ライフサイエンスコーパス: Xenopus laevis oocyte

1 ctivities measured through expression in the Xenopus laevis oocyte.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

17 el activity when heterologously expressed in Xenopus laevis oocytes.

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

19 eta2beta3 nAChRs heterologously expressed in Xenopus laevis oocytes.

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

21 recombinant mouse CFTR channels expressed in Xenopus laevis oocytes.

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

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

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

25 + channel complexes transiently expressed in Xenopus laevis oocytes.

26 al recombinant mutant receptors expressed in Xenopus laevis oocytes.

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

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

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

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

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

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

33 recognized essential regulator of meiosis in Xenopus laevis oocytes.

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

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

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

37 GirK potassium channel currents expressed in Xenopus laevis oocytes.

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

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

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

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

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

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

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

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

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

47 ed hERG channels heterologously expressed in Xenopus laevis oocytes.

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

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

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

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

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

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

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

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

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

57 an intestine and expressed heterologously in Xenopus laevis oocytes.

58 beta2gamma2 subunit combination expressed in Xenopus laevis oocytes.

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

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

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

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

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

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

65 ) sodium channel heterologously expressed in Xenopus laevis oocytes.

66 us receptor when expressed heterologously in Xenopus laevis oocytes.

67 eterologously expressed Cx30 hemichannels in Xenopus laevis oocytes.

68 nit subcellular distributions using mice and Xenopus laevis oocytes.

69 supported by electrophysiological studies in Xenopus laevis oocytes.

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

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

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

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

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

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

76 water transport activity when coexpressed in Xenopus laevis oocytes.

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

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

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

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

81 GABAAR were expressed in Xenopus laevis oocytes.

82 conformational changes of SUT1 expressed in Xenopus laevis oocytes.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

101 1, LdNT1.2, and LdNT2 have been expressed in Xenopus laevis oocytes and found to be electrogenic in t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

160 8-mediated transport of OTC was monitored in Xenopus laevis oocytes by electrophysiological means.

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

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

163 In Xenopus laevis oocytes, channels formed by the GluClalph

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

184 Using Xenopus laevis oocytes expressing NBCe1 variants, we hav

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 In Xenopus laevis oocytes microinjected with PCFT cRNA, upt

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

249 In the Xenopus laevis oocyte system, extracellular AqF026 poten

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

282 In Xenopus laevis oocytes, we monitored proteolytic activat

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

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

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

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

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

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

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

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