ライフサイエンスコーパス: Xenopus laevis

1 aling components in the African clawed frog (Xenopus laevis).

2 of identified cells in the live frog embryo (Xenopus laevis).

3 afish (Danio rerio) and clawed African frog (Xenopus laevis).

4 do not produce foot flags (Rana pipiens and Xenopus laevis).

5 developmentally regulated retrotransposon in Xenopus laevis.

6 nstructive factor during brain patterning in Xenopus laevis.

7 MHC class Ib molecule XNC10 in the amphibian Xenopus laevis.

8 ryonic expression and morphant phenotypes in Xenopus laevis.

9 lar development throughout the life cycle of Xenopus laevis.

10 f developing retinal ganglion cells (RGC) in Xenopus laevis.

11 yury of the protist Capsaspora owczarzaki in Xenopus laevis.

12 the nuclei of intestinal epithelium cells of Xenopus laevis.

13 al communication in the African clawed frog, Xenopus laevis.

14 ncreasing N/C ratios in vitro and in vivo in Xenopus laevis.

15 in contrast to the single locus condition of Xenopus laevis.

16 role of TRPM6 during early embryogenesis in Xenopus laevis.

17 been suggested to control eye development in Xenopus laevis.

18 ptides found in the skin of the African frog Xenopus laevis.

19 ient absorption spectroscopy measurements on Xenopus laevis (6-4) photolyase have shown that the four

20 The utility of Xenopus laevis, a common research subject for developmen

21 elated to the well-known developmental model Xenopus laevis, a pseudotetraploid amphibian.

22 ying this technique to study gastrulation in Xenopus laevis (African clawed frog) embryos.

23 ction from 2-, 4-, 8-, 16-, 32-, and 50-cell Xenopus laevis (African clawed frog) embryos.

24 neural induction and normal eye formation in Xenopus laevis Although sufficient for neural induction,

25 ighly related species, the pseudo-tetraploid Xenopus laevis and diploid Xenopus tropicalis, as a mode

26 The amphibian Xenopus laevis and Frog Virus 3 (FV3) were established a

27 e mesoderm is best characterised in the frog Xenopus laevis and has been well studied both experiment

28 e expression in two distantly related frogs, Xenopus laevis and Mantidactylus betsileanus, with patte

29 e a prominent iT population in the amphibian Xenopus laevis and show the requirement of the class Ib

30 nalysis of differentially localizing RNAs in Xenopus laevis and Xenopus tropicalis oocytes, revealing

31 Hermes loss of function in both Xenopus laevis and zebrafish embryos leads to a signific

32 the cleft-like ectoderm-mesoderm boundary in Xenopus laevis and zebrafish gastrulae.

33 binations on three genomes, human, yeast and Xenopus laevis , and found that about 2.5-35% of the pro

34 ll embryos of the South African clawed frog (Xenopus laevis) and microextraction of their metabolomes

35 nochemistry on transfected cells, transgenic Xenopus laevis, and knock-in mice.

36 stream mechanisms in Caenorhabditis elegans, Xenopus laevis, and mouse embryos, in each species, it r

37 progesterone-stimulated oocytes of the frog Xenopus laevis, and recent evidence has revealed Musashi

38 rio, Pimephales promelas, Takifugu rubripes, Xenopus laevis, and Xenopus tropicalis, as well as subpo

39 The Xenopus laevis APE2 (apurinic/apyrimidinic endonuclease

40 Anuran tadpoles, including those of Xenopus laevis, are particularly susceptible to infectio

41 sholds for early life stage Se toxicities in Xenopus laevis as a consequence of in ovo exposure throu

42 This study introduces Xenopus laevis as a model to determine the cellular and

43 Using Xenopus laevis as model organism, we demonstrate that ch

44 that were microinjected into the oocytes of Xenopus laevis, as an example of a non-dividing cell, is

45 ronmental stressors in most cases, including Xenopus laevis at stages 24, 32 and 34 exposed to a sali

46 In Xenopus laevis, bone morphogenetic proteins (Bmps) induc

47 hanisms underlying this process, we isolated Xenopus laevis Brca2.

48 velopment of testes in African clawed frogs (Xenopus laevis), but little is known about molecular cha

49 daptive inflammatory swelling in the feet of Xenopus laevis by injection of killed bacteria or phytoh

50 w in two evolutionarily distant vertebrates (Xenopus laevis cell culture and mouse nerve-muscle ex-vi

51 g nanobody-labeled nuclear pore complexes in Xenopus laevis cells showed that MINFIELD-STED microscop

52 lly, expression and knockdown experiments in Xenopus laevis confirmed an evolutionarily conserved rol

53 Xenopus laevis craniofacial development is a good system

54 ieuwkoop and Faber's classic Normal Table of Xenopus laevis (Daudin) The lack of standardized images

55 stem for investigating nuclear size is early Xenopus laevis development, during which reductions in n

56 In the frog Xenopus laevis, dorsal-ventral axis specification involv

57 to deplete the LICs in human cell lines and Xenopus laevis early embryos to dissect the LICs' role i

58 Despite the large size of the Xenopus laevis egg (approximately 1.2 mm diameter), a fe

59 umvent this limitation by studying nuclei in Xenopus laevis egg and embryo extracts, open biochemical

60 ns with 99% confidence from the unfertilized Xenopus laevis egg and estimate protein abundance with a

61 ated the hydrodynamic behavior of the CPC in Xenopus laevis egg cytosol using sucrose gradient sedime

62 of their individual activities, and how the Xenopus laevis egg extract system has been utilized as a

63 Using Xenopus laevis egg extract, we found that increases in c

64 By using Xenopus laevis egg extract, we found that SUMOylation of

65 Using Xenopus laevis egg extract, we have shown that blocking

66 Previous studies in Xenopus laevis egg extracts and in highly proliferative

67 By combining studies in Xenopus laevis egg extracts and mouse embryonic fibrobla

68 uired for mitotic chromosome architecture in Xenopus laevis egg extracts and, unlike core histones, e

69 Depletion-reconstitution experiments in Xenopus laevis egg extracts indicate that NCOA4 acts as

70 In this study we have used Xenopus laevis egg extracts to analyse Uhrf1 function in

71 nsional structure of Listeria actin tails in Xenopus laevis egg extracts using cryo-electron tomograp

72 ined experiments in tissue culture cells and Xenopus laevis egg extracts with a mathematical model.

73 n higher eukaryotes is inferred from data in Xenopus laevis egg extracts, but its identity remains el

74 ing 3D structured illumination microscopy to Xenopus laevis egg extracts, here we reveal that in the

75 Through biochemical analysis in Xenopus laevis egg extracts, we establish that the MRN (

76 the cell cycle using crude and fractionated Xenopus laevis egg extracts.

77 The metabolism of the Xenopus laevis egg provides a cell survival signal.

78 itiation sites in extracts of human cells or Xenopus laevis eggs.

79 es of both bicc1 mRNA and Bicc1 protein from Xenopus laevis eggs.

80 getal and marginal zones of the pre-gastrula Xenopus laevis embryo.

81 ed and remodeled during cell division in the Xenopus laevis embryo.

82 es that were isolated from the 16-cell frog (Xenopus laevis) embryo, amounting to a total of 1709 pro

83 stigated the function of hepatocystin during Xenopus laevis embryogenesis and identified hepatocystin

84 During early Xenopus laevis embryogenesis both nuclear and cell volum

85 Early Xenopus laevis embryogenesis is a robust system for inve

86 ify mechanisms that scale the spindle during Xenopus laevis embryogenesis, we established an in vitro

87 in causes neural tube closure defects during Xenopus laevis embryogenesis.

88 endent signaling modulates phenotypes during Xenopus laevis embryonic development.

89 Xenopus laevis embryonic epidermal lectin (XEEL), an int

90 characterize mitotic spindle dynamics in the Xenopus laevis embryonic epithelium.

91 We identified in Xenopus laevis embryos a novel posttranscriptional mecha

92 Using Xenopus laevis embryos as a model system to examine Anil

93 Here, using gastrula-stage Xenopus laevis embryos as a model system, we examine Mgc

94 dial intercalation of cells into the skin of Xenopus laevis embryos as a model to study directed cell

95 The dorsal half of bisected Xenopus laevis embryos can regenerate a well-proportione

96 e observed that depletion of hepatocystin in Xenopus laevis embryos decreased TRPM7 expression, indic

97 Xenopus laevis embryos from adult female frogs fed n-3 P

98 -catenin-induced secondary axis formation in Xenopus laevis embryos in vivo.

99 Biochemical tests and in vivo assays in Xenopus laevis embryos suggest that these mutations may

100 Here, we use Xenopus laevis embryos to analyze the spatial and tempor

101 arly development, overexpression of TRPM7 in Xenopus laevis embryos was sufficient to fully rescue th

102 During the early development of Xenopus laevis embryos, the first mitotic cell cycle is

103 and testing the effects of phosphomutants in Xenopus laevis embryos, we identify the novel site S267

104 ibitory neural markers xVGlut1 and xVIAAT in Xenopus laevis embryos.

105 ccurs at the midblastula transition in early Xenopus laevis embryos.

106 ysed for enhancer activity by injection into Xenopus laevis embryos.

107 Frog (here Xenopus laevis) embryos are more than 1 mm in diameter a

108 kdown of nphp4 in multiciliated cells of the Xenopus laevis epidermis compromised ciliogenesis and di

109 nesis in both murine airway epithelia and in Xenopus laevis epidermis.

110 We took advantage of the Xenopus laevis expression system to determine the indivi

111 n GLT1a or GLT1b separately, we employed the Xenopus laevis expression system.

112 semi-intact in vitro preparations of larval Xenopus laevis Extracellular nerve recordings during sin

113 Xenopus laevis fibres (n = 21) were suspended in a seale

114 ntified form of deep-brain photoreception in Xenopus laevis frog tadpoles.

115 Data obtained using Xenopus laevis gastrulae have shown that integrin-fibron

116 in the African clawed frog, we sequenced the Xenopus laevis genome and compared it to the related dip

117 ription of the 43,673 genes annotated in the Xenopus laevis genome under a variety of conditions that

118 Recent updates to the database include the Xenopus laevis genome, a new Xenopus tropicalis genome b

119 e we present X-ray crystal structures of the Xenopus laevis GluN1-GluN2B NMDA receptor with the allos

120 Furthermore, NEIL3 from Xenopus laevis has been shown to cleave psoralen- and ab

121 heterogametic sex, as in the related species Xenopus laevis, has yet to be presented.

122 cobasally polarized neuroepithelial cells in Xenopus laevis have a shorter cell cycle than nonpolar p

123 can act as +TIPs to regulate MT dynamics in Xenopus laevis Here we characterize TACC2 as a +TIP that

124 ng DNA and monitor protein dissociation from Xenopus laevis histones reconstituted with two model NCP

125 The African clawed frog Xenopus laevis is an important model organism for studie

126 neages, the v2r gene family of the amphibian Xenopus laevis is expressed in the main olfactory as wel

127 The amphibian Xenopus laevis is extensively utilized as an infection m

128 Xenopus laevis is one of the most widely used model orga

129 While Xenopus laevis is the leading model for studies of immun

130 mparison, these lysines are not conserved in Xenopus laevis Ku, and Ku from this species has negligib

131 Here, we show that self-association of Xenopus laevis Mcm10 is mediated by a conserved coiled-c

132 sponse to optic nerve (ON) shortening during Xenopus laevis metamorphic remodeling.

133 We investigated the effects of VPA on Xenopus laevis models of RP expressing human P23H, T17M,

134 Pertinently, amphibian (Xenopus laevis) Mphis differentiated by CSF-1 and IL-34

135 based approach, here we demonstrate that the Xenopus laevis Npm tail domain controls the binding of h

136 adjacent homology (BAH) domain bound to the Xenopus laevis nucleosome core particle and the crystal

137 A) as the key metabolic signal that inhibits Xenopus laevis oocyte apoptosis by directly activating C

138 Human AQP1 was analyzed in the Xenopus laevis oocyte expression system by two-electrode

139 In the context of the Xenopus laevis oocyte expression system, this technique

140 roquine resistance transporter" (PfCRT) in a Xenopus laevis oocyte expression system.

141 ern of microtubule-interacting proteins upon Xenopus laevis oocyte maturation by quantitative proteom

142 In the Xenopus laevis oocyte system, extracellular AqF026 poten

143 Here we use a Xenopus laevis oocyte-based automated 2-electrode voltag

144 mal and vegetal pole RNAs in the fully grown Xenopus laevis oocyte.

145 implicated in KID syndrome when expressed in Xenopus laevis oocytes (IC50 approximately 16 muM), usin

146 Expression of AtINT2 in Xenopus laevis oocytes also induced arsenite import.

147 Expression of OCT1 variants in Xenopus laevis oocytes and determination of quinine-sens

148 Expression of SthK channels in Xenopus laevis oocytes and functional characterization u

149 rial rhodopsin Gloeobacter violaceus (GR) in Xenopus laevis oocytes and HEK-293 cells.

150 racterization of the mutant channels in both Xenopus laevis oocytes and human HEK293T cells showed a

151 two-electrode voltage clamp recordings from Xenopus laevis oocytes and imaging of mammalian BHK cell

152 lar folded peptidyl-prolyl isomerase Pin1 in Xenopus laevis oocytes and in native-like crowded oocyte

153 ctrophysiological and fluorescence assays in Xenopus laevis oocytes and protein interaction assays.

154 gene, we investigated functional effects in Xenopus laevis oocytes and screened a follow-up cohort.

155 The mutants were expressed in Xenopus laevis oocytes and tagged with environmentally s

156 D and N variants) subunits were expressed in Xenopus laevis oocytes and tested with or without LYPD6B

157 pe and mutant transporters were expressed in Xenopus laevis oocytes and two-electrode voltage-clamp e

158 te genes that were subsequently confirmed in Xenopus laevis oocytes and zebrafish.

159 as proven to be inert in in-cell extracts of Xenopus laevis oocytes at 18 degrees C for more than 24

160 LjNPF8.6 achieves nitrate uptake in Xenopus laevis oocytes at both 0.5 and 30 mm external co

161 Here we study membrane dynamics in wounded Xenopus laevis oocytes at high spatiotemporal resolution

162 dependent sensitization of TRPV4 currents in Xenopus laevis oocytes by adenylyl cyclase- and protein

163 quiescent (G0) mammalian cells and immature Xenopus laevis oocytes by an FXR1a-associated microRNA-p

164 encodes a nitrate transporter: expression in Xenopus laevis oocytes conferred upon the oocytes the ab

165 mplete disruption of spindle microtubules in Xenopus laevis oocytes did not affect the bivalent-to-dy

166 ither CPK2 or CPK20 (but not CPK17/CPK34) in Xenopus laevis oocytes elicited S-type anion channel cur

167 Transport assays in Xenopus laevis oocytes established that indeed all human

168 luorescence signals and gating currents from Xenopus laevis oocytes expressing ASAP1.

169 two-electrode voltage clamp recordings from Xenopus laevis oocytes expressing GluN1/GluN2A(N615K) (N

170 d with experimental records from emptied-out Xenopus laevis oocytes expressing hAQP1.

171 g were selected for functional validation in Xenopus laevis oocytes expressing hGlyR-alpha1.

172 Cage to mediate the uptake of (65) Zn(2+) by Xenopus laevis oocytes expressing hZIP4 demonstrates the

173 Two-electrode voltage-clamp recordings of Xenopus laevis oocytes expressing mutant KV 1.2 channels

174 Using Xenopus laevis oocytes expressing NBCe1 variants, we hav

175 ation in a simplified preparation comprising Xenopus laevis oocytes expressing proteins that underlie

176 Injecting RS1 fragments into Xenopus laevis oocytes expressing SGLT1 or CNT1 and meas

177 D.The uptake of radiolabeled substrates into Xenopus laevis oocytes expressing the 2 GLUT14 isoforms

178 Upon treatment of Xenopus laevis oocytes expressing the W441C/K269C double

179 Functional expression in Xenopus laevis oocytes followed by two-electrode voltage

180 Functional analyses were performed in Xenopus laevis oocytes for eight missense and two nonsen

181 ng two-electrode voltage clamp techniques in Xenopus laevis oocytes indicates that the investigated c

182 a prerequisite for the re-entry of immature Xenopus laevis oocytes into MI.

183 it phosphorylated KCC3 at Ser-96 and that in Xenopus laevis oocytes Ser-96 of human KCC3 is phosphory

184 Functional analysis in Xenopus laevis oocytes showed that both NRT1.11 and NRT1

185 esponses measured from transfected cells and Xenopus laevis oocytes shows the same disparity in poten

186 Electrophysiological analysis of NPF2.4 in Xenopus laevis oocytes suggested that NPF2.4 catalyzed p

187 N, and S364D were expressed in HEK cells and Xenopus laevis oocytes to measure radioactive substrate

188 volume-sensing, we expressed the channel in Xenopus laevis oocytes together with AQP4.

189 f CO donors (CORMs) on Cx46 HCs expressed in Xenopus laevis oocytes using two-electrode voltage clamp

190 iffusing fluorescent spots on the surface of Xenopus laevis oocytes when expressed alone, coexpressio

191 ha3beta4 nAChRs heterogeneously expressed in Xenopus laevis oocytes with a calculated IC50 of 2.3 nM

192 channels (GluCls) recombinantly expressed in Xenopus laevis oocytes with electrophysiology.

193 hysiology revealed that, when coexpressed in Xenopus laevis oocytes with various potassium channels,

194 ogous expression systems (HEK-293T cells and Xenopus laevis oocytes), an enhanced activation of the G

195 In Xenopus laevis oocytes, activation of group I mGlu recep

196 In Xenopus laevis oocytes, an increase in Kv7.2/3 function

197 inhibits KAT2 and/or KAT1 when expressed in Xenopus laevis oocytes, and (3) closely interacts in pla

198 annel types were heterologously expressed in Xenopus laevis oocytes, and K(+) currents were measured

199 ion of TRPA1 was studied in in HEK293 cells, Xenopus laevis oocytes, and primary sensory neurons by m

200 ell-known stiffness, were microinjected into Xenopus laevis oocytes, and the Gd(III)-Gd(III) distance

201 perties heterologously expressed in yeast or Xenopus laevis oocytes, and their in planta cellular and

202 ns A382T, T459R, and Q386E were expressed in Xenopus laevis oocytes, and their transport and anion ch

203 Receptors were expressed heterologously in Xenopus laevis oocytes, and whole-cell electrophysiology

204 In Xenopus laevis oocytes, CTSB triggered alpha- and gammaE

205 nt receptor potential vanilloid 4 (TRPV4) in Xenopus laevis oocytes, HEK cells and nociceptive neuron

206 o have reduced general translation: immature Xenopus laevis oocytes, mouse ES cells, and the transiti

207 electrode voltage-clamp electrophysiology in Xenopus laevis oocytes, NS206 was observed to positively

208 he activation of cyclin-dependent kinases in Xenopus laevis oocytes, suggesting a role in cell cycle

209 When expressed in Xenopus laevis oocytes, two bacteriocyte amino acid tran

210 In Xenopus laevis oocytes, VviCCC targeted to the plasma me

211 In Xenopus laevis oocytes, we monitored proteolytic activat

212 ux experiments conducted on PfCRT-expressing Xenopus laevis oocytes, we show here that both wild-type

213 nsport and localization of mRNA molecules in Xenopus laevis oocytes, where active transport processes

214 line does not evoke ion current responses in Xenopus laevis oocytes, which heterologously express fun

215 plants and CYBDOM complementary RNA-injected Xenopus laevis oocytes.

216 and efflux of glutamate were investigated in Xenopus laevis oocytes.

217 water transport activity when coexpressed in Xenopus laevis oocytes.

218 facilitates the movement of B and water into Xenopus laevis oocytes.

219 ed by a biotinylation assay in cRNA-injected Xenopus laevis oocytes.

220 several types of cloned nAChRs expressed in Xenopus laevis oocytes.

221 ransport CQ when expressed at the surface of Xenopus laevis oocytes.

222 GABAAR were expressed in Xenopus laevis oocytes.

223 conformational changes of SUT1 expressed in Xenopus laevis oocytes.

224 current of human ASIC3 channels expressed in Xenopus laevis oocytes.

225 mbrane proteins and in vivo expression using Xenopus laevis oocytes.

226 duced when coexpressed with IDF1 in yeast or Xenopus laevis oocytes.

227 n, expressed in transfected HEK 293 cells or Xenopus laevis oocytes.

228 crose (Suc) after heterologous expression in Xenopus laevis oocytes.

229 ion of the chimera in the plasma membrane of Xenopus laevis oocytes.

230 to mediate ionic currents when expressed in Xenopus laevis oocytes.

231 eterologously expressed Cx30 hemichannels in Xenopus laevis oocytes.

232 nit subcellular distributions using mice and Xenopus laevis oocytes.

233 supported by electrophysiological studies in Xenopus laevis oocytes.

234 CELL HYDROGEN PEROXIDE-RESISTANT1 (GHR1) in Xenopus laevis oocytes.

235 rdiac Kv channel alpha subunits expressed in Xenopus laevis oocytes.

236 MB, and AO when expressed at the surface of Xenopus laevis oocytes.

237 s that localize to the vegetal cortex during Xenopus laevis oogenesis have been reported to function

238 nously relative to neighboring inputs in the Xenopus laevis optic tectum.

239 on of Hif-1alpha by antisense morpholinos in Xenopus laevis or zebrafish embryos led to complete inhi

240 c modification at amino acid position 131 in Xenopus laevis p60 decreases severing and microtubule-st

241 Expression of EGFP-rab11a fusion proteins in Xenopus laevis photoreceptors revealed that the nucleoti

242 ly this alpha-helix in stable cell lines and Xenopus laevis photoreceptors.

243 A long-standing model in the frog, Xenopus laevis, posits that MBT timing is controlled by

244 The larval head skeleton of the frog Xenopus laevis possesses a unique combination of ancestr

245 that neither full-length human PRMT5 nor the Xenopus laevis PRMT5 catalytic domain has appreciable pr

246 d biochemical analysis of both the human and Xenopus laevis RecQ4 cysteine-rich regions, and showed b

247 systems, axons of single receptor neurons of Xenopus laevis regularly bifurcate and project into more

248 otoreceptors using adeno-associated virus in Xenopus laevis rod photoreceptors using a transgene and

249 In ciliated cells, including bovine and Xenopus laevis rod photoreceptors, P/rds was robustly se

250 luorescent protein Dendra2 and expressing in Xenopus laevis rod photoreceptors.

251 uorescent protein, Dendra2, and expressed in Xenopus laevis rod photoreceptors.

252 dissected nerves following extraction of the Xenopus laevis sciatic nerve.

253 e (FAK) as proteolytic targets of calpain in Xenopus laevis spinal cord neurons both in vivo and in v

254 Down-regulating PTEN expression in Xenopus laevis spinal neurons selectively abolished grow

255 factors essential for assembly of the larger Xenopus laevis spindles: RanGTP, which functions in chro

256 salinity of 5); (ii) the African clawed toad Xenopus laevis (stages 24, 32 and 34 exposed to a salini

257 in cultured rat cortical neurons and in the Xenopus laevis tadpole visual system.

258 red filopodial motility in the intact albino Xenopus laevis tadpole.

259 ral dependence of MSI in the optic tectum of Xenopus laevis tadpoles is mediated by the network dynam

260 Here we use the optic tectum of awake Xenopus laevis tadpoles to determine how a neuron become

261 rodevelopmental disorders in which we expose Xenopus laevis tadpoles to valproic acid (VPA) during a

262 ty found in the olfactory system of mice and Xenopus laevis tadpoles, a discussion arose about the in

263 In swimming Xenopus laevis tadpoles, gaze stabilization is achieved

264 Using semi-intact preparations of Xenopus laevis tadpoles, we determined the cellular subs

265 rived from single tectal progenitor cells in Xenopus laevis tadpoles.

266 lease of endogenous D-serine in the brain of Xenopus laevis tadpoles.

267 isual system and visually-guided behavior in Xenopus laevis tadpoles.

268 azipropofol, a potent analog of propofol, in Xenopus laevis tadpoles.

269 velopment of the optic tectum in stage 46-49 Xenopus laevis tadpoles.

270 ctric activities during tail regeneration in Xenopus laevis tadpoles.

271 the beta-glomerulus in the olfactory bulb of Xenopus laevis tadpoles.

272 Here we show in Xenopus laevis that developmental activation of the chec

273 species are represented: the allotetraploid Xenopus laevis that is widely used for microinjection an

274 We have previously shown in oocytes from Xenopus laevis that the mRNA-binding protein Musashi tar

275 In the fully aquatic larvae of Xenopus laevis, the main olfactory epithelium specialize

276 s were analyzed in the basal hypothalamus of Xenopus laevis throughout development by means of combin

277 R) immunoreactive structures in the brain of Xenopus laevis throughout development, conducted with th

278 rs were analyzed in the alar hypothalamus of Xenopus laevis throughout development.

279 Here, the authors use an amputation assay in Xenopus laevis to demonstrate that removal of the brain

280 ate mapping using GFP-transgenic axolotl and Xenopus laevis to document the contribution of individua

281 In this study, we used transgenic Xenopus laevis to investigate the pathogenic mechanism c

282 Here we use an amputation assay in Xenopus laevis to show that absence of brain alters subs

283 dels, such as fathead minnow, zebrafish, and Xenopus laevis, to understand modes of action and to scr

284 We establish the domain organization of Xenopus laevis TPX2 and define the minimal TPX2 version

285 ally and functionally compared the amphibian Xenopus laevis type I (IFN) and III (IFN-lambda) IFNs in

286 In Xenopus laevis, ventrovegetal expression of PAF hyperact

287 al crest cell migration cell autonomously in Xenopus laevis via the Scar/WAVE complex.

288 In contrast, the frog (Xenopus laevis) vocal CPG contains a functionally unexpl

289 ression dynamics of nearly 4,000 proteins of Xenopus laevis was generated from fertilized egg to neur

290 Using the pronephric kidney of Xenopus laevis we discovered that the G-protein modulato

291 role of Tctp in retinal axon development in Xenopus laevis We report that Tctp deficiency results in

292 Using RNA-Seq in Xenopus laevis we screened for presumptive direct placod

293 xicanum), and the South African clawed toad (Xenopus laevis), we traced the origins of fin mesenchyme

294 g in vivo imaging in the developing brain of Xenopus laevis, we show that ATP release from damaged ce

295 /or glucose on SGLT1 expressed in oocytes of Xenopus laevis were investigated.

296 We report a new step in the fertilization in Xenopus laevis which has been found to involve activatio

297 ent vertebrate genome duplication is that in Xenopus laevis, which resulted from the hybridization of

298 r structure that closely resembles that from Xenopus laevis (xIKKbeta): an N-terminal kinase domain (

299 s to RNAs, we focused on a putative TUT from Xenopus laevis, XTUT7.

300 1274 peptides were identified from 50 ng of Xenopus laevis zygote homogenate, which is comparable wi