ライフサイエンスコーパス: catesbeiana

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1 an anuran amphibian, the male bullfrog (Rana catesbeiana).

2 m2 gene from the brain of the bullfrog (Rana catesbeiana).

3 t ganglia (DRGs) of juvenile bullfrogs (Rana catesbeiana).

4 ily ribonuclease genes of the bullfrog, Rana catesbeiana.

5 tures, olive oil, and the belly skin of Rana catesbeiana.

6 ympathetic stimulation in the bullfrog, Rana catesbeiana.

7 o identify putative O2-sensing cells in Rana catesbeiana.

8 transmission in the inner ear of frogs (Rana catesbeiana and Rana pipiens).

9 in expressed in the lenses of bullfrog (Rana catesbeiana) and European common frog (Rana temporaria)

10 transposase sequences in the bull frog (Rana catesbeiana) and in the clawed frog (Xenopus laevis), wh

11 C (RTKC), were named for their source, Rana catesbeiana, and their homology to the tachykinin peptid

12 entified in the North American bullfrog Rana catesbeiana; and the temporin family, first identified i

13 arly in regions where both Phragmites and R. catesbeiana are invasive.

14 trangers by territorial male bullfrogs (Rana catesbeiana) could result from habituation of the aggres

15 s concordant with that of rat and frog (Rana catesbeiana) CPSase I, which have been suggested to have

16 The ammonia-specific CPS of Rana catesbeiana (fCPS) presents an interesting anomaly in th

17 channels, using the wild-type bullfrog Rana catesbeiana H' protein and some of its variants as case

18 aggressive response of male bullfrogs (Rana catesbeiana) habituates with repeated broadcasts of acou

19 g of a recombinant RcC/EBP-1 protein (the R. catesbeiana homolog of the mammalian C/EBP alpha) to the

20 ion, we used the North American species Rana catesbeiana in a cultured tadpole tailfin (C-fin) assay

21 ave cloned the full-length fCPS gene from R. catesbeiana liver.

22 The isolated brainstem of larval Rana catesbeiana maintained in vitro generates neural bursts

23 ng positive influences of Phragmites on Rana catesbeiana (North American bullfrog) larval performance

24 14 ribonucleases from three Rana species (R. catesbeiana, R. japonica, and R. pipiens), we have const

25 -standing hair bundles of the bullfrog (Rana catesbeiana) sacculus have exhibited spontaneous oscilla

26 y dissociated hair cells from bullfrog (Rana catesbeiana) sacculus resonate at frequencies well above

27 ile the LC50 of IBF for pre-metamorphic Rana catesbeiana tadpoles is 41.5 mg/L (95% confidence interv

28 thin the liver of exposed pre-metamorphic R. catesbeiana tadpoles within 6 d.

29 Here we demonstrate that bullfrog (Rana catesbeiana) tadpoles avoid infected conspecifics becaus

30 r K+ on membrane currents of bull frog (Rana catesbeiana) taste receptor cells (TRCs) was investigate

31 .) predator on large bullfrog tadpoles (Rana catesbeiana), through nonlethal effects on competing sma

32 The ability of 73 male bullfrogs (Rana catesbeiana) to detect single mistuned harmonics in an o

33 recording chorus activity in bullfrogs (Rana catesbeiana) using multiple, closely spaced acoustic sen

34 ) neurons in postmetamorphic bullfrogs (Rana catesbeiana) was found to occur in the absence of neuron

35 rations from the brain of the bullfrog, Rana catesbeiana, was investigated in kinetic, saturation, an

36 itro brainstem preparation using larval Rana catesbeiana which generates two rhythmic neural activiti

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