ライフサイエンスコーパス: cotransfect

1 ocal adhesions and was released when Akt was cotransfected.

2 affected when both HDV-L and HDV-S RNA were cotransfected.

3 expression plasmids for both receptors were cotransfected.

4 nd exogenous GFP-AKR1B10 fusion protein when cotransfected.

5 hird reacted only when CNTN1 and CASPR1 were cotransfected.

6 ecipitation of an Oatp1a1-PDZK1 complex from cotransfected 293T cells as well as from native rat live

7 splicing at the upstream 3' splice sites in cotransfected 293T cells.

8 VSV-G)-pseudotyped viruses were generated by cotransfecting 293T cells with expression plasmids encod

9 In undifferentiated MEL cells, cotransfected Abcb10 specifically interacts with Mfrn1 t

10 tors of the two-hybrid system, and they were cotransfected along with a chloramphenicol acetyltransfe

11 f AP-2 on Mn-SOD promoter transactivation we cotransfected AP-2-deficient HepG2 cells with a human Mn

12 the nucleus of transfected cells, recruited cotransfected ARP1 to these foci and potentiated ARP1-me

13 Reporter assays revealed that cotransfected C/EBPalpha activated the ZTA promoter even

14 autoregulation of the C/EBPalpha promoter by cotransfected C/EBPalpha in transient luciferase reporte

15 reporter gene assays, but in the presence of cotransfected C/EBPalpha, ZTA enhanced the level of C/EB

16 In cells, both cotransfected CARMA1/Bcl10 complex and the endogenous CB

17 acing the CCV ORF5 with the BAC cassette and cotransfecting CCO cells.

18 This was due to the transfer of PD from the cotransfected CD mutants to the DeltaPD mutant.

19 tivate Erag-dependent reporter constructs in cotransfected cell lines.

20 alternative SUMO-1 conjugation sites in both cotransfected cells and an in vitro sumoylation assay an

21 efficiently modified by SUMO-1 or SUMO-2 in cotransfected cells and in cells infected with a recombi

22 ein-dependent trafficking of DAT, we treated cotransfected cells and primary mesencephalic neurons wi

23 lled and adhered onto substrates composed of cotransfected cells bearing E-selectin and intercellular

24 ions were confirmed to occur in infected and cotransfected cells by coimmunoprecipitation assays foll

25 emoval of contactin from the cell surface of cotransfected cells does not reduce the elevated levels

26 ining microNS and micro2 protein from T1L in cotransfected cells mimicked the morphology difference b

27 Vaccination with these cotransfected cells provided a significant degree of pro

28 inylated DAT levels were decreased by 40% in cotransfected cells relative to cells expressing only DA

29 Confocal microscopy of cotransfected cells revealed that this mutant colocalize

30 tion, immunofluorescence assays performed on cotransfected cells showed that there was colocalization

31 he interaction of the M2-1 and N proteins in cotransfected cells was found to be sensitive to RNase A

32 ERs could regulate CRH promoter activity, we cotransfected cells with a CRH promoter construct and ei

33 Treatment of cotransfected cells with platelet-derived growth factor

34 ntly modified by SUMO-1 in both infected and cotransfected cells, as well as in in vitro assays, with

35 rtion of B-Myb formed complexes with p107 in cotransfected cells, however, B-Myb bound weakly to the

36 MPP(+)/MPTP models of Parkinsonism (SH-SY5Y cotransfected cells, mesencephalic neurons, transgenic m

37 In cotransfected cells, the two proteins colocalized in thi

38 n and DAT, in specific rat brain regions and cotransfected cells, through specific amino acid motifs

39 Kif15 and EspW colocalized in cotransfected cells, while ectopically expressed Kif15 l

40 AP with the EP4 receptor from the lysates of cotransfected cells.

41 lutamate receptor activation in Kv3.1/mGluR1-cotransfected cells.

42 -immunoadsorbs with myc-CHIP from cytosol of cotransfected cells.

43 h a 3-fold increase in basal NO release from cotransfected cells.

44 y mild trypsinization (0.1%, 30 s) of Ltk(-) cotransfected cells.

45 AT levels, in both mesencephalic neurons and cotransfected cells.

46 dative stress and cell death were reduced in cotransfected cells.

47 eplication compartments in both infected and cotransfected cells.

48 rom both the C/EBPalpha and p21 promoters in cotransfected cells.

49 5 colocalized with SKIP within the nuclei of cotransfected cells.

50 uced the calcium response in D(1)R and D(2)R cotransfected cells.

51 the cytoplasmic aggregation of p190RhoGEF in cotransfected cells.

52 ze extensively in a vesicular compartment in cotransfected cells.

53 with the PtdIns(3)P markers FYVE and SetA in cotransfected cells.

54 was found to colocalize poorly with UL11 in cotransfected cells.

55 and form a physical complex in A(3)AR/hSERT cotransfected cells.

56 tion from the Sema3a and Sema3d promoters in cotransfected cells.

57 s) to facilitate Cl(-)-HCO(3)(-) exchange in cotransfected cells.

58 nslated proteins and extracts of transiently cotransfected Chinese hamster ovary (CHO)-K1 cells confi

59 Treatment of A(3)AR/SERT-cotransfected Chinese hamster ovary cells with the A(3)A

60 er NECA or sildenafil stimulation of AR/SERT-cotransfected Chinese hamster ovary cells.

61 Cotransfected cJUN plus cFOS or TPA treatment transactiv

62 l cycle and that this arrest is abrogated by cotransfecting constitutively active beta-catenin or cyc

63 We cotransfected COS-1 cells (that provide viral large T an

64 mem147/M3R interaction occurred in the ER of cotransfected COS-7 cells, resulting in impaired traffic

65 In cotransfected COS-7 cells, wild-type and constitutively

66 endogenous CTCF in vivo was accomplished by cotransfecting COS-1 cells with a plasmid overexpressing

67 promoter-driven reporter gene expression in cotransfected CV-1 cells in which the beta-promoter has

68 ation of tumor-bearing mice using OX40L mRNA-cotransfected DCs resulted in significant enhancement of

69 We report here that cotransfected DNA molecules commonly transfer enhancer e

70 Conversely, cotransfected dominant-negative IRE1-alpha or small inte

71 Cotransfecting dozens of vectors into the haploid blood

72 were then analyzed in transient assays with cotransfected E1 or E2 expression vectors.

73 We find that stimulation by cotransfected EKLF is retained with the mutant promoter,

74 ion of these epitopes on the cell surface by cotransfecting Envs containing either the V2 or the V3 d

75 When IEBP and ERE-BP were cotransfected, ERE promoter-reporter activity was reduce

76 ression of WNK1 led to increased activity of cotransfected ERK5 in HEK293 cells.

77 endogenous Foxj1 expression and stimulate a cotransfected Foxj1 reporter in heterologous cells, and

78 nhibiting constructs, and in the presence of cotransfected Galpha subunits.

79 activity could be significantly augmented by cotransfected Galpha(i), Galpha(q), and Galpha(12/13) su

80 nces of PA-X also play a role in suppressing cotransfected gene expression.

81 lease active site, is sufficient to suppress cotransfected gene expression.

82 h specific shRNAs, increased expression of a cotransfected gene relative to standard plasmid vectors.

83 the ability to give increased expression of cotransfected genes (superinduction).

84 RT-PCRs revealed that RNA levels of cotransfected genes were unchanged during superinduction

85 ructs in HepG2 cells only in the presence of cotransfected glucocorticoid receptor (GR), whereas the

86 t the infectivity and plaquing efficiency of cotransfected GPCMV viral DNA was enhanced by GP82.

87 nd we visualized the neuronal processes with cotransfected green fluorescent protein.

88 Furthermore, cotransfecting HA-p70S6K1 with 4E-BP1, but not 4E-BP1(F1

89 CoR/mSin3A corepressor complexes, suppresses cotransfected HCF-1 complement-ation of a temperature le

90 The cotransfected HEK cells were then treated with doxorubic

91 s confirmed by coimmunoprecipitation in both cotransfected HEK293 cells and prostate cancer cells.

92 Electrophysiologic recordings of cotransfected HEK293 cells were performed to analyze the

93 In cotransfected HEK293 cells, Pcdh-gammaC5 promotes the tr

94 and naturally glycosylated m152 and RAE-1 in cotransfected HEK293T cells.

95 accumulate the receptor in the cytoplasm of cotransfected HepG2 cells.

96 uman constitutive active receptor (hCAR), in cotransfected HepG2 cells.

97 sal promoter region that is cis-activated by cotransfected HNF4alpha.

98 gged EV marker, CD63, after LPC treatment of cotransfected Huh-7 cells.

99 ct the generation of reassortant viruses, we cotransfected human embryonic kidney cells with plasmids

100 04A but not SC2-K208A inhibited secretion of cotransfected human growth hormone and of noradrenalin.

101 The ORF35-37 transcript was upregulated by cotransfected hypoxia-inducible factor (HIF).

102 When cotransfected in equal quantities with the wild-type com

103 When cotransfected in HEK293 cells, calmodulin bound to NCKX4

104 ract with histone deacetylase 1 (HDAC1) when cotransfected in human cell lines and by in vitro bindin

105 , hINV promoter linked to CAT reporter gene, cotransfected in human corneal simian virus 40-transform

106 When rbslo1 and 2 are cotransfected in non-polarized cells, they colocalized p

107 en tau and active kinase (Cdk5 and p25) were cotransfected in to COS cells, there was robust tau phos

108 viral genes involved in DNA replication were cotransfected into cells along with the mutant gfp-conta

109 onsiveness on TLR4 when mutant and TLR4 were cotransfected into cells expressing an NF-kappaB reporte

110 expressed normally on the cell surface when cotransfected into Chinese hamster ovary (CHO) cells.

111 SOCS-3 cDNA was cotransfected into cultured C2C12 myotubes with either t

112 ains alpha(IIb) K118C and beta(3) E171C were cotransfected into HEK 293 cells.

113 ephosphorylation at Thr-75 in DARPP-32 (also cotransfected into HEK293 cells).

114 s (HBV) replication, a 1.3mer HBV genome was cotransfected into HepG2 or Huh7 cells with plasmid expr

115 When M and N expression plasmids were cotransfected into human 293 renal epithelial cells, pse

116 To test this hypothesis, CCR1 was cotransfected into human embryonic kidney (HEK)293 cells

117 mphenicol acetyltransferase (CAT), they were cotransfected into human HeLa cells.

118 ctin can be secreted as heterooligomers when cotransfected into mammalian cells, and in vivo, adipone

119 This reporter construct was cotransfected into TM cells with a mammalian expression

120 ides and a TGMV A replicon encoding AL1 were cotransfected into tobacco protoplasts, and viral DNA re

121 We thus cotransfected Jurkat T cells with CEACAM1 isoform-encodi

122 fusion lymphoma (PEL) cells, as well as in a cotransfected KSHV-negative cell line.

123 alpha-synuclein in mesencephalic neurons and cotransfected Ltk- cells.

124 In cotransfected Ltk-, HEK 293, and SK-N-MC cells, alpha-sy

125 7 could be coimmunoprecipitated with M3Rs in cotransfected mammalian cells (COS-7 cells).

126 xpression does not reduce the aggregation of cotransfected mutant TBP containing 105 glutamines, it p

127 V) phenotypic assay has been investigated by cotransfecting mutant HIV clones expressing the firefly

128 K mutant Y576F/Y577F prevented activation of cotransfected myc-ERK2 by cyclic strain.

129 Cotransfecting NF-kappaB1 with RelA further increased ac

130 In cotransfected NMCs, AQP4 dominant negative reduced P(f)

131 5 and ZDHHC8 robustly palmitoylated Gp130 in cotransfected nonneuronal cells, supporting the possibil

132 of Keap1, and measurement of the ability of cotransfected Nrf2 to repress an ARE-luciferase reporter

133 Furthermore, we show that cotransfected Oct-1 augments BRLF1 binding to a variety

134 We show that cotransfected Oct-1 enhances the ability of BRLF1 to act

135 differentiation, but only in the presence of cotransfected Pbx and Meis Hox cofactors.

136 it does not affect the replication of other cotransfected plasmids containing only the SV40 origin.

137 ome and LCMV L and NP proteins supplied from cotransfected plasmids driven by the T7 RNA polymerase p

138 We cotransfected plasmids encoding a common origin of repli

139 in MDCK cells and suppressed expression from cotransfected plasmids in MDCK cells.

140 factors (NP and L), expressed from separated cotransfected plasmids.

141 gene transcription system was established by cotransfecting plasmids containing T7 promoter-driven la

142 Functional promoter analysis was examined by cotransfecting plasmids containing variable portions of

143 ependent promoter activity in the absence of cotransfected PPARgamma.

144 esulted in an induction of the activity of a cotransfected rat iNOS promoter-reporter (iNOS-luciferas

145 urface are segregated from clusters of other cotransfected receptor tyrosine kinases.

146 We found that cotransfecting replication constructs with a small dose

147 hypothesis, FAST promotes the expression of cotransfected reporter proteins, a process that requires

148 Cotransfected RTA also increased positive C/EBPalpha aut

149 perate to activate Dorsal synergistically in cotransfected Schneider cells.

150 At least five different genes can be cotransfected simultaneously including reporters, allowi

151 ined depending on the presence or absence of cotransfected Smad4.

152 C class II antigen presentation machinery by cotransfecting T84d with the MHC class I transactivator

153 RIG-I-like receptors on HBV replication, we cotransfected the HBV replicative plasmid with RIG-I or

154 we constructed deletion mutants of NF180 and cotransfected them with L-NFL.

155 separately in different NKCC1 constructs and cotransfected these in HEK cells, we observed FRET betwe

156 as not observed when ZTA and C/EBPalpha were cotransfected together in either HeLa or DG75 cells.

157 When cotransfected together with the wild-type vector into IF

158 vity, and reduced promoter responsiveness to cotransfected TR2/TR4.

159 , and they coimmunoprecipitate with Fyn from cotransfected tsA-201 cells.

160 repressive effects of these compounds on the cotransfected tyrosinase promoter.

161 We cotransfected various IE1-72 and p107 constructs into C3

162 ein to the mitochondria in the presence of a cotransfected wild-type, but not mutant Ku70 (S6A/S51A)

163 In cells transiently or stably cotransfected with 5-HT1A (G(alpha)i/o-coupled) and TRH-

164 78) compared with patches excised from cells cotransfected with a cDNA encoding the PKA peptide inhib

165 plasmid expressing either Mlx or ChREBP was cotransfected with a ChoRE-containing reporter plasmid i

166 ivity was partially restored when cells were cotransfected with a constitutively active form of Akt.

167 duced more than 10-fold when this mutant was cotransfected with a construct specifying an RNA molecul

168 rter were activated by 1,25-D3 only in cells cotransfected with a human VDR expression plasmid.

169 When cotransfected with a luciferase reporter construct conta

170 Neurons were cotransfected with a mitochondrially targeted cyan fluor

171 increased SOCS-3 expression, SOCS-3 cDNA was cotransfected with a NF-kappa B (NF-kappaB) luciferase c

172 e decrease of luciferase activities in cells cotransfected with a plasmid carrying APC promoter/lucif

173 ontrol of an RNA polymerase II promoter were cotransfected with a plasmid containing an LCMV minigeno

174 activate the IFN-inducible Mx promoter when cotransfected with a plasmid containing the zebrafish Mx

175 RBL-2H3 cells were cotransfected with a plasmid encoding a human growth hor

176 ontaining this CRE site was induced in cells cotransfected with a plasmid encoding the protein kinase

177 a B (NF-kappaB)-dependent transcription when cotransfected with a plasmid expressing retinoic acid-in

178 re dissociated, cultured at low density, and cotransfected with a plasmid expressing the green fluore

179 HepG2 cells were cotransfected with a reporter construct and one of sever

180 romoter vector expression was curtailed when cotransfected with a REST expressing plasmid.

181 nhanced luciferase activity when transiently cotransfected with a wild-type (wt) p53 expression vecto

182 nhanced luciferase activity when transiently cotransfected with a wild-type p53 expression vector in

183 If cotransfected with ActRII/IIB and ALK4, Cripto inhibited

184 g alpha(1) molecules, alpha(1C).beta(2b) was cotransfected with alpha(1B) (Ca(V)2.2), and pharmacolog

185 t produce functional AChRs unless cells were cotransfected with alpha5, beta3, or alpha6 to replace a

186 However, in cells cotransfected with AMN and the cubilin construct, cubili

187 When SKBr3 cells were cotransfected with an ARHI/luciferase reporter and E2F-e

188 When CIITA was cotransfected with an IL-10 promoter-reporter into a mou

189 -6 to alpha7A was abolished, when cells were cotransfected with an Src-related kinase, which is known

190 ells stably transfected with Cx40 or Cx43 or cotransfected with both connexins.

191 ore typical NFs were observed when NF180 was cotransfected with both NF-L and NF-M.

192 Human embryonic kidney 293 cells were cotransfected with c-Src and green fluorescent protein-R

193 Wild-type (wt) and mutated NKG2A were then cotransfected with CD94 into rat basophilic leukemia 2H3

194 the phosphorylation of tau in HEK293 cells, cotransfected with Cdk5/p25 and CIP, is effectively redu

195 r A3 receptor cDNA individually or they were cotransfected with cDNAs encoding either receptor plus I

196 genesis was performed, and CHO-K1 cells were cotransfected with cDNAs encoding wild-type or mutant CA

197 a large three-dimensional set of fixed cells cotransfected with CFP/YFP pairs of proteins that either

198 on and activity measurements in HEK293 cells cotransfected with cPLA(2)alpha and p11 also showed that

199 In cells cotransfected with CPR and PGRMC1, strong binding of CPR

200 Chinese hamster ovarian cells were cotransfected with CTLA4-Ig vector and a dihydrofolate r

201 293 cells were cotransfected with different proportions of plasmids enc

202 rent density and [(3)H]RTX affinity in cells cotransfected with different ratios of wild-type and mut

203 HFO, or HTR11 overexpression constructs were cotransfected with double- or single-stranded forms of a

204 s significantly suppressed when CTLA-4BP was cotransfected with either CD80 or CD28BP.

205 COS-1 cells were cotransfected with either wild-type (WT) RDS or RDS cont

206 HUVECs were cotransfected with enhanced Green Fluorescent Protein (e

207 ither eNOS alone and then treated with PV or cotransfected with eNOS and constitutively active v-Src

208 ing analysis of individual endothelial cells cotransfected with eNOS-ECFP and calmodulin-EYFP shows t

209 Epo stimulation of CHO cells cotransfected with Epo-R and TRPC2 resulted in a rise in

210 calcium influx through TRPC2, CHO cells were cotransfected with Epo-R subcloned into pTracer-CMV and

211 an increase in SNAT2 promoter activity when cotransfected with estrogen receptor alpha (ER-alpha) af

212 trusion by the pump, model cells (HeLa) were cotransfected with expression plasmids encoding its muta

213 A20 IIA1.6 B cells cotransfected with FcalphaR and wild-type gamma-chain (w

214 contain detectable endogenous FGF-2 protein, cotransfected with FGF-2 and LMP1.

215 discovery was designed using dendritic cells cotransfected with full-length transcripts of self-TAA a

216 e transfected stably with functional AQP4 or cotransfected with functional AQP4 and a transport-defic

217 However, when these cells were cotransfected with G protein-coupled receptor kinase 2,

218 Moreover, EBNA3C when cotransfected with Gal4-Nm23-H1 enhanced the transcripti

219 laced into the pcDNA-3 expression vector and cotransfected with Galpha16 cDNA into COS-1 cells, 8C10

220 ritic cells from HLA-A2-negative donors were cotransfected with GPC3 and HLA-A2 RNA to stimulate and

221 sured whole-cell Cl(-) currents in BHK cells cotransfected with GPCRs and CFTR.

222 on of eNOS and dynamin in both Clone 9 cells cotransfected with green fluorescent protein-dynamin and

223 In cells cotransfected with green fluorescent protein-tagged ASBT

224 HeLa cells were cotransfected with HIV-1 constructs producing pseudoviru

225 odest increase in promoter activity in cells cotransfected with hPXR.

226 In 293 cells cotransfected with htt exon 1 containing an expanded pol

227 Analysis of ER Ca(2+) uptake in cells cotransfected with human wild-type SERCA2a (SERCA2a(WT))

228 For validation, C33 cells were cotransfected with increasing amounts of selected TF exp

229 lones and subclones of the CJ394 genome were cotransfected with intact OD4 DNA into Vero cells, the t

230 s (which lack K(v)beta subunits) transiently cotransfected with K(v)1.5+K(v)beta1.3 and also rat vent

231 Using a FcgammaRI-p85 receptor chimera cotransfected with kinase-inactive mutants of Syk or app

232 ined rat heart cryosections and HEK293 cells cotransfected with Kir2.1 and WT-Cav3 both demonstrated

233 When the same SUR1 was cotransfected with Kir6.2, functional K(ATP) channels we

234 In cells cotransfected with Kir6.2, SUR1, and TRPM4, we measured

235 beta(2)WT3'UTR had decreased expression when cotransfected with let-7f, but a mutated luc-beta(2)3'UT

236 When cotransfected with luciferase reporter vectors containin

237 ells (HCE-T, RCB1384) and HEK-293 cells were cotransfected with mammalian expression vectors containi

238 in HEK293 (human embryonic kidney 293) cells cotransfected with mGluR1 or mGluR5.

239 Allogeneic T cells cotransfected with mRNAs encoding the alpha and beta cha

240 lyzed IFNB1 reporter levels in HEK293T cells cotransfected with mutant or nonmutant STING constructs.

241 Cells cotransfected with Na(+) channel Na(v)1.2alpha and beta1

242 When cotransfected with normal VWF, Cys1149Arg or the double

243 n transfected cells formed trimers only when cotransfected with NSP4.IMPORTANCE Rotavirus, a member o

244 f p12 and p17 accumulated in cells that were cotransfected with p12 and a caspase inactive mutant of

245 ent mediated transcriptional repression when cotransfected with pcDNA3.1/HOXA10 in transient-transfec

246 When pNV-GFP was cotransfected with pCI-LC in MVA-T7-infected cells, we o

247 ired for its degradation, HEK293T cells were cotransfected with plasmids containing cDNAs of human iN

248 uman hepatoma cell line Huh7 was transiently cotransfected with plasmids containing the HBV genome an

249 ISA and immunoprecipitation in HEK 293 cells cotransfected with plasmids encoding the alpha- and beta

250 However, vhs does accumulate in cells cotransfected with plasmids expressing two other tegumen

251 When rabbit skin cells were cotransfected with plasmids that express LAT sRNA1 and H

252 The modified GAL4-containing constructs were cotransfected with plasmids that expressed GAL4 fusion p

253 ts own, was translocated to the nucleus when cotransfected with PPF.

254 Protoplasts transiently cotransfected with promoter-luciferase and gene-specific

255 to monitor rat hippocampal pyramidal neurons cotransfected with PSD-95-GFP and DsRed-Express, and we

256 revented NMDA-mEPSC amplitude reduction when cotransfected with PSD-95gfp.

257 ckaging, we examined virus produced in cells cotransfected with PTC-bearing retroviral clones and wil

258 When cotransfected with rat NF-L into SW13c1.2vim(-) cells, N

259 l lytic replication, purified virion DNA was cotransfected with Rd1 or Rd2 into fibroblasts.

260 Cells cotransfected with RDH1 and any one of three retinal deh

261 We demonstrate here that these PNAs, when cotransfected with recombinatory donor DNA fragments, ca

262 ter activity by over 5-fold when transiently cotransfected with reporter constructs.

263 n 10T1/2 fibroblasts unless these cells were cotransfected with Runx2.

264 DCA further repressed reporter activity when cotransfected with RXRalpha/FXR.

265 When HEK293T cells were cotransfected with S1P(5) and G protein DNAs, prepared m

266 R-targeted Ca(2+) sensor R-CEPIA1er in cells cotransfected with SERCA2a and ryanodine receptor.

267 tivity also occurred in opossum kidney cells cotransfected with SGLT2 and MAP17.

268 he siRNA-induced apoptosis, LnCaP cells were cotransfected with siRNA specific to the HOXC6 3'UTR and

269 was even more pronounced in cells that were cotransfected with siRNAs directed against both collagen

270 and developed more rapidly when olf186-F was cotransfected with Stim.

271 BHK cells were either cotransfected with TGEV-Rep(AvrII) (E gene deletion) and

272 When cotransfected with the full-length EGFR, but not Y992Del

273 eration of inositol phosphates in COS7 cells cotransfected with the Gbetagamma-regulated effector pho

274 In the case of the 293 cells cotransfected with the HIV-1 pNL4-3 proviral DNA and the

275 When AP2 was cotransfected with the hRFC-A reporter construct into HT

276 rcentage of cardiac cells killed in myocytes cotransfected with the human A3 receptor than in those c

277 ls that do not express DNA-PKcs and in cells cotransfected with the immediate early protein ICP0, whi

278 he luciferase activity dose-dependently when cotransfected with the mouse or human notch3 3'-untransl

279 helial cells to H. pylori, HEK293 cells were cotransfected with the NF-kappa B-Luc reporter, CD14 and

280 s reduced enzyme activity when the cells are cotransfected with the Nfluc (1-475) fragment expressed

281 However, when cotransfected with the other glycoproteins required for

282 s Cdk5 activity in vitro and in HEK293 cells cotransfected with the peptide and Cdk5/p25, but had no

283 Cells cotransfected with the resultant PKDgalvp fusion protein

284 a partial increase in promoter activity when cotransfected with the TLR2 promoter with one of the Sp1

285 Cells cotransfected with the VPAC(1) receptor (VPAC(1)R) and G

286 ia-induced reporter gene expression in cells cotransfected with the wild type leptin -116/HRE constru

287 Cells cotransfected with these plasmids and delta env genomes

288 uc-3'-UTR mutants decreased drastically when cotransfected with Tis11b plasmid, correlating with an a

289 Human colonic epithelial cells cotransfected with TLR1 and -2 preferentially respond to

290 ation in human microvessel endothelial cells cotransfected with TLR2 cDNA.

291 ial cells (MAECs) and HEK293 cells that were cotransfected with TRPV4, TRPC1, and TRPP2.

292 eased V1bR promoter activity by 11-fold when cotransfected with V1bRp2.5-Luc and increased endogenous

293 the full-length EP4 receptor in HEK293 cells cotransfected with V5-tagged EPRAP and FLAG-tagged EP4 r

294 However, when the K88E DNA was cotransfected with wild type PITX2, analogous to the pat

295 by using the luciferase assay in 293T cells cotransfected with wild-type and mutant TACI.

296 Expression of such mutants in BJAB cells cotransfected with wild-type K1 results in dramatic inhi

297 Furthermore, we observed in HEK cells cotransfected with wild-type, Y14D, or Y14F Cav1-CFP and

298 FRET signals did not occur in cells cotransfected with YFP-apoE4 and apoE4-CFP, suggesting t

299 In addition, cotransfected YY-1 enhanced both IL-4 promoter activity

300 the ZTA promoter even more effectively than cotransfected ZTA.