ライフサイエンスコーパス: bullfrog

1 ous to human OTOR in the mouse, chicken, and bullfrog.

2 ments on hair cells from the sacculus of the bullfrog.

3 s within lumbar paravertebral ganglia of the bullfrog.

4 ential firing from CO2 -sensitive neurons in bullfrogs acclimatized to semi-terrestrial (air-breathin

5 electrophysiology, we demonstrate that adult bullfrogs acclimatized to water-breathing conditions do

6 us repetition rate and stimulus intensity on bullfrog aggressive responses were tested in a field exp

7 Supporting cells in adult sharks and bullfrogs also retained thin belts, but were not tested

8 onstructions and capacitance measurements of bullfrog amphibian papilla hair cells dialyzed with high

9 erence between the absorption maximum of the bullfrog and newt pigments, 44 nm.

10 d higher Bd inhibition than rare bacteria in bullfrog and newt populations, in which Bd was prevalent

11 e relative abundance of cultured bacteria on bullfrogs and newts was comprised of inhibitory bacteria

12 ion of whole brain rem2 expression levels in bullfrogs at different stages of development revealed gr

13 , we report evidence for proton release from bullfrog auditory hair cells when they are held at more

14 on, using recordings from gerbil, mouse, and bullfrog auditory organs, we find that the spatial coupl

15 Paired recordings from adult bullfrog auditory synapses demonstrate that CP-AMPARs me

16 hykinin-like peptides has been isolated from bullfrog brain and gut.

17 ificity of [3H]muscimol binding sites in the bullfrog brain support the hypothesis that this amphibia

18 Bullfrog brain thus possesses binding sites with signifi

19 secretomotor B neurons were assessed in the bullfrog by recording intracellularly from isolated prep

20 sly monitored so that the cumulative dose to bullfrogs could be accurately estimated throughout the e

21 ression between neighboring territorial male bullfrogs could result from long-term, stimulus-specific

22 Acutely dissociated bullfrog dorsal root ganglion (DRG) cells could be divid

23 Zn2+ on ATP-activated current was studied in bullfrog dorsal root ganglion (DRG) neurones using the w

24 ls collected from 13 hindlimb muscles of the bullfrog during swimming and jumping, before and after d

25 ted from the skin of four amphibian species: bullfrogs, Eastern newts, spring peepers and American to

26 We used an optical trap to deflect bullfrog hair bundles and to measure bundle movement whi

27 Previous work on bullfrog hair cells showed an effect of phosphoinositol-

28 Bullfrogs in their natural environment were presented wi

29 ty of the bullfrog rem2 gene showed that the bullfrog is similar to both mammals and fish in that the

30 and which differed between the newt and the bullfrog (lambda(max) = 430 nm) wild-type SWS2 pigments:

31 ragmites on Rana catesbeiana (North American bullfrog) larval performance.

32 Tadpoles of the American bullfrog, Lithobates catesbeianus, breathe water at earl

33 arterial tone was studied in preparations of bullfrog lumbar sympathetic ganglia 7-10 and the dorsal

34 kinetics studies with homopolymer ferritins (bullfrog M-chain, human H-chain and Escherichia coli bac

35 nm is fairly close to that of the wild-type bullfrog pigment.

36 olated from 15 systemically diseased African bullfrogs (Pyxicephalus edulis), and were initially iden

37 e two ferritin channels, using the wild-type bullfrog Rana catesbeiana H' protein and some of its var

38 mily, first identified in the North American bullfrog Rana catesbeiana; and the temporin family, firs

39 om rho-crystallin expressed in the lenses of bullfrog (Rana catesbeiana) and European common frog (Ra

40 onditions, free-standing hair bundles of the bullfrog (Rana catesbeiana) sacculus have exhibited spon

41 e, enzymatically dissociated hair cells from bullfrog (Rana catesbeiana) sacculus resonate at frequen

42 Here we demonstrate that bullfrog (Rana catesbeiana) tadpoles avoid infected cons

43 uence of the rem2 gene from the brain of the bullfrog (Rana catesbeiana).

44 n the brain of an anuran amphibian, the male bullfrog (Rana catesbeiana).

45 this issue, we cloned transporter cDNAs from bullfrog (Rana catesbiana) paravertebral sympathetic gan

46 neighbors and strangers by territorial male bullfrogs (Rana catesbeiana) could result from habituati

47 The aggressive response of male bullfrogs (Rana catesbeiana) habituates with repeated br

48 The ability of 73 male bullfrogs (Rana catesbeiana) to detect single mistuned h

49 methodology for recording chorus activity in bullfrogs (Rana catesbeiana) using multiple, closely spa

50 ot ganglion (DRG) neurons in postmetamorphic bullfrogs (Rana catesbeiana) was found to occur in the a

51 n the dorsal root ganglia (DRGs) of juvenile bullfrogs (Rana catesbeiana).

52 in artificial soil media and fed to juvenile bullfrogs (Rana catesbeina).

53 membrane preparations from the brain of the bullfrog, Rana catesbeiana, was investigated in kinetic,

54 ostganglionic sympathetic stimulation in the bullfrog, Rana catesbeiana.

55 Nase A superfamily ribonuclease genes of the bullfrog, Rana catesbeiana.

56 As adults, bullfrogs rely on lungs for gas exchange, but spend mont

57 Tissue specificity of the bullfrog rem2 gene showed that the bullfrog is similar t

58 amino acid sequence analysis showed that the bullfrog Rem2 protein possesses the unique 5' extension

59 Although the bullfrog's amphibian papilla lacks the flexible basilar

60 s synapse, we developed a preparation of the bullfrog's amphibian papilla.

61 operties of individual hair bundles from the bullfrog's ear, we found that an oscillatory bundle disp

62 s thought to mediate this adaptation; in the bullfrog's hair cell, the relevant isozyme may be the 11

63 oreceptive hair bundles of hair cells in the bullfrog's sacculus have the ability to amplify mechanic

64 When a hair cell of the bullfrog's sacculus is maintained in vitro under native

65 glass fiber, an active hair bundle from the bullfrog's sacculus oscillates spontaneously.

66 estigated the ability of hair bundles in the bullfrog's sacculus to produce oscillations that might u

67 When a hair bundle from the bullfrog's sacculus was abruptly deflected in the positi

68 By pulling directly on tip links of the bullfrog's sacculus we have evoked transduction currents

69 al resonance in an intact preparation of the bullfrog's sacculus, a receptor organ sensitive to low-f

70 Using dual-beam interferometry in the bullfrog's sacculus, we found that thermal movements of

71 t library directed against proteins from the bullfrog's sacculus.

72 By screening a bullfrog saccular cDNA library, we identified abundant P

73 the type-Mb goldfish bipolar neuron and the bullfrog saccular hair cell.

74 operties of voltage-gated Ca(2+) channels in bullfrog saccular hair cells by means of perforated and

75 stinct single voltage-gated Ca2+ channels in bullfrog saccular hair cells to assess the roles of the

76 viously, confocal and electron microscopy of bullfrog saccular hair cells using an anti-myosin-Ibeta

77 cal and electrophysiological recordings from bullfrog saccular hair cells with such spontaneously osc

78 We used dissociated hair cells from the bullfrog saccule and high-speed video imaging to charact

79 tment in mitotically blocked cultures of the bullfrog saccule.

80 scillations displayed by hair bundles of the bullfrog sacculus have complex temporal profiles, not fu

81 bited by free-standing hair bundles from the Bullfrog sacculus suggest the existence of an active pro

82 mmunoprecipitation experiments, we showed in bullfrog sacculus that PMCA1b is the major isozyme of ha

83 ly soft gating springs, such as those of the bullfrog sacculus, the need for membrane reinforcement b

84 ing position of the hair cell bundles of the bullfrog sacculus.

85 e genome analysis of the most diverse of the bullfrog strains verified affiliation with the genus Bru

86 These species included bovine, chicken, bullfrog, striped bass, thresher shark, and Pacific hagf

87 er ovarian cells stably transfected with the bullfrog substance P receptor (bfSPR).

88 ion of nicotinic transmission was studied in bullfrog sympathetic ganglia by recording synaptic curre

89 19 serially reconstructed nerve terminals in bullfrog sympathetic ganglia.

90 depolarizations in the ganglionic neurons of bullfrog sympathetic ganglia.

91 ed by action potentials was tested in intact bullfrog sympathetic ganglia.

92 perforated-patch recordings from dissociated bullfrog sympathetic ganglion cells.

93 on Ca2+(-)induced Ca2+ release alone in the bullfrog sympathetic neuron.

94 Currents were recorded from bullfrog sympathetic neurons using whole-cell patch-clam

95 o) on whole-cell calcium channel currents in bullfrog sympathetic neurons.

96 arval dragonfly (Anax sp.) predator on large bullfrog tadpoles (Rana catesbeiana), through nonlethal

97 through nonlethal effects on competing small bullfrog tadpoles, were large relative to indirect effec

98 we utilized the respiratory motor circuit in bullfrogs that normally remains inactive for several mon

99 ls in the low-frequency hearing organ of the bullfrog, the amphibian papilla, sinusoidally oscillates

100 We exposed a second group of bullfrogs to equivalent doses of Au NPs by oral gavage t

101 ution of myosin Ibeta in hair bundles of the bullfrog utricle.

102 Confocal imaging of isolated bullfrog vestibular hair cells shows that the bundle mem

103 Bullfrogs were more aggressive at the higher stimulus in

104 d inner ears from dogfish sharks, zebrafish, bullfrogs, Xenopus, turtles, and the lizard, Anolis.