1 arkov model and maximum likelihood molecular
phylogenetic analyses.
2 ransmission dynamics were investigated using
phylogenetic analyses.
3 atterns, transposable element insertions and
phylogenetic analyses.
4 tion and transmission were investigated with
phylogenetic analyses.
5 ously suggested to be very young by standard
phylogenetic analyses.
6 gain of an intron has only been suggested by
phylogenetic analyses.
7 ermined using the Stanford HIVdb program and
phylogenetic analyses.
8 s that were highly related, as determined by
phylogenetic analyses.
9 ssessed using multilocus sequence typing and
phylogenetic analyses.
10 d the isolated pathogen by morphological and
phylogenetic analyses.
11 fied products were sequenced and analyzed by
phylogenetic analyses.
12 ARC domain sequence can directly be used for
phylogenetic analyses.
13 OTUs by combining local BLAST searches with
phylogenetic analyses.
14 e-of-the-art maximum-likelihood and Bayesian
phylogenetic analyses.
15 hs, is roughly half the rate estimated using
phylogenetic analyses,
a difference in magnitude similar
16 ing developmental genetics with chemical and
phylogenetic analyses across a broad sample of species,
17 in simultaneously conducting behavioral and
phylogenetic analyses across an entire group.
18 Genomic and
phylogenetic analyses across ascomycetes suggest that th
19 Phylogenetic analyses across New World flycatchers (Tyra
20 Structure-based
phylogenetic analyses also provide insight into the orig
21 Phylogenetic analyses also showed that the multiple inse
22 Together, our
phylogenetic analyses and ancestral state reconstruction
23 In this study, we used a combination of
phylogenetic analyses and bioinformatics to investigate
24 es long reads with sufficient depth for many
phylogenetic analyses and can therefore provide insights
25 We combined
phylogenetic analyses and conserved domain identificatio
26 unction was modified as land plants evolved,
phylogenetic analyses and cross-species complementation
27 We conducted
phylogenetic analyses and divergence time estimation usi
28 sing studies, bulk-segregant RNA sequencing,
phylogenetic analyses and functional tests to identify t
29 Phylogenetic analyses and hypothesis testing support its
30 ch was located within Poales on the basis of
phylogenetic analyses and its association with the 'sigm
31 Using
phylogenetic analyses and mixing experiments of single-c
32 opod fossils, however, impedes comprehensive
phylogenetic analyses and species descriptions according
33 Phylogenetic analyses and their Sinemurian age indicate
34 fossil record, by the results of comparative
phylogenetic analyses and through insights from evolutio
35 Phylogenetic analyses and trait diffusion process of the
36 ial function in rice (Oryza sativa) based on
phylogenetic analyses and transgenic experiments, respec
37 when combined with sequence data that allow
phylogenetic analyses,
and estimates of when these regio
38 mily classification, transcriptome analyses,
phylogenetic analyses,
and pathogenicity experiments wer
39 However,
phylogenetic analyses,
and rare emergent drug resistance
40 is study combined biochemical, molecular and
phylogenetic analyses,
and uncovered coordinated evoluti
41 nd IE isolates could not be distinguished by
phylogenetic analyses,
and we did not succeed in identif
42 Phylogenetic analyses applying different optimality crit
43 Phylogenetic analyses assigned the vap multigene family
44 We performed
phylogenetic analyses based on five loci on 31 isolates
45 ella The remaining six isolates are shown by
phylogenetic analyses based on four loci to represent tw
46 Phylogenetic analyses based on homologs of these two dom
47 Our
phylogenetic analyses,
based on 11 novel xenacoelomorph
48 Genomic and
phylogenetic analyses can give insight into a patient's
49 Phylogenetic analyses classified the isolates in the P.
50 Phylogenetic analyses clearly distinguish historical iso
51 Multiple
phylogenetic analyses confirm the new virus to be a nove
52 Phylogenetic analyses confirmed close relationships amon
53 Phylogenetic analyses confirmed that distinct from BioH,
54 Phylogenetic analyses confirmed WSHBV as distinct from p
55 Additionally, Bayesian
phylogenetic analyses corroborate several lineage-specif
56 ent, also for the first time, the results of
phylogenetic analyses covering extinct and extant lineag
57 Our
phylogenetic analyses date the origin of the pandemic li
58 In-depth sequence searches and
phylogenetic analyses demonstrate convergent evolution b
59 Phylogenetic analyses demonstrated geographic clustering
60 Phylogenetic analyses demonstrated that 44 of these GPCR
61 Phylogenetic analyses demonstrated that the virus repres
62 ontogenetic information from Limusaurus into
phylogenetic analyses demonstrates surprisingly little e
63 nitiase and, through combined structural and
phylogenetic analyses,
engineer TTLL6 into a branch-init
64 Bayesian
phylogenetic analyses estimate the jump to the US at aro
65 Phylogenetic analyses estimated that the isolates shared
66 Phylogenetic analyses firmly place the palmophyllalean V
67 Phylogenetic analyses further identify groups (New World
68 A combination of
phylogenetic analyses,
gene silencing, and biochemical a
69 Based on domain architecture and
phylogenetic analyses grape homeobox genes can be classi
70 sequencing, the number of loci available for
phylogenetic analyses has increased by orders of magnitu
71 Indeed,
phylogenetic analyses have indicated their acquisition b
72 Furthermore,
phylogenetic analyses have led to the inference that fel
73 20% sequence identity with eukaryotic actin,
phylogenetic analyses have placed it much closer to euka
74 Phylogenetic analyses have placed the pangolins, order P
75 Recent
phylogenetic analyses have retrieved aglaspidids within
76 Comparative
phylogenetic analyses have shown that unequal sex ratios
77 ecially given that most previous comparative
phylogenetic analyses have tended to use both limited ta
78 has obscured their evolutionary origins, and
phylogenetic analyses have traditionally been hindered b
79 r challenge in the early 21(st) century, and
phylogenetic analyses have uncovered the dramatic effect
80 function between dicots and monocots, while
phylogenetic analyses highlight distinct evolutionary pa
81 leles within multiple tumour regions enables
phylogenetic analyses,
identification of differentially
82 Phylogenetic analyses identified 32 independent incursio
83 Phylogenetic analyses identified a genetically related c
84 q), in vitro (surface plasmon resonance) and
phylogenetic analyses identified an astonishing plastici
85 Phylogenetic analyses identified five geographically dis
86 Phylogenetic analyses identified groups of related melan
87 Phylogenetic analyses identified multiple introductions
88 Our
phylogenetic analyses identified stabilizing selection a
89 Phylogenetic analyses identified TcyP homologues in many
90 Phylogenetic analyses identified two polyphyletic cluste
91 Phylogenetic analyses identify eight distinct lineages g
92 For example, genome-wide studies and
phylogenetic analyses identify genes related in sequence
93 Phylogenetic analyses indicate a highly dynamic evolutio
94 Extant-only
phylogenetic analyses indicate freshwater ancestry, but
95 Combined epidemiological and
phylogenetic analyses indicate multiple independent intr
96 Our
phylogenetic analyses indicate strong cranial support fo
97 Phylogenetic analyses indicate that almost all the gene
98 Our
phylogenetic analyses indicate that cytonuclear discorda
99 Phylogenetic analyses indicate that domesticated potato
100 Our
phylogenetic analyses indicate that environmental isolat
101 Finally, our
phylogenetic analyses indicate that premeiotic functions
102 Recent
phylogenetic analyses indicate that RNA virus population
103 Phylogenetic analyses indicate that THBs of eukaryotic S
104 However, comparative genomic and
phylogenetic analyses indicate that the mat chromosomes
105 Phylogenetic analyses indicate that the tuatara lineage
106 Phylogenetic analyses indicate that they are paralogous
107 Phylogenetic analyses indicate that this motif is conser
108 Phylogenetic analyses indicate that Val76 is not monophy
109 In addition, genome content and
phylogenetic analyses indicate that YSLV5 and YSLV7 are
110 ene and morphological analyses, genome-scale
phylogenetic analyses indicate the sister taxon of land
111 Phylogenetic analyses indicated that four of these core
112 lowly than those from the United States, and
phylogenetic analyses indicated that isolates from Europ
113 Phylogenetic analyses indicated that the ancestral state
114 Phylogenetic analyses indicated that the CSLC genes are
115 Phylogenetic analyses indicated that the sampled metasta
116 This is in line with
phylogenetic analyses indicating that JMJ24 (with the mu
117 A surprising result of
phylogenetic analyses is the relatively small proportion
118 Using extensive
phylogenetic analyses,
mathematical modeling of NAD meta
119 Maximum-likelihood and Bayesian inference
phylogenetic analyses of 13 PCGs and 68 terminals suppor
120 Here, we performed
phylogenetic analyses of 164 whole BTV-8 genomes sampled
121 Phylogenetic analyses of 16S rRNA, recA, nodA, nodC and
122 Phylogenetic analyses of 17 representative angiosperm ge
123 Phylogenetic analyses of 63 mitochondrial genomes sugges
124 means of nucleotide sequencing and extensive
phylogenetic analyses of a 400-nucleotide region of the
125 We performed
phylogenetic analyses of ARF GEFs in eukaryotes, defined
126 e 1a for location and genotype, and then did
phylogenetic analyses of available North American sequen
127 Phylogenetic analyses of bilateral tumors indicated that
128 Phylogenetic analyses of cellulose synthase (CesA) and c
129 With these data in hand, we performed
phylogenetic analyses of complete genome and VP1 capsid
130 Phylogenetic analyses of extant ferredoxins support the
131 Morphological characteristics and
phylogenetic analyses of five-gene and whole-genome sequ
132 Phylogenetic analyses of G12 sequences and their geograp
133 ptome analysis of gene age distributions and
phylogenetic analyses of gene duplications.
134 otein domains across the genome, followed by
phylogenetic analyses of gene families, did not identify
135 For example, in-depth
phylogenetic analyses of hormone signaling components ar
136 We conducted
phylogenetic analyses of key K. pneumoniae multi-locus s
137 Phylogenetic analyses of L. bostrychophila individuals r
138 Our
phylogenetic analyses of miRNAs in bryophytes, lycophyte
139 y history has mainly been reconstructed from
phylogenetic analyses of morphological characters.
140 e ancestry of one of these older polyploids,
phylogenetic analyses of multiple populations of the all
141 Genetic and
phylogenetic analyses of newfound hantaviruses, detected
142 ates of chemoautotrophic carbon fixation and
phylogenetic analyses of nitrogen cycling genes and tran
143 Phylogenetic analyses of Nrf2 sequences are used here to
144 ere assigned to species based on multi-locus
phylogenetic analyses of nrITS, GAPDH and TUB2 for CASC,
145 Phylogenetic analyses of NumtS derived from two differen
146 Both the biochemical and
phylogenetic analyses of OsONS1 suggest convergent evolu
147 We performed substantially expanded
phylogenetic analyses of peritrichs that incorporated SS
148 Molecular
phylogenetic analyses of protein markers and 18S ribosom
149 tructural and biochemical data together with
phylogenetic analyses of Rb and E2F proteins support the
150 Phylogenetic analyses of rrs, gltA, groEL, msp2, and msp
151 Phylogenetic analyses of selected matrices, ranging from
152 Whole genome sequence and
phylogenetic analyses of selected strains showed close g
153 Phylogenetic analyses of sequences of the partial 18S ri
154 Phylogenetic analyses of the 11 available membracoid mit
155 We performed population genetic and
phylogenetic analyses of the CHC22-encoding CLTCL1 gene,
156 Finally,
phylogenetic analyses of the Grs proteins reveal that ma
157 We performed
phylogenetic analyses of the HEV sequence (partial and f
158 uantification of cell-associated HIV DNA and
phylogenetic analyses of the highly variable EnvV1V3 reg
159 By combining sequence similarity network and
phylogenetic analyses of the replication proteins (Rep)
160 s retroviruses into two main groups based on
phylogenetic analyses of the reverse transcriptase (RT)
161 Subsequent
phylogenetic analyses of the rrs, groEL and gltA genes r
162 Phylogenetic analyses of the variable beta-domain sequen
163 Here we used
phylogenetic analyses of the vision genes involved in th
164 In silico and
phylogenetic analyses of these protein families revealed
165 Based on
phylogenetic analyses of these receptors, we predicted t
166 Phylogenetic analyses of these sequences revealed more t
167 Phylogenetic analyses of these sequences were performed
168 ts that infect plants, and in some cases the
phylogenetic analyses of these virus families indicate t
169 Phylogenetic analyses of three concatenated nucleotide d
170 Phylogenetic analyses of traits for 259 lepidosaur speci
171 Phylogenetic analyses of viral genomes from two cases re
172 Here, we perform comparative
phylogenetic analyses on Australian rodents (Muridae: Hy
173 d microRNA (miRNA) candidates, and performed
phylogenetic analyses on small RNA pathways as well as m
174 Here, combined with biological and
phylogenetic analyses,
our results provide new insights
175 In
phylogenetic analyses,
partitioning strategies involve e
176 were identified as Sapajus apella, based on
phylogenetic analyses,
pelage pattern and geographic pro
177 Here, we propose a new paradigm:
Phylogenetic analyses performed on a local level (munici
178 Phylogenetic analyses place both species within the Psit
179 Phylogenetic analyses place the enigmatic orthonectids w
180 Phylogenetic analyses place this new taxon as a proximat
181 Our morphological comparisons and
phylogenetic analyses place this specimen confidently in
182 Molecular
phylogenetic analyses place this Stephanorhinus as a sis
183 Phylogenetic analyses placed this population from northe
184 te Triassic deposits despite time-calibrated
phylogenetic analyses predicting an Early Triassic diver
185 repositories of resistance-causing variants,
phylogenetic analyses,
quality control and standardized
186 Our
phylogenetic analyses recover Clevosaurus hadroprodon as
187 ation is shared with extant Magelonidae, and
phylogenetic analyses recover Dannychaeta within Palaeoa
188 ddressing nonindependence of characters, our
phylogenetic analyses recovered hagfish and lampreys in
189 Phylogenetic analyses recovered multiple deep lineages i
190 Our
phylogenetic analyses render Gnathifera paraphyletic wit
191 Phylogenetic analyses resolve C. kroegeri as a stem-grou
192 Phylogenetic analyses resulted in the separation of two
193 Phylogenetic analyses reveal a pattern of serial introdu
194 Phylogenetic analyses reveal Homotherium as highly diver
195 Phylogenetic analyses reveal that DAH evolved independen
196 Phylogenetic analyses reveal that ray-finned fish FLERVs
197 Phylogenetic analyses reveal that the ISC and CIA pathwa
198 Phylogenetic analyses reveal that these form-function as
199 Our
phylogenetic analyses reveal that unsuspected dental hom
200 Phylogenetic analyses reveal two sets of homologous chro
201 Phylogenetic analyses revealed 2 dominant clades that se
202 Phylogenetic analyses revealed a large diversity of alph
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 Comprehensive
phylogenetic analyses revealed that ISE2 is a non-canoni
210 Phylogenetic analyses revealed that magnoliids were sist
211 Phylogenetic analyses revealed that paralogs found in ma
212 Phylogenetic analyses revealed that photosynthetic eukar
213 Phylogenetic analyses revealed that RTH6 is part of a mo
214 Phylogenetic analyses revealed that the ancestral change
215 Previous molecular
phylogenetic analyses revealed that the black type is on
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 Phylogenetic analyses revealed that this infectious agen
221 Phylogenetic analyses revealed that two of the genomes b
222 Phylogenetic analyses revealed that while a few genes cl
223 Phylogenetic analyses revealed the cryptic introduction
224 Phylogenetic analyses revealed the presence of 8 diverge
225 Genome mining and
phylogenetic analyses revealed two Ahr-encoding genes in
226 during the aquatic-to-land transition, with
phylogenetic analyses revealing the presence of numerous
227 Phylogenetic analyses show a close relationship with Nor
228 Phylogenetic analyses show that intensive reassortment w
229 Strain genotyping and
phylogenetic analyses show that noroviruses often recomb
230 Our
phylogenetic analyses show that Platyhelminthes consist
231 However,
phylogenetic analyses show that strigolactone signalling
232 Our
phylogenetic analyses show that substitution T401A occur
233 Furthermore,
phylogenetic analyses show that these recent virulent is
234 The
phylogenetic analyses show the presence of several disti
235 Sequence and
phylogenetic analyses showed 94% to 97% nucleotide ident
236 Phylogenetic analyses showed an intrahost virus variatio
237 Phylogenetic analyses showed that major shifts of divers
238 Phylogenetic analyses showed that megabat bufavirus 1 cl
239 Multilocus
phylogenetic analyses showed that MRE form a previously
240 Phylogenetic analyses showed that other segments were mo
241 Phylogenetic analyses showed that subjects treated durin
242 Phylogenetic analyses showed that the ICEclc regulatory
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 Phylogenetic analyses strongly suggest that G2/M arrest/
247 As
phylogenetic analyses suggest a sister group relationshi
248 Phylogenetic analyses suggest it diverged from a human S
249 Phylogenetic analyses suggest location-specific evolutio
250 Our
phylogenetic analyses suggest multiple acquisitions of t
251 Phylogenetic analyses suggest species-specific diversifi
252 Phylogenetic analyses suggest that "chilihueque" was a l
253 Phylogenetic analyses suggest that divergent flavinylate
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 the last common ances
258 Phylogenetic analyses suggest that the origin of rebound
259 Phylogenetic analyses suggest that the regulation of G56
260 Our
phylogenetic analyses suggest that this major retroviral
261 Phylogenetic analyses suggest that titin, the largest kn
262 Phylogenetic analyses suggested that G-LSR2 was acquired
263 ysis of available whole-genome sequences and
phylogenetic analyses suggested that increased virulence
264 Phylogenetic analyses support a scenario of vertical inh
265 Phylogenetic analyses support co-speciation as having a
266 Our subfamily reconstruction and
phylogenetic analyses support Platy-1 propagation throug
267 Morphology-based
phylogenetic analyses support the monophyly of the Scali
268 However, new fossil discoveries and
phylogenetic analyses tend to imply a multiple-shift mod
269 Three independent
phylogenetic analyses that incorporate new data from the
270 cialized characteristics, and the results of
phylogenetic analyses that support the hypothesis that h
271 In Bayesian and parsimony-based
phylogenetic analyses,
the majority of trees place Parma
272 According to
phylogenetic analyses,
these enzymes are proposed to con
273 ion of molecular, genetic, bioinformatic and
phylogenetic analyses to determine the role of HgGLAND18
274 aterian and bilaterian Metazoa and performed
phylogenetic analyses to gain insight into the evolution
275 hodology that combines such predictions with
phylogenetic analyses to identify genetic loci (epitopes
276 he diversification of PP2A subunits, we used
phylogenetic analyses to reconstruct the evolutionary hi
277 We performed
phylogenetic analyses to reveal the evolutionary history
278 We combine comparative anatomical and
phylogenetic analyses to test whether fundamental trade-
279 phical range polygons and then used Bayesian
phylogenetic analyses to test whether niche evolution wa
280 events, population structure and comparative
phylogenetic analyses,
to examine evidence for this mode
281 ide study of this family in B. distachyon by
phylogenetic analyses,
transactivation assays and transc
282 Phylogenetic analyses used maximum likelihood estimation
283 Phylogenetic analyses using both mitochondrial and nucle
284 Comprehensive
phylogenetic analyses using parsimony, Bayesian inferenc
285 Phylogenetic analyses using SNPs as well as gene express
286 of protein characterization, expression and
phylogenetic analyses we identified a novel class of Ara
287 Through full-genome sequencing and
phylogenetic analyses,
we could identify the source of i
288 rough a series of BLAST searches, as well as
phylogenetic analyses,
we estimate that fully 15 differe
289 Using homology modeling and
phylogenetic analyses,
we present evidence that SDH6 and
290 Based on
phylogenetic analyses,
we propose the linkage specificit
291 By sequence and
phylogenetic analyses,
we show that it is a betaherpesvi
292 ies with ancestral state reconstructions and
phylogenetic analyses,
we show that mating plug transfer
293 Using genomic and
phylogenetic analyses,
we show that plasmids are widespr
294 WGS and
phylogenetic analyses were performed on a sample of USA3
295 Phylogenetic analyses were performed to compare the clin
296 Comprehensive sequence and
phylogenetic analyses were performed to evaluate viral p
297 Phylogenetic analyses were performed to study linkages b
298 Phylogenetic analyses with PdPV-1 RdRp and CP sequences
299 In this study, we have used a combination of
phylogenetic analyses with syntenic alignment of mammali
300 Comparative genomics and
phylogenetic analyses within the Malassezia genus reveal