1 , gelatinase B (gelB; MMP-9) in cell culture
transfection studies.
2 ined by in vitro reporter/promoter construct
transfection studies.
3 showed reduced levels of colony formation in
transfection studies.
4 ive different cell lines utilizing transient
transfection studies.
5 tro and is activated by LXR/RXR in transient-
transfection studies.
6 AR promoter-luciferase activity in transient
transfection studies.
7 ompared with those hitherto revealed through
transfection studies.
8 nificantly increased EDA transcription in co-
transfection studies.
9 ession of the reporter cat gene in transient
transfection studies.
10 ht affect the function of ARNT, we performed
transfection studies.
11 lands and exhibits bidirectional activity in
transfection studies.
12 activity of a reporter gene was measured in
transfection studies.
13 tivate ERK2, SAPK, and p38 MAPK in transient
transfection studies.
14 of miRs in MDSC activation was confirmed by
transfection studies.
15 to be functionally impaired in reporter gene
transfection studies.
16 ion and conformation in transient COS-7 cell
transfection studies.
17 onferred TTP sensitivity to the mRNA in cell
transfection studies.
18 box, we tested nine constructs in transient
transfection studies.
19 ctivation of specific HCMV gene promoters in
transfection studies.
20 duced by BimEL but not BimL and BimS in gene
transfection studies.
21 xpression of the Nmyc1 promoter in transient
transfection studies.
22 On the basis of in vitro and
transfection studies,
5'ppp RNA produced during virus re
23 In
transfection studies,
a phosphorylation-deficient Ser316
24 Cell
transfection studies also demonstrated that the expressi
25 Transfection studies also show that IAFGP increased the
26 Consistent with the
transfection studies,
analysis of knockout mice demonstr
27 In vitro
transfection studies and chromatin immunoprecipitation a
28 henobarbital induction in previous transient
transfection studies and consistent with mediation of ph
29 Using transient
transfection studies and deletion constructs of the huma
30 Reporter gene
transfection studies and electrophoretic mobility gel sh
31 Transient
transfection studies and electrophoretic mobility shift
32 In vitro
transfection studies and gene ontology revealed involvem
33 Transfection studies and genetic analysis revealed that
34 In vivo
transfection studies and in vitro characterization of pu
35 ssessed by both coimmunoprecipation and cell
transfection studies and it is presumed that it function
36 Transfection studies and mutagenesis indicate that the -
37 idney epithelial 293T cells for transient co-
transfection studies and the nerve growth factor (NGF)-r
38 in the cleavage of core proteins, based on a
transfection study and the presence of an HXXEH motif fo
39 Transfection studies assessed the response of isolated p
40 e based liposome-AuNP-DNA composite for cell
transfection studies at reduced reagents and costs.
41 racted with B5 as predicted by the transient-
transfection studies but had a small-plaque phenotype.
42 Because
transfection studies can lead to imprecise or erroneous
43 ins and co-immunoprecipitation and transient
transfection studies,
Cdc42 was shown to be an upstream
44 Transfection studies confirm the presence of GnRH- and a
45 Cardiomyocyte
transfection studies confirmed that COUP-TF repressed th
46 Transfection studies confirmed that DES-mediated downreg
47 Transfection studies confirmed that plasmid homologous r
48 Transfection studies confirmed the expression of similar
49 Transfection studies confirmed this result by demonstrat
50 In transient
transfection studies,
Crx transactivates rhodopsin promo
51 In co-
transfection studies,
cyclin A expression stimulated tra
52 In in vitro
transfection studies,
DAX-1 repressed the SF-1-mediated
53 In
transfection studies,
deletion of exonic sequences downs
54 It is surprising that
transfection studies demonstrate aberrant cytoplasmic lo
55 Immunocytochemistry and
transfection studies demonstrate colocalization of PDE4D
56 Transient
transfection studies demonstrate further that TCR-stimul
57 Transient co-
transfection studies demonstrate that A-SREBP-1 can inhi
58 Site-directed mutagenesis and
transfection studies demonstrate that calcineurin-induci
59 Transfection studies demonstrate that cap-independent tr
60 Transient
transfection studies demonstrate that overexpression of
61 entic AGGAWG Ets DNA cognates, and transient
transfection studies demonstrate that PE1 represses MMP1
62 Cell
transfection studies demonstrate that TBX5 activates the
63 Transfection studies demonstrate that translation initia
64 Cell
transfection studies demonstrate that Wnt7b can activate
65 Cell
transfection studies demonstrated a dominant-negative ef
66 Furthermore, transient
transfection studies demonstrated a loss of GM-CSF respo
67 Moreover, inhibitor and siRNA
transfection studies demonstrated an apparent effect of
68 The current transient
transfection studies demonstrated by confocal microscopy
69 AhR sense/antisense
transfection studies demonstrated that AhR contents infl
70 Co-
transfection studies demonstrated that constitutively ac
71 Transient
transfection studies demonstrated that LPS represses SR-
72 Cardiac myocyte
transfection studies demonstrated that M-CPT I promoter
73 First,
transfection studies demonstrated that overexpression of
74 Transient
transfection studies demonstrated that Puralpha and JCV
75 Furthermore, co-
transfection studies demonstrated that Sp3 abolished tra
76 Transfection studies demonstrated that synaptojanin 2, l
77 Transfection studies demonstrated that TAO2 stimulates p
78 Transient
transfection studies demonstrated that the combination o
79 Transfection studies demonstrated that the Ets family me
80 The results of mutation analysis and
transfection studies demonstrated that the interaction o
81 ophoretic mobility shift assay and transient
transfection studies demonstrated that the NeuroD1 and E
82 Nuclear run-on experiments and transient
transfection studies demonstrated that the suppression o
83 These data coupled with results of transient
transfection studies demonstrated that transcriptional a
84 Subsequent kinetic analyses and
transfection studies demonstrated that VHR specifically
85 Subsequent in vitro
transfection studies determined a higher transfection ef
86 Cell
transfection studies disclosed a dual behavior of R406W-
87 s 587-636 have been deleted and, in parallel
transfection studies,
DRIP205Delta587-636 also coactivat
88 In
transfection studies,
either constitutively active Vav o
89 Transfection studies further implicate Bright in facilit
90 Contrary to the results of our
transfection studies,
GFP expression could not be detect
91 Based on
transfection studies,
GM-CSF mRNA was 2.5 times more sta
92 Although
transfection studies have established that human MRP3 co
93 Transfection studies have established that MRP confers r
94 Transfection studies have indicated that the variant chi
95 Transfection studies have now proven that pfcrt mutation
96 Recently, transient
transfection studies have shown that overexpression of c
97 -rich element-containing transcripts in cell
transfection studies;
however, its physiological importa
98 Transient
transfection studies illustrate that HNF3alpha can activ
99 In vitro and in vivo shRNA
transfection studies implied that one such factor, share
100 In
transfection studies in 3T3/L1 cells, stable expression
101 Transient
transfection studies in cardiac myocytes and in CV-1 cel
102 Early
transfection studies in cell cultures revealed predomina
103 Transfection studies in cell cultures using methylated t
104 ered BMPR-II function, we employed transient
transfection studies in cell lines and primary cultures
105 Transfection studies in COS cells demonstrated that both
106 Transfection studies in COS-1 cells demonstrated that in
107 Co-
transfection studies in Drosophila SL2 cells indicated t
108 Transfection studies in head and neck squamous cell carc
109 Transfection studies in HEK 293 cells demonstrated that
110 be dependent on the presence of TLR4 through
transfection studies in HEK cells, which do not normally
111 In vitro
transfection studies in HEK-293 cells established the sp
112 Transfection studies in HeLa cells revealed AVP localize
113 Transient
transfection studies in HeLa cells, an E(2) receptor-neg
114 Transfection studies in HepG2 cells demonstrate that AGL
115 Transient
transfection studies in Jurkat cells showed that the G a
116 Moreover,
transfection studies in liver- and kidney-derived cells
117 Transfection studies in murine pancreatic beta-cells sug
118 In transient
transfection studies in NIH3T3 cells, the LARG(Cys1306)
119 Transfection studies in placental and nonplacental cells
120 Transfection studies in primary hippocampal neurons show
121 In
transfection studies in rat adipocytes, transient expres
122 ut protein-dependent yeast growth assays and
transfection studies in the HT29 human CRC cell line to
123 fusion (p alpha A 111aCAT) in competitive co-
transfection studies in the mouse alpha TN4-1 lens cell
124 nd mutational analysis as well as functional
transfection studies in the murine gonadotrope-derived a
125 Transient
transfection studies in time courses (24-72 h) and diffe
126 Transfection studies in yeast, which lack nuclear hormon
127 Transfection studies indicate that 1,25(OH)(2)D(3) induc
128 Both in vitro import studies and in vivo
transfection studies indicate that deletion of the YGG(C
129 The results of transient
transfection studies indicate that HNF1alpha is required
130 Nuclear run-on and
transfection studies indicate that IL-4-mediated repress
131 Transfection studies indicate that synemin requires the
132 Transfection studies indicate that the NFARs regulate ge
133 Results from co-
transfection studies indicated superactivation of LTR by
134 Site directed mutagenesis and
transfection studies indicated that both Sp1 sites are f
135 Previous
transfection studies indicated that F13L induces the for
136 Previous
transfection studies indicated that fusion of GFP to the
137 Transfection studies indicated that mutation of both the
138 Results from co-
transfection studies indicated that overexpression of wi
139 Northern blotting, immunoblotting, and
transfection studies indicated that the ATG-to-AAG mutat
140 Transfection studies indicated that the EEV protein enco
141 Nuclear run-on analysis and
transfection studies indicated that the effects of Ang I
142 These observations corroborated results from
transfection studies indicating the ability of JCV T-ant
143 DUX4 expression in
transfection studies induces apoptosis and interferes wi
144 In addition,
transfection studies involving Sp1, Sp2, Sp3, CREB, and
145 Evidence from in vitro
transfection studies is often assumed to be sufficient e
146 cysteine methyl ester and, in agreement with
transfection studies,
is more active with the farnesylat
147 Transient
transfection studies localized its promoter, lacking a c
148 These studies suggest that microarray
transfection studies may be useful in functional charact
149 In transient
transfection studies,
Myc effectively repressed p21 prom
150 Transfection studies of bronchial epithelial cells were
151 Transient
transfection studies of CHO cells with Nhs1-GFP fusion p
152 Transfection studies of cultured cells revealed that a t
153 Also, in contrast to previous observations,
transfection studies of PtK2 cells showed that mouse K16
154 Transient
transfection studies of the human, mouse, and rat ASBT p
155 Induction is attenuated in similar
transfection studies of the mouse promoter.
156 DNA
transfection studies on the NIH3T3 cell line confirmed t
157 er, we found that reexpression of miR-200 by
transfection studies or treatment of gemcitabine-resista
158 However, all of the
transfection studies (
over 2350 PAEs) have been limited
159 In gene
transfection studies PAN1 manifests an inhibitory influe
160 In dominant-negative
transfection studies,
patch clamp analysis of Mz-ChA1 ch
161 analysis of the mRNA steady-state levels and
transfection studies performed with a plasmid containing
162 Gel retardation experiments and cell
transfection studies provided evidence for the repressio
163 In
transfection studies,
PTP1B dephosphorylates the leptin
164 In co-
transfection studies PU.1 represses MOR promoter reporte
165 Remarkably,
transfection studies reveal that expression of either th
166 Transient
transfection studies reveal that PPARgamma ligands, in a
167 Transfection studies reveal that TRF can differentially
168 In vitro
transfection studies revealed a higher and longer lastin
169 Transfection studies revealed that 15d-PGJ2 stimulated H
170 Site-directed mutagenesis and
transfection studies revealed that all these binding sit
171 Transfection studies revealed that AML1-ETO, a dominant-
172 Transfection studies revealed that DKK1 decreased melano
173 Transfection studies revealed that overexpression of GLU
174 However,
transfection studies revealed that SRA enhances thyroid
175 Transfection studies revealed that the 5'-flanking seque
176 Co-
transfection studies revealed that the phosphorylation o
177 Site-specific mutagenesis and
transfection studies revealed that this region contains
178 Biochemical and co-
transfection studies revealed that TIP120B, but not the
179 Transient-
transfection studies revealed that UL116 is efficiently
180 In vitro
transfection studies revealed that wild-type gammaD prot
181 Transfection studies show codominant expression of the m
182 Transient
transfection studies show that a 1.4-kb promoter fragmen
183 Transfection studies show that a dominant-negative ERM c
184 Co-
transfection studies show that ARP-1/COUP-TFII repressed
185 Transient
transfection studies show that collagenase-3 promoter ac
186 Transfection studies show that FP1 and FP2 Sp1/Sp3 sites
187 Also,
transfection studies show that IgD functions as a typica
188 In addition, transient
transfection studies show that KLF2 directly inhibits PP
189 In vivo colocalization and
transfection studies show that pp32 INHAT domains are re
190 In vitro cultures and
transfection studies show that the nuclear localization
191 In vitro
transfection studies show that the reversibly shielded p
192 Previous cell line
transfection studies show that ubiquitination of these l
193 Co-
transfection studies showed no effect of the 5-HT(2A-tr)
194 Transfection studies showed that BMPRII modulated Gc act
195 Results of transient
transfection studies showed that GKLF-induced repression
196 Transfection studies showed that Hoxa-9 is a strong tran
197 Quantitative PCR, immunoblotting, and
transfection studies showed that IL8-S cells or IL-8-tre
198 Transient
transfection studies showed that native osteopontin prom
199 NIH 3T3
transfection studies showed that overexpression of full-
200 Finally, results of co-
transfection studies showed that overexpression of IKLF/
201 Transient
transfection studies showed that the ability of MTF1 to
202 Transfection studies showed that the basal promoter acti
203 Promoter deletion and transient
transfection studies showed that the estrogen response e
204 Transfection studies showed that the G-7A and T-138C pol
205 Co-
transfection studies showed that the mutants affected ne
206 Transient
transfection studies showed that the region spanning -77
207 Cellular
transfection studies showed that the two mutations resul
208 Transfection studies showed that, in contrast with Bgp1,
209 In
transfection studies,
stable overexpression of wild-type
210 Transfection studies suggest that inactive caspase-8 ado
211 al histone H4 acetylation in eukaryotes, and
transfection studies suggest that Ing4 may regulate a wi
212 Transient
transfection studies suggest that LPS-induced phosphoryl
213 In vitro biochemical and cellular
transfection studies suggest that RAG1/2 may also play p
214 Although the results of
transfection studies suggest that the level of PTEN and
215 site abolished all reporter activity in cell
transfection studies,
suggesting that this element is es
216 Transfection studies support the presence of a bidirecti
217 Here, we show by coimmunoprecipitation and
transfection studies that CD44 associates with VLA-4 but
218 ymes, we have demonstrated through transient
transfection studies that long pro-CART gives rise to an
219 Transfection studies that modulate N-Myc levels also res
220 er and intestine, as well as biochemical and
transfection studies that support its function as an ene
221 ecipitation assay and small interference RNA
transfection studies that the POU2 family transcription
222 In
transfection studies,
the isolated variable domain of PK
223 In
transfection studies,
the PAX3-FKHR fusion activates tra
224 In both cell-free translation and
transfection studies,
the rate of translation decreased
225 In transient
transfection studies,
the truncated AR is three to five
226 our previous morphological observations and
transfection studies,
these data suggest that pinin may
227 t and deaminase-defective APO3G in transient-
transfection studies to achieve similar levels of virus-
228 Finally,
transfection studies to analyze NF-kappaB-directed gene
229 In transient-
transfection studies,
transcriptional activity of an hCY
230 Transfection studies,
typically of tagged RGS proteins,
231 Based largely on
transfection studies,
UL50 and UL53 have been proposed t
232 Transient
transfection studies using 5'-deletion mutants of the hu
233 Transient
transfection studies using a fully functional HLA-DRA pr
234 e were constructed and employed in transient
transfection studies using a line of SV40 transformed mo
235 on by intact COS-phox cells, on the basis of
transfection studies using a p67(phox) (Val204Ala) mutan
236 Transfection studies using a series of deleted tissue fa
237 Transfection studies using a series of reporter construc
238 Transfection studies using an hPTH promoter construct in
239 statin gene in neural cells was confirmed in
transfection studies using embryonic cerebral cortex-der
240 Additionally,
transfection studies using ERRalpha-null primary fibrobl
241 In transient
transfection studies using HEK 293 cells, both NR2E3 and
242 Further
transfection studies using Huh7 hepatoma cells indicate
243 Transient
transfection studies using kinase-dead and rapamycin-res
244 Transient
transfection studies using luciferase reporter construct
245 Transfection studies using mature miR mimics of miR-490
246 Further
transfection studies using mutant constructs of these ci
247 Transfection studies using reporter constructs and chrom
248 Co-
transfection studies using Sp1 and/or Sp3 expression pla
249 tivation by MAZ and Sp1 also was observed in
transfection studies using the complete adenovirus type
250 differentiation inducers is corroborated by
transfection studies using the promoter region of mda-7
251 Transfection studies using these constructs indicated th
252 Transfection studies using TRAP220 mutants revealed that
253 Transient
transfection studies using various VCAM-1 promoter const
254 horylation experiments, as well as transient
transfection studies using wild type and mutant SHP-2 co
255 Transfection studies,
using either full-length hLXRalpha
256 Using bioinformatic analysis and co-
transfection studies we further identified the EGR1 tran
257 I footprinting, gel retardation assays, and
transfection studies,
we also detect occupancy in vivo o
258 In reporter gene
transfection studies,
we found that among a panel of Sma
259 In
transfection studies,
we showed that the 5-kb RNA can be
260 Using co-
transfection studies,
we showed that the NRSE of the MOR
261 the human CRALBP gene in the RPE, transient
transfection studies were carried out with three CRALBP-
262 alysis, in situ hybridization, and transient
transfection studies were performed using standard metho
263 stochemistry, Western blotting, and in vitro
transfection studies were used to characterize mutant le
264 Transfection studies were used to identify specific regi
265 Transient
transfection studies were used to investigate the transc
266 correlates with functional cooperativity in
transfection studies where AML1 and BSAP synergistically
267 ta thus help to deconvolute previous in vivo
transfection studies which have debated the role of a di
268 In co-
transfection studies,
wild-type PTPN13 inhibited Ras/RAF
269 Transient
transfection studies with 5' deletion mutants localized
270 Nuclear run-on assays and transient
transfection studies with a -1.6 kb ecNOS promoter const
271 Transient
transfection studies with a series of 5'-deleted cyclin
272 trophoretic mobility shift assays (EMSA) and
transfection studies with cJun and PEA3 expression vecto
273 Transfection studies with deletion mutants of Par-4 reve
274 Transfection studies with different deletion constructs
275 Co-
transfection studies with dominant-negative arrestins an
276 Transfection studies with E1A, which binds to and inacti
277 Transfection studies with epitope-tagged KLHL1 demonstra
278 Transient
transfection studies with FGFR3 mutant constructs show t
279 We have combined
transfection studies with gene targeting in mice to iden
280 Transfection studies with human C3 promoter-luciferase r
281 DNA binding analysis and
transfection studies with IkappaB kinase cDNA revealed t
282 s demonstrated by the following: 1) EMSA; 2)
transfection studies with IL-8 promoter reporter constru
283 Co-
transfection studies with individual miR mimics along wi
284 Transient
transfection studies with luciferase reporter constructs
285 Transfection studies with luciferase reporter constructs
286 As a result, in transient
transfection studies with MCF-7 cells, resveratrol showe
287 Additional
transfection studies with mutated Rad cDNAs revealed tha
288 nscriptional level, as revealed by transient
transfection studies with plasmid constructs (pDTD-1097C
289 Additional
transfection studies with progressively COOH-terminally
290 Transfection studies with reporter constructs and variou
291 Transient
transfection studies with reporter gene constructs in 29
292 titive gel mobility supershift assays and co-
transfection studies with SF-1 produced in vitro indicat
293 An array analysis of microRNAs (miRNAs) and
transfection studies with specific miRNA inhibitors and
294 Transfection studies with the apoA-I promoter suggested
295 Co-
transfection studies with USF proteins and the varicella
296 Transient
transfection studies with wild-type and dominant-negativ
297 Transient
transfection studies with wild-type and E3-defective c-I
298 Transient-
transfection studies with wild-type and kinase-inactive
299 Transfection studies with wild-type and mutated RET dete
300 of LDLR promoted NV replication in trans by
transfection study with pNV-GFP.