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1 and tumorigenesis mediated by the adenovirus E1A protein.
2 arkedly diminished by expression of the 12 S E1A protein.
3 nase promoter as efficiently as the wildtype E1A protein.
4 the domain of CBP/p300 that binds adenovirus E1A protein.
5 s examined by in vitro binding to adenovirus E1A protein.
6 een for cellular proteins that interact with E1A protein.
7 activation by cellular factors and the viral E1A protein.
8 terminal binding protein binding site in the E1A protein.
9 he p160 coactivators and with the adenovirus E1A protein.
10 o either E1A-Myc chimeras, or the native 12S E1A protein.
11 not only by Myc, but also by the adenovirus E1A protein.
12 E1 and fails to produce the immediate-early E1a protein.
13 antigen, by oncogenic ras, or by adenovirus E1a protein.
14 qually sensitive to inhibition by adenovirus E1A protein.
15 n of E2F could not be reversed by adenovirus E1A protein.
16 cked in HeLa cells expressing the adenovirus E1A proteins.
17 functionally conserved in E2F and adenovirus E1A proteins.
18 performed with recombinant HPV16 E7 and Ad5 E1A proteins.
19 2 and 3 within the HAdV-A12 early region 1A (E1A) protein.
20 C terminus of adenovirus early region 1A (Ad E1A) proteins.
21 ssion of CBP/p300 function by the adenoviral E1A protein abolishes c-fos activation by EWS, indicatin
25 ted i.v. with LPD-E1A, and the expression of E1A protein and effects on tumor growth were assessed.
26 r subunit that interacts with the adenovirus E1A protein and functions in a mitogen-activated protein
27 ated to conserved region 1 of the adenovirus E1A protein and importantly contributes to cellular tran
28 in vivo by overexpression of the adenovirus E1A protein and mutant forms of E1A that lack p300-bindi
29 idenced by inhibition with overexpressed 12S E1A protein and reversal of this inhibition with exogeno
30 because it bound normally to the adenovirus E1A protein and showed nuclear localization by immunosta
31 s (p5, p19, and p40) requires the adenovirus E1a protein and the AAV nonstructural (Rep) proteins.
32 bolished by the NO donors: the appearance of E1A protein and the cleavage of cytokeratin 18 by AVP.
34 y reduced by cotransfection of the wild-type E1A protein and variably reduced by the cotransfection o
35 his activation is enhanced by the adenovirus E1A protein, and evidence for interaction between E1A an
36 steroid receptor co-activator, as well as by E1A proteins, and attenuated by Smad nuclear interacting
37 ponse as a result of expression of the viral E1A proteins, and this process is suppressed by the vira
43 nal machinery is inhibited by the adenovirus E1A protein as a result of E1A's binding to the p300 coa
46 ed with proteasomes and that the larger Ad12 E1A protein binds strongly to at least three components
47 force the general conclusion that adenovirus E1A proteins block IFN signaling pathways by lowering th
50 repressed by E1A, these studies suggest that E1A protein can repress cellular and viral promoter/enha
51 ll established, however, that the adenovirus E1A protein can sensitize these cells to the induction o
53 ith the use of purified wild type and mutant E1A proteins confirmed that CBP, p300, and pRB were targ
64 ntrast, the nontumorigenic adenovirus type 5 E1A protein (E1A-5) and other E1A-12 mutants lacking the
65 adenovirus-infected cells, the expression of E1A protein enhances the accumulation of p53 during earl
66 ult suggests that an inhibiting effect on wt E1A protein expression and/or E1A function might account
69 ort to the idea that the p202 and adenovirus E1A protein functionally counteract each other and E1A p
78 nd DP-1 proteins or microinjected adenovirus E1A protein, however, could induce S phase in cells arre
80 t proteins have been shown to bind stably to E1A proteins in adenovirus-infected and -transformed cel
81 that transactivation of the promoter by the E1A proteins in cycling cells is mediated through the tw
82 l gene transfer to express various E2F-1 and E1A proteins in neonatal rat cardiac myocytes that are a
83 adenoviruses to express wild-type and mutant E1A proteins in primary cultures from embryonic day 20 r
86 s reduced by competition with the adenovirus E1a protein, indicating that binding occurs through the
93 ffinity chromatography studies show that the E1A protein interacts with the DNA binding/dimerization
95 tified by its ability to bind the adenovirus E1A protein, interacts both with gene-specific transcrip
98 property of the adenovirus (Ad) transforming E1A protein is linked to its capacity to induce cellular
100 r at 48 degrees C or with the adenovirus 13S E1a protein; (iv) this domain of Tag cannot bind concurr
101 nd p21 through the binding of the adenovirus E1A protein leads to the induction of DNA replication in
103 These results support the conclusion that E1A protein mediates optimal transactivation of the huma
106 ave previously shown that the adenoviral 12S E1A protein modulates the phosphorylation status of p130
107 engineering the expression of the adenoviral E1A protein, necessary for viral replication, under the
108 Despite data suggesting that the adenovirus E1A protein of 243 amino acids creates an S-phase enviro
116 have revealed that human adenovirus-encoded E1A protein promotes cell proliferation through the targ
121 ovary and L-cells, HPV E7 and the adenovirus E1A protein repressed the transduced hPCNA promoter, but
122 , we demonstrated that the adenovirus type 5 E1A proteins repressed stimulation by the E-box activato
123 found that overexpression of the adenovirus E1A protein represses expression of a reporter gene dire
124 nds to Stat1 and CBP/p300, and by the mutant E1A protein RG2, which binds to Stat1 but not to CBP/p30
125 18 and the oncogenic adenovirus (Ad) type 12 E1A protein share the ability to down-regulate the expre
126 ino acids in the conserved region 2 (CR2) of E1A protein significantly reduced the binding of E1A to
128 R3 activation domain of the human adenovirus E1A protein stimulates transcription by forming protein-
129 egion 1 (CR1) of the adenovirus type 5 (Ad5) E1A protein synergizes with CR3 in the transactivation o
130 otein functionally counteract each other and E1A protein targets p202 to promote cell proliferation.
131 teins, we analyzed the functional regions of E1A proteins that are required for muscle gene repressio
133 xpression of wild-type and mutant adenovirus E1a proteins that sequester p300/CBP eliminated IFN-gamm
134 hat ivermectin disrupts binding of the viral E1A protein to Imp-alpha without affecting the interacti
135 /p300-binding is required for the adenovirus E1A protein to regulate transcription of many genes duri
136 protein also cooperates with the adenovirus E1A protein to transform primary baby rat kidney cells,
138 E1A 243R, as shown by the ability of mutant E1A proteins to repress the promoter, and correlated wit
139 n the MDA-MB-361 breast model, expression of E1A protein was detected in the tumors after LPD-E1A tre
141 ted through direct binding by the adenovirus E1A protein, we overexpressed E1A in cardiac myocytes us