ライフサイエンスコーパス: crayfish

1 d activity in primary sensory neurons in the crayfish.

2 , whereas crabs lost mass in the presence of crayfish.

3 p in the opener muscle of the walking leg in crayfish.

4 eparations of neuromuscular junctions in the crayfish.

5 ponse of LG in both dominant and subordinate crayfish.

6 onse of the cell in dominant and subordinate crayfish.

7 ed the response of LG in the social dominant crayfish.

8 dominant, subordinate, and socially isolate crayfish.

9 LG neurons' responses in all three types of crayfish.

10 ersistently enhanced it in socially isolated crayfish.

11 they were fed on either dragonfly larvae or crayfish.

12 ed crayfish increased their response only to crayfish.

13 he underlying evolutionary history for these crayfish.

14 ent lineages of arthropods: grasshoppers and crayfish.

15 ystems such as the receptors in crickets and crayfish.

16 s of swimmerets on different segments of the crayfish abdomen is conducted by interneurons that origi

17 he swimmerets on neighboring segments of the crayfish abdomen make periodic power-stroke movements th

18 mmerets are limbs on several segments of the crayfish abdomen that are used for forward swimming and

19 from parasitism/commensalism to mutualism as crayfish age.

20 ion to remembering the location of the exit, crayfish also remembered the overall configuration of th

21 gous to a metalloendopeptidase isolated from crayfish, an epidermal growth-factor-like domain, and th

22 Study results show that crayfish and aqueous phase samples collected within the

23 mocytes as a source of adult-born neurons in crayfish and demonstrate that the immune system is a key

24 sing neuronal function in the invertebrates (crayfish and Drosophila).

25 recorded at neuromuscular junctions (NMJ) of crayfish and Drosophila, indicated a reduction in the nu

26 hypothesis in the cleaning symbiosis between crayfish and ectosymbiotic branchiobdellidan worms.

27 d the LG neurons in dominant and subordinate crayfish and had no effect in isolates, whereas a verteb

28 ) that showed similarity to the LGBP gene of crayfish and insects.

29 ociated with action potential propagation in crayfish and lobster nerves.

30 that drives coordinated swimmeret beating in crayfish and modulated this pattern in a dose-dependent

31 a neurogenic niche, are not self-renewing in crayfish and must be replenished.

32 ntly increased the response of LG in isolate crayfish and reversibly increased the response of the ce

33 The symbiosis between crayfish and their worms can shift from parasitism/comme

34 nts, fishes, molluscs, odonates, amphibians, crayfish and turtles alongside key features within and b

35 lar to rectifying electrical synapses in the crayfish and were eliminated in shaking-B2 mutants.

36 In eureptantian crustaceans (lobsters, crayfish, and crabs), these projection neurons also form

37 ng Daphnia magna, rainbow trout and juvenile crayfish, and is able to capture the observed size-speci

38 ni respond equally to dragonfly larvae, hard crayfish, and soft crayfish before feeding experience.

39 m near-field hydrodynamic sensilla along the crayfish antennules at their synaptic contacts with cent

40 The mechanisms of TRP action in crayfish are not known, but a plausible pathway is a TRP

41 The abdominal extensor muscles in crayfish are separated into parallel deep and superficia

42 articularly well characterized in freshwater crayfish (Arthropoda, Crustacea), although the identity

43 demonstrates the potential to use freshwater crayfish as a benthic-zone indicator of nanosilver and i

44 odels, based on the crystal structure of the crayfish astacin, showed electrostatic differences withi

45 Analysis of European crayfish (Astacus astacus) taken from L. Steinsfjorden r

46 of beluga sturgeon (Huso huso) on freshwater crayfish (Astacus leptodactylus) muscle subjected to dif

47 e reflex of socially dominant and submissive crayfish at rest and during agonistic encounters was stu

48 suggested that this shift is attributable to crayfish availability rather than an initial preference

49 In severed crayfish axons we used the exclusion of hydrophilic, flu

50 dance declined at those sites invaded by the crayfish, becoming locally extinct at one.

51 to dragonfly larvae, hard crayfish, and soft crayfish before feeding experience.

52 Crayfish burrows and molluscan body fossils, abundant be

53 ure were found in the genomes of lobster and crayfish, but not in other species of the genus Penaeus.

54 In experiments, crayfish, but not mosquitofish, became infected with B.

55 s (GFs) and motor giant neurone (MoG) in the crayfish can be blocked by depolarising postsynaptic che

56 Here, we report that adult-born neurons in crayfish can be derived from hemocytes.

57 e method when applied to the dynamics of the crayfish caudal photoreceptor (subject to stimuli repres

58 A local interneuron of a crayfish central pattern generator serves as a hub that

59 ic gland (AG) cDNA library prepared from the crayfish Cherax quadricarinatus, we have identified a no

60 stomatogastric nervous system (STNS) of the crayfish Cherax quadricarinatus.

61 citatory synapses with target neurons in the crayfish CNS.

62 ract with the insulin-like AG hormone of the crayfish (Cq-IAG).

63 m wavelength absorption (lambdamax) found in crayfishes (Decapoda: Cambaridae and Parastacidae) and t

64 pposite to that used during training trials, crayfish did not display a preference for either respons

65 Conversely, adult crayfish did not exhibit grooming responses to any worm

66 We report that dominant and subordinate crayfish differ in their behavioral orienting response t

67 We found that crayfish display such a complex ritual, when two males e

68 rgo a dietary shift from dragonfly larvae to crayfish during ontogeny.

69 Crayfish escape from threats by either giant neuron-medi

70 In laboratory experiments, young crayfish exhibited a directed grooming response to all w

71 Among crayfish, fighting between size-matched animals leads to

72 rado revealed that zoosporangia occur within crayfish gastrointestinal tracts, that B. dendrobatidis

73 s Cambarus is one of three most species rich crayfish genera in the Northern Hemisphere.

74 Studies of the crayfish genus Orconectes have shown gonopod morphology

75 independent manner, but had no effect on the crayfish glutamate junction.

76 At crayfish glutamatergic neuromuscular junctions, hyperpol

77 The invasive crayfish had a dramatic effect on ecosystem structure an

78 of this study show that ROS are involved in crayfish hematopoiesis, in which a low ROS level is requ

79 ntal Cell, Benton et al. (2014) show that in crayfish, hemolymph-derived cells enter a neurogenic nic

80 Older crayfish hosted two additional larger species.

81 f the globally widespread invasive red swamp crayfish in an African river ecosystem.

82 eeding dynamics of a population of red swamp crayfish in Lake Naivasha, Kenya, after the crash of sub

83 We injected melatonin or saline into crayfish in scotophase and monitored activity and hemoly

84 s to exogenously applied 5-HT at the NMJs of crayfish in which the animals have altered endogenous 5-

85 nfly larvae and crayfish, whereas snakes fed crayfish increased their response only to crayfish.

86 nificant similarity to homologous genes from crayfish, insects, earthworms, and sea urchins.

87 r of cells composing the neurogenic niche in crayfish is tightly correlated with total hemocyte count

88 Crayfish, krill, prawns, lobsters, and other long-tailed

89 are localized in the amacrine neurons of the crayfish lamina ganglionaris.

90 ping significantly decreased indicating that crayfish learned to escape from the maze more rapidly an

91 organ from the coxobasal joint (CBCO) of the crayfish leg.

92 that replacement of native crabs by invasive crayfish likely alters the structure and functioning of

93 Although some invertebrates, including crayfish, lobsters, and ants, display dominance postures

94 In spite of this, crayfish maintained positive growth rates in the presenc

95 proteins (HSPs) of the 70-kDa family in the crayfish medial giant axon (MGA), we analyzed axoplasmic

96 Crayfish medial giant axons (MGAs) transected in physiol

97 erfusion; (3) we examined transected GAs and crayfish medial giant axons (MGAs) with time-lapse confo

98 Following severance of crayfish medial giant axons in physiological saline, ves

99 of calpain activity inhibits the sealing of crayfish medial giant axons.

100 The lateral giant (LG) escape circuit of crayfish mediates a coordinated escape triggered by stro

101 Crayfish melatonin production occurs in the eyestalks, a

102 eld B. dendrobatidis also caused significant crayfish mortality and gill recession.

103 of IP3 as a second messenger cascade within crayfish motor neurons in response to application of 5-H

104 ion of GABA and glutamate, transmitters that crayfish motor neurons release at neuromuscular junction

105 ed the amplitude of the action potentials in crayfish motor neurons.

106 polypeptides could lower the denaturation of crayfish myosin heavy chain when compared to the control

107 rotonin receptor, 5-HT1crust, throughout the crayfish nerve cord and on abdominal superficial flexor

108 rsma established that the giant axons of the crayfish nerve cord drive tail-flip escape responses.

109 The inhibitory synapse of the crayfish neuromuscular junction was used to examine mech

110 ith the experimental properties of SF at the crayfish neuromuscular junction, and find that the satur

111 Serotonin, a neuromodulator at the crayfish neuromuscular junction, regulates neurotransmis

112 g-term modulation of synaptic release at the crayfish neuromuscular junction.

113 thin axons and terminal varicosities of the crayfish neuromuscular junction.

114 contrary to experimental observations at the crayfish neuromuscular junction.

115 asynchronous transmitter release at "phasic" crayfish neuromuscular junctions (NMJs) showing depressi

116 cilitation (LTF) of synaptic transmission at crayfish neuromuscular junctions (NMJs) that is accompan

117 r data suggested that transmitter release at crayfish neuromuscular junctions is a non-linear functio

118 acological properties of calcium currents at crayfish neuromuscular junctions resemble those found at

119 At crayfish neuromuscular junctions, basal transmission and

120 At crayfish neuromuscular junctions, cAMP increases transmi

121 At crayfish neuromuscular junctions, several inhibitors of

122 ration of post-tetanic potentiation (PTP) at crayfish neuromuscular junctions, using spectrophotometr

123 From the synaptic delay of crayfish neuromuscular synapses the time for a few Ca(2+

124 t, we examined the influence of melatonin on crayfish neurophysiology.

125 uces an increase in synaptic strength at the crayfish NMJ and an increase in activity of sensory neur

126 ide synthase (NOS)-containing neurons in the crayfish olfactory midbrain.

127 Long-term facilitation at the crayfish opener muscle is elicited by prolonged high fre

128 acid (OA) on the inhibitory junction of the crayfish opener muscle.

129 Benthic invertebrates Crayfish (Orcoescties spp.) had larger body burdens of S

130 e to study the spatial learning abilities of crayfish (Orconectes rusticus), using tactile stimuli as

131 function of ROS during hematopoiesis in the crayfish Pacifastacus leniusculus was examined.

132 pling devices (SPMDs) and collected resident crayfish (Pacifastacus leniusculus) at nine locations wi

133 limbs on different abdominal segments of the crayfish, Pacifastacus leniusculus.

134 controls limbs on abdominal segments of the crayfish, Pacifastacus leniusculus.

135 ot established, the results indicate that in crayfish photoreceptors TRP displays actions on two time

136 es in this genus are A. astaci, the cause of crayfish plague and its close relative, A. invadans, whi

137 equence, and indeed, for the majority of the crayfish population caught from the lake, we saw a conco

138 etary niche constriction within the invasive crayfish population.

139 class Malacostraca (which includes lobsters, crayfishes, prawns and shrimps) shifted toward the forma

140 evalence in crayfish was up to 29%, and that crayfish presence in Colorado wetlands was a positive pr

141 cells maintaining adult neurogenesis in the crayfish Procambarus clarkii are glial cells.

142 A phasic stimulus directed to the rear of a crayfish (Procambarus clarkii) creates mechanosensory in

143 with stimulation at 0.2 Hz in both isolated crayfish (Procambarus clarkii) neuromuscular junction (N

144 In cultured nerve cord explants from the crayfish (Procambarus clarkii), the normal impulse activ

145 hether mosquitofish (Gambusia holbrooki) and crayfish (Procambarus spp. and Orconectes virilis), whic

146 nhibitory nerve terminals that innervate the crayfish (Procambarus spp.) opener muscle.

147 The presynaptic terminals at crayfish (Procambarus spp.) opener neuromuscular junctio

148 ptantian decapod crustaceans: the freshwater crayfish, Procambarus clarkii and Orconectes rusticus, a

149 tailflip command neuron in socially dominant crayfish, reversibly inhibited it in subordinate animals

150 The crayfish's decision to escape, previously thought to lie

151 In standard crayfish saline at room temperature, the average Ca(2+)

152 ustaceans of the Class Malacostraca (such as crayfish) share a set of homologous neurons.

153 Striped crayfish snakes (Regina alleni) undergo a dietary shift

154 t use of terrestrial resources by an aquatic crayfish species and further highlight the traits that m

155 ver 60% of North America's fish, mussel, and crayfish species.

156 producing neurons are likely to exist in the crayfish STNS.

157 orrelate with the habitat differences of the crayfishes studied.

158 her highlight the traits that make red swamp crayfish such opportunistic and successful invaders.

159 The motor pattern that drives each crayfish swimmeret consists of alternating bursts of imp

160 swimming, motor neurons that innervate each crayfish swimmeret fire periodic coordinated bursts of i

161 modified version of an existing model of the crayfish swimmeret system that is based on three known c

162 The modular local circuits that control crayfish swimmerets are distributed in four segments of

163 presynaptic mechanosensory afferents in the crayfish tailfan.

164 Here we describe a pathway feature in the crayfish tailflip reflex: A position-dependent linear gr

165 morphological diagnoses based on traditional crayfish taxonomy might be confounded by convergent evol

166 ions based on morphology used in traditional crayfish taxonomy to the underlying evolutionary history

167 y enhances the differential survival of male crayfish that engage in this behavior.

168 However, we also caught individual crayfish that had occupied the footprints of hippopotamu

169 rent axons in the last abdominal ganglion of crayfish that produces nonlinear amplification of the se

170 In crayfish, the effect of serotonin on the neural circuit

171 pils in the central olfactory pathway of the crayfish: the accessory lobe and its target neuropil, th

172 ted by low molecular weight PAHs compared to crayfish tissues.

173 This coincidence detection enables crayfish to produce reflex escape responses only to very

174 the ability of the lateral giant neurons of crayfish to sum synchronous inputs, but not inputs separ

175 Young crayfish typically hosted only two relatively small worm

176 ses of the lateral giant (LG) interneuron in crayfish was found to depend on the social status of the

177 tracts, that B. dendrobatidis prevalence in crayfish was up to 29%, and that crayfish presence in Co

178 In a previous study of lobsters and crayfish we showed that whereas projection neurons inner

179 Crayfish were acclimated to 20 L aquaria filled with Hud

180 If, however, two dominant crayfish were paired and one became subordinate, the enh

181 Crayfish were significantly more active in photophase ve

182 e power for estimating PAH concentrations in crayfish, where the model explained >/=72% of the variat

183 ensory response to both dragonfly larvae and crayfish, whereas snakes fed crayfish increased their re

184 transmission to the lateral giant neurons of crayfish, which are command neurons for escape behavior.

185 In the crayfish, which has been developed as a model for nervou