ライフサイエンスコーパス: Xenopus

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

2 entity in the secondarily aquatic frog genus Xenopus.

3 s pivotal for CNC induction and migration in Xenopus.

4 ur long-standing research program focused on Xenopus, a frog genus which has provided valuable insigh

5 ails in the tuatara and regenerated limbs in Xenopus adult frogs, which have a cartilaginous endoskel

6 This effect was not observed in Xenopus alphabetagamma-ENaC or human ENaC orthologs.

7 evolutionary relationship with humans, makes Xenopus an attractive model to uncover the mechanisms un

8 A comparison of Xenopus and Discoglossus reveals a relatively conserved

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

10 DAPLE, MPDZ is induced during neurulation in Xenopus and is required for apical constriction of neuro

11 DNA demethylation in non-mammalian species (Xenopus and medaka) despite their evolutionary divergenc

12 Here, we combine Xenopus and mouse genetic models to identify that the tr

13 expression patterns in the thalamus between Xenopus and mouse, however, the dynamic changes in gene

14 results in decreased levels of rfx3 mRNA in Xenopus, and exogenous rfx3 can rescue the Rnf20 depleti

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

16 XR1 depletion is perinatally lethal in mice, Xenopus, and zebrafish; however, the mechanisms driving

17 Here, we present an overview of Xenopus as a key model organism for regeneration researc

18 Here, using Xenopus as a model, we analyzed the post-translational r

19 positively regulates vegfa expression during Xenopus blood stem cell development through multiple tra

20 a stiffness gradient arose in the developing Xenopus brain, and retinal ganglion cell axons turned to

21 The frog, Xenopus, can achieve both scar-free healing and tissue r

22 Finally, Hspb1 knockdown in Xenopus causes eye/lens defects.

23 s species, their ratio is shared within each Xenopus clade providing information on species identity

24 In a Xenopus daam2-CRISPR knockout model, we demonstrate acti

25 We propose that Xenopus deltabetagamma-ENaC can serve as a model for inv

26 ma-subunit combinations, we demonstrate that Xenopus deltabetagamma-ENaC is profoundly activated by e

27 ue-specific splicing of fxr1 is required for Xenopus development and alters the disordered domain of

28 we discover SNX9 at specialized filopodia in Xenopus development and that SNX9 is an endogenous compo

29 lear size reductions that occur during early Xenopus development.

30 s of Cadherin3 (Cdh3; formerly C-cadherin in Xenopus) disrupts contact inhibition of locomotion.

31 Overexpressed Rspo2 inhibited elongation of Xenopus ectoderm explants and Erk1 activation in respons

32 Using Xenopus egg extract and in vitro reconstitution systems,

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

34 ysical model by titrating dynein activity in Xenopus egg extract spindles and quantifying the shape a

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

36 Using Xenopus egg extracts and biochemical reconstitution, we

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

38 the polarity-independent sliding observed in Xenopus egg extracts and in vitro experiments with purif

39 movement by dynein and actomyosin forces in Xenopus egg extracts and observed outward co-movement of

40 tion that occur at mitotic entry and exit in Xenopus egg extracts back to their origins.

41 orks, generated by encapsulating cytoplasmic Xenopus egg extracts into cell-sized 'water-in-oil' drop

42 Using Xenopus egg extracts that recapitulate replication-coupl

43 We used Xenopus egg extracts to recapitulate DNA replication inv

44 We use Xenopus egg extracts to study the nucleation and dynamic

45 te the signal that triggers CMG unloading in Xenopus egg extracts using single-molecule and ensemble

46 In Xenopus egg extracts, the collision of replication forks

47 Using Xenopus egg extracts, we previously showed that replicat

48 inks and determine their repair mechanism in Xenopus egg extracts.

49 developed an in vitro import system based on Xenopus egg extracts.

50 ns that regulate nuclear and spindle size in Xenopus egg extracts.

51 itosis might affect DNA replication, we used Xenopus egg extracts.

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

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

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

55 at reduces DNA damage in oxidative stress in Xenopus egg extracts.

56 Soluble extracts prepared from Xenopus eggs have been used extensively to study various

57 o complement TMTC3 rescue of gastrulation in Xenopus embryo development.

58 deo-rate 4D microscopic imaging of a beating Xenopus embryo heart at a rate of 30 volumes/s.

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

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

61 ion of a subset of mesodermal markers in the Xenopus embryo.

62 We have identified a case of regeneration in Xenopus embryonic aggregates that restores a mucociliate

63 Neil-deficiency in Xenopus embryos and differentiating mouse embryonic stem

64 Studies with Xenopus embryos and individuals with the congenital resp

65 of a set of innate immune response genes in Xenopus embryos and that splicing-blocking morpholinos l

66 ulated by Lef1 in the involuting mesoderm of Xenopus embryos at gastrula stages.

67 CRISPR/Cas9-mediated TBX4 deletion in Xenopus embryos confirmed its restricted role during leg

68 esis in human fetuses, and sox4 knockdown in Xenopus embryos diminishes brain and whole-body size.

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

70 Examination of global H2Bub1 level in Xenopus embryos shows that H2Bub1 is developmentally reg

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

72 phenotypes were further confirmed in MCCs of Xenopus embryos when CAMSAP3 expression was knocked down

73 t gene programs in human in vitro models and Xenopus embryos, and cause craniofacial defects.

74 In Xenopus embryos, Bicc1 binds and represses specific mate

75 re experiments, promoted axis duplication in Xenopus embryos, stimulated low-density lipoprotein rece

76 ll imaging of large-scale ZGA in whole-mount Xenopus embryos.

77 ed enzymatic activities and abnormal CNSs in Xenopus embryos.

78 tegrity of the epidermal layer in developing Xenopus embryos.

79 cancer cells and in the Spemann organizer of Xenopus embryos.

80 erior neural development and gastrulation in Xenopus embryos.

81 e germ plasm associated protein DDX4/VASA in Xenopus embyos.

82 chnique for cells (Xenopus oocyte), tissues (Xenopus epithelium and rat cornea), organs (Xenopus gill

83 In Xenopus explants, in the presence of Wnt5a, these recept

84 wn to unhook interstrand crosslinks (ICL) in Xenopus extracts, how NEIL3 participants in ICL repair i

85 Consistent with these Xenopus findings, PABPC1 remained associated with Musash

86 s in tubulin populations between two related Xenopus frog species influence microtubule dynamics and

87 Xenopus frog species possess a variety of egg and meioti

88 dynamics in embryonic mesendoderm cells from Xenopus gastrula.

89 e repressors to potential Wnt targets in the Xenopus gastrula.

90 we define the Sox17-governed endoderm GRN in Xenopus gastrulae.

91 During Xenopus gastrulation, Wnt and FGF signaling pathways coo

92 trives to integrate the body of knowledge on Xenopus genomics and biology together with the visualiza

93 (Xenopus epithelium and rat cornea), organs (Xenopus gills and mouse skin) and appendages (Xenopus ta

94 Recent work in Xenopus has identified an epidermal cell population crit

95 ration research and highlight how studies of Xenopus have led to new insights into the mechanisms gov

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

97 corrected by the addition of exogenous Xkid (Xenopus homolog of human Kid/KIF22), indicating a role f

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

99 We show that Xenopus Kinesin-14, XCTK2, and importin alpha/beta form

100 and phosphorylation of targeting protein for Xenopus Klp2 (TPX2) on serine 121.

101 In Xenopus, knockdown of rnf20 and rnf40 results in abnorma

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

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

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

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

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

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

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

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

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

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

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

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

114 Using Xenopus laevis egg extracts and biochemical reconstituti

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

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

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

118 In Xenopus laevis egg extracts, GWL-mediated phosphorylatio

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

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

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

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

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

124 During early Xenopus laevis embryogenesis both nuclear and cell volum

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

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

127 endent signaling modulates phenotypes during Xenopus laevis embryonic development.

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

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

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

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

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

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

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

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

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

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

138 illin contributes to epithelial mechanics in Xenopus laevis embryos.

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

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

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

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

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

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

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

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

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

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

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

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

151 ctivities measured through expression in the Xenopus laevis oocyte.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

169 eta2beta3 nAChRs heterologously expressed in Xenopus laevis oocytes.

170 us receptor when expressed heterologously in Xenopus laevis oocytes.

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

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

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

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

175 Using purified Xenopus laevis proteins we biochemically reconstitute br

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

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

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

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

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

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

182 Using the frog Xenopus laevis to expand gnathostome phylogenetic repres

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

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

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

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

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

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

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

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

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

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

193 ring early embryonic development in the frog Xenopus laevis.

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

195 been suggested to control eye development in Xenopus laevis.

196 so used mutagenesis and electrophysiology in Xenopus laevisoocytes to functionally map the determinan

197 establish that germ-line mutations in Kcp in Xenopus lead to valve defects and, ultimately, cardiac f

198 Moreover, in Xenopus, loss of Strap leads to impeded lineage differen

199 Here, we show that Xenopus M18BP1 localizes to centromeres during metaphase

200 Finally, we tested patient variants in our Xenopus model and found the majority to be loss-of-funct

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

202 teins reside on the plasma membranes of live Xenopus muscle cells.

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

204 In this study, we show that Xenopus nucleoplasmic extract (NPE) supports robust tran

205 In Xenopus oocyte assays TaNRT2.5 requires a partner protei

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

207 Using Xenopus oocyte meiosis as a well-established physiologic

208 ing factor Ascl1 is injected directly into a Xenopus oocyte nucleus which has been preloaded with a l

209 hen TRPV4 is heterologously expressed in the Xenopus oocyte or yeast.

210 We use injected Xenopus oocyte with two-electrode voltage clamp techniqu

211 describe how to use the technique for cells (Xenopus oocyte), tissues (Xenopus epithelium and rat cor

212 Here, using a Xenopus oocyte-based system to express and functionally

213 In conclusion, using Xenopus oocytes allowed us for the first time, to focus

214 Experiments in Xenopus oocytes and flies indicate that Hodor is a pH-se

215 cterized 7 dicarboxylic acid transporters in Xenopus oocytes and in Saccharomyces cerevisiae engineer

216 high suppression potency in mammalian cells, Xenopus oocytes and mice in vivo, producing PTC repair i

217 i function is required for the maturation of Xenopus oocytes and specifically for translational activ

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

219 and brain (alpha4beta2) nAChRs expressed in Xenopus oocytes by using a two-electrode voltage clamp a

220 All 3 mutants cloned in Xenopus oocytes caused an aberrant modulation of the mec

221 duration current-voltage (I-V) protocol with Xenopus oocytes expressing eGFP-tagged NBCe1-A, our grou

222 cell and single-channel electrophysiology of Xenopus oocytes expressing ENaC isoforms assembled from

223 ked the compounds for rapid activation using Xenopus oocytes expressing human alpha7 nAChR with a two

224 l, as hyperpolarization of CNGC19-expressing Xenopus oocytes in the presence of both cyclic adenosine

225 maging conducted in murine retinal cells and Xenopus oocytes indicated that cell swelling in the phys

226 mistry and functional expression analysis in Xenopus oocytes indicates that the capacity of this H(+)

227 Expression of GFP-OsPIP1;3 alone in Xenopus oocytes or rice protoplasts showed OsPIP1;3 misl

228 lectrode voltage clamp (TEVC) of transfected Xenopus oocytes revealed that the M2 S31N channel is ess

229 Electrophysiological characterization in Xenopus oocytes revealed that these derivatives differ i

230 kinases and because Nav1.7 had been shown in Xenopus oocytes to be affected by protein kinases C and

231 bunits and/or concatamers were injected into Xenopus oocytes to obtain receptors of defined subunit c

232 Expression of THIK-1 channels in Xenopus oocytes was used to compare wild-type channels w

233 Xenopus oocytes were injected with RNA encoding 5-HT(3)A

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

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

236 siological measurements in HEK-293 cells and Xenopus oocytes with pulldown experiments, we analyzed t

237 ethods, electrophysiological measurements in Xenopus oocytes, and fluorescent microscopy of mammalian

238 ionally following heterologous expression in Xenopus oocytes, and mediates both inward and outward tr

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

240 cal range activated TRPV4 in Muller glia and Xenopus oocytes, but required phospholipase A(2) (PLA(2)

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

242 arious heterologous cell expression systems (Xenopus oocytes, CHO cells, and rat atrial cardiomyocyte

243 ort function by expressing these proteins in Xenopus oocytes, Drip, Prip, and Eglp2 show significant

244 We observed that, in Xenopus oocytes, expression of Ggamma alone activated ho

245 Using ion-selective microelectrodes and Xenopus oocytes, here we studied Cl(-)/H(+) coupling pro

246 In Xenopus oocytes, the IRBITs substantially increase the a

247 In HeLa cells and Xenopus oocytes, we show that Cx43-G8V, Cx43-A44V and Cx

248 K(2P) channels, expressed heterologously in Xenopus oocytes, were measured by two-electrode voltage

249 tivities of human AQP1 channels expressed in Xenopus oocytes.

250 otassium ionic channels (Kv1.3) expressed in Xenopus oocytes.

251 ents when it was heterologously expressed in Xenopus oocytes.

252 tor PMA (phorbol 12-myristate 13-acetate) in Xenopus oocytes.

253 es, and (iv) recombinant NMDARs expressed in Xenopus oocytes.

254 and extending into the vegetal hemisphere of Xenopus oocytes.

255 odified with azide-reactive alkyne probes in Xenopus oocytes.

256 ing duct cell line, mirroring the results in Xenopus oocytes.

257 a1beta2gamma2 GABA(A) receptors expressed in Xenopus oocytes.

258 temeric ternary GABAA receptors expressed in Xenopus oocytes.

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

260 onal effects of IRBITs on NBCn1 and NBCn2 in Xenopus oocytes.

261 isoforms of NBCn1 and NBCn2 as expressed in Xenopus oocytes.

262 imulate NBCe1-A, heterologously expressed in Xenopus oocytes.

263 an alpha1beta3gamma2L receptors expressed in Xenopus oocytes.

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

265 thin vertebrate vocal communication systems, Xenopus provides insights that can inform social communi

266 Deficiency of Xenopus Ptprk increases Wnt signaling, leading to reduce

267 Cue stimulation of growing Xenopus retinal ganglion cell axons induces rapid dissoc

268 resent an analysis of all publicly available Xenopus RNA sequencing (RNA-seq) data in a reexamination

269 iously charged linkers and expressed them in Xenopus rod photoreceptors.

270 r transplantations from knockdown to control Xenopus showed that it is the Fzd3 expressed within the

271 In Xenopus skin, multiciliated cells (MCCs), which contain

272 Here we show that Xenopus sprouty2 is expressed in the optic vesicle at la

273 In vivo, studies in the Xenopus system showed that TFG is required for endogenou

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

275 In a small fraction of Xenopus tadpoles, a single retinal ganglion cell (RGC) a

276 ent and -incompetent developmental stages of Xenopus tadpoles.

277 enopus gills and mouse skin) and appendages (Xenopus tail), and provide recommendations on how to ada

278 Xenopus thus provides a vertebrate model in which to stu

279 Here, we use mouse and Xenopus to define the HH/Gli-dependent processes orchest

280 Here, we use in vivo imaging in Xenopus to show that inner dynein arm (IDA) and outer dy

281 present the cryo-EM structure of OTOP3 from Xenopus tropicalis (XtOTOP3) along with functional chara

282 ebrates, with two members in elephant shark, Xenopus tropicalis and Anolis lizard and three members i

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

284 hizosaccharomyces pombe, Xenopus laevis, and Xenopus tropicalis formed stable homotetramers, the mtSS

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

286 the egg cytoplasm between Xenopus laevis and Xenopus tropicalis have been shown to account for spindl

287 rod photoreceptors in retinas of developing Xenopus tropicalis heterozygous, but not homozygous muta

288 6-expressing NPCs isolated from regenerating Xenopus tropicalis tails.

289 ction of this gene, we used the diploid frog Xenopus tropicalis We discover that Dyrk1a is expressed

290 s musculus), and 2 frogs (Xenopus laevis and Xenopus tropicalis).

291 wo closely related frogs, Xenopus laevis and Xenopus tropicalis, have surprisingly different microtub

292 we show that the genetically tractable frog Xenopus tropicalis, paired with optical coherence tomogr

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

294 orecast CRISPR/Cas9 gene editing outcomes in Xenopus tropicalis, Xenopus laevis, and zebrafish.

295 in to specify initial competence in the frog Xenopus tropicalis.

296 nic effects of aquatic exposure of Silurana (Xenopus) tropicalis embryos to commercial NA extracts an

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

298 Results refute the current theory for Xenopus vocalization, cavitation, and favor instead soun

299 s CRISPR/Cas9 approaches to target CTNND1 in Xenopus, we identified a subset of phenotypes that can b

300 Using Xenopus, we identified defects in neural crest cells (NC