ライフサイエンスコーパス: Danio rerio

1 otion across early development in zebrafish (Danio rerio) .

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

3 ponsiveness using male and female zebrafish (Danio rerio).

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

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

6 reparations on developing zebrafish embryos (Danio rerio).

7 heart malformations in developing zebrafish (Danio rerio).

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

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

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

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

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

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

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

15 lino oligonucleotide knockdown in zebrafish (Danio rerio).

16 ce of ordinal numerical skills in zebrafish (Danio rerio).

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

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

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

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

21 nematode Caenorhabditis elegans to the fish Danio rerio.

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

23 of mitochondrial function and morphology in Danio rerio.

24 nserved in another vertebrate, the zebrafish Danio rerio.

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

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

27 cycle of laboratory populations of zebrafish Danio rerio.

28 dopsis thaliana, Caenorhabditis elegans, and 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 ment has been most studied in the zebrafish, Danio rerio.

37 ferented olfactory bulbs of adult zebrafish, Danio rerio.

38 mammalian vertebrates such as the zebrafish, Danio rerio.

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

40 ively studied member of the CCC family, from Danio rerio.

41 pharmaceuticals in embryos of the zebrafish Danio rerio.

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

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

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

45 Zebrafish (Danio rerio), a distantly related teleost with a well-kn

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

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

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

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

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

51 ells contribute to heart repair, we examined Danio rerio adult heart regeneration in the neural crest

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

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

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

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

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

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

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

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

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

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

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

63 thesis by generating germline-free zebrafish Danio rerio and testing the effect of the presence and a

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

65 Smn from Danio rerio and Xenopus laevis significantly prevent dis

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

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

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

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

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

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

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

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

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

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

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

77 ated IL-4/13A and IL-4/13B mutant zebrafish (Danio rerio) and, together with an existing IL-10 mutant

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

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

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

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

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

83 orhabditis elegans, Drosophila melanogaster, Danio rerio, and Mus musculus.

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

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

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

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

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

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

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

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

92 Using zebrafish (Danio rerio) as a model, we observed replicated shoals b

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

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

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

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

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

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

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

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

101 Embryonic zebrafish (Danio rerio) at 4 h post fertilization were exposed to w

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

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

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

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

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

107 osition alters larval behavior in zebrafish (Danio rerio), but the mechanisms were unknown.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

122 GenBank accession number for Danio rerio disc1: EU273350.

123 earning and memory differences in zebrafish (Danio rerio) displaying proactive and reactive stress co

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

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

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

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

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

129 sulfonic and carboxylic acid) in zebrafish ( Danio rerio) embryo.

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

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

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

133 851 single cells from dissociated zebrafish (Danio rerio) embryos and generated a transcriptome-wide

134 ation of heart rate from multiple zebrafish (Danio rerio) embryos per imaging field, which is capable

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

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

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

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

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

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

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

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

143 ine-2,4-dione (BQD) in developing zebrafish (Danio rerio) embryos.

144 logical activity using developing zebrafish (Danio rerio) embryos.

145 for their effects on developing zebrafish ( Danio rerio) embryos.

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

147 and fecundity measured in female zebrafish (Danio rerio) exposed to fadrozole for 21 days but not th

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

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

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

151 We used zebrafish Danio rerio from four populations to test if color prefe

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

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

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

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

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

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

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

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

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

161 The zebrafish species Danio rerio has become one of the major vertebrate model

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

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

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

165 The zebrafish (Danio rerio) has been widely used in the study of human

166 The zebrafish embryo (Danio rerio) has developed into one of the most importan

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

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

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

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

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

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

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

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

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

176 azine inhibitor with catalytic domain 2 from Danio rerio HDAC6.

177 Here, we show that zebrafish (Danio rerio) hmx2 and hmx3a are coexpressed in spinal dI

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

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

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

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

182 The recently published TRPM2 structures from Danio rerio in the ligand-free and the ADPR/Ca(2+)-bound

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

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

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

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

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

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

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

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

191 The zebrafish Danio rerio is a powerful model system to study the gene

192 Danio rerio is a recently characterized model host for p

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

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

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

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

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

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

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

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

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

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

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

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

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

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

207 Zebrafish (Danio rerio) is rapidly becoming a model for human aging

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

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

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

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

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

213 Zebrafish (Danio rerio) larvae are widely recognized for studying h

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

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

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

217 study we developed a mutant dguok zebrafish (Danio rerio) line using CRISPR/Cas9 mediated mutagenesis

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

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

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

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

222 eta) in a facile, high-throughput zebrafish (Danio rerio) model using casein coated-gold nanoparticle

223 ugh development and validation of zebrafish (Danio rerio) models of VWM, we demonstrate that zebrafis

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

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

226 ptic pH in retina from transgenic zebrafish (Danio rerio) of either sex.

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

228 y different lifestyles such as Mus musculus, Danio rerio, Oryzias latipes and Xiphophorus maculatus.

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

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

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

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

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

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

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

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

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

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

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

240 The zebrafish (Danio rerio) rnasel-1, 2 and 3 are orthologues of hANG a

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

242 Danio rerio SelL, transiently expressed in mammalian cel

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

244 show that, across the lifespan of zebrafish (Danio rerio), social isolation specifically decreased th

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

246 Zebrafish (Danio rerio) swim within days of fertilization, powered

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

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

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

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

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

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

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

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

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

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

257 lected offspring from wild-caught zebrafish (Danio rerio) to increase (Up-selected) or decrease (Down

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

259 1, col1a2 and col1a1a function in zebrafish (Danio rerio) to phenocopy skeletal reduction in Antarcti

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

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

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

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

264 t the cryo-electron microscopy structures of Danio rerio TRPM2 in the absence of ligands, in complex

265 Correspondingly, zebrafish (Danio rerio) TRPM2 (drTRPM2) and hsTRPM2 channels inacti

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

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

268 complex I (rotenone) and complex IV (azide) Danio rerio vertebrate zebrafish disease models from bra

269 First, by using a Danio rerio voltage-sensing phosphatase (DrVSP), we show

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 vey of Danio fishes, including the zebrafish Danio rerio, we identified two populations of white pigm

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

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

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

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

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

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

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

283 we describe an infection model of zebrafish (Danio rerio) with Trypanosoma carassii.

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

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

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

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

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

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

290 Danio rerio (Zebrafish) tbx20 morphants show defects in

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

292 s musculus (mouse), Rattus norvegicus (rat), Danio rerio (zebrafish), and Macaca mulatta (macaque), a

293 raries: Drosophila melanogaster (fruit fly), Danio rerio (zebrafish), and Oryza sativa (rice).

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

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

296 he early divisions of the vertebrate embryo, Danio rerio (zebrafish).

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

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

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

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