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1 (B. spinosus) than the northern species (B. bufo).
2 feeding movements in the marine toad (genus Bufo).
6 ansfer of trace elements in southern toads ( Bufo[Anaxyrus] terrestris) residing in two locations: (1
7 haracterization of a galectin from the toad (Bufo arenarum Hensel) ovary in its primary structure, ca
10 ansects along the 900 km hybrid zone between Bufo bufo and B. spinosus, in northern and southern Fran
11 mporaria) and Bufonidae (Anaxyrus boreas and Bufo bufo) families, which diverged more than 100 Mya an
12 substantially lower in one common amphibian (Bufo bufo) than in another with similar life history tra
14 its were investigated in two anuran species (Bufo calamita and Rana temporaria) under controlled labo
15 berian toad species (Pelobates cultripes and Bufo calamita) emerged significantly earlier than contro
16 n exception that the cardiac muscle of toad (Bufo) expresses exclusively slow skeletal muscle TnT (ss
20 th muscle cells from the stomach of the toad Bufo marinus using standard patch clamp and microfluorim
21 icrotubules, eyecup preparations of the toad Bufo marinus were treated with the microtubule depolymer
22 y reported that during the dry season, toad (Bufo marinus) NMJs display decreased sensitivity to extr
27 he extinction of the Monteverde golden toad (Bufo periglenes) appears to have coincided with an excep
29 our analysis of field data, the presence of Bufo spp. and Gastrophryne spp. were significant positiv
30 the risk of chytridiomycosis for tadpoles of Bufo terrestris and Hyla cinerea, whereas tadpoles of B.
31 on-model amphibian, the European green toad, Bufo(tes) viridis, with ddRAD- and whole genome pool-seq