戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

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 al tests rejected both Archonta and microbat monophyly.
2 no individual nuclear gene tree supports dog monophyly.
3 erally strong phylogenetic support for their monophyly.
4 have not consistently supported deuterostome monophyly.
5 econciling molecular support for the group's monophyly.
6  under evolutionary models about features of monophyly.
7 mertea but are unable to reject deuterostome monophyly.
8 me phylogenomic studies support lophophorate monophyly,(1)(,)(2) others group bryozoans with entoproc
9  indicating a lack of mitochondrial sequence monophyly among species.
10 ugh recent studies unambiguously support bat monophyly and consensus is rapidly emerging about evolut
11               Our analyses recover bryophyte monophyly and demonstrate that the guard cell toolkit is
12 nt classes further confirms siliceous sponge monophyly and demosponge-hexactinellid spicule homology,
13                                 However, the monophyly and early emergence of the various DPANN clade
14    This finding is consistent with Chromista monophyly and implicates secondary endosymbiosis as an i
15 me molecular studies also challenge microbat monophyly and instead support an alliance between megaba
16              We found strong phylogeographic monophyly and large genetic distances between N. n. nebu
17                                 However, the monophyly and placement of DPANN within the archaeal tre
18            Our analyses robustly support the monophyly and placement within Euryarchaeota, and we ide
19 ic analyses confirm hypotheses of lemuriform monophyly and provide robust resolution of the phylogene
20 simony analyses all contradict macroglossine monophyly and provide support for an African clade that
21 ve innovations that strongly support unikont monophyly and the primary bikont/unikont bifurcation.
22 epth phylogenomic analyses to reassess DPANN monophyly and their relationships to other archaea.
23 lationships in the Acercaria, supporting its monophyly, and questioning the position of Psocodea as s
24 ence among isolates, nearly complete species monophyly, and widespread geographic distribution sugges
25                                   Aspects of monophyly are therefore central to fields that examine a
26 s as sister to all other animals, and sponge monophyly, are strongly supported under multiple analyse
27  + matK and rbcL + matK + trnH-psbA) using a monophyly-based method (GARLI).
28                                         This monophyly can be divided into four subfamilies, and each
29        Parametric bootstrapping tests reject monophyly for Arthropoda and Nemertea but are unable to
30  Coleoptera, and Diptera) but do not support monophyly for Deuterostomia, Arthropoda, or Nemertea.
31               The ATPase-based trees support monophyly for several clades (including Lophotrochozoa,
32                                              Monophyly for suborder Annulipalpia sensu stricto also i
33 u stricto also is widely acknowledged, as is monophyly for suborder Integripalpia sensu stricto.
34                                              Monophyly for Trichoptera seems well argued.
35                                              Monophyly for Yponomeutoidea was supported very strongly
36                           This assumption of monophyly has been generally validated by independent da
37 hylogenetically and structurally distinctive monophyly in Archaeplastida.
38 lineages in the Caucasus as the cause of non-monophyly in Primula.
39 se results and supports traditional microbat monophyly, inclusive of representative rhinolophoids fro
40 o acid composition-we find that deuterostome monophyly is strongly supported.
41 atic statistical analyses have shown whether monophyly is the rule across all HPV open reading frames
42 have been tacitly assumed, although microbat monophyly is uncorroborated by molecular data.
43         Resolution of the microbat paraphyly/monophyly issue is essential for reconstructing the temp
44 viruses, that are reported to share the same monophyly lineage as chloroviruses.
45                               The respective monophylies of the two suborders have been tacitly assum
46             Our results strongly support the monophyly of 11 subfamilies; however, the subfamily Puel
47 erful statistical evidence corroborating the monophyly of all known life.
48 es, the trees neither refute nor support the monophyly of Apusozoa.
49 ith the addition of these sequences indicate monophyly of Archaea, with modest bootstrap support.
50 ly as the cetacean sister group and supports monophyly of artiodactyls.
51     LSU and SSU data agree in supporting the monophyly of Bilateria, Cnidaria, Ctenophora, and Metazo
52  polyphyletic, however we fail to reject the monophyly of Cambarus with a topology test.
53 ced within the order Pleuronematida; (6) the monophyly of classes Phyllopharyngea, Karyorelictea, Arm
54 ut without true shells, and they support the monophyly of Conchifera.
55                                          The monophyly of Copepoda (including Platycopioida Fosshagen
56 analysis of conserved genes demonstrates the monophyly of crAss-like phages, a putative virus order,
57  investigated by estimating their support to monophyly of cultivars.
58 us with regard to nonmolecular characters as monophyly of Cyanocorax.
59             Together, these data support the monophyly of cyclostomes and suggest that the last commo
60                   The topologies support the monophyly of Delphacinae and its basal split into three
61 analyses have questioned the support for the monophyly of Deuterostomia, however, showing that the br
62 ees in their strong support for the separate monophyly of domains as well as the early evolution of t
63                     Our analyses support the monophyly of DPANN (Diapherotrites, Parvarchaeota, Aenig
64                                          The monophyly of each order is well established, but interre
65                                          The monophyly of Ecdysozoa, molting organisms, was not suppo
66  (elephants) and Sirenia (sea cows), and the monophyly of echolocating Chiroptera (bats).
67 s Avialae, with implications for, first, the monophyly of Enantiornithes and Sauriurae; second, the p
68 rived from these subfossils corroborates the monophyly of endemic Malagasy primates.
69 Analyses of 185 genes resulted in reciprocal monophyly of Enteropneusta and Pterobranchia, placed the
70 ents (30 taxa, 129 characters), supports the monophyly of Equus, denies the recognition of Plesippus
71 cate an age of 4.0-4.5 Ma for the origin and monophyly of Equus.
72 re well resolved with strong support for the monophyly of Evacanthinae and its four previously includ
73                                              Monophyly of exportation cases and the Bayelsa sample, a
74                                              Monophyly of exportation cases and the Bayelsa sample, a
75               This convincingly supports the monophyly of Facetotecta and its sister relationship wit
76          There is strong support overall for monophyly of families previously recognized on morpholog
77 es A and B recapitulate the species-specific monophyly of FIV marked by high levels of genetic divers
78                                              Monophyly of Glanapteryginae and Sarcoglanidinae was not
79 bfamilies reveals high levels of support for monophyly of Hominidae, tribe Hominini and subtribe Homi
80 hyletic Lethrinidae did not resolve, but the monophyly of Lethrinus is well supported.
81  gene transfer, leading some to question the monophyly of life.
82 l the remaining Lygaeoidea, and supports the monophyly of Lygaeoidea.
83 ns include four gene markers and support the monophyly of Meioglossus.
84 wo cicadomorphan superfamilies supported the monophyly of Membracoidea, and indicated that treehopper
85 lthough the phylogenetic results support the monophyly of Menneus and the single reduction of PME siz
86 ese studies have concluded that the observed monophyly of metastatic subclones favored metastasis-to-
87 pods), and provide molecular support for the monophyly of molluscs, a group long recognized by morpho
88 helming presence of diderm phyla and the non-monophyly of monoderm ones, pointing to an early origin
89 d 11 well-supported clades and supported the monophyly of most genera (except Malus, Sorbus, and Pour
90  sister to other euarthropods, and indicates monophyly of Myriapoda and Mandibulata.
91  of interfamilial relationships and supports monophyly of neotropical tapirs.
92 spider tree and all reject the long-accepted monophyly of Orbiculariae, by placing the cribellate orb
93  psbA tree shows significant support for the monophyly of peridinin- and fucoxanthin-containing dinof
94                          Our analyses reject monophyly of plant R-proteins and NLRs and suggest that
95 support for clade L and weak support for the monophyly of Pleuronectiformes.
96 lies as evolutionary characters supports the monophyly of poxviruses, asfarviruses, iridoviruses, and
97                      The results confirm the monophyly of Premna and reveal two primary clades which
98                                              Monophyly of Pycnogonida, Euchelicerata, Myriapoda, Tetr
99 p between passerines and parrots and the non-monophyly of raptorial birds in the hawk and falcon fami
100 yze 60,000 novel red algal genes to test the monophyly of red + green (RG) algae and their extent of
101 dentified 30 trees that support the expected monophyly of red and green algae/plants (i.e. the Planta
102 GS: A new phylogenetic analysis supports the monophyly of saber-toothed cats (Machairodontinae) exclu
103                   Our model robustly rejects monophyly of SAR11, classifying all but one strain as Rh
104                                              Monophyly of Staphylininae and its sister relationship t
105        Recent molecular phylogenies rejected monophyly of Staphylininae and regarded Paederinae as a
106 oversial ascaridomorph clades, including the monophyly of superfamilies and families, except for Asca
107                      Our results support the monophyly of Tetrarogidae and Synanceiidae, placing them
108                     This result supports the monophyly of the "robust" australopiths and suggests tha
109  show that endocranial form fails to support monophyly of the 'chirodipterids'.
110                                 However, the monophyly of the Acantharea and the separate monophyly o
111 ses of 13 PCGs and 68 terminals supports the monophyly of the Caridea and the family Alpheidae.
112 alysis of nucleic acid sequences support the monophyly of the cyanobacteria and actinobacteria but no
113                         Analyses support the monophyly of the Cyanobacteria, alphabetagamma-Proteobac
114   Other nif analyses resolve and support the monophyly of the cyanobacteria, proteobacteria, and acti
115      The debate centers on the placement and monophyly of the cyanobacteria, proteobacteria, and Gram
116         Extended RdRP phylogeny supports the monophyly of the five established phyla and reveals two
117  American, and African Morus, supporting the monophyly of the genus.
118                         We also examined the monophyly of the group considered as the eggplant relati
119           Systematic conclusions support the monophyly of the infraorder Pecora, the monophyly of the
120                                              Monophyly of the M, C, and O lineages is strongly suppor
121                                          The monophyly of the major subgroups of Copepoda, including
122 netic studies on mtDNA have shown reciprocal monophyly of the matrilines among seven of the nine assu
123 ar phylogeny provided strong support for the monophyly of the Mucorales, exclusive of Echinosporangiu
124  Cervinae and confirm for the first time the monophyly of the Old World Capreolinae (including the Ch
125 monophyly of the Acantharea and the separate monophyly of the Polycystinea (Spumellarida) are well su
126           Phylogenetic analysis supports the monophyly of the Ptolemaiida, including Kelba, and recov
127 logy-based phylogenetic analyses support the monophyly of the Scalidophora (Kinorhyncha, Loricifera,
128                                          The monophyly of the so-called "problematic" Gonideinae taxa
129  the monophyly of the infraorder Pecora, the monophyly of the subfamily Bovinae (containing the Bosel
130                                  To test the monophyly of the two genera, we generated molecular data
131 genetic analysis of these sequences supports monophyly of the two Hawaiian genera but, surprisingly,
132 evidence for convergence of the orb web, the monophyly of the two typical orb web taxa, the cribellat
133 e) within the Xag that strongly supports the monophyly of the Xag.
134 ow an early-branching position of Noctiluca, monophyly of thecate (plate-bearing) dinoflagellates, an
135  nucleotide and amino-acid sequence indicate monophyly of these talitrid taxa.
136 mical characters, additional support for the monophyly of this clade comes from geography and the fos
137  robustus from South Africa, questioning the monophyly of this genus.
138 e traditional morphology-based taxonomy; the monophyly of three of four major groups is rejected.
139 s of 37 spider fibroin sequences support the monophyly of TuSp1 within the spider fibroin gene family
140 ips mitochondrial sequence data supports the monophyly of two suborders, a sister-group relationship
141  some basal felids, but does not support the monophyly of various saber-toothed tribes and genera.
142 t and epidermal tissues, consistent with the monophyly of Xenacoelomorpha.
143 orphisms, we identify strong support for the monophyly of, and subsequent sympatric divergence within
144 ld eliminate shared polymorphism, leading to monophyly or exclusivity of populations, when the elapse
145 strongly indicates that the ancestor of this monophyly originated by a de novo fusion of a kinase gen
146 ior, including the maintenance of nontrivial monophyly probabilities for gene lineage samples that sp
147 cies tree topology and branch lengths on the monophyly probability.
148 random, under 3 different models of expected monophyly rates: approximately 63% of 425 surveyed morph
149                          Lastly, genome-wide monophyly supported the South China tiger as a distinct
150 e approach, we find an emerging signal of RG monophyly (supported by approximately 50% of the examine
151  or other approaches dependent on population monophyly, they provide important insights into the hist
152  Hesperiinae formed a clade, but support for monophyly was weak.
153 nal; conflicting, strong support for tineoid monophyly when synonymous signal was added back is shown
154                                          The monophyly with haptophytes is robustly recovered in the
155 f Hadrosaurinae, Edmontosaurini, and forms a monophyly with Laiyangosaurus and Kerberosaurus from the
156 omesticated crops appear to be associated by monophyly with only a single geographic locality.
157 described non-bioluminescent strains exhibit monophyly within the V. fischeri clade.

 
Page Top