Yanling Yang

This study shows that viral replication byproducts called cbVGs drive changes in circadian gene expression during infection through distinct immune pathways, with ARNTL2 playing a key role in amplifying antiviral responses.

The paper uses single-cell RNA-sequencing to study how copy-back viral genomes drive host cell responses during Sendai virus infection, revealing dynamic transcriptional changes over time.

This study investigates copy-back viral genomes (cbVGs) generated during Sendai virus infection, finding conserved and variable features in their generation and accumulation across different viral stocks.

The paper optimizes Direct RNA Sequencing to obtain full-length copyback viral genomes and introduces a BLAST-based tool for their detection.

This study identifies SLC35A2 as a host factor essential for paramyxovirus fusion during infection, showing its role in virus-cell and cell-to-cell fusion events.

This paper develops minigenome systems for Nipah and Hendra viruses and shows that their polymerase complex proteins can replicate both minigenomes regardless of origin, suggesting potential targets for antivirals.

This study identifies a carbapenem-resistant Pseudomonas aeruginosa strain co-harboring blaKPC-2 and blaVIM-2 genes, revealing their genetic environment and plasmid-mediated transmission.

The paper identifies a Tn7-like transposon carrying blaIMP-1 in carbapenem-resistant Pseudomonas aeruginosa strains and describes its genetic structure and potential role in intrahospital dissemination.