ライフサイエンスコーパス: human embryonic kidney cell

1 y and fidelity of DNA replication in HEK293T human embryonic kidney cells.

2 ) receptor function transiently expressed in human embryonic kidney cells.

3 erties of the peroxidase stably expressed in human embryonic kidney cells.

4 protein-tagged tau were co-transfected into human embryonic kidney cells.

5 II voltage-gated sodium channel expressed in human embryonic kidney cells.

6 n in primary mouse embryonic fibroblasts and human embryonic kidney cells.

7 , N182Y, L186F, and C191Y, were expressed in human embryonic kidney cells.

8 ters which could not have been studied using human embryonic kidney cells.

9 l vein endothelial cells and eNOS-expressing human embryonic kidney cells.

10 pression and plasma membrane localization in human embryonic kidney cells.

11 oxia on hTREK-1 channels stably expressed in human embryonic kidney cells.

12 otein in the nucleus after transfection into human embryonic kidney cells.

13 m-selective inhibition of Abeta secretion in human embryonic kidney cells.

14 A or GluR6 subunits excised from transfected human embryonic kidney cells.

15 conserved rat ortholog subunits expressed in human embryonic kidney cells.

16 etween CLCA1 and KCNMB1 when co-expressed in human embryonic kidney cells.

17 were overexpressed in LPS non-responsive 293 human embryonic kidney cells.

18 tosis induction by Fas ligand in transfected human embryonic kidney cells.

19 ulin-stimulated or -activated AKT-expressing human embryonic kidney cells.

20 wild-type channels transiently expressed in human embryonic kidney cells.

21 imulates TCF-dependent gene transcription in human embryonic kidney cells.

22 he human heart G(h)/transglutaminase (TG) in human embryonic kidney cells.

23 a5beta1 integrin-mediated cell attachment in human embryonic kidney cells.

24 eptor both in vivo and when cotransfected in human embryonic kidney cells.

25 ifically to the hPTH1-Rc stably expressed in human embryonic kidney cells.

26 ized by DNA replication machinery in HEK293T human embryonic kidney cells.

27 y component of the Wnt signaling pathway, in human embryonic kidney cells.

28 D45K and K51S, were expressed transiently in human embryonic kidney cells.

29 sphorylation of PHAS-I in insulin-stimulated human embryonic kidney cells.

30 amma subunits of GABAA receptor expressed in human embryonic kidney cells.

31 We validated this sensor in human embryonic kidney cells.

32 channel is highly degraded by proteasome in human embryonic kidney cells.

33 4 was confirmed in TLR2- or TLR4-transformed human embryonic kidney cells.

34 mouse keratocytes in vivo and of transfected human embryonic kidney cells.

35 ic hiPSC-CMs as well as hESC-CMs, but not in human embryonic kidney cells.

36 ase 2, a contaminant in our preparation from human embryonic kidney cells.

37 (S198A, S199A, and S202A) D(1) receptors in human embryonic kidney cells.

38 on N-methyl d-aspartate receptor-expressing human embryonic kidney cells.

39 pe and mutant ferroportin fusion proteins in human embryonic kidney cells.

40 V)3.3 T-channels heterologously expressed in human embryonic kidney cells.

41 subunit concatemeric constructs expressed in human embryonic kidney cells.

42 These effects also occurred in human embryonic kidney cells.

43 s for SFRS1 in the transcriptome of cultured human embryonic kidney cells.

44 uman homologs of Orai together with STIM1 in human embryonic kidney cells.

45 A receptor transiently expressed in HEK-293 (human embryonic kidney) cells.

46 ndent stimulation of GPRC6A overexpressed in human embryonic kidney cells 293 cells.

47 nocyte calcium-sensing receptor expressed in human embryonic kidney cells 293.

48 ain of human TSHR (TBP), or TBP expressed on human embryonic kidney cells (293 cells) (293-TBP cells)

49 om human lung cancer was stably expressed in human embryonic kidney cells (293 cells) to evaluate eff

50 en recombinant mevalonate kinase produced in human embryonic kidney cells (293 cells) was tested, it

51 To examine receptor internalization, human embryonic kidney cells (293 T) expressing wild typ

52 r TBX2, we generated stable transfectants of human embryonic kidney cells (293) that express a TBX2-e

53 Human embryonic kidney cells (293) were transiently tran

54 Human embryonic kidney cells (293T) were transfected wit

55 Human embryonic kidney cells (293T) were transfected wit

56 transactivate an AP-1 promoter construct in human embryonic kidney cells (293T).

57 In this work, we expressed in human embryonic kidney cells a KV-containing recombinant

58 ar interaction was observed in C6 glioma and human embryonic kidney cells after co-transfection with

59 When expressed in human embryonic kidney cells, all three new mutations re

60 cells incapable of BgtR expression, such as human embryonic kidney cells, alpha7 subunits are not si

61 Stable expression of NBCn1-E in human embryonic kidney cells also evoked an inward curre

62 NA is co-expressed with the APP cDNA in 293 (human embryonic kidney) cells, amyloidogenic fragments a

63 cDNAs of P2XA, P2XB, P2XC, P2XD, and P2XE in human embryonic kidney cells and altered the ionic and p

64 (12) proteins were individually expressed in human embryonic kidney cells and analyzed for interactio

65 For human embryonic kidney cells and B cells at least, optim

66 effect of AP301 in A549 cells as well as in human embryonic kidney cells and Chinese hamster ovary c

67 regates in the endoplasmic reticulum (ER) of human embryonic kidney cells and differentiated primary

68 Human embryonic kidney cells and foreskin fibroblasts we

69 To achieve high expression in 293 human embryonic kidney cells and formation of homo-oligo

70 M1-R669H mutant Na channel experimentally in human embryonic kidney cells and found that it has no si

71 When CFP-Kir6.2-YFP was expressed in human embryonic kidney cells and illuminated at 440 nm t

72 close spatial arrangement of the channels in human embryonic kidney cells and in hippocampal neuron m

73 expression of ERICE induces apoptosis of 293 human embryonic kidney cells and MCF7 breast carcinoma c

74 We expressed the rat P2X7 receptor in human embryonic kidney cells and measured membrane curre

75 dependent means on two different cell lines: human embryonic kidney cells and mouse embryonic fibrobl

76 ublication by Kim et al. on penetrating both human embryonic kidney cells and mouse embryonic stem ce

77 videnced by a biophotonic assay performed in human embryonic kidney cells and Nicotiana benthamiana l

78 Human embryonic kidney cells and NIH 3T3 fibroblasts tra

79 ort fibulins were recombinantly expressed in human embryonic kidney cells and purified by immobilized

80 Factor X was expressed in human embryonic kidney cells and purified from condition

81 tive immunoblotting of protein extracts from human embryonic kidney cells and rat organs reveals that

82 nits with the clustering protein, rapsyn, in human embryonic kidney cells and tested for binding of a

83 escence and biotinylation techniques in both human embryonic kidney cells and the human microvascular

84 A-coated colloids were allowed to adsorb on human embryonic kidney cells and then detached one by on

85 type or specifically mutated TRP channels in human embryonic kidney cells and used calcium imaging or

86 A species through AChR expression studies in human embryonic kidney cells and Xenopus oocytes.

87 itions using three cell lines: parental HEK (human embryonic kidney) cells and transfected HEK cells

88 inant (murine receptor subunits expressed in human embryonic kidney cells) and rat neuronal GABAA rec

89 by mutagenesis, transiently transfected into human embryonic kidney cells, and characterized electrop

90 Receptors were expressed in human embryonic kidney cells, and disulfide formation wa

91 adelta(2) pentameric form of the AChR in 293 human embryonic kidney cells, and measured binding of th

92 and mouse P2X(1) receptors were expressed in human embryonic kidney cells, and membrane currents evok

93 revented activation by overexpressed HNF1 in human embryonic kidney cells, and reduced by >80% the ma

94 idea, MRP1-Phe594 mutants were expressed in human embryonic kidney cells, and their properties were

95 more than 50% in a dual-luciferase assay in human embryonic kidney cells, and they strongly inhibit

96 o-alpha1(V) homotrimers produced in 293-EBNA human embryonic kidney cells, and this cleavage is shown

97 ion with beta2a and alpha2/delta subunits in human embryonic kidney cells, and used 2 mM Ca2+ as the

98 holine receptors (nAChRs) are expressed when human embryonic kidney cells are permanently transfected

99 activity associated with ABCB19 expressed in human embryonic kidney cells as measured by patch-clamp

100 d complement on glycine receptor-transfected human embryonic kidney cells at room temperature, and ca

101 Furthermore, Nrf2 activators were tested in human embryonic kidney cells bearing the Swedish mutatio

102 ot assay, binding to contactin-1-transfected human embryonic kidney cells, binding to paranodes of mu

103 cantly enhanced the fusion of CHO cells with human embryonic kidney cells but not B lymphocytes.

104 found that prostaglandin E(1) stimulation of human embryonic kidney cells caused a transient increase

105 When human embryonic kidney cells (cell line 293) over-expres

106 human umbilical vein endothelial cells, and human embryonic kidney cells (cell line HEK293).

107 receptor agonist quinpirole (0.1-10 muM) to human embryonic kidney cells coexpressing human DAT and

108 of sFRP-2 and sFRP-3 produced in transfected human embryonic kidney cells confer cell-surface binding

109 Transient expression of the cDNA in human embryonic kidney cells confirmed that it encodes h

110 ed transcription of a luciferase reporter in human embryonic kidney cells (EBNA) and mouse Leydig- (T

111 e-induced currents in chromaffin cells or in human embryonic kidney cells ectopically expressing func

112 pression of KvLQT1 in Xenopus oocytes and in human embryonic kidney cells elicits a rapidly activatin

113 Using human embryonic kidney cells enabled the purification of

114 ited significantly higher activation of both human embryonic kidney cells engineered to express TLR2

115 ild-type RyR1, following their expression in human embryonic kidney cells, enhances [(3)H]ryanodine b

116 Human embryonic kidney cells express several isoforms of

117 hemistry on rat brain, cultured neurons, and human embryonic kidney cells expressing GAD65, GAD67, al

118 n of l-glutamate to outside-out patches from human embryonic kidney cells expressing GLT-1 transporte

119 amino)styryl]-1-methylpyridinium (ASP(+)) in human embryonic kidney cells expressing human dopamine t

120 We recorded membrane currents from human embryonic kidney cells expressing P2X subunits and

121 Human embryonic kidney cells expressing P2X7 exhibited a

122 rescence and membrane currents in individual human embryonic kidney cells expressing rat P2X7 recepto

123 ith the whole cell patch clamp techniques in human embryonic kidney cells expressing recombinant rece

124 cohols on nnAChRs was further analyzed using human embryonic kidney cells expressing the alpha 4 beta

125 The amount of caveolin-1 in the human embryonic kidney cells expressing the highest cave

126 ere potently inhibited by KN-62 and KN-04 in human embryonic kidney cells expressing the human P2X7R

127 here in studies in striatal suspensions and human embryonic kidney cells expressing the human transp

128 effects on potassium channel currents using human embryonic kidney cells expressing the potassium ch

129 riments and whole-cell current recordings in human embryonic kidney cells expressing the wild-type or

130 which contain Wolbachia, directly stimulated human embryonic kidney cells expressing TLR2, but not TL

131 d that the A561T mutant channel expressed in human embryonic kidney cells failed to generate HERG cur

132 Biosynthesis of normal MPO by human embryonic kidney cells faithfully mirrored events

133 its data from cultured human fibroblasts and human embryonic kidney cells for two free parameters wel

134 When uPAR was expressed in human embryonic kidney cells, hamster melanoma cells, or

135 and Kir6.2 were investigated in transfected human embryonic kidney cells (HEK 293) by combined imagi

136 Heterologous expression of hTRPM3 in human embryonic kidney cells (HEK 293) showed that hTRPM

137 Human alphavbeta3 was isolated from human embryonic kidney cells (HEK 293) that stably expre

138 glycine subunits were in vitro expressed in human embryonic kidney cells (HEK 293).

139 embrane patches from transiently transfected human embryonic kidney cells (HEK 293).

140 lpha 2) expressed in transiently transfected human embryonic kidney cells (HEK 293).

141 ual luminescent SWNTs on the surface of live human embryonic kidney cells (HEK cells).

142 using human uveal melanoma cells (MEL 270), human embryonic kidney cells (HEK) and breast cancer cel

143 Viral stocks were used to infect human embryonic kidney cells (HEK) that were selected by

144 mide activates the SAPK signaling pathway in human embryonic kidney cells (HEK-293).

145 hPTH/PTHrP receptor stably transfected into human embryonic kidney cells (HEK-293/C-21 cells, approx

146 In our setup, drug binding to human embryonic kidney cell (HEK293) homogenate was meas

147 ecombinant rho1 receptors after infection of human embryonic kidney cells (HEK293 cell line), human e

148 f the CaR to Ca2+i dynamics in fura-2-loaded human embryonic kidney cells (HEK293 cells) transiently

149 Gene expression was monitored in human embryonic kidney cells (HEK293) after attachment o

150 Rings of human embryonic kidney cells (HEK293) and tracheal smoot

151 tracellular cadmium was detected in cultured human embryonic kidney cells (HEK293) expressing heterol

152 ors were expressed in Xenopus oocytes and in human embryonic kidney cells (HEK293) in order to examin

153 sates of mCLCA1 cDNA-transfected transformed human embryonic kidney cells (HEK293) reveals proteins o

154 nd in vivo, and expression of QKI mutants in human embryonic kidney cells (HEK293) significantly decr

155 We generated human embryonic kidney cells (HEK293) that stably expres

156 Human embryonic kidney cells (HEK293) transfected with A

157 wild type and C-terminal mutant receptors in human embryonic kidney cells (HEK293) with respect to tr

158 studies a single cell line, E1A-immortalized human embryonic kidney cells (HEK293), has been used.

159 Human embryonic kidney cells (HEK293/VR1 cells) and Chin

160 of cytochrome c from mitochondria in lysates human embryonic kidney cells HEK293T.

161 Using human embryonic kidney cells (HEKs) as a model cell syst

162 We used whole-cell recordings of human embryonic kidney cells heterologously expressing e

163 modestly transactivated this promoter in 293 human embryonic kidney cells; however, mutation of CRE h

164 ppaB p65 activity caused by interleukin-1 in human embryonic kidney cells in vitro.

165 Transfection of mZip14 cDNA into human embryonic kidney cells increased zinc uptake as me

166 itive microvesicles derived from transfected human embryonic kidney cells induced a significant neutr

167 DSTYK knockdown in human embryonic kidney cells inhibited FGF-stimulated ph

168 ype and delta exon5 CFTR were expressed in a human embryonic kidney cell line (293 HEK).

169 I with the flap loop deletion expressed in a human embryonic kidney cell line (HEK 293) revealed no e

170 sed whole-cell TRPC6 current in cells from a human embryonic kidney cell line (HEK 293) stably expres

171 eric 5-HT3 receptor (h5-HT3A) expressed in a human embryonic kidney cell line (HEK 293) was character

172 in (A2780S/R), as well in the nontumorigenic human embryonic kidney cell line (HEK-293T), showing in

173 cancer cells (MCF7) and in a nontumorigenic human embryonic kidney cell line (HEK-293T).

174 nce Ca2+-activated K+ (BKCa) currents from a human embryonic kidney cell line (HEK293) expressing wil

175 electrophysiology-based safety testing using human embryonic kidney cell line 293 cells expressing hu

176 rd, electrophysiology in Xenopus oocytes and human embryonic kidney cell line 293 cells in which we c

177 n(2+)]free in cancer (TOV112D) and noncancer human embryonic kidney cell line 293 to 15.8 and 18.1 nM

178 a human colon cancer cell line HCT116 and a human embryonic kidney cell line 293, which are sensitiv

179 epithelial cell lines (AGS and SCC68) or the human embryonic kidney cell line 293-P.

180 e stably expressed in cells derived from the human embryonic kidney cell line 293.

181 n of multinucleated cells in the mononuclear human embryonic kidney cell line 293.

182 ce Ca(2+) mobilization via endogenous M3R in human embryonic kidney cell line 293T (HEK293T) or mouse

183 Utilizing the human embryonic kidney cell line 293T, it was possible t

184 roducts of RAG-mediated transposition in the human embryonic kidney cell line 293T.

185 ion of TauT in cisplatin nephrotoxicity in a human embryonic kidney cell line and in LLC-PK1 cells, a

186 inant CLC-3 stably expressed in tsA cells, a human embryonic kidney cell line derivative, and nativel

187 ical studies are produced in the 293 cell, a human embryonic kidney cell line expressing E1 functions

188 Many of these studies have used the human embryonic kidney cell line HEK 293.

189 ere we examine the biogenesis of AQP1 in the human embryonic kidney cell line HEK-293T.

190 Transient expression of GAUT1 cDNA in the human embryonic kidney cell line HEK293 yielded uridine

191 d by coimmunoprecipitation assays within the human embryonic kidney cell line HEK293, which identifie

192 uronal-type channels stably expressed in the human embryonic kidney cell line HEK293.

193 However, by utilizing the human embryonic kidney cell line HEK293T, it was possibl

194 on regulates the homeostasis of hMSH4 in the human embryonic kidney cell line HEK293T.

195 eterokaryons between primary monocytes and a human embryonic kidney cell line restored Tat transactiv

196 alpha1-antitrypsin was stably expressed in a human embryonic kidney cell line to elucidate the mechan

197 bules assembled from tubulin purified from a human embryonic kidney cell line with isoform compositio

198 bition of N-type channels in HEK293 cells (a human embryonic kidney cell line) by coexpressing cloned

199 rsal root ganglia (DRG) and in HEK293 cells (human embryonic kidney cell line) transiently or stably

200 Using the human embryonic kidney cell line, 293, we show in the cu

201 ssary for wild-type levels of adherence to a human embryonic kidney cell line, biofilm formation, and

202 ppaB-dependent reporter gene activity in the human embryonic kidney cell line, HEK293, only if the ce

203 human D(1) receptors in a stably transfected human embryonic kidney cell line.

204 osophila (Dslo) were expressed in the HEK293 human embryonic kidney cell line.

205 arcoma) cell line and 2 pM against HEK 293T (human embryonic kidney) cell line], and a set of valuabl

206 wild-type hSkM1 channels were expressed in a human embryonic kidney cell lines (tsA201) using recombi

207 Cell density studies were performed on human embryonic kidney cell lines expressing human P2X7R

208 angiogenesis factor, we established several human embryonic kidney cell lines that constitutively se

209 energy transfer (FRET) in stably expressing human embryonic kidney cell lines.

210 with beta2 in permanently transfected tsA201 human embryonic kidney cell lines.

211 energy transfer (FRET) in stably expressing human embryonic kidney cell lines.

212 lls as well as in SY5Y neuroblastoma and 293 human embryonic kidney cell lines.

213 In HEK-293 human embryonic kidney cells, LPA and thrombin receptor-

214 hat the errant KCNE1 trafficking observed in human embryonic kidney cells may be due, in part, to the

215 ck of four Na+ channel isoforms expressed in human embryonic kidney cells: Nav1.5 (cardiac), Nav1.4 (

216 Overexpression in human embryonic kidney cells of either PPIP5K1 or PPIP5K

217 Coexpression in human embryonic kidney cells of specific pairs of mutant

218 ncreased the NP(o) of Slo alpha expressed in human embryonic kidney cells only in the presence of the

219 y fura-2 imaging of intracellular calcium in human embryonic kidney cells or electrophysiologically i

220 plantation of HT1080 fibrosarcoma cells, 293 human embryonic kidney cells, or human skin fibroblasts.

221 phomimicking Y14D-Cav-1 mutant transduced in human embryonic kidney cells overexpressing eNOS and red

222 Human embryonic kidney cells overexpressing p.R489K ferr

223 Expression of cyclin E1 in human embryonic kidney cells prevents Cdk5-mediated phos

224 stimulated neutrophils and 5-LOX-transfected human embryonic kidney cells, propofol attenuated the pr

225 his hypothesis, overexpression of viperin in human embryonic kidney cells reduces the intracellular r

226 Overexpression of beta-arrestins in human embryonic kidney cells rescued the sequestration o

227 Expression studies in human embryonic kidney cells reveal that shark kidney se

228 o the enhanced green fluorescence protein in human embryonic kidney cells revealed its location in th

229 In human embryonic kidney cells stably expressing a Flag-ta

230 Human embryonic kidney cells stably expressing beta3 and

231 When expressed in human embryonic kidney cells stably expressing Ca(v)2.3,

232 Internal dialysis of human embryonic kidney cells stably expressing CLCA1 wit

233 ties of antisera were determined by staining human embryonic kidney cells stably transfected with eit

234 annel gating, we transfected beta4 into HEK (human embryonic kidney) cells stably expressing Na(V)1.1

235 hole-cell recordings were made from HEK 293 (human embryonic kidney) cells stably transfected with cD

236 APOL1 G1 variant, or the APOL1 G2 variant in human embryonic kidney cells (T-REx-293) using a tetracy

237 When 5-HT(2A) receptors were expressed in human embryonic kidney cells, taurine and AL34662, a non

238 In 293-pTP cells (human embryonic kidney cells that express pTP in additio

239 We identified 11 proteins in human embryonic kidney cells that interact with the rat

240 , with the use of heterologous expression in human embryonic kidney cells, that it encodes a membrane

241 receptor subunits expressed recombinantly in human embryonic kidney cells; the effects of the recepto

242 ditionally, we observe dynamic variations of human embryonic kidney cells, through a silicon substrat

243 nt rat skeletal muscle (mu1) Na+ channels in human embryonic kidney cells to investigate the state-de

244 y, in experimental preparations ranging from human embryonic kidney cells to neurons in culture, slic

245 se 8 recruitment and sensitized immortalized human embryonic kidney cells to TRAIL-induced death.

246 Drosophila olfactory sensory neurones and in human embryonic kidney cells, together with electrophysi

247 n human umbilical vein endothelial cells and human embryonic kidney cells transfected or infected wit

248 eneity of the heterodimer synthesized by 293 human embryonic kidney cells transfected with EvIL-12 by

249 hain reaction analysis of RNA extracted from human embryonic kidney cells transfected with exon trapp

250 transport in human red cells or transport in human embryonic kidney cells transfected with GLUT1-HA-H

251 d hormone binding and signal transduction in human embryonic kidney cells transfected with hPTH/PTHrP

252 l patch-clamp and whole-cell recordings from human embryonic kidney cells transfected with rat GABA(A

253 Whole cell recordings were made from human embryonic kidney cells transfected with the human

254 nts, but not from a control subject, stained human embryonic kidney cells transfected with the TRPM1

255 Human monocytes, human embryonic kidney cells transfected with TLR2, and

256 noprecipitation studies of cell lysates from human embryonic kidney cells transfected with wild-type

257 explored by recording chloride currents from human embryonic kidney cells transiently expressing homo

258 711 is phosphorylated by PKC in vitro and in human embryonic kidney cells treated with a PKC activato

259 serine phosphorylation of IRS-1 observed in human embryonic kidney cells treated with an activator o

260 Release of PRDX2 is also observed in human embryonic kidney cells treated with TNF-alpha.

261 oltage-dependent capacitance were studied in human embryonic kidney cells (TSA201 cell line) transien

262 alterations of the global kinome of HEK293T human embryonic kidney cells upon treatment with methylg

263 athione production) and nitric oxide-induced human embryonic kidney cell using 2 labeling reagents: t

264 tudied after transient transfection into 293 human embryonic kidney cells using 5 mM Ca(2+) as charge

265 observed in Neuro2A cells and replicated in human embryonic kidney cells using a radioligand uptake

266 interactions and dynamics directly in living human embryonic kidney cells using fluorescence fluctuat

267 A receptors expressed in Xenopus oocytes and human embryonic kidney cells using site-directed mutagen

268 ombinant plasmid DNA was introduced into 293 human embryonic kidney cells using the calcium phosphate

269 1beta2gamma2S GABA(A) receptors expressed in human embryonic kidney cells using the following series

270 ular domain of TLR3 (hTLR3 ECD) expressed in human embryonic kidney cells was found to inhibit TLR3-d

271 A line of human embryonic kidney cells was stably transfected with

272 That a distinct GERAD program operates in human embryonic kidney cells was supported by the extent

273 cetylcholine receptor, stably transfected in human embryonic kidney cells, was examined using the who

274 locks p53-mediated induction of p21/Waf-1 in human embryonic kidney cells, we observed no inhibition

275 ta-amyloid precursor protein in vitro and in human embryonic kidney cells, we show that gamma-secreta

276 Importantly, using experiments in human embryonic kidney cells, we show that specific para

277 n and characterization with GluN1-expressing human embryonic kidney cells were confirmed to be agains

278 , human alpha 4 beta 2 subunits expressed in human embryonic kidney cells were inhibited rather than

279 Human embryonic kidney cells were stably transfected wit

280 human ether-a-go-go-related gene expressing human embryonic kidney cells were used as controls.

281 tiated alphabeta4 BK currents in transfected human embryonic kidney cells, whereas it failed to alter

282 ers of this mutant channel when expressed in human embryonic kidney cells, whereas VTD completely fai

283 We expressed eight concatenated cDNAs in human embryonic kidney cells, which encoded three serial

284 between our results and a previous study in human embryonic kidney cells, which showed wild type KCN

285 Furthermore, transfection of human embryonic kidney cells with a rat liver AO express

286 cell line that was generated by transforming human embryonic kidney cells with human adenovirus type

287 When expressed in human embryonic kidney cells with M2 muscarinic acetylch

288 ion of reassortant viruses, we cotransfected human embryonic kidney cells with plasmids for the synth

289 Transfection of human embryonic kidney cells with ZAC subunit cDNA cause