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