ライフサイエンスコーパス: zebra finch

1 spectrotemporal modulations in the songs of zebra finches).

2 ound in another avian lineage, the passerine zebra finch.

3 erally available cell lines derived from the zebra finch.

4 a high-resolution genetic linkage map of the zebra finch.

5 mparative maps of the genomes of chicken and zebra finch.

6 phalic enlargement in passerines such as the zebra finch.

7 sparrow and was essentially undetectable in zebra finch.

8 similar, suggesting no heterochiasmy in the zebra finch.

9 of the avian vocal organ, the syrinx, in the zebra finch.

10 nse elements in orthologous promoters in the zebra finch.

11 ion in the developing embryonic beaks of the zebra finch.

12 s been retained in other bird lineages, like zebra finch.

13 dynamic control of subsyringeal pressure in zebra finches.

14 log FoxP2 disrupts song learning in juvenile zebra finches.

15 upper-vocal-tract filtering to the songs of zebra finches.

16 generated neurons into the brain of juvenile zebra finches.

17 ingle HVC axons innervating RA in adult male zebra finches.

18 essary for vocal variability and learning in zebra finches.

19 ing, we analyzed the songs of young juvenile zebra finches.

20 f complex, learned acoustic signals in awake zebra finches.

21 n the auditory and sensorimotor forebrain of zebra finches.

22 of the arcopallium in brain slices from male zebra finches.

23 rial sections in embryonic and post-hatching zebra finches.

24 ed lentivirus to produce germline transgenic zebra finches.

25 ed in NIf and HVC of anesthetized adult male zebra finches.

26 mary auditory area field L of unanesthetized zebra finches.

27 wo neural pathways generates learned song in zebra finches.

28 perceptual responses might be lateralized in zebra finches.

29 he first utilized 25-day-old male and female zebra finches.

30 telencephalon of developing male and female zebra finches.

31 computational complexity of song learning in zebra finches.

32 physiological studies of selected neurons in zebra finches.

33 that ketolation occurs in the integument in zebra finches.

34 oxP2 disrupts song learning in juvenile male zebra finches.

35 erization that could impact song behavior in zebra finches.

36 identified HVC projection neurons in singing zebra finches.

37 protein in brains of juvenile and adult male zebra finches.

38 controls learning and production of song in zebra finches.

39 and chronic recording methods in the singing zebra finch, a small songbird that relies on auditory fe

40 tnap2 protein expression in the brain of the zebra finch, a songbird species in which males, but not

41 The zebra finch, a songbird, presents a unique opportunity t

42 programs in the four key song nuclei of the zebra finch, a vocal learning songbird.

43 Here, in male and female zebra finches, a combination of aromatase immunohistoche

44 (DCX), a microtubule-associated protein, in zebra finch adult and nestling (P9-11) brains.

45 he present study we actively immunized adult zebra finches against VIP conjugated to KLH and compared

46 Furthermore, within the zebra finch, all receptors, except for D4, showed differ

47 The zebra finch also does not show the reduced male-to-femal

48 characterize transcript distribution in the zebra finch, an experimentally tractable songbird for wh

49 all structures of the genomes are similar in zebra finch and chicken, but they differ in many intrach

50 In both zebra finch and chicken, the D1A, D1B, and D2 receptors

51 ies being found in chicken, turkey, duck and zebra finch and its expression profile confirmed in both

52 pulation in Africa, and tens of genomes from zebra finch and long-tailed finch populations in Austral

53 whose sequences are highly conserved between zebra finch and other species.

54 Zebra finch and rat CBG crystal structures in complex wi

55 One is inspired by the zebra finch and successfully reproduces songbird singing

56 f interchromosomal rearrangement between the zebra finch and the chicken genomes.

57 of 8,424 orthologs in both falcons, chicken, zebra finch and turkey identified consistent evidence fo

58 in the high vocal center of both adult male zebra finches and canaries (Serinus canaria).

59 Studies in zebra finches and canaries have now identified the gene

60 ture functional studies we cloned FoxP4 from zebra finches and compared regional and cellular coexpre

61 nations were similar in accuracy to those of zebra finches and humans.

62 hicle was administered peripherally to adult zebra finches and sickness behavior was recorded 2 or 24

63 udy we tested these abilities in a songbird (zebra finch) and a parrot species (budgerigar).

64 ional and experimental data from chicken and zebra finch, and acts to equalize male-to-female express

65 ve immune gene repertoire, as in chicken and zebra finch, and this repertoire has been shaped through

66 m neurons in area X of singing juvenile male zebra finches, and directly compared their firing patter

67 energic receptors was investigated in quail, zebra finches, and rats.

68 postnatal auditory environment of developing zebra finches, and then assessed effects on hemispheric

69 llular basis of telencephalic enlargement in zebra finches, and then to compare these findings with w

70 nucleus LMAN during development as juvenile zebra finches are actively engaged in evaluating feedbac

71 s in a forebrain auditory area of adult male zebra finches are selectively tuned to the song of a tut

72 Zebra finches are widely used for studying the basic bio

73 at single neurons, in the auditory cortex of zebra finches, are capable of discriminating the individ

74 nglia-projecting dopamine neurons in singing zebra finches as we controlled perceived song quality wi

75 from this work is that the telencephalon of zebra finches at hatching contains a thick proliferative

76 Here, we infused norepinephrine into the zebra finch auditory cortex and performed extracellular

77 , we describe a population of neurons in the zebra finch auditory cortex that represent vocalizations

78 In the zebra finch auditory forebrain, the concentration of cas

79 pectrograms by combining the spike trains of zebra finch auditory midbrain neurons with information a

80 e neurons and the neuronal population in the zebra finch auditory midbrain.

81 osome painting and cytogenetic mapping of 15 zebra finch BAC clones to the standard (ZAL2) and altern

82 is enrichment in song control neurons of the zebra finch basal ganglia impairs tutor song imitation,

83 We end-sequenced cDNAs from zebra finch brain and incorporated additional sequences

84 ffective estrogen receptor antagonist in the zebra finch brain and that estrogens may influence sexua

85 Here we cloned from zebra finch brain cDNAs of all avian dopamine receptors:

86 The zebra finch brain features a set of clearly defined and

87 This atlas of the zebra finch brain is expected to become an important too

88 o cDNAs from the same set of male and female zebra finch brain samples, both arrays detected a common

89 ings from pairs of HVC neurons in adult male zebra finch brain slices and used spike-triggered averag

90 VZ cell proliferation, male and female adult zebra finch brain slices containing the VZ were exposed

91 Cntnap2 protein expression in zebra finch brain supports the hypothesis that this mole

92 iour engages gene regulatory networks in the zebra finch brain, altering the expression of long non-c

93 tein expression in song-related areas of the zebra finch brain.

94 d an acute regulation of auditory neurons in zebra finches by (1) delineating the extent of the brain

95 ulated NR2B expression in LMAN of adult male zebra finches by increasing its protein levels to those

96 cts on RA projection neurons, but that adult zebra finches can partially compensate for this deficit

97 nd that the dopaminergic reward circuitry of zebra finches can simultaneously promote social cohesion

98 Zebra finches categorized test stimuli with previously h

99 term potentiation, is rapidly induced within zebra finch caudal medial nidopallium (NCM) following no

100 ied polyclonal antibody directed against the zebra finch CB(1) cannabinoid receptor, we have studied

101 main site of plasma CBG production, and anti-zebra finch CBG antibodies cross-react with CBGs in othe

102 Glycosylation of this asparagine in zebra finch CBG does not influence its steroid-binding a

103 Recombinant zebra finch CBG steroid-binding properties reflect those

104 Substitutions of amino acids within zebra finch CBG that are conserved only in birds reveal

105 Here we show that Zebra Finch chicks (Taeniopygia guttata) are capable of

106 Zebra finches communicate with each other in ways that a

107 Like other songbirds, the zebra finch communicates through learned vocalizations,

108 Experiment 3 found that juvenile zebra finches could discriminate songs on the basis of s

109 neural tracers in the TeO and the Ipc of the zebra finch demonstrated that neurons from the external

110 neuroestrogen levels in the forebrain of the zebra finch depend on calcium influx within presynaptic

111 This study shows that the zebra finch differs from the chicken because it lacks a

112 more challenging 8-range task, pigeons, like zebra finches, discriminated shifts from reward to nonre

113 probes, and mappings from turkey, condor and zebra finch DNA and EST sequences to the chicken genome.

114 We found that subsong production in zebra finches does not require HVC (high vocal center),

115 uit is enhanced in male compared with female zebra finches due to differential rates of incorporation

116 Additional experiments in the gregarious zebra finch (Estrildidae: Taeniopygia guttata) underscor

117 In the highly gregarious zebra finch (Estrildidae: Taeniopygia guttata), blockade

118 We now show that in male zebra finches (Estrildidae: Taeniopygia guttata), Fos ac

119 scrimination and song perception in juvenile zebra finches, even in birds with little experience with

120 ffect of ovulation order on TL in embryos of zebra finches experiencing the same controlled incubatio

121 vaeformis (Uva) of the posterior thalamus in zebra finches extend farther rostrally than to Uva, as g

122 vaeformis (Uva) of the posterior thalamus in zebra finches extend farther rostrally than to Uva, as g

123 w well neural spike trains recorded from the zebra finch field L (an analog of mammalian primary audi

124 s tested song responsiveness of adult female zebra finches for three acoustically different song type

125 The zebra finch, for example, sings a highly stereotyped son

126 und that activation of HTR2 receptors in the zebra finch forebrain song premotor structure the robust

127 ts demonstrate spatial coding of song in the zebra finch forebrain, based on developmental familiarit

128 s vocal patterns, we recorded in the singing zebra finch from populations of neurons in the robust nu

129 ivo intracellular recordings in anesthetized zebra finches from the input (nucleus HVC, used here as

130 A complete draft sequence of the zebra finch genome is imminent, yet a need remains for a

131 ing path microarray and identify CNVs in the zebra finch genome relative to chicken; 32 interspecific

132 or any passerine and a valuable tool for the zebra finch genome sequence project and for studies of q

133 Access to the zebra finch genome sequence will, therefore, prompt new

134 The wild-type zebra finch genome was found to have three intact genes

135 apped the majority to the recently assembled zebra finch genome.

136 aping patterns of molecular evolution in the zebra finch genome.

137 arrangements were reported; (2) to hybridize zebra finch genomic DNA to a chicken tiling path microar

138 st exploited differences between chicken and zebra finch gut morphology to identify the BMP pathway a

139 The zebra finch has long been an important model system for

140 to its basal ganglia part, Area X, in adult zebra finches has been noted to have no strong effects o

141 Songbirds like the zebra finch have become important models to understand t

142 e is mounting that both developing and adult zebra finches have the capacity for neurosteroidogenesis

143 nderstand this phenomenon better, we studied zebra finches hearing playbacks of birdsong.

144 The addition of HVC-RA neurons happens in zebra finches housed singly, but becomes more acute if t

145 in seasonal songbirds, neurons added to the zebra finch HVC are not part of a replacement process.

146 onses to intracellular current injections of zebra finch HVC neurons.

147 Here we examined the circuit anatomy of zebra finch HVC, a cortical region that generates sequen

148 tire chromosomes between chicken, turkey and zebra finch, identifying syntenic blocks of at least 250

149 ed full-length cDNA libraries from brains of zebra finches in 57 developmental and behavioral conditi

150 The zebra finch is an important model organism in several fi

151 h the imminent sequencing of its genome, the zebra finch is now poised to become a model system for p

152 The neural song system in zebra finches is highly sexually dimorphic; only males s

153 sexually dimorphic vocal repertoire of adult zebra finches is paralleled by structural and functional

154 Zebra finch isolates, unexposed to singing males during

155 onal progenitors in different regions of the zebra finch lateral ventricle.

156 Zebra finches learn song during distinct developmental s

157 We found that juvenile zebra finches living in flocks socially learned novel fo

158 supports 51 species including marmoset, pig, zebra finch, lizard, gorilla and wallaby, which were add

159 In normal adult zebra finches, LMAN neurons exhibit highly selective res

160 We found that the zebra finch LSt projects to the GP, substantia nigra par

161 Adult male zebra finches maintain highly stable songs via auditory

162 Socially reared zebra finch males imitate a song they hear during postha

163 Zebra finch males learn their song by imitation, a proce

164 te early gene ZENK) during sleep in juvenile zebra finch males that were still learning their songs f

165 , a letter-based name) of juvenile and adult zebra finch males, independent of the song stimulus pres

166 Here we show that in the zebra finch, many auditory midbrain neurons have extra-c

167 In zebra finches, many features of the neural song system a

168 The elastic modulus of the zebra finch ML is 18 kPa at 5% strain, which is comparab

169 Here, we addressed these issues in the zebra finch model by combining intracerebral pharmacolog

170 halamus exerts diverse behavioral effects in zebra finches, most of which are sexually differentiated

171 We measured telomere length in zebra finches (n = 99) from the nestling stage and at va

172 Much as children learn language, young male zebra finches need to interact socially with an adult tu

173 In the adult zebra finch, new projection neurons are added to the nuc

174 Birdsong learning in the zebra finch occurs during a sensitive period similar to

175 aHVC based on expression of zRalDH for adult zebra finches of both sexes and for males during the son

176 Here, we show, however, that juvenile zebra finches partway through song learning, singing imm

177 ted by Pseudomonas aeruginosa cleaves CBG in zebra finch plasma within its reactive center loop and d

178 Here we show that, in juvenile zebra finches, playback during the day of an adult 'tuto

179 ns of polymorphism and divergence among wild zebra finch populations.

180 field L (primary auditory cortex analog) of zebra finches, previous studies identified a limited set

181 Thus, zebra finches prioritize efficient learning of syllable

182 Male zebra finches produce long, spectrally complex, learned

183 These findings indicate that male and female zebra finches produce their disparate vocal repertoires

184 es for two bird species, the chicken and the zebra finch, provides, for the first time, an ideal oppo

185 In contrast, male zebra finches reared in isolation from other males have

186 lencephalic neurogenesis are both delayed in zebra finches relative to quail (Galliformes).

187 Dopaminergic neurons in anesthetized zebra finches respond more strongly to the bird's own so

188 leus DLM of urethane-anesthetized adult male zebra finches responded selectively to playback of the b

189 parison of FnTm2 expression between mice and zebra finches revealed a conserved pattern of expression

190 A study of zebra finches reveals the potential advantages of idiosy

191 output nucleus of this circuit in adult male zebra finches reverses moderate changes in song structur

192 In the zebra finch, singing behavior is driven by a sequence of

193 luence sexually dimorphic development of the zebra finch song circuit.

194 g techniques, on their ability to identify a zebra finch song in the presence of a background masker

195 atal exposure to cannabinoid agonists alters zebra finch song learning, we have sought to identify br

196 thin the spectral and temporal dimensions of zebra finch song structure.

197 sms regulating sexual differentiation of the zebra finch song system appear to include both genetic a

198 e-related morphological changes in the adult zebra finch song system by focusing on two cortical proj

199 id hormones in sexual differentiation of the zebra finch song system have produced complicated and at

200 esponsible for sexual differentiation of the zebra finch song system remains unknown but likely invol

201 modulate the sexually differentiation of the zebra finch song system.

202 recisely timed learned motor sequence, adult zebra finch song, to examine motor preparation.

203 ent amounts of statistical information about zebra finch song.

204 s have been reported in adult and developing zebra finch song.

205 he timescale for the representation of adult zebra finch song.

206 in ovo in poultry, and apply it to posthatch zebra finch songbird chicks.

207 Here, we investigated mTOR in juvenile zebra finch songbirds.

208 Adult zebra finch songs consist of stereotyped sequences of sy

209 tions matched to those found across multiple zebra finch songs to yield song spectrograms similar to

210 In the case of the zebra finch, steroids that impact song system masculiniz

211 Lesion studies in adult zebra finches suggest that the avian basal ganglia are i

212 Recent work in zebra finches suggests that genes and hormones may act t

213 , mounting evidence in one such species, the zebra finch, suggests that forms of plasticity common du

214 ow that inbreeding causes early death in the zebra finch Taeniopygia guttata, and among inbred indivi

215 A comparison with zebra finch Taeniopygia guttata, chicken Gallus gallus a

216 in the caudomedial nidopallium (NCM) of the zebra finch (Taeniopygia guttata) brain.

217 We made cDNA libraries from zebra finch (Taeniopygia guttata) brains at different de

218 We examined neural responses in zebra finch (Taeniopygia guttata) field L (homologous to

219 The recent sequencing of the zebra finch (Taeniopygia guttata) genome allowed an asse

220 kers against the chicken (Gallus gallus) and zebra finch (Taeniopygia guttata) genomes places the Ppu

221 A young male zebra finch (Taeniopygia guttata) learns to sing by copy

222 Sexual differentiation of the zebra finch (Taeniopygia guttata) neural song circuit is

223 Here we use the yellowbeak mutation in the zebra finch (Taeniopygia guttata) to investigate the gen

224 describe a genome-wide analysis of LD in the zebra finch (Taeniopygia guttata) using 838 single nucle

225 alysis of a whole-genome linkage map for the zebra finch (Taeniopygia guttata) using a 354-bird pedig

226 lation of Cck in the brain of the adult male zebra finch (Taeniopygia guttata), a songbird species.

227 hroated sparrow (Zonotrichia albicollis) and zebra finch (Taeniopygia guttata), we labeled putative V

228 ative analysis of the genome sequence of the zebra finch (Taeniopygia guttata), which is a songbird b

229 ddress this question, we use a songbird, the zebra finch (Taeniopygia guttata), whose learned song an

230 bird species: the pigeon (Columba livia) and zebra finch (Taeniopygia guttata).

231 e extend such an analysis to a songbird, the zebra finch (Taeniopygia guttata).

232 call-like, harmonic sounds were measured in zebra finches (Taeniopygia guttata) and budgerigars (Mel

233 histological sections from the brain of male zebra finches (Taeniopygia guttata) and make them public

234 Male zebra finches (Taeniopygia guttata) are vocal learners t

235 udomedial auditory forebrain of anesthetized zebra finches (Taeniopygia guttata) at 32 sites simultan

236 we recorded the vocalisations of individual zebra finches (Taeniopygia guttata) behaving freely in s

237 tory inputs from vocal effectors of juvenile zebra finches (Taeniopygia guttata) during the stage of

238 ow that short bouts of singing in adult male zebra finches (Taeniopygia guttata) induce persistent in

239 Song development in juvenile zebra finches (Taeniopygia guttata) is characterized by

240 ors found that song responsiveness in female zebra finches (Taeniopygia guttata) is strongly modulate

241 Zebra finches (Taeniopygia guttata) learn to produce son

242 New neurons are added, too, to the HVC of zebra finches (Taeniopygia guttata) that do not learn ne

243 a model for a migrating songbird, we fasted zebra finches (Taeniopygia guttata) that had been dosed

244 In the vocal control system of zebra finches (Taeniopygia guttata) the pre-motor mechan

245 photon calcium imaging in anesthetized adult zebra finches (Taeniopygia guttata) to examine how learn

246 sive functional MRI method in mildly sedated zebra finches (Taeniopygia guttata) to localize and char

247 rners, combining an experimental approach in zebra finches (Taeniopygia guttata) with an analysis of

248 d-eared turtles (Trachemys scripta elegans), zebra finches (Taeniopygia guttata), and mice (Mus muscu

249 ong from reversed song in juvenile and adult zebra finches (Taeniopygia guttata), and to test for pos

250 The songs of adult male zebra finches (Taeniopygia guttata), produced as rapid s

251 In adult zebra finches (Taeniopygia guttata), the telencephalon o

252 e temporal structure of learned song in male zebra finches (Taeniopygia guttata).

253 ellular recordings of HVC neurons in singing zebra finches (Taeniopygia guttata).

254 ame) encodes the learned songs of adult male zebra finches (Taeniopygia guttata).

255 enriched in the song control system of adult zebra finches (Taeniopygia guttata).

256 cellular nucleus of the nidopallium) of male zebra finches (Taeniopygia guttata).

257 ia, a nonsongbird species) with results from zebra finches (Taeniopygia guttata, a songbird species)

258 resequencing data for two bird species: the zebra finch, Taeniopygia guttata, and the long-tailed fi

259 with an identified partial sequence from the zebra finch, Taeniopygia guttata, as well as the previou

260 ion of CART-immunoreactivity in the brain of zebra finch, Taeniopygia guttata, its interaction with N

261 basal ganglia circuit of juvenile songbirds (zebra finches, Taeniopygia guttata) during vocal learnin

262 in prairie voles (Microtus ochrogaster) and zebra finches (Taenioypygia guttata), and also reduces t

263 onlinear dynamics to test whether adult male zebra finches (Taenopygia guttata) use the intrinsic non

264 We developed germline transgenic songbirds, zebra finches (Taneiopygia guttata) expressing human mut

265 n mRNA was widely distributed throughout the zebra finch telencephalon, overlapping with song control

266 nd learning-related (Area X) song regions of zebra finch telencephalon.

267 sumptive tectum is proportionally smaller in zebra finches than quail before neurogenesis begins, thi

268 g stereotypy is persistently reduced in male zebra finches that have been developmentally exposed to

269 ere we investigated in a songbird model, the zebra finch, the neural substrate for ranging and identi

270 Measurements of CBG mRNA in zebra finch tissues indicate that liver is the main site

271 We exposed zebra finches to aversively reinforcing white noise stim

272 ork analysis on microarray data from singing zebra finches to discover gene ensembles regulated durin

273 We manipulated song learning in zebra finches to experimentally control the requirements

274 chloride (DSP-4) to estradiol-treated female zebra finches to investigate if estrogenic effects on so

275 oped a spatial orientation assay and trained zebra finches to magnetic and/or overhead polarized ligh

276 We exposed male zebra finches to tutor or unfamiliar song.

277 phogen Sonic hedgehog (SHH) in the chick and zebra finch, two species that differ in size during the

278 the ascending projections of the nTTD in the zebra finch, using in vivo injections of biotinylated de

279 ntified as important to specific features of zebra finch vocal learning and production.

280 a size) within brain regions associated with zebra finch vocal learning are affected by late-postnata

281 the lateral septum, and sociality in female zebra finches was reduced by OT antagonist infusions int

282 cellular recordings in urethane-anesthetized zebra finches, we characterized the auditory properties

283 Using intracellular recordings in singing zebra finches, we found that DAF failed to perturb singi

284 In zebra finches, we found that exposure to a tutor's song

285 Using in vivo microdialysis in male zebra finches, we found that local estradiol levels incr

286 bilateral coordination for vocal learning in zebra finches, we investigated the anatomical organizati

287 In sleeping zebra finches, we observed slow wave sleep (SWS), rapid

288 ransported fluorescent tracers in adult male zebra finches, we show that Area X and other song contro

289 Budgerigars and zebra finches were tested, using operant conditioning te

290 In our first study, juvenile zebra finches were trained to perform one song and then

291 Male and female zebra finches were treated with E2 or control vehicle fr

292 regarious, non-territorial songbirds such as zebra finches, where females have access to numerous mal

293 in vivo imaging to measure spine dynamics in zebra finches, which learn to sing by imitating a tutor

294 manipulating the brain activity of juvenile zebra finches, which learn to sing by memorizing and voc

295 We deafened adult zebra finches, which rely on auditory feedback to mainta

296 , we sectioned the vocal nerve in adult male zebra finches, which spectrally distorted the birds' son

297 We evaluated this question in adult zebra finches, whose premotor neurons in the nucleus rob

298 ly from auditory neurons in awake adult male zebra finches with multiple microelectrodes during repea

299 on between two bird species, the chicken and zebra finch, with regard to sex bias of autosomal versus

300 of histone 4 lysine 16 (H4K16) near MHM, the zebra finch Z chromosome appears to lack the MHM sequenc