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1 ments on hair cells from the sacculus of the bullfrog.
2 s within lumbar paravertebral ganglia of the bullfrog.
3 ous to human OTOR in the mouse, chicken, and bullfrog.
4 wing oxygen and glucose deprivation in adult bullfrogs.
5 espiratory-related motor outflow in American bullfrogs.
6  amphibian papillae of either male or female bullfrogs.
7 ential firing from CO2 -sensitive neurons in bullfrogs acclimatized to semi-terrestrial (air-breathin
8 electrophysiology, we demonstrate that adult bullfrogs acclimatized to water-breathing conditions do
9 us repetition rate and stimulus intensity on bullfrog aggressive responses were tested in a field exp
10         Supporting cells in adult sharks and bullfrogs also retained thin belts, but were not tested
11 s the hair cell to afferent fiber synapse in bullfrog amphibian papilla adjust to a wide range of phy
12 onstructions and capacitance measurements of bullfrog amphibian papilla hair cells dialyzed with high
13 erence between the absorption maximum of the bullfrog and newt pigments, 44 nm.
14 d higher Bd inhibition than rare bacteria in bullfrog and newt populations, in which Bd was prevalent
15 tion loads across approximately 1,500 farmed bullfrogs and in the water that is released from farms i
16 e relative abundance of cultured bacteria on bullfrogs and newts was comprised of inhibitory bacteria
17 y impacting the invasive success of American bullfrogs and this study gives us insight on management
18 ly tested whether Bd genotypes isolated from bullfrogs are more virulent in native anuran hosts compa
19                                              Bullfrogs are tolerant to Bd, meaning that they can carr
20 ion of whole brain rem2 expression levels in bullfrogs at different stages of development revealed gr
21 , we report evidence for proton release from bullfrog auditory hair cells when they are held at more
22 on, using recordings from gerbil, mouse, and bullfrog auditory organs, we find that the spatial coupl
23                 Paired recordings from adult bullfrog auditory synapses demonstrate that CP-AMPARs me
24 represents either the presence or absence of bullfrogs based on observations.
25 hykinin-like peptides has been isolated from bullfrog brain and gut.
26 ificity of [3H]muscimol binding sites in the bullfrog brain support the hypothesis that this amphibia
27                                              Bullfrog brain thus possesses binding sites with signifi
28  secretomotor B neurons were assessed in the bullfrog by recording intracellularly from isolated prep
29 ino acid, and fatty acid profile of American Bullfrog byproducts (whole frogs (WF), legs (LF), and sk
30 sly monitored so that the cumulative dose to bullfrogs could be accurately estimated throughout the e
31 ression between neighboring territorial male bullfrogs could result from long-term, stimulus-specific
32 study analyzes data from national surveys on bullfrog distribution.
33                          Acutely dissociated bullfrog dorsal root ganglion (DRG) cells could be divid
34 Zn2+ on ATP-activated current was studied in bullfrog dorsal root ganglion (DRG) neurones using the w
35 ls collected from 13 hindlimb muscles of the bullfrog during swimming and jumping, before and after d
36 ted from the skin of four amphibian species: bullfrogs, Eastern newts, spring peepers and American to
37                                  In American bullfrogs, excitatory synapses scale up to regulate brea
38                                              Bullfrog farming and trade practices are well-establishe
39                     To test the potential of bullfrog farms as reservoirs for diverse and virulent ch
40                    Our results indicate that bullfrog farms can harbor high Bd genotypic diversity an
41 t Bd monitoring and mitigation strategies in bullfrog farms to aid in the conservation of native amph
42                      The hair bundles of the bullfrog, for example, exhibit all four attributes by op
43           We used an optical trap to deflect bullfrog hair bundles and to measure bundle movement whi
44                             Previous work on bullfrog hair cells showed an effect of phosphoinositol-
45                       The spread of American Bullfrog has a significant impact on the surrounding eco
46 th males and females was smaller relative to bullfrogs in their native range as well as in population
47                                              Bullfrogs in their natural environment were presented wi
48 itability to create an overall assessment of bullfrog invasion risk.
49 ty of the bullfrog rem2 gene showed that the bullfrog is similar to both mammals and fish in that the
50  and which differed between the newt and the bullfrog (lambda(max) = 430 nm) wild-type SWS2 pigments:
51 ragmites on Rana catesbeiana (North American bullfrog) larval performance.
52 wn tree snake Boiga irregularis and American bullfrog Lithobates catesbeianus), with 10.3 and 6.0 bil
53  four independent experiments using American bullfrogs (Lithobates catesbeianus) and green frogs Lith
54                     Tadpoles of the American bullfrog, Lithobates catesbeianus, breathe water at earl
55  the brainstem respiratory network of female bullfrogs, Lithobates catesbeianus Contrary to our expec
56 arterial tone was studied in preparations of bullfrog lumbar sympathetic ganglia 7-10 and the dorsal
57 kinetics studies with homopolymer ferritins (bullfrog M-chain, human H-chain and Escherichia coli bac
58                                 The American bullfrog, native to the eastern U.S. (Lithobates catesbe
59 ons of hair cells in the sacculi of American bullfrogs of both genders.
60  nm is fairly close to that of the wild-type bullfrog pigment.
61 mphibian populations as an invasive species, bullfrogs play a key role in spreading the frog-killing
62 olated from 15 systemically diseased African bullfrogs (Pyxicephalus edulis), and were initially iden
63 e two ferritin channels, using the wild-type bullfrog Rana catesbeiana H' protein and some of its var
64 mily, first identified in the North American bullfrog Rana catesbeiana; and the temporin family, firs
65                                     American bullfrog (Rana castesbeiana) saxiphilin (RcSxph) is a hi
66 om rho-crystallin expressed in the lenses of bullfrog (Rana catesbeiana) and European common frog (Ra
67                  Here, we show that American bullfrog (Rana catesbeiana) RcSxph and High Himalaya fro
68 onditions, free-standing hair bundles of the bullfrog (Rana catesbeiana) sacculus have exhibited spon
69 e, enzymatically dissociated hair cells from bullfrog (Rana catesbeiana) sacculus resonate at frequen
70                     Here we demonstrate that bullfrog (Rana catesbeiana) tadpoles avoid infected cons
71 uence of the rem2 gene from the brain of the bullfrog (Rana catesbeiana).
72 n the brain of an anuran amphibian, the male bullfrog (Rana catesbeiana).
73 this issue, we cloned transporter cDNAs from bullfrog (Rana catesbiana) paravertebral sympathetic gan
74  neighbors and strangers by territorial male bullfrogs (Rana catesbeiana) could result from habituati
75              The aggressive response of male bullfrogs (Rana catesbeiana) habituates with repeated br
76                       The ability of 73 male bullfrogs (Rana catesbeiana) to detect single mistuned h
77 res on the susceptibility of larval American bullfrogs (Rana catesbeiana) to echinostomes.
78 methodology for recording chorus activity in bullfrogs (Rana catesbeiana) using multiple, closely spa
79 ot ganglion (DRG) neurons in postmetamorphic bullfrogs (Rana catesbeiana) was found to occur in the a
80 n the dorsal root ganglia (DRGs) of juvenile bullfrogs (Rana catesbeiana).
81 in artificial soil media and fed to juvenile bullfrogs (Rana catesbeina).
82  membrane preparations from the brain of the bullfrog, Rana catesbeiana, was investigated in kinetic,
83 ostganglionic sympathetic stimulation in the bullfrog, Rana catesbeiana.
84 Nase A superfamily ribonuclease genes of the bullfrog, Rana catesbeiana.
85                                   As adults, bullfrogs rely on lungs for gas exchange, but spend mont
86                    Tissue specificity of the bullfrog rem2 gene showed that the bullfrog is similar t
87 amino acid sequence analysis showed that the bullfrog Rem2 protein possesses the unique 5' extension
88                                 Although the bullfrog's amphibian papilla lacks the flexible basilar
89 s synapse, we developed a preparation of the bullfrog's amphibian papilla.
90 operties of individual hair bundles from the bullfrog's ear, we found that an oscillatory bundle disp
91 s thought to mediate this adaptation; in the bullfrog's hair cell, the relevant isozyme may be the 11
92 oreceptive hair bundles of hair cells in the bullfrog's sacculus have the ability to amplify mechanic
93                      When a hair cell of the bullfrog's sacculus is maintained in vitro under native
94  glass fiber, an active hair bundle from the bullfrog's sacculus oscillates spontaneously.
95 estigated the ability of hair bundles in the bullfrog's sacculus to produce oscillations that might u
96                  When a hair bundle from the bullfrog's sacculus was abruptly deflected in the positi
97      By pulling directly on tip links of the bullfrog's sacculus we have evoked transduction currents
98 al resonance in an intact preparation of the bullfrog's sacculus, a receptor organ sensitive to low-f
99        Using dual-beam interferometry in the bullfrog's sacculus, we found that thermal movements of
100  hair bundles from the rat's cochlea and the bullfrog's sacculus, we observed that extensive recovery
101 t library directed against proteins from the bullfrog's sacculus.
102                               By screening a bullfrog saccular cDNA library, we identified abundant P
103  the type-Mb goldfish bipolar neuron and the bullfrog saccular hair cell.
104 operties of voltage-gated Ca(2+) channels in bullfrog saccular hair cells by means of perforated and
105 stinct single voltage-gated Ca2+ channels in bullfrog saccular hair cells to assess the roles of the
106 viously, confocal and electron microscopy of bullfrog saccular hair cells using an anti-myosin-Ibeta
107 cal and electrophysiological recordings from bullfrog saccular hair cells with such spontaneously osc
108      We used dissociated hair cells from the bullfrog saccule and high-speed video imaging to charact
109 tment in mitotically blocked cultures of the bullfrog saccule.
110 scillations displayed by hair bundles of the bullfrog sacculus have complex temporal profiles, not fu
111 bited by free-standing hair bundles from the Bullfrog sacculus suggest the existence of an active pro
112 mmunoprecipitation experiments, we showed in bullfrog sacculus that PMCA1b is the major isozyme of ha
113       We use a preparation from the American bullfrog sacculus which preserves the active motility of
114 ly soft gating springs, such as those of the bullfrog sacculus, the need for membrane reinforcement b
115 ing position of the hair cell bundles of the bullfrog sacculus.
116 es and found that Bd genotypes cultured from bullfrogs showed similar virulence in native toads when
117 e genome analysis of the most diverse of the bullfrog strains verified affiliation with the genus Bru
118      These species included bovine, chicken, bullfrog, striped bass, thresher shark, and Pacific hagf
119 er ovarian cells stably transfected with the bullfrog substance P receptor (bfSPR).
120 ion of nicotinic transmission was studied in bullfrog sympathetic ganglia by recording synaptic curre
121 depolarizations in the ganglionic neurons of bullfrog sympathetic ganglia.
122 ed by action potentials was tested in intact bullfrog sympathetic ganglia.
123 19 serially reconstructed nerve terminals in bullfrog sympathetic ganglia.
124 perforated-patch recordings from dissociated bullfrog sympathetic ganglion cells.
125  on Ca2+(-)induced Ca2+ release alone in the bullfrog sympathetic neuron.
126                  Currents were recorded from bullfrog sympathetic neurons using whole-cell patch-clam
127 o) on whole-cell calcium channel currents in bullfrog sympathetic neurons.
128 arval dragonfly (Anax sp.) predator on large bullfrog tadpoles (Rana catesbeiana), through nonlethal
129 through nonlethal effects on competing small bullfrog tadpoles, were large relative to indirect effec
130 we utilized the respiratory motor circuit in bullfrogs that normally remains inactive for several mon
131 ls in the low-frequency hearing organ of the bullfrog, the amphibian papilla, sinusoidally oscillates
132                 We exposed a second group of bullfrogs to equivalent doses of Au NPs by oral gavage t
133 ution of myosin Ibeta in hair bundles of the bullfrog utricle.
134                 Confocal imaging of isolated bullfrog vestibular hair cells shows that the bundle mem
135                                              Bullfrogs were more aggressive at the higher stimulus in
136 haracterized reproductive characteristics of bullfrogs with emphasis on the minimum size at which mal
137 d inner ears from dogfish sharks, zebrafish, bullfrogs, Xenopus, turtles, and the lizard, Anolis.

 
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