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1 tures of its genome suggest that it is a new DNA tumor virus.
2  steroid receptor superfamily and the HPV-16 DNA tumor virus.
3 r similar to that of T antigens of the small DNA tumor viruses.
4 or suppressor pathway in a manner similar to DNA tumor viruses.
5 s also targeted by oncoproteins expressed by DNA tumor viruses.
6 effects associated with infections with many DNA tumor viruses.
7 made through the use of GEM models for human DNA tumor viruses.
8 the mechanisms of transformation employed by DNA tumor viruses.
9 apillomaviruses are a family of nonenveloped DNA tumor viruses.
10 ession of transforming proteins derived from DNA tumor viruses.
11 ement in latent replication of these related DNA tumor viruses.
12 equired to mediate transformation induced by DNA tumor viruses.
13 c single-stranded DNA elements and mammalian DNA tumor viruses.
14 plication of mammalian cells and their small DNA tumor viruses.
15  by the transforming oncoproteins of several DNA tumor viruses.
16  to have onco-suppressive properties against DNA tumor viruses.
17 ered in many cancers and is also targeted by DNA tumor viruses.
18 om studies using immediate-early proteins of DNA tumor viruses.
19                      The oncoproteins of the DNA tumor viruses, adenovirus E1A, simian virus 40 T ant
20          While oncoproteins encoded by small DNA tumor viruses and Epstein-Barr virus (EBV) latent an
21 ression is critical for persistence of these DNA tumor viruses and most likely involved in mediating
22 n factors, bind to origins of replication in DNA tumor viruses and stimulate viral DNA replication in
23 teract with the transforming oncoproteins of DNA tumor viruses and this led to rapid advances in our
24 be effective in malignant diseases for which DNA tumor viruses are etiologic agents and that antitumo
25                                    All known DNA tumor viruses are known to target and inactivate two
26                            Oncoproteins from DNA tumor viruses associate with critical cellular prote
27 is a key target of oncoproteins expressed by DNA tumor viruses, but RNA viruses are not known to regu
28  into the host genome, is a critical step in DNA tumor virus carcinogenesis.
29       Human papillomaviruses (HPV) are small DNA tumor viruses causally associated with cervical canc
30                       The study of the small DNA tumor viruses continues to provide valuable new insi
31 xtensively to our understanding of how these DNA tumor viruses directly contribute to human cancers.
32                                         Most DNA tumor viruses disturb the cell cycle pathways by ess
33 ically interact with oncoproteins encoded by DNA tumor viruses (E7, T-Ag, E1A).
34                                        Small DNA tumor viruses encode gene products which can functio
35                            Many of the small DNA tumor viruses encode transforming proteins that func
36                               Viruses of the DNA tumor virus family share the ability to transform ve
37                                    SV40 is a DNA tumor virus found in some studies to be associated a
38                         Evolution of minimal DNA tumor virus' genomes has selected for small viral on
39                                 The study of DNA tumor viruses has been invaluable in uncovering the
40     Human papillomavirus type 16 (HPV-16), a DNA tumor virus, has a causal role in cervical cancer, a
41                The origins of replication of DNA tumor viruses have a highly conserved feature, namel
42                                   Studies of DNA tumor viruses have provided important insights into
43                                              DNA tumor viruses have provided major insights into how
44 sive properties of AAV against adenovirus, a DNA tumor virus, have been well documented.
45 in required for T-cell transformation by the DNA tumor virus herpesvirus saimiri (HVS) and designated
46 in required for T-cell transformation by the DNA tumor virus herpesvirus saimiri (HVS) strain 484, de
47                         Intervention by this DNA tumor virus in cellular translational controls is li
48 dy of the transforming proteins derived from DNA tumor viruses in experimental models of transformati
49  Polyoma virus (Py) differs from other small DNA tumor viruses in not encoding a protein that inactiv
50       Here, we identify the oncogenes of the DNA tumor viruses, including E7 from human papillomaviru
51                              Infections with DNA tumor viruses, including members of the polyomavirus
52  factors, and associate with oncoproteins of DNA tumor viruses, including simian virus 40 (SV40) larg
53 te with the transforming proteins of several DNA tumor viruses, including the large T antigen encoded
54 ctions of transforming proteins from several DNA tumor viruses, including two papillomaviruses and tw
55 The papillomavirus (PV) is a double-stranded DNA tumor virus infecting cervix, mouth, and throat tiss
56 f the best-studied oncoproteins encoded by a DNA tumor virus is adenovirus E1A, which modifies the fu
57 neral theme that has emerged from studies of DNA tumor viruses is that otherwise unrelated oncoprotei
58 i's sarcoma-associated herpesvirus (KSHV), a DNA tumor virus, is an etiological agent linked to sever
59                                          The DNA tumor virus Kaposi's sarcoma associated herpesvirus
60              Infection of cells with SV40, a DNA tumor virus known to abrogate formation of p130- and
61                  Simian virus 40 (SV40) is a DNA tumor virus known to induce cancers in laboratory an
62 ex, a hallmark of cellular transformation by DNA tumor viruses, leads to cell proliferation.
63 y that the oncoproteins encoded by the small-DNA tumor viruses may use this mechanism to induce c-Myc
64                                         Many DNA tumor virus oncogenes are capable of activating and
65 hat shares a subset of the properties of the DNA tumor virus oncoproteins but maintains important dif
66                                              DNA tumor virus oncoproteins reduce Rb function by eithe
67 t can physically interact with two mammalian DNA tumor virus oncoproteins, simian virus 40 large-T an
68                                 Unlike other DNA tumor virus oncoproteins, which possess immortalizin
69 critical for growth regulation interact with DNA tumor virus oncoproteins.
70 1 HR1 and HR3 and short regions of two other DNA tumor virus origin-binding proteins, SV40 T antigen
71                       In cells infected with DNA tumor viruses, p53 is bound to the viral tumor antig
72 TP-binding proteins in transformation by the DNA tumor virus polyomavirus, the GTP-binding activities
73                  Next, we found that SV40, a DNA tumor virus present in approximately 50% of mesothel
74                    The oncoproteins of small DNA tumor viruses promote tumorigenesis by complexing wi
75  is the first report of STAT activation by a DNA tumor virus protein.
76                               The ability of DNA tumor virus proteins to trigger apoptosis in mammali
77                    However, unlike the small DNA tumor virus proteins, individual HCMV IE proteins ta
78 ry cells in which RB has been inactivated by DNA tumor virus proteins.
79                            It is unclear how DNA tumor viruses regulate these enzymes and how these i
80  T Ag, which suggests yet another reason why DNA tumor viruses require actively cycling host cells.
81 therefore postulated that immortalization by DNA tumor viruses results in the induction of PTKs funda
82 is increasing evidence that the transforming DNA tumor virus simian virus 40 (SV40) is associated wit
83        Infection of quiescent cells with the DNA tumor virus simian virus 40 induces expression of th
84 ies with oncoproteins encoded by other small DNA tumor viruses such as adenovirus E1A and SV40 large
85 action can be disrupted by oncoproteins from DNA tumor viruses such as adenovirus E1a that bind p107.
86                            Oncoproteins from DNA tumor viruses such as adenovirus E1a, simian virus 4
87 ed as the binding site for oncoproteins from DNA tumor viruses such as adenovirus E1a.
88                                              DNA tumor viruses such as Kaposi's sarcoma-associated he
89                                        Small DNA tumor viruses such as simian virus 40 (SV40) and pol
90                                              DNA tumor viruses such as simian virus 40 (SV40) express
91             It is widely accepted that small DNA tumor viruses, such as adenovirus, simian virus 40 a
92 s (HCMV) and IE equivalents encoded by small DNA tumor viruses, such as adenovirus.
93                           Although the small DNA tumor virus SV40 (simian virus 40) fails to replicat
94 and KS.IMPORTANCE Here we show that HHV-8, a DNA tumor virus that causes Kaposi's sarcoma, infects th
95 ociated herpesvirus (KSHV) is a lymphotropic DNA tumor virus that induces Kaposi's sarcoma and AIDS-r
96                        Adenovirus is a small DNA tumor virus that is a global human pathogen and key
97           Simian virus 40 (SV40) is a potent DNA tumor virus that is known to induce primary brain ca
98      Human papillomaviruses (HPVs) are small DNA tumor viruses that are the causative agent of warts
99 KSHV) and Epstein-Barr virus (EBV) are human DNA tumor viruses that express nuclear antigens [latency
100  also the binding site for oncoproteins from DNA tumor viruses that inactivate Rb.
101  The human papillomaviruses (HPVS) are small DNA tumor viruses that infect epithelial cells and induc
102                 Thus, like many of the small DNA tumor viruses, the first protein expressed upon HCMV
103                    The mechanism employed by DNA tumor viruses to inhibit p53-dependent transcription
104 terpretation of the p53-Tag complexes and of DNA tumor virus transformation in general.
105 s is also the first demonstration of a human DNA tumor virus upregulating TLR3, a TLR that thus far h
106       In benign lesions induced by the small DNA tumor viruses, viral genomes are typically maintaine
107       The results indicate that unlike other DNA tumor viruses which block apoptosis by inactivation

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