ライフサイエンスコーパス: Danio rerio

1 rtilization (2-d.p.f.) embryos in zebrafish (Danio rerio).

2 osis in dark-adapted adult albino zebrafish (Danio rerio).

3 network-driven ones in the larval zebrafish (Danio rerio).

4 ty acid (FA) metabolism in larval zebrafish (Danio rerio).

5 equired for normal development of zebrafish (Danio rerio).

6 tations and psychotropic drugs in zebrafish (Danio rerio).

7 cloned and characterized Sp2 from zebrafish (Danio rerio).

8 lino oligonucleotide knockdown in zebrafish (Danio rerio).

9 0 days postfertilization (dpf) in zebrafish (Danio rerio).

10 ontogeny of aminergic systems in zebrafish (Danio rerio).

11 sh (Fugu rubripes), and, in part, zebrafish (Danio rerio).

12 dissect PI cycle function in the zebrafish (Danio rerio).

13 ns, mouse, and more recently, the zebrafish (Danio rerio).

14 a single species of teleost fish, zebrafish (Danio rerio).

15 ynchus kisutch) and embryo-larval zebrafish (Danio rerio).

16 racterization of Mate proteins in zebrafish (Danio rerio).

17 wed frog (Xenopus tropicalis) and zebrafish (Danio rerio).

18 in muscle, liver, and brain from zebrafish (Danio rerio).

19 ehavior of several PPCPs in adult zebrafish (Danio rerio).

20 n viability of inbred and outbred zebrafish (Danio rerio).

21 es to hypoxia in adult and larval zebrafish (Danio rerio).

22 reparations on developing zebrafish embryos (Danio rerio).

23 heart malformations in developing zebrafish (Danio rerio).

24 of mitochondrial function and morphology in Danio rerio.

25 nserved in another vertebrate, the zebrafish Danio rerio.

26 mes are conserved in the genome of zebrafish Danio rerio.

27 (GBT) insertional mutants in the zebrafish, Danio rerio.

28 cycle of laboratory populations of zebrafish Danio rerio.

29 ed to assess gene function in the vertebrate Danio rerio.

30 ins with low similarity to ferroportin1 from Danio rerio.

31 ctural and biochemical studies of TIGAR from Danio rerio.

32 ct (E) values <10(-5) (95), in the zebrafish Danio rerio.

33 ells from the lateral line of the zebrafish, Danio rerio.

34 entiation in the zebrafish model vertebrate, Danio rerio.

35 ls in the olfactory bulb of adult zebrafish, Danio rerio.

36 ferented olfactory bulbs of adult zebrafish, Danio rerio.

37 mammalian vertebrates such as the zebrafish, Danio rerio.

38 a melanogaster, but is first detected in the Danio rerio.

39 of two eIF4E family members in the zebrafish Danio rerio.

40 ife stages of fish, including the zebrafish, Danio rerio.

41 We have cloned the Ptf1a-p48 ortholog in Danio rerio.

42 larval-to-adult transformation of zebrafish, Danio rerio.

43 or vascular development using the zebrafish, Danio rerio.

44 rization of the IFN gene from the zebrafish, Danio rerio.

45 nematode Caenorhabditis elegans to the fish Danio rerio.

46 system using a novel psen1 mutant zebrafish, Danio rerio.

47 tected in the brain of G0 zebrafish embryos (Danio rerio) 4 days after fertilisation following egg in

48 we identify in sperm of the freshwater fish Danio rerio a novel CNGK family member featuring non-can

49 Here we report that feeding adult zebrafish (Danio rerio) a high-cholesterol diet (HCD) resulted in h

50 Here we have developed, in the zebrafish (Danio rerio), a combination of fluorescent reporter tran

51 Zebrafish (Danio rerio), a freshwater vertebrate, has a well-charac

52 ng-term expression studies in the zebrafish (Danio rerio), a popular organism for clinical disease, v

53 ent in the adult forebrain of the zebrafish (Danio rerio), a species known to possess widespread neur

54 We show that zebrafish (Danio rerio) Abcd1 is highly conserved at the amino acid

55 in short-term habituation of the zebrafish (Danio Rerio) acoustic startle response (ASR).

56 n the tractable model system, the zebrafish (Danio rerio), additionally examining the evolutionary re

57 formities in early life stages of zebrafish (Danio rerio) after exposure to excess selenomethionine (

58 yces cerevisiae, Caenorhabditis elegans, and Danio rerio all retain high viability after prolonged ar

59 Interestingly, native Danio rerio alpha3(IV)NC1 does not bind Goodpasture auto

60 cloned, sequenced, and generated recombinant Danio rerio alpha3(IV)NC1 domain.

61 sence of autoantibody binding to recombinant Danio rerio alpha3(IV)NC1.

62 In the zebrafish, Danio rerio, alternating horizontal stripes of black mel

63 of genetic manipulation make the zebrafish (Danio rerio) an excellent model for studying hematopoies

64 We report here that zebrafish (Danio rerio), an important developmental model species,

65 brate system, we performed gene knockdown in Danio rerio and assessed the cardinal features of BBS an

66 nvironmentally relevant and model organisms (Danio rerio and Caenorhabditis elegans) and bacterial sp

67 primary taste centers of two cyprinid fish, Danio rerio and Carassius auratus, i.e., in their vagal,

68 erform in vivo experimental investigation in Danio rerio and confirm the regulatory role of our top p

69 we show, despite 90% sequence identity, that Danio rerio and Mus musculus alphaE-catenin have strikin

70 und in the Bmp7 genes of vertebrates such as Danio rerio and Takifugu rubripes indicating that this m

71 genesis, and polarity in the lateral line of Danio rerio and the embryo of Caenorhabditis elegans.

72 tenuated and immune protective in zebrafish (Danio rerio) and catfish (Ictalurus punctatus), triggeri

73 nium based ionic liquids (ILs) on zebrafish (Danio rerio) and Chinese hamster ovary cells (CHO) was i

74 ertebrate model organisms such as zebrafish (Danio rerio) and clawed African frog (Xenopus laevis).

75 model organisms, early life stage zebrafish (Danio rerio) and Daphnia magna.

76 tive imaging of entire developing zebrafish (Danio rerio) and Drosophila melanogaster embryos and per

77 cated HoxAa and HoxAb clusters of zebrafish (Danio rerio) and extended the 5' (posterior) part of the

78 ors by comparing the responses of zebrafish (Danio rerio) and fathead minnow (Pimephales promelas) to

79 distributions in different sized zebrafish (Danio rerio) and goldfish (Carassius auratus) and find t

80 f the pectoral fins of the larval zebrafish (Danio rerio) and its ontogeny.

81 to readily introduce mutations in zebrafish (Danio rerio) and livestock through non-homologous end jo

82 ficiently mutate specific loci in zebrafish (Danio rerio) and screen for genes involved in vertebrate

83 years of divergent evolution: the zebrafish (Danio rerio) and the ascidian Ciona intestinalis, an inv

84 t-sensitive model vertebrate, the zebrafish (Danio rerio), and characterized their tissue distributio

85 sea squirt (Ciona intestinalis), zebrafish (Danio rerio), and chicken (Gallus gallus) and, using phy

86 ule in decision experiments using zebrafish (Danio rerio), and in existing rich datasets of argentine

87 te in a diurnal lower vertebrate, zebrafish (Danio rerio), and this effect is mediated through activa

88 Key individuals in groups of 3-4 zebrafish (Danio rerio), and to measure the impact of removing thos

89 y, we followed the development of zebrafish, Danio rerio, and found that larvae turn toward each othe

90 Thus Xiphophorus, in contrast to zebrafish, Danio rerio, and several other vertebrate species, does

91 The zebrafish (Danio rerio) animal model offers a unique opportunity to

92 nerated ZFNs, we rapidly altered 20 genes in Danio rerio, Arabidopsis thaliana and Glycine max.

93 Zebrafish (Danio rerio) are a genetically tractable system to inves

94 zation distributions of groups of zebrafish (Danio rerio) are bimodal, showing two distinct modes of

95 Adult zebrafish (Danio rerio) are capable of regenerating retinal neurons

96 Zebrafish (Danio rerio) are emerging as a powerful new vertebrate m

97 Zebrafish (Danio rerio) are emerging as a useful model organism for

98 Zebrafish (Danio rerio) are rapidly emerging as a promising model o

99 l of embryonic melanocytes in the zebrafish (Danio rerio) are temporally and functionally independent

100 ogs among 15 claudin genes in the zebrafish, Danio rerio, are expressed in the otic and lateral-line

101 To use the zebrafish (Danio rerio) as a model to study 2,3,7,8-tetrachlorodibe

102 Hence, using zebrafish (Danio rerio) as a model, we examined the evolutionary ro

103 Using zebrafish (Danio rerio) as a model, we show that the lens-averted e

104 s developmental programming using zebrafish (Danio rerio) as a model.

105 Here, we describe the zebrafish (Danio rerio) as a vertebrate model system to study liver

106 owing importance and relevance of zebrafish (Danio rerio) as an alternate cancer model, we have gener

107 he embryonic and larval stages of zebrafish (Danio rerio) as an animal model to study ptpn6 function

108 ous teleost model organism is the zebrafish, Danio rerio, as a significant amount of work has been do

109 t pigment pattern formation in the zebrafish Danio rerio, as well as studies of how these mechanisms

110 s 24, 32 and 34 exposed to a salinity of 20, Danio rerio at 33 hpf exposed to 1.5% ethanol, and Radix

111 or the complete brain of a larval zebrafish (Danio rerio) at 5.5 days post-fertilization.

112 data showing that embryos of the zebrafish, Danio rerio, at 1.5 h post fertilization (hpf) subjected

113 uding a Drosophila melanogaster embryo and a Danio rerio beating heart.

114 ntal toxicity using the embryonic zebrafish (Danio rerio) bioassay.

115 human RPGR (ZFRPGR1, ZFRPGR2) in zebrafish (Danio rerio), both of which are expressed within the nas

116 form the stripe pattern of adult zebrafish (Danio rerio), but their molecular nature is poorly under

117 hologs are present in Xenopus tropicalis and Danio rerio, but apparently not in birds or mammals.

118 to AgRP was mapped in a teleost (zebrafish, Danio rerio) by double-label immunocytochemistry.

119 ) trophic transfer and fate in a model fish, Danio rerio, by combining natural isotopic fractionation

120 , Rattus novegicus, Drosophila melanogaster, Danio rerio, Caenorhabditis elegans and Saccharomyces ce

121 Rattus norvegicus, Drosophila melanogaster, Danio rerio, Caenorhabditis elegans, and Saccharomyces c

122 We found that embryos of the zebrafish Danio rerio can survive for 24 h in the absence of oxyge

123 genomes, we cloned and sequenced zebrafish (Danio rerio) cDNAs and/or genomic BAC clones orthologous

124 Here we identify and characterize zebrafish, Danio rerio, CHL (Chl).

125 nts in vivo using male and female zebrafish (Danio rerio) confirm a mutual antagonism between slit si

126 opy revealed that the eyes of the zebrafish (Danio rerio) contain high levels of 11-cis-retinyl ester

127 otide mitochondrial genome of the zebrafish (Danio rerio); contained are 13 protein genes, 22 tRNAs,

128 Here we show that the zebrafish, Danio rerio, contains a highly conserved gene, otop1, th

129 The coupling efficiency of five zebrafish (Danio rerio) CYP1 isoforms with a series of fluorogenic

130 oodei (Fundulidae) and wild-caught zebrafish Danio rerio (Cyprinidae), the average numbers of recessi

131 neuronal cell types during early zebrafish (Danio rerio) development is well-studied, little is know

132 orodibenzo-p-dioxin (TCDD) during zebrafish (Danio rerio) development results in altered heart morpho

133 During early zebrafish (Danio rerio) development zygotic transcription does not

134 mine the effects of coated NPs on zebrafish (Danio rerio) development, we tested aqueous poly(acrylic

135 to 30 h post-fertilization during zebrafish (Danio rerio) development.

136 GenBank accession number for Danio rerio disc1: EU273350.

137 bditis elegans, Drosophila melanogaster, and Danio rerio do not bind Goodpasture autoantibodies, whil

138 and characterization of two Cmas enzymes in Danio rerio (dreCmas), one of which is exclusively local

139 al lability is conserved among Mus musculus, Danio rerio, Drosophila melanogaster and Caenorhabditis

140 xylate cotransporters (SMCT) from zebrafish (Danio rerio), electrogenic (zSMCTe) and electroneutral (

141 types of axons in the developing zebrafish (Danio rerio) embryo, with frequent accumulation at the g

142 growth during development of the zebrafish (Danio rerio) embryo.

143 sms, metabolomic perturbations in zebrafish (Danio rerio) embryo/larvae were measured following 24 h

144 ction (up to 94%) and increased mortality of Danio rerio embryos (up to 100%) after exposure to extra

145 We examined the toxicity to zebrafish ( Danio rerio ) embryos of CdSecore/ZnSshell quantum dots

146 851 single cells from dissociated zebrafish (Danio rerio) embryos and generated a transcriptome-wide

147 In vivo ORF119L overexpression in zebrafish (Danio rerio) embryos resulted in myocardial dysfunctions

148 ts of hypoxia on the responses of zebrafish (Danio rerio) embryos to copper, a widespread aquatic con

149 ashing experiment supernatants to zebrafish (Danio rerio) embryos was negligible, with the exception

150 labeled cells isolated from live zebrafish (Danio rerio) embryos without using costly, commercially

151 ce (HRMAS NMR), applied to intact zebrafish (Danio rerio) embryos, as a model of vertebrate developme

152 ) was less toxic in an assay with zebrafish (Danio rerio) embryos, causing no adverse developmental e

153 Here, using zebrafish (Danio rerio) embryos, we investigated (i) whether hypoxi

154 blocks primitive hematopoiesis in zebrafish (Danio rerio) embryos, while increasing expression of the

155 on protein cadherin in developing zebrafish (Danio rerio) embryos.

156 ioavailability of Hg(2+) in larval zebrafish Danio rerio, evaluated by assessment of metallothionein

157 Zebrafish (Danio rerio) exhibit periodic tooth replacement througho

158 minnow (Pimephales promelas) and zebrafish (Danio rerio), exposed in parallel using matched experime

159 esis of Muller glial cells during zebrafish (Danio rerio) eye development.

160 evidence supports the utility of zebrafish (Danio rerio) for studying various pharmacological manipu

161 We employed embryos of the zebrafish, Danio rerio, for our studies on the in vivo bystander ef

162 n non-mammalian species including zebrafish (Danio rerio), fruitflies (Drosophila melanogaster) and r

163 de worm (Caenorhabditis elegans), zebrafish (Danio rerio), fruitfly (Drosophila melanogaster) and mou

164 Mus musculus, Bos taurus, Rattus norvegicus, Danio rerio, Gallus gallus and Arabidopsis thaliana).

165 o oligonucleotides to target the orthologous Danio rerio gene, dlx4b, and found reduced cranial size

166 ogenetic analysis and chromosomal mapping of Danio rerio genes indicate that tandem duplications are

167 abase is the central resource for zebrafish (Danio rerio) genetic, genomic, phenotypic and developmen

168 chromosomes and around 40% of the zebrafish Danio rerio genome.

169 ar approaches to characterize the zebrafish (Danio rerio) genome, which contains orthologoues of each

170 he pufferfish (Fugu rubripes) and zebrafish (Danio rerio) genomes for GCAP-related gene sequences (fu

171 of a subset of ov-serpin genes in zebrafish (Danio rerio) gives insight into the ancestral locus.

172 The zebrafish (Danio rerio) has become a useful model for studying earl

173 topoietic progenitor cells in the zebrafish (Danio rerio) has been hindered by a lack of functional a

174 The zebrafish (Danio rerio) has been used extensively in cardiovascular

175 The zebrafish (Danio rerio) has been widely used as a model vertebrate

176 The zebrafish (Danio rerio) has emerged as an ideal organism for the st

177 The zebrafish (Danio rerio) has two ABCC6-related sequences.

178 The zebrafish, Danio rerio, has become recognized as a valuable model f

179 Zebrafish (Danio rerio) have a number of strengths as a host model

180 high genetic homology to mammals, zebrafish (Danio rerio) have emerged as a powerful model organism i

181 Genetic screens in zebrafish (Danio rerio) have identified mutations that define the r

182 emical mutagenesis screens in the zebrafish (Danio rerio) have led to the identification of novel gen

183 Larval zebrafish (Danio rerio) have recently been suggested as a high-thro

184 Zebrafish (Danio rerio) have traditionally been used to study embry

185 The zebrafish (Danio rerio) Hb9 genomic region was then found to have t

186 lution structures of catalytic domain 2 from Danio rerio HDAC6 (henceforth simply "HDAC6") complexed

187 abidopsis thaliana, Drosophila melanogaster, Danio rerio, Homo sapiens, Mus musculus, Oryza sativa, S

188 ne expression in Drosophila melanogaster and Danio rerio identified 20 genes at 11 loci that are rele

189 Morpholino-based silencing in Danio rerio identified a modest role for commd7 and a si

190 lopment and metabolic function in zebrafish (Danio rerio), impacting hepatic differentiation, but not

191 he tropical freshwater vertebrate zebrafish (Danio rerio) in studying hepatogenesis.

192 toxicity of TiO2NPs to developing zebrafish (Danio rerio) in the dark and under simulated sunlight il

193 ly conserved immune system of the zebrafish (Danio rerio), in combination with its genetic tractabili

194 d germline disruption of genes in zebrafish (Danio rerio), in which targeted mutagenesis was previous

195 namniotes, represented by Xenopus laevis and Danio rerio, include an absence of lunatic fringe (lfng)

196 Loss of retinal neurons in adult zebrafish (Danio rerio) induces a robust regenerative response medi

197 demonstrate that social status in zebrafish (Danio rerio) influences behavioral decisions by shifting

198 Although the zebrafish Danio rerio is a major model for studies of development,

199 Danio rerio is a recently characterized model host for p

200 The zebrafish Danio rerio is an excellent model system for mammalian g

201 Zebrafish (Danio rerio) is a model organism that is used to study t

202 oning strategy, the small teleost zebrafish (Danio rerio) is a particularly appealing model.

203 The zebrafish (Danio rerio) is a popular vertebrate model for biomedica

204 The zebrafish (Danio rerio) is a useful vertebrate model system in whic

205 The zebrafish (Danio rerio) is a well-known developmental model that pr

206 Zebrafish (Danio rerio) is a widely used model for toxicological st

207 The developing zebrafish (Danio rerio) is an animal model that circumvents these p

208 Zebrafish (Danio rerio) is an emergent strategy for pre-clinical dr

209 The zebrafish (Danio rerio) is an emerging vertebrate model system for

210 Zebrafish (Danio rerio) is an excellent model organism for the stud

211 The larval zebrafish (Danio rerio) is an excellent vertebrate model for in viv

212 The zebrafish (Danio rerio) is emerging as a new important species for

213 The zebrafish (Danio rerio) is increasingly being used to study basic v

214 The zebrafish, Danio rerio, is a well-characterized and genetically tra

215 Although the zebrafish, Danio rerio, is an emerging model for studying hematopoi

216 The zebrafish, Danio rerio, is an established genetic and developmental

217 rate that the GC3 of genes in the zebrafish, Danio rerio, is correlated with that in humans, suggesti

218 The zebrafish, Danio rerio, is emerging as an important model organism

219 isotropic whole-brain functional imaging in Danio rerio larvae and spatially isotropic multicolor im

220 y stages of bone formation in the zebrafish (Danio rerio) larvae because the zebrafish has emerged as

221 acterial treatment in vivo, using zebrafish (Danio rerio) larvae infected with an antibiotic-resistan

222 Zebrafish (Danio rerio) larvae, broadly expressing halorhodopsin (N

223 overexpressed in the obligate suction feeder Danio rerio, mandibular morphology exhibits specific tra

224 In zebrafish (Danio rerio), mechanosensory organs called neuromasts ar

225 established the first transgenic zebrafish (Danio rerio) model of MJD by expressing human ataxin-3 p

226 rtebrate development, we used the zebrafish (Danio rerio) model system.

227 a heat-inducible VEGF transgenic zebrafish (Danio rerio) model through which VP can be monitored in

228 orhabditis elegans, Drosophila melanogaster, Danio rerio, Mus musculus and Arabidopsis thaliana.

229 structural architecture of larval zebrafish (Danio rerio) neuromuscular junctions in three dimensions

230 addition, new genetic model systems such as Danio rerio now make large-scale vertebrate early develo

231 Pigment cells of the zebrafish, Danio rerio, offer an exceptionally tractable system for

232 The zebrafish, Danio rerio, offers an opportunity to identify genes ess

233 We cloned the zebrafish (Danio rerio) ortholog of BCOR and found that knock-down

234 alpha3(IV)NC1 domain, as it evolved from the Danio rerio over 450 million years.

235 d MWCNTs ((14)C-MWCNT; 1 mg/L) by zebrafish (Danio rerio) over time.

236 models in Caenorhabditis elegans (Lis-1) and Danio rerio (pentylenetetrazole) highlight a reductionis

237 nce of visual information, larval zebrafish (Danio rerio) perform rheotaxis by using flow velocity gr

238 In zebrafish, Danio rerio, pigment-cell autonomous interactions genera

239 targets to their corresponding orthologs in Danio rerio, Pimephales promelas, Takifugu rubripes, Xen

240 ch show specific binding to three zebrafish (Danio rerio) proteins, namely suppression of tumorigenic

241 The zebrafish (Danio rerio) provides an opportunity to investigate the

242 oad set of electrical synapses in zebrafish, Danio rerio, require two gap-junction-forming Connexins

243 describe the miRNA profile of the zebrafish Danio rerio resolved in a developmental and cell-type-sp

244 progressed normally, silencing of arhgef3 in Danio rerio resulted in microcytic and hypochromic anemi

245 Expression of Fpn(D157G)-GFP in Danio rerio results in a severe growth defect, which can

246 GCAP3, is expressed in human and zebrafish (Danio rerio) retinas, and a guanylate cyclase-inhibitory

247 Knockdown and overexpression of klc2 in Danio rerio revealed mild to severe curly-tail phenotype

248 rabidopsis thaliana, Caenorhabditis elegans, Danio rerio, Saccharomyces cerevisiae, and Plasmodium fa

249 Danio rerio SelL, transiently expressed in mammalian cel

250 ELW1, were not toxic to embryonic zebrafish (Danio rerio), single compound standards of minor OHPHE m

251 of each of three species: (i) the zebrafish Danio rerio (stages 19 h, 21.5 h and 33 h exposed to 1.5

252 n E(2) was removed from embryonic zebrafish (Danio rerio) system using the aromatase inhibiter (AI) 4

253 ntributing to relapse, we studied zebrafish (Danio rerio) T-ALL samples using array comparative genom

254 In the developing zebrafish (Danio rerio), the muscle pioneers (MPs) are intermediate

255 As previously found for zebrafish (Danio rerio), the use of MS-222 and benzocaine also appe

256 Experimental analysis in Danio rerio, the zebrafish, is providing mechanistic ins

257 is study, we describe the role of zebrafish (Danio rerio) TICAM1 in activating NF-kappaB and zebrafis

258 s lethal muscular dystrophy in the zebrafish Danio rerio to a genomic interval containing the titin g

259 rformed antisense morpholino (MO) studies in Danio rerio to characterize the developmental effects of

260 ted a 21-day exposure of breeding zebrafish (Danio rerio) to 0.01, 0.5, and 10 mg/L (glyphosate acid

261 A genetic screen was performed in zebrafish (Danio rerio) to find mutations that cause genomic instab

262 sive analysis of the responses of zebrafish (Danio rerio) to MPA, DDG, and their binary mixtures at m

263 ogy and in vivo imaging in larval zebrafish (Danio rerio) to reveal a systematic relationship between

264 nitrosourea mutagenesis screen in zebrafish (Danio rerio) to search for mutants with defective defini

265 To test this, we exposed zebrafish (Danio rerio) to two commercial TiO2NP preparations at co

266 We used zebrafish, Danio rerio, to comprehensively investigate the preferen

267 from medaka (Oryzias latipes) and zebrafish (Danio rerio), two distantly related teleosts separated b

268 bulk-, and ionic forms on zebrafish embryos (Danio rerio) using a Next Generation Sequencing approach

269 ranial neurogenic placodes in the zebrafish, Danio rerio, using bHLH transcription factors as molecul

270 SAS-6 from Chlamydomonas reinhardtii and Danio rerio was shown to form ninefold symmetric, ring-s

271 m of the dorsal and caudal fin of zebrafish, Danio rerio, was studied, including the anatomy of fin m

272 The zebrafish, Danio rerio, was suggested as a promising model system f

273 Using small colonies of zebrafish (Danio rerio), we evaluated the impacts of estrogen expos

274 neurons in unanesthetized larval zebrafish (Danio rerio), we unequivocally demonstrate bistability i

275 olecules on the heart rate of the zebrafish, Danio rerio, we found that drugs that cause QT prolongat

276 the density of a gene map of the zebrafish, Danio rerio, we have placed 3119 expressed sequence tags

277 Using the zebrafish Danio rerio, we show that selection on phenotypic variat

278 Loss of function for crb2b and nphs1 in Danio rerio were previously shown to result in loss of t

279 iles of ovary and brain of female zebrafish (Danio rerio) were characterized after exposure to 55, 55

280 eral visceral system of the adult zebrafish (Danio rerio) were examined by means of carbocyanine dye

281 Zebra fish (Danio rerio) were infected with the NV deletion mutant o

282 ification of apo A-I derived from zebrafish (Danio rerio), which combines with phospholipids to form

283 el system for this purpose is the zebrafish (Danio rerio), which is endowed with special qualities fo

284 d genomes of Homo sapiens, Mus musculus, and Danio rerio with nonmethylated genomes of Drosophila mel

285 In Danio rerio (zebrafish) and Xenopus laevis (African claw

286 enetic processes that drive epiboly in early Danio rerio (zebrafish) development.

287 In the current study, the transparent Danio rerio (zebrafish) embryo was used as a model for i

288 through replicate enrichments of a wild-type Danio rerio (zebrafish) lysate.

289 ts of SOD1 in primary motor neurons and in a Danio rerio (zebrafish) model of ALS.

290 ion of fully compartmentalised models of the Danio rerio (zebrafish) on a global scale.

291 Danio rerio (Zebrafish) tbx20 morphants show defects in

292 n in Drosophila melanogaster (fruit fly) and Danio rerio (zebrafish) to quantify signaling changes ca

293 quatic and terrestrial eukaryotic organisms (Danio rerio (zebrafish), Fundulus heteroclitus (killifis

294 aquatic species, Xenopus laevis (frogs) and Danio rerio (zebrafish), specifically focusing on the ef

295 ild-caught population (Bangladesh, BLD01) of Danio rerio (zebrafish).

296 pe receptor (nitr) genes has been defined in Danio rerio (zebrafish).

297 binant enzymes from Homo sapiens (human) and Danio rerio (zebrafish).

298 to knockout the two mcoln1 genes present in Danio rerio (zebrafish).

299 tically encoded system in the model organism Danio rerio (zebrafish).

300 ranch of the FOXO sub-class, which includes: Danio rerio zFKHR (foxo5), Homo sapiens FKHR-L1 (FoxO3a)