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1 ly protein activates expression of the other immediate-early protein.
2 domain found in a bovine herpesvirus 4 major immediate-early protein.
3 l cells) or BRLF1 (in epithelial cells only) immediate-early protein.
4 miR-UL112-1 inhibits expression of the major immediate-early protein.
5 oma-associated herpesvirus (KSHV) encodes an immediate-early protein.
6 reased and prolonged expression of the viral immediate early proteins.
7 ecognition of virion input proteins or viral immediate early proteins.
8 accumulates at ND10 before the production of immediate-early proteins.
9 s normally overcome by viral tegument and/or immediate-early proteins.
10 ranscriptional activation by cytomegalovirus immediate-early proteins.
11 mutants deleted for various combinations of immediate-early proteins.
12 n 65 (pp65), phosphoprotein 150 (pp150), and immediate early protein 1 (IE1) immunodominant antigens
13 8(+) T cell responses to the pp65 (UL83) and immediate early protein 1 (IE1; UL123) gene products in
14 lls recognized the CMV phosphoprotein 65 and immediate early protein 1, which have been considered ma
18 patients, stratified by their baseline CMV (immediate-early protein 1)-specific CMI risk, were rando
20 ve characterized the mechanisms by which the immediate early protein 2 (IE2 or IE86), a master transc
22 R-200 miRNA family members target the UL122 (immediate early protein 2) 3' untranslated region, resul
25 n did not require VZV replication; the viral immediate-early protein 62 (IE62) alone was sufficient t
27 racterized by the abundant expression of the immediate early protein 63 (IE63), whereas other viral p
28 hibition of CaMKK has a negligible impact on immediate-early-protein accumulation yet severely attenu
29 ins are transcriptional activators, and each immediate-early protein activates expression of the othe
30 utant virus accumulated representative viral immediate-early proteins and early proteins normally.
32 st CD8+ cytotoxic T lymphocytes specific for immediate-early protein are present in seropositive indi
33 e previously demonstrated that ORF45, a KSHV immediate-early protein as well as a tegument protein of
34 ription factor Oct-1 cooperates with the EBV immediate-early protein BRLF1 (R, Rta) to induce lytic v
37 t, unexpectedly, expression of another viral immediate-early protein, BRLF1, can disrupt viral latenc
38 ired virus resulted in similar levels of VZV immediate-early proteins but reduced levels of glycoprot
42 xpression of either Epstein-Barr virus (EBV) immediate-early protein BZLF1 (Z) or BRLF1 (R) is suffic
47 re we show that the Epstein-Barr virus (EBV) immediate-early protein BZLF1 prevents TNF-alpha activat
50 c EBV infection is mediated by the two viral immediate-early proteins BZLF1 (Z) and BRLF1 (R), which
52 the ability of rAd vectors encoding the EBV immediate-early proteins BZLF1 and BRLF1 to induce the l
53 of EBV infection, expression of either viral immediate-early protein (BZLF1 or BRLF1) is sufficient t
54 s gene silencing, yet the Epstein-Barr virus immediate-early protein, BZLF1 (Z), converts the virus f
57 emonstrate that the Epstein-Barr virus (EBV) immediate-early protein, BZLF1, inhibits the IFN-gamma s
58 t is known that expression of a single viral immediate-early protein, BZLF1, is sufficient to initiat
59 erentially affect the ability of the two EBV immediate-early proteins, BZLF1 (Z) and BRLF1 (R), to in
60 However, expression of either of the EBV immediate-early proteins, BZLF1 and BRLF1, is sufficient
62 ment, an immunohistochemical analysis of the immediate early protein c-Fos was performed as a marker
64 follow-up experiment, expression of a second immediate early protein, egr-1, was blocked as well, sug
65 ycin-D, which results in accumulation of the immediate-early protein, failed to down-regulate class I
66 C-5 cells with a virus that does not express immediate-early proteins, followed by superinfection wit
67 s all required prior expression of the viral immediate early proteins for activation in fibroblasts.
69 26-95 except K3 and K5 (bovine herpesvirus-4 immediate-early protein homologues), K7 (nut-1), and K12
73 DNA-PKcs and in cells cotransfected with the immediate early protein ICP0, which degrades DNA-PKcs.
74 larities with herpes simplex virus 1 (HSV-1) immediate early protein ICP0, which stimulates lytic HSV
76 the interaction between the C-USP7 and HSV-1 immediate-early protein ICP0 (infected cell protein 0),
78 of the late viral proteins gE and gD and the immediate-early protein ICP0 but did not have discernibl
79 When expressed in the infected cell, the HSV immediate-early protein ICP0 has E3 ubiquitin ligase act
80 SV-1) mutants that fail to express the viral immediate-early protein ICP0 have a pronounced defect in
88 In herpes simplex virus type 1 (HSV-1), the immediate-early protein ICP0 serves as a counterdefense
89 Using mutant viruses, we determined that the immediate-early protein ICP0 was necessary for the inhib
93 , in the absence of the "nonessential" viral immediate-early protein, ICP0, HSV-1 is severely impaire
94 s, US11 and gC, and increased amounts of two immediate-early proteins, ICP0 and ICP4, as well as prot
97 that the herpes simplex virus type 1 (HSV-1) immediate-early protein ICP22 alters the phosphorylation
99 ro cells and that certain mutations in viral immediate early protein ICP27 can confer LMB resistance.
103 The herpes simplex virus type 1 (HSV-1) immediate-early protein ICP27 is required posttranscript
104 of the HSV genome, we provide evidence that immediate-early protein ICP4 is involved in the process
105 infected with DeltaU(L)31, expression of the immediate-early protein ICP4, early protein ICP8, and la
106 ific viral DNA sequence, OriS, and the viral immediate-early proteins ICP4 and ICP27 are sufficient f
108 le component, granzyme B, degrades the HSV-1 immediate early protein, ICP4, which is essential for fu
111 implex virus serotype 1 (HSV-1) expresses an immediate-early protein, ICP47, that effectively blocks
112 s types 1 and 2 (HSV-1 and HSV-2) express an immediate-early protein, ICP47, that effectively inhibit
119 d through individual expression of the viral immediate-early protein IE1-72, mimicking full virus inf
123 ting a transactivator plasmid expressing the immediate early protein (IE1) from the Bombyx mori nucle
125 rnica multicapsid nuclear polyhedrosis virus immediate-early protein, IE1, is a 582-amino-acid phosph
127 ndent DNA replication and interacts with the immediate-early protein IE2 in lytically infected cells.
129 ally identified as a binding element for the immediate-early protein IE2, was essential for oriLyt(PM
131 Peptides corresponding to residues of the immediate early protein, IE62, of varicella-zoster virus
132 oclonal antibody (rec-MAb 63P4) that detects immediate-early protein IE63 encoded by varicella-zoster
133 viral major immediate promoter (MIEP) by its immediate-early protein IE72 (determined by cotransfecti
134 fic for either HCMV tegument protein pp65 or immediate-early protein IE72 are found in both CD45RO(hi
137 Stimulation of this promoter by the 86-kDa immediate-early protein (IE86) is controlled by sequence
138 R2 protein (IR2P) is a truncated form of the immediate-early protein (IEP) lacking the essential acid
143 resistant translation, the presence of viral immediate-early proteins is sufficient to establish a st
144 iral transcription factor, the 72K principal immediate-early protein, is abundantly expressed before
146 n.IMPORTANCE HSV-1 ICP0 is a multifunctional immediate early protein key to effective replication in
147 iRNAs targeted to sequences encoding Rta, an immediate-early protein known as an initiator of the lyt
149 that the human cytomegalovirus (HCMV) major immediate-early proteins (MIEPs) can rescue the transcri
157 ein interactions between ICP4 and ICP27, two immediate-early proteins of HSV-1 that are essential for
159 copy studies indicated that Rosco caused the immediate-early proteins ORF4 and IE62 to abnormally loc
160 of KSHV lytic proteins demonstrated that the immediate early proteins ORF45 and replication and trans
161 ansactivation was also mediated by the viral immediate-early protein Orf50/Rta, suggesting that the K
162 cient to reactivate latent VZV or target the immediate-early protein ORF62p to the nucleus in culture
167 minutes of infection, herpes simplex virus 1 immediate early proteins repurpose cellular RNA polymera
168 HV genome, including repression of the viral immediate-early protein Rta and a cellular factor, Rbl2,
169 rpes simplex virus (HSV) infection relies on immediate early proteins that initiate viral replication
171 ssential herpes simplex virus type 1 (HSV-1) immediate-early protein that stimulates viral mRNA expre
172 1 (R) is one of two Epstein-Barr virus (EBV) immediate-early proteins that mediate the switch from th
176 rus type 1 infection revealed that the viral immediate-early protein Vmw110 (also known as ICP0) form
181 ability to interact with the mammalian TIS21 immediate-early protein, was then shown to have protein
184 viral proteins expressed upon infection, the immediate early proteins, which play a key role in creat
185 rus IRS1 and TRS1 open reading frames encode immediate-early proteins with identical N-terminal domai
186 and replication function of the EBV-encoded immediate-early protein Zta (also referred to as ZEBRA,