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1 e protein is the primary oncogene product of bovine papillomavirus.
2 nt involving a conserved tyrosine (Y) in the bovine papillomavirus 1 (BPV-1) E2 protein at amino acid
3                                              Bovine papillomavirus 1 (BPV-1) E6 has served as a model
4             Here we have discovered that the bovine papillomavirus 1 (BPV-1) transcription and replic
5 UTRs) of human papillomavirus 16 (HPV16) and bovine papillomavirus 1 (BPV1) contain a negative regula
6                Recent biochemical studies on bovine papillomavirus 1 (BPV1) E1 showed that the AR and
7 f the H+ vacuolar ATPase and cooperates with bovine papillomavirus 1 E5 oncoprotein in cell transform
8                                              Bovine papillomavirus 1 E6 interacts with two similar pr
9 PV16, HPV 18, HPV31, HPV 45, HPV 52, HPV 58, bovine papillomavirus 1, and HPV11 native virions.
10  transformed with the E5 genes of RhPV 1 and bovine papillomavirus 1.
11 ein Brd4 is implicated in the hitchhiking of bovine papillomavirus-1 (BPV-1), and the viral protein E
12 s by which E2 from the related viral strains bovine papillomavirus-1 and human papillomavirus-16 disc
13 n is similar to the crystal structure of the bovine papillomavirus-1 E2 protein when complexed to DNA
14 uch as Fos and Jun (activator protein-1) and bovine papillomavirus-1 E2 protein.
15 or the double-stranded DNA-binding domain of bovine papillomavirus-1 E2 that has a three-dimensional
16 ific for HPV-11, since SIs generated against bovine papillomavirus and HPV-16 VLPs were not generally
17 ene and has features similar to those of the bovine papillomavirus and human papillomavirus E5 genes.
18 ons from electron cryomicroscopy (cryoEM) of bovine papillomavirus at 9 A resolution with coordinates
19                  The E1 and E2 proteins from bovine papillomavirus bind cooperatively to binding site
20                  The E1 and E2 proteins from bovine papillomavirus bind cooperatively to the viral or
21              The 44-amino acid E5 protein of bovine papillomavirus binds to and activates the PDGFbet
22 s of diverse papillomavirus types, including bovine papillomavirus (BPV) and human papillomavirus 16
23      A new electrochemical DNA biosensor for bovine papillomavirus (BPV) detection that was based on
24                                          The bovine papillomavirus (BPV) E2 enhancer protein plays a
25  We previously showed that expression of the bovine papillomavirus (BPV) E2 gene results in a dramati
26                                          The bovine papillomavirus (BPV) E2 protein, when phosphoryla
27 8 E7 gene in these cells is repressed by the bovine papillomavirus (BPV) E2 protein.
28                           Here, we show that bovine papillomavirus (BPV) E2-induced growth arrest of
29    Transformed bovine fibroblasts expressing bovine papillomavirus (BPV) E5 are highly vacuolated and
30           The E2 protein segregates episomal bovine papillomavirus (BPV) genomes to daughter cells by
31                            The E1 protein of bovine papillomavirus (BPV) is a site-specific DNA bindi
32                     In this study, we made a bovine papillomavirus (BPV) L1-HIV-1 gp41 fusion protein
33 localization of structural and nonstructural bovine papillomavirus (BPV) proteins in cultured cells t
34                           DNA replication of bovine papillomavirus (BPV) requires two viral proteins
35        The small transmembrane E5 protein of bovine papillomavirus (BPV) transforms cells by forming
36 expression of a reporter gene, Tn5, within a bovine papillomavirus (BPV) vector.
37 ilize the virion or promote capsid assembly, bovine papillomavirus (BPV) virions were subjected to bu
38 e interaction with E1, we have used chimeric bovine papillomavirus (BPV)/human papillomavirus type 11
39       E1 and T-antigen of the tumour viruses bovine papillomavirus (BPV-1) and Simian virus 40 (SV40)
40 he DNA-binding domain of the E2 protein from bovine papillomavirus (BPV-1).
41     Both human papillomavirus 16 (HPV16) and bovine papillomavirus (BPV1) E7 proteins are capable of
42  only been available for high-risk HPV18 and bovine papillomavirus (BPV1).
43          We have determined the structure of bovine papillomavirus by electron cryomicrosopy (cryoEM)
44 sist in the rapid and efficient detection of bovine papillomavirus DNA and help in the prevention and
45 2 controls the biochemical activities of the bovine papillomavirus E1 and E2 proteins by modifying th
46                                Serine 584 of bovine papillomavirus E1 is in a conserved motif resembl
47                                    Recently, bovine papillomavirus E1 was shown to be post-translatio
48 y other cellular proteins that interact with bovine papillomavirus E1, an HeLa cDNA library was scree
49   Mutations, which impair the sumoylation of bovine papillomavirus E1, prevent normal nuclear accumul
50  peptides derived from the CDK/NLS region of bovine papillomavirus E1.
51 osed of two protein dimers bound to DNA, the bovine papillomavirus E1E2-ori complex.
52                            Expression of the bovine papillomavirus E2 protein in cervical carcinoma c
53                                              Bovine papillomavirus E2 protein is phosphorylated at tw
54                                          The bovine papillomavirus E2 protein maintains and segregate
55 elicase ChlR1 is required for loading of the bovine papillomavirus E2 protein onto chromatin during D
56                                          The bovine papillomavirus E2 protein tethers the viral genom
57      To address these questions, we used the bovine papillomavirus E2 protein to repress the expressi
58 rd4 as the mitotic chromosome anchor for the bovine papillomavirus E2 protein, which tethers the vira
59  with a recombinant virus that expresses the bovine papillomavirus E2 protein.
60 hift analyses demonstrate that human but not bovine papillomavirus E2 proteins recognize this sequenc
61                                          The bovine papillomavirus E2 proteins regulate viral transcr
62                            Expression of the bovine papillomavirus E2 regulatory protein in human cer
63       The major phosphorylation sites of the bovine papillomavirus E2 transactivator protein are two
64 gene in HeLa cervical carcinoma cells by the bovine papillomavirus E2 transcription factor activates
65  a major cellular interacting partner of the bovine papillomavirus E2.
66              Here we show that expression of bovine papillomavirus E5 causes the retention of MHC I i
67                                          The bovine papillomavirus E5 gene encodes a 44-amino-acid, h
68 ze to cellular endomembranes, cooperate with bovine papillomavirus E5 in transformation, as well as b
69                                          The bovine papillomavirus E5 protein (BPV E5) is a 44-amino-
70                                          The bovine papillomavirus E5 protein activates the cellular
71 omodimers of the transmembrane 44-amino acid bovine papillomavirus E5 protein bind the transmembrane
72                                          The bovine papillomavirus E5 protein binds to the cellular p
73                                          The bovine papillomavirus E5 protein forms a stable complex
74                                          The bovine papillomavirus E5 protein forms a stable complex
75                                          The bovine papillomavirus E5 protein is a 44-aa transmembran
76                                          The bovine papillomavirus E5 protein is a 44-amino-acid tran
77                                          The bovine papillomavirus E5 protein is a dimeric, 44-amino
78                                          The bovine papillomavirus E5 protein is a small, homodimeric
79                                          The bovine papillomavirus E5 protein, a 44-amino acid homodi
80                                    The 44-aa bovine papillomavirus E5 protein, which binds to the TM
81                          The E1 protein from bovine papillomavirus has site-specific DNA binding acti
82 us VLPS: Exposure to fully assembled VLPs of bovine papillomavirus, human papillomavirus (HPV)16 or H
83 ein E1 binds to the origin of replication of bovine papillomavirus in several forms.
84 sed electrochemical signal corresponded to a bovine papillomavirus infection.
85                            The E5 protein of bovine papillomavirus is a 44-amino acid, Golgi-resident
86              The 44-amino-acid E5 protein of bovine papillomavirus is a dimeric transmembrane protein
87                The oncogenic E5 protein from bovine papillomavirus is a short (44 amino acids long) i
88         The dimeric 44-residue E5 protein of bovine papillomavirus is the smallest known naturally oc
89                              Coexpression of bovine papillomavirus L1 with L2 mutants lacking either
90 din that, when conjugated at high density to bovine papillomavirus major capsid protein L1 VLPs, indu
91                                          The bovine papillomavirus protein E2 serves dual functions i
92                                          The bovine papillomavirus replication initiator protein E1 i
93 ic resolution structures of complexes of the bovine papillomavirus strain 1 (BPV-1) E2 protein and DN
94 man papillomavirus strain 16 (HPV-16) E2 and bovine papillomavirus strain 1 (BPV-1) E2 to discriminat
95 he DNA-binding domain of the E2 protein from bovine papillomavirus strain 1 and its complex with DNA
96      The transmembrane E5 protein encoded by bovine papillomavirus transforms cells by activating the
97     We have found that the E6 oncoprotein of Bovine Papillomavirus Type 1 (BE6) as well as the E6 pro
98  mutants that prevent phosphorylation of the bovine papillomavirus type 1 (BPV) E2 protein are transf
99  transcription factors was examined by using bovine papillomavirus type 1 (BPV).
100 milar to previously determined structures of bovine papillomavirus type 1 (BPV-1) and human papilloma
101               The full-length product of the bovine papillomavirus type 1 (BPV-1) E1 translational op
102 nimal DNA-binding and dimerization domain of bovine papillomavirus type 1 (BPV-1) E2 alone or this bi
103                                              Bovine papillomavirus type 1 (BPV-1) E2 binds cellular c
104                                 For example, bovine papillomavirus type 1 (BPV-1) E2 binds to all chr
105              We have recently shown that the bovine papillomavirus type 1 (BPV-1) E6 and E7 genes ind
106 6 oncoproteins of cutaneous papillomaviruses Bovine Papillomavirus Type 1 (BPV-1) E6 and human papill
107                                          The bovine papillomavirus type 1 (BPV-1) E6 oncoprotein can
108                                          The bovine papillomavirus type 1 (BPV-1) E7 does not bind pR
109 ted bovine fibropapillomas were examined for bovine papillomavirus type 1 (BPV-1) E7 localization.
110                                          The bovine papillomavirus type 1 (BPV-1) E7 oncoprotein is r
111                                          The bovine papillomavirus type 1 (BPV-1) exonic splicing sup
112 an important mechanism for the regulation of bovine papillomavirus type 1 (BPV-1) gene expression dur
113 an important mechanism for the regulation of bovine papillomavirus type 1 (BPV-1) gene expression dur
114 ing plays an important role in regulation of bovine papillomavirus type 1 (BPV-1) gene expression.
115       While murine C127 cells containing the bovine papillomavirus type 1 (BPV-1) genome were reporte
116                        The E6 oncoprotein of bovine papillomavirus type 1 (BPV-1) has been shown to t
117                                              Bovine papillomavirus type 1 (BPV-1) induces fibropapill
118                                              Bovine papillomavirus type 1 (BPV-1) is a small DNA viru
119                           The E6 gene of the bovine papillomavirus type 1 (BPV-1) is expressed in fib
120                        The E7 oncoprotein of bovine papillomavirus type 1 (BPV-1) is required for the
121                                              Bovine papillomavirus type 1 (BPV-1) late gene expressio
122                                              Bovine papillomavirus type 1 (BPV-1) late pre-mRNAs are
123 ich SE4 element regulates the selection of a bovine papillomavirus type 1 (BPV-1) late-specific splic
124                                              Bovine papillomavirus type 1 (BPV-1) requires viral prot
125                                 Furthermore, bovine papillomavirus type 1 (BPV-1) transformation was
126  a model for high-risk type genital HPV, and bovine papillomavirus type 1 (BPV-1), a papillomavirus k
127                                           In bovine papillomavirus type 1 (BPV-1), a switch in 3' spl
128 he best-characterized E2 protein, encoded by bovine papillomavirus type 1 (BPV-1), has been shown to
129 elix is significantly different from that of bovine papillomavirus type 1 (BPV-1).
130 teins encoded by HPV-16, HPV-18, HPV-11, and bovine papillomavirus type 1 (BPV-1).
131                            Complexes between bovine papillomavirus type 1 (BPV1) and examples of two
132                                        Using bovine papillomavirus type 1 (BPV1) and human papillomav
133 iologic agent of cervical carcinoma, whereas bovine papillomavirus type 1 (BPV1) causes benign fibrop
134     In addition to viral proteins E1 and E2, bovine papillomavirus type 1 (BPV1) depends heavily on h
135            Here, we show that, surprisingly, bovine papillomavirus type 1 (BPV1) E2 but not RNA inter
136 ly demonstrated that acute expression of the bovine papillomavirus type 1 (BPV1) E2 protein in HeLa a
137 ells, we fused the DNA binding domain of the bovine papillomavirus type 1 (BPV1) E2 protein to the ca
138  structurally more similar to the HPV 18 and bovine papillomavirus type 1 (BPV1) E2 proteins than it
139    Tax1BP1 also interacts with the HPV16 and bovine papillomavirus type 1 (BPV1) E2 proteins, with th
140                    A structural model of the bovine papillomavirus type 1 (BPV1) E2 transactivation d
141                                              Bovine papillomavirus type 1 (BPV1) entry into cells has
142 E-1 cells harboring autonomously replicating bovine papillomavirus type 1 (BPV1) genomes were infecte
143 syntaxin 18 as a protein that interacts with bovine papillomavirus type 1 (BPV1) L2.
144 that syntaxin 18 colocalizes with infectious bovine papillomavirus type 1 (BPV1) pseudovirions during
145 psidate viral genome and generate infectious bovine papillomavirus type 1 (BPV1) upon coexpression of
146 ues 1 to 88 or 11 to 200 derived from HPV16, bovine papillomavirus type 1 (BPV1), or cottontail rabbi
147 ng mechanism has been best characterized for bovine papillomavirus type 1 (BPV1), where the E2 protei
148 of the nuclear import of the E1 protein from bovine papillomavirus type 1 (BPV1).
149                                 We show that bovine papillomavirus type 1 and beta-HPV E6 repress Not
150                                              Bovine papillomavirus type 1 and HPV6b, -11, -16, -18, a
151 6 proteins of the beta-genus HPVs and of the bovine papillomavirus type 1 associated with cutaneous f
152 ell spreading, while E6 genes from HPV-11 or bovine papillomavirus type 1 did not.
153                               Replication of bovine papillomavirus type 1 DNA absolutely requires the
154 e absence of E2, is sufficient for low-level bovine papillomavirus type 1 DNA replication in C-33A ce
155 rthermore, SV40 Tag was able to compete with bovine papillomavirus type 1 E1 for binding to RPA.
156                                          The bovine papillomavirus type 1 E1 protein is important for
157 stablished that it participates in tethering bovine papillomavirus type 1 E2 and viral genomes to hos
158                                              Bovine papillomavirus type 1 E2 binds to chromosomes in
159 ces between the activation properties of the bovine papillomavirus type 1 E2 protein and those of eit
160                 The N-terminal domain of the bovine papillomavirus type 1 E2 protein is important for
161           The transactivation domain (AD) of bovine papillomavirus type 1 E2 stimulates gene expressi
162                                          The bovine papillomavirus type 1 E2 transactivator protein i
163                                          The bovine papillomavirus type 1 E6 (BE6) binds to LXXLL pep
164                                              Bovine papillomavirus type 1 E6 (BE6) interacts with thr
165                 We have generated mutants of bovine papillomavirus type 1 E6 (BE6) that are defective
166                               The E2 gene of bovine papillomavirus type 1 encodes at least three nucl
167                                              Bovine papillomavirus type 1 encodes two proteins requir
168 re generated in the background of the entire bovine papillomavirus type 1 genome.
169                           We have found that bovine papillomavirus type 1 genomes are also associated
170                        Specifically, JCV and bovine papillomavirus type 1 have been shown to enter ce
171                        The E5 oncoprotein of bovine papillomavirus type 1 is a 44-amino-acid, hydroph
172                        The E5 oncoprotein of bovine papillomavirus type 1 is a Golgi-resident, 44-ami
173                        The E5 oncoprotein of bovine papillomavirus type 1 is a Golgi-resident, hydrop
174                            The E2 protein of bovine papillomavirus type 1 is tethered to the mitotic
175 nding target through which the E2 protein of bovine papillomavirus type 1 links the viral genome to m
176 d trimeric L1 species, whereas the capsid of bovine papillomavirus type 1 matures into more extensive
177      Here we demonstrate that melting of the bovine papillomavirus type 1 ori is a sequence-dependent
178                                              Bovine papillomavirus type 1 replication was previously
179        The small transmembrane E5 protein of bovine papillomavirus type 1 transforms cells by a uniqu
180 gene expression of the E6 promoter of BPV-1 (bovine papillomavirus type 1) and HPV types 16 and 18.
181 V), cottontail rabbit papillomavirus (CRPV), bovine papillomavirus type 1, and human papillomavirus t
182 nd HPV-18, wart-causing low risk HPV-11, and bovine papillomavirus type 1, in part through enhancing
183 -interacting protein and, in the case of the bovine papillomavirus type 1, serves to tether E2 and th
184 ts counterpart from the related viral strain bovine papillomavirus type 1, the precise placement of t
185 conserved among E1 proteins of many HPVs and bovine papillomavirus type 1.
186 ion is conserved in HPV-11, -16, and -18 and bovine papillomavirus type 4 (BPV-4) E2 and is also requ
187                            The expression of bovine papillomavirus type 4 (BPV-4) E7 overcame this ar
188                            The E1 protein of bovine papillomavirus type-1 is the viral replication in
189                                           In bovine papillomavirus type-1, DNA replication begins whe
190                                              Bovine papillomavirus, type 1 (BPV-1), E1, and E2 bind c
191 es were recently hypothesized to be sites of bovine papillomavirus virion assembly, our observation s
192 transcription after infection with authentic bovine papillomavirus virions was similarly elevated in
193 orporated into an immunodominant site of the bovine papillomavirus virus L1 coat protein, which self-
194 ) effectively bound and rapidly internalized bovine papillomavirus VLPS: Exposure to fully assembled
195                               L2 of HPV16 or bovine papillomavirus was shown to bind to a 43-kDa cell
196 he crystal structure of the E1 helicase from bovine papillomavirus, where asymmetric assembly is for
197 n four viral oncoproteins: the E5 protein of bovine papillomavirus, which activates the platelet-deri

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