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1 he rem2 gene from the brain of the bullfrog (Rana catesbeiana).
2 l root ganglia (DRGs) of juvenile bullfrogs (Rana catesbeiana).
3 n of an anuran amphibian, the male bullfrog (Rana catesbeiana).
4 erfamily ribonuclease genes of the bullfrog, Rana catesbeiana.
5 mperatures, olive oil, and the belly skin of Rana catesbeiana.
6 HT) to identify putative O2-sensing cells in Rana catesbeiana.
7 nic sympathetic stimulation in the bullfrog, Rana catesbeiana.
9 stallin expressed in the lenses of bullfrog (Rana catesbeiana) and European common frog (Rana tempora
10 ered transposase sequences in the bull frog (Rana catesbeiana) and in the clawed frog (Xenopus laevis
11 kinin C (RTKC), were named for their source, Rana catesbeiana, and their homology to the tachykinin p
12 st identified in the North American bullfrog Rana catesbeiana; and the temporin family, first identif
13 and strangers by territorial male bullfrogs (Rana catesbeiana) could result from habituation of the a
14 ene is concordant with that of rat and frog (Rana catesbeiana) CPSase I, which have been suggested to
16 ritin channels, using the wild-type bullfrog Rana catesbeiana H' protein and some of its variants as
17 The aggressive response of male bullfrogs (Rana catesbeiana) habituates with repeated broadcasts of
18 ) action, we used the North American species Rana catesbeiana in a cultured tadpole tailfin (C-fin) a
20 strong positive influences of Phragmites on Rana catesbeiana (North American bullfrog) larval perfor
21 free-standing hair bundles of the bullfrog (Rana catesbeiana) sacculus have exhibited spontaneous os
22 ically dissociated hair cells from bullfrog (Rana catesbeiana) sacculus resonate at frequencies well
23 While the LC50 of IBF for pre-metamorphic Rana catesbeiana tadpoles is 41.5 mg/L (95% confidence i
25 llular K+ on membrane currents of bull frog (Rana catesbeiana) taste receptor cells (TRCs) was invest
26 ax sp.) predator on large bullfrog tadpoles (Rana catesbeiana), through nonlethal effects on competin
28 for recording chorus activity in bullfrogs (Rana catesbeiana) using multiple, closely spaced acousti
29 (DRG) neurons in postmetamorphic bullfrogs (Rana catesbeiana) was found to occur in the absence of n
30 preparations from the brain of the bullfrog, Rana catesbeiana, was investigated in kinetic, saturatio
31 in vitro brainstem preparation using larval Rana catesbeiana which generates two rhythmic neural act
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