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Fulvia Bono

Researcher at Max Planck Society

Publications -  37
Citations -  3018

Fulvia Bono is an academic researcher from Max Planck Society. The author has contributed to research in topics: Hepatitis C virus & Exon junction complex. The author has an hindex of 21, co-authored 35 publications receiving 2868 citations. Previous affiliations of Fulvia Bono include University of Exeter & University of Milan.

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Journal ArticleDOI

Structural biology of nucleocytoplasmic transport.

TL;DR: The molecular mechanisms underlying nucleocytoplasmic transport as they have been revealed by structural studies of the receptors and regulators in different steps of transport cycles are described.
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The Crystal Structure of the Exon Junction Complex Reveals How It Maintains a Stable Grip on mRNA

TL;DR: Comparison with the structure of the eIF4AIII-Btz subcomplex that is determined reveals that large conformational changes are required upon EJC assembly and disassembly.
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Hepatitis C virus genotypes and risk of hepatocellular carcinoma in cirrhosis: a prospective study

TL;DR: Cirrhotic patients infected with HCV type 1b carry a significantly higher risk of developing HCC than patients infected by other HCV types, and the latter may require a less intensive clinical surveillance for the early detection of neoplasia.
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Differential distribution of hepatitis C virus genotypes in patients with and without liver function abnormalities.

TL;DR: Virological features of HCV infection might be associated with different clinical manifestations, suggesting a potential prognostic significance on disease outcome, and isolated genotype II was progressively more represented in advanced liver disease, such as cirrhosis and HCC.
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Hepatitis C virus core protein binds to apolipoprotein AII and its secretion is modulated by fibrates.

TL;DR: The results show the direct binding of the viral protein to apolipoprotein AII (apoAII) and map the interaction domain to the C‐terminal of HCV core protein and show that the intervention of fenofibric acid in cellular lipid metabolism directly affects the expression pattern of HCv core protein.