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

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

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

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

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

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

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

9 into a human mini-chromosome within a human-Chinese hamster hybrid cell line.

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

11 Chinese hamster lung V79 cells and its mutant cell lines

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

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

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

15 Chinese hamster ovarian cells were cotransfected with CT

16 Expression of the mutant proteins in Chinese hamster ovarian-K1 cells revealed that a majorit

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

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

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

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

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

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

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

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

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

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

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

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

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

30 etrotransposition pathway (EN(i)) in certain Chinese hamster ovary (CHO) cell lines that are defectiv

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

61 Short-term activation of MOR in Chinese hamster ovary (CHO) cells stably transfected wit

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

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

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

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

66 tudy mechanisms, we engineered alphaIIbbeta3 Chinese hamster ovary (CHO) cells to conditionally expre

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

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

69 ivator, on hERG channels stably expressed in Chinese hamster ovary (CHO) cells using the patch-clamp

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

106 lecules, and in null versus AQP4-transfected Chinese hamster ovary (CHO)-K1 cells and Fisher rat thyr

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

108 ane protein gp41 when the Ab was produced in Chinese hamster ovary (CHO)-K1 cells.

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

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

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

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

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

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

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

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

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

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

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

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

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

122 1 antibody, generated during production in a Chinese hamster ovary cell culture, was observed in the

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

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

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

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

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

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

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

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

131 Stably transfected Chinese hamster ovary cell lines expressing increasing l

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

154 Chinese Hamster Ovary cells are the most popular host ex

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

171 Chinese hamster ovary cells expressing the muscarinic ac

172 Using Chinese hamster ovary cells expressing the PTH1R, where

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

190 Chinese hamster ovary cells proliferated after cleavage

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

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

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

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

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

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

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

198 50) = 0.2 microM) and whole-cell currents in Chinese hamster ovary cells stably expressing heteromult

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

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

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

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

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

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

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

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

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

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

209 Second, in Chinese hamster ovary cells that heterologously express

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

228 Chinese hamster ovary cells were transfected with alpha(

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

259 -1 K(+) channels heterologously expressed in Chinese hamster ovary cells, which are silent in physiol

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

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

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

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

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

265 -100 nm) manner in human ChemR23-transfected Chinese hamster ovary cells.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

280 eta42 secreted from human APP-overexpressing 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 ion and cell retention was confirmed using a Chinese hamster ovary model, in which cellular sphingoli

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

285 Overexpression of Nek3 in Chinese hamster ovary transfectants potentiated cytoskel

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

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

288 0), 1A(1)) allele variants expressed by CHO (Chinese hamster ovary) mammalian cells to study their ef

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

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

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

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

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

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

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

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

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

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

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

300 Chinese hamsters were orally immunized with four weekly