ライフサイエンスコーパス: Xenopus laevis oocyte

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

2 nit subcellular distributions using mice and Xenopus laevis oocytes.

3 channels and 4 Na(V) channels), expressed in Xenopus laevis oocytes.

4 of rat Na(v)1.4 sodium channels expressed in Xenopus laevis oocytes.

5 nvestigated WT and WT/mutant combinations in Xenopus laevis oocytes.

6 quiescent (G0) mammalian cells and immature Xenopus laevis oocytes.

7 were similar findings in OATP2B1-expressing Xenopus laevis oocytes.

8 water, glycerol, and urea when expressed in Xenopus laevis oocytes.

9 mutant subunits expressed in cell lines and Xenopus laevis oocytes.

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

11 e1-A in inside-out macropatches excised from Xenopus laevis oocytes.

12 el activity when heterologously expressed in Xenopus laevis oocytes.

13 (TIRF) microscopy to image Ca(2+) influx in Xenopus laevis oocytes.

14 pression and control of maternal mRNAs using Xenopus laevis oocytes.

15 recombinant mouse CFTR channels expressed in Xenopus laevis oocytes.

16 sed rat NBCe1-A in excised macropatches from Xenopus laevis oocytes.

17 cetylcholine receptors (nAChRs) expressed in Xenopus laevis oocytes.

18 t has strong uric acid transport activity in Xenopus laevis oocytes.

19 + channel complexes transiently expressed in Xenopus laevis oocytes.

20 supported by electrophysiological studies in Xenopus laevis oocytes.

21 al recombinant mutant receptors expressed in Xenopus laevis oocytes.

22 on of KA and glutamate-activated currents in Xenopus laevis oocytes.

23 with wild-type beta2 and gamma2 subunits in Xenopus laevis oocytes.

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

25 and the efflux directions when expressed in Xenopus laevis oocytes.

26 fter expression of the cloned transporter in Xenopus laevis oocytes.

27 s and coexpressed these with NR1 subunits in Xenopus laevis oocytes.

28 R2A and NR1/NR2B NMDA receptors expressed in Xenopus laevis oocytes.

29 recognized essential regulator of meiosis in Xenopus laevis oocytes.

30 ion by ibuprofen (K(i) = 73 +/- 9 microM) in Xenopus laevis oocytes.

31 with wild-type beta2 and gamma2 subunits in Xenopus laevis oocytes.

32 iant squid axon and in cytosolic extracts of Xenopus laevis oocytes.

33 GirK potassium channel currents expressed in Xenopus laevis oocytes.

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

35 et high-sensitivity alpha4beta2 expressed in Xenopus laevis oocytes.

36 specific genes from the nuclei injected into Xenopus laevis oocytes.

37 recombinant NR1/NR2A receptors expressed in Xenopus laevis oocytes.

38 n Kv1.5 channels heterologously expressed in Xenopus laevis oocytes.

39 g of localized RNAs at the vegetal cortex of Xenopus laevis oocytes.

40 two proteins was performed by expression in Xenopus laevis oocytes.

41 nnels (Kv2.1, Kv3.4, and Kv4.2) expressed in Xenopus laevis oocytes.

42 n heterologous systems, and most commonly in Xenopus laevis oocytes.

43 tive currents when co-expressed with ENaC in Xenopus laevis oocytes.

44 ed hERG channels heterologously expressed in Xenopus laevis oocytes.

45 ed, cotransporter activity in NKCC1-injected Xenopus laevis oocytes.

46 y expressing the mutated Kir6.2 with SUR1 in Xenopus laevis oocytes.

47 made in these three domains and evaluated in Xenopus laevis oocytes.

48 deletion, were constructed and expressed in Xenopus laevis oocytes.

49 d TM3 (A288C) were individually expressed in Xenopus laevis oocytes.

50 cked by alpha-bungarotoxin when expressed in Xenopus laevis oocytes.

51 alpha6(*) nAChRs heterologously expressed in Xenopus laevis oocytes.

52 oexpressed with wild-type alpha1 subunits in Xenopus laevis oocytes.

53 an intestine and expressed heterologously in Xenopus laevis oocytes.

54 beta2gamma2 subunit combination expressed in Xenopus laevis oocytes.

55 to those described in our previous study in Xenopus laevis oocytes.

56 voltage clamp to record channel currents in Xenopus laevis oocytes.

57 (GABA) transporter (mouse GAT3) expressed in Xenopus laevis oocytes.

58 ard rectifier K+ (Kir) channels expressed in Xenopus laevis oocytes.

59 sion of their pore-forming alpha subunits in Xenopus laevis oocytes.

60 f equal amounts of alpha4 and beta2 mRNAs in Xenopus laevis oocytes.

61 ) sodium channel heterologously expressed in Xenopus laevis oocytes.

62 ymerase II when microinjected into nuclei of Xenopus laevis oocytes.

63 T310I pathogenic mutant, expressing them in Xenopus laevis oocytes.

64 atases of cloned Kv1.5 channels expressed in Xenopus laevis oocytes.

65 o the agonist binding site were expressed in Xenopus laevis oocytes.

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

67 receptor, alpha(4)beta(2)delta, by 40-50% in Xenopus laevis oocytes.

68 mammalian NR1 subunit is expressed alone in Xenopus laevis oocytes.

69 s fast N-type inactivation when expressed in Xenopus laevis oocytes.

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

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

72 water transport activity when coexpressed in Xenopus laevis oocytes.

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

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

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

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

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

78 GABAAR were expressed in Xenopus laevis oocytes.

79 conformational changes of SUT1 expressed in Xenopus laevis oocytes.

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

81 eterologously expressed Cx30 hemichannels in Xenopus laevis oocytes.

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

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

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

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

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

87 Enhancing presenilin levels in Xenopus laevis oocytes accelerates clearance of cytosoli

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

89 nicotine on HS and LS receptors expressed in Xenopus laevis oocytes after cDNA injections or microtra

90 When expressed in Xenopus laevis oocytes, AgAQP1 transports water but not

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

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

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

94 this process, we expressed TrkA receptors in Xenopus laevis oocytes and analyzed their response to NG

95 )beta(2)gamma(2) GABA(A)Rs were expressed in Xenopus laevis oocytes and analyzed using a two-electrod

96 at neuronal nicotinic receptors expressed in Xenopus laevis oocytes and assayed under two-electrode v

97 n of G-protein-coupled K+ channels (Kir3) in Xenopus laevis oocytes and AtT20 cells, confocal microsc

98 Two heterologous expression systems, Xenopus laevis oocytes and cell monolayers, were used to

99 c (CNGA3 + CNGB3) human cone CNG channels in Xenopus laevis oocytes and characterized the alterations

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

101 We show that, in Xenopus laevis oocytes and early embryos, double-strande

102 sporter type 3 (hSGLT3), using expression in Xenopus laevis oocytes and electrophysiology.

103 We have now expressed the mutant D454C in Xenopus laevis oocytes and examined the role of charge o

104 1, LdNT1.2, and LdNT2 have been expressed in Xenopus laevis oocytes and found to be electrogenic in t

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

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

107 ingated ion channels (5-HT(3A)) expressed in Xenopus laevis oocytes and human embryonic kidney 293 ce

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

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

110 gth dependence with C12 being optimum in the Xenopus laevis oocytes and in LPA(3)-expressing RH7777 c

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

112 PCFT, expressed at high levels in Xenopus laevis oocytes and in transporter-competent HepG

113 igh agonist concentrations when expressed in Xenopus laevis oocytes and larger peak currents when exp

114 pha(1)beta(2)gamma(2) GABA(A)Rs expressed in Xenopus laevis oocytes and native GABA(A)Rs of isolated

115 otentiation of alpha7 receptors expressed in Xenopus laevis oocytes and outside-out patches from BOSC

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

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

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

119 ere examined using hSGLT1 Q457C expressed in Xenopus laevis oocytes and tagged with tetramethylrhodam

120 The mutants were expressed in Xenopus laevis oocytes and tested for sensitivities of G

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

122 Channels were expressed in Xenopus laevis oocytes and the effects of the pyrethroid

123 sporter (hCHT) has allowed its expression in Xenopus laevis oocytes and the simultaneous measurement

124 Its expression in Xenopus laevis oocytes and the use of a glucose analogue

125 T692A) NMDA receptors have been expressed in Xenopus laevis oocytes and their pharmacological and sin

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

127 s of inner cavity residues were expressed in Xenopus laevis oocytes and were used to characterize the

128 r Na(+) and K(+) transport when expressed in Xenopus laevis oocytes and yeast.

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

130 PAT1 function was measured in isolation ( Xenopus laevis oocytes) and in intact epithelia (Caco-2

131 oth in vivo (heterologous cRNA expression in Xenopus laevis oocytes) and in vitro ((32)P-phosphorylat

132 a(2)gamma(2L) GABA(A) receptors expressed in Xenopus laevis oocytes, and (3) as tadpole anesthetics.

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

134 a(2)gamma(2L) GABA(A) receptors expressed in Xenopus laevis oocytes, and (3). as tadpole anesthetics.

135 rRNA quality control based on experiments in Xenopus laevis oocytes, and a Ro ortholog enhances survi

136 Concatemers were expressed in Xenopus laevis oocytes, and activation by GABA, potentia

137 ffinity for rat alpha7 homomers expressed in Xenopus laevis oocytes, and antagonism is slowly reversi

138 Channels were heterologously expressed in Xenopus laevis oocytes, and currents were measured by us

139 Channels were heterologously expressed in Xenopus laevis oocytes, and currents were recorded using

140 expressed with wild-type beta(2) subunits in Xenopus laevis oocytes, and examined using two-electrode

141 ediates uptake of ammonium when expressed in Xenopus laevis oocytes, and functional studies indicate

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

143 rch-rho subunits expressed heterologously in Xenopus laevis oocytes, and on native GABA(C) receptors

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

145 combination of studies with mammalian cells, Xenopus laevis oocytes, and RS1-null mice, evidence that

146 ned from liver mRNA, sequenced, expressed in Xenopus laevis oocytes, and tested for their ability to

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

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

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

150 nction, cRNA encoding GmN70 was expressed in Xenopus laevis oocytes, and two-electrode voltage clamp

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

152 aliana) L. Heynh., was expressed in Xenopus (Xenopus laevis) oocytes, and transport activity was anal

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

154 on of vertebrate DAZL proteins, we have used Xenopus laevis oocytes as a model system.

155 PAK/WNK4, the NKCC1-mediated Cl(-) uptake in Xenopus laevis oocytes, as measured using (36)Cl, is twi

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

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

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

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

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

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

162 8-mediated transport of OTC was monitored in Xenopus laevis oocytes by electrophysiological means.

163 ucleoside transporter 3 (hCNT3) expressed in Xenopus laevis oocytes by measuring substrate-induced in

164 the cloned maxi-K channel hSlo expressed in Xenopus laevis oocytes by utilizing electrophysiological

165 In Xenopus laevis oocytes, channels formed by the GluClalph

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

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

168 Following expression of the mutants in Xenopus laevis oocytes, cysteines were labeled with tetr

169 egulated expression of reporters in immature Xenopus laevis oocytes, dependent on Xenopus AGO or huma

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

171 des a protein (Kcnj1) that when expressed in Xenopus laevis oocytes displayed pH- and Ba2+-sensitive

172 of action, Kv4.1 or Kv4.3 were expressed in Xenopus laevis oocytes, either alone or together with KC

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

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

175 When expressed in Xenopus laevis oocytes, EXP-1 forms a GABA receptor that

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

177 two electrode voltage clamp recordings from Xenopus laevis oocytes expressing cloned mKCNQ2 channels

178 e studied gap junction formation in pairs of Xenopus laevis oocytes expressing connexins that form fu

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

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

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

182 DM-induced activation was studied further in Xenopus laevis oocytes expressing human epithelial CFTR.

183 from rat ventral tegmental area (VTA) and in Xenopus laevis oocytes expressing human homomeric (alpha

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

185 p and inside-out patch clamp recordings from Xenopus laevis oocytes expressing Kir2.3 channels, we fo

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

187 Using Xenopus laevis oocytes expressing NBCe1 variants, we hav

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

189 Xenopus laevis oocytes expressing rat Oat1 showed increa

190 two-electrode voltage-clamp recordings from Xenopus laevis oocytes expressing recombinant NMDARs to

191 Here, we used Xenopus laevis oocytes expressing rho(1)Rs as a model sy

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

193 Pre-incubation of Xenopus laevis oocytes expressing TaALMT1 with protein k

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

195 -Hg(2+) conjugate was also shown to occur in Xenopus laevis oocytes expressing the hOAT1 or the rOAT3

196 Transport studies in Xenopus laevis oocytes expressing the P. falciparum nucl

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

198 microinjecting them together with inulin in Xenopus laevis oocytes expressing this pump.

199 apoE(141-148), experiments were conducted in Xenopus laevis oocytes expressing wild-type and mutated

200 changes in pH using giant patch clamping of Xenopus laevis oocytes expressing WT or mutant ROMK, and

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

202 Functional studies using the Xenopus laevis oocyte expression system showed that hSGL

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

204 sistance transporter' were investigated in a Xenopus laevis oocyte expression system.

205 potentiation of steady-state currents in the Xenopus laevis oocyte expression system.

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

207 that in both cerebellar granule cells and in Xenopus laevis oocytes expression system, surface delive

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

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

210 introduce a eukaryotic cellular system, the Xenopus laevis oocyte, for in-cell NMR analyses of biomo

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

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

213 ng provided by Cx50, but not Cx46, in paired Xenopus laevis oocytes in vitro, as well as between fres

214 acetylcholine (ACh) from nAChRs expressed in Xenopus laevis oocytes increase up to 8-fold in the pres

215 Expression of VvPIP2;4N in Xenopus laevis oocytes increased their swelling rate 54-

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

217 nexpectedly, expression of wild-type RhAG in Xenopus laevis oocytes induced a monovalent cation leak;

218 Expression of the mutated genes in Xenopus laevis oocytes induced abnormal Na and K fluxes

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

220 subunit (alphaR205A,R208A,R231Abetagamma) in Xenopus laevis oocytes led to increases in whole cell cu

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

222 Progesterone-induced Xenopus laevis oocyte maturation is mediated via a plasm

223 ound that oncogenic (Val 12)-ras-p21 induces Xenopus laevis oocyte maturation that is selectively blo

224 o undergo cytoplasmic polyadenylation during Xenopus laevis oocyte maturation.

225 Xenopus laevis oocytes microinjected with either AQP7 or

226 In Xenopus laevis oocytes microinjected with PCFT cRNA, upt

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

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

229 croinjection assays in 2 eukaryotic systems, Xenopus laevis oocyte nuclei and Drosophila melanogaster

230 al to mediate RNA transport in microinjected Xenopus laevis oocyte nuclei.

231 tion of fluorescein-labeled transcripts into Xenopus laevis oocyte nuclei.

232 its and pol III transcription factors in the Xenopus laevis oocyte nucleus.

233 l as eukaryotic cells and extracts employing Xenopus laevis oocytes or egg extracts.

234 quences for these proteins were expressed in Xenopus laevis oocytes or HEK 293 cells.

235 sion of the candidate solute transporters in Xenopus laevis oocytes: PAT1 (SLC36A1) is a H(+)-coupled

236 essed in Madin-Darby canine kidney cells and Xenopus laevis oocytes, PMAT efficiently transports sero

237 Expression of GPR3 or GPR12 in Xenopus laevis oocytes prevented progesterone-induced me

238 n of G(q)-coupled P2Y receptors expressed in Xenopus laevis oocytes produces the activation of an end

239 ted down-regulation of treacle expression in Xenopus laevis oocytes reduced 2'-O-methylation of pre-r

240 Finally, heterologous studies in Xenopus laevis oocytes reveal that FRD3 mediates the tra

241 Expression of LmPOT1 cRNA in Xenopus laevis oocytes revealed LmPOT1 to be a high affi

242 Expression in Xenopus laevis oocytes revealed that TbNT2/927, TbNT5, T

243 d Cl(-)-dependent (86)Rb(+) uptake assays in Xenopus laevis oocytes revealed that WNK2 promotes Cl(-)

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

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

246 voltage clamp recordings after expression in Xenopus laevis oocytes showed that only two chimeras wer

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

248 When T1 or T2 was expressed in Xenopus laevis oocytes, small whole-cell currents were a

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

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

251 r previous gene expression studies using the Xenopus laevis oocyte system suggested that tyrosine pho

252 Truncated forms of AQP0 were expressed in a Xenopus laevis oocyte system, and the effect of truncati

253 In the Xenopus laevis oocyte system, extracellular AqF026 poten

254 Ca(2+) transport in the intestine using the Xenopus laevis oocyte system.

255 idenced from GABA-induced inward currents in Xenopus laevis oocytes that express ceGAT-1 heterologous

256 T1) gave a protein at the plasma membrane of Xenopus laevis oocytes that was able to transport the no

257 We have systematically tested in Xenopus laevis oocytes the effects of coexpressing human

258 pression of the human SLC6A14 transporter in Xenopus laevis oocytes, the key functional characteristi

259 In the Xenopus laevis oocyte there is a million fold more trans

260 of the cockroach sodium channel expressed in Xenopus laevis oocytes to all eight structurally diverse

261 tinic acetylcholine receptors was studied in Xenopus laevis oocytes to identify key structures of put

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

263 itamin C transport, we expressed SVCT1(h) in Xenopus laevis oocytes to study the mechanism of transpo

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

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

266 Whereas in Xenopus laevis oocytes, two NR3 subunits coassemble with

267 transporter when expressed heterologously in Xenopus laevis oocytes: under hypotonic conditions that

268 Down-regulation of xGu in Xenopus laevis oocyte using an antisense oligodeoxynucle

269 the cloned maxi-K channel mSlo expressed in Xenopus laevis oocytes using electrophysiological method

270 of various recombinant GABA(A) receptors in Xenopus laevis oocytes using the two-electrode voltage c

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

272 ene (ERG) K(+) channel subtypes expressed in Xenopus laevis oocytes using two-electrode voltage-clamp

273 e studied inactivation of Kv4.3 expressed in Xenopus laevis oocytes, using the two-electrode voltage-

274 T310I human GLUT1 mutants for expression in Xenopus laevis oocytes via cRNA injection.

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

276 from wheat (Triticum aestivum) expressed in Xenopus laevis oocytes was conducted.

277 and fructose transport by GLUT2 expressed in Xenopus laevis oocytes was produced by the flavonols myr

278 mately 400 microm in diameter) isolated from Xenopus laevis oocytes was studied by scanning electroch

279 Transport in OSTalpha-OSTbeta-expressing Xenopus laevis oocytes was unaffected by depletion of in

280 els cloned from mouse brain and expressed in Xenopus laevis oocytes, we demonstrate that ethanol, eve

281 esis of channels heterologously expressed in Xenopus laevis oocytes, we discovered that 2 of the 8 Mi

282 In contrast to previous studies in Xenopus laevis oocytes, we find a strong correlation bet

283 Using Xenopus laevis oocytes, we have previously shown that ta

284 In Xenopus laevis oocytes, we monitored proteolytic activat

285 proteins of known stoichiometry expressed in Xenopus laevis oocytes, we resolved the composition of N

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

287 By expression in Xenopus laevis oocytes, we show that WNK4 also inhibits

288 and mutant human AQP1 channels expressed in Xenopus laevis oocytes were characterized by two-electro

289 cofactors or heterologous partner proteins, Xenopus laevis oocytes were injected with cRNA of wild-t

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

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

292 docaine inhibits TRPV1 channels expressed in Xenopus laevis oocytes, whereas the neutral local anesth

293 emonstrate the technique with a freeze-dried Xenopus laevis oocyte, which is a single cell.

294 This contrasts with Xenopus laevis oocytes, which express a large amount of

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

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

297 Treatment of Xenopus laevis oocytes with cholesterol-depleting methyl

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

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

300 In Xenopus laevis oocytes, WNK4 is required for modulation