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1 alpha-1-mediated expression of the reporter chloramphenicol acetyltransferase.
2 transfection assays with plasmids expressing chloramphenicol acetyltransferase.
3 er gene such as green fluorescent protein or chloramphenicol acetyltransferase.
4 orase 5' region upstream of a reporter gene, chloramphenicol acetyltransferase.
5 e transcriptional activation of the gene for chloramphenicol acetyltransferase.
6 lso possessed the cat2 gene, which encodes a chloramphenicol acetyltransferase.
9 CHN) resulted in repression of IL-6 promoter chloramphenicol acetyltransferase activity (P < 0.05).
10 a-2 cells led to an increase in RII promoter-chloramphenicol acetyltransferase activity and RII expre
12 P 1/2A, stimulated the iNOS promoter-derived chloramphenicol acetyltransferase activity in astrocytes
13 the pineal hormone, melatonin, can stimulate chloramphenicol acetyltransferase activity in Drosophila
14 ortmannin also induced iNOS promoter-derived chloramphenicol acetyltransferase activity in LPS- or IL
15 ytes and inhibited the iNOS promoter-derived chloramphenicol acetyltransferase activity in macrophage
16 S gene transcription activity as assessed by chloramphenicol acetyltransferase activity in Raw264.7 c
18 was attributed to a decrease in RII promoter-chloramphenicol acetyltransferase activity that was asso
21 repinephrine-induced cAMP-regulated enhancer-chloramphenicol acetyltransferase activity was inhibited
27 kbone fold, which is also similar to that of chloramphenicol acetyltransferase and dihydrolipoyl tran
28 ervations were further supported by chimeric chloramphenicol acetyltransferase and Epo-3'-UTR constru
29 sRobo) that expressed reporter genes such as chloramphenicol acetyltransferase and green fluorescent
31 ferent proteins, bovine rhodanese, bacterial chloramphenicol acetyltransferase and MS2 coat protein,
32 found in the structurally unrelated type III chloramphenicol acetyltransferase and suggest that His 7
33 n were fused to the reporter gene, bacterial chloramphenicol acetyltransferase, and relative expressi
34 dition, successful co-expression of GFP with chloramphenicol acetyltransferase, and thioredoxin with
35 to diacetyl chloramphenicol, the product of chloramphenicol acetyltransferase, as it was to chloramp
37 7D nuclear extracts in vitro, in a transient chloramphenicol acetyltransferase assay, as well as defe
38 if as measured in transient-transfection and chloramphenicol acetyltransferase assays and also inhibi
41 Nuclear run-on and TSP 2 promoter-reporter (chloramphenicol acetyltransferase) assays showed similar
42 ic liposome-DNA complexes (CLDCs) containing chloramphenicol acetyltransferase, beta-galactosidase (b
43 t a 293-base pair betaMyHC promoter fused to chloramphenicol acetyltransferase (beta293) responds to
44 ng partners of an insoluble protein fused to chloramphenicol acetyltransferase by monitoring the surv
45 ns of various APE1 promoter fragments to the chloramphenicol acetyltransferase CAT reporter gene indi
46 ere cotransfected with plasmids containing a chloramphenicol acetyltransferase (CAT ) reporter gene u
47 corporation of [3H]uridine and a decrease in chloramphenicol acetyltransferase (CAT) activity in a de
48 nic acid capsule genes (hasABC) by measuring chloramphenicol acetyltransferase (CAT) activity in a re
49 by the ability of BK to stimulate increased chloramphenicol acetyltransferase (CAT) activity in A549
50 ion of JNK and p38 correlated with increased chloramphenicol acetyltransferase (CAT) activity in repo
53 nting analysis of transcripts encoded by the chloramphenicol acetyltransferase (CAT) and beta-galacto
54 uence is inserted between the reporter genes chloramphenicol acetyltransferase (CAT) and beta-glucuro
57 n, each cell line was transfected with pRARE-chloramphenicol acetyltransferase (CAT) and treated with
58 residues were appended to the C terminus of chloramphenicol acetyltransferase (CAT) and were tested
59 to activate both RRE-mediated reporter gene [chloramphenicol acetyltransferase (CAT) and/or gag] expr
62 on cells fail to express a TbetaR-2 promoter/chloramphenicol acetyltransferase (CAT) construct but ov
63 tat expression plasmid with the JDV promoter chloramphenicol acetyltransferase (CAT) construct pJDV-U
65 transfected with a chimeric gene expressing chloramphenicol acetyltransferase (CAT) driven by the pr
67 um were noted to be the dominant inducers of chloramphenicol acetyltransferase (CAT) expression in MC
68 ors required for insulin-increased prolactin-chloramphenicol acetyltransferase (CAT) expression while
69 and ARM-COOH was sufficient for redirecting chloramphenicol acetyltransferase (CAT) from the cytosol
72 ulin on the basal expression of mouse G6Pase-chloramphenicol acetyltransferase (CAT) fusion genes tra
74 it of glucose-6-phosphatase (G6Pase), G6Pase-chloramphenicol acetyltransferase (CAT) fusion genes wer
75 ) gene transcription a series of collagenase-chloramphenicol acetyltransferase (CAT) fusion genes wer
76 of the IGRP gene, a series of truncated IGRP-chloramphenicol acetyltransferase (CAT) fusion genes wer
77 c and intestinal expressions of the reporter chloramphenicol acetyltransferase (CAT) gene (which subs
78 tream flanking sequences using the bacterial chloramphenicol acetyltransferase (CAT) gene as a report
79 ted mutagenesis were fused to a promoterless chloramphenicol acetyltransferase (CAT) gene as a report
80 ndent transactivation of human hARE-mediated chloramphenicol acetyltransferase (cat) gene expression
82 A-deleted Ad7a reporter virus expressing the chloramphenicol acetyltransferase (CAT) gene from the cy
83 (VLPs) in which a functional viral RNA-like chloramphenicol acetyltransferase (CAT) gene is delivere
84 d transgenic mice in which expression of the chloramphenicol acetyltransferase (CAT) gene is driven b
85 either P1 or P2 was linked to the bacterial chloramphenicol acetyltransferase (CAT) gene resulted in
86 eporter genes were developed consisting of a chloramphenicol acetyltransferase (CAT) gene the native
87 rivative (PureIDelta100), and a promoterless chloramphenicol acetyltransferase (CAT) gene were constr
88 n HepG2 cells transiently transfected with a chloramphenicol acetyltransferase (CAT) gene whose expre
92 ansient expression of two reporter proteins, chloramphenicol acetyltransferase (CAT) or luciferase, w
93 The HS2 enhancer in transfected recombinant chloramphenicol acetyltransferase (CAT) plasmids was als
94 Thus, the effect of RPTPalpha on prolactin-chloramphenicol acetyltransferase (CAT) promoter activit
95 liver thiolase (rthio) and various chimeric chloramphenicol acetyltransferase (CAT) proteins were ex
96 hancer binding protein (C/EBP)/NFIL-6-driven chloramphenicol acetyltransferase (CAT) reporter activit
98 ctivity using cotransfection with ferritin H-chloramphenicol acetyltransferase (CAT) reporter constru
100 Mutagenized E-boxes in M6P/IGFIIR promoter-chloramphenicol acetyltransferase (CAT) reporter constru
101 3'UTRs of these transcripts were mapped and chloramphenicol acetyltransferase (CAT) reporter constru
102 pendent transcription from an egr-1 promoter/chloramphenicol acetyltransferase (CAT) reporter constru
103 e transiently transfected with CDT6 promoter-chloramphenicol acetyltransferase (CAT) reporter constru
105 omoters for these genes were analysed with a chloramphenicol acetyltransferase (CAT) reporter gene an
107 Activation of a CRE-dependent junB promoter/chloramphenicol acetyltransferase (CAT) reporter gene by
108 ibroblasts with a battery of 5' end deletion/chloramphenicol acetyltransferase (CAT) reporter gene co
110 e consisting of a negative-sense copy of the chloramphenicol acetyltransferase (CAT) reporter gene fl
111 if (kappaL-kappaR)-dependent VCAM-1 promoter-chloramphenicol acetyltransferase (CAT) reporter gene la
112 r genes and an NFkappaB motif containing the chloramphenicol acetyltransferase (CAT) reporter gene ma
113 kb fragment, of the mE-RABP gene driving the chloramphenicol acetyltransferase (CAT) reporter gene re
114 events, paclitaxel stimulated AP-1-dependent chloramphenicol acetyltransferase (CAT) reporter gene tr
115 oxynitrosohydrazone)bis-) had no effect on a chloramphenicol acetyltransferase (CAT) reporter gene un
117 anscriptional start site) fused to a LacZ or chloramphenicol acetyltransferase (CAT) reporter gene we
118 he MMP-2 promoter was linked upstream of the chloramphenicol acetyltransferase (CAT) reporter gene, C
119 he rat FAS 5'-flanking sequence fused to the chloramphenicol acetyltransferase (CAT) reporter gene.
120 nit alone was unable to induce an NF-kappa B/chloramphenicol acetyltransferase (CAT) reporter gene.
121 al regulation by IL-1alpha and IL-1beta to a chloramphenicol acetyltransferase (CAT) reporter gene.
122 myc promoter constructs cloned upstream of a chloramphenicol acetyltransferase (CAT) reporter gene.
123 ES and Lab-Lb intervening segment fused to a chloramphenicol acetyltransferase (CAT) reporter has bee
124 n retinoblastoma cells were transfected with chloramphenicol acetyltransferase (CAT) reporter plasmid
125 gene promoter sequence were subcloned into a chloramphenicol acetyltransferase (CAT) reporter vector
126 em, and they were cotransfected along with a chloramphenicol acetyltransferase (CAT) reporter vector
128 ne promoter, robust in vitro expression of a chloramphenicol acetyltransferase (CAT) reporter was det
129 oid activation of the promoter attached to a chloramphenicol acetyltransferase (CAT) reporter, but in
132 Transcriptional fusions to the reporter gene chloramphenicol acetyltransferase (CAT) revealed that re
133 CAT element led to significant reductions in chloramphenicol acetyltransferase (CAT) specific activit
134 amster galectin-3 to the cytoplasmic protein chloramphenicol acetyltransferase (CAT) supported the ra
137 ed by a shortened version of intron 1 to the chloramphenicol acetyltransferase (CAT) vector showed th
139 , including green fluorescent protein (GFP), chloramphenicol acetyltransferase (CAT), and luciferase.
143 the third vector containing a reporter gene, chloramphenicol acetyltransferase (CAT), they were cotra
144 fine the underlying mechanism, we prepared a chloramphenicol acetyltransferase (CAT)-p21(waf1/cip1) 3
145 ctively eliminated the replication of the DI-chloramphenicol acetyltransferase (CAT)-reporter, as dem
149 rent marrow cells, carrying a reporter gene [chloramphenicol acetyltransferase (CAT)] under the contr
151 wnstream cistron encoded a reporter protein (chloramphenicol acetyltransferase [CAT]) under translati
153 modified to recognize various target mRNAs (chloramphenicol acetyltransferase [CAT], beta-galactosid
154 in, netilmicin, and tobramycin resistance; a chloramphenicol acetyltransferase, catB8; and gene aadA1
155 n expression relative to cells infected with chloramphenicol acetyltransferase (CATneo) as a control.
156 ked plasmid DNA containing the luciferase or chloramphenicol acetyltransferase cDNA directly to mouse
157 ments, but not MYC 3'-untranslated region or chloramphenicol acetyltransferase coding sequences, medi
159 otein inhibited basal expression of the SP-A/chloramphenicol acetyltransferase construct in MLE-15 ce
160 ivated a transiently expressed PCNA promoter chloramphenicol acetyltransferase construct through p53
161 , and Smads, within the p-560Col7a1 promoter/chloramphenicol acetyltransferase construct, coupled wit
163 ed transcriptional activity of SP-A promoter-chloramphenicol acetyltransferase constructs containing
164 ion at p19, we made a series of p19 promoter chloramphenicol acetyltransferase constructs in which th
166 sfected with various SM alpha-actin promoter/chloramphenicol acetyltransferase deletion mutants and s
167 c promoter/enhancer regulating expression of chloramphenicol acetyltransferase demonstrated 50-250-fo
168 rive transcription of the bacterial gene for chloramphenicol acetyltransferase demonstrated that the
170 hares unexpected similarity to structures of chloramphenicol acetyltransferase, dihydrolipoyl transac
171 nding affinity between YAP and p53BP-2 using chloramphenicol acetyltransferase/enzyme-linked immunoso
172 disrupted terminal complementarity abolished chloramphenicol acetyltransferase expression and RNA syn
173 nhibited IL-4, but not IL-2, promoter-driven chloramphenicol acetyltransferase expression in transien
175 -fold increase in expression of a UV-damaged chloramphenicol acetyltransferase expression vector tran
176 sequence and first intron were ligated into chloramphenicol acetyltransferase expression vectors, tr
177 enhances interleukin (IL)-4 promoter-driven chloramphenicol acetyltransferase expression, while repr
180 hepatoma cells that express a PEPCK promoter-chloramphenicol acetyltransferase fusion gene that is re
181 ently co-transfected with a series of G6Pase-chloramphenicol acetyltransferase fusion genes and an ex
182 to replace the an open reading frame with a chloramphenicol acetyltransferase gene (cat) and a bacmi
183 To determine the pattern of translation, a chloramphenicol acetyltransferase gene (cat) reporter wa
184 constructed, respectively, by insertion of a chloramphenicol acetyltransferase gene and the tetM tetr
186 rik5 (3.4 kb) inhibited transcription of the chloramphenicol acetyltransferase gene driven by the 2-k
187 lements that confer hormonal inducibility to chloramphenicol acetyltransferase gene expression both i
188 DNA, resulting in enhanced expression of the chloramphenicol acetyltransferase gene in most tissues e
189 ssay for (CAG)(n)*(CTG)(n) deletion from the chloramphenicol acetyltransferase gene integrated into t
191 ch a firefly luciferase gene was linked to a chloramphenicol acetyltransferase gene using a segment o
192 of the has operon promoter to a promoterless chloramphenicol acetyltransferase gene were constructed
193 5' or 3' to the promoter, and a promoterless chloramphenicol acetyltransferase gene were used (i) to
195 of the gamma-fibrinogen promoter coupled to chloramphenicol acetyltransferase gene, an IL-6 responsi
196 e for the expression of a reporter gene, the chloramphenicol acetyltransferase gene, in a mouse liver
197 ansformed an exthemophilic red alga with the chloramphenicol acetyltransferase gene, rendering this o
198 ansformed an exthemophilic red alga with the chloramphenicol acetyltransferase gene, rendering this o
199 t ribosomal gene (rDNA) promoter linked to a chloramphenicol acetyltransferase gene, we show that at
203 muscle cells by binding to myocyte-specific chloramphenicol acetyltransferase heptamer elements in t
205 e estrogen receptor a-mediated expression of chloramphenicol acetyltransferase in SK-BR-3 cells.
206 direct the expression of the reporter gene, chloramphenicol acetyltransferase, in airway epithelial
207 mblance of catalysis by the EntF C domain to chloramphenicol acetyltransferase, including an active s
210 rmore, addition of -AKM to the C terminus of chloramphenicol acetyltransferase is sufficient to targe
211 transfected reporter gene (the gene encoding chloramphenicol acetyltransferase) linked to the promote
212 lation using three separate reporter assays (chloramphenicol acetyltransferase, luciferase, and red f
213 smid containing a Himar1 transposon encoding chloramphenicol acetyltransferase, mCherry fluorescent p
214 tant to chloramphenicol due to production of chloramphenicol acetyltransferase mediated by catP.
215 ts on VSV in vitro transcription and in vivo chloramphenicol acetyltransferase minigenome replication
216 integrated with a mouse mammary tumor virus-chloramphenicol acetyltransferase (MMTV-CAT) reporter, w
217 e RNase protection assay shows that HIV-1 U5-chloramphenicol acetyltransferase mRNA expressed intrace
218 erase chain reaction was used to measure the chloramphenicol acetyltransferase mRNA levels before and
221 o reflected at the levels of cytoplasmic RRE-chloramphenicol acetyltransferase mRNAs, indicating that
222 nsactivation of the E2F-1 promoter linked to chloramphenicol acetyltransferase or green fluorescent p
223 l coumarin caused an accumulation of nascent chloramphenicol acetyltransferase peptides in the mass r
226 ted with an mouse mammary tumor virus (MMTV) chloramphenicol acetyltransferase reporter (Cat0) synchr
227 r Delta-35 decreased cAMP responsive element-chloramphenicol acetyltransferase reporter activity, dem
229 in Drosophila SL-3 cells transfected with a chloramphenicol acetyltransferase reporter construct con
231 of a mutated or deleted residue 1 of a cRNA chloramphenicol acetyltransferase reporter construct, su
232 s, in marked contrast to its effect on a DBH-chloramphenicol acetyltransferase reporter construct.
233 nd to confer B-Myb responsiveness to a bcl-2/chloramphenicol acetyltransferase reporter construct.
235 ffected the transcriptional activity of PCNA-chloramphenicol acetyltransferase reporter constructs in
237 e EICP0 protein independently transactivated chloramphenicol acetyltransferase reporter constructs un
238 by transient cotransfection with ferritin H-chloramphenicol acetyltransferase reporter constructs.
239 trolled by a collagenase AP-1 sequence and a chloramphenicol acetyltransferase reporter controlled by
240 enerated double transgenic mice carrying the chloramphenicol acetyltransferase reporter driven by the
241 thermore, phenserine reduced expression of a chloramphenicol acetyltransferase reporter fused to the
242 ucocorticoid response elements (GRE) and the chloramphenicol acetyltransferase reporter gene (AdGRE.C
243 e stimulated a 14-fold increase in NF-kappaB-chloramphenicol acetyltransferase reporter gene activity
244 The minimal promoter sufficient to drive chloramphenicol acetyltransferase reporter gene activity
245 the betaB1-crystallin promoter fused to the chloramphenicol acetyltransferase reporter gene and a pl
246 expression vectors were cotransfected with a chloramphenicol acetyltransferase reporter gene and, in
247 ctions with a series of 5'-deletion promoter/chloramphenicol acetyltransferase reporter gene construc
248 II distal promoter constructed upstream of a chloramphenicol acetyltransferase reporter gene demonstr
249 lso suppressed the NDV-mediated induction of chloramphenicol acetyltransferase reporter gene driven b
250 t to bind AP-2 proteins and failed to target chloramphenicol acetyltransferase reporter gene expressi
251 strongly synergized with Tat on Tat-mediated chloramphenicol acetyltransferase reporter gene expressi
252 placement of ORF-2 with the major ORF of the chloramphenicol acetyltransferase reporter gene followed
253 sitive) inhibited MCAM/MUC18 promoter-driven chloramphenicol acetyltransferase reporter gene in a dos
254 e is sufficient for high level expression of chloramphenicol acetyltransferase reporter gene in NCI-H
255 , to support tissue-specific expression of a chloramphenicol acetyltransferase reporter gene in trans
256 an directly activate an IL-4 promoter-driven chloramphenicol acetyltransferase reporter gene in trans
257 he Egr1 protein in PC12 cells stimulates the chloramphenicol acetyltransferase reporter gene placed u
258 lymphoid cell-specific virus upstream of the chloramphenicol acetyltransferase reporter gene showed t
259 Increases in blk promoter activity using a chloramphenicol acetyltransferase reporter gene system s
260 m transgenic mice carrying a type I collagen-chloramphenicol acetyltransferase reporter gene to follo
261 Consistent with this, transcription of a chloramphenicol acetyltransferase reporter gene was cons
262 B expression, the seb promoter fused to the chloramphenicol acetyltransferase reporter gene was intr
263 moter-variants were compared in vitro with a chloramphenicol acetyltransferase reporter gene, and in
264 ith a strong 5' erythroid enhancer driving a chloramphenicol acetyltransferase reporter gene, rho-CAT
274 s flanking the Bmp2 gene were screened using chloramphenicol acetyltransferase reporter genes in F9 c
275 ty of a somatostatin cAMP-regulated enhancer-chloramphenicol acetyltransferase reporter in these cell
276 and Ets2 indeed transactivate a PS1 promoter-chloramphenicol acetyltransferase reporter including the
277 wild-type p53-mediated transactivation of a chloramphenicol acetyltransferase reporter linked to a c
278 lved replacing the CRE of the PEPCK promoter/chloramphenicol acetyltransferase reporter plasmid (pPL3
279 ogen response element as measured by using a chloramphenicol acetyltransferase reporter plasmid.
281 on was further evaluated via transfection of chloramphenicol acetyltransferase reporter plasmids with
282 eated cells by using GAL4-Sp1 chimera or Sp1-chloramphenicol acetyltransferase reporter revealed a si
283 the transcription of a presenilin-1 promoter-chloramphenicol acetyltransferase reporter synthetic gen
286 In co-transfection experiments, the col-chloramphenicol acetyltransferase reporter with a mutage
290 sed of MCAD gene promoter fragments fused to chloramphenicol acetyltransferase reporters in different
291 for His-tagged green fluorescent protein and chloramphenicol acetyltransferase, respectively) and wer
292 The cap-dependent translation of a reporter (chloramphenicol acetyltransferase) RNA or naturally capp
293 ansfected RII promoter-reporter element (RII-chloramphenicol acetyltransferase) showed an increase in
294 polar expression of fluorescent proteins and chloramphenicol acetyltransferase substitutions for the
295 pment of a method, based on the transport of chloramphenicol acetyltransferase, that allows positive
296 terminal tail was not sufficient for sorting chloramphenicol acetyltransferase to peroxisomes via pER
297 peroxisomal APX C-terminal tail also sorted chloramphenicol acetyltransferase to peroxisomes via pER
299 During growth in THB, the reporter activity (chloramphenicol acetyltransferase) was first detected in
300 the c-met promoter and the coding region for chloramphenicol acetyltransferase, we have identified tw
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