ライフサイエンスコーパス: goldfish

1 important resource for selective breeding of goldfish.

2 ell triggers an escape response (C-start) in goldfish.

3 raction with telencephalic NMDA receptors in goldfish.

4 ng bipolar cells isolated from the retina of goldfish.

5 inhibitor 7-NI in avoidance conditioning in goldfish.

6 hey might regulate development and growth in goldfish.

7 en in explanted retinal tissue taken from PC goldfish.

8 take and elimination rates of Hg and PCBs in goldfish.

9 nal cord tracts occur spontaneously in adult goldfish.

10 feration of retinal progenitors in the adult goldfish.

11 ied to track the 3D position of a live comet goldfish.

12 g bipolar cells isolated from the retinae of goldfish.

13 in, has been identified and characterized in goldfish.

14 reticular and motor basal hindbrain of adult goldfish.

15 nd koi and cyprinid herpesvirus 2 (CyHV2) in goldfish.

16 uce strong estrogen-like effects in the male goldfish.

17 issociated horizontal cells from catfish and goldfish.

18 ut not learning of avoidance conditioning in goldfish.

19 y simple and inexpensive MPTP model of PD in goldfish.

20 imulated uptake of Co++ in the vagal lobe of goldfish.

21 e that Hg has a bioaccumulation potential in goldfish 118% higher than the highest PCB BMF observed f

22 ted innervation patterns in the heart of the goldfish, a species representative of a large group of c

23 terlamellar cell mass (ILCM) on the gills of goldfish acclimated to 7 degrees C leads to preferential

24 sly that a 1.696 kb upstream fragment of the goldfish alpha1-tubulin promoter was capable of driving

25 vision in a wide range of mammalian species, goldfish, American chameleon (Anolis carolinensis), and

26 The ligand tuning properties of the goldfish amino acid odorant receptor provide information

27 re absent from mammalian injured CNS; but in goldfish and lamprey CNS, expression of several nIFs inc

28 nd clathrin, were examined in the retinas of goldfish and mouse by using immunocytochemical methods.

29 sive S-nitrosylation that takes place in the goldfish and mouse retinas under physiologically relevan

30 highly restricted to the retina in the adult goldfish and overlaps with Vsx-1 expression in the matur

31 In both goldfish and rat retinal ganglion cells, 6-TG completely

32 ted in chicken eggs and tested in retinae of goldfish and rat, and rat caudate putamen, by using immu

33 effects on social approach responses in male goldfish and that endogenous VT, at least, is associated

34 Suspension-feeding fishes such as goldfish and whale sharks retain prey without clogging t

35 ped body bend has been described in depth in goldfish and zebrafish [1, 2] and is thought to occur in

36 "C family" of G-protein-coupled receptors in goldfish and zebrafish.

37 d to ultraviolet cone photoreceptors in both goldfish and zebrafish.

38 retinas of rhesus monkey, mouse, rat, chick, goldfish, and tiger salamander by using a subtype-specif

39 aquatic species, such as Xenopus tropicalis, goldfish, and zebrafish, and in Arabidopsis and chickpea

40 hat the IR is expressed in the retina of the goldfish, and, on the basis of the cellular pattern of e

41 The olfactory organ of goldfish appears as a rosette, with the sensory epitheli

42 Goldfish are injected intraperitoneally with doses betwe

43 or black carp, grass carp, and a common carp/goldfish are reported and details of the marker testing

44 we have imaged optic fibers in living adult goldfish at 2-4 weeks of regeneration.

45 in mammal, the MCH and hypocretin systems in goldfish barely innervate these aminergic populations re

46 y have been identified, and their effects on goldfish behavior have been studied in depth.

47 action potentials (APs) but the Mb1 class of goldfish bipolar cell exhibits Ca(2+)-dependent APs and

48 Here, we report that glutamate release from goldfish bipolar cell terminals activates first AMPA rec

49 brane capacitance measurements from isolated goldfish bipolar cell terminals, we found that the kinet

50 r different sodium channel alpha subunits in goldfish bipolar cells, putatively corresponding to the

51 ry sites and synaptic ribbons in the type-Mb goldfish bipolar neuron and the bullfrog saccular hair c

52 In goldfish, both hypocretin and MCH immunoreactive cell bo

53 scending axonal projection patterns in adult goldfish brain nuclei.

54 eatly abbreviated blood-brain barrier of the goldfish brain, make it an attractive system for study o

55 than calpain activity in control and severed goldfish brain, spinal cord, muscle, or M-axons.

56 ediated electrical transmission is common in goldfish brain.

57 lpha) induced a multitude of changes in male goldfish brain.

58 ned during fixation behavior from neurons in goldfish brainstem area I, a key element of the integrat

59 rm wash vapor, fish water vapor, earthworms, goldfish) but not water vapor.

60 n C-start behavior compared with that of the goldfish, but the correlations in morphology, physiology

61 F-I binding sites in the retina of the adult goldfish by performing receptor-binding autoradiography

62 velopment of new rods and cones in the adult goldfish by using a combination of bromodeoxyuridine imm

63 rmined in the retina and ON bipolar cells of goldfish by using double-label light and electron micros

64 al structure in the crista ampullaris of the goldfish Carassius auratus.

65 different sized zebrafish (Danio rerio) and goldfish (Carassius auratus) and find that, as both spec

66 as a possible addition to AEP techniques in goldfish (Carassius auratus) and poikilothermic vertebra

67 onian syndrome can be elicited in the common goldfish (Carassius auratus) by a single dose of MPTP.

68 Studies with goldfish (Carassius auratus) have suggested that N-methy

69 0, a G-protein-coupled estrogen receptor, in goldfish (Carassius auratus) neural tissue and used reve

70 ntly, toxicant-induced nephron neogenesis in goldfish (Carassius auratus) parallels nephron developme

71 Goldfish (Carassius auratus) use reproductive hormones a

72 A high-density linkage map of goldfish (Carassius auratus) was constructed using RNA-s

73 Goldfish (Carassius auratus) were conditioned to suppres

74 he silver perch is comparable to that in the goldfish (Carassius auratus), a hearing "specialist." Th

75 sed peptides on social approach behaviors in goldfish (Carassius auratus), a social teleost.

76 bution of these peptides in the brain of the goldfish (Carassius auratus), focusing on those regions

77 e also regenerated the "true" red pigment of goldfish (Carassius auratus), which has a lambdamax valu

78 reen, blue, and ultraviolet cone opsins from goldfish (Carassius auratus).

79 olitrix), common carp (Cyprinus carpio), and goldfish (Carassius auratus).

80 vestigate the primary gustatory afferents in goldfish (Carassius auratus).

81 Studies on the Mauthner cell (M-cell) of goldfish, Carassius auratus, have facilitated our unders

82 nnervate taste buds of the oropharynx of the goldfish, Carassius auratus, project to the vagal lobe,

83 The Mauthner (M-) cell of the goldfish, Carassius auratus, triggers the rapid escape r

84 he area dorsalis of the telencephalon of the goldfish, Carassius auratus.

85 ogenesis using Mycobacterium marinum and the goldfish, Carassius auratus.

86 "periaxoplasmic plaques," were described in goldfish CNS myelinated axons.

87 The ultrastructural similarities of the goldfish crista afferents to calyx afferents found in am

88 against the 18 C-terminal amino acids of the goldfish D1 receptor (gfD1r) was generated in chicken eg

89 activity are produced in the retina of adult goldfish during activity-dependent refinement by regener

90 ns in an oculomotor neural integrator of the goldfish during spontaneous saccades and fixations.

91 tes that these proteins directly interact at goldfish electrical synapses.

92 e their expression patterns in zebrafish and goldfish embryos.

93 To address this question, we analyzed goldfish escapes in response to distinct visual looming

94 r to those reported for the commonly studied goldfish, except that DC is larger and better differenti

95 VTG protein was increased in the plasma from goldfish exposed to EE2, FLX, and FLX plus EE2.

96 ed by extracellular recordings in the intact goldfish eye.

97 is first genetic map enables us to study the goldfish genome evolution and provides an important reso

98 The study also showed that goldfish genome had one more round of whole genome dupli

99 igh sequence homology to the recently cloned goldfish GluR2a receptor, was used for light- and electr

100 The retina of the adult goldfish grows throughout the life of the animal, in par

101 tinal progenitors in the retina of the adult goldfish have yet to be identified.

102 ish of the genus Carassius (crucian carp and goldfish) have evolved a specialized metabolic system th

103 We have shown that the goldfish heart possesses the necessary neuroanatomical s

104 containing Cx35 at mixed synapses across the goldfish hindbrain.

105 ponses were observed in a high percentage of goldfish horizontal cells.

106 Normoxic 7 degrees C goldfish (ILCM present) possessed significantly greater

107 lian and nonmammalian vertebrates, including goldfish, in which it rapidly stimulates approach respon

108 s within the primary gustatory nuclei of the goldfish, including the vagal lobe, which is a large, la

109 Depletion of retinal dopamine in goldfish increases light sensitivity at photopic backgro

110 data suggest that in the retina of the adult goldfish, insulin-related peptides regulate proliferatio

111 from neurons in a "neural integrator" of the goldfish involved in maintaining eye position.

112 These clones were designated goldfish IR-1 (gfIR-1) and goldfish IR-2 (gfIR-2).

113 s were designated goldfish IR-1 (gfIR-1) and goldfish IR-2 (gfIR-2).

114 the pufferfish, Fugu rubrides, identified a goldfish ISG15 (gfISG15) homologue with an IFN-stimulate

115 In this study, two previously cloned goldfish kainate receptor subunits (GFKAR alpha and GFKA

116 ate receptor subtype, a low molecular weight goldfish kainate-binding protein, GFKARbeta.

117 extend 90 microm in 10 s, but an epithelial goldfish keratocyte can only glide a few microns in the

118 Forces generated by goldfish keratocytes and Swiss 3T3 fibroblasts have been

119 fast enough to support the observed speed of goldfish keratocytes, but previous models have indicated

120 y analysis of control and gentamicin-treated goldfish kidney.

121 The goldfish M-cell initial segment/axon hillock is surround

122 Regenerating optic fibers in goldfish make large-scale errors when they invade tectum

123 Our results illustrated that most goldfish markers were orthologous to genes in common car

124 ied at the axo-axonic connection between the goldfish Mauthner axon and identified cranial relay inte

125 e examined in the distal segments of severed goldfish Mauthner axons (M-axons), which do not degenera

126 nsmission between auditory afferents and the goldfish Mauthner cell is mediated by coexisting gap jun

127 ed (electrical and chemical) synapses on the goldfish Mauthner cell, we show here that gap junction h

128 rical and chemical) synaptic contacts on the goldfish Mauthner cell.

129 ical synapses between auditory afferents and goldfish Mauthner cells are constructed by apposition of

130 nating as "large myelinated club endings" on goldfish Mauthner cells are identifiable "mixed" (electr

131 mixed" (electrical and chemical) contacts on goldfish Mauthner cells, a model synapse for the study o

132 istal portion of the lateral dendrite of the goldfish Mauthner cells, a pair of large reticulospinal

133 Here we analyzed axonal RNA transport in goldfish Mauthner neurons in vivo.

134 or neuronal progenitors in the retina of the goldfish may contain hybrid IGF-1/insulin receptors.

135 Using patch-clamp recordings from axotomized goldfish Mb bipolar cell (BC) terminals with paired-puls

136 Here we report that glutamate release from goldfish Mb-type bipolar cell terminals can trigger fast

137 another retinal ribbon synapse, that of the goldfish Mb1 bipolar cell, less is known about endocytos

138 stem, responses by second-order cells in the goldfish medulla are mediated by N-methyl-D-aspartate (N

139 The accessibility of the goldfish nervous system, neural density, the evolutionar

140 e show here that, in the adult retina of the goldfish, neuroD is expressed by putative amacrine cells

141 We showed previously that, in goldfish, neuroD is expressed in the rod photoreceptor l

142 attempt to identify in the normal retina of goldfish neuronal progenitors intrinsic to the retina, p

143 In a companion paper, we reported that the goldfish oculomotor neural integrator could be trained t

144 in a model system for persistent firing, the goldfish oculomotor neural integrator.

145 tested predictions of this hypothesis in the goldfish oculomotor velocity-to-position integrator by m

146 an expression cloning strategy to identify a goldfish odorant receptor that is activated by amino aci

147 We have cloned goldfish olfactory epithelium cDNAs belonging to two mul

148 The goldfish opsins include rod opsin and four different con

149 on visual recovery following axotomy of the goldfish optic nerve were investigated.

150 bers were less reliably affected compared to goldfish or adult mouse, suggesting a developmentally re

151 ateral (Dl) and medial (Dm) divisions of the goldfish pallium.

152 in detail how individual, axially orientated goldfish photoreceptors absorb linearly polarized light.

153 s between escape and swimming in a paralyzed goldfish preparation in which we can activate the networ

154 n Vibrio fischeri and the toxicity effect on goldfish primary kidney macrophages (PKMs) were both red

155 However, the OSPW toxicity toward goldfish primary kidney macrophages after solar/chlorine

156 The Mauthner cell of goldfish receives auditory and visual information via tw

157 ybridization showed that the two families of goldfish receptors are differentially expressed in the o

158 er the experimental conditions used, control goldfish recovered vision, measured behaviorally, within

159 phosphodiesterases (CNPases), hence the name goldfish regeneration-induced CNPase homolog (gRICH).

160 Goldfish reproduction is coordinated by pheromones that

161 h nerve (NVIII) EPSP recorded in vivo in the goldfish reticulospinal neuron, the Mauthner cell, can b

162 erminals: bipolar cell synaptic terminals in goldfish retina and the calyx of Held in rat auditory br

163 cer labeling and electrical recording in the goldfish retina and tracer labeling in the mouse retina,

164 ental retina support the hypothesis that new goldfish retina arises via two spatially and cellularly

165 zation of sodium channel immunoreactivity in goldfish retina confirmed the expression of voltage-gate

166 The goldfish retina displays a characteristic arrangement of

167 proteins that are selectively induced in the goldfish retina during optic nerve regeneration.

168 The onset of opsin expression in goldfish retina follows a highly ordered spatio-temporal

169 eases output of Mb-type bipolar cells in the goldfish retina in response to weak inputs but leaves th

170 x gene, Vsx-1, whose expression in the adult goldfish retina is restricted to the inner nuclear layer

171 has demonstrated that photoreceptors in the goldfish retina regenerate selectively after laser ablat

172 ion by intraocular injection of ouabain, the goldfish retina regenerates, but little is known about t

173 Immunoblot analysis of goldfish retina revealed a single band at about 101 kDa.

174 measure the extracellular pH of the in vitro goldfish retina superfused with a bicarbonate-based Ring

175 m of temporal filtering in the zebrafish and goldfish retina that is not dynamic but is in fact a str

176 is, we exposed isolated bipolar neurons from goldfish retina to cationized ferritin.

177 trastructure of the giant bipolar synapse in goldfish retina to the jump in capacitance that accompan

178 otoreceptor differentiation in the embryonic goldfish retina to understand how the retinal cone mosai

179 micrometer diameter) of bipolar neurons from goldfish retina were used to directly investigate calciu

180 ccurs in bipolar cell terminals in slices of goldfish retina, and we investigate the effect that this

181 In goldfish retina, gfD1r-IR was most intense over cell bod

182 he extent of biocytin tracer coupling in the goldfish retina.

183 ifferent dopamine systems are present in the goldfish retina.

184 calized to dendrites of OFF bipolar cells in goldfish retina.

185 observed in a subset of bipolar neurons from goldfish retina.

186 minal of depolarizing bipolar cells from the goldfish retina.

187 s of large, alpha-like ganglion cells in the goldfish retina.

188 red class homeobox gene, Vsx-2, in the adult goldfish retina.

189 at endogenous dopamine release from isolated goldfish retinae cultured in continuous darkness for 56

190 ions in a ribbon-type synaptic terminal, the goldfish retinal bipolar cell.

191 recordings from the large axon terminals of goldfish retinal bipolar cells (BCs) have revealed detai

192 ts, the ribbon-type presynaptic terminals of goldfish retinal bipolar cells were coaxed to release a

193 At the axon terminal of goldfish retinal bipolar cells, GABA(C) receptors have b

194 uanosine in the low micromolar range induced goldfish retinal ganglion cells to extend lengthy neurit

195 In normal and experimental models of goldfish retinal growth, the patterns of tyrosine hydrox

196 es that were cloned originally from an adult goldfish retinal library.

197 eptor currents directly from BC terminals in goldfish retinal slices, I show that spontaneous GABA re

198 minals of ON-type mixed rod/cone BCs (Mb) in goldfish retinal slices.

199 neurons in the ganglion cell layer (GCL) in goldfish retinal slices.

200 bipolar cell terminals and amacrine cells in goldfish retinal slices.

201 nt APs in isolated bipolar-cell terminals in goldfish retinal slices.

202 r any other cone type, in both zebrafish and goldfish retinas, and the pattern of expression was iden

203 sicle cycling in bipolar cells isolated from goldfish retinas.

204 the CNPase activity detected in regenerating goldfish retinas.

205 the underlying program of gene expression in goldfish RGCs are mediated via a common, purine-sensitiv

206 In culture, goldfish RGCs regenerate their axons in response to two

207 Goldfish RGCs showed far less selectivity, responding st

208 Using cultured goldfish RGCs, RNA sequencing and de novo transcriptome

209 We show here that in goldfish RGCs, the effects of several trophic factors co

210 n of expression was identical to that of the goldfish rod opsin probe.

211 opsin, goldfish ultraviolet cone opsin, and goldfish rod opsin.

212 d characterize partial cDNAs that encode the goldfish's insulin receptor (IR) and to establish the ce

213 The goldfish sacculus gives rise to the vast majority of inp

214 he general distribution of these peptides in goldfish shows many similarities to those described prev

215 sis of the M-region of myosin filaments from goldfish skeletal muscle under relaxing conditions and a

216 studied the Mauthner cells (M-cells) in the goldfish startle circuit, which receive visual and audit

217 function of the serotonin 5-HT5A receptor in goldfish startle plasticity and sensorimotor gating.

218 -dependent refinement of optic fibers in the goldfish tectum.

219 Furthermore, microinjections of D-AP5 to the goldfish telencephalon immediately following training di

220 ino-5-phosphonopentanoic acid (D-AP5) to the goldfish telencephalon on avoidance conditioning.

221 o assays for androgenic activity (binding to goldfish testis androgen receptors), estrogenic activity

222 issue was addressed by using optic fibers of goldfish that have the capacity to regenerate a retinoto

223 In goldfish, the primary gustatory nucleus (equivalent to t

224 scribes the lineage of rod photoreceptors in goldfish; the second is a consensus model of neurogenesi

225 on, body form, and habitat compared with the goldfish, they display the correlation of axon cap morph

226 After 1 week of exposure of goldfish to hypoxia, the pool of branchial ionocytes was

227 ish and medaka, common carp, grass carp, and goldfish to study the genome evolution events in the Cyp

228 We used the retinotectal projection of goldfish to test this idea in the intact adult CNS.

229 ining cDNAs for zebrafish ultraviolet opsin, goldfish ultraviolet cone opsin, and goldfish rod opsin.

230 The goldfish ultraviolet opsin, in contrast, hybridized to u

231 etail the cytoarchitecture of the MON in the goldfish using Golgi staining and HRP histochemical tech

232 (L-NOARG), nitric oxide (NO) inhibitors, in goldfish, using active-avoidance conditioning as the lea

233 rs in the neurons of the sensory zone of the goldfish vagal lobe, but even within this limited region

234 In the adult goldfish visual pathway, expression of the neuronal inte

235 n alpha-internexin-like nIF protein from the goldfish visual system.

236 n with 55% overall identity to zebrafish and goldfish Vsx1 and 35% overall identity to goldfish Vsx2

237 e the RINX gene is likely an ortholog of the goldfish Vsx1 gene, it has been named VSX1 by the Human

238 nd goldfish Vsx1 and 35% overall identity to goldfish Vsx2 and murine Chx10.

239 The optic nerve of goldfish was crushed, and at various times later, a smal

240 of regenerating optic fibers in living adult goldfish was used to visualize arbor restructuring durin

241 o generate refinement during regeneration in goldfish, we examined its effect on tectal activity.

242 l patterns persist in the hindbrain of adult goldfish, we hypothesize that a permanent "hindbrain fra

243 atory, photoreceptors in the retina of adult goldfish were ablated with an argon laser.

244 and possible interactions between them, male goldfish were exposed to an ethanol control or to nomina

245 Goldfish were maintained on a 12-hr light/12-hr dark cyc

246 Previously retinal progenitors in the adult goldfish were shown to proliferate vigorously when expos

247 explants and on retinal explants from adult goldfish, which normally regenerate in vivo.

248 sensory layer of the vagal gustatory lobe of goldfish, while both peptidergic systems distribute to t

249 ustatory function is especially important in goldfish, who utilize a sophisticated oropharyngeal sort

250 have a composite axon cap, like that of the goldfish, will perform C-start behavior with primarily u

251 in two locations in the retina of the adult goldfish, within the inner plexiform layer of the differ

252 gle cell RGCs, mouse hippocampal neurons and goldfish, zebrafish and chick retinal explants.

253 polylysine-(Plys)-only lanes, RGC axons from goldfish, zebrafish, and chick retinal explants avoided