ライフサイエンスコーパス: synapomorphy

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1 e set of sequence and structural signatures (synapomorphies).

2 opment, it possesses no definitive hylobatid synapomorphies.

3 ld clades which have no opportunity to share synapomorphies.

4 th T. vaginalis gap1 and shared with it as a synapomorphy a 10- to 11-residue insertion not found in

5 genetic analyses (RASA, or relative apparent synapomorphy analysis), we demonstrate that comparison o

6 , United States, with a melange of caecilian synapomorphies and general lissamphibian plesiomorphies.

7 of covariant sites, annotation of trees with synapomorphies and homoplasies, and motif detection.

8 The taphonomic loss of synapomorphies and relatively higher preservation potent

9 st, the absence of midbrain is a urochordate synapomorphy and not a peculiarity of ascidians, perhaps

10 re in the lateral body wall is a gnathostome synapomorphy, and the redistribution of LPM was a key st

11 Five synapomorphies are also evident between them and monophy

12 Several morphological synapomorphies between the galeae, which constitute the

13 ed, whereas other characters could emerge as synapomorphies for an expanded conifer group including G

14 to conduct a largescale search for molecular synapomorphies for bacterial clades.

15 y, the mtDNA sequence data do not reveal any synapomorphies for either G. pennsylvanicus or G. firmus

16 lian mouthparts, and providing an anatomical synapomorphy for the ecdysozoan supergroup.

17 feration of genetic sequence data, molecular synapomorphies have assumed great importance, yet there

18 r defining relationships, with rearrangement synapomorphies identified across multiple orders and at

19 s and pitfalls for identifying rearrangement synapomorphies in each group.

20 several tissues considered to be vertebrate synapomorphies, including the forebrain, cranial neural

21 A synapomorphy is a phylogenetic character that provides e

22 Ideally a synapomorphy is ubiquitous within the clade of related o

23 ures that previously have been identified as synapomorphies of Bilateria and Ctenophora, e.g., mesode

24 adanius has a tubular ectotympanic but lacks synapomorphies of either group of crown Catarrhini, and

25 nally, although triploid endosperm remains a synapomorphy of angiosperms, inclusive fitness analysis

26 t here that this head/trunk distinction is a synapomorphy of the Bilateria as a whole, and that it re

27 ng degrees among the genera, appears to be a synapomorphy of the Rafflesiaceae.

28 If the anterior pillar is a true synapomorphy of these two species, the evidence for a so

29 ocated next to each other and are possibly a synapomorphy of these two taxa.

30 rs, forming retinal pigment epithelium, is a synapomorphy of vertebrates.

31 ionary relationships because they constitute synapomorphies or cladistic characters.

32 These synapomorphies partition sets of aaRSs with the same spe

33 tereon, and Smilodon ( = Smilodontini) share synapomorphies relative to their sister-taxon Machairodo

34 ast five of the conserved genes appear to be synapomorphies (shared derived characters) that unite th

35 le alignments resulted in the delineation of synapomorphies-shared derived characters, such as extra

36 rly retracted nares and numerous postcranial synapomorphies that are unique compared with all other c

37 A number of euryarchaeal synapomorphies (unique shared characters) were identifie

38 fate, was previously thought to be an animal synapomorphy, we demonstrate that S. rosetta produces ch

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