Moonhee Park

This study identifies VIRMA as an HCV RNA-targeting factor that recruits the m6A-MTC to the viral genome through a WTAP-independent mechanism.

This paper identifies IFIT3's preference for m⁶A-modified RNA to restrict HCV infection and reveals structural regions critical for RNA binding and antiviral activity.

This study shows UFMylation enhances orthoflavivirus infection by promoting virion assembly, but not RNA replication or translation.

This study identifies UFMylation sites on 14-3-3ϵ that regulate MAVS complex assembly and RIG-I signaling to enhance antiviral innate immunity.

The paper shows that cellular RNA interacts with MAVS to scaffold signaling proteins and promote antiviral signaling by facilitating IRF3 phosphorylation.

The paper shows FTO suppresses proinflammatory ISG expression by inhibiting STAT3 activation during the type I IFN response.