1 growth of S. aureus and Escherichia coli on
ectopic overexpression.
2 Ectopic overexpression also promotes the development of
3 ne and phenotype characterizations following
ectopic overexpression and endogenous silencing experime
4 or complexes with CXCR4 and CD74, both after
ectopic overexpression and in endogenous conditions in a
5 nal analyses of the Npr1 promoter along with
ectopic overexpression and inhibition of Sp1 confirmed t
6 Ectopic overexpression and silencing experiments reveale
7 However, both
ectopic overexpression and siRNA-mediated knockdown of C
8 f TCF7L2 or JMJD6 reversed BETi-P/R, whereas
ectopic overexpression conferred BETi-P/R in sAML cells,
9 dance through mRNA stabilization upon TbZFP3
ectopic overexpression,
dependent upon the integrity of
10 Inhibitory RNA (RNAi)-mediated knockdown and
ectopic overexpression established a critical functional
11 MiR-181b-1
ectopic overexpression further diminishes Bcl-2 expressi
12 uman lung cancer cell lines by both RNAi and
ectopic overexpression further substantiates an oncogeni
13 ning p21WAF1/CIP1 (Adp21WAF1/CIP1) to effect
ectopic overexpression in a p53-defective human astrocyt
14 RAGE
ectopic overexpression in breast cancer cells increased
15 PR-1 by small interfering RNA (siRNA) and by
ectopic overexpression in endothelial cells showed that
16 icrotubules and neurite outgrowth, while its
ectopic overexpression in the cytoplasm blocked both of
17 Increasing MDM2 by
ectopic overexpression in the cytoplasm enhanced both mR
18 Ectopic overexpression in zebrafish resulted in an expan
19 Conversely, EZH 2
ectopic overexpression induces growth factor independenc
20 uired for v-Rel-mediated transformation, its
ectopic overexpression is inhibitory.
21 is that, unlike endogenous vasohibin-1, the
ectopic overexpression is not regulated by VEGF and ther
22 the clearance of aggregated proteins, whose
ectopic overexpression is sufficient to capture the neur
23 ants, and creating CRISPR-Cas9 knockouts and
ectopic overexpression lines in poplar.
24 s is the first report demonstrating that the
ectopic overexpression of a Cdk inhibitor such as p21 or
25 germination via the GR manipulated, although
ectopic overexpression of a D gene had no effect on over
26 Notably,
ectopic overexpression of a deacetylated PKM2 mutant in
27 apoptosis but could be sensitized following
ectopic overexpression of a superdominant I kappa B.
28 However,
ectopic overexpression of ABCG2 in MCF7 cells could not
29 Ectopic overexpression of AIF1 in macrophages provided p
30 Ectopic overexpression of alpha4 is associated with hepa
31 Third,
ectopic overexpression of AMA1 is able to stimulate ubiq
32 Ectopic overexpression of AMF/PGI results in its secreti
33 Ectopic overexpression of an uninhibitable GSK3beta muta
34 Ectopic overexpression of ANAC012 in Arabidopsis (35S::A
35 We previously demonstrated that
ectopic overexpression of angiopoietin-2 (Ang-2) comprom
36 Importantly,
ectopic overexpression of ANGPTL4 restored maternal bloo
37 Ectopic overexpression of Apaf-1 (2.5-fold) in human acu
38 Conversely,
ectopic overexpression of ARC in a PyMT-derived metastat
39 ted topoisomerase I that complexes with ARF,
ectopic overexpression of ARF causes sensitization to ca
40 By
ectopic overexpression of ARR10, Arabidopsis lines hyper
41 Ectopic overexpression of asd, adiY and folE is specific
42 Ectopic overexpression of aurora kinase A in mammalian c
43 In contrast,
ectopic overexpression of B-myb blocked the ability of 3
44 Ectopic overexpression of Bach2 in murine Tfh cells resu
45 n of BAM3 expression upon CLE45 application,
ectopic overexpression of BAM3 in brx root meristems, an
46 The
ectopic overexpression of Bcl-2 restricts both influenza
47 wn of Bim (but not Puma or Noxa) by shRNA or
ectopic overexpression of Bcl-2, Bcl-x(L), or Mcl-1 dimi
48 Ectopic overexpression of bcl-x(L) and bcl-2 prevents th
49 Ectopic overexpression of Bcl-XL in parental U87MG cells
50 Ectopic overexpression of beta-catenin in 293 cells also
51 Ectopic overexpression of BHLHE40 prevented induction of
52 sion of mRNA encoding BiP was phenocopied by
ectopic overexpression of BiP protein, and was also obse
53 n in living animals, we have determined that
ectopic overexpression of both human and C. elegans tors
54 sed upon incubation of cells with MG132, and
ectopic overexpression of c-Jun mimicked the effect of M
55 Furthermore,
ectopic overexpression of c-Jun renders breast cancer ce
56 cells and E2F1-overexpressing cells, whereas
ectopic overexpression of c-myb activates the COX-2 prom
57 We show that the
ectopic overexpression of c-Myb in 32Dcl3 cells results
58 While
ectopic overexpression of c-myb in 32Dcl3 cells results
59 Ectopic overexpression of c-Myc has been shown to sensit
60 The
ectopic overexpression of CagA significantly increased t
61 er of PEX7 depends on cargo binding and that
ectopic overexpression of cargo protein stimulates this
62 Thus,
ectopic overexpression of caveolin in this heterologous
63 Conversely,
ectopic overexpression of CHD7 in LN-428 and A172 gliobl
64 stages of erythroid differentiation and that
ectopic overexpression of CHOP enhances this process.
65 WT plants transformed with a construct for
ectopic overexpression of CLE45 could not be recovered,
66 Ectopic overexpression of constitutively active Akt prot
67 Conversely,
ectopic overexpression of constitutively active PKD1 in
68 Ectopic overexpression of constitutively active STAT1 in
69 gnificantly reduces internalization, whereas
ectopic overexpression of CPn0678-GFP results in a domin
70 s ceramide reverted the KO phenotype, as did
ectopic overexpression of CPT1C, indicating that CPT1C r
71 ant axillary meristems into thorns, although
ectopic overexpression of CsCEN represses TI1 expression
72 This study demonstrates that
ectopic overexpression of cyclin D1 in a rat liver epith
73 irk-dependent manner, as G1 was shortened by
ectopic overexpression of cyclin D1 mutated at the Mirk
74 The
ectopic overexpression of cytosolic GS1 in tobacco leave
75 Ectopic overexpression of DinR causes depletion of ftsZ
76 Ectopic overexpression of dnmt3bb.1 in non-hematopoietic
77 hibitors to prevent their phosphorylation or
ectopic overexpression of dominant-negative IkappaBalpha
78 Use of an IKKalpha/beta inhibitor or
ectopic overexpression of dominant-negative IkappaBalpha
79 Ectopic overexpression of dominant-negative soluble ephr
80 ly prevent uptake by proliferating cells, as
ectopic overexpression of DPP4 in HeLa cells rendered DP
81 lation of sub-G(0)/G(1) cells resulting from
ectopic overexpression of E2F1.
82 RF, and the effect was partially reversed by
ectopic overexpression of E2F1.
83 Ectopic overexpression of each of the five closely relat
84 Ectopic overexpression of EDN1 in cells with mutated EGF
85 Ectopic overexpression of Egr-1 in H35 cells decreased P
86 On the other hand,
ectopic overexpression of either a Gab1 mutant incapable
87 Our data also demonstrate that
ectopic overexpression of either cyclin is sufficient to
88 Ectopic overexpression of either GNC or CGA1 promotes ch
89 Furthermore,
ectopic overexpression of either htl or fz in the mesode
90 key regulators of plant cell totipotency, as
ectopic overexpression of either transcription factor in
91 In contrast,
ectopic overexpression of EN1 in normal cells activated
92 nduced-at a conserved sequence motif-via the
ectopic overexpression of eukaryotic acetyltransferase c
93 Ectopic overexpression of ezrin in low-ezrin-expressing
94 Here we show that
ectopic overexpression of F5H in Arabidopsis abolishes t
95 In Drosophila,
ectopic overexpression of Fbxo7 rescued loss of Parkin,
96 Ectopic overexpression of FDPS promotes oncogenic phenot
97 Ectopic overexpression of FGF-3 in pubescent mammary gla
98 In mice,
ectopic overexpression of FGF19 drives HCC development i
99 multiple myeloma (MM) and is associated with
ectopic overexpression of fibroblast growth factor recep
100 Ectopic overexpression of FOXC1 in breast cancer cells i
101 In support of this finding, we show that
ectopic overexpression of FOXO3 can reduce the sensitivi
102 Here, by gene expression analysis upon
ectopic overexpression of FOXP1 in primary human memory
103 uggestion relied on in vitro experiments and
ectopic overexpression of Gadd45 protein, we examined wh
104 Ectopic overexpression of GADD45alpha during repair incr
105 vide further support for the notion that the
ectopic overexpression of genes for cytosolic GS1 can po
106 Ectopic overexpression of GFP-MLL5 induced cell cycle ar
107 Ectopic overexpression of GIRK2 alone mimics the effect
108 Conversely, the
ectopic overexpression of HDAC6 inhibited LAQ824-induced
109 Similarly, depletion of ZBRK1, or
ectopic overexpression of HMGA2, in MCF10A cells induces
110 Moreover,
ectopic overexpression of Hsf1 enhanced 17-AAG effects u
111 n of eIF4F was enhanced during heat shock by
ectopic overexpression of Hsp25, the murine homolog of h
112 Here, we show that
ectopic overexpression of hsp70 in human acute myelogeno
113 Ectopic overexpression of HuD dramatically inhibits RNA
114 Ectopic overexpression of HuR potently enhanced the tran
115 Ectopic overexpression of Id-1 in the SCp2 nontumorigeni
116 Ectopic overexpression of IFT80 rescued osteolysis in a
117 Ectopic overexpression of INPP4B conferred leukemic resi
118 Ectopic overexpression of IRF-7 partially rescued dsRNA
119 of cyclin D1 expression, when accompanied by
ectopic overexpression of its partner Cdk4, resulted in
120 -6 (IL-6) in macrophage differentiation, and
ectopic overexpression of Jak3 accelerates monocytic dif
121 In addition,
ectopic overexpression of Jak3 appears to result in the
122 ak3 is a primary response gene for G-CSF and
ectopic overexpression of Jak3 can accelerate granulocyt
123 Ectopic overexpression of Jak3 in 32Dcl3 cells resulted
124 Although
ectopic overexpression of K1 in cultured fibroblasts can
125 oss-of-function studies, we demonstrate that
ectopic overexpression of kek1 mimics a loss of EGFR act
126 Ectopic overexpression of KLF-4 and RNAi-mediated inhibi
127 Ectopic overexpression of KLF8 in the non-invasive MCF-1
128 Conversely,
ectopic overexpression of LeHB-1 by viral delivery to de
129 Ectopic overexpression of let-7 in SMCs inhibited inflam
130 Here we show that
ectopic overexpression of menin via adenoviruses induces
131 nd 'gain'-of-function approaches showed that
ectopic overexpression of MIC-1 (PC-3-MIC-1) and forced
132 f the developmentally down-regulated miRNAs,
ectopic overexpression of miR-191 blocks erythroid enucl
133 Transcriptomic analysis of cSCC cells with
ectopic overexpression of miR-203 showed dramatic change
134 Ectopic overexpression of miR-23b in normal renal cells
135 Ectopic overexpression of miR-26b in rat primary postmit
136 Loss of LBR by
ectopic overexpression of miR-340-5p derepressed heteroc
137 Ectopic overexpression of miR-503 promotes cell growth a
138 Ectopic overexpression of miR-621 promoted apoptosis and
139 , miR-222-3p, and miR-432-5p was analyzed by
ectopic overexpression of miRNA mimics.
140 Although
ectopic overexpression of miRNAs can influence mammary n
141 genesis of MDS/AML in part by enforcing the
ectopic overexpression of MLF1 within hematopoietic tiss
142 Conversely,
ectopic overexpression of MORC-1 in the wild-type germ l
143 Interestingly,
ectopic overexpression of Mst77Y caused decompaction of
144 Ectopic overexpression of MUC4 in OC cells (SKOV3-MUC4)
145 glioma cell lines and could be suppressed by
ectopic overexpression of mutant IDH1 in immortalized hu
146 Biologic investigations showed that
ectopic overexpression of NEFL inhibited cell growth spe
147 Conversely,
ectopic overexpression of NHS inhibited lamellipod forma
148 Ectopic overexpression of NmU in drug-sensitive cells co
149 ediated protection was not observed, whereas
ectopic overexpression of Notch1 diminished TNFalpha-ind
150 Consequently,
ectopic overexpression of NS activates p53, induces G(1)
151 Ectopic overexpression of NtERF32 increases expression o
152 In contrast,
ectopic overexpression of NtMYC2a and NtMYC2b had no eff
153 Ectopic overexpression of OmpA in S. Typhimurium Deltasi
154 Importantly,
ectopic overexpression of OsPHO1;2 enhanced grain yield,
155 Ectopic overexpression of p27 in serum-stimulated VSMCs
156 Adenovirally mediated
ectopic overexpression of p27(Kip1) in exponentially gro
157 Notably,
ectopic overexpression of p27KIP1 was associated with a
158 (in contrast to wild-type macrophages); (3)
ectopic overexpression of p50 reduces transcriptional ac
159 er anchorage-independent conditions, whereas
ectopic overexpression of p62 enhanced the self-renewal
160 Our results show that while
ectopic overexpression of p75 c-Myb results in the accel
161 ced cell death similar to that seen with the
ectopic overexpression of p89 c-Myb.
162 th a functional role for par-4 in apoptosis,
ectopic overexpression of par-4 in prostate cancer cell
163 cells acquire bone-metastatic potential upon
ectopic overexpression of PDGFRalpha.
164 emonstrated that the absence of Sirt1 or the
ectopic overexpression of Per2 in the liver resulted in
165 Ectopic overexpression of PGI results in the acquisition
166 The
ectopic overexpression of PhFT4 and PhFT5 promotes flowe
167 Moreover,
ectopic overexpression of PIGN restored the expression o
168 Whereas
ectopic overexpression of PKCalpha in parental H1650 cel
169 An earlier report showed that
ectopic overexpression of PML precludes the disaggregati
170 Silencing PpBL in peach fruit and
ectopic overexpression of PpBL in tomatoes confirm that
171 apoptosis mediated by Ad-p53 infection, and
ectopic overexpression of procaspase-9 sensitized cells
172 Ectopic overexpression of Prox1 in blood vascular endoth
173 postsynaptic compartment of SGN fibers with
ectopic overexpression of PSD95 far outside the synaptic
174 r the interaction between PEX7 and PEX5L and
ectopic overexpression of PTS2-carrying cargo protein dr
175 Ectopic overexpression of PttPXY and PttCLE41 genes in h
176 Ectopic overexpression of PvMYB4 in transgenic switchgra
177 Ectopic overexpression of RAF enhanced BLR1 expression i
178 sistent with this possibility, we found that
ectopic overexpression of Ras-GAP in a Ras-GAP-insensiti
179 Ectopic overexpression of Rdd-BRCA1 promoted partial PAR
180 In addition,
ectopic overexpression of Rem2 both inhibited L-type Ca2
181 Ectopic overexpression of rpr in the developing retina r
182 Ectopic overexpression of S-3B drove tumorigenesis by fa
183 f its own promoter as DNMT corepressors, and
ectopic overexpression of SALL4 led to increased CpG isl
184 HP-1 cells enhanced HSV-1 replication, while
ectopic overexpression of SAMHD1 in U937 cells repressed
185 Ectopic overexpression of SEIPIN1 in Arabidopsis resulte
186 Ectopic overexpression of SET domain mutant (F681Y) almo
187 down-modulates NK-cell cytotoxicity, whereas
ectopic overexpression of SET enhances cytotoxicity.
188 Furthermore,
ectopic overexpression of SET significantly enhanced IFN
189 Furthermore, while
ectopic overexpression of sgrS mutant alleles lacking on
190 Ectopic overexpression of sigma(E) stimulated transcript
191 This was further confirmed by
ectopic overexpression of sirt1, which induced expressio
192 Ectopic overexpression of SIRT2, but not its catalytical
193 Ectopic overexpression of SKP2 led to reduction of p27 p
194 Here we show that
ectopic overexpression of slo-1 in pharyngeal muscle con
195 ng with the increased activity of caspase-3,
ectopic overexpression of Smac/DIABLO or cotreatment wit
196 While it had no activity alone,
ectopic overexpression of Smac/DIABLO or treatment with
197 treatment induced SMAD3 phosphorylation, and
ectopic overexpression of SMAD3 resulted in a significan
198 Ectopic overexpression of Smad7 inhibited Smad2 activati
199 ta-induced inhibition of lung morphogenesis,
ectopic overexpression of Smad7 was introduced into embr
200 Ectopic overexpression of SND1 results in activation of
201 was associated with their upregulation upon
ectopic overexpression of SOX4.
202 Enforced
ectopic overexpression of Sp1 in H35 rat hepatoma cells
203 Both in vitro and in vivo
ectopic overexpression of SPRR1A protected cardiomyocyte
204 Additionally,
ectopic overexpression of Stat3 enhanced Jak3 promoter a
205 positive regulators of leaf senescence, but
ectopic overexpression of SUB1A dampened responsiveness
206 Genotypes with conditional and
ectopic overexpression of SUB1A significantly delayed lo
207 ion of TBXT and induction of cell death, but
ectopic overexpression of TBXT increased viability, ther
208 as the result of a deletion that results in
ectopic overexpression of the Agouti gene mRNA in all ti
209 Arabidopsis thaliana lines with constitutive
ectopic overexpression of the AtNBR1 gene (OX lines) and
210 We show here that
ectopic overexpression of the E3 ubiquitin ligase Rad18
211 partly because studies have so far relied on
ectopic overexpression of the gene in cell lines.
212 Ectopic overexpression of the glutathione S-transferase
213 Ectopic overexpression of the hetRR223W allele in the he
214 Increased JunD levels by
ectopic overexpression of the junD gene or by depleting
215 rm1)EPv develops spontaneous melanoma due to
ectopic overexpression of the metabotropic glutamate rec
216 Furthermore,
ectopic overexpression of the mutant proteins fails to r
217 Ectopic overexpression of the newly cloned AA-enriched v
218 Ectopic overexpression of the short prodomain caspases-3
219 iRNAs that are differentially expressed upon
ectopic overexpression of the splicing factor SF2/ASF.
220 ile floral induction system that is based on
ectopic overexpression of the transcription factor LEAFY
221 dwf5 plant could be restored to wild type by
ectopic overexpression of the wild-type copy of the gene
222 frame 50 (ORF50) in such reactivation, since
ectopic overexpression of this protein induces reactivat
223 allowing for the execution of cell death, as
ectopic overexpression of this protein protects multiple
224 Ectopic overexpression of TIMP-3 in cultured leiomyosarc
225 levels of Aurora-A gene expression and that
ectopic overexpression of TRAP220/MED1 coactivates trans
226 eal maize plant architecture originated from
ectopic overexpression of tru1 in axillary branches, a c
227 Ectopic overexpression of two components of AP-1 (c-jun
228 Knockdown of UHRF1 upregulates whereas
ectopic overexpression of UHRF1 downregulates protein ab
229 Conversely,
ectopic overexpression of UHRF2 in non-tumorigenic MCF10
230 Ectopic overexpression of ULK2-induced autophagy, which
231 Ectopic overexpression of uPAR in human MDA-MB-468 breas
232 Ectopic overexpression of UQCRH in KMRC2 restored mitoch
233 Conversely,
ectopic overexpression of vimentin in osteoblasts inhibi
234 Ectopic overexpression of wild type and a constitutive a
235 Conversely,
ectopic overexpression of wild-type PAR-1b results in ec
236 Ectopic overexpression of wnt5b reduced shh expression,
237 We demonstrate that
ectopic overexpression of WOR3 results in mass conversio
238 Ectopic overexpression of WT 14-3-3sigma in Er/Er kerati
239 of dynamin phenocopies loss of Nm23-H1, and
ectopic overexpression of WT dynamin complements the los
240 Ectopic overexpression of XBP1 induced collagen 1-alpha
241 Both
ectopic overexpression of XOR cDNA and uric acid supplem
242 Ectopic/overexpression of ABCB19 (B19OE) greatly increas
243 I31 levels were either increased by moderate
ectopic overexpression or decreased by RNA interference
244 oliferation mechanism is disrupted by either
ectopic overexpression or mutation of CYCA2;1, the hypon
245 Modulation of beta-catenin levels via
ectopic overexpression or small interference RNA-mediate
246 ets involved in this reprogramming, as their
ectopic overexpression partly phenocopies the dedifferen
247 on of RITMO1 expression levels and timing by
ectopic overexpression results in lines with deregulated
248 Ectopic overexpression results in the development of ect
249 Ectopic overexpression studies have implicated G2A as a
250 In vitro
ectopic overexpression studies implicated GPR4 in sensin
251 nd stem cell neurosphere formation, with its
ectopic overexpression sufficient to shorten survival in