and then did phylogenetic analyses of available North American sequen
127 cterial isolates is enabling high resolution phylogenetic analyses of bacterial populations leading t
128                                              Phylogenetic analyses of both genes recovered the majori
129                                              Phylogenetic analyses of cellulose synthase (CesA) and c
130                                              Phylogenetic analyses of Coleopteran MtD genome show clu
131        With these data in hand, we performed phylogenetic analyses of complete genome and VP1 capsid
132 rences in gene content and organization plus phylogenetic analyses of conserved core proteins that ha
133                                        While phylogenetic analyses of datasets containing 1000-5000 s
134 omparative approach combining phenotypic and phylogenetic analyses of E. coli isolates from crops and
135                                              Phylogenetic analyses of each transcription factor famil
136                                              Phylogenetic analyses of gag and env genes suggest that
137 ptome analysis of gene age distributions and phylogenetic analyses of gene duplications.
138                                              Phylogenetic analyses of isolates from 2 cases of equine
139                                              Phylogenetic analyses of L. bostrychophila individuals r
140                                              Phylogenetic analyses of local HIV-1 subtype D sequences
141                          From sequencing and phylogenetic analyses of MAVS from 21 simian primates, w
142                                          Our phylogenetic analyses of miRNAs in bryophytes, lycophyte
143 e ancestry of one of these older polyploids, phylogenetic analyses of multiple populations of the all
144                                  Genetic and phylogenetic analyses of newfound hantaviruses, detected
145                                              Phylogenetic analyses of Nrf2 sequences are used here to
146                                        Using phylogenetic analyses of nuclear genes and leaf transcri
147                                              Phylogenetic analyses of NumtS derived from two differen
148                                      Using a phylogenetic analyses of Nymphalidae and of other Lepido
149                                              Phylogenetic analyses of organelle- and nucleus-encoded
150                     Both the biochemical and phylogenetic analyses of OsONS1 suggest convergent evolu
151          We performed substantially expanded phylogenetic analyses of peritrichs that incorporated SS
152                                    Molecular phylogenetic analyses of protein markers and 18S ribosom
153 tructural and biochemical data together with phylogenetic analyses of Rb and E2F proteins support the
154                                              Phylogenetic analyses of rrs, gltA, groEL, msp2, and msp
155                                              Phylogenetic analyses of selected matrices, ranging from
156                    Whole genome sequence and phylogenetic analyses of selected strains showed close g
157                                              Phylogenetic analyses of the 11 available membracoid mit
158   The following results are supported in our phylogenetic analyses of the data: (1) the Atypoidea (i.
159                                 We performed phylogenetic analyses of the HEV sequence (partial and f
160 uantification of cell-associated HIV DNA and phylogenetic analyses of the highly variable EnvV1V3 reg
161                                              Phylogenetic analyses of the RdRps encoded in these cont
162 s retroviruses into two main groups based on phylogenetic analyses of the reverse transcriptase (RT)
163                                          Our phylogenetic analyses of the RPE65/BCMO and N1pC/P60 (LR
164                                   Subsequent phylogenetic analyses of the rrs, groEL and gltA genes r
165                                              Phylogenetic analyses of the variable beta-domain sequen
166                                 Here we used phylogenetic analyses of the vision genes involved in th
167                                              Phylogenetic analyses of these data demonstrate that mos
168                  Whole-genome sequencing and phylogenetic analyses of these geographic CpGV variants
169                                In silico and phylogenetic analyses of these protein families revealed
170                                     Based on phylogenetic analyses of these receptors, we predicted t
171                                              Phylogenetic analyses of these sequences indicated that
172                                              Phylogenetic analyses of these sequences revealed more t
173                                              Phylogenetic analyses of these sequences were performed
174                                              Phylogenetic analyses of these sequences with homologs f
175                                              Phylogenetic analyses of this family indicate that GPAT4
176                                              Phylogenetic analyses of three concatenated nucleotide d
177                                              Phylogenetic analyses of three families of arthropod apy
178                                              Phylogenetic analyses on four new bat genomes provide co
179 d microRNA (miRNA) candidates, and performed phylogenetic analyses on small RNA pathways as well as m
180           Here, combined with biological and phylogenetic analyses, our results provide new insights
181                    Consistent with data from phylogenetic analyses, our results support the existence
182                                              Phylogenetic analyses (parsimony, Bayesian, maximum like
183                                           In phylogenetic analyses, partitioning strategies involve e
184  were identified as Sapajus apella, based on phylogenetic analyses, pelage pattern and geographic pro
185                                              Phylogenetic analyses place the AcMADS1 protein in the s
186                                              Phylogenetic analyses place the enigmatic orthonectids w
187                                              Phylogenetic analyses placed the Micromonas GSIIs in a l
188                                              Phylogenetic analyses placed these sequences as distinct
189                                              Phylogenetic analyses placed this population from northe
190 easily incorporated into gene tree parsimony phylogenetic analyses, potentially producing more credib
191 te Triassic deposits despite time-calibrated phylogenetic analyses predicting an Early Triassic diver
192 rial and archaeal sequence data, large-scale phylogenetic analyses present both opportunities and cha
193                                          Our phylogenetic analyses recognize Euharamiyida as the sist
194                                              Phylogenetic analyses recovered multiple deep lineages i
195                                              Phylogenetic analyses resolve C. kroegeri as a stem-grou
196                                              Phylogenetic analyses reveal a pattern of serial introdu
197                                              Phylogenetic analyses reveal that ray-finned fish FLERVs
198                          Moreover, molecular phylogenetic analyses reveal that tetherins of the genus
199                                              Phylogenetic analyses reveal that the ISC and CIA pathwa
200                                          Our phylogenetic analyses reveal that unsuspected dental hom
201                                              Phylogenetic analyses revealed 2 dominant clades that se
202                                Gene-specific phylogenetic analyses revealed a great deal of variation
203 sis factor (TNF) superfamily, and subsequent phylogenetic analyses revealed its extraordinary diversi
204                                              Phylogenetic analyses revealed O. priapus n. sp. as a de
205                                              Phylogenetic analyses revealed several cryptic Hepatocys
206                                              Phylogenetic analyses revealed that all paramyxoviruses
207                               Structural and phylogenetic analyses revealed that although RACK1 is hi
208                                              Phylogenetic analyses revealed that an ancestral PIF-lik
209                                              Phylogenetic analyses revealed that four internal genes
210                                Comprehensive phylogenetic analyses revealed that ISE2 is a non-canoni
211                                              Phylogenetic analyses revealed that photosynthetic eukar
212                                              Phylogenetic analyses revealed that RTH6 is part of a mo
213                                              Phylogenetic analyses revealed that SbnG forms a separat
214                                     Finally, phylogenetic analyses revealed that the acquisition of a
215                                              Phylogenetic analyses revealed that the ancestral change
216                                              Phylogenetic analyses revealed that the Elaphomyces line
217                                              Phylogenetic analyses revealed that the five STs have in
218                                              Phylogenetic analyses revealed that the single-stranded
219                                    Molecular phylogenetic analyses revealed that the strains comprise
220                                 Sequence and phylogenetic analyses revealed that the U.S. rabbit HEV
221                                              Phylogenetic analyses revealed that this infectious agen
222                                              Phylogenetic analyses revealed that WMoV formed an evolu
223                               Concomitantly, phylogenetic analyses revealed the existence of two dist
224                 Sequence and structure-based phylogenetic analyses revealed two distinct groups of L1
225 rens proto-MHC was based on macrosynteny and phylogenetic analyses revealing approximately one third
226                                              Phylogenetic analyses show a close relationship with Nor
227                   Full genome sequencing and phylogenetic analyses show that IND1982/01 is a reassort
228                        Strain genotyping and phylogenetic analyses show that noroviruses often recomb
229                                          Our phylogenetic analyses show that Platyhelminthes consist
230                                          Our phylogenetic analyses show that substitution T401A occur
231                                Molecular and phylogenetic analyses show that these novel members of t
232                                 Furthermore, phylogenetic analyses show that these recent virulent is
233                                              Phylogenetic analyses show that three genera of beewolf
234                                              Phylogenetic analyses show that ves1 genes are transpose
235                                          The phylogenetic analyses show the presence of several disti
236                                              Phylogenetic analyses showed an intrahost virus variatio
237                       Genomic sequencing and phylogenetic analyses showed that both phages belong to
238                                              Phylogenetic analyses showed that major shifts of divers
239                                              Phylogenetic analyses showed that megabat bufavirus 1 cl
240                                   Multilocus phylogenetic analyses showed that MRE form a previously
241                                              Phylogenetic analyses showed that subjects treated durin
242                                              Phylogenetic analyses showed that the genome segments of
243                                              Phylogenetic analyses showed that this virus, tentativel
244                                              Phylogenetic analyses showed that WGS correlated well wi
245                                              Phylogenetic analyses showed the existence of 4 major PW
246     Activity assays, as well as sequence and phylogenetic analyses, showed that the majority of funga
247                                              Phylogenetic analyses strongly suggest that G2/M arrest/
248                                     Bayesian phylogenetic analyses strongly support ENV7 as an orthol
249                                              Phylogenetic analyses suggest it diverged from a human S
250                                              Phylogenetic analyses suggest species-specific diversifi
251                                              Phylogenetic analyses suggest that "chilihueque" was a l
252                                              Phylogenetic analyses suggest that class Ia subunits are
253                                              Phylogenetic analyses suggest that genes encoding glutam
254                         Although genomic and phylogenetic analyses suggest that genetic evolution may
255                                              Phylogenetic analyses suggest that land plant TAL genes
256                                     Bayesian phylogenetic analyses suggest that most of these attribu
257                                              Phylogenetic analyses suggest that RSL proteins evolved
258                                              Phylogenetic analyses suggest that the last common ances
259                                              Phylogenetic analyses suggest that the origin of rebound
260                                  Genetic and phylogenetic analyses suggest that the pandemic H1N1/200
261                                              Phylogenetic analyses suggest that the regulation of G56
262                        Structurally informed phylogenetic analyses suggest that the role of prolyl-hy
263                                          Our phylogenetic analyses suggest that this major retroviral
264                                              Phylogenetic analyses suggest that titin, the largest kn
265                                              Phylogenetic analyses suggested that G-LSR2 was acquired
266 ysis of available whole-genome sequences and phylogenetic analyses suggested that increased virulence
267                                        These phylogenetic analyses support a key role for infanticide
268                                              Phylogenetic analyses support co-speciation as having a
269             Our subfamily reconstruction and phylogenetic analyses support Platy-1 propagation throug
270                             Morphology-based phylogenetic analyses support the monophyly of the Scali
271 sites is likely to be far more important for phylogenetic analyses than accounting for rare shifts in
272                    This conclusion relies on phylogenetic analyses that fail to discriminate between
273                            Three independent phylogenetic analyses that incorporate new data from the
274 ne in invertebrates, together with molecular phylogenetic analyses that indicate the encoded proteins
275 cialized characteristics, and the results of phylogenetic analyses that support the hypothesis that h
276                                 According to phylogenetic analyses, these enzymes are proposed to con
277                                      We used phylogenetic analyses to classify the Ms5HTRs and to est
278 ion of molecular, genetic, bioinformatic and phylogenetic analyses to determine the role of HgGLAND18
279 he diversification of PP2A subunits, we used phylogenetic analyses to reconstruct the evolutionary hi
280                                 We performed phylogenetic analyses to reveal the evolutionary history
281                        In this study, we use phylogenetic analyses to test this idea in 739 Amazonian
282 phical range polygons and then used Bayesian phylogenetic analyses to test whether niche evolution wa
283 ide study of this family in B. distachyon by phylogenetic analyses, transactivation assays and transc
284                                              Phylogenetic analyses used maximum likelihood estimation
285                                              Phylogenetic analyses using 59 carefully selected low-co
286                                              Phylogenetic analyses using different genes of PEDV sugg
287                                              Phylogenetic analyses using SNPs as well as gene express
288                                     However, phylogenetic analyses using the Hofstenia transcriptome
289  of protein characterization, expression and phylogenetic analyses we identified a novel class of Ara
290           Through full-genome sequencing and phylogenetic analyses, we could identify the source of i
291                  Using homology modeling and phylogenetic analyses, we present evidence that SDH6 and
292                                     Based on phylogenetic analyses, we propose the linkage specificit
293                              By sequence and phylogenetic analyses, we show that it is a betaherpesvi
294 ies with ancestral state reconstructions and phylogenetic analyses, we show that mating plug transfer
295                                              Phylogenetic analyses were based on sequence data from t
296                                      WGS and phylogenetic analyses were performed on a sample of USA3
297                                              Phylogenetic analyses were performed on their genomic re
298                                              Phylogenetic analyses were performed to compare the clin
299  with particular relevance for morphological phylogenetic analyses which generally use the parsimony
300 In this study, we have used a combination of phylogenetic analyses with syntenic alignment of mammali

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