ライフサイエンスコーパス: Chinese hamster ovary cell

1 ough Ca2+-activated K+ channels expressed in Chinese hamster ovary cells.

2 -100 nm) manner in human ChemR23-transfected Chinese hamster ovary cells.

3 oth muscle, neuroblastoma, glioblastoma, and Chinese hamster ovary cells.

4 ed at Asn positions in proteins expressed in Chinese hamster ovary cells.

5 f hsEH in transiently and stably transfected Chinese hamster ovary cells.

6 y site-directed mutagenesis and expressed in Chinese hamster ovary cells.

7 pha2 homomeric GlyRs stably transfected into Chinese hamster ovary cells.

8 ChR subtypes 1-5 heterologously expressed in Chinese Hamster Ovary cells.

9 atin)-8 (TRPM8), heterologously expressed in Chinese hamster ovary cells.

10 -FPR and recombinant FPR (rFPR) expressed in Chinese hamster ovary cells.

11 t of PMCA4a on the shape of a Ca2+ signal in Chinese hamster ovary cells.

12 ored cholesterol transport to NPC1-deficient Chinese hamster ovary cells.

13 pe of a Ca2+ signal in PMCA4b-overexpressing Chinese hamster ovary cells.

14 GP Ib-IX complex in transiently transfected Chinese hamster ovary cells.

15 the receptor complex has been reproduced in Chinese hamster ovary cells.

16 12 mouse myoblasts and IGF-II-overexpressing Chinese hamster ovary cells.

17 s beta3 G708N or alphaIIb G972N expressed on Chinese hamster ovary cells.

18 amicin-invasion/gentamicin-survival assay in Chinese hamster ovary cells.

19 All prodrugs were evaluated in Chinese hamster ovary cells.

20 letely rescue the transporter defect of Lec2 Chinese hamster ovary cells.

21 inding domain of FGFR1-IIIc were produced in Chinese Hamster Ovary cells.

22 neuroglial cultures and human APP-expressing Chinese hamster ovary cells.

23 our irradiated, genetically unstable GM10115 Chinese hamster ovary cells.

24 lls, primary human alveolar macrophages, and Chinese hamster ovary cells.

25 human beta3-adrenoceptor stably expressed in Chinese hamster ovary cells.

26 resulted in ectodomain cleavage of beta2 in Chinese hamster ovary cells.

27 activity of ENaC heterologously expressed in Chinese hamster ovary cells.

28 am antibiotics) to inhibit OAT1 expressed in Chinese hamster ovary cells.

29 hin the cell following expression in COS7 or Chinese hamster ovary cells.

30 ytes and in control versus ClC-3-transfected Chinese hamster ovary cells.

31 cle cells (A10 cells) and stably transfected Chinese hamster ovary cells.

32 elenomethionyl-substituted HER-1 produced in Chinese hamster ovary cells.

33 le in mediating Wnt-3a-dependent motility in Chinese hamster ovary cells.

34 fluorescein, in OATP1B1- or 1B3-transfected Chinese hamster ovary cells.

35 eta42 secreted from human APP-overexpressing Chinese hamster ovary cells.

36 ng (14)C-urate transport assays in mammalian Chinese hamster ovary cells.

37 in wild-type and glycoengineered plants and Chinese hamster ovary cells.

38 into the full-length integrins expressed in Chinese hamster ovary cells.

39 ed in heparan sulfate proteoglycan-deficient Chinese hamster ovary cells.

40 sufficient to confer infectibility onto CHO (Chinese hamster ovary) cells.

41 By Western blot of Chinese hamster ovary cells, 130C037 selectively induced

42 Forces obtained with Chinese hamster ovary cells, a malignant human brain tum

43 ore, using alphaIIbbeta3 integrin-expressing Chinese hamster ovary cells, a well described model syst

44 cular, in both Xenopus oocytes and mammalian Chinese hamster ovary cells, AaTXKbeta(2)(-)(6)(4), but

45 lso found to induce morphological changes in Chinese hamster ovary cells, an epithelial cell line.

46 inant SGN-40 was expressed and purified from Chinese hamster ovary cells and characterized based on b

47 fragments [Fab, F(ab')(2)] were expressed in Chinese hamster ovary cells and evaluated in vitro and i

48 e and mutant S1P receptors were expressed in Chinese hamster ovary cells and examined for their abili

49 acromolecular channel complex in transfected Chinese hamster ovary cells and found a dominant-negativ

50 position tool, and we tested the adhesion of Chinese Hamster Ovary cells and Human Embrionic Kidney c

51 or explaining activation of this integrin in Chinese hamster ovary cells and human platelets.

52 r of calcineurin, increased ASIC currents in Chinese hamster ovary cells and in cortical neurons, sug

53 P9 significantly reduced Abeta generation in Chinese hamster ovary cells and in primary neurons, demo

54 lag in the induction of cytotoxicity towards Chinese hamster ovary cells and is attenuated for virule

55 nding of the purified recombinant protein to Chinese hamster ovary cells and loss of binding to the f

56 ted after fMLF activation of rFPR-expressing Chinese hamster ovary cells and neutrophils.

57 of extracellular signal-regulated kinase in Chinese hamster ovary cells and permits chemokine and pr

58 In this study hDK has been overexpressed in Chinese hamster ovary cells and shown to be a polytopic

59 resistant to c-Cbl-mediated degradation, in Chinese hamster ovary cells and the UMSCC11B human head

60 Produced in stably transduced Chinese hamster ovary cells and used to immunize New Zea

61 e the uptake of silver nanoparticles by CHO (Chinese hamster ovary) cells and their subsequent fate a

62 ukaryotic cells (up to approximately 36% for Chinese hamster ovary cells) and bacterial cells (up to

63 efficiency for transfection (up to ~71% for Chinese hamster ovary cells) and permeabilization sugges

64 dly incorporates into the plasma membrane of Chinese hamster ovary cells, and 9AcGD3 is detected afte

65 n sulfate isolated from mutant and wild-type Chinese hamster ovary cells, and select tissues from mut

66 ly localized to the endoplasmic reticulum in Chinese hamster ovary cells, and this intracellular loca

67 Chinese Hamster Ovary cells are the most popular host ex

68 70%) localized on the surface of transfected Chinese hamster ovary cells, as determined by biotinylat

69 ished potencies based on the comet assay for Chinese hamster ovary cells (assesses the level of DNA s

70 clamp recordings from channels expressed in Chinese Hamster Ovary Cells at different temperatures (3

71 iggered gating of BKCa channels expressed in Chinese hamster ovary cells at distinct membrane potenti

72 Human ALDH7A1 expression in Chinese hamster ovary cells attenuated osmotic stress-in

73 In TRPV3-expressing Chinese hamster ovary cells, both extracellular and intr

74 ction of misfolded TPP I mutant expressed in Chinese hamster ovary cells, but not in human embryonic

75 helial Na(+) channel (ENaC) reconstituted in Chinese hamster ovary cells by PI3K.

76 calpain cleavage-resistant beta(3) mutant in Chinese hamster ovary cells causes defective clot retrac

77 of various cell types in culture, including Chinese hamster ovary cells, chicken DF1 fibroblasts, pr

78 on the stabilities of Escherichia coli- and Chinese hamster ovary cell (CHO)-derived IgG1 Fc high-or

79 liquids (ILs) on zebrafish (Danio rerio) and Chinese hamster ovary cells (CHO) was investigated with

80 ndocytic/phagocytic pathway was reported for Chinese hamster ovary cells (CHO-K1 cells).

81 hnology was used to localize the subunits in Chinese hamster ovary cells (CHO-K1).

82 oprecipitated with the I(Ks) channel only in Chinese hamster ovary cells co-expressing AKAP-9, and PD

83 When ADAP was heterologously expressed in Chinese hamster ovary cells co-expressing alphaIIbbeta3,

84 en prostasin and HAI-1B were co-expressed in Chinese hamster ovary cells, complexes of prostasin with

85 adipose tissue, and expression of GPIHBP1 in Chinese hamster ovary cells confers upon those cells the

86 a recombinant inside-out signaling system in Chinese hamster ovary cells confirmed the ability of fim

87 ng to recombinant alphaIIbbeta3 expressed by Chinese hamster ovary cells, confirming that its effect

88 In this study, a high-producing Chinese hamster ovary cell culture which was transfected

89 1 antibody, generated during production in a Chinese hamster ovary cell culture, was observed in the

90 rane vesicles isolated from AQP1-transfected Chinese hamster ovary cell cultures.

91 ide attachment sites will not be secreted by Chinese hamster ovary cells deficient in xylosyltransfer

92 assays that use human receptors expressed in Chinese hamster ovary cells demonstrate that NDD-713 and

93 ts from nanoparticles incorporated in living Chinese hamster ovary cells demonstrate that the nanopar

94 ntrosome duplication in hydroxyurea-arrested Chinese hamster ovary cells, demonstrating that Stat3 is

95 report the isolation of a new mutant line of Chinese hamster ovary cells, designated SRD-14, in which

96 report the isolation of a new line of mutant Chinese hamster ovary cells, designated SRD-15, deficien

97 When expressed in Chinese hamster ovary cells, dKCNQ gives rise to a slowl

98 of the three homologs that are expressed in Chinese hamster ovary cells (DPY19L1, DPY19L3, and DPY19

99 pus oocytes (EC(50) approximately 200 pM) or Chinese hamster ovary cells (EC(50) approximately 75 pM)

100 ethylammonium transport by OCT2 expressed in Chinese hamster ovary cells, effects that were largely r

101 epatocytes are induced on cocultivation with Chinese hamster ovary cells engineered to express T-cadh

102 reviously described beta(3)G708N mutation in Chinese hamster ovary cells enhanced ligand binding affi

103 In Chinese hamster ovary cells, Erb increased the inactivat

104 Wild-type Chinese hamster ovary cells express abundant Xylt2 mRNA

105 lite trends from a bioreactor cultivation of Chinese hamster ovary cells expressing a recombinant ant

106 Functional experiments in Chinese hamster ovary cells expressing AKAP-9 and either

107 In Chinese hamster ovary cells expressing APP, BMS-561392 s

108 on in a wound healing assay carried out with Chinese hamster ovary cells expressing beta2.

109 In transfected Chinese hamster ovary cells expressing ClC-3A, endosomal

110 dies showed that H. pylori adhered avidly to Chinese hamster ovary cells expressing human DAF but not

111 rand break (SSB) repair capacity of isogenic Chinese hamster ovary cells expressing human forms of XR

112 Mice were injected with Chinese hamster ovary cells expressing human IL-6 or no

113 was evaluated before and after adsorption to Chinese hamster ovary cells expressing human TSHRs using

114 virus (MV-Edm), but it selectively infected Chinese hamster ovary cells expressing integrin alpha(v)

115 Here, we show that Chinese hamster ovary cells expressing Mgat3 and the pol

116 [3H]Palmitate labeling of Chinese hamster ovary cells expressing MUC1 with mutatio

117 Studies using Chinese hamster ovary cells expressing SR-BI showed that

118 Chinese hamster ovary cells expressing the D447V exchang

119 We found that in Chinese hamster ovary cells expressing the hDOR, deltorp

120 In Chinese hamster ovary cells expressing the human A3-AR,

121 Chinese hamster ovary cells expressing the muscarinic ac

122 Using Chinese hamster ovary cells expressing the PTH1R, where

123 When the Chinese hamster ovary cells expressing VEGF plasmid were

124 on of MO-evoked calcium accumulation using a Chinese hamster ovary cell expression system.

125 Paclitaxel resistance mutations in Chinese hamster ovary cells frequently alter a cluster o

126 r Abeta binding and uptake were confirmed in Chinese hamster ovary cells genetically deficient in HSP

127 ibodies as well as significantly enhanced in Chinese hamster ovary cells genetically modified to expr

128 We show that fucosylation-deficient Lec13 Chinese hamster ovary cells have wild type levels of Pof

129 well as in human embryonic kidney cells and Chinese hamster ovary cells heterologously expressing hu

130 icited NF-kappaB and MAPK activities in RAGE-Chinese hamster ovary cells; however, after cotransfecti

131 localize in the region of the plasmalemma of Chinese hamster ovary cells; however, both are locked in

132 In living Chinese hamster ovary cells, imaging showed that sensors

133 CFTR currents expressed in NIH 3T3 cells or Chinese hamster ovary cells in a dose-dependent manner w

134 demonstrated that ExsE was translocated into Chinese hamster ovary cells in a T3SS-dependent manner.

135 eta3 enhanced IGF-1-induced proliferation of Chinese hamster ovary cells in serum-free conditions (in

136 ultrasound on the intracellular [Ca(2+)] of Chinese hamster ovary cells in the presence of albumin-e

137 adherence of E. histolytica trophozoites to Chinese hamster ovary cells in vitro (P, <0.001 for each

138 g in response to MSU crystals in transfected Chinese hamster ovary cells in vitro.

139 se to the agonist uridine 5'-triphosphate in Chinese hamster ovary cells, in both microfluidic and mi

140 ADPH: cytochrome c (P450) reductase (NPR) in Chinese hamster ovary cells increases the hypoxic/aerobi

141 etylglucosaminyltransferase I-deficient Lec1 Chinese hamster ovary cells, indicating that N-glycosyla

142 ction in T3SS-dependent cytotoxicity towards Chinese hamster ovary cells, indicating that the translo

143 t transient expression of kindlin-1 or -2 in Chinese hamster ovary cells inhibits the activation of e

144 nnels, which are heterologously expressed in Chinese hamster ovary cells, into the depolarizing direc

145 ant human TWEAK binding to CD163-transfected Chinese hamster ovary cells is inhibited by the presence

146 In HNF4alpha-null Chinese hamster ovary cells, IsoNAM and resveratrol fail

147 no acids 354-493, expressed these mutants in Chinese hamster ovary cells lacking ACAT1, and prepared

148 In the present study, Chinese hamster ovary cells lacking DHFR were transfecte

149 yed a previously described GALE-null line of Chinese hamster ovary cells, ldlD.

150 in a human retinal cell line (ARPE-19) and a Chinese hamster ovary cell line (CHO-K1) to study the fu

151 ath, we generated and characterized a mutant Chinese hamster ovary cell line that is resistant to pal

152 ot cholesterol levels per se, by utilizing a Chinese hamster ovary cell line that overexpressed trans

153 Revertants of a colcemid-resistant Chinese hamster ovary cell line with an altered (D45Y) b

154 Here we used a Chinese hamster ovary cell line with three different lac

155 A mutant Chinese hamster ovary cell line, glyB, that required exo

156 his mutated form of XPF in the XPF-deficient Chinese hamster ovary cell line, UV41, only partially re

157 In a Chinese hamster ovary cell-line (CHO-lac-mGlu5a), none o

158 of human endothelial kidney 293, HepG2, and Chinese hamster ovary cell lines decreases cellular LDL

159 Through the use of mutant Chinese hamster ovary cell lines defective in glycosamin

160 at transduction occurs efficiently in mutant Chinese hamster ovary cell lines deficient in glycosamin

161 ist, was characterized in vitro using stable Chinese hamster ovary cell lines expressing each of the

162 apid endocytosis of LRP, we generated stable Chinese hamster ovary cell lines expressing either a wil

163 Stably transfected Chinese hamster ovary cell lines expressing increasing l

164 Stable Chinese hamster ovary cell lines expressing PKGIalpha or

165 promoter trap mutagenesis to generate mutant Chinese hamster ovary cell lines resistant to lipotoxic

166 Here we treated Chinese hamster ovary cell lines with lovastatin (a hydr

167 Utilizing Chinese hamster ovary cell lines, we demonstrate that Th

168 ining (NHEJ) in Msh2-deficient and wild-type Chinese hamster ovary cell lines.

169 etic conservation, and functional studies on Chinese hamster ovary cell lines.

170 prt gene at its endogenous locus in isogenic Chinese hamster ovary cell lines.

171 which endogenously expresses DRD2) and CHO (Chinese hamster ovary) cell lines, decreasing luciferase

172 ipodial dynamics of EGF receptor-transfected Chinese hamster ovary cells migrating on fibronectin-coa

173 p91(phox) and p22(phox), we demonstrate in a Chinese hamster ovary cell model system and in RAW 264.7

174 In a Chinese hamster ovary cell model system, adhesion to fib

175 In Chinese hamster ovary cells, MPS-1 forms stable complexe

176 Using Chinese hamster ovary cell mutants defective in heparan

177 vation allowed the utilization of a panel of Chinese hamster ovary cell mutants with defined glycosam

178 and function of COG using Cog1 or Cog2 null Chinese hamster ovary cell mutants, fibroblasts from a p

179 xhibited reduced toxoplasma infectivity like Chinese hamster ovary cell mutants.

180 Ibbeta3 integrins by talin head fragments in Chinese hamster ovary cells, nor do I observe affinity i

181 cellular gangliosides and incorporated into Chinese hamster ovary cell O-glycans.

182 We determined that electroporation of Chinese hamster ovary cells occurred when the local fiel

183 Transfection into Chinese hamster ovary cells of a cDNA representing only

184 etabolism, using RNA interference to deplete Chinese hamster ovary cells of NPC1 alone or in combinat

185 -linked fluorophore to these compartments in Chinese hamster ovary cells or Jurkat lymphocytes, membr

186 n wild-type and D1275N channels expressed in Chinese hamster ovary cells or tsA201 cells in the absen

187 eficiency, complementation group 1-deficient Chinese hamster ovary cells over a 24 h period.

188 I purified to homogeneity from secretions of Chinese hamster ovary cells overexpressing TPP I cDNA.

189 CaK in fusion with enhanced GFP in mammalian Chinese hamster ovary cells' plasma membrane gave rise t

190 ses formed between primary T lymphocytes and Chinese hamster ovary cells presenting major histocompat

191 TGF-mediated control of beta-AR sensitivity, Chinese hamster ovary cells pretreated with rec-hCTGF di

192 icient uptake of Hsp70 when transfected into Chinese hamster ovary cells previously null for uptake.

193 Expression of either isoform in Chinese hamster ovary cells produced Ca2+ - and voltage-

194 Heterologous expression of Kv4.3 in Chinese hamster ovary cells produced small I(to); I(to)

195 Chinese hamster ovary cells proliferated after cleavage

196 b/IIIa (integrin alphaIIbbeta3) expressed on Chinese hamster ovary cells promoted melanoma cell adhes

197 We expressed mutant forms of GPIHBP1 in Chinese hamster ovary cells, rat and human endothelial c

198 ene promoter; overexpression of HNF4alpha in Chinese hamster ovary cells re-established transcription

199 mpetition assays at membrane preparations of Chinese hamster ovary cells recombinantly expressing the

200 In Chinese Hamster Ovary cells, redox-modifying agents only

201 ivated Teffs with Sn(+) macrophages or Sn(+) Chinese hamster ovary cells resulted in increased cell d

202 Studies with transporter-transfected Chinese hamster ovary cells reveal that SERT stimulation

203 at the human beta1-adrenoceptor expressed in Chinese hamster ovary cells revealed negative cooperativ

204 In Chinese hamster ovary cells, SAA promoted cellular chole

205 In modeled ischemia using Chinese hamster ovary cells, serum depletion caused a si

206 Expression studies in Chinese hamster ovary cells showed that the splice site

207 eic acid with aromatase mutants expressed in Chinese hamster ovary cells showed that these fatty acid

208 capability of our setup on fixed and living Chinese hamster ovary cells, showing the cytoskeleton dy

209 We used Chinese hamster ovary cells stably expressing 5-HT2C rec

210 Galpha(q) and Galpha(i) pathways in vitro on Chinese hamster ovary cells stably expressing FFA2.

211 substrate for PKC, and this was confirmed in Chinese hamster ovary cells stably expressing full-lengt

212 50) = 0.2 microM) and whole-cell currents in Chinese hamster ovary cells stably expressing heteromult

213 or binding of fluorescently labeled Abeta to Chinese hamster ovary cells stably expressing human CD36

214 In Chinese hamster ovary cells stably expressing PKGIalpha

215 Chinese hamster ovary cells stably expressing the entire

216 stimulated cAMP accumulation was measured in Chinese hamster ovary cells stably expressing the human

217 terfering RNA knockdown of endogenous SET in Chinese hamster ovary cells stably expressing the M3 mus

218 Chinese hamster ovary cells stably expressing wild-type

219 ed from the serum-free conditioned medium of Chinese hamster ovary cells stably transfected with a pS

220 ophosphate-, and Rap1-independent pathway in Chinese hamster ovary cells stably transfected with the

221 agonist 5'-(N-ethylcarboxamido)adenosine in Chinese hamster ovary cells stably transfected with the

222 increased plasmalogen synthesis in wild-type Chinese hamster ovary cells, strongly suggesting that Fa

223 tes and its binding to the LDLR expressed on Chinese hamster ovary cells, suggesting a direct interac

224 educes ASIC currents in cortical neurons and Chinese hamster ovary cells, suggesting a role of AKAP15

225 ing electrode to Kv2.1 channels expressed in Chinese hamster ovary cells, suggesting against an inter

226 nt Kv3.4 channel heterologously expressed in Chinese hamster ovary cells, supporting our findings in

227 ular endothelial cell line and a transfected Chinese hamster ovary cell system were used to determine

228 a membrane of intact rabbit erythrocytes and Chinese hamster ovary cells that can be explained by the

229 ection technique to generate a population of Chinese hamster ovary cells that display a global defici

230 When Chinese hamster ovary cells that exhibit a temperature-s

231 a colcemid resistant beta-tubulin mutant of Chinese hamster ovary cells that exhibits hypersensitivi

232 with a role in cell cycling, we observe that Chinese hamster ovary cells that express a tetracycline-

233 horage-independent conditions in transformed Chinese hamster ovary cells that express alphavbeta3 (be

234 ADAMs were expressed in Chinese hamster ovary cells that express defined integri

235 In Chinese hamster ovary cells that express the channels, K

236 tion of PKCI with HmuOR was recapitulated in Chinese hamster ovary cells that express the full-length

237 ) and selective inhibitory activities toward Chinese hamster ovary cells that expressed FRalpha or FR

238 ulated release of arachidonic acid (AA) from Chinese hamster ovary cells that expressed M(3) muscarin

239 Second, in Chinese hamster ovary cells that heterologously express

240 Using Chinese hamster ovary cells that inducibly overexpress e

241 to block the binding of ligands to pgsA-745 Chinese hamster ovary cells that overexpress GPIHBP1.

242 Transport was measured in Chinese hamster ovary cells that stably expressed the hu

243 is functional for IP-10 expression in vivo, Chinese hamster ovary cells that were designed to secret

244 Expression of wild-type hCTR1 in mutant Chinese hamster ovary cells that were unable to initiate

245 Th2 receptor (1.14 +/- 0.44 nM) expressed in Chinese hamster ovary cells, the binding being reversibl

246 m clone 2.27 was cloned and transfected into Chinese hamster ovary cells, the cells expressed human C

247 In Chinese hamster ovary cells, the loss of G alpha(q/11) b

248 in WIN-induced dephosphorylation of TRPV1 in Chinese hamster ovary cells through targeted expression

249 pUL128-131 pentameric complex and gH/gL from Chinese hamster ovary cells to >95% purity.

250 pressed mutant forms of full-length JAM-A in Chinese hamster ovary cells to assess reovirus binding a

251 ssembly of RAD51 recombinase, and sensitized Chinese hamster ovary cells to cisplatin when added to g

252 ession of TREM-2-DAP12 enables nonphagocytic Chinese hamster ovary cells to internalize bacteria.

253 lations to bind and/or infect HL-60 cells or Chinese hamster ovary cells transfected to express PSGL-

254 ndent decrease in the luciferase activity in Chinese Hamster Ovary cells transfected with CACNA1C and

255 t using human peripheral blood monocytes and Chinese hamster ovary cells transfected with CD14 cells

256 We also reported that Chinese hamster ovary cells transfected with GD3 synthas

257 ma1, expresses Fibtail-T3Dsigma1 and infects Chinese hamster ovary cells transfected with human or mo

258 nzyme assays and flow cytometric analyses of Chinese hamster ovary cells transfected with plasmids co

259 Chinese hamster ovary cells transfected with recombinant

260 tent stem cell-derived cardiomyocytes and in Chinese hamster ovary cells transfected with SCN5A, enco

261 In Chinese hamster ovary cells transfected with SCN5A, whic

262 Chinese hamster ovary cells transfected with TF(C186S),

263 acterized a series of rigid D(2) agonists in Chinese hamster ovary cells transfected with the human D

264 Moreover, Chinese hamster ovary cells transfected with TLR13, but

265 to inhibit MO-evoked calcium accumulation in Chinese hamster ovary cells transfected with TRPV1 and T

266 A or fibronectin bound to DC and Mphi and to Chinese hamster ovary cells transfected with VLA-5.

267 ological relevance, because LEC29 and parent Chinese hamster ovary cells transiently expressing a Fut

268 Forster resonance energy transfer (FRET) on Chinese hamster ovary cells under total internal refecti

269 nt protein-tagged KCNQ subunits expressed in Chinese hamster ovary cells under total internal reflect

270 ools to analyze proteins in situ in cultured Chinese hamster ovary cells using fluorescence recovery

271 These proteins were imaged in Chinese hamster ovary cells using single-molecule fluore

272 and expression in C-mannosylation-defective Chinese hamster ovary cell variants.

273 First, we demonstrated that in Chinese hamster ovary cells we could distinguish three d

274 /Cys-labeled MUC1 in glycosylation-defective Chinese hamster ovary cells, we found previously that tr

275 upernatant following transient expression in Chinese hamster ovary cells were analyzed by immunoblot

276 rvival rates of scraped Capns1+/+, HFL-1, or Chinese hamster ovary cells were decreased by the calpai

277 Chinese hamster ovary cells were transfected with alpha(

278 hilled platelets could be reconstituted when Chinese hamster ovary cells were transfected with alpha(

279 Chinese hamster ovary cells were transfected with full-l

280 ocell" particles are taken up efficiently by Chinese hamster ovary cells, where, due to a reduced pH

281 ated JAM family members JAM-B and JAM-C into Chinese hamster ovary cells, which are poorly permissive

282 -1 K(+) channels heterologously expressed in Chinese hamster ovary cells, which are silent in physiol

283 as investigated after overexpressing RAGE in Chinese hamster ovary cells, which lack RAGE.

284 ized co-expression of FcepsilonRI and Lyn in Chinese hamster ovary cells, which results in high basal

285 leasing intracellular proteins from adherent Chinese hamster ovary cells while preserving the cell vi

286 imulated 2D diffusion conditions and in live Chinese hamster ovary cells with a GFP-tagged transmembr

287 human IgG in vitro by stable transfection of Chinese hamster ovary cells with expression plasmids con

288 ropermeabilization of suspended and adherent Chinese hamster ovary cells with green DNA dye SYTOX is

289 ER, we transfected McArdle RH7777, HepG2, or Chinese hamster ovary cells with human albumin (ALB)/hum

290 Transfection of Chinese hamster ovary cells with human MARCO supported t

291 ced uptake of (45)Ca(2+) in TRPV1-expressing Chinese hamster ovary cells with IC(50) values of 17 +/-

292 Moreover, Chinese hamster ovary cells with mutant XRCC1 (EM9) were

293 Treatment of A(3)AR/SERT-cotransfected Chinese hamster ovary cells with the A(3)AR agonist N(6)

294 Stable transfection of Chinese hamster ovary cells with the MC-1 receptor showe

295 uman p22phox were generated and expressed in Chinese hamster ovary cells with transgenes for gp91phox

296 tive to E2F1-induced apoptosis compared with Chinese hamster ovary cells with wild-type XRCC1 (AA8).

297 iate Wnt-dependent cell motility, we treated Chinese hamster ovary cells with Wnt-3a-conditioned medi

298 nescence and storage lesion, was assessed in Chinese hamster ovary cells with/without functional GPIb

299 Analysis of a previously described Chinese hamster ovary cell xylosyltransferase mutant (ps

300 Ectopic expression of SREC-I in Chinese hamster ovary cells yielded chaperone recognitio