Unveiling the role of PUS7-mediated pseudouridylation in host protein interactions specific for the SARS-CoV-2 RNA genome: Molecular Therapy - Nucleic Acids

PUS7: a targetable epitranscriptomic regulator of glioblastoma growth: Trends in Pharmacological Sciences

Large scale discovery of coronavirus-host factor protein interaction motifs reveals SARS-CoV-2 specific mechanisms and vulnerabilities

tRNA renovatio: Rebirth through fragmentation - ScienceDirect

Pseudouridine synthases modify human pre-mRNA co-transcriptionally and affect splicing

Regulatory roles of tRNA-derived RNA fragments in human pathophysiology: Molecular Therapy - Nucleic Acids

Unveiling the role of PUS7-mediated pseudouridylation in host protein interactions specific for the SARS-CoV-2 RNA genome: Molecular Therapy - Nucleic Acids

Unveiling the role of PUS7-mediated pseudouridylation in host protein interactions specific for the SARS-CoV-2 RNA genome: Molecular Therapy - Nucleic Acids

Targeting PUS7 suppresses tRNA pseudouridylation and glioblastoma tumorigenesis

Pseudouridine synthases modify human pre-mRNA co-transcriptionally and affect splicing

Frontiers Epitranscriptomics of SARS-CoV-2 Infection

The SARS-CoV-2 RNA–protein interactome in infected human cells

Frontiers A Journey From SARS-CoV-2 to COVID-19 and Beyond: A Comprehensive Insight of Epidemiology, Diagnosis, Pathogenesis, and Overview of the Progress into Its Therapeutic Management

Host cell entry mediators implicated in the cellular tropism of SARS‑CoV‑2, the pathophysiology of COVID‑19 and the identification of microRNAs that can modulate the expression of these mediators (Review)

Targeting PUS7 suppresses tRNA pseudouridylation and glioblastoma tumorigenesis

Pseudouridine-modified tRNA fragments repress aberrant protein synthesis and predict leukaemic progression in myelodysplastic syndrome