ライフサイエンスコーパス: zebra

1 t one of the 12 best-sampled species (plains zebra).

2 known hybrid issue in the endangered Grevy's zebra.

3 d two of its subspecies, as well as mountain zebra.

4 's zebra E. grevyi and the mountain zebra E. zebra.

5 id not block the transcriptional function of ZEBRA.

6 g and Asiatic wild ass, to 14 in the Grevy's zebra.

7 host shutoff that is activated downstream of ZEBRA.

8 ptionally upregulated temporally upstream of ZEBRA.

9 enomes from each living species of asses and zebras.

10 Between 52 and 87% of zebra, 0-15% of springbok and 3-52% of elephants had mea

11 ZEBReplication Activator (ZEBRA), a viral basic zipper protein that initiates the

12 nt, depends on the molecular switch protein, ZEBRA, a viral bZIP transcription factor that initiates

13 ne in 'Orange', those of phenolics in 'Green Zebra', all of them common tomatoes.

14 While ZEBRA also plays an obligatory role as an activator of r

15 ZEBrA also provides unique opportunities for linking gen

16 of the lytic switch, sustains expression of ZEBRA, amplifies the lytic cascade, increasing virus pro

17 ssor enables retrograde regulation by vPK of ZEBRA, an observation that is counter to the unidirectio

18 terized 28 microsatellite markers in Grevy's zebra and assessed cross-amplification in plains zebra a

19 reported for two related avian species, the zebra and Bengalese finches.

20 rger, water-dependent grazers as wildebeest, zebra and buffalo-dominant species in savanna ecosystems

21 ndicated greater genetic variation in plains zebra and its subspecies than Grevy's zebra, despite pot

22 Two transcription factors, ZEBRA and Rta, switch Epstein-Barr virus (EBV) from the

23 n the early dry season, and grazers, such as zebra and suids, contributing more to female diet in the

24 The Grevy's zebra and the mountain zebra are endangered, and hybridi

25 gered, and hybridization between the Grevy's zebra and the plains zebra has been documented, leading

26 a and assessed cross-amplification in plains zebra and two of its subspecies, as well as mountain zeb

27 into captive population genetic diversity in zebras and support the use of these markers for identify

28 The Grevy's zebra and the mountain zebra are endangered, and hybridization between the Grev

29 Zebras are members of the horse family.

30 Tim Caro introduces why zebras are striped.

31 This work contributes to the assessment of ZEBRA as a potential therapeutic target for antiviral an

32 Although ZEBRA batteries are considered one of the promising cand

33 Cl(2) battery surpasses that of a Na-FeCl(2) ZEBRA battery over 25%, to 576 Wh kg(-1) and 2216 Wh L(-

34 Horses, asses, and zebras belong to a single genus, Equus, which emerged 4.

35 and/or PDD for all but four species (Grevy's zebra, buffalo, elephant, Grant's gazelle); however, the

36 There, zebras can forage in large patches of open grasslands lo

37 uidae, including horses, donkeys, mules, and zebras, caused by either of two protozoan parasites, The

38 Zebra changes in night-time selection for vegetation cov

39 ive causal agents of citrus greening, potato zebra chip and tomato vein greening diseases.

40 therapies to control citrus greening, potato zebra chip and tomato vein greening diseases.

41 For zebra chip disease control, aggressive psyllid managemen

42 North American haplotype (F) associated with zebra chip disease in potatoes.

43 associated with psyllid yellows disease and zebra chip disease, especially in potato.

44 eases, including Huanglongbing in citrus and zebra chip in potato.

45 nner and cause damaging plant diseases (e.g. Zebra chip in potatoes).

46 es including tomato vein-greening and potato zebra chip.

47 ive species: quagga (Dreissena bugensis) and zebra (D. polymorpha) mussels.

48 tests on E. coli, A. thaliana and Maylandia zebra data sets, HALC was able to obtain 6.7-41.1% highe

49 This work advances our understanding of ZEBRA-dependent activation of the viral lytic cascade.IM

50 plains zebra and its subspecies than Grevy's zebra, despite potential ascertainment bias.

51 d that the ancestor of present-day asses and zebras dispersed into the Old World 2.1-3.4 Mya.

52 One of these patterns is zebra dolomite that is frequently hosting economically i

53 : the plains zebra Equus quagga, the Grevy's zebra E. grevyi and the mountain zebra E. zebra.

54 the Grevy's zebra E. grevyi and the mountain zebra E. zebra.

55 viral bZIP transcription factor, Zta (BZLF1, ZEBRA, EB1), drives some of these changes.

56 We found out that zebras employ a DM anti-predator strategy.

57 here are three species of zebras: the plains zebra Equus quagga, the Grevy's zebra E. grevyi and the

58 We investigated whether plains zebras Equus quagga perform DM in Hwange National Park (

59 lis), wildebeest (Connochaetes taurinus) and zebra (Equus quagga) were most affected by VTOL approach

60 , we collected 154 serum samples from plains zebra (Equus quagga), 21 from springbok (Antidorcas mars

61 units establishing infection in wild plains zebra (Equus quagga).

62 vulnerability across vegetation types, with zebras favouring low vulnerability once DM has reduced e

63 ined myelin development in the brains of the zebra finch (Taeniopygia guttata) from chick at posthatc

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

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

66 the first evidence that song learning in the zebra finch (Taeniopygia guttata), the most common model

67 y, we investigated a passerine songbird, the zebra finch (Taeniopygia guttata), with a biparental car

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

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

70 ate important differences in the PGCs of the zebra finch and advance the first stage of creating PGC-

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

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

73 Zebra finch and rat CBG crystal structures in complex wi

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

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

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

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

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

81 Recording from adult zebra finch brain slices we show that within each bird b

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

83 erved in a high-level auditory region of the zebra finch brain, we addressed this question at the neu

84 secondary auditory cortex-like region of the zebra finch brain.

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

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

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

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

89 Recombinant zebra finch CBG steroid-binding properties reflect those

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

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

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

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

94 sequences in HVC (proper name) of the adult zebra finch forebrain that are central to the performanc

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

96 We show that the zebra finch GRC contains >115 genes paralogous to single

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

98 Although transgenesis in the zebra finch has been accomplished, it is with a very low

99 The zebra finch has been used as a valuable vocal learning a

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

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

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

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

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

105 n-specific neuronal activation in the VMH of zebra finch parents.

106 roved conditions for isolating and culturing zebra finch PGCs in vitro and were able to transfect the

107 rences between the 2 species, including that zebra finch PGCs were more numerous, more widely distrib

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

109 und in a long sequence of sounds (canary and zebra finch song syllables) patterned in either an alter

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

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

112 Juvenile male zebra finch songbirds (females cannot sing) learn to sin

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

114 thms of wild thrush nightingale and domestic zebra finch songs.

115 opy to optically section oviduct tissue from zebra finch Taeniopygia guttata females label free by ha

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

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

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

119 situ hybridization effort, we show that the zebra finch vocal robust nucleus of the arcopallium (RA)

120 We identified a vocal-motor pathway in the zebra finch where memories that guide learning of song-e

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

122 rds (chicken, duck, pigeon, ostrich, emu and zebra finch), early postnatal marsupial mammals (fat-tai

123 r characterization of the arcopallium in the zebra finch, a passerine songbird species and a major mo

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

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

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

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

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

129 the dynamics of Hoxb genes activation during zebra finch, chicken, and ostrich gastrulation, we provi

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

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

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

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

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

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

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

137 To improve germ-line transmission in the zebra finch, we identified and characterized its primord

138 In both carrion crow and zebra finch, we identified four different subareas of hi

139 the NCL in pigeon, chicken, carrion crow and zebra finch.

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

141 y/associative forebrain of the highly social zebra finch.

142 nse elements in orthologous promoters in the zebra finch.

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

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

145 umber of brain regions were activated in the zebra finch.

146 lls in a vocal learning Neoaves species, the zebra finch.

147 mutual mate choice in captive populations of Zebra finches (r = -0.020, 95% CI -0.148-0.107, 1,414 pa

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

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

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

151 emotor nucleus HVC (proper name) in juvenile zebra finches (Taeniopygia guttata) during auditory lear

152 Zebra finches (Taeniopygia guttata) learn to produce son

153 Song learning in zebra finches (Taeniopygia guttata) requires exposure to

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

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

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

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

158 between Anna's hummingbirds (Calypte anna), zebra finches (Taeniopygia guttata), and pigeons (Columb

159 We PIT-tagged wild zebra finches (Taeniopygia guttata), monitoring their re

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

161 Adult female zebra finches (Taeniopygia guttata), which do not produc

162 involved with the regulation of immunity, in zebra finches (Taeniopygia guttata).

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

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

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

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

167 at a social feedback loop between young male zebra finches and adult females guides the process of so

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

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

170 gulated FoxP1 or FoxP4 in Area X of juvenile zebra finches and compared the resulting song phenotypes

171 In zebra finches and other songbirds, there is a sensitive

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

173 ous measurement of neuronal activity of male zebra finches and vocalizations of males and females tha

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

175 te experimentally that the songs of juvenile zebra finches are guided toward mature vocal forms by re

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

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

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

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

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

181 Zebra finches categorized test stimuli with previously h

182 Zebra finches communicate with each other in ways that a

183 he oculomotor cerebellum in hummingbirds and zebra finches do not originate in the medial LM (as in p

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

185 Imaging with song analyses in juvenile male zebra finches during song learning and beyond, we reveal

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

187 ripheral tissues (liver, spleen, and fat) of zebra finches exposed to 12 h light:12 h darkness (LD),

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

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

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

191 eginning of the sensitive period, just after zebra finches have fledged from the nest, there is an in

192 emotor cortex (HVC, acronym is name) in male zebra finches identified prominent efferent pathways fro

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

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

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

196 Thus, zebra finches prioritize efficient learning of syllable

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

198 In this study, we show that in young zebra finches that are just beginning to learn the struc

199 avian cortical auditory neurons recorded in zebra finches that were listening to a large set of call

200 We exposed zebra finches to aversively reinforcing white noise stim

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

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

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

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

205 vity in the auditory forebrain of awake male zebra finches while presenting rare repetitions of a sin

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

207 These results suggest that zebra finches' tectofugal pathway predominately processi

208 spectrotemporal modulations in the songs of zebra finches).

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

210 ive during call-based vocal communication of zebra finches, a highly social songbird species.

211 ert multiple long-term phenotypic effects in zebra finches, and we here test for effects of these man

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

213 In male zebra finches, experimental manipulation of FoxP2 in Are

214 This circuit is incomplete in female zebra finches, hence only males sing.

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

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

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

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

219 In nightingales, but not in zebra finches, we found universal rhythm categories, wit

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

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

222 n vocal production learning in juvenile male zebra finches.

223 computational complexity of song learning in zebra finches.

224 physiological studies of selected neurons in zebra finches.

225 n the auditory and sensorimotor forebrain of zebra finches.

226 that ketolation occurs in the integument in zebra finches.

227 eural processing of vocal sounds, using male zebra finches.

228 nctionally changes over vocal development in zebra finches.

229 oxP2 disrupts song learning in juvenile male zebra finches.

230 erization that could impact song behavior in zebra finches.

231 identified HVC projection neurons in singing zebra finches.

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

233 ise known for being essential for singing in zebra finches.

234 controls learning and production of song in zebra finches.

235 dynamic control of subsyringeal pressure in zebra finches.

236 log FoxP2 disrupts song learning in juvenile zebra finches.

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

238 thalamofugal and the tectofugal pathways, of zebra finches.

239 an elegant ability for red discrimination in zebra finches.

240 whether a comparable transmission occurs in zebra finches.

241 human keratinocyte, monocyte, and embryonic zebra fish assays revealed no cytotoxicity.

242 tive erythropoiesis in the rps29(-/-) mutant zebra fish DBA model.

243 l imaging of H2S and in vivo imaging in live zebra fish demonstrated FEPO's potential biological appl

244 dels exist for FPD/AML, as Runx11/2 mice and zebra fish do not develop bleeding disorders or leukemia

245 l with the N-terminal ADPR binding pocket in zebra fish DrTRPM2.

246 esterol efflux in endothelial cells controls zebra fish embryonic angiogenesis.

247 in mouse macrophages as well as infection of zebra fish embryos.

248 both mouse developing cerebral cortices and zebra fish embryos.

249 a defective erythropoiesis phenotype using a zebra fish model.

250 maging in positive ion mode of rat brain and zebra fish tissues allowed enhanced detection of compoun

251 Rat brain and zebra fish tissues were investigated with reactive DESI-

252 Vertebrates, from zebra fish to humans, have an innate immune recognition

253 crystal structures of these compounds in the zebra fish zVDR ligand binding domain as complexes with

254 dopsis thaliana, Drosophila melanogaster, or zebra fish, in which a majority of genes have broad-shap

255 pombe, D. melanogaster, C. elegans, Xenopus, zebra fish, mouse and human, for a total of 12,877 tRFs.

256 imetry to measure heat dissipation by living zebra-fish embryos and to estimate the energetics of spe

257 Zebras forage near waterholes during the day but move aw

258 onditions, most herbivores (primarily plains zebra, Grant's gazelle and hartebeest) favoured sites wi

259 ion between the Grevy's zebra and the plains zebra has been documented, leading to a requirement for

260 s still equivocal, our results indicate that zebra in ENP often survive sublethal anthrax infections,

261 ptionally repressed temporally downstream of ZEBRA, indicating an additional mode of virus-mediated h

262 ZEBrA is a first of its kind gene expression brain atlas

263 binding to the origin of viral replication, ZEBRA is also an essential replication protein.

264 A component of the biologic action of ZEBRA is attributable to binding methylated CpGs in ZREs

265 triggering expression of the switch protein ZEBRA is essential to lytic cycle entry, sustaining its

266 on of the EBV latent-to-lytic switch protein ZEBRA is turned on.

267 Gazelle and zebra made decisions based on current light levels and l

268 d experimental samples, both assays detected zebra mussel in 94% of spiked samples and 0% of negative

269 f uninfested ballast and harbor samples with zebra mussel tissue to further test each assay's detecti

270 In unmanipulated samples, zebra mussel was not detected, while quagga mussel was d

271 e could detect the bioaccumulation of NPs in zebra mussels (Dreissena polymorpha) exposed for 1 h at

272 e focused on whether the grazing activity of zebra mussels (Dreissena polymorpha) would result in a c

273 as that in axenic mixed species co-cultures, zebra mussels had a significantly greater negative effec

274 The zebra mussels' putative preference for Synechocystis ove

275 Initially, we searched for a ZEBRA mutant that supports viral replication but not tra

276 , we identified a novel DNA-binding motif of ZEBRA, N terminal to the canonical bZIP domain.

277 key player is the viral protein Zta (BZLF1, ZEBRA, or Z).

278 endogenous methoxykaempferol glucoronide in zebra plant (Aphelandra squarrosa) leaves producing a lo

279 -wide gene expression assessments in a bird, ZEBrA provides important substrates for comparative neur

280 der radiation, Lake Tanganyika), Metriaclima zebra (recent radiation, Lake Malawi), Pundamilia nyerer

281 se methods, we identified significantly more zebras responding immunologically to anthrax than have p

282 and activates transcription through heptamer ZEBRA response elements (ZREs) related to AP-1 sites.

283 o a lytic trigger turns on the expression of ZEBRA, resulting in responsive and refractory subpopulat

284 ZEBrA's >3,200 high-resolution digital images of in situ

285 over a century of interest, the function of zebra stripes has never been examined systematically.

286 n regular, highly structured and unexpected 'zebra stripes', even when the solar-wind activity is low

287 A solution to the riddle of zebra stripes, discussed by Wallace and Darwin, is at ha

288 We compared populations of zebra-tailed lizards and western banded geckos, which ar

289 In a perissodactyl ungulate (Burchell's zebra) the distal end of CA1 is so large that it forms a

290 There are three species of zebras: the plains zebra Equus quagga, the Grevy's zebra

291 ZEBRA then transcriptionally activates other EBV genes a

292 lation of KAP1 renders it unable to restrain ZEBRA, thereby further derepressing and sustaining its e

293 se mutant AP-1 proteins acquire functions of ZEBRA; they activate expression of many viral early lyti

294 iral lytic cascade.IMPORTANCE The binding of ZEBRA to methylated and unmethylated viral DNA triggers

295 ead abundance (RRA) ranged from >99% (plains zebra) to <1% (dik-dik).

296 We found that Z(S186A), a mutant of ZEBRA unable to activate transcription of Rta or viral g

297 Our work thoroughly examines how ZEBRA uses a previously unrecognized basic motif to bind

298 ybrid populations between Grevy's and plains zebra were simulated to investigate subspecies and hybri

299 men to characterize the genome of the quagga zebra, which was driven to extinction in the early 1900s

300 Residue S186 of ZEBRA, Z(S186), which is absolutely required for disrupt