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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
7 olyploid occurrences in three animal clades (Amphibia, Actinopterygii, and Insecta).
8 taxonomic classes (Mammalia, Aves, Reptilia, Amphibia and Actinopterygii), of which the majority were
9  the likely ancestral condition of teleosts, amphibia and amniotes.
10     Heart regeneration is well documented in amphibia and fish and in developing mammals.
11 d lower organisms, particularly mammals, and amphibia and fish.
12 tal biology, concentrating on new studies of amphibia and Homo.
13 ibits ACh release by different mechanisms at amphibia and mammalian neuromuscular junctions, it is al
14                    WIF-1 is present in fish, amphibia and mammals, and is expressed during Xenopus an
15 general principles have emerged from work in amphibia and mammals.
16 ss, three are expressed in the hair cells of amphibia and mammals.
17 y function in response to light in teleosts, amphibia and primates.
18 te markers in natural tetraploids of Rorippa amphibia and R. sylvestris is tetrasomic, confirming the
19  with higher values observed in Actinopteri, Amphibia and Reptilia.
20          Here, we demonstrate that eggs from amphibia and teleost fish also release zinc.
21 e body appear to be highly conserved between amphibia and teleosts.
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
24                     Genetic studies in fish, amphibia, and mice have shown that deficiency of Nodal s
25 y major myelin constituents in bony fish and amphibia, and so are coexpressed with P0.
26 brates was duplicated after the emergence of amphibia, and that the resulting alphaI gene was preserv
27 ers of the hymenoptera, the lepidoptera, and amphibia) are highly mobile.
28 st defense systems of plants, insects, fish, amphibia, birds, and mammals.
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
31             In contrast to mammals, fish and amphibia functionally regenerate axons in the central ne
32                          Studies in fish and amphibia have shown that graded Bmp signalling activity
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.
35  defined in numerous other species including amphibia, insects, plants, and microbials.
36 t As content measured in roots of Persicaria amphibia (L.) Gray (87.2 mg kg(-1)) greatly exceeded the
37 ore strongly induced in the less tolerant R. amphibia than in R. sylvestris.
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