Titlebook: Hepadnaviruses; Molecular Biology an William S. Mason,Christoph Seeger Book 1991 The Editor(s) (if applicable) and The Author(s), under exc

mandatory

书目名称Hepadnaviruses影响因子(影响力)




书目名称Hepadnaviruses影响因子(影响力)学科排名




书目名称Hepadnaviruses网络公开度




书目名称Hepadnaviruses网络公开度学科排名




书目名称Hepadnaviruses被引频次




书目名称Hepadnaviruses被引频次学科排名




书目名称Hepadnaviruses年度引用




书目名称Hepadnaviruses年度引用学科排名




书目名称Hepadnaviruses读者反馈




书目名称Hepadnaviruses读者反馈学科排名

军火

grenade

使饥饿

Assembly of Hepadnaviral Virions and Subviral Particles,ding large numbers of noninfections subviral particles as well as complete virions. Although this unusual property was among the first aspects of the viral life cycle to be discovered, it remains one of its least well understood aspects. Why do infected cells produce subviral particles? What factors

侵略主义

Analysis of Hepadnavirus Gene Expression, Biology, and Pathogenesis in the Transgenic Mouse,ion the virus replicates episomally within infected cells. In chronic infection the virus may also integrate into the host cell genome. In HBV-induced hepatocellular carcinoma, integrated viral DNA sequences are virtually always present, and the viral and flanking cellular sequences may be rearrange

ELUDE

思考才皱眉

Human Hepatitis Delta Virus,s been recently reviewed (B. et al. 1990; H. 1989; T. 1990a, b). The present chapter will emphasize those areas in which our perspective has recently changed and those questions about HDV which are (almost) accessible to laboratory research.

枯燥

Development of Antiviral Therapy for Chronic Infection with Hepatitis B Virus,isting chronic carriers there is no effective treatment to clear the virus and thus limit the high risk of liver diseases associated with long-term infection; chronic hepatitis, cirrhosis, and hepatocellular carcinoma. A number of recent reviews have described the limited success of current antivira

Mucosa

Inherited Hepatic Enzyme Defects as Candidates for Liver-Directed Gene Therapy,developmental disability. For these defects, serious consideration must be given to any new treatment that offers the possibility of altering the extremely poor prognosis. In the desparate clinical setting of these single gene defects, two forms of therapy have recently been considered—hepatic trans

摘要

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