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1 ted with HBV and of woodchucks infected with woodchuck hepatitis virus.
2 woodchuck that was chronically infected with woodchuck hepatitis virus.
3 h includes human Hepatitis B virus (HBV) and Woodchuck hepatitis virus.
4 cacy in woodchucks chronically infected with woodchuck hepatitis virus.
5 et-like region in the mammalian hepadnavirus woodchuck hepatitis virus.
6 e cultures following in vitro infection with woodchuck hepatitis virus and treatment with inhibitors
7 ed from woodchucks chronically infected with woodchuck hepatitis virus and vaccinated with woodchuck
8 ), two hepadnaviruses (hepatitis B virus and woodchuck hepatitis virus), and an intron-retaining tran
9 ree woodchucks chronically infected with the woodchuck hepatitis virus before and during 30 weeks of
10 recancerous lesions observed in the liver of woodchuck hepatitis virus carrier woodchucks, and these
12 ks (Marmota monax) chronically infected with woodchuck hepatitis virus contained at least 100,000 clo
13 replication, and intrahepatic expression of woodchuck hepatitis virus core antigen (WHcAg) in a dose
14 that in the livers chronically infected with woodchuck hepatitis virus, (i) hepadnavirus superinfecti
15 tory acting RNA element (WPRE), derived from woodchuck hepatitis virus in combination with an antibod
17 of hepatocellular carcinoma in woodchucks by woodchuck hepatitis virus is associated with the activat
19 ciated virus-mouse phenylalanine hydroxylase-woodchuck hepatitis virus post-transcriptional response
20 th 4 erythroid enhancers with or without the woodchuck hepatitis virus postregulatory element (WPRE)
22 on than its sc counterpart, which lacked the woodchuck hepatitis virus posttranscriptional regulatory
24 oodchuck hepatitis virus and vaccinated with woodchuck hepatitis virus surface antigen could be induc
25 ed when woodchucks chronically infected with woodchuck hepatitis virus were treated with L-FMAU [1-(2
27 t were chronically infected with HBV-related woodchuck hepatitis virus (WHV) and already developed HC
28 but not other animal hepadnaviruses, such as woodchuck hepatitis virus (WHV) and duck hepatitis B vir
31 (HCC) associated with chronic infection with woodchuck hepatitis virus (WHV) and serve as a model of
32 g woodchuck hepatocytes were infectable with woodchuck hepatitis virus (WHV) and showed WHV replicati
33 demonstrated that the X-deficient mutants of woodchuck hepatitis virus (WHV) are not completely repli
34 When woodchucks chronically infected with woodchuck hepatitis virus (WHV) are superinfected with H
36 an initial experiment, groups of six chronic woodchuck hepatitis virus (WHV) carrier woodchucks recei
38 rs from woodchucks chronically infected with woodchuck hepatitis virus (WHV) contained covalently clo
44 of woodchucks chronically infected with the woodchuck hepatitis virus (WHV) elicited differential T-
46 hucks that were experimentally infected with woodchuck hepatitis virus (WHV) for 4 weeks by intraperi
47 201 to 205 of the pre-S envelope protein of woodchuck hepatitis virus (WHV) form a conserved amino a
48 cil) to woodchucks chronically infected with woodchuck hepatitis virus (WHV) induces a transient decl
49 es of neonatal woodchucks with self-limiting woodchuck hepatitis virus (WHV) infection to those woodc
50 xamined and compared with other markers of a woodchuck hepatitis virus (WHV) infection using rabbit a
51 Liver tissue from woodchucks with chronic woodchuck hepatitis virus (WHV) infection was assayed fo
58 Woodchucks (Marmota monax) infected with the woodchuck hepatitis virus (WHV) represent the best anima
59 ks, and then the immunogenicity of an analog woodchuck hepatitis virus (WHV) surface antigen (WHsAg)
60 red by testing the ability of the virions of woodchuck hepatitis virus (WHV) to induce productive acu
61 reared woodchucks chronically infected with woodchuck hepatitis virus (WHV) were treated with N-nony
62 Woodchucks chronically infected with the woodchuck hepatitis virus (WHV) were treated with the an
65 ubcellular distribution and the stability of woodchuck hepatitis virus (WHV) X protein (WHx) in prima
67 k (Marmota monax) is naturally infected with woodchuck hepatitis virus (WHV), a hepadnavirus closely
68 nfected with a closely related hepadnavirus, woodchuck hepatitis virus (WHV), serve as a model for HB
69 Using woodchucks chronically infected with woodchuck hepatitis virus (WHV), we investigated the con
71 cal biopsies of the liver were obtained from woodchuck hepatitis virus (WHV)-infected neonatal woodch
72 er tumors from X/c-myc bitransgenic mice and woodchuck hepatitis virus (WHV)-infected woodchucks.
74 chuck ( Marmota monax ) harbors a DNA virus (Woodchuck hepatitis virus [WHV]) that is similar in stru
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