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1 rom a part of the radiation of living birds (Aves).
2 existence across an entire vertebrate class (Aves).
3 although absent in mammals, is common in the Aves.
4 rn demand identification of traits unique to Aves.
5 kely have a long evolutionary history within Aves.
7 ebrate species (mammalia = 11, reptilia = 4, aves = 2, and amphibia = 1), accuracy (range 0.57-0.94)
9 ebrates, and understanding why extant birds (Aves) alone among dinosaurs survived the Cretaceous-Pale
11 ter, the latter of which was prevalent among Aves and relatively abundant in species with higher body
12 nvolved in odontogenesis remain inducible in Aves and suggest that loss of odontogenic Bmp4 expressio
13 ng Cretaceous lineages of crown clade birds (Aves) are exceptionally rare but are crucial to elucidat
15 or this secondary loss of tooth formation in Aves by analyzing in chick embryos the status of molecul
17 halized brains of crown birds (Neornithes or Aves) compared to their stem taxa-the non-avialan coelur
18 ntergeneric relationships of New World Jays (Aves: Corvidae), we sequenced the entire mitochondrial D
21 frequent in long bones of New Zealand's moa (Aves: Dinornithiformes), a recently extinct ratite order
26 ed that endocranial morphology varies across Aves; however, variation of those systems among closely
30 Here we show that in the mockingbird family (Aves: Mimidae), species subject to more variable and unp
31 ed and evaluated a series of class-specific (Aves), order-specific (Rodentia), and species-specific (
34 that span five taxonomic classes (Mammalia, Aves, Reptilia, Amphibia and Actinopterygii), of which t
35 nce for a fundamental dichotomy in the class Aves that may antedate the temporal occurrence of the La
37 B-allele isolates, and the relative rates of Aves-to-Mammalia transmission were not significantly dif