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1 an parvovirus B19, Chlamydia trachomatis, or human papillomavirus type 16.
2 ing CTL, Th cell, and B cell epitopes of the human papillomavirus type 16.
3 chose cervical carcinoma cells positive for human papillomavirus type 16.
4 of human papillomavirus type 16 and 18, and human papillomavirus type 16, 18, 6, and 11 virus-like p
5 udy using a prototype, lateral-flow test for human papillomavirus type 16, 18, and/or 45 (HPV16/18/45
6 together with DNA encoding the E7 protein of human papillomavirus type 16, a model cervical cancer an
7 with invasive cancers infected by high-risk human papillomavirus type 16 and 18 (rs9296925, P = 0.01
8 effective prophylactic vaccines composed of human papillomavirus type 16 and 18, and human papilloma
10 in HIV-infected women suggest that although human papillomavirus types 16 and 18 dominate, multiple
12 ogous promoters, including those of c-H-ras, human papillomavirus types 16 and 18, and HIV type 1.
14 sing bovine papillomavirus type 1 (BPV1) and human papillomavirus type 16 as model papillomaviruses,
15 hown previously that the E7 oncoprotein from human papillomavirus type 16, dependent upon its binding
17 atinocytes immortalized by transfection with human papillomavirus type-16 Dna became tumorigenic afte
18 d screen for proteins that interact with the human papillomavirus type 16 E1 replication protein.
19 alanine-scanning substitution mutants of the human papillomavirus type 16 E2 N-terminal transactivati
21 pulated A549 cells by transfecting them with human papillomavirus type 16 E6 (designated A549-E6) to
23 ry-HPV16E6/E7 transgenic mice expressing the human papillomavirus type 16 E6 and E7 oncogenes (HPV-16
26 to interactions of other DNA virus proteins (human papillomavirus type 16 E6 and E7, simian virus 40
27 ry and sufficient for complex formation with human papillomavirus type 16 E6 has been mapped to a 25-
30 hich p53 was eliminated by transduction with human papillomavirus type 16 E6 showed that treatment wi
32 on in diploid human fibroblasts that express human papillomavirus type 16 E6, which inactivates p53.
33 , following retroviral transduction with the human papillomavirus type 16 E6/E7 oncogenes, are altere
36 ression by retroviral-mediated expression of human papillomavirus type-16 E6 protein (HPV-16 E6) in h
37 sage HMEC (prior to M0) were transduced with human papillomavirus type-16 E6, E7, or E6/E7 by using r
38 cted to cell-bound protein and unaffected by human papillomavirus type 16/E6E7 immortalization and pr
40 omes from the observation that expression of human papillomavirus type 16 E7 alleviates the M0 prolif
44 NA vaccine containing an HLA-A2.1-restricted human papillomavirus type 16 E7 epitope (amino acid resi
45 polycomb-mediated epigenetic methylations in human papillomavirus type 16 E7 expressing cells, and in
46 encoding SPI-6 with DNA constructs encoding human papillomavirus type 16 E7 linked to these intracel
47 l human diploid fibroblasts that express the human papillomavirus type 16 E7 oncoprotein have a decre
49 e defective in binding to adenovirus E1A and human papillomavirus type 16 E7 protein but exhibit wild
51 biologically relevant, we tested whether the human papillomavirus type 16 E7 protein, which inactivat
52 he coadministration of DNA vaccines encoding human papillomavirus type 16 E7 with siRNA targeting key
53 ated a novel fusion of VP22 with a model Ag, human papillomavirus type 16 E7, in a DNA vaccine that g
54 l fusion of VP22 with a model tumor antigen, human papillomavirus type 16 E7, in a Sindbis virus RNA
55 xin A (ETA(dII)) with a model tumor antigen, human papillomavirus type 16 E7, in the context of a DNA
56 cells, but this function can be replaced by human papillomavirus type 16 E7, which targets pRb for d
57 ne into one with significant potency against human papillomavirus type 16 E7-expressing murine tumors
64 Essential to the oncogenic properties of human papillomavirus type 16 (HPV-16) are the activities
65 here that the E6 protein from the oncogenic human papillomavirus type 16 (HPV-16) binds to three reg
66 ism by which the E6 and E7 oncoproteins from human papillomavirus type 16 (HPV-16) can be translated
69 rved glutamic acid residue at position 39 of human papillomavirus type 16 (HPV-16) E2 to alanine (E39
79 of human skin fibroblasts by expressing the human papillomavirus type 16 (HPV-16) E6 oncoprotein to
82 live vector, we show that the expression of human papillomavirus type 16 (HPV-16) E7 fused to a nonh
86 trosomal marker, with a model tumor antigen, human papillomavirus type 16 (HPV-16) E7, in a DNA vacci
91 tionship between serum antibody response and human papillomavirus type 16 (HPV-16) infection, a cohor
96 high-risk cervical cancer-associated strain human papillomavirus type 16 (HPV-16) is described here.
101 on would occur in human cells transformed by human papillomavirus type 16 (HPV-16) oncoproteins.
106 ompared for their capacities to detect mixed human papillomavirus type 16 (HPV-16) variant infections
107 rological assays for measuring antibodies to human papillomavirus type 16 (HPV-16) virus-like particl
108 sensitive luminescence immunoassay (LIA) for human papillomavirus type 16 (HPV-16) was developed and
110 ignal, we found that the E7 oncoprotein from human papillomavirus type 16 (HPV-16), the etiological a
112 tiveness of prophylactic vaccination against human papillomavirus types 16 (HPV-16) and 18 (HPV-18) i
113 teins from high-risk human papillomaviruses (human papillomavirus type 16 [HPV-16] and HPV-18) are mu
114 ractions between the L2 protein of high-risk human papillomavirus type 16 (HPV16) and nuclear import
117 blished a cell-free in vitro system to study human papillomavirus type 16 (HPV16) assembly, a poorly
119 inocytes (HKc) immortalized with full-length human papillomavirus type 16 (HPV16) DNA (HKc/HPV16), bu
121 tro binding assays to map the domains of the human papillomavirus type 16 (HPV16) E1 and E2 proteins
126 (E6-targeted protein 1) as a novel high-risk human papillomavirus type 16 (HPV16) E6-binding protein.
129 e (hTERT) in keratinocytes can be induced by human papillomavirus type 16 (HPV16) E6/E6AP ubiquitin l
135 e simian virus 40 (SV40) large T antigen and human papillomavirus type 16 (HPV16) E7 protein also bin
136 r to identify cellular factors that regulate human papillomavirus type 16 (HPV16) gene expression, ce
137 In this study, we map the elements in the human papillomavirus type 16 (HPV16) genome that can sub
138 xperiments investigating the capacity of the human papillomavirus type 16 (HPV16) genome to replicate
159 ents infection of the mouse genital tract by human papillomavirus type 16 (HPV16) pseudovirions.
160 o examine the rate of and risks for cervical human papillomavirus type 16 (HPV16) redetection in wome
161 0, H16.U4, and H16.V5, neutralize pseudotype human papillomavirus type 16 (HPV16) virions in vitro.
163 primary causative agent of cervical cancer, human papillomavirus type 16 (HPV16), must first cross t
165 ortal 184A1 HMEC line to the viral oncogenes human papillomavirus type 16 (HPV16)-E6, -E7, or SV40T,
169 DEK message and protein levels in senescing human papillomavirus type 16- (HPV16-) and HPV18-positiv
170 n repair (NER) capacity of normal (NHOK) and human papillomavirus type-16 immortalized oral keratinoc
171 e epidermal growth factor receptor (EGFR) in human papillomavirus type 16-immortalized human keratino
172 CIN II/III among American Indian women were human papillomavirus type 16 infection (adjusted odds ra
175 ructure of small virus-like particles of the human papillomavirus type 16 L1 protein to generate an a
177 tes of a single papillomavirus type (such as human papillomavirus type 16) may contribute to a collec
178 corneal endothelial cells, transformed with human papillomavirus type 16 oncogenes E6 and E7, showed
183 ciation between serum antibodies against the human papillomavirus type 16 protein E6 and anal cancer
186 c E2F expression or Rb inactivation by E7 of human papillomavirus type 16 signals apoptosis by induci
187 We report the isolation and propagation of human papillomavirus type 16, the main agent of cervical
189 for optimal Ab responses to a model vaccine, human papillomavirus type 16 virus-like particles (HPV 1
190 use with transgenes for the highly oncogenic human papillomavirus type 16, we asked whether a diet hi
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