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1 or structure, they are all recognized by the virus-encoded 3C protein.
2  the ORF1 polyprotein was generated, and the virus-encoded 3C-like (3CL) proteinase (Pro) mediated cl
3 at undergoes autocatalytic processing by the virus-encoded 3C-like proteinase.
4 ORFs of equine H3N8 and avian H3N2 influenza viruses encoded 61 amino acids but were truncated after
5                                         This virus encoded a single mutation, H316N (numbered relativ
6       Mouse T cells specific to the vaccinia virus-encoded a11r(198-205) could be cross-reactive with
7 ful infection of adult Drosophila requires a virus-encoded activity to suppress RVI.
8 secreting potential unless stimulated with a virus-encoded Ag.
9         The influenza A virus NS1 protein, a virus-encoded alpha/beta interferon (IFN-alpha/beta) ant
10                                  L4-33K is a virus-encoded alternative RNA splicing factor which acti
11 ion between corresponding family clusters of virus-encoded ANK and Skp1 proteins from three chlorovir
12 ated in myeloid cells despite the actions of virus-encoded antagonists.
13 e triggered at mitochondria and modulated by virus-encoded anti-apoptotic B cell leukemia (BCL)2-like
14 selection for the evolution of sophisticated virus-encoded anti-CRISPR mechanisms.
15 pase-8, cytokine response modifier A (cowpox virus-encoded antiapoptotic protein), or DN Fas-associat
16                                Unexpectedly, virus-encoded antigen was detectable more than 6 weeks a
17 e efficiency difference between cellular and virus-encoded antigens is based on whether the antigen i
18 red thirty-six of the proteins were vaccinia virus-encoded ( approximately 64% of the known vaccinia
19 view the discovery of viral master circuits: virus-encoded autoregulatory gene networks that autonomo
20 by notable sequence homology to the vaccinia virus-encoded B1 kinase (vvB1).
21 wed that CBP interacts with the Epstein-Barr virus-encoded basic region zipper (b-zip) protein, Zta,
22       We previously showed that the vaccinia virus-encoded Bcl-2-like protein, F1L, which suppresses
23    Virulence in animal models depends on the virus-encoded bifunctional Z-DNA/double-stranded RNA (ds
24  (GILGFVFTL) and the dissimilar Epstein-Barr virus-encoded BMLF1(280-288) epitope (GLCTLVAML), that,
25 ression of immune subversion proteins of the virus encoded by genes belonging to the US gene family.
26       RNA transcripts from this cDNA and the viruses encoded by them were infectious for cells of bot
27                                              Virus-encoded capsid proteins play a major role in the l
28 CMV growth by blocking the expression of the virus-encoded capsid proteins.
29                                   Given that virus-encoded cation channels play a crucial role in the
30 ecruits new macrophages to the tumor via the virus-encoded chemokine MCK2, and viruses lacking this c
31 d a chemokine-binding domain called smallpox virus-encoded chemokine receptor (SECRET) domain.
32                                  While these virus-encoded chemokine receptors are necessary for the
33  with diversity-generating retroelements and virus-encoded Clustered Regularly Interspaced Short Pali
34          Recent studies suggest that several virus-encoded components that antagonize RLR signaling i
35               Here we show that unlike other virus-encoded countermeasures, such as those from primat
36 mmunomodulatory activities in the ectromelia virus-encoded CrmD.
37                                          The virus-encoded cysteine proteinase mediated at least five
38 relevant to understanding the potential of a virus-encoded cytokine-like molecule, HHV8 vIL6, to indu
39  intramolecular disulfide bond formed by the virus-encoded cytoplasmic redox pathway, and is incorpor
40 the formation of which required the vaccinia virus-encoded cytoplasmic redox pathway, and was localiz
41 iated proteins localized to the periphery of virus-encoded cytoplasmic structures, termed virus facto
42                                 The vaccinia virus-encoded D5 protein is an essential ATPase involved
43 ncy virus type 1, which is counteracted by a virus-encoded degradation mechanism(1-4).
44 progress is leading to the identification of virus-encoded determinants responsible for altering fung
45                   Finally, identification of virus-encoded dissimilatory sulfite reductase suggests S
46  ori-Lyt in the presence of the Epstein-Barr virus-encoded DNA binding initiator protein, ZTA.
47 ous amounts of methylated nucleotides due to virus-encoded DNA methyltransferases (MTases); about 25%
48 inding protein (OBP), one of seven essential virus-encoded DNA replication proteins, to specific sequ
49 evaded by transcription of highly structured virus-encoded dsRNA inhibitors that bind to and inactiva
50  circumvent PKR function by transcription of virus-encoded dsRNA inhibitors that bind to and inactiva
51 tethering, mediated by Brd4 interaction with virus-encoded E2 protein, facilitates viral genome segre
52 understanding of the mechanisms by which the virus-encoded E6 oncoproteins contribute to cell transfo
53 hile their direct autoregulatory activity on virus-encoded early gene products is completely preserve
54                                          The virus-encoded EBNA-1 (EBV nuclear antigen 1) and latent
55 ex mechanism involving interactions with the virus-encoded EBNA1 protein.
56                        The identification of virus-encoded effectors of SIE and their transgenic expr
57                                      The two viruses encoded either wild-type (WT) VP35 protein (recE
58 ircle-like mechanism initiated by a distinct virus-encoded endonuclease.
59                                          The virus-encoded envelope proteins of human immunodeficienc
60 somal DNA of a host cell and is one of three virus-encoded enzymes that are required for replication.
61  acid motifs as a result of glycosylation by virus-encoded enzymes.
62 es, episome maintenance requires a dedicated virus-encoded episome maintenance protein (EMP), namely
63 adapter-mediated substrate recruitment for a virus-encoded ERAD E3 ligase, mK3.
64  analysis indicated that the mutation in the virus-encoded external scaffolding protein was primarily
65 tein, whereas the fourth mutation alters the virus-encoded external scaffolding protein.
66                      We report that vaccinia virus-encoded F1L protein, previously recognized as anti
67 ssociated proteins around the peripheries of virus-encoded factories, interrupting the normal formati
68      The contributions of major Epstein-Barr virus-encoded factors, including proteins, small RNAs, a
69 s previously identified as fcr-1, a putative virus-encoded FcR.
70 both plant and invertebrate hosts requires a virus-encoded function to block the RNA silencing antivi
71 eptibility to cucumber mosaic virus when the virus-encoded function to suppress RNAi was disrupted.
72 ted, by an immediate-early (IE) or early (E) virus-encoded function(s).
73 es is transcribed, including one of the four virus-encoded G protein-coupled receptors (GPCRs), US28.
74 ite of budding by the late (L) domain of the virus-encoded Gag protein.
75 ess ERK activity in the absence of any other virus-encoded gene products.
76 d cells that express a broad spectrum of the virus-encoded genes (type III latency; EBV+/III), EBV-po
77 c analysis reveals that 65% of the predicted virus-encoded genes are expressed during lytic infection
78 ce, host-cell-derived tissue factor (TF) and virus-encoded glycoprotein C (gC) can stimulate protease
79 s initiated by the interaction of the Friend virus-encoded glycoprotein gp55 with the erythropoietin
80                                              Virus-encoded glycoproteins in the envelope are responsi
81 nd tegument, and a lipid envelope containing virus-encoded glycoproteins.
82       Here, we identified the roles of three virus-encoded glycosyltransferases (GTs) that have four
83 s expressing only US28 but not the remaining virus-encoded GPCRs is phenotypically similar to that of
84 s, in a process that is probably driven by a virus-encoded helicase.
85 acterization of the aptamers showed that the virus-encoded hemagglutinin, a protein expressed on the
86               Moreover, we observed that the virus-encoded HIV transactivator protein Tat cooperated
87                                          The virus-encoded Holliday junction resolvase is required to
88 s and vaccinia virus specifically, utilize a virus-encoded host range factor(s), such as a member of
89 ropism at the cellular level is regulated by virus-encoded host range proteins acting downstream of v
90 ed of the minor capsid protein (CPm) and the virus-encoded Hsp70 homolog.
91 hermore, the absence of analogous degrons in virus-encoded IAPs explains their relative stability and
92                           Over 170 different virus-encoded IFN antagonists from 93 distinct viruses h
93 tiple factors, indicating robustness against virus-encoded immune evasion genes.
94 t has resulted in a delicate balance between virus-encoded immune evasion mechanisms and host antivir
95 rus, extending the known diversity of insect virus-encoded immune inhibitors.IMPORTANCE Coevolution o
96      PA-X is a fusion protein of influenza A virus encoded in part from a +1 frameshifted X open read
97   However, the relative contribution of each virus-encoded innate immune antagonist has not been full
98                                  Transmitted viruses encoded intact canonical genes (gag-pol-vif-vpr-
99   This enzymatic process is catalyzed by the virus-encoded integrase protein, which is conserved amon
100 ces correlate with the sequence/structure of virus-encoded integrases, supporting the idea that integ
101 he retroviral life cycle and is catalyzed by virus-encoded integrases.
102                      Here we report that the virus-encoded interferon regulatory factor 3 (vIRF3) lat
103                         Viroporins are small virus-encoded ion channel proteins.
104 es suggested that HCV p7 could function as a virus-encoded ion channel.
105 e class of agent has been licensed targeting virus-encoded ion channels, or 'viroporins', contrasting
106                                       The M1 virus-encoded K1 toxin is primarily but not solely respo
107 ation that bind the origin-binding domain of virus-encoded large T antigen.
108 rs (vTAs) coordinate to direct expression of virus-encoded late genes, which are critical for viral a
109 he latter, (iii) neither viral DNA nor other virus-encoded late proteins are required for the interac
110                                  In general, virus-encoded late stage structural proteins, such as gB
111 virus (EBV) nuclear antigen 3C (EBNA3C) is a virus-encoded latent antigen essential for primary B-cel
112                             The Epstein-Barr virus-encoded latent infection membrane protein 1 (LMP1)
113 al tumor nasopharyngeal carcinoma (NPC), the virus-encoded latent membrane protein LMP2A is consisten
114 nd transmembrane domains of the Epstein-Barr virus-encoded latent membrane protein-1 (LMP1) fused to
115 ng infected cells to differentiate using the virus-encoded LMP1 and LMP2a proteins, which act as func
116 ed that several nonenveloped viruses utilize virus-encoded lytic peptides for host membrane disruptio
117 ty between the HLA-A2-restricted influenza A virus-encoded M1(58-66) epitope (GILGFVFTL) and the diss
118 We propose that the NEC functions as minimal virus-encoded membrane-budding machinery during nuclear
119  transforms host metabolism, in part through virus-encoded metabolic genes; the functions performed b
120 e identification and characterization of two virus-encoded methyltransferases (MTases) involved in RN
121 wn-regulated at late times by miR-UL112-1, a virus-encoded microRNA.
122          To date, the vast majority of known virus-encoded microRNAs (miRNAs) are derived from polyme
123 genes in the animal kingdom, although animal virus-encoded microRNAs (miRNAs) are known to guide effi
124                                  Hundreds of virus-encoded microRNAs (miRNAs) have been uncovered, bu
125 e expression, and there have been reports of virus-encoded microRNAs.
126 n, we report the discovery of three herpes B virus-encoded microRNAs.
127                             The Epstein-Barr virus-encoded miR-BART20-5p inhibits T-bet (TBX21), the
128 ese findings imply that some host targets of virus-encoded miRNAs are likely to be of little selectiv
129                                              Virus-encoded miRNAs have garnered much interest, althou
130                                      Several virus-encoded miRNAs have unique aspects to their biogen
131 s are continuing but the recent discovery of virus-encoded miRNAs indicates that viruses also use thi
132                                              Virus-encoded miRNAs seem to evolve rapidly and regulate
133 miRNAs and there is evidence to suggest that virus-encoded miRNAs target specific host genes and path
134 ain LMP1, signal transduction molecules, and virus-encoded miRNAs.
135 ies, and a number of previously unidentified virus-encoded miRNAs.
136 similar to those reported for other vaccinia virus-encoded model antigens.
137                                        These virus-encoded molecules promote cell entry, facilitate d
138 h plasmodesmata (PD), a process depending on virus-encoded movement protein (MP).
139 itiation factor eIF4E and VP39 (the vaccinia virus-encoded mRNA cap-specific 2'-O-methyltransferase),
140 e antigen is synthesized from transgene- vs. virus-encoded mRNA.
141         KSHV genomes expressing latent state virus-encoded mRNAs and the LANA1 (latent nuclear antige
142 pect to virus production and accumulation of virus-encoded mRNAs measured by real-time PCR when K-Rta
143                               Poxviruses use virus-encoded multisubunit RNA polymerases (vRNAPs) and
144 mbinant fusion protein comprised of a cowpox virus encoded NKG2D binding protein (OMCP) and a mutated
145 ied, little is known about the structures of virus-encoded non-structural proteins that are essential
146 involves the contribution of a wide array of virus encoded noncoding RNAs.
147                                          The virus-encoded nonstructural protein 5B (NS5B) of hepatit
148 rsistent insect reovirus took advantage of a virus-encoded nonstructural protein, P10, for efficient
149                                            A virus-encoded nonstructural protein, termed NSs, is a ma
150                           It is thought that virus-encoded nonstructural proteins and RNA genomes int
151 s observed as discrete foci, associated with virus-encoded NS5A and core proteins and identical in mo
152                                          The virus-encoded NSs protein acts as a virulence factor by
153 oliferation and the EBV latency Epstein-Barr virus-encoded nuclear antigen (EBNA)2 transcriptional tr
154 -alanine repeat domain (GAr) of Epstein-Barr virus-encoded nuclear antigen 1 (EBNA1) prevents major h
155 a repeat (GAr) within the viral Epstein-Barr virus-encoded nuclear antigen 1 protein.
156 ive sense RNA that are encapsidated with the virus-encoded nucleocapsid (N) protein to form a ribonuc
157 t C6 in the 2'-deoxynucleoside series showed virus-encoded nucleoside kinase-sensitive anti-VZV activ
158 RB) family of tumor suppressor proteins, and virus-encoded oncogenes disrupt the RB-E2F repressor com
159 nd the carcinogenic mechanism of hepatitis B virus-encoded oncoprotein HBx, we explored the function
160 factor receptor family, and the Epstein-Barr virus-encoded oncoprotein latent membrane protein 1 (LMP
161                    The human T-cell leukemia virus-encoded oncoprotein Tax is a potent activator of v
162 nducing kinase and the human T-cell leukemia virus-encoded oncoprotein Tax or be constitutively turne
163 liomas in vertebrates through the actions of virus-encoded oncoproteins.
164 ombinant PABP in vitro in the absence of any virus-encoded or eukaryotic cellular cofactors.
165 egative costimulatory signal to T cells by a virus-encoded orthologue of CD200.
166                       The Tomato bushy stunt virus-encoded P19 forms dimers that bind duplex short in
167 ose induced by p55(gag), which recognize the virus encoded p24(gag) protein.
168    MERS-CoV replication depends in part on a virus-encoded papain-like protease (PL(pro)) that cleave
169  to characterize the functional role of this virus-encoded pathway during lytic viral infection.
170 onformation of gamma, a membrane-disrupting, virus-encoded peptide usually sequestered inside the cap
171  opposite roles in generating an influenza A virus-encoded peptide.
172 ormation to generate ISVP*s and releases two virus-encoded peptides, mu1N and Phi.
173           This is the first description of a virus-encoded PERK-specific effector and defines a new s
174                         In general, the same virus-encoded polymerase is responsible for both genome
175                       However, an additional virus-encoded polypeptide referred to as the RPO-associa
176 ermediate transcription factor, comprised of virus-encoded polypeptides A8 and A23, was previously id
177 provide direct evidence that AC4 is a unique virus-encoded posttranscriptional gene-silencing suppres
178 s from cellular transcription in requiring a virus-encoded preinitiation complex that binds to TATT m
179 ved after CVB3 infection at G175 and G436 by virus-encoded protease 2A(pro), independent of caspase a
180                                              Virus-encoded proteases play diverse roles in the effici
181 ting that 2C is indeed capable of regulating virus-encoded proteases.
182                                       Cowpox virus encoded protein CPXV203 blocks MHCI surface expres
183  terminal alpha-l-Rha is achieved by another virus-encoded protein A061L, which requires an O-2 methy
184 e mechanism of STAT signaling evasion, but a virus-encoded protein called V plays a central role in t
185                  We identified the Kallithea virus-encoded protein gp83 as a potent inhibitor of Toll
186 mplexes (RNPs) formed by these RNAs with the virus-encoded protein hepatitis delta antigen (HDAg) per
187 during their lytic replication cycle through virus-encoded protein kinases.
188                                          The virus-encoded protein pUS9 promotes axonal dissemination
189  assemble in the host cell membrane from the virus-encoded protein PVAP and open at the end of the in
190 nsactivator of transcription (Tat), an early virus-encoded protein required for the efficient transcr
191 to the ability to phosphorylate H5, the only virus-encoded protein shown to be a B1 substrate in vivo
192           The tegument consists of multiple, virus-encoded protein species that together can account
193                         We have identified a virus-encoded protein termed gp37/Dip, which directly bi
194           EBV nuclear antigen 1 (EBNA1) is a virus-encoded protein that is critical for the replicati
195 hondria-localized inhibitor of apoptosis), a virus-encoded protein with a unique, albeit poorly under
196 otic function of NSP4 is balanced by another virus-encoded protein, NSP1, which is implicated in PI3K
197 reproduced by ectopic expression of a single virus-encoded protein, Tat.
198 icornaviral RNA replication utilizes a small virus-encoded protein, termed 3B or VPg, as a primer to
199 ific cleavage of the host factor Gemin3 by a virus-encoded proteinase, 2A(pro).
200 oteins that are proteolytically processed by virus-encoded proteinases to produce mature replicase pr
201 on, several cellular proteins are cleaved by virus-encoded proteinases.
202                                      Several virus-encoded proteins and an activity designated VLTF-X
203 f the human nervous system that uses its own virus-encoded proteins and the normal cellular ESCRT mac
204                               Representative virus-encoded proteins and viral DNA accumulated with no
205                           (d) Many chlorella virus-encoded proteins are either the smallest or among
206                                 At least six virus-encoded proteins are required for synthesis and pr
207 Combined, these analyses revealed 148 unique virus-encoded proteins associated with the virion (about
208                                              Virus-encoded proteins counteract this innate antiviral
209                         The tip contains the virus-encoded proteins genome-linked protein and helper-
210                   Despite these findings, no virus-encoded proteins have been identified that directl
211 al response that inhibits the translation of virus-encoded proteins in Nicotiana benthamiana.
212 d heterologous viruses to express individual virus-encoded proteins in wheat.
213 udies have uncovered new mechanisms by which virus-encoded proteins inhibit Ub and Ub-like (Ubl) modi
214          UL25 is one of seven herpes simplex virus-encoded proteins involved specifically in DNA enca
215 duce a restrictive defense response but that virus-encoded proteins may be involved in differential i
216 e focusing on agents that block Epstein-Barr virus-encoded proteins or induce lytic cycle agents.
217 man cytomegalovirus (HCMV), contains over 70 virus-encoded proteins that are incorporated during a nu
218 of herpesvirus late genes depends on several virus-encoded proteins whose function is not completely
219                                    Two other virus-encoded proteins, an HSP70 homolog (HSP70h) and an
220  HCMV gB is also one of the most immunogenic virus-encoded proteins, and a significant fraction of vi
221                       Here, we show that two virus-encoded proteins, US2 and US3, coordinate their fu
222 ng live-cell imaging of viral RNA (vRNA) and virus-encoded proteins, we show that the TGB proteins ha
223 xpression, modification, and localization of virus-encoded proteins.
224 pect for therapeutic interventions targeting virus-encoded proteins.
225 localization of active ERK can be altered by virus-encoded proteins.
226 esumed to be RNA, and is suppressed by plant virus-encoded proteins.
227 kaging them into an outer shell or capsid of virus-encoded proteins.
228 kaging them into an outer shell or capsid of virus-encoded proteins.
229 ific peptides from vaccinia- and influenza A virus-encoded proteins.
230 strains the functional analysis of influenza virus-encoded proteins.
231 eparations, >88% of the theoretical vaccinia virus-encoded proteome was detected with high confidence
232         The PBCV-1 proteome reveals that two virus-encoded REases, but not their companion MTases, ar
233 homologous recombination in the absence of a virus-encoded RecA-type protein.
234                  During latency, a subset of virus-encoded regulatory proteins is detected; however,
235 lving interactions between the viral genome, virus-encoded replication factors, and host factors.
236 luding a requirement of two PCV Oris and the virus-encoded replication initiator Rep protein, suggest
237 auses G(1) cell cycle arrest mediated by the virus-encoded replication-associated protein (RAP) (or K
238  A(1) was found to block the expression of a virus-encoded reporter gene in both infection and transf
239 Holliday junctions, which are cleaved by the virus-encoded resolvase enzyme to form unit-length genom
240 eflects a multistep process catalyzed by the virus-encoded reverse transcriptase (RT).
241           HBV is a DNA virus that utilizes a virus-encoded reverse transcriptase to convert an RNA in
242                                 Packaging of virus-encoded RNA is selective, with virions virtually d
243 se is a multiprotein complex, containing the virus-encoded RNA polymerase L and P proteins, and two c
244  belonging to the Picornaviridae, requires a virus-encoded RNA polymerase.
245  provide evidence for a mechanism by which a virus-encoded RNA silencing suppressor represses the tra
246       Neither Bcl-6 protein nor Epstein-Barr virus-encoded RNA was expressed.
247 (HCV) nonstructural protein 5B (NS5B) is the virus-encoded RNA-dependent RNA polymerase (RdRp) essent
248 ation of nearly all RNA viruses depends on a virus-encoded RNA-dependent RNA polymerase (RdRp).
249 ein complexes, on the regulation of VP1, the virus-encoded RNA-dependent RNA polymerase (RdRp).
250 ination occurs via template switching by the virus-encoded RNA-dependent RNA polymerase (RdRP).
251 n the nucleocapsid must be accessible by the virus-encoded RNA-dependent RNA polymerase in order to s
252 perforin, TIA-1, Granzyme B and Epstein-Barr virus-encoded RNA.
253                   Ecological distribution of virus-encoded RPs suggests some level of ecosystem adapt
254 onal assays confirm that the two most common virus-encoded RPs, bS21 and bL12, are incorporated into
255 equence similarity with RuvC, the absence of virus-encoded RuvA and RuvB to interact with, and the di
256 factors that are produced by the activity of virus-encoded serine palmitoyltransferase (SPT).
257 ted by differential substrate specificity of virus-encoded serine palmitoyltransferase, a key enzyme
258 ted herpesvirus (KSHV) lytic infection, many virus-encoded signaling molecules (e.g., viral G protein
259                           Moreover, when the virus encoded SIINFEKL, T cells specific for nonrecombin
260 VX, was not dependent on the presence of the virus-encoded silencing suppressor protein, 25K.
261 ted by rising temperatures but suppressed by virus-encoded silencing suppressors.
262 plication, we recently demonstrated that the virus-encoded single-stranded (ss) DNA-binding protein (
263 d with a multisubunit complex containing the virus-encoded single-stranded DNA-binding protein ICP8.
264  that functioned as binding partners for the virus-encoded Skp1, proteins A682L and A607R.
265  virus (HDV) genome replication requires the virus-encoded small delta protein (deltaAg).
266 ASFV growth, indicating that ASFV utilizes a virus-encoded small RNA to disrupt its own replication.I
267 ovirus-associated (VA) RNAs and Epstein-Barr virus-encoded small RNAs (EBERs) with respect to RNA seq
268 gest a potential role for either cellular or virus-encoded SSB protein in improving the processivity
269 ing to a better understanding of the role of virus-encoded structural proteins not only in KSHV-relat
270 en1 mutant plants and in plants expressing a virus-encoded suppressor of RNA silencing (P1/HC-Pro), w
271  clearance in the absence of expression of a virus-encoded suppressor.
272                                   eHAV lacks virus-encoded surface proteins, and how it enters cells
273  of how early protein interactions involving virus-encoded tegument proteins are critical for virus a
274          Suppression of viral replication by virus-encoded temperance factors represents a novel mech
275                           The genome of this virus encoded the replicative enzymes and the cis-acting
276 acute infection, even after stimulation with virus-encoded TLR7/8 ligand.
277                                          The virus-encoded transactivating HTLV-I tax gene was demons
278 tes by Epstein-Barr virus (EBV) requires the virus-encoded transactivator EBNA2 and the products of b
279 V gene 62, is the major immediate-early (IE) virus-encoded transactivator of viral gene transcription
280  (HTLV-1) gene expression is mediated by the virus-encoded transactivator protein Tax and three imper
281 responsible for localization of at least one virus-encoded transcript, IRS1 mRNA.
282 coding changes in the core components of the virus-encoded transcription and replication apparatus.
283          This sequence element is bound by a virus-encoded transcription and replication factor E2, w
284                     EBNA2 is an Epstein-Barr virus-encoded transcriptional transactivator that mimics
285 irus-transposon vector that stably maintains virus-encoded transgenes in vivo through integration int
286 othelial cell infectivity was dependent on a virus-encoded tropism factor.
287 sform vertebrate cells through the action of virus-encoded tumor antigens that interfere with normal
288                            Thus, EBNA3B is a virus-encoded tumor suppressor whose inactivation promot
289 SV40) large tumor antigen (Tag) represents a virus-encoded tumor-specific antigen expressed in many t
290             This is the first structure of a virus-encoded tumour necrosis factor receptor (TNFR).
291 ntrol of PABP1, Paip2, and EDD1 required the virus-encoded UL38 mTORC1 activator and resulted in augm
292 observations together with the presence of a virus-encoded uracil DNA glycosylase indicates that HSV-
293 -early kinetics, and requires the functional virus-encoded Us3 Ser/Thr protein kinase.
294 annel-forming protein, placing it within the virus-encoded "viroporin" family.
295 ne responses likely drove the evolution of a virus-encoded virulence factor that regulates complement
296 acking MISTRAV or expressing the squirrelpox virus-encoded vMISTRAV exhibit resistance to the same in
297                                 In addition, virus-encoded VP3 antagonizes RNase L activity both in v
298 n of translation initiation factors with the virus-encoded VPg protein covalently linked to the 5' en
299 ate transcription factor (VITF)-1 and -3 are virus-encoded, whereas VITF-2 was partially purified fro
300 e expression interferes with the function of virus-encoded wild-type Vif.

 
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