Kevin Tsai

This study shows that N6-methyladenosine (m6A) is abundant on IAV mRNAs but rare on genomic RNA, and m6A promotes mRNA stability and viral replication.

This study uses Nanopore DRS to show m6A modification on HBV RNA enhances stability by protecting long poly(A) tails, supporting m6A as an antiviral target.

The paper introduces PA-{Psi}-seq, a technique to map pseudouridine residues on cellular and viral transcripts, and shows that HIV-1 transcripts are not affected by PUS enzyme inactivation.

This paper shows that m6A methylation regulates HIV-1 RNA stability and alternative splicing through YTHDC1 and YTHDF2.