ライフサイエンスコーパス: woodchuck hepatitis virus

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 We found that woodchuck hepatitis virus capsid protein undergoes struc

11 recancerous lesions observed in the liver of woodchuck hepatitis virus carrier woodchucks, and these

12 Analysis of several HBV/woodchuck hepatitis virus chimeras corroborated the find

13 ks (Marmota monax) chronically infected with woodchuck hepatitis virus contained at least 100,000 clo

14 replication, and intrahepatic expression of woodchuck hepatitis virus core antigen (WHcAg) in a dose

15 nsgene expression compared to a conventional woodchuck hepatitis virus element (WPRE).

16 that in the livers chronically infected with woodchuck hepatitis virus, (i) hepadnavirus superinfecti

17 tory acting RNA element (WPRE), derived from woodchuck hepatitis virus in combination with an antibod

18 gulation was similarly observed during acute woodchuck hepatitis virus infection.

19 of hepatocellular carcinoma in woodchucks by woodchuck hepatitis virus is associated with the activat

20 A related element from woodchuck hepatitis virus is known as the woodchuck post

21 ciated virus-mouse phenylalanine hydroxylase-woodchuck hepatitis virus post-transcriptional response

22 th 4 erythroid enhancers with or without the woodchuck hepatitis virus postregulatory element (WPRE)

23 The woodchuck hepatitis virus posttranscriptional regulatory

24 on than its sc counterpart, which lacked the woodchuck hepatitis virus posttranscriptional regulatory

25 in nonhepatoma cells are not able to support woodchuck hepatitis virus replication.

26 oodchuck hepatitis virus and vaccinated with woodchuck hepatitis virus surface antigen could be induc

27 ed when woodchucks chronically infected with woodchuck hepatitis virus were treated with L-FMAU [1-(2

28 The cis-acting element found in the woodchuck hepatitis virus (WHV) (the WHV posttranscripti

29 t were chronically infected with HBV-related woodchuck hepatitis virus (WHV) and already developed HC

30 but not other animal hepadnaviruses, such as woodchuck hepatitis virus (WHV) and duck hepatitis B vir

31 The woodchuck hepatitis virus (WHV) and its natural host, th

32 The woodchuck hepatitis virus (WHV) and its natural host, th

33 (HCC) associated with chronic infection with woodchuck hepatitis virus (WHV) and serve as a model of

34 g woodchuck hepatocytes were infectable with woodchuck hepatitis virus (WHV) and showed WHV replicati

35 demonstrated that the X-deficient mutants of woodchuck hepatitis virus (WHV) are not completely repli

36 When woodchucks chronically infected with woodchuck hepatitis virus (WHV) are superinfected with H

37 chucks were infected experimentally with the woodchuck hepatitis virus (WHV) at 3 days of age.

38 an initial experiment, groups of six chronic woodchuck hepatitis virus (WHV) carrier woodchucks recei

39 Woodchucks infected at birth with woodchuck hepatitis virus (WHV) cleared viremia and deve

40 rs from woodchucks chronically infected with woodchuck hepatitis virus (WHV) contained covalently clo

41 A small region in the capsid protein of woodchuck hepatitis virus (WHV) contains four hydrophobi

42 from hepatitis B virus (HBV) and the related woodchuck hepatitis virus (WHV) determined by cryo-elect

43 Integrations of woodchuck hepatitis virus (WHV) DNA and rearrangements o

44 WH44KA cells contain a single woodchuck hepatitis virus (WHV) DNA integration in the 3

45 We have recently described HBV and woodchuck hepatitis virus (WHV) dominant negative (DN) c

46 Woodchuck hepatitis virus (WHV) efficiently induces hepa

47 of woodchucks chronically infected with the woodchuck hepatitis virus (WHV) elicited differential T-

48 Woodchuck hepatitis virus (WHV) enhancer II (EnII) is lo

49 hucks that were experimentally infected with woodchuck hepatitis virus (WHV) for 4 weeks by intraperi

50 201 to 205 of the pre-S envelope protein of woodchuck hepatitis virus (WHV) form a conserved amino a

51 cil) to woodchucks chronically infected with woodchuck hepatitis virus (WHV) induces a transient decl

52 es of neonatal woodchucks with self-limiting woodchuck hepatitis virus (WHV) infection to those woodc

53 xamined and compared with other markers of a woodchuck hepatitis virus (WHV) infection using rabbit a

54 Liver tissue from woodchucks with chronic woodchuck hepatitis virus (WHV) infection was assayed fo

55 self-limited (resolved) and chronic neonatal woodchuck hepatitis virus (WHV) infection.

56 -mediated immunity (vCMI) following neonatal woodchuck hepatitis virus (WHV) infection.

57 ions of these cytokines during the course of woodchuck hepatitis virus (WHV) infection.

58 ocyte turnover during clearance of transient woodchuck hepatitis virus (WHV) infections.

59 Accordingly, several woodchuck hepatitis virus (WHV) inocula were characteriz

60 Woodchuck hepatitis virus (WHV) is prone to aberrant ass

61 Here, we found that the woodchuck hepatitis virus (WHV) precore/core gene produc

62 Woodchucks (Marmota monax) infected with the woodchuck hepatitis virus (WHV) represent the best anima

63 rth American woodchucks (Marmota monax) with woodchuck hepatitis virus (WHV) represents the most valu

64 ks, and then the immunogenicity of an analog woodchuck hepatitis virus (WHV) surface antigen (WHsAg)

65 red by testing the ability of the virions of woodchuck hepatitis virus (WHV) to induce productive acu

66 reared woodchucks chronically infected with woodchuck hepatitis virus (WHV) were treated with N-nony

67 Woodchucks chronically infected with the woodchuck hepatitis virus (WHV) were treated with the an

68 The woodchuck hepatitis virus (WHV) X gene (WHx) is required

69 In this study, we generated a series of woodchuck hepatitis virus (WHV) X mutants, including mut

70 ubcellular distribution and the stability of woodchuck hepatitis virus (WHV) X protein (WHx) in prima

71 Woodchuck hepatitis virus (WHV), a close relative of hum

72 9688 in woodchucks chronically infected with woodchuck hepatitis virus (WHV), a hepadnavirus closely

73 k (Marmota monax) is naturally infected with woodchuck hepatitis virus (WHV), a hepadnavirus closely

74 nfection in an estimated 240 million people; woodchuck hepatitis virus (WHV), an HBV homologue, has b

75 nfected with a closely related hepadnavirus, woodchuck hepatitis virus (WHV), serve as a model for HB

76 Using woodchucks chronically infected with woodchuck hepatitis virus (WHV), we investigated the con

77 We find that the closely related woodchuck hepatitis virus (WHV), which has been shown to

78 cal biopsies of the liver were obtained from woodchuck hepatitis virus (WHV)-infected neonatal woodch

79 er tumors from X/c-myc bitransgenic mice and woodchuck hepatitis virus (WHV)-infected woodchucks.

80 was not demonstrated for HBV or HBV-related woodchuck hepatitis virus (WHV).

81 chuck ( Marmota monax ) harbors a DNA virus (Woodchuck hepatitis virus [WHV]) that is similar in stru

82 -transcriptional regulatory element from the woodchuck hepatitis virus (WPRE).

83 Cotranslation of woodchuck p53 with woodchuck hepatitis virus X antigen, followed by immunop

84 Expression of the woodchuck hepatitis virus X gene in alpha ML cells does

85 The expression and localization of the woodchuck hepatitis virus X-antigen (WHxAg) was examined