ライフサイエンスコーパス: Xenopus oocyte

1 the influx of carbon dioxide (CO(2)) into a Xenopus oocyte.

2 at a desired distance from the membrane of a Xenopus oocyte.

3 analysis of glutamate receptor responses in Xenopus oocytes.

4 nt channels were heterologously expressed in Xenopus oocytes.

5 ue proteins between nucleus and cytoplasm of Xenopus oocytes.

6 fluence the timescale of RNA localization in Xenopus oocytes.

7 nd the mutants were functionally examined in Xenopus oocytes.

8 ng both human (h) and mouse (m) subunits, in Xenopus oocytes.

9 tructs with the alpha5 subunit, expressed in Xenopus oocytes.

10 g progesterone-induced meiotic maturation of Xenopus oocytes.

11 g of somatic nuclei after transplantation to Xenopus oocytes.

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

13 ngth of S4 from engineered VSDs expressed in Xenopus oocytes.

14 r-mediated ionic currents in SERT-expressing Xenopus oocytes.

15 ivity of MCT1/4, heterologously expressed in Xenopus oocytes.

16 and in ouabain-resistant pumps expressed in Xenopus oocytes.

17 r (FRET) and recording of Cav1.2 currents in Xenopus oocytes.

18 ponses to injections of Abeta oligomers into Xenopus oocytes.

19 variants, DmNav9-1, DmNav22, and DmNav26, in Xenopus oocytes.

20 nt potentiation of NMDA receptor currents in Xenopus oocytes.

21 he human cardiac Na(V) channel, Na(V)1.5, in Xenopus oocytes.

22 mediates a highly electrogenic transport in Xenopus oocytes.

23 ed transport of RNA to the vegetal cortex in Xenopus oocytes.

24 a gliclazide with KATP channels expressed in Xenopus oocytes.

25 not impact on sugar transport as assayed in Xenopus oocytes.

26 various insect sodium channels expressed in Xenopus oocytes.

27 ant alpha1beta2gamma2 GABA(A)Rs expressed in Xenopus oocytes.

28 2;4 functional properties were reassessed in Xenopus oocytes.

29 temeric ternary GABAA receptors expressed in Xenopus oocytes.

30 essed in yeast (Saccharomyces cerevisiae) or Xenopus oocytes.

31 d following expression of SLC2A1 variants in Xenopus oocytes.

32 or for the TCS in maternal mRNAs in immature Xenopus oocytes.

33 the thermal sensitivity of CFTR channels in Xenopus oocytes.

34 nt populations of alpha3beta4alpha5 nAChR in Xenopus oocytes.

35 Slo2.1 channels heterologously expressed in Xenopus oocytes.

36 est at metaphases I and II in Drosophila and Xenopus oocytes.

37 nt channels were heterologously expressed in Xenopus oocytes.

38 nd pharmacology in ion channels expressed in Xenopus oocytes.

39 orters permeable to Ca(2+) when expressed in Xenopus oocytes.

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

41 wild-type AQP1 and the mutants expressed in Xenopus oocytes.

42 or all-mouse alpha6beta4*-nAChR expressed in Xenopus oocytes.

43 f K(o)(+) sensitivity of Kir4.2 expressed in Xenopus oocytes.

44 tutive kinase activity to promote M phase in Xenopus oocytes.

45 ver, SecA-liposomes elicit ionic currents in Xenopus oocytes.

46 ional consequences in receptors expressed in Xenopus oocytes.

47 inG, form functional gap junctions in paired Xenopus oocytes.

48 tiates recombinant NMDA receptor currents in Xenopus oocytes.

49 ock rodent Na(V)1.1 through 1.8 expressed in Xenopus oocytes.

50 s very poorly if at all after injection into Xenopus oocytes.

51 ng the resulting receptors when expressed in Xenopus oocytes.

52 rminus converted Aqp0b to a water channel in Xenopus oocytes.

53 f Cl(-) on the activity of ENaC expressed in Xenopus oocytes.

54 Cx46 hemichannel currents recorded in single Xenopus oocytes.

55 determined using RDL receptors expressed in Xenopus oocytes.

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

57 alyses of Na(+) self-inhibition responses in Xenopus oocytes.

58 ei into the germinal vesicle (GV) of growing Xenopus oocytes.

59 effect of full-length WNK1 when expressed in Xenopus oocytes.

60 pseudouridine leads to a splicing defect in Xenopus oocytes.

61 pe inactivation) heterologously expressed in Xenopus oocytes.

62 dence of fast inactivation when expressed in Xenopus oocytes.

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

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

65 s of embryonic muscle receptors expressed in Xenopus oocytes.

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

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

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

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

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

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

72 -electrode voltage clamp after expression in Xenopus oocytes.

73 93 and 82%, respectively, when expressed in Xenopus oocytes.

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

75 the mitochondria, and p38/JNK activation in Xenopus oocytes.

76 rdly rectifying potassium (GIRK) channels in Xenopus oocytes.

77 ities of GIRK1/2 and Gbetagamma expressed in Xenopus oocytes.

78 abditis elegans homomeric ACR-20 receptor in Xenopus oocytes.

79 ompounds on recombinant 5-HT3Rs expressed in Xenopus oocytes.

80 ion, functional GABA(A) Rs were expressed in Xenopus oocytes after microinjection with membrane fract

81 In Xenopus oocytes, all of the disease-associated mutant ch

82 alpha6/alpha3beta2beta3 nAChRs expressed in Xenopus oocytes (alpha6/alpha3 is a subunit chimera that

83 yeast S. cerevisiae, approximately 1000 from Xenopus oocytes and >1050 from human cells.

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

85 s measured by two-electrode voltage clamp in Xenopus oocytes and cleaved ASIC1 expressed in oocytes o

86 USP8 increased ENaC current in Xenopus oocytes and collecting duct epithelia and enhanc

87 burst of MPM-2 reactivity can be induced in Xenopus oocytes and egg extracts in the absence of MAPK

88 erizing the mitotic MPM-2 epitope kinases in Xenopus oocytes and egg extracts, we have determined tha

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

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

91 Kv1.2 with the hERG channel for function in Xenopus oocytes and for overexpression in Pichia.

92 xt we examined channel surface expression in Xenopus oocytes and HeLa cells using a chemiluminescence

93 xpressed with the cardiac alpha1c subunit in Xenopus oocytes and human embryonic kidney (HEK) 293 cel

94 Third, electrophysiology in Xenopus oocytes and human embryonic kidney cell line 293

95 PCSK9 reduced ENaC current in Xenopus oocytes and in epithelia.

96 n of these proteins (and mutants thereof) in Xenopus oocytes and in mammalian cell lines.

97 diated increases of intracellular calcium in Xenopus oocytes and in neurons, and the latter is also d

98 nd Panx2 formed active homomeric channels in Xenopus oocytes and in vitro vesicle assays.

99 a functional water channel when expressed in Xenopus oocytes and in yeast, whereas Aqp0b was not.

100 racellular Cu(2+) on human ENaC expressed in Xenopus oocytes and investigated the structural basis fo

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

102 In particular, in both Xenopus oocytes and mammalian Chinese hamster ovary cell

103 dulation, upregulates the Kv7.2/3 current in Xenopus oocytes and mammalian human embryonic kidney HEK

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

105 We expressed ROMK2 channels in Xenopus oocytes and measured unitary currents in the ins

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

107 Using 2-microelectrode experiments on Xenopus oocytes and patch-clamp electrophysiology on HEK

108 we expressed homotetrameric HCN2 channels in Xenopus oocytes and performed single-channel experiments

109 esses currents as an undocked hemichannel in Xenopus oocytes and provides a model system to study the

110 ombined electrophysiological measurements in Xenopus oocytes and pulldown experiments to analyze the

111 We expressed rat TRPV4 in Xenopus oocytes and repeatedly examined >200 excised pat

112 ubtle effects are observed when expressed in Xenopus oocytes and studied with electrophysiology, does

113 USERs, expressed in Xenopus oocytes and tested using two-electrode voltage c

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

115 Channels were heterologously expressed in Xenopus oocytes and the two-microelectrode voltage clamp

116 rected mutation constructs were expressed in Xenopus oocytes and their functionality and pharmacology

117 Binding studies in Xenopus oocytes and transfected HEK-293 cells revealed t

118 ediates translational repression in immature Xenopus oocytes and translational activation in mature o

119 hR subtypes were heterologously expressed in Xenopus oocytes and two-electrode voltage clamp recordin

120 s investigated by heterologous expression in Xenopus oocytes and yeast cells.

121 Although microinjected Xenopus oocytes and/or transfected cells indicate overla

122 er NBCe1-A in an excised macropatch from the Xenopus oocyte, and indirectly stimulates NBCe1-B and -C

123 2 were studied by heterologous expression in Xenopus oocytes, and by homology modelling.

124 ns activate or repress the targeted mRNAs in Xenopus oocytes, and elicit poly(A) addition or removal.

125 e of human cardiac NKA isozymes expressed in Xenopus oocytes, and of native NKA isozymes in rat ventr

126 oral cortices of control and AD brains, into Xenopus oocytes, and recorded the electrophysiological a

127 dentified, synthesized, cloned, expressed in Xenopus oocytes, and studied by two-electrode voltage cl

128 cies) function of alpha6*-nAChR expressed in Xenopus oocytes, and that nAChR halpha6 subunit residues

129 and alpha1beta3 receptors were expressed in Xenopus oocytes, and the effects of substitutions of sel

130 ium channel, AaNav1-1, from Aedes aegypti in Xenopus oocytes, and the functional examination of nine

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

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

133 These residues were mutated, expressed in Xenopus oocytes, and their functions assessed using elec

134 Homomeric MPTL-1 channels reconstituted in Xenopus oocytes are gated by microM concentrations of be

135 is necessary and sufficient for maintaining Xenopus oocytes arrested in prophase.

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

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

138 ith the different beta subunits expressed in Xenopus oocytes (beta1, beta2IR, beta3b, and beta4).

139 Similarly, injection of CFTR-1420-57 into Xenopus oocytes blocked the inhibition of cAMP-stimulate

140 e, in two-electrode voltage clamp studies in Xenopus oocytes, both Ca(2+) and Na(+) illicit 5-HT-indu

141 OS-7 cells, and voltage-clamp fluorimetry in Xenopus oocytes, both heterologously expressing the volt

142 PIAS2b is restricted to the cytoplasm of Xenopus oocytes but relocates to the nucleus immediately

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

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

145 sis for human DMT1 expressed in RNA-injected Xenopus oocytes by using radiotracer assays and the cont

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

147 ation by in vitro and ex vivo analysis using Xenopus oocyte, cell culture, and kidney tissue assays d

148 ously in both an Escherichia coli strain and Xenopus oocyte cells, AtDTX50 was found to facilitate AB

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

150 Using expression cloning in Xenopus oocytes coexpressing the cystic fibrosis transme

151 Similarly, in paired Xenopus oocytes, coexpression with wild-type restored fu

152 Expression of AE1-M909T in Xenopus oocytes confirmed preservation of its anion exch

153 The Xenopus oocyte contains components of both the planar ce

154 Human NBCe1 heterologously expressed in Xenopus oocytes could be activated by adding 1-3 mm HCO3

155 from fluorophore-labeled hSERT expressed in Xenopus oocytes could be robustly detected at four posit

156 studies of PIEZO1 mutant R2488Q expressed in Xenopus oocytes demonstrated changes in ion-channel acti

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

158 Expression in Xenopus oocytes demonstrates that LGC-35 is a homopentam

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

160 se initiation and maintenance in Drosophila, Xenopus oocytes/eggs, and mammalian cells.

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

162 In Xenopus oocytes, ERp29 overexpression increased the func

163 ter, we recorded currents in voltage-clamped Xenopus oocytes expressing EAATs and used concentration

164 Our data demonstrate that in Xenopus oocytes expressing either OAT4 or OATP2B1 efflux

165 Xenopus oocytes expressing ENaC with a beta C43A,C557A m

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

167 nts (I(Na) and I(amil), respectively) across Xenopus oocytes expressing human alpha-, beta-, and gamm

168 pounds were profiled by electrophysiology in Xenopus oocytes expressing human nicotinic acetylcholine

169 inylation and two-electrode voltage-clamp on Xenopus oocytes expressing NBCe1, we demonstrate that th

170 AQP2 and AQP2-mediated water permeability in Xenopus oocytes expressing P2X(2), P2Y(2,) or P2Y(4) rec

171 amino acids, were tested on voltage-clamped Xenopus oocytes expressing rat Na(V)1.2 or Na(V)1.4.

172 inhibition of glutamate-evoked currents from Xenopus oocytes expressing recombinant homo- or heterome

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

174 cordance, elevated currents were observed in Xenopus oocytes expressing the Kir3.1/Kir3.4 heteromer t

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

176 Using Xenopus oocyte expression and two-electrode voltage clam

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

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

179 lamp technique and alpha4beta2 nAChRs in the Xenopus oocyte expression system, we demonstrate that in

180 degradation in human, HEK293 cells, and in a Xenopus oocyte expression system.

181 Using Xenopus oocyte expression, we investigated whether facil

182 Using the Xenopus oocytes expression system and two microelectrode

183 ading MCM2-7 onto replication origins in the Xenopus oocyte extract system.

184 f-organization of stabilized microtubules in Xenopus oocyte extracts and find that they can form macr

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

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

187 In Xenopus oocytes, furin and PC6 function redundantly to c

188 ation of ATP to hP2X7 receptors expressed in Xenopus oocytes gave rise to a current that had a biphas

189 In Xenopus oocytes, Gem suppresses the activity of P/Q-type

190 ts and concatemeric constructs, expressed in Xenopus oocytes, HEK 293 cells, and cultured hippocampal

191 curately recapitulates Ibasal and Ievoked in Xenopus oocytes, HEK293 cells and hippocampal neurons; c

192 ly blocked acetylcholine-induced currents in Xenopus oocytes heterologously expressing human muscle-t

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

194 RNA injection of K(+)-transporter genes into Xenopus oocytes, however, both putative K(+) transporter

195 In Xenopus oocytes, HvHKT2;1 co-transports Na+ and K+ over

196 duced currents in this receptor expressed in Xenopus oocytes (IC50 = 236 nm) and less potently inhibi

197 lters the membrane conductance properties of Xenopus oocytes in a manner consistent with a large non-

198 membranolytic activity could be measured for Xenopus oocytes, in which CsTx-1 and CT1-long increase i

199 YD7 could translocate to the cell surface of Xenopus oocytes independently of the coexpression of alp

200 Mutation studies in Xenopus oocytes indicate that CAIX, via its intramolecul

201 ansfer of mammalian somatic cell nuclei into Xenopus oocytes induces transcriptional reprogramming of

202 enous PIP(2) in inside-out macropatches from Xenopus oocytes inhibited heterologously expressed Slo3

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

204 oximal domain, hERG variant were explored in Xenopus oocytes injected with the same amount of RNA enc

205 When expressed in Xenopus oocytes, IR64a and IR8a formed a functional ion

206 Overexpression of Ano1 in HEK cells or Xenopus oocytes is sufficient to generate Ca(2+)-activat

207 ion-induced translation of mRNAs in maturing Xenopus oocytes is the cytoplasmic polyadenylation eleme

208 When tested in Xenopus oocytes, kappaM-RIIIJ has an order of magnitude

209 ulating translation of reporter mRNAs during Xenopus oocyte maturation.

210 f testosterone-induced MAPK-signaling during Xenopus oocyte maturation.

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

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

213 on of human aquaporin 1 (hAQP1) expressed in Xenopus oocyte membranes.

214 d intervals) induced GABA current rundown in Xenopus oocytes microinjected with HH membrane proteins,

215 s confirmed in the heterologously expressing Xenopus oocyte model.

216 In Xenopus oocytes, mutant TRESK subunits exert a dominant-

217 When co-expressed in Xenopus oocytes, NaDC-1 enhanced Slc26a6 transport activ

218 After injection into Xenopus oocyte nuclei, representative GANP-dependent tra

219 Functional expression in Xenopus oocytes of concatenated pentameric (alpha7)5-, (

220 Expression of AQP1 with CAII in Xenopus oocytes or mammalian cells increased water flux

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

222 electrode voltage-clamp electrophysiology in Xenopus oocytes, oxytocin was found to completely block

223 Surface expression of PLM in Xenopus oocytes requires coexpression with the Na(+)/K(+

224 cycle progression in progesterone-stimulated Xenopus oocytes requires that the translation of pre-exi

225 Wounded cells such as Xenopus oocytes respond to damage by assembly and closur

226 ly, microinjection of KCNE3 in bicelles into Xenopus oocytes resulted in functional co-assembly with

227 Coinjection of Rab14 in Xenopus oocytes results in a decrease of UT-A1 urea tran

228 d that coexpression of ASIC2b with ASIC1a in Xenopus oocytes results in novel proton-gated currents w

229 Heterologous expression of both genes in Xenopus oocytes revealed a strong conservation of charac

230 Electrophysiological characterization in Xenopus oocytes revealed that activity exclusively resid

231 ctional expression and analysis of AaCAT1 in Xenopus oocytes revealed that it acts as a sodium-indepe

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

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

234 For nAChRs expressed in Xenopus oocytes, S- and R-mTFD-MPAB inhibited ACh-induce

235 Although successful in Xenopus oocytes, single subunit counting, manually count

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

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

238 Electrophysiological experiments in Xenopus oocytes support this notion and suggest that con

239 bility of both proteins was tested using the Xenopus oocyte swelling assay and a yeast shrinkage assa

240 tics of each rescue protein were tested in a Xenopus oocyte swelling assay.

241 Here, we show in a heterologous Xenopus oocyte system as well as in Arabidopsis thaliana

242 Using the heterologous Xenopus oocyte system combined with molecular dynamics s

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

244 ode voltage clamp technique using a standard Xenopus oocyte system.

245 We performed patch clamp studies in Xenopus oocytes that co-expressed BK channel-forming (cb

246 rrents of the Shaker Kv channel expressed in Xenopus oocytes that F184 not only interacts directly wi

247 Here, we investigated in Xenopus oocytes the impact of RasGAP and its fragments o

248 Similar to M phase progression in maturing Xenopus oocytes, the destruction of CPEB during the mamm

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

250 When transplanted into Xenopus oocytes, the nuclei of mammalian somatic cells a

251 m at alpha6beta2,3delta GABAARs expressed in Xenopus oocytes, the pronounced agonism exhibited by the

252 tionality for Si transport when expressed in Xenopus oocytes, thus confirming the genetic capability

253 t responses in CquiOR136*CquiOrco-expressing Xenopus oocytes, thus suggesting a possible link between

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

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

256 s and heterologous expression of channels in Xenopus oocytes to characterize the structural basis for

257 ecule imaging and stepwise photobleaching in Xenopus oocytes to directly determine the subunit stoich

258 The hDAT constructs were expressed in Xenopus oocytes to investigate if heightened membrane po

259 activation of BgNa(v) channels expressed in Xenopus oocytes to more negative membrane potentials but

260 two-electrode voltage clamp measurements in Xenopus oocytes together with targeted mutagenesis to in

261 We show that, when expressed in Xenopus oocytes, TRPV4 with the L596P or W733R mutation

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

263 gh K(+) affinity) of Na/K pumps expressed in Xenopus oocytes, under voltage clamp.

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

265 idea, we recorded NaV1.5 gating currents in Xenopus oocytes using a cut-open voltage-clamp with extr

266 M2-V27A mutant ion channels were measured in Xenopus oocytes using two-electrode voltage clamp (TEV)

267 mutant forms of the channel were measured in Xenopus oocytes using two-electrode voltage clamp assays

268 1 cells in a fluorescence-based assay and in Xenopus oocytes using two-electrode voltage clamp electr

269 eceptor (AgOR) repertoire was carried out in Xenopus oocytes using two-electrode, voltage-clamp elect

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

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

272 g studies in both sperm and voltage clamp of Xenopus oocytes, we define a molecular mechanism for GM1

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

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

275 Using single molecule optical imaging in Xenopus oocytes, we found that MEC-4 forms homotrimers a

276 I(4,5)P(2)-sensitive KCNQ2/KCNQ3 channels in Xenopus oocytes, we identified four positions (A242C, R2

277 es ENaC functional and surface expression in Xenopus oocytes, we investigated the mechanism by which

278 Upon coexpression of ASIC1a and ASIC2a in Xenopus oocytes, we observed the formation of heteromers

279 A isoform IV was heterologously expressed in Xenopus oocytes, we observed, by measuring H(+) at the o

280 In Xenopus oocytes, we show that a genetically encoded vers

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

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

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

284 d CNGC18 resulted in activation of CNGC18 in Xenopus oocytes where expression of CNGC18 alone did not

285 MEC evoked inward current in SERT-expressing Xenopus oocytes, whereas 4-MePPP was inactive in this re

286 mma2S GABAA receptors (GABAARs) expressed in Xenopus oocytes, whereas it displayed highly diverse fun

287 The cloned acHCN gene was expressed in Xenopus oocytes, which displayed a hyperpolarization-ind

288 inositol trisphosphate receptors (IP(3)R) in Xenopus oocytes, which lack RyR.

289 work affect ion channels in the membrane of Xenopus oocytes, which shows the possibility to access a

290 specific, inhibiting KcsA-Shaker channels in Xenopus oocytes with a Ki of 0.5 nM whereas Shaker, Kv1.

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

292 currents or of Slo3 channels co-expressed in Xenopus oocytes with epidermal growth factor receptor, d

293 We expressed (alpha4beta2)2 concatamers in Xenopus oocytes with free accessory subunits to obtain d

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

295 edo (alphabetagammadelta) nAChR expressed in Xenopus oocytes with IC50 values of approximately 1 muM.

296 urally altered TaALMT1 proteins expressed in Xenopus oocytes with phylogenic analyses of the ALMT fam

297 ge clamp electrophysiology, we found that in Xenopus oocytes with RACK1 overexpression Pkd2L1 channel

298 and screened this library by coexpression in Xenopus oocytes with TRPA1.

299 nd segregation of Rho and Cdc42 zones during Xenopus oocyte wound repair and the role played by Abr,

300 In RNA-injected Xenopus oocytes, ZIP8-mediated (55)Fe(2+) transport was