ライフサイエンスコーパス: zebrafish embryo

1 ures, that migrates from head to tail in the zebrafish embryo.

2 dividing cells and the neuromast organ of a zebrafish embryo.

3 g of hindbrain segments (rhombomeres) in the zebrafish embryo.

4 ditis elegans embryo and in the gastrulating zebrafish embryo.

5 genesis, both in vitro and in the developing zebrafish embryo.

6 for screening of androgenic compounds in the zebrafish embryo.

7 enes at the single cell level in whole-mount zebrafish embryo.

8 tic stem and progenitor cells (HSPCs) in the zebrafish embryo.

9 nd organizer specification in the developing zebrafish embryo.

10 collectively migrate along the trunk of the zebrafish embryo.

11 lk syncytial layer (YSL) in the gastrulating zebrafish embryo.

12 ermlayers simultaneously within a developing zebrafish embryo.

13 hich controls body axis morphogenesis in the zebrafish embryo.

14 lar development in wild-type and etv2 mutant zebrafish embryos.

15 olecular analysis of fully intact and living zebrafish embryos.

16 xplain the enantioselectivity of fipronil to zebrafish embryos.

17 of fluorescently tagged BMP2b and Chordin in zebrafish embryos.

18 characterize candidate genes for HRV in live zebrafish embryos.

19 hed in cytosolic puncta in ciliated cells in zebrafish embryos.

20 of a legacy AFFF sample and its toxicity in zebrafish embryos.

21 imposed to trapped red blood cells of living zebrafish embryos.

22 nositol (PI), in newly fertilized individual zebrafish embryos.

23 even signals in time-lapse imaging of living zebrafish embryos.

24 -like cells and corneal endothelium of early zebrafish embryos.

25 stem to deplete specific mRNA transcripts in zebrafish embryos.

26 de larvae and embryos, Drosophila brain, and zebrafish embryos.

27 scale expression screening of human cDNAs in zebrafish embryos.

28 ein we report such a method using developing zebrafish embryos.

29 unction of the GOF TRPP2 was investigated in zebrafish embryos.

30 al cells, and analyzed expression pattern in zebrafish embryos.

31 g phenotype in Delta-like 4 (Dll4) knockdown zebrafish embryos.

32 tumor suppression in basal keratinocytes of zebrafish embryos.

33 ed transient gene knockdown was performed in zebrafish embryos.

34 Lgp2 deficiency enhanced, HSPC emergence in zebrafish embryos.

35 ion, and led to potent angiogenic defects in zebrafish embryos.

36 xpression analysis and time-lapse imaging of zebrafish embryos.

37 ription factors in real-time in gastrulating zebrafish embryos.

38 an AKAP, recruits PKA RI to primary cilia in zebrafish embryos.

39 he use of human hematopoietic stem cells and zebrafish embryos.

40 and mitotic dysfunction compared to wildtype zebrafish embryos.

41 ed pesticide ziram is synuclein-dependent in zebrafish embryos.

42 l monitoring of the wound response in living zebrafish embryos.

43 markably decreased in ORF119L-overexpressing zebrafish embryos.

44 ivilege and transparent nature of developing zebrafish embryos.

45 is sufficient to expand definitive HSPCs in zebrafish embryos.

46 with pronephric cysts and microphthalmia in zebrafish embryos.

47 its overexpression results in excess PGCs in zebrafish embryos.

48 te, development, and biological functions of zebrafish embryos.

49 ng of sialylated glycoconjugates within live zebrafish embryos.

50 lyphenol compounds in a red wine extract and zebrafish embryos.

51 ells, xenografts of mice, budding yeast, and zebrafish embryos.

52 em and progenitor cell (HSPC) development in zebrafish embryos.

53 human ECs and during vascular development in zebrafish embryos.

54 y inducing a series of in-frame deletions in zebrafish embryos.

55 ific nuclear proteins in mammalian cells and zebrafish embryos.

56 n is that of primordial germ cells (PGCs) in zebrafish embryos.

57 ort UCHL1 activity during the development of zebrafish embryos.

58 tial for the development of the body axis in zebrafish embryos.

59 lecular information extracted from unlabeled zebrafish embryos.

60 c activity when grafted in syngeneic mice or zebrafish embryos.

61 sh cell lines (hepatocytes, fibroblasts) and zebrafish embryos.

62 ng zygotic genome activation (ZGA) in living zebrafish embryos.

63 luripotent stem cells and blood formation in zebrafish embryos.

64 of myosin protein levels in muscle cells of zebrafish embryos.

65 targeted mutagenesis in mammalian cells and zebrafish embryos.

66 achment of an amine group were identified in zebrafish embryos.

67 in the mouse and human embryonic gut and in zebrafish embryos.

68 pression of HA-tagged proteins in developing zebrafish embryos.

69 de promotes the ST phenotype in myotubes and zebrafish embryos.

70 ology to be scalable to single cells in live zebrafish embryos.

71 quired for ciliation both in human cells and zebrafish embryos.

72 count for diminished CRISPR-Cas9 activity in zebrafish embryos.

73 tion of arterial fate, and HSPC formation in zebrafish embryos.

74 mitotic spindle [1], is notably large in the zebrafish embryo (246.44 +/- 11.93 mum(2) in a 126.86 +/

75 FISH method that is suitable for whole-mount zebrafish embryo, a popular vertebrate model organism fo

76 ile manipulation of protein function in live zebrafish embryos, a transparent and commonly used model

77 d the biotransformation of fluoxetine in the zebrafish embryo - an aquatic model organism of intermed

78 In zebrafish embryos, an induced loss of function in snap29

79 matopoietic datasets, adult planaria and the zebrafish embryo and benchmark computational performance

80 Analysis of loss of function in the zebrafish embryo and larva showed that pomk function is

81 tant role for zebrafish Mate transporters in zebrafish embryos and adults and provide a basis for det

82 Both proteins are expressed in the cornea of zebrafish embryos and adults.

83 cell apoptosis in central nervous system of zebrafish embryos and adults.

84 e early morphogenetic movement of epiboly in zebrafish embryos and caused microtubule defects.

85 of-function effect by functional analyses in zebrafish embryos and cultured hippocampal neurons from

86 an be carefully implanted in the yolk sac of zebrafish embryos and display excellent biocompatibility

87 Loss of miR-144-mediated Dicer repression in zebrafish embryos and human cells leads to increased can

88 e required to maintain Warburg metabolism in zebrafish embryos and in both primary and malignant mamm

89 scriptional adaptation have been reported in zebrafish embryos and in mouse cell lines, it is not kno

90 ivate a typical human oncogene, kRASG12V, in zebrafish embryos and investigate the developmental and

91 Intriguingly, ORF119L-overexpressing zebrafish embryos and ISKNV-infected mandarin fish devel

92 Here we report genetic code expansion in zebrafish embryos and its application to the optogenetic

93 e central canal of the spinal cord of 30 hpf zebrafish embryos and its impact on development.

94 metry has been applied for the first time to zebrafish embryos and larvae to study five neurotransmit

95 act, ERSE, comprised of 36 detected PAHs) to zebrafish embryos and larvae.

96 32 is required for normal cilia formation in zebrafish embryos and mammalian cell culture, arguing th

97 ergence and extension movements in wild-type zebrafish embryos and mutants for the Wnt/PCP core compo

98 in zebrafish liver cells (ZFL) cells and in zebrafish embryos and novel insights into their molecula

99 We depleted wt1a in zebrafish embryos and observed glomerular injury and fil

100 splanted melanoma-derived cells into G2 tert zebrafish embryos and observed that tissue environment w

101 increased MG concentrations in tg(fli:EGFP) zebrafish embryos and rapidly induced several additional

102 a set of genes that are highly expressed in zebrafish embryos and systematically analyzed for enrich

103 these advances to deliver BE3 RNPs into both zebrafish embryos and the inner ear of live mice to achi

104 -EGFP in cerebellar cells of live transgenic zebrafish embryos and the role of palmitoylation in its

105 eter to measure heat flow between developing zebrafish embryos and the surrounding medium.

106 ocal imaging, parabiotic surgical pairing of zebrafish embryos, and blastula transplantation assays,

107 ubcellular behaviours in live C. elegans and zebrafish embryos, and show how TLS-SPIM can facilitate

108 ecting mRNAs in cell culture and whole-mount zebrafish embryos, and that combined with SPIM and PACT

109 tic chemical probes has been demonstrated in zebrafish embryos, and these reagents have been employed

110 Zebrafish embryos are rapidly injected with calibrated d

111 Using the zebrafish embryo as a model for thyroid axis development

112 ose V2 neural progenitor cells in developing zebrafish embryo as their successive shape changes can b

113 rgence of hematopoietic stem cells (HSCs) in zebrafish embryos as a model to investigate the role of

114 cular beacon to detect miR-430 in developing zebrafish embryos as a proof of principle.

115 propionate (CLO), cortisol and cortisone in zebrafish embryos as single compounds and binary mixture

116 dine reduces heart rate and increases HRV in zebrafish embryos, as it does in humans; and highlighted

117 ockdown of Kapbeta2 affected Hh signaling in zebrafish embryos, as well as in vitro cultured cerebell

118 nome-wide 3D atlas of gene expression in the zebrafish embryo at three developmental stages.

119 ordings of beating atria in 381 live, intact zebrafish embryos at 2 and 5 days post-fertilization hig

120 In situ hybridization of early zebrafish embryos at 24 hr postfertilization (hpf) demon

121 ss-correlation analysis to the blood flow in Zebrafish embryos at 4 days after fertilization, measuri

122 ging of sialylation and fucosylation in live zebrafish embryos at distinct developmental stages.

123 metabolite of fluoxetine that accumulates in zebrafish embryos at environmentally relevant exposure s

124 gged sialic acid and fucose into the yolk of zebrafish embryos at the one-cell stage enables systemat

125 Zebrafish embryos bearing mutations in genes required fo

126 teractome capture, we identified 227 RBPs in zebrafish embryos before and during ZGA, hereby named th

127 We found that although zebrafish embryos begin neurulation without a convention

128 the glycosyltransferase domain Afp18(G) into zebrafish embryos blocks cytokinesis, actin-dependent mo

129 In zebrafish embryos, bnc2 was expressed in the pronephric

130 as an early marker of HSC commitment in the zebrafish embryo, but recent studies have suggested that

131 ort the birth of hematopoietic stem cells in zebrafish embryos, but their cellular source in mammals

132 on glioblastoma U251-MG cells and in vivo on zebrafish embryos, but they were not significantly toxic

133 simulate cardiac hemodynamics in developing zebrafish embryos by coupling 4-D light sheet imaging wi

134 f Nodal ligands and Lefty inhibitors in live zebrafish embryos by fluorescence correlation spectrosco

135 Here we examine sarcolemmal repair in live zebrafish embryos by real-time imaging.

136 g, we introduce a method to tune the size of zebrafish embryos by reducing varying amounts of vegetal

137 RNA-seq analysis of zebrafish embryos carrying a missense variant detected s

138 Knockdown of slc24a46 expression in zebrafish embryos caused brain malformation, spinal moto

139 In vivo, depletion of NDPK-C in zebrafish embryos caused cardiac edema and ventricular d

140 Overexpression of OTG in zebrafish embryos caused dorso-anteriorized phenotype, i

141 ression of nesprin-1alpha2 WT and mutants in zebrafish embryos caused heart developmental defects tha

142 -tocopherol transfer protein (alpha-TTP)] in zebrafish embryos causes death within 24 h post-fertiliz

143 In the zebrafish embryo, chromatophores derive from the neural

144 The subintestinal plexus of the zebrafish embryo comprises vessels that vascularize the

145 is restricted to fast-twitch myocytes in the zebrafish embryo; consistent with this, fro mutant embry

146 Here, we conducted a screen in primary zebrafish embryo cultures for chemicals that disrupt neu

147 The zebrafish embryo (Danio rerio) has developed into one of

148 Removal of Ythdf2 in zebrafish embryos decelerates the decay of m(6)A-modifie

149 Here, we show zebrafish embryos deficient for Cyp26a1 and Cyp26c1 enzy

150 ties, recapitulating some of the features of zebrafish embryos deficient in the glaucoma-related gene

151 Loss- and gain-of-function experiments in zebrafish embryos demonstrate that col15a1b expression a

152 coupled with immunofluorescence performed on zebrafish embryos demonstrate that enox1 message and tra

153 Functional analysis in the developing zebrafish embryo demonstrated that both THAP11 and HCFC1

154 Exposure of zebrafish embryos demonstrated negligible effects of pre

155 the cranial neural crest in little skate and zebrafish embryos demonstrated that the transcriptional

156 active in an in vivo overexpression assay in zebrafish embryos demonstrating that the HP1 interaction

157 also track migrating cells in the developing zebrafish embryo, demonstrating the utility of this syst

158 Zebrafish embryos depleted of Atr resembled ATR-SS morph

159 Zebrafish embryos develop rapidly; all of their digestiv

160 Downregulation of INPP5K orthologs in zebrafish embryos disrupted muscle fiber morphology and

161 In zebrafish embryos disruption of lzap increases the expre

162 ese compounds show no off-target toxicity in zebrafish embryos, do not cause haematological, biochemi

163 high spatiotemporal specificity in cells and zebrafish embryos, excellent off-to-on switching, and st

164 pH values, a kinetic ion-trap model for the zebrafish embryo explained the pH dependence of biouptak

165 tified putative androgen-responsive genes in zebrafish embryos exposed to 0.05-5000 nM 11-ketotestost

166 Translucent zebrafish embryos express extraretinal opsins early on,

167 cts indicative of aberrant cell migration in zebrafish embryos, further demonstrating the function of

168 eduction of sox9b expression in TCDD-exposed zebrafish embryos has been shown to contribute to heart

169 Heart rate assays in wild-type zebrafish embryos have been limited to analysis of one e

170 ent lineage-tracing experiments in chick and zebrafish embryos have shown that cNCCs can also give ri

171 behavioral tests using in vivo models (e.g., zebrafish embryo) have been proposed as complementary ap

172 In zebrafish embryos, hemoglobin expression was significant

173 In Ldb2a-deficient zebrafish embryos, homeostasis of TGFbeta signalling is

174 We show that Fat1 knockout mice and zebrafish embryos homozygous for truncating fat1a mutati

175 recovery after photobleaching experiments in zebrafish embryos identified a pool of dynamic F-actin w

176 nal lethal concentrations killing 50% of the zebrafish embryos (ILC(50)) were calculated from the mea

177 Targeted inhibition of Plk1 in zebrafish embryos illustrates how centrosomal Plk1 under

178 AFFF toxicity was assessed in zebrafish embryos in comparison with four major constitu

179 lex sensory organ, the inner ear, by imaging zebrafish embryos in vivo over an extended timespan, com

180 Using live imaging of zebrafish embryos, in combination with photoconvertable

181 Suppression of clpb in zebrafish embryos induced a central nervous system pheno

182 or CRISPR-mediated deletions of sec61al2 in zebrafish embryos induced convolution defects of the pro

183 harboring any of three patient mutations in zebrafish embryos induced defects in axon guidance, conf

184 found to be required for pathogenesis in the zebrafish embryo infection model.

185 x gangliosides in patient fibroblasts and in zebrafish embryos injected with antisense morpholinos th

186 The zebrafish embryo is a highly interesting biological mode

187 nd that overexpression of hand2 in the early zebrafish embryo is able to enhance cardiomyocyte produc

188 In the current study, we showed that the zebrafish embryo is permissive to M. kansasii infection,

189 e neurodevelopmental toxicity of BMAA in the zebrafish embryo is presented in relation to the potenti

190 The zebrafish embryo is transcriptionally mostly quiescent d

191 fy molecules that affect MCC ontogeny in the zebrafish embryo kidney, and found prostaglandin signali

192 The ability of zebrafish embryos lacking both maternal and zygotic ezh2

193 y in wild-type but also in immunocompromised zebrafish embryos lacking either macrophages or neutroph

194 of the bisphenols BPA, BPS, BPF, and BPAF in zebrafish embryo-larvae and an assessment on their estro

195 s were confirmed by experimental analysis of zebrafish embryo LC50 according to OECD guideline 236.

196 y human and mouse kidney cells as well as in zebrafish embryos leads to enhanced DNA damage signaling

197 We found that radial glia ablation in zebrafish embryos leads to excessive sprouting of the tr

198 We found that deletion of Dab2 in zebrafish embryos led to a significant reduction in card

199 ADPGK knockdown in zebrafish embryos led to short, dorsalized body axis ind

200 D1 mutant Mycobacterium marinum strains in a zebrafish embryo model of tuberculosis and (iv) in vivo

201 ed ROS-induced toxicity as demonstrated in a zebrafish embryo model system.

202 In this study, we used a germ-free zebrafish embryo model to show that osmotic stress regul

203 wed significant antineoplastic activity in a zebrafish embryo model.

204 tible to digestive enzymes and did not alter zebrafish embryos' morphology and development.

205 Data from zebrafish embryos, murine and human cell melanoma lines,

206 We found that in Wdr1-deficient zebrafish embryos, neutrophils display F-actin cytoplasm

207 ition, we describe the acute toxicity toward zebrafish embryos of Dysoxylum alkaloids, comparing thei

208 Within maturing fibres of host zebrafish embryos, our analysis reveals a pool of diffus

209 FRET nanoprobes can be imaged in developing zebrafish embryos over seven days with toxicity similar

210 aled the induction of cellular senescence in zebrafish embryos overexpressing mutant, but not wild-ty

211 d of the activity of wild-type GRHL3, and in zebrafish embryos, perturbed periderm development.

212 ofiled for bioavailability and toxicity in a zebrafish embryo phenotype assay.

213 d anthocyanin metabolites were determined in zebrafish embryos previously exposed to the red wine ext

214 Zebrafish embryos provide a unique opportunity to visual

215 Zebrafish embryos provide an excellent model system to s

216 In zebrafish embryos, RAP-011 likely stimulates erythropoie

217 th knockdown and genome editing of znhit3 in zebrafish embryos recapitulate the patients' cerebellar

218 ssion or CRISPR-mediated deletion of brf1 in zebrafish embryos recapitulated key neurodevelopmental p

219 Expression of the histone H4 mutants in zebrafish embryos recapitulates the developmental anomal

220 ting yielded red fluorescent erythrocytes in zebrafish embryos, recapitulating the phenotype observed

221 rotoxicity, whereas MMP-13 overexpression in zebrafish embryos rendered the skin vulnerable to injury

222 Constitutive expression of these mutants in zebrafish embryos resulted in a heart failure phenotype

223 Knockdown of nansa in zebrafish embryos resulted in abnormal skeletal developm

224 ound that inactivation of bdh2 in developing zebrafish embryo results in heme deficiency and delays e

225 The loss of THAP11 in zebrafish embryos results in craniofacial abnormalities

226 Studies in zebrafish embryos reveal that wnt9b expression is simila

227 In vivo imaging of live zebrafish embryos revealed that loss of muscle-specific

228 Intravital imaging in live zebrafish embryos revealed that YAP influenced the distr

229 spindle size scales with cell size in early zebrafish embryos reveals fundamental principles of spin

230 ian liver and intestinal epithelium, fly and zebrafish embryos, sections from the mammalian cerebellu

231 Assessment of cell proliferation across zebrafish embryo segmentation, using the FUCCI transgeni

232 In zebrafish embryos, sema3 knockdowns show reduction of mi

233 cell cycle of single cells in culture and in zebrafish embryos showed that the total surface increase

234 Knockdown of mog1 expression in zebrafish embryos significantly decreased the heart rate

235 We show that sphk2 maternal-zygotic mutant zebrafish embryos (sphk2(MZ)) display early developmenta

236 elanoblast and melanocyte differentiation in zebrafish embryos, suggesting a possible role for GALC i

237 significantly retarded granule formation in zebrafish embryos, suggesting that any combination of at

238 rm differentiation upon forced expression in zebrafish embryos, suggesting that they have dominant-ne

239 ading and immobilization of large numbers of zebrafish embryos suspended in a continuous microfluidic

240 ino or the coexpression of ror2 and wnt11 in zebrafish embryos synergetically induced more severe con

241 transgenic perturbations, 4D imaging of the zebrafish embryo, systematic analysis of cell motion, an

242 Genetic studies in mouse and zebrafish embryos that are deficient in RA-generating en

243 In addition, we show in zebrafish embryos that filamin plays a positive role in

244 Finally, we demonstrate in zebrafish embryos that the improved LbCas12a and FnoCas1

245 Here, we show in zebrafish embryos, that (i) pUL97 can be expressed in ze

246 sing mammalian cultured epithelial cells and zebrafish embryos, that prior to apical extrusion of Ras

247 Here, we show that in the zebrafish embryo, the homeodomain transcription factor R

248 In zebrafish embryos, the bioconcentration factor of FLX wa

249 and rapid framework that relies on the early zebrafish embryo to assess mutational effects on a commo

250 , by exploiting the unique properties of the zebrafish embryo to capture the dynamics of signaling an

251 Exposure of zebrafish embryos to 17beta-estradiol (E2) during liver

252 ifferent combinations of steroid mixtures in zebrafish embryos to assess their joint activities on ph

253 ty of Pdots were evaluated on HeLa cells and zebrafish embryos to demonstrate their great biocompatib

254 Here we used zebrafish embryos to examine toxicities and transcriptio

255 We used mosaic zebrafish embryos to investigate the formation of the en

256 ng the week-long experiments, students raise zebrafish embryos to learn principles of development and

257 gentle mechanical deformation of developing zebrafish embryos to probe the role of physical forces i

258 We use the transparency of zebrafish embryos to reveal the de novo generation of a

259 Using tegmental hindbrain nuclei neurons in zebrafish embryos together with subcellular imaging, opt

260 can supplement existing methods, such as the Zebrafish Embryo Toxicity assay (OECD TG236), with molec

261 y against selected human cell lines and in a zebrafish embryo toxicity model.

262 b-on-a-Chip technology for automation of the zebrafish embryo toxicity test common in aquatic ecotoxi

263 on channel and show reduced cytotoxicity and zebrafish-embryo toxicity.

264 We show here that in zebrafish embryos, transient overexpression of editing-d

265 We present a kinetic digital model of zebrafish embryos up to 16 h of development.

266 o the embryonic body and the yolk sac of the zebrafish embryo using TK experiments, a dialysis approa

267 Expression of rad21 was suppressed in zebrafish embryos using a splice-blocking morpholino (ra

268 k dynamics in the anterior PSM in developing zebrafish embryos using an in vivo clock reporter, her1:

269 ole in vascular development was validated in zebrafish embryos using morpholino oligonucleotides.

270 , in vivo microangiography imaging on living zebrafish embryos using Pdots.

271 CRISPR/Cas9 activity in mammalian cells and zebrafish embryos using photochemically activated, caged

272 Delivery of 8-oxo-dGTP and 2-OH-dATP to zebrafish embryos was highly toxic in the absence of MTH

273 indbrain regions by sensory afferents in the zebrafish embryo, we mapped the fine-grained topographic

274 Using live imaging and transplantation in zebrafish embryos, we additionally reveal that axon init

275 of Escherichia coli (E. coli) and transgenic zebrafish embryos, we are able to design optimized antib

276 netically encoded calcium indicators in live zebrafish embryos, we show that ICOs depend on Pkd2 and

277 mbination of in vitro and in vivo studies in zebrafish embryos, we show that PAK3(N389) escapes its p

278 ying a multi-scalar morphometric analysis in zebrafish embryos, we show that posterior body elongatio

279 e partitioning to lipids and proteins in the zebrafish embryo were found to be suitable to predict th

280 Zebrafish embryos were exposed to 0.1, 1.0, 10, 50, and

281 cts of EETs were conserved in the developing zebrafish embryo, where 11,12-EET promoted HSPC specific

282 Wnt3 and subsequently, its secretion in live zebrafish embryos, where chemical inhibition of Porcupin

283 nockdown abolishes nodal signalling in early zebrafish embryos, whereas overexpression of rab5ab mRNA

284 the region where hematopoiesis occurs in the zebrafish embryo, which recapitulates a BM-like niche.

285 endothelial cell behavior in alk1-deficient zebrafish embryos, which develop cranial AVMs.

286 ed secreted signaling protein, Wnt3, in live zebrafish embryos, which is necessary for the investigat

287 expressed in wild-type or dmd(ta222a/ta222a) zebrafish embryos, which lack Dystrophin, and in Gt(dmd-

288 ing to assess the functional architecture of zebrafish embryos with a retrospective cardiac synchroni

289 tegrative approach, we have ablated cells in zebrafish embryos with both spatial and temporal control

290 Here, we report that zebrafish embryos with compound homozygous mutations in

291 transcripts during embryogenesis, we treated zebrafish embryos with ethanol during pre-gastrulation p

292 Treatment of zebrafish embryos with fluoxetine significantly blocked

293 Zebrafish embryos with global DNA hypomethylation caused

294 9 activity by comparing mutagenesis rates in zebrafish embryos with in vitro cleavage assays.

295 Treatment of early zebrafish embryos with NCI-65828, or with terrein, a fun

296 re physiological relevance, we microinjected zebrafish embryos with the same oligonucleotides, as a s

297 Furthermore, we show that zebrafish embryos with zfcoa6 knockdown display reduced

298 halts SRC-associated neuromast migration in zebrafish embryos without inducing life-threatening hear

299 Here we report that zebrafish embryos without maternally provided vg1 fail t

300 ) with a diversity of functional groups into zebrafish embryos (ZFE) was studied over 96 h of exposur