ライフサイエンスコーパス: Chinese hamster

1 we evaluated XRCC1-deficient and -proficient Chinese hamster and human cancer cells for synthetic let

2 ive replication of several OPXV species in a Chinese hamster cell line was caused by a species-specif

3 ray repair complementing defective repair in Chinese hamster cells 3 (XRCC3), 4 CpGs) birth weight.

4 ray repair complementing defective repair in Chinese hamster cells 4 (XRCC4).

5 ray repair complementing defective repair in Chinese hamster cells 5 (XRCC5).

6 g in potent inhibition against FR-expressing Chinese hamster cells and human KB tumor cells in cultur

7 in binding in G1-synchronized populations of Chinese hamster cells harboring amplified copies of the

8 (CHO-S and CHO DG44) and compared with seven Chinese hamster (Cricetulus griseus) tissues (brain, hea

9 t a 2.4-Gb draft genome sequence of a female Chinese hamster, Cricetulus griseus, harboring 24,044 ge

10 We created browsers for new species (Chinese hamster, elephant shark, minke whale), 'mined th

11 ompetitive binding assay was performed using Chinese hamster lung (CHL) cells transfected with GLP-1R

12 ompetitive binding assay was performed using Chinese hamster lung (CHL) cells transfected with the GL

13 type 2, early onset- (BRCA2-) deficient V79 Chinese hamster lung fibroblast cell line derivative (VC

14 Chinese hamster lung V79 cells and its mutant cell lines

15 n by RNA polymerase I promoters of human and Chinese hamster origin performed equally well.

16 Sialylation-deficient Chinese hamster ovarian (CHO) epithelial cell lines Lec1

17 hich led to higher uptake of 4-(18)F-T140 by Chinese hamster ovarian (CHO)-CXCR4 tumors.

18 ized LDL and acLDL to CR1 on CR1-transfected Chinese Hamster Ovarian cells (CHO-CR1) was tested by fl

19 Chinese hamster ovarian cells were cotransfected with CT

20 has been demonstrated from both E. coli and Chinese hamster ovaries (CHO) cell expression platforms;

21 In Chinese hamster ovary (CHO cells), coexpression of rat O

22 for inhibition of proliferation in isogenic Chinese hamster ovary (CHO) and HeLa cells expressing PC

23 bit the import of spermidine in DFMO-treated Chinese hamster ovary (CHO) and L3.6pl human pancreatic

24 Using Chinese hamster ovary (CHO) APP751SW cells, we identifie

25 city of the nine NOCs was quantified using a Chinese hamster ovary (CHO) cell assay, and the descendi

26 re, we present an effort to create a "clean" Chinese hamster ovary (CHO) cell by disrupting multiple

27 re mAb) and competitive conditions (mAb in a Chinese Hamster Ovary (CHO) cell culture harvest).

28 ant interferon gamma (IFN-gamma) produced in Chinese hamster ovary (CHO) cell culture.

29 Using a Chinese hamster ovary (CHO) cell line (PAT active) and i

30 e human amyloid precursor protein (APP) in a Chinese hamster ovary (CHO) cell line by cleaving APP at

31 s/mL) perfusion culture of an IgG1-producing Chinese hamster ovary (CHO) cell line for 18-25 days.

32 the dihydrofolate reductase (DHFR) gene in a Chinese hamster ovary (CHO) cell line.

33 d-type and glycosaminoglycan (GAG)-deficient Chinese hamster ovary (CHO) cell lines and soluble GAGs,

34 Chinese hamster ovary (CHO) cell lines are widely used i

35 al binding and transduction assays on mutant Chinese hamster ovary (CHO) cell lines defective in vari

36 vity were evaluated as expressed in a set of Chinese hamster ovary (CHO) cell lines under conditions

37 , we engineered and characterized a panel of Chinese hamster ovary (CHO) cell lines with inducible tr

38 ifficult in the case of genetically unstable Chinese hamster ovary (CHO) cell lines with only draft g

39 For Chinese Hamster ovary (CHO) cell lines, key indicators o

40 Chinese hamster ovary (CHO) cell-derived recombinant hum

41 he heavy chain and the light chain (LC) of a Chinese hamster ovary (CHO) cell-expressed monoclonal an

42 Mitochondria purified from wild-type Chinese hamster ovary (CHO) cells and HepG2 cells conver

43 We have previously reported the use of Chinese hamster ovary (CHO) cells and its PAT-deficient

44 om Schistosoma mansoni (Platyhelminthes), in Chinese hamster ovary (CHO) cells and use fluorescence-b

45 etection platform to image endogenous H2S in Chinese hamster ovary (CHO) cells and use the developed

46 fractions, here we show that, when parental Chinese hamster ovary (CHO) cells are briefly exposed to

47 e a broad host range in mammalian cells, but Chinese hamster ovary (CHO) cells are nonpermissive for

48 While parental Chinese hamster ovary (CHO) cells are permissive for bot

49 Chinese hamster ovary (CHO) cells are the predominant pr

50 Chinese hamster ovary (CHO) cells are widely used for th

51 ckdown with small interfering RNA (siRNA) in Chinese hamster ovary (CHO) cells augments M3-MR signali

52 o generate any current when transfected into Chinese hamster ovary (CHO) cells but, surprisingly, exe

53 The McKbac virus entered efficiently into Chinese hamster ovary (CHO) cells constitutively express

54 Furthermore, Rxt1/NTT4-transfected Chinese hamster ovary (CHO) cells exhibited significant

55 sibility of a nuclear-translocation assay in Chinese hamster ovary (CHO) cells expressing an NFkappaB

56 the binding of 5,6-EET-EA to membranes from Chinese hamster ovary (CHO) cells expressing either reco

57 shift in neonatal mouse cardiac myocytes or Chinese hamster ovary (CHO) cells expressing the mouse o

58 o demonstrate that somatostatin treatment of Chinese hamster ovary (CHO) cells expressing the wild ty

59 Chinese hamster ovary (CHO) cells expressing wild type o

60 ion of PS on the plasma membrane of isolated Chinese Hamster Ovary (CHO) cells following exposure to

61 hich KCNQ subunits are targeted by AKAP79 in Chinese hamster ovary (CHO) cells heterologously express

62 activation of human DORs stably expressed in Chinese hamster ovary (CHO) cells increased AMPK activit

63 this study, we evaluated the genotoxicity to Chinese hamster ovary (CHO) cells induced by municipal s

64 how that overexpression of TREK-1 in NPE and Chinese hamster ovary (CHO) cells leads to a significant

65 Recombinant antibodies produced in Chinese hamster ovary (CHO) cells often exhibit a slight

66 e of exporting the diamine putrescine in the Chinese hamster ovary (CHO) cells selected for resistanc

67 Chinese hamster ovary (CHO) cells stably expressing a Te

68 n embryonic kidney (HEK) 293, C6 glioma, and Chinese hamster ovary (CHO) cells stably expressing this

69 In mutant Chinese hamster ovary (CHO) cells that do not add galact

70 ition, compounds 3-6 inhibited the growth of Chinese hamster ovary (CHO) cells that expressed FRs but

71 beta-GlcNAc on the complex N-glycans of Lec8 Chinese hamster ovary (CHO) cells that lack UDP-Gal tran

72 ronic cytotoxicity and acute genotoxicity in Chinese hamster ovary (CHO) cells to compare the toxicit

73 We show that Chinese hamster ovary (CHO) cells used to express recomb

74 an amphotericin B loss-of-function screen in Chinese hamster ovary (CHO) cells using insertional muta

75 Single cell suspensions of Chinese hamster ovary (CHO) cells were plated on flasks

76 Treatment of fibroblasts or Chinese hamster ovary (CHO) cells with 25OH caused a 50-

77 LDL increased cytosolic G protein by 350% in Chinese hamster ovary (CHO) cells with genetically induc

78 accomplish glycomic survey of bioengineered Chinese Hamster Ovary (CHO) cells with knock-in/out enzy

79 Treating Chinese hamster ovary (CHO) cells with monoHANs followed

80 er cells were created by stably transfecting Chinese Hamster Ovary (CHO) cells with plasmids encoding

81 The mutant proteins were expressed in Chinese hamster ovary (CHO) cells, and their expression

82 Chinese hamster ovary (CHO) cells, first isolated in 195

83 and duration of reporter gene expression in Chinese Hamster Ovary (CHO) cells, Human Immortalized My

84 ter) obtained from red blood cells (RBC), or Chinese hamster ovary (CHO) cells, were immobilized on t

85 re assayed as luciferase reporter fusions in Chinese hamster ovary (CHO) cells, where the putative ci

86 re caused by EGFR expression, we transfected Chinese hamster ovary (CHO) cells, which lack EGFR expre

87 Here we describe a procedure to vesiculate Chinese hamster ovary (CHO) cells, widely used for the e

88 toward folate receptor (FR) alpha-expressing Chinese hamster ovary (CHO) cells.

89 binant antibody produced in tyrosine-limited Chinese hamster ovary (CHO) cells.

90 t human erythropoietin (rHuEPO) expressed in Chinese hamster ovary (CHO) cells.

91 recombinant monoclonal antibody expressed in Chinese hamster ovary (CHO) cells.

92 Caveolae were isolated from Chinese hamster ovary (CHO) cells.

93 TGF-beta-mediated cell growth inhibition in Chinese hamster ovary (CHO) cells.

94 roxides demonstrated low cytotoxicity toward Chinese hamster ovary (CHO) cells.

95 of several non-hepatic cancer cell lines and Chinese hamster ovary (CHO) cells.

96 increase in cyclic AMP (cAMP) production by Chinese hamster ovary (CHO) cells.

97 when all three subunits are reconstituted in Chinese hamster ovary (CHO) cells.

98 , SH-SY5Y, and when ectopically expressed in Chinese hamster ovary (CHO) cells.

99 reen fluorescent protein (EGFP) plasmid into Chinese hamster ovary (CHO) cells.

100 expressed in mammalian cell lines including Chinese hamster ovary (CHO) cells.

101 abolite profiles in samples from recombinant Chinese hamster ovary (CHO) cells.

102 aged interacting with the plasma membrane of Chinese hamster ovary (CHO) cells.

103 d hDAT fused to monomeric GFP (mGFP-hDAT) in Chinese hamster ovary (CHO) cells.

104 tis from invertebrate B. mori and vertebrate Chinese hamster ovary (CHO) cells.

105 terol distribution in the plasma membrane of Chinese hamster ovary (CHO) cells.

106 ssed in human embryonic kidney (HEK 293) and Chinese hamster ovary (CHO) cells.

107 ll many cells used in bioreactors, including Chinese Hamster Ovary (CHO) cells.

108 Therefore, we generated rhC7 from Chinese hamster ovary (CHO) cells.

109 We show in a Chinese hamster ovary (CHO) disease model cell line and

110 89%) of mouse-human heterohybridoma (HH) and Chinese hamster ovary (CHO) mAb-Ds blocked ADCC and clea

111 CD36 expressed in Chinese hamster ovary (CHO) or HEK 293 cells was found t

112 These analogues inhibited proliferation of Chinese hamster ovary (CHO) sublines expressing folate r

113 alysis was performed on mouse myeloma SP2/0, Chinese hamster ovary (CHO), and human embryonic kidney

114 the first N-glycosylation gene, DPAGT1, from Chinese hamster ovary (CHO), Madin-Darby canine kidney (

115 Chinese hamster ovary (CHO)- and human embryonic kidney

116 ryptamine 6 (5-HT(6)) receptors expressed in Chinese hamster ovary (CHO)-Dukx and HeLa cells.

117 InvD1L expressed in Chinese hamster ovary (CHO)-K1 cells was activated by do

118 RNA-based pathway inhibition in recombinant Chinese hamster ovary (CHO)-S1P2 cells as well as human

119 -expressing human WT or p.P888L SAP97 and in Chinese hamster ovary (CHO)-transfected cells.

120 ut not in other cell lines, such as HeLa and Chinese hamster ovary (CHO).

121 on was confirmed using human CR3-transfected Chinese hamster ovary (CHO-CR3) cells.

122 AIRS enzyme by analysis of mutations in the Chinese hamster ovary (CHO-K1) cell that require purines

123 arly ranking the cytotoxicity of the HBQs in Chinese hamster ovary (CHO-K1) cells.

124 study, we found that knockdown of cofilin in Chinese hamster ovary 7WD10 cells and primary neurons si

125 s (c13C6, h-13F6, and c6D8) were produced in Chinese hamster ovary and in whole plant (Nicotiana bent

126 CR3 affects the generation of cAMP, we used Chinese hamster ovary and K562 cells transfected to expr

127 ion of folate receptor (FR) alpha-expressing Chinese hamster ovary and KB human tumor cells.

128 in relation to endogenous Notch receptors of Chinese hamster ovary and murine embryonic stem (ES) cel

129 at were and were not associated with CSBS in Chinese Hamster Ovary and T84 cells and generated a zebr

130 was assayed in vitro by the transduction of Chinese hamster ovary and trabecular meshwork cells.

131 In transfected Chinese hamster ovary AP-1 cells, the Leu515Phe mutant p

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

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

134 1 antibody, generated during production in a Chinese hamster ovary cell culture, was observed in the

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

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

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

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

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

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

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

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

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

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

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

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

147 ected against membrane protein antigens in a Chinese hamster ovary cell system.

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

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

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

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

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

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

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

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

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

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

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

159 We expressed human CTRP6 in Chinese hamster ovary cells and investigated the binding

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

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

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

163 Chinese Hamster Ovary cells are the most popular host ex

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

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

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

167 affinity was measured in P2Y(14)R-expressing Chinese hamster ovary cells by flow cytometry.

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

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

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

171 nant human beta-gal (rhbeta-gal) produced in Chinese hamster ovary cells enabled direct and precise r

172 nant human Beta-Gal (rhBeta-Gal) produced in Chinese hamster ovary cells enabled direct and precise r

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

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

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

176 ning this exon promote serotonin uptake into Chinese hamster ovary cells expressing either vesicular

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

178 Chinese hamster ovary cells expressing marmoset or human

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

180 Chinese hamster ovary cells expressing the muscarinic ac

181 a synthetic naive human scFv library against Chinese hamster ovary cells expressing the oncogenic tar

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

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

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

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

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

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

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

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

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

191 emperature dependence of hERG kinetics using Chinese hamster ovary cells overexpressing hERG1a on the

192 ents as well as single-channel recordings on Chinese hamster ovary cells overexpressing I(Ks) channel

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

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

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

196 Chinese hamster ovary cells proliferated after cleavage

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

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 n, and competition assays using membranes of Chinese hamster ovary cells recombinantly expressing the

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

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

203 Expression of p.T224M KCNQ1 in Chinese hamster ovary cells showed near complete loss of

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

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

206 ated patch-clamp platform, by applying it to Chinese hamster ovary cells stably expressing hERG1a.

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

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

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

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

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

212 t a comprehensive gene engineering screen in Chinese hamster ovary cells that enables production of l

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

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

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

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

217 Second, in Chinese hamster ovary cells that heterologously express

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

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

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

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

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

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

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

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

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

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

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

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

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

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

232 Chinese hamster ovary cells were transfected with alpha(

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

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

235 We transfected Chinese hamster ovary cells with plasmids carrying wild

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

237 Conversely, transfection of Chinese hamster ovary cells with the core 2 GlcNAc trans

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

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

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

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

242 al epithelial cells) and a cancer cell line (Chinese hamster ovary cells) were exposed to liquid and

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

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

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

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

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

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

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

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

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

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

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

254 development of filopodia and lamellipodia in Chinese hamster ovary cells, stimulate their motility, a

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

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

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

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

259 In Chinese hamster ovary cells, three classes of adhesion c

260 when coexpressing ficolin-2 and ficolin-3 in Chinese hamster ovary cells, we could detect ficolin-2/-

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

262 -1 K(+) channels heterologously expressed in Chinese hamster ovary cells, which are silent in physiol

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

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

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

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

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

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

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

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

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

272 -100 nm) manner in human ChemR23-transfected Chinese hamster ovary cells.

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

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

275 in which hERG1a current was measured in nine Chinese hamster ovary cells.

276 for Puromycin resistance gene expression in Chinese Hamster Ovary cells.

277 tabolic reconstructions of human, mouse, and Chinese hamster ovary cells.

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

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

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

281 igate this possibility utilizing recombinant Chinese hamster ovary K1 cells.

282 ans to modify protein glycosylation, we used Chinese hamster ovary ldl-D cells defective in UDP-Gal/U

283 hanced binding to FcgammaRIIIa compared with Chinese hamster ovary or wild-type plant-derived 2G12.

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

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

286 ssessed in the arrestin recruitment assay in Chinese hamster ovary-K(1) cells expressing the long iso

287 etition binding assays using hB1R-expressing Chinese hamster ovary-K1 cell membranes.

288 In Chinese hamster ovary-K1 cells expressing the variant D3

289 g to platelets from P1 but absent binding to Chinese hamster ovary-K1 cells expressing variant D304N

290 Ca(2+) upregulation; however, in HEK293T or Chinese hamster ovary-K1 cells overexpressing M3R, piloc

291 single-point mutations were transfected into Chinese hamster ovary-K1 cells, and affinity and functio

292 type and mutants heterologously expressed in Chinese hamster ovary-K1 cells.

293 either the human endothelial kidney 293-F or Chinese hamster ovary-K1 systems.

294 tion of human erythrocytes when expressed in Chinese hamster ovary-K1, but not in human endothelial k

295 ne receptors (H1R and H2R) in U937 cells and Chinese hamster ovary-transfected cells.

296 screening assay using the GeneBridge4 human/Chinese hamster radiation hybrid panel and found to be t

297 s a unique inhibitor capable of antagonizing Chinese hamster SAMD9L (chSAMD9L).

298 While the Chinese hamster SAMD9L could not be inhibited by two pre

299 rget cells (Salmonella typhimurium TA100 and Chinese hamster V79) of standard mutagenicity tests trea

300 region of the genome, in two cell lines, the Chinese hamster V79-derived G12 and G10 cells, respectiv