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