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Jens Bukh

Researcher at University of Copenhagen

Publications -  302
Citations -  22917

Jens Bukh is an academic researcher from University of Copenhagen. The author has contributed to research in topics: Hepatitis C virus & Virus. The author has an hindex of 71, co-authored 270 publications receiving 21051 citations. Previous affiliations of Jens Bukh include Copenhagen University Hospital & Hvidovre Hospital.

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Hepatitis C virus RNA in southern African blacks with hepatocellular carcinoma.

TL;DR: A significant number of southern African Blacks with HCC had a current HCV infection but not a current HBV infection, further suggesting that infection with HCV plays a role, albeit minor, in the development of HCC in this population.
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Breadth of neutralization and synergy of clinically relevant human monoclonal antibodies against HCV genotypes 1a, 1b, 2a, 2b, 2c, and 3a

TL;DR: The neutralization synergism obtained when pooling the most potent HMAbs could have significant implications for developing novel strategies to treat and control HCV.
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How Escherichia coli can bias the results of molecular cloning: Preferential selection of defective genomes of hepatitis C virus during the cloning procedure

TL;DR: There was a strong cloning selection for defective genomes and that most clones generated initially were incapable of expressing the HCV proteins, finding this has enormous implications for the study of viral heterogeneity.
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Studies of Hepatitis C Virus in Chimpanzees and Their Importance for Vaccine Development

TL;DR: Of relevance for vaccine evaluation was the titration in chimpanzees of different HCV variants to provide well-characterized challenge pools, and monoclonal virus pools generated from chimpanzees infected with cloned viruses make it possible to examine immunity to HCV without the confounding factor of antigenic diversity of the challenge virus (quasispecies).
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Highly efficient infectious cell culture of three hepatitis C virus genotype 2b strains and sensitivity to lead protease, nonstructural protein 5A, and polymerase inhibitors.

TL;DR: Highly efficient HCV full‐length 2b culture systems can be established by using consensus clones with defined mutations, and lead protease and NS5A inhibitors, as well as polymerase inhibitors sofosbuvir, mericitabine, and BI207127, show cross‐activity against full-length 1a, 2a, and 2b viruses, but important sensitivity differences exist at the isolate level.