ライフサイエンスコーパス: Xenopus laevis

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

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

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

4 role of TRPM6 during early embryogenesis in Xenopus laevis.

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

6 developmentally regulated retrotransposon in Xenopus laevis.

7 nstructive factor during brain patterning in Xenopus laevis.

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

9 ryonic expression and morphant phenotypes in Xenopus laevis.

10 lar development throughout the life cycle of Xenopus laevis.

11 ring early embryonic development in the frog Xenopus laevis.

12 ent in cell-cycle-associated proteins within Xenopus laevis.

13 been suggested to control eye development in Xenopus laevis.

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

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

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

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

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

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

20 dy, we have analyzed in the anuran amphibian Xenopus laevis (an anamniote vertebrate), through larval

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

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

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

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

25 ate post-anaphase microtubule (MT) asters in Xenopus laevis and other large eggs remains unclear.

26 ciated proteins in the egg cytoplasm between Xenopus laevis and Xenopus tropicalis have been shown to

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

28 ofa), the mouse (Mus musculus), and 2 frogs (Xenopus laevis and Xenopus tropicalis).

29 ins purified from two closely related frogs, Xenopus laevis and Xenopus tropicalis, have surprisingly

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

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

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

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

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

35 Bs and those from Schizosaccharomyces pombe, Xenopus laevis, and Xenopus tropicalis formed stable hom

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

37 gene editing outcomes in Xenopus tropicalis, Xenopus laevis, and zebrafish.

38 The Xenopus laevis APE2 (apurinic/apyrimidinic endonuclease

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

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

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

42 Using Xenopus laevis as a model, we document that zinc reversi

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 We thus assessed heart regeneration in Xenopus laevis before, during, and after TH-dependent me

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

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

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

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

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

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

52 Xenopus laevis craniofacial development is a good system

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

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

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

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

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

58 transient protein interactions in cell-free Xenopus laevis egg extract identified the dimeric histon

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

60 that combines microfluidics, hydrogels, and Xenopus laevis egg extract to investigate the mechanics

61 Here, we use Xenopus laevis egg extract to investigate the role of th

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

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

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

65 Using Xenopus laevis egg extracts and biochemical reconstituti

66 We showed in both Xenopus laevis egg extracts and mammalian cells that a c

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 Here, we demonstrate biochemically using Xenopus laevis egg extracts that the Cdk1-counteracting

71 We used Xenopus laevis egg extracts to show that homogenized int

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

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

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

75 In Xenopus laevis egg extracts, GWL-mediated phosphorylatio

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

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

78 The large length scale of Xenopus laevis eggs facilitates observation of bulk cyto

79 ere, we used cell-free extracts derived from Xenopus laevis eggs to recapitulate different phases of

80 In cell-free extracts of Xenopus laevis eggs, we find that nuclei define such pac

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

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

83 for improved tracking of calcium flux in the Xenopus laevis embryo, lowering the barrier for in vivo

84 Using the Xenopus laevis embryo, we show that Dishevelled (Dvl), a

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

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

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

88 During early Xenopus laevis embryogenesis both nuclear and cell volum

89 Early Xenopus laevis embryogenesis is a robust system for inve

90 ctions in both cell and nuclear sizes during Xenopus laevis embryogenesis provide a robust scaling sy

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

92 ing analysis of >1600 proteins from ~130 mum Xenopus laevis embryonic cells containing <6 nL of cytop

93 endent signaling modulates phenotypes during Xenopus laevis embryonic development.

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

95 d associated with mitotic spindles in intact Xenopus laevis embryonic epithelia.

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

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

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

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

100 Here, we show that growing Xenopus laevis embryos at cold temperatures results in a

101 Single blastomeres from Xenopus laevis embryos at the 50-cell stage (~200 ng yol

102 The knockdown of the Tmtcs in Xenopus laevis embryos caused a delay in gastrulation th

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

104 dermal cells and tissues from gastrula stage Xenopus laevis embryos demonstrate that deletion of extr

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

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

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

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

109 xpressed specifically in the neural plate of Xenopus laevis embryos to trigger a G protein signaling

110 pic Barrier Assay (ZnUMBA), which we used in Xenopus laevis embryos to visualize short-lived, local b

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

112 Here, we observed toxicity in early Xenopus laevis embryos when using such a conventional op

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

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

115 cance was further demonstrated in vivo using Xenopus laevis embryos.

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

117 illin contributes to epithelial mechanics in Xenopus laevis embryos.

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

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

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

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

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

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

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

125 n content from individual cells in a 16-cell Xenopus laevis (frog) embryo.

126 ng distinct between the limbs of chicken and Xenopus laevis frogs.

127 y visualize nucleation of a MT from purified Xenopus laevis gamma-TuRC.

128 ion of all 15 formins in epithelial cells of Xenopus laevis gastrula-stage embryos.

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

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

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

132 We report that the recombinant Xenopus laevis H3-H4 tetramer is an oxidoreductase enzym

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

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

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

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

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

138 brain slices, and Caenorhabditis elegans and Xenopus laevis in vivo.

139 FP), hSGLT2-YFP and hSGLT3-YFP in oocytes of Xenopus laevis, injected hRS1-Reg(S20E), QEP, DFMO, and/

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

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

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

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

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

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

146 In this manuscript, we took advantage of Xenopus laevis models of both sexes expressing wild-type

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

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

149 the other DNA glycosylases NEIL1 and NEIL2, Xenopus laevis NEIL3 C terminus has two highly conserved

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

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

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

153 By employing a Xenopus laevis oocyte kinase activity assay, we demonstr

154 Functional analysis was performed using a Xenopus laevis oocyte model system.

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

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

157 ctivities measured through expression in the Xenopus laevis oocyte.

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

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

160 PIP2;1 in the plant and upon coexpression in Xenopus laevis oocytes and activated AtPIP2;1, preferent

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

162 od pressure values"Functional experiments in Xenopus laevis oocytes and HEK293T cells demonstrated th

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

164 localize to the tonoplast; when expressed in Xenopus laevis oocytes and Nicotiana benthamiana cells,

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

166 electrode voltage clamp electrophysiology in Xenopus laevis oocytes and radioligand displacement assa

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

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

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

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

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

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

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

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

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

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

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

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

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

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

181 Using Xenopus laevis oocytes expressing NBCe1 variants, we hav

182 spinal cord neurons, spinal cord slice, and Xenopus laevis oocytes expressing recombinant human glyc

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

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

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

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

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

188 Functional analysis of Xenopus laevis oocytes injected with PIC30 cRNA demonstr

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

190 cted in the parasite and in PfCRT-expressing Xenopus laevis oocytes linked phosphomimetic substitutio

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

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

193 ologous expression of the mutant proteins in Xenopus laevis oocytes to measure TREK-1 current.

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

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

196 heteromeric 5-HT(3AB) receptors expressed in Xenopus laevis oocytes using two-electrode voltage clamp

197 died their effects on GABA(A)Rs expressed in Xenopus laevis oocytes using two-microelectrode voltage

198 es including placental villous fragments and Xenopus laevis oocytes were used to investigate UDCA tra

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

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

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

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

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

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

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

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

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

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

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

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

211 ecific glycosylation sites were expressed in Xenopus laevis oocytes, HEK-293T cells, and HeLa cells.

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

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

214 able to interact with the cell membranes of Xenopus laevis oocytes, to alter their electrical membra

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

216 by endogenous TMEM16A channels expressed in Xenopus laevis oocytes, using the inside-out configurati

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

218 In Xenopus laevis oocytes, we monitored proteolytic activat

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

220 ce, and analysis of EAG currents recorded in Xenopus laevis oocytes, we show that a small molecule ch

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

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

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

224 eterologously expressed Cx30 hemichannels in Xenopus laevis oocytes.

225 nit subcellular distributions using mice and Xenopus laevis oocytes.

226 supported by electrophysiological studies in Xenopus laevis oocytes.

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

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

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

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

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

232 us receptor when expressed heterologously in Xenopus laevis oocytes.

233 water transport activity when coexpressed in Xenopus laevis oocytes.

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

235 e shown to reduce co-transporter function in Xenopus laevis oocytes.

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

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

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

239 GABAAR were expressed in Xenopus laevis oocytes.

240 eta2beta3 nAChRs heterologously expressed in Xenopus laevis oocytes.

241 ated MCT6 substrate/inhibitor specificity in Xenopus laevis oocytes; however, these data remain limit

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

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

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

245 We tested this idea in Xenopus laevis photoreceptors, and found that transgenic

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

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

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

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

250 Using purified Xenopus laevis proteins we biochemically reconstitute br

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

252 In vitro Xenopus laevis replication systems showed that OGRE/G4 s

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

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

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

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

257 Smn from Danio rerio and Xenopus laevis significantly prevent disease, whereas Sm

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

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

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

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

262 Without food, Xenopus laevis tadpoles enter a period of stasis during

263 Unlike mammals, Xenopus laevis tadpoles have a high regenerative potenti

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

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

266 y we examined the ability of pre-metamorphic Xenopus laevis tadpoles to self-correct malformed cranio

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

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

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

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

271 ctric activities during tail regeneration in Xenopus laevis tadpoles.

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

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

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

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

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

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

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

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 Using the frog Xenopus laevis to expand gnathostome phylogenetic repres

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

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

284 d an infection model system in the amphibian Xenopus laevis to study host responses to M. marinum at

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

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

287 t in ENaC isoforms of the aquatic pipid frog Xenopus laevis Using whole-cell and single-channel elect

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

289 In Xenopus laevis, vocal signals differ between the sexes,

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

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 in Saccharomyces cerevisiae, C. elegans, and Xenopus laevis, we present studies identifying a novel d

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

296 Here, using Xenopus laevis, we show that SSRP1 stimulates replicatio

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

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

299 revisiae Kar3, Saccharomyces pombe Pkl1, and Xenopus laevis XCTK2) are characterized by a C-terminal

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