Subhash G. Vasudevan

Secreted dengue virus NS1 from infection is predominantly dimeric and in complex with high-density lipoprotein

Non-nucleoside Inhibitors of Zika Virus RNA-Dependent RNA Polymerase

Luteolin escape mutants of dengue virus map to prM and NS2B and reveal viral plasticity during maturation

Current Status of Dengue Therapeutics Research and Development

Luteolin restricts dengue virus replication through inhibition of the proprotein convertase furin

NS3 helicase from dengue virus specifically recognizes viral RNA sequence to ensure optimal replication

Characterization of RyDEN (C19orf66) as an Interferon-Stimulated Cellular Inhibitor against Dengue Virus Replication

The C-terminal 18 Amino Acid Region of Dengue Virus NS5 Regulates its Subcellular Localization and Contains a Conserved Arginine Residue Essential for Infectious Virus Production

Novel antiviral activity of bromocriptine against dengue virus replication

Extended Evaluation of Virological, Immunological and Pharmacokinetic Endpoints of CELADEN: A Randomized, Placebo-Controlled Trial of Celgosivir in Dengue Fever Patients

A Crystal Structure of the Dengue Virus NS5 Protein Reveals a Novel Inter-domain Interface Essential for Protein Flexibility and Virus Replication

Molecular basis for specific viral RNA recognition and 2′-O-ribose methylation by the dengue virus nonstructural protein 5 (NS5)

Animal models for studying dengue pathogenesis and therapy

Structural insight and flexible features of NS5 proteins from all four serotypes of<i>Dengue virus</i>in solution

The C-terminal 50 Amino Acid Residues of Dengue NS3 Protein Are Important for NS3-NS5 Interaction and Viral Replication

Chikungunya virus nsP3 &amp; nsP4 interacts with HSP-90 to promote virus replication: HSP-90 inhibitors reduce CHIKV infection and inflammation in vivo

Differential unfolded protein response during Chikungunya and Sindbis virus infection: CHIKV nsP4 suppresses eIF2α phosphorylation

Sulfated Polysaccharide, Curdlan Sulfate, Efficiently Prevents Entry/Fusion and Restricts Antibody-Dependent Enhancement of Dengue Virus Infection In Vitro: A Possible Candidate for Clinical Application