1 red with WT membranes from cells in the same
transfection experiment.
2 ease in PNRC2 promoter activity in transient
transfection experiments.
3 BEC3G or APOBEC3F when assessed in transient-
transfection experiments.
4 fer the activity of FXR ligands in transient
transfection experiments.
5 shift assays, site-directed mutagenesis, and
transfection experiments.
6 e expression of a reporter gene in transient
transfection experiments.
7 able to induce Ov gene promoter activity in
transfection experiments.
8 tem and TTP-induced mRNA instability in cell
transfection experiments.
9 on factors on SP-B promoter expression by co-
transfection experiments.
10 Reverb(alpha) promoter activity in transient
transfection experiments.
11 nscription and secretion of PSA in transient
transfection experiments.
12 e-stimulated hiNOS transcription in promoter
transfection experiments.
13 state levels of ARE-containing mRNAs in cell
transfection experiments.
14 ated transcriptional activation in transient
transfection experiments.
15 s the factor X promoter 28-fold in transient
transfection experiments.
16 aling in SLP-76-deficient Jurkat cells in co-
transfection experiments.
17 site in vitro and activate transcription in
transfection experiments.
18 trial and non-endometrial cells in transient
transfection experiments.
19 ctivator of transcription when tested in DNA
transfection experiments.
20 e for type II collagen (Col2a1) in transient
transfection experiments.
21 e minimum alpha1(I) collagen promoter in DNA
transfection experiments.
22 cer promoter-reporter construct in transient-
transfection experiments.
23 rease in CD34 promoter activity in transient
transfection experiments.
24 ted by addition of flavopiridol in transient
transfection experiments.
25 ly repressing synthetic targets in transient
transfection experiments.
26 were subjected to acid treatment and used in
transfection experiments.
27 protein aggregates both in vitro and in cell-
transfection experiments.
28 in an IF-cubilin mediated fashion via siRNA
transfection experiments.
29 sts, based on both phylogenetic analyses and
transfection experiments.
30 oxf2 repressed Foxf1 promoter activity in co-
transfection experiments.
31 vates transcription of the STAT3 promoter in
transfection experiments.
32 ells in vivo and activates its expression in
transfection experiments.
33 s not ligand-activate PPARalpha in transient
transfection experiments.
34 dictions through mutational analyses in cell
transfection experiments.
35 vation of the cyclin A promoter in transient-
transfection experiments.
36 ctivity of the Ddelta2 promoter in transient
transfection experiments.
37 f the Optimedin promoter activity by Pax6 in
transfection experiments.
38 In
transfection experiments,
10 microM TMPyP4 reduced the a
39 n protein to Gal4-responsive promoters in co-
transfection experiments activated transcription 5-6-fol
40 Transfection experiments also suggest that RasGRP4 is a
41 or siRNA knockdown of these proteins in cell
transfection experiments altered the levels of NF1 exon
42 Transient
transfection experiments analyzing the function of SHIP
43 Transient
transfection experiments and chromatin immunoprecipitati
44 Transient
transfection experiments and DNA-protein interaction ass
45 ferase activity measurements in transient co-
transfection experiments and electro-mobility shift assa
46 DNA
transfection experiments and electrophoretic mobility sh
47 Transient
transfection experiments and EMSAs showed that induction
48 Transfection experiments and molecular modeling showed t
49 en fluorescence protein (GFP)-tagged IKLF in
transfection experiments and western analysis.
50 Claudin-1 associated with claudin-7 in co-
transfection experiments,
and claudin-7 was required for
51 ncreases beta-promoter activity in transient
transfection experiments,
and mutations in the PCS that
52 niques (clonal analysis, immunofluorescence,
transfection experiments,
and patch-clamp recordings) in
53 alpha1(I) collagen promoter fragment in DNA
transfection experiments as well as in transgenic mice.
54 Transient
transfection experiments as well as mRNA stability studi
55 In co-
transfection experiments,
Barx2 repressed N-CAM promoter
56 In
transfection experiments,
both Skn-1a and Tst-1 repress
57 p2-mediated trans-activation in transient co-
transfection experiments but also revealed Sp2 to be a r
58 unctional characterization were performed in
transfection experiments by using immunoblotting and imm
59 With transient
transfection experiments conducted with Ishikawa cells,
60 MEK5
transfection experiments confirm its ability to induce p
61 Transfection experiments confirmed that the extent of in
62 Transient
transfection experiments confirmed the ability of this T
63 eed for caution when interpreting results of
transfection experiments containing more than one plasmi
64 molecules driven by TH promoter in transient
transfection experiments,
data that provide additional s
65 As shown by transient
transfection experiments,
deletion or site-specific muta
66 The results from cell line-based
transfection experiments demonstrate that APeg3 has the
67 Transfection experiments demonstrate that efficient cell
68 Transfection experiments demonstrate that modulating HuD
69 Transfection experiments demonstrate that SRCAP is able
70 ent with this idea, the results of transient
transfection experiments demonstrate that the four FXR i
71 Transfection experiments demonstrated specific binding o
72 Transient
transfection experiments demonstrated that a 1.7-kb mous
73 Transfection experiments demonstrated that all three reg
74 Transfection experiments demonstrated that CKA1/CKA1S se
75 Transfection experiments demonstrated that Cn directly a
76 Co-
transfection experiments demonstrated that dominant nega
77 Co-
transfection experiments demonstrated that expression of
78 Transient
transfection experiments demonstrated that intact MTF-1
79 Transfection experiments demonstrated that polyhistidine
80 Transient
transfection experiments demonstrated that the hypoxia-m
81 Transient
transfection experiments demonstrated that two different
82 Previous transient-
transfection experiments detected cis-acting elements (t
83 In
transfection experiments,
dominant-negative N17Rac1 inhi
84 In transient
transfection experiments,
DP-1 polypeptides that stably
85 ZO-1 small interfering RNA and cDNA
transfection experiments emphasized regulation of CXCL8/
86 Transient
transfection experiments establish that NOR1 transactiva
87 Transient
transfection experiments established that follistatin-lu
88 In co-
transfection experiments expressing EDG-1 and eNOS cDNAs
89 Third, because of
transfection experiments followed by immunoprecipitation
90 n of BiFC and FRET assays and how to perform
transfection experiments for acquisition of fluorescent
91 c Stat3 complex was found to be essential in
transfection experiments for maximal interleukin-6-induc
92 In co-
transfection experiments,
Foxm1 directly bound to and in
93 In co-
transfection experiments,
Foxm1 directly bound to and tr
94 In co-
transfection experiments,
Foxm1 protein-induced Cox-2 pr
95 Co-
transfection experiments further established that Sp1 an
96 Transfection experiments further show that CBP stimulate
97 In
transfection experiments,
GAPDH overexpression significa
98 In co-
transfection experiments,
GKLF transactivated a reporter
99 In transient
transfection experiments,
glucagon receptor mutants that
100 Transient
transfection experiments have demonstrated that, by inte
101 Transfection experiments have shown that Sup35p filament
102 In transient
transfection experiments,
Hcy significantly inhibited cy
103 In co-
transfection experiments,
Hes-1, up-regulated by over-ex
104 In co-
transfection experiments,
high levels of phosphotyrosine
105 In
transfection experiments,
HNF-1 alpha activated the SI p
106 antly reduces receptor activity in transient
transfection experiments,
however, and effectively elimi
107 Mutagenesis and
transfection experiments identified an antioxidant respo
108 Transfection experiments identified the LMW-PTP as a neg
109 Transfection experiments in 293T and SLK cells demonstra
110 DDX58
transfection experiments in 293T cells confirmed a biolo
111 ar to destabilise the wildtype protein in co-
transfection experiments in a human RPE cell line.
112 Transient
transfection experiments in B cell lines indicate that Y
113 e chicken beta-globin insulator in transient
transfection experiments in both erythroid and nonerythr
114 In vitro association assays and co-
transfection experiments in both MDCK and HeLa cells con
115 Transient
transfection experiments in both myeloid and lymphoid ce
116 Transfection experiments in cell culture indicated that
117 ted-region reporter construct and subsequent
transfection experiments in cell cultures.
118 Cell
transfection experiments in combination with DNA binding
119 ivated the 20alpha-HSD promoter in transient
transfection experiments in corpus luteum-derived cells
120 Co-
transfection experiments in COS cells demonstrated that
121 Transfection experiments in COS-1 cells with various vim
122 Transient
transfection experiments in COS-7 cells indicated that o
123 characterized these constructs in transient
transfection experiments in COS-7 cells.
124 Transient
transfection experiments in ES cells suggest that Goosec
125 Transient
transfection experiments in HCT116 and SW480 human colon
126 our analysis of a panel of vIL-6 mutants in
transfection experiments in Hep3B cells (that express IL
127 Transfection experiments in HSC with reporter constructs
128 and mRNA expression data obtained from miRNA
transfection experiments in human cell lines.
129 Transient
transfection experiments in human foreskin fibroblasts d
130 mes and 14 core promoter mutants analyzed by
transfection experiments in human hepatoma cell lines, 6
131 Our co-
transfection experiments in human neuroblastoma SH-SY5Y
132 specimens express elevated HRPAP20, which in
transfection experiments in MCF-7 and MDA-MB-231 cells,
133 Transient
transfection experiments in MDCK cells using sequential
134 eins from 3T3-F442A adipocytes and transient
transfection experiments in NIH3T3 cells were utilized.
135 Transient
transfection experiments in pancreatic beta-cell lines s
136 Co-
transfection experiments in postnatal rat explant cultur
137 Finally, in vitro
transfection experiments in primary dorsal root ganglion
138 h CHIT1 siRNA transfection and CHIT1 plasmid
transfection experiments in primary macrophages.
139 wide transcript responses from 151 published
transfection experiments in seven different human cell t
140 es were recreated through a series of staged
transfection experiments in the MC38 mouse colon cancer
141 Transfection experiments in the SL2 Drosophila cell line
142 on signaling were demonstrated in transient
transfection experiments,
in which SopE2 enhanced the ab
143 Further
transfection experiments including expression of constit
144 Co-
transfection experiments indicate that GRG proteins regu
145 Furthermore,
transfection experiments indicate that K8 and K19 may as
146 Transfection experiments indicated that each mutant gene
147 Transfection experiments indicated that MCF-7 cells tran
148 Transfection experiments indicated that miRNA-17 and miR
149 In vivo ChIP and
transfection experiments indicated that Pitx2 directly b
150 Co-
transfection experiments indicated that Sp1 and Sp3 were
151 Transfection experiments indicated that the COOH-termina
152 The
transfection experiment is further complicated by PCR er
153 In cellular
transfection experiments,
L1-luciferase reporter constru
154 In a transient
transfection experiment,
miR-298 directly bound to the M
155 In co-
transfection experiments,
miR-BART20-5p inhibited T-bet
156 Furthermore, in transient
transfection experiments,
Nkx2.5 colocalized outside the
157 In neither in-vitro HC11
transfection experiments nor transgenic mice was hormona
158 Transient
transfection experiments of a reporter gene construct co
159 Transient
transfection experiments of a reporter gene construct co
160 Transient
transfection experiments of COS-7 cells revealed that th
161 Transfection experiments of HeLa cells and biochemical a
162 In
transfection experiments of the GR-deficient mouse fibro
163 However, in
transfection experiments,
only telomestatin significantl
164 In co-
transfection experiments p73alpha, but not p73beta, atte
165 Furthermore, in
transfection experiments,
Pep3 also blocked the nuclear
166 Transfection experiments performed in vitro and in vivo
167 In
transfection experiments,
REA suppressed ERalpha transcr
168 In
transfection experiments,
reporter plasmids containing t
169 In transient
transfection experiments,
REST-VP16 was found to operate
170 Transient
transfection experiments revealed a approximately 20-nuc
171 Indeed,
transfection experiments revealed accumulation of JAM-A
172 Transfection experiments revealed further characteristic
173 Transfection experiments revealed that 1,25(OH)(2)D(3) a
174 Transient
transfection experiments revealed that 2.0 kilobase pair
175 Transient
transfection experiments revealed that Cux-1 is an inhib
176 Transient
transfection experiments revealed that HBO1 specifically
177 Transient
transfection experiments revealed that LXR ligands suppr
178 Further, co-
transfection experiments revealed that the amount of c-m
179 DNA binding assays and cell
transfection experiments revealed that the bipartite cor
180 The mammalian cell
transfection experiments revealed that the ERRalpha-1 mu
181 Transfection experiments revealed that the mutation caus
182 In vivo
transfection experiments revealed that the presence of t
183 Transfection experiments show that BHLHB4 can repress tr
184 Transient
transfection experiments show that both mouse and rat my
185 In support of these results, COS cell
transfection experiments show that phosphomimetic mutati
186 Data from transient-
transfection experiments show that the filamentous patte
187 escent protein (GFP) gene as the reporter in
transfection experiments show that the U3 region of the
188 Transient
transfection experiments showed an androgen-dependent en
189 Transfection experiments showed significantly increased
190 Transfection experiments showed that a 936-bp promoter f
191 Transfection experiments showed that an N-terminal mutan
192 Co-
transfection experiments showed that binding sites for b
193 Transfection experiments showed that both promoter activ
194 Transient
transfection experiments showed that C/EBPalpha transact
195 Moreover,
transfection experiments showed that dexamethasone reduc
196 Transient
transfection experiments showed that DHA also activated
197 Co-
transfection experiments showed that full-length C/EBPbe
198 Transient-
transfection experiments showed that full-length CD163 c
199 Gene
transfection experiments showed that HN (but not an inac
200 Co-
transfection experiments showed that KLF4 repressed the
201 shift analysis, promoter mutagenesis and co-
transfection experiments showed that NeuroD, a pro-neuro
202 Transient
transfection experiments showed that NMTS fusions to gre
203 Transient
transfection experiments showed that PAK6 specifically r
204 Transfection experiments showed that rec-RC IgG recogniz
205 Transfection experiments showed that synthesis of gas5-e
206 Transient
transfection experiments showed that the A allele of thi
207 Transient
transfection experiments showed that the DNA segment loc
208 rthern blot analysis of A3AR mRNA, transient
transfection experiments showed that the promoter activi
209 9, MMP14, and MMP15 promoters, and transient
transfection experiments showed that these promoters are
210 Transient
transfection experiments showed that these promoters wer
211 Co-
transfection experiments showed that transcription facto
212 Further co-
transfection experiments showed that two of the SOX/Sry-
213 Transfection experiments showed that, when expressed ind
214 by results from IFIT3-small interfering RNA
transfection experiments showing decreased expression of
215 in some of the mouse cell lines in transient
transfection experiments,
similar to the observation mad
216 Using mammalian cell
transfection experiments,
SnaH was found to act as a rep
217 In
transfection experiments,
subcellular localization of al
218 Results of RNA
transfection experiments suggest that cytoplasmic protei
219 nding domains, and DNA binding and transient
transfection experiments suggest that it functions as a
220 The
transfection experiments suggest that KIDS Cx26(D50N) im
221 However, co-
transfection experiments suggest that other proteins tha
222 Transfection experiments suggest that TGTCTC AuxREs are
223 vely regulated by Kruppel-like factors in co-
transfection experiments suggesting a possible mechanism
224 on analysis, luciferase reporter assays, and
transfection experiments support a role of targeting of
225 tically active state in vitro, thus enabling
transfection experiments that altered gene expression to
226 In the cell
transfection experiments,
the average level of beta-gala
227 In
transfection experiments,
the CARD6 protein suppressed N
228 In cell
transfection experiments,
the D816H mutant protein was a
229 In co-
transfection experiments,
the effects of A1E proteins on
230 In transient
transfection experiments,
the human and murine E-cadheri
231 In transient
transfection experiments,
the mutant protein showed sign
232 In
transfection experiments,
the time courses for appearanc
233 c activity to a heterologous promoter in DNA
transfection experiments;
this enhancing ability was con
234 target prediction is combined with the miRNA
transfection experiment to systematically identify the g
235 , three of which have been shown in previous
transfection experiments to disrupt the V-mediated block
236 s been used in adenovirus-mediated transient
transfection experiments to study the properties of this
237 lear receptors were found, by mammalian cell
transfection experiments,
to act as negative regulatory
238 In transient
transfection experiments using a luciferase reporter gen
239 Co-
transfection experiments using a luciferase reporter lin
240 In transient cell
transfection experiments using a neuroblastoma cell line
241 Transfection experiments using an AF1q promoter lucifera
242 In transient
transfection experiments using an NF-kappaB driven secre
243 In
transfection experiments using chicken pineal cells, an
244 Transient
transfection experiments using constructs encoding FGF r
245 Double
transfection experiments using dominant negative mutants
246 In co-
transfection experiments using Drosophila SL2 cells that
247 Transfection experiments using fluorescent protein and l
248 Transfection experiments using GADD153 to create C/EBP-n
249 Results from
transfection experiments using human myelocytic cell lin
250 In
transfection experiments using mammalian cell lines, suc
251 Transient
transfection experiments using NF-kappaB reporter constr
252 Transient
transfection experiments using reporter constructs conta
253 RNA
transfection experiments using several schistosome stage
254 Transfection experiments using synthetic miRNAs showed t
255 In transient
transfection experiments,
virtually all of the transfect
256 sion of predicted targets, and through miRNA
transfection experiments,
we could suggest mechanistic l
257 In transient
transfection experiments,
we demonstrate that IFNalpha i
258 By reporter gene
transfection experiments,
we found that approximately 2.
259 ent protein-Bombyx mori G-actin in transient
transfection experiments,
we identified six AcMNPV early
260 In cell culture
transfection experiments,
we identified two promoter reg
261 Using transient
transfection experiments,
we now show that overexpressio
262 the reduction in apo A-I expression by DHA,
transfection experiments were conducted with plasmid con
263 Co-
transfection experiments were performed in which AQP3 or
264 Kinase assay or transient
transfection experiments were performed to study the bid
265 Kinase assays and transient
transfection experiments were performed to study the sig
266 a luciferase reporter plasmid and transient
transfection experiments were performed using H630 human
267 Estrogen receptor (ER) transient
transfection experiments were performed using the SK-BR-
268 rectly transactivates the CD1 promoter in co-
transfection experiments,
whereas electrophoretic mobili
269 Transfection experiments which overexpressed the full-le
270 Transient
transfection experiments with 5'-deletion CRP promoter c
271 Transient
transfection experiments with a minimal TYRP1 promoter s
272 Co-
transfection experiments with a SOX9 expression plasmid
273 Transient
transfection experiments with a vector containing a muri
274 Transient
transfection experiments with A549 lung adenocarcinoma c
275 Transfection experiments with adult schistosomes further
276 anscriptional activity of ERs was studied in
transfection experiments with an estrogen-responsive rep
277 Moreover, co-
transfection experiments with both mutant and WT transpo
278 Transient
transfection experiments with CaCo-2 and HepG2 cells ind
279 recapitulated in HepG2 cells using transient
transfection experiments with CAT reporter constructs co
280 In cDNA
transfection experiments with Chinese hamster ovary cell
281 phoretic mobility shift assays and transient
transfection experiments with deleted and mutated varian
282 oth pharmacological inhibitors and transient
transfection experiments with dominant-negative and cons
283 Transient
transfection experiments with epitope tagged proteins ha
284 Transfection experiments with full-length and progressiv
285 Transient
transfection experiments with HepG2 cells revealed a tra
286 Site-directed mutagenesis and
transfection experiments with human hepatoma cell lines
287 ng intestinal enhancer activity in transient
transfection experiments with intestine-derived CaCo-2 c
288 Transient
transfection experiments with luciferase-aromatase promo
289 Using transient cell
transfection experiments with M-MITF promoter constructs
290 ast, in the absence of DNA replication or in
transfection experiments with ORF62, only ORF63 transcri
291 Transfection experiments with OvCAT (chloramphenicol ace
292 ed functional promoter activity in transient
transfection experiments with PC12, C6, and CV-1 cells.
293 Furthermore,
transfection experiments with RANK and its deletion muta
294 Transfection experiments with recombinant constructs sho
295 Transfection experiments with reporter constructs contai
296 Transfection experiments with reporter gene constructs d
297 Transient
transfection experiments with RXRalpha promoter-lucifera
298 r activities in chondrocytes, as revealed in
transfection experiments with site-directed CpG mutants
299 Furthermore, co-
transfection experiments with Stat3 beta demonstrate gam
300 In transient-
transfection experiments with the alpha(2)-macroglobulin