ライフサイエンスコーパス: Xenopus

1 sidue near the carboxyl terminus (Ser-883 in Xenopus).

2 ific mutations for human disease modeling in Xenopus.

3 ibuted over a 329 kbp wide genomic region in Xenopus.

4 ation on Dvl during CE in both the mouse and Xenopus.

5 allow efficient mutagenesis in zebrafish and Xenopus.

6 In the brain of larval and juvenile Xenopus, 5hmC is also detected in neurons, while ventric

7 similarity to human (93%), mouse (93%), and Xenopus (88%) UCN3.

8 C cells, are required for NC delamination in Xenopus and chick embryos, whereas they do not affect th

9 A comparison of Xenopus and Discoglossus reveals a relatively conserved

10 We have analyzed Xenopus and human MTBP to assess its role in DNA replica

11 ypes as well, including cartilage defects in Xenopus and misalignment of inner ear hair cells in mous

12 We show that KCNJ2 is expressed in Xenopus and mouse during the earliest stages of craniofa

13 g conditional gain-of-function approaches in Xenopus and mouse to maintain Gsc expression in the orga

14 comprehension of the diencephalic region of Xenopus and show that the organization of the pretectum

15 The similarities of CSF-c cells in chicken, Xenopus, and zebrafish suggest that these characteristic

16 organization of the CSF-c cells in chicken, Xenopus, and zebrafish, by analyzing the expression of s

17 to the cell membrane was inhibited by Gsc in Xenopus animal cap assays and key Wnt/PCP factors (RhoA,

18 The embryos and tadpoles of the frog Xenopus are increasingly important subjects for studies

19 We propose that Xenopus Balbiani bodies form by amyloid-like assembly of

20 n-like domain, is an abundant constituent of Xenopus Balbiani bodies.

21 acid-sensitive olfactory sensory neurons of Xenopus commonly function in a cAMP-independent manner.

22 The earliest event in Xenopus development is the dorsal accumulation of nuclea

23 ctivator for thyroid hormone receptor during Xenopus development.

24 lear size reductions that occur during early Xenopus development.

25 F-beta signaling in keratinocytes and during Xenopus development; however, potential involvement of P

26 Xenopus egg extracts and immunodepletion of Xenopus DNA2 also strongly inhibited resection.

27 We show that in Xenopus early ectoderm, the Prickle3/Vangl2 complex was

28 the Tetrahymena group I ribozyme embedded in Xenopus egg extract demonstrate the ability of M2-seq to

29 Using Xenopus egg extract, we show that direct, cell-cycle-reg

30 Depletion of PP1 impairs NHEJ in both Xenopus egg extracts and human cells.

31 Here, using Xenopus egg extracts and human somatic cells, we show th

32 odel 5' adducts were efficiently resected in Xenopus egg extracts and immunodepletion of Xenopus DNA2

33 is recruited to a DSB-mimicking substrate in Xenopus egg extracts and sites of laser microirradiation

34 optical reconstruction microscopy (STORM) to Xenopus egg extracts and tissue culture cells, we report

35 ein binding assays and functional studies in Xenopus egg extracts to show that TopBP1 makes a direct

36 ere, we use repair of a site-specific ICL in Xenopus egg extracts to study the mechanism of lesion by

37 otubule assembly in tissue culture cells and Xenopus egg extracts using two-photon microscopy with FL

38 id-based DSB templates that were repaired in Xenopus egg extracts via the canonical, Ku-dependent NHE

39 Using Xenopus egg extracts, we describe here a replication-cou

40 Using a proteomic screen in Xenopus egg extracts, we identified factors that are enr

41 icating nuclei from transcriptionally silent Xenopus egg extracts, we identified numerous actin regul

42 Depletion of MTBP from Xenopus egg extracts, which also removes Treslin, abolis

43 R pathway in response to oxidative stress in Xenopus egg extracts.

44 ndles at interaction zones between asters in Xenopus egg extracts.

45 this hypothesis with model DNA substrates in Xenopus egg extracts.

46 domain are defective for DNA replication in Xenopus egg extracts.

47 pindle localization, and spindle assembly in Xenopus egg extracts.

48 not translation, leads to spindle defects in Xenopus egg extracts.

49 ve psoralen- and abasic site-induced ICLs in Xenopus egg extracts.

50 ors in kinetochore-microtubule attachment in Xenopus egg extracts.

51 we have studied neuronal development in the Xenopus embryo in the absence of n1-src, while preservin

52 The ectoderm of the Xenopus embryo is permeated by a network of channels tha

53 tl4 is expressed in the Spemann organizer of Xenopus embryos and acts as a Wnt antagonist to promote

54 Similarly, depletion of CCDC11 in Xenopus embryos causes defective assembly and motility o

55 ally, we analyze mRNA expression patterns in Xenopus embryos for each TACC protein and observe neural

56 ansiently inhibits neural crest migration in Xenopus embryos in a Snail1-dependent manner, indicating

57 Exposure of Xenopus embryos to AChE-inhibiting chemicals results in

58 In Xenopus embryos, knockdown of Rusc1 or overexpression of

59 When Foxn4 activity is inhibited in Xenopus embryos, MCCs show transient ciliogenesis defect

60 In Xenopus embryos, the three TBP family factors are all es

61 When applied to Xenopus embryos, this system enables blue light-dependen

62 e and extent of injury caused to the skin of Xenopus embryos.

63 Here we identified the transcriptomes of Xenopus foregut and hindgut progenitors, which are conse

64 ons, and showed by NMR spectroscopy that the Xenopus fragment indeed assumes the canonical Zn knuckle

65 rtebrate homologue of Drosophila Prickle, in Xenopus gastrocoel roof plate (GRP).

66 for morphogenesis and papc expression during Xenopus gastrulation.

67 T imaging planes to visualize and quantitate Xenopus heart and facial structures establishing normati

68 y well understood, but neither zebrafish nor Xenopus is electroreceptive and our molecular understand

69 Finally, overexpression of human or Xenopus Ki-67 induced ectopic heterochromatin formation.

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

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

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

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

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

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

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

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

78 The Xenopus laevis APE2 (apurinic/apyrimidinic endonuclease

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

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

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

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

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

84 Xenopus laevis craniofacial development is a good system

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

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

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

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

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

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

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

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

93 During early Xenopus laevis embryogenesis both nuclear and cell volum

94 endent signaling modulates phenotypes during Xenopus laevis embryonic development.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

137 eterologously expressed Cx30 hemichannels in Xenopus laevis oocytes.

138 nit subcellular distributions using mice and Xenopus laevis oocytes.

139 supported by electrophysiological studies in Xenopus laevis oocytes.

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

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

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

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

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

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

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

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

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

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

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

151 ctric activities during tail regeneration in Xenopus laevis tadpoles.

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

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

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

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

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

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

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

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

160 1274 peptides were identified from 50 ng of Xenopus laevis zygote homogenate, which is comparable wi

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

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

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

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

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

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

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

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

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

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

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

172 role of TRPM6 during early embryogenesis in Xenopus laevis.

173 been suggested to control eye development in Xenopus laevis.

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

175 We demonstrate that Xenopus M18BP1 binds CENP-A nucleosomes using a motif th

176 Xenopus mesendoderm cells migrate collectively along a f

177 ng intestinal remodeling during T3-dependent Xenopus metamorphosis as a model for organ maturation an

178 If these findings in the Xenopus model extend to P. falciparum in vivo, our data

179 Here, we analyzed a Xenopus model of conversion of melanocytes to a metastat

180 maternal-to-zygotic transition in zebrafish, Xenopus, mouse, and Drosophila, and gene expression duri

181 In this study, working with Xenopus, mouse, and human systems, we identified a cis e

182 In Xenopus multiciliated cells, zeta-tubulin is a component

183 ions and promotes adhesion to fibronectin in Xenopus neural crest, a highly migratory embryonic cell

184 Using the Xenopus nuclear extract system, here we show that the Dn

185 Misexpression in Xenopus of KCNJ2 carrying ATS-associated mutations cause

186 vestigation of the anatomical changes of the Xenopus olfactory organ during metamorphosis.

187 e the structural and cellular changes of the Xenopus olfactory organ during metamorphosis.

188 Using the Xenopus oocyte assay, we found an absence of GABA-A rece

189 In this study we utilized the Xenopus oocyte expression system to shed light on how CF

190 copa monnieri Screening was conducted in the Xenopus oocyte expression system, using quantitative swe

191 Lysosome acidification also occurs during Xenopus oocyte maturation; thus, a lysosomal switch that

192 Kv1.3 disrupts the channel expression on the Xenopus oocyte membrane, suggesting a potential role as

193 luding TREK-1, TREK-2, TRAAK; NaV1.5) in the Xenopus oocyte system.

194 Functional studies using a Xenopus oocyte two-microelectrode voltage clamp system r

195 ned the outward currents of TRPV4-expressing Xenopus oocyte upon depolarizations as well as phenotype

196 co (odorant receptor co-receptor subunit) in Xenopus oocytes and assayed by two-electrode voltage cla

197 erin channels comprising MEC-4 and MEC-10 in Xenopus oocytes and examined their response to laminar s

198 ium channels (ENaC) in H441 and expressed in Xenopus oocytes and exposed mice in vivo.

199 Human CFTR was heterologously expressed in Xenopus oocytes and its activity was electrophysiologica

200 We expressed Kv4.2 channels in Xenopus oocytes and measured the onset of low-voltage in

201 Functional studies of mutant NaPi-IIa in Xenopus oocytes and opossum kidney (OK) cells demonstrat

202 Using heterologous expression in Xenopus oocytes and the engineered cysteine-less hCNT3 p

203 Here, we used Xenopus oocytes as a simple system to study LRRC8 protei

204 ese data indicate that H2S activates CFTR in Xenopus oocytes by inhibiting phosphodiesterase activity

205 hat increased SGLT2 activity in RNA-injected Xenopus oocytes by two orders of magnitude.

206 over, the purified alpha7nAChR injected into Xenopus oocytes can be activated by acetylcholine, choli

207 Assay on expression in Xenopus oocytes demonstrated that SlPIP2s protein displa

208 Here we observe that AQP4-expressing Xenopus oocytes display a reflection coefficient <1 for

209 cholesterol enrichment were also observed in Xenopus oocytes expressing GIRK2 channels, the primary G

210 they inhibited uptake of (14)C-glucose into Xenopus oocytes expressing the human glucose transporter

211 g an endocytosis-defective Fpn mutant (K8R), Xenopus oocytes expressing wild-type or K8R Fpn, and mat

212 Expressing SjAQP in Xenopus oocytes facilitated the permeation of water, gly

213 Utilizing inside-out patches from Xenopus oocytes heterologously expressing NKA, we observ

214 We used a voltage-clamp assay on Xenopus oocytes injected with the RNAs that encode the a

215 orter in vivo However, functional studies in Xenopus oocytes revealed that MCT12 transports creatine

216 a1beta1epsilondelta AChRs (epsilon-AChRs) in Xenopus oocytes revealed that PEA selectively affected t

217 ity of mosquito sodium channels expressed in Xenopus oocytes to both type I and type II pyrethroids.

218 y) renal cell lines and electrophysiology on Xenopus oocytes to characterize the mutant transporters

219 Functional Nav-LBT channels expressed in Xenopus oocytes were voltage-clamped, and distinct LRET

220 he channel, mouse ENaCs were co-expressed in Xenopus oocytes with each of the 23 mouse DHHCs.

221 method for CRISPR-mediated genome editing in Xenopus oocytes with homology-directed repair (HDR) that

222 AQP0 were performed on protein expressed in Xenopus oocytes, and the results may therefore also refl

223 The mutants were expressed in Xenopus oocytes, and the unitary water and urea permeabi

224 displayed robust repair capacity, including Xenopus oocytes, Chlamydomonas, and Stentor coeruleus Al

225 When PON-2 was co-expressed with ENaC in Xenopus oocytes, ENaC activity was reduced, reflecting a

226 cid membrane protein that, when expressed in Xenopus oocytes, functions as an Na-Cl cotransporter wit

227 that reconstitution of NMDA-gated current in Xenopus oocytes, or C. elegans muscle cells, depends on

228 C remodeling and glycogen uptake in maturing Xenopus oocytes, suggesting that these processes are evo

229 ecule Na(+) /HCO3(-) cotransport activity in Xenopus oocytes, suggesting that they are suitable candi

230 In Xenopus oocytes, the interaction of AtPP2CA with "phosph

231 d-type and chimeric Kv channels expressed in Xenopus oocytes, using the voltage-clamp technique.

232 n coexpression of tandem PIP2-PIP1 dimers in Xenopus oocytes, we can address, for the first time to o

233 Using heterologous expression in Xenopus oocytes, we demonstrate that NAM is a soluble ag

234 When expressed in Xenopus oocytes, we find that the R510H and Q913R-mutant

235 le membranes from selected ALS patients into Xenopus oocytes, we show that PEA reduces the desensitiz

236 notropic glutamate receptor AMPA subunits in Xenopus oocytes, we show that this effect is through dir

237 mediates a highly electrogenic transport in Xenopus oocytes.

238 nt channels were heterologously expressed in Xenopus oocytes.

239 temeric ternary GABAA receptors expressed in Xenopus oocytes.

240 ine flux measurements in mutant RNA-injected Xenopus oocytes.

241 (and unmodified controls) were expressed in Xenopus oocytes.

242 active muscle using human ClC-1 expressed in Xenopus oocytes.

243 and 5-HT3A serotonin receptors expressed in Xenopus oocytes.

244 s of embryonic muscle receptors expressed in Xenopus oocytes.

245 ally with GORK and inhibits GORK activity in Xenopus oocytes.

246 d TREK-1 and TREK-2 subunits, coexpressed in Xenopus oocytes.

247 ne for fluorophore labeling, as expressed in Xenopus oocytes.

248 ast two different ways and expressed them in Xenopus oocytes.

249 lters the gating of human ClC-1 expressed in Xenopus oocytes.

250 D)-, and (alpha3beta4)2alpha5(398N)-nAChR in Xenopus oocytes.

251 d SLC26A6-mediated Cl(-)-oxalate exchange in Xenopus oocytes.

252 fluence the timescale of RNA localization in Xenopus oocytes.

253 o reduced ENaC activity when co-expressed in Xenopus oocytes.

254 melanopsin (OPN4), encoded by two genes: the Xenopus (Opn4x) and mammalian (Opn4m) orthologs.

255 Here we tested whether FMRP knockdown in Xenopus optic tectum affects local protein synthesis in

256 In Xenopus patterning, loss of the 11-bp negative regulator

257 MEK1 was required to make Xenopus pluripotent cells competent to respond to all ce

258 ain protein Lhx9 is transiently expressed in Xenopus proepicardial cells and is essential for the pos

259 3749 peptides were identified from 50 ng of Xenopus protein using the online sample preparation meth

260 In both the human and Xenopus proteins, the presence of this region strongly e

261 hat are not fully represented in the beloved Xenopus resource, Nieuwkoop and Faber's classic Normal T

262 Knockdown of PWWP2A in Xenopus results in severe cranial facial defects, arisin

263 rate stiffness determined growth patterns of Xenopus retinal ganglion cell axons.

264 is of progenitor domains in the pretectum of Xenopus revealed three molecularly distinct anteroposter

265 lticilin required for MCC differentiation in Xenopus skin.

266 Here, we show in Xenopus spinal neurons that RF is reduced in rapidly mig

267 Using the Xenopus system, we show that RARbeta2 plays a specific r

268 l model of the development of neurons in the Xenopus tadpole spinal cord to include interactions betw

269 evels in the developing visual system of the Xenopus tadpole.

270 Using Xenopus tadpoles as an experimental system to investigat

271 These findings were corroborated in Xenopus tadpoles by EFhd2 knockdown.

272 Xenopus tadpoles exhibit a visual avoidance behavior tha

273 ing a dot avoidance assay in freely swimming Xenopus tadpoles, we demonstrate that CB1R activation ma

274 mechanosensory inputs in the optic tectum of Xenopus tadpoles.

275 olling locomotory swimming in post-embryonic Xenopus tadpoles.

276 s that include start codons of zebrafish and Xenopus Tgs and experimentally proved that these are ful

277 Here, we show in mouse and Xenopus that the mechanisms that drive the curvature of

278 Similar rings are observed in Xenopus tissue culture cells at a lower frequency but ar

279 tified that ZNF143, the human homolog of the Xenopus transcriptional activator STAF, specifically bin

280 ethylation profiles in developing zebrafish, Xenopus tropicalis and mice and suggests roles for Tet p

281 s during the phylotypic period in zebrafish, Xenopus tropicalis and mouse.

282 Using the T3-dependent metamorphosis in Xenopus tropicalis as a model, we show here that high le

283 g the predicted transcription start sites in Xenopus tropicalis for genome wide identification of TR

284 Here we use a library of Xenopus tropicalis genomic sequences in bacterial artifi

285 Here, we coupled the frog Xenopus tropicalis with Optical Coherence Tomography (OC

286 Tg coding sequence from western clawed frog (Xenopus tropicalis) and zebrafish (Danio rerio).

287 rc in the early development of the amphibian Xenopus tropicalis, and found that n1-src expression is

288 pseudo-tetraploid Xenopus laevis and diploid Xenopus tropicalis, as a model for postembryonic develop

289 We show that in Xenopus tropicalis, these processes are connected to the

290 Tested using Xenopus tropicalis, we show that founders containing tra

291 The expression of Xenopus TRPM6 (XTRPM6) is elevated at the onset of gastr

292 well-studied systems such as Drosophila and Xenopus use maternally inherited germ determinants to sp

293 mily of cell signaling ligands that includes Xenopus Vg1 and mammalian Gdf1/3.

294 Using Xenopus we show that Cp110 inhibits cilia formation at h

295 In Xenopus, we have been studying the gene regulatory netwo

296 alyses demonstrate analogous interactions in Xenopus, which are further supported by residue-swapping

297 erived from the cleavage motifs of Wnt3a and Xenopus wnt8 (Xwnt8).

298 Indeed, in Xenopus, zebrafish, and lamprey Tgs, key residues, inclu

299 Both the human and Xenopus Zn knuckles bind to a variety of nucleic acid su

300 The cleavage furrow in Xenopus zygotes is positioned by two large microtubule a