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