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1 common with regeneration in lepidosaurs and amphibia.
2 s by an effect on the secretory apparatus in amphibia.
3 s that there are DNA-mediated transposons in Amphibia.
4 R. sylvestris surviving much longer than R. amphibia.
5 two species, Rorippa sylvestris and Rorippa amphibia.
6 (mammalia = 11, reptilia = 4, aves = 2, and amphibia = 1), accuracy (range 0.57-0.94) is influenced
8 taxonomic classes (Mammalia, Aves, Reptilia, Amphibia and Actinopterygii), of which the majority were
13 ibits ACh release by different mechanisms at amphibia and mammalian neuromuscular junctions, it is al
18 te markers in natural tetraploids of Rorippa amphibia and R. sylvestris is tetrasomic, confirming the
22 ammals, but bursts of rapid evolution in the amphibia and the elasmobranchs, and several bursts in th
23 e of biofluorescent sexual dimorphism within Amphibia and the first documentation of the biofluoresce
26 brates was duplicated after the emergence of amphibia, and that the resulting alphaI gene was preserv
29 to a model based on embryological studies in amphibia, dorsoventral patterning is regulated by the an
30 that are found in all vertebrates (reptilia, amphibia, fish, and mammals), whereas more distantly rel
33 rtebrate representatives as well as fish and amphibia in addition to mammals, the molecular diversity
34 of the Schlafen family in Chondrichthyes and Amphibia, indicating an ancient origin of these genes.
36 t As content measured in roots of Persicaria amphibia (L.) Gray (87.2 mg kg(-1)) greatly exceeded the
38 in mammals, but AFP and ALF are not found in amphibia, which diverged from reptiles about 360 Myr ago
39 me that biofluorescence is widespread across Amphibia, with a focus on salamanders (Caudata), which a