Literature DB >> 29387656

HCV genetics and genotypes dictate future antiviral strategies.

Louis Papageorgiou1,2, Chrisanthy Vlachakis3, Konstantina Dragoumani3, Sofia Raftopoulou4, Dimitrios Brouzas5, Nicolas C Nicolaides6,7, George P Chrousos6,7,8, Evangelia Charmandari6,7, Vasileios Megalooikonomou9, Dimitrios Vlachakis6,9,10.   

Abstract

At the end of the 1980s, the hepatitis C virus (HCV) was cloned and formally identified as the cause of the majority of non-A and non-B hepatitis cases. Today, around 170 million people worldwide are infected with HCV, making it five times more common than infection with the human immunodeficiency virus (HIV). Several methods exist which mediate the spread of infection. One of the most common and efficient is sharing or re-using injecting equipment; studies have indicated that 80-90% of individuals in some populations of intravenous drug users test positive in serum HCV assays. Contracting HCV from infected blood transfusions was also a major cause of infection before screening tests were introduced in the early 1990s. Other possible, but less common, methods of infection transmission include mother-to-child during pregnancy, sexual contact and nosocomial acquisition (for example between surgical or dialysis patients). It appears that concurrent HIV-1 infection increases the risk of HCV transmission via the mother-to-child or sexual routes.

Entities:  

Year:  2017        PMID: 29387656      PMCID: PMC5788192     

Source DB:  PubMed          Journal:  J Mol Biochem        ISSN: 2241-0090


  42 in total

1.  Hepatitis C viral IRES inhibition by phenazine and phenazine-like molecules.

Authors:  W Wang; P Préville; N Morin; S Mounir; W Cai; M A Siddiqui
Journal:  Bioorg Med Chem Lett       Date:  2000-06-05       Impact factor: 2.823

2.  Biological evaluation of hepatitis C virus helicase inhibitors.

Authors:  C W Phoon; P Y Ng; A E Ting; S L Yeo; M M Sim
Journal:  Bioorg Med Chem Lett       Date:  2001-07-09       Impact factor: 2.823

3.  Crystal structure of the RNA-dependent RNA polymerase of hepatitis C virus.

Authors:  S Bressanelli; L Tomei; A Roussel; I Incitti; R L Vitale; M Mathieu; R De Francesco; F A Rey
Journal:  Proc Natl Acad Sci U S A       Date:  1999-11-09       Impact factor: 11.205

4.  Probing the relationship between RNA-stimulated ATPase and helicase activities of HCV NS3 using 2'-O-methyl RNA substrates.

Authors:  T Hesson; A Mannarino; M Cable
Journal:  Biochemistry       Date:  2000-03-14       Impact factor: 3.162

5.  Solution structure and dynamics of the single-chain hepatitis C virus NS3 protease NS4A cofactor complex.

Authors:  M A McCoy; M M Senior; J J Gesell; L Ramanathan; D F Wyss
Journal:  J Mol Biol       Date:  2001-02-02       Impact factor: 5.469

6.  The solution structure of the N-terminal proteinase domain of the hepatitis C virus (HCV) NS3 protein provides new insights into its activation and catalytic mechanism.

Authors:  G Barbato; D O Cicero; M C Nardi; C Steinkühler; R Cortese; R De Francesco; R Bazzo
Journal:  J Mol Biol       Date:  1999-06-04       Impact factor: 5.469

7.  Identification and characterization of a histone binding site of the non-structural protein 3 of hepatitis C virus.

Authors:  P Borowski; R Kühl; R Laufs; J Schulze zur Wiesch; M Heiland
Journal:  J Clin Virol       Date:  1999-06       Impact factor: 3.168

8.  Hepatitis C virus: an overview of current approaches and progress.

Authors: 
Journal:  Drug Discov Today       Date:  1999-11       Impact factor: 7.851

9.  Replication of subgenomic hepatitis C virus RNAs in a hepatoma cell line.

Authors:  V Lohmann; F Körner; J Koch; U Herian; L Theilmann; R Bartenschlager
Journal:  Science       Date:  1999-07-02       Impact factor: 47.728

10.  Crystal structure of the RNA-dependent RNA polymerase from hepatitis C virus reveals a fully encircled active site.

Authors:  C A Lesburg; M B Cable; E Ferrari; Z Hong; A F Mannarino; P C Weber
Journal:  Nat Struct Biol       Date:  1999-10
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