Mark A. Feitelson's Hepatitis C Virus: From Laboratory to Clinic (Biomedical PDF

By Mark A. Feitelson

ISBN-10: 0511041322

ISBN-13: 9780511041327

ISBN-10: 0521799597

ISBN-13: 9780521799591

This multidisciplinary review covers easy innovations with regards to the invention of the Hepatitis C virus, improvement of serological and nucleic acid checks to become aware of an infection, the constitution of the virus genome, new release of virus gene items, and proposed replication scheme. the amount discusses the epidemiology, transmission, pathogenesis of an infection, the advance of hepatocellular carcinoma linked to continual virus an infection, and present suggestions for therapy. It additionally discusses advances in telephone tradition platforms, animal versions of an infection, and rising remedies and vaccine improvement.

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Hepatitis C Virus: From Laboratory to Clinic (Biomedical by Mark A. Feitelson PDF

This multidisciplinary review covers easy suggestions relating to the invention of the Hepatitis C virus, improvement of serological and nucleic acid assessments to observe an infection, the constitution of the virus genome, new release of virus gene items, and proposed replication scheme. the amount discusses the epidemiology, transmission, pathogenesis of an infection, the improvement of hepatocellular carcinoma linked to persistent virus an infection, and present thoughts for therapy.

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1989). , 1997). Hence, the primary sequence of HCV NS5B isolates has provided clues as to the regions of the protein that may be functionally important. Building upon this knowledge, expression systems have been generated to characterize NS5B further (Ch. 23). , 1998) yielded products with RdRp activity, proving that NS5B is the HCVencoded polymerase. 5 and was Mg2+ dependent.

1998). , 1999). These studies imply that core antigen expression is directly related to the levels of HCV replication. , 1999); the impression from this work is that replication is supported but less eYcient in HCC cells compared with that in surrounding nontumor liver (Ch. 6). , 1992) raises the question as to the origin of the RT/PCR products. , 1995). This may be true for some patients but may also reXect the diYculty in assuring speciWc minus strand ampliWcation and detection using RT/PCR, even when precautions are taken (Sangar & Carroll, 1998) (Ch.

Hence, cleavage of the HCV structural proteins is followed by a rapid, autocatalytic cleavage of the NS2–NS3 sequences, which releases NS3. As explained below, NS3 plays a number of roles in virus maturation and virus replication. , 1995). , 1994b). , 1995). Another rapid cleavage then occurs at the NS5A–NS5B site, resulting in the appearance of the virus RdRp, NS5B. , 1994b). , 1995a), which may contribute to protease activation. , 1994). These cleavage sites were also observed using appropriate synthetic peptide substrates, suggesting that processing speciWcity is related to the primary sequence around the cleavage site and is not conformationally dependent.

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Hepatitis C Virus: From Laboratory to Clinic (Biomedical Research Topics S.) by Mark A. Feitelson


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