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 e set of sequence and structural signatures (synapomorphies).
2 ially, a dorsal nerve cord-a robust chordate synapomorphy.
3 opment, it possesses no definitive hylobatid synapomorphies.
4 ld clades which have no opportunity to share synapomorphies.
5 th T. vaginalis gap1 and shared with it as a synapomorphy a 10- to 11-residue insertion not found in
6 describe chromatin in hornworts to establish synapomorphies across bryophytes and approach a definiti
7 sister group of pterosaurs, sharing numerous synapomorphies across the entire skeleton.
8 genetic analyses (RASA, or relative apparent synapomorphy analysis), we demonstrate that comparison o
9 , United States, with a melange of caecilian synapomorphies and general lissamphibian plesiomorphies.
10 of covariant sites, annotation of trees with synapomorphies and homoplasies, and motif detection.
11                       The taphonomic loss of synapomorphies and relatively higher preservation potent
12 st, the absence of midbrain is a urochordate synapomorphy and not a peculiarity of ascidians, perhaps
13 re in the lateral body wall is a gnathostome synapomorphy, and the redistribution of LPM was a key st
14                                         Five synapomorphies are also evident between them and monophy
15  elusive given the difficulty of recognizing synapomorphies between Cambrian forms and extant represe
16                        Several morphological synapomorphies between the galeae, which constitute the
17 ed, whereas other characters could emerge as synapomorphies for an expanded conifer group including G
18 to conduct a largescale search for molecular synapomorphies for bacterial clades.
19 two species, and 24 of these are unambiguous synapomorphies for clades identified by phylogenetic ana
20 y, the mtDNA sequence data do not reveal any synapomorphies for either G. pennsylvanicus or G. firmus
21 rrangements show some MGOs to be informative synapomorphies for some taxonomic groups providing stron
22 ibule and enabling the proposal of potential synapomorphies for various hominoid clades, our results
23  an evolutionary relic and could represent a synapomorphy for an as-yet undetermined terrestrial clad
24 icanthus has apical flaps, the only existing synapomorphy for sea anemones.
25 lian mouthparts, and providing an anatomical synapomorphy for the ecdysozoan supergroup.
26 feration of genetic sequence data, molecular synapomorphies have assumed great importance, yet there
27 r defining relationships, with rearrangement synapomorphies identified across multiple orders and at
28 s and pitfalls for identifying rearrangement synapomorphies in each group.
29  several tissues considered to be vertebrate synapomorphies, including the forebrain, cranial neural
30                                            A synapomorphy is a phylogenetic character that provides e
31                                    Ideally a synapomorphy is ubiquitous within the clade of related o
32 scaphoid is among the clearest morphological synapomorphies of African apes and hominins.
33 ures that previously have been identified as synapomorphies of Bilateria and Ctenophora, e.g., mesode
34 om another locality that display unambiguous synapomorphies of crouzeliid pliopithecoids.
35 adanius has a tubular ectotympanic but lacks synapomorphies of either group of crown Catarrhini, and
36                          Instead, they are a synapomorphy of a clade we term the circinatophytes that
37 nally, although triploid endosperm remains a synapomorphy of angiosperms, inclusive fitness analysis
38 he load-bearing dentary-squamosal joint is a synapomorphy of mammaliaforms.
39 only known in osteichthyans and considered a synapomorphy of that group.
40 noderms have a calcite-based endoskeleton, a synapomorphy of the Ambulacraria.
41 t here that this head/trunk distinction is a synapomorphy of the Bilateria as a whole, and that it re
42 e modified wedged sacrum, likely a potential synapomorphy of the clade and key in the evolutionary hi
43 ng degrees among the genera, appears to be a synapomorphy of the Rafflesiaceae.
44             If the anterior pillar is a true synapomorphy of these two species, the evidence for a so
45 ocated next to each other and are possibly a synapomorphy of these two taxa.
46 ific to the Cellia and therefore represent a synapomorphy of this subgenus.
47 rs, forming retinal pigment epithelium, is a synapomorphy of vertebrates.
48 ionary relationships because they constitute synapomorphies or cladistic characters.
49                                        These synapomorphies partition sets of aaRSs with the same spe
50 tereon, and Smilodon ( = Smilodontini) share synapomorphies relative to their sister-taxon Machairodo
51 ast five of the conserved genes appear to be synapomorphies (shared derived characters) that unite th
52 le alignments resulted in the delineation of synapomorphies-shared derived characters, such as extra
53 rly retracted nares and numerous postcranial synapomorphies that are unique compared with all other c
54                    It is therefore a hominid synapomorphy that can be used to assess the presence and
55 rphies, 12 homoplastic characters, and seven synapomorphies, the latter of which are reproductive fea
56                     A number of euryarchaeal synapomorphies (unique shared characters) were identifie
57 fate, was previously thought to be an animal synapomorphy, we demonstrate that S. rosetta produces ch