Area of research
Cardiology and Cardiovascular Medicine · Infectious Diseases
Research interest
Research interests include Viral Infections and Immunology Research, Animal Disease Management and Epidemiology, SARS-CoV-2 and COVID-19 Research, and Viral gastroenteritis research and epidemiology.
Recombinant expression systems for production of stabilised virus-like particles as next-generation polio vaccines.
The SARS-CoV-2 neutralizing antibody response to SD1 and its evasion by BA.2.86.
Emerging variants develop total escape from potent monoclonal antibodies induced by BA.4/5 infection.
A broadly reactive ultralong bovine antibody that can determine the integrity of foot-and-mouth disease virus capsids
The impact of exchanging the light and heavy chains on the structures of bovine ultralong antibodies.
Structural plasticity of 2A proteins in the Parechovirus family
Generation of SARS-CoV-2 escape mutations by monoclonal antibody therapy.
Isolation of a pair of potent broadly neutralizing mAb binding to RBD and SD1 domains of SARS-CoV-2
Emerging variants develop total escape from potent monoclonal antibodies induced by BA.4/5 infection
A conserved glutathione binding site in poliovirus is a target for antivirals and vaccine stabilisation.
Genome-first detection of emerging resistance to novel therapeutic agents for SARS-CoV-2
Switching of Receptor Binding Poses between Closely Related Enteroviruses.
Publisher Correction: A conserved glutathione binding site in poliovirus is a target for antivirals and vaccine stabilisation.
Reduced neutralization of SARS-CoV-2 B.1.1.7 variant by convalescent and vaccine sera.
The antigenic anatomy of SARS-CoV-2 receptor binding domain.
Mammalian expression of virus-like particles as a proof of principle for next generation polio vaccines.
Neutralization of SARS-CoV-2 by Destruction of the Prefusion Spike
Structural basis for the neutralization of SARS-CoV-2 by an antibody from a convalescent patient
Structural basis for the neutralization of SARS-CoV-2 by an antibody from a convalescent patient.
Neutralization of SARS-CoV-2 by Destruction of the Prefusion Spike.
Hand-foot-and-mouth disease virus receptor KREMEN1 binds the canyon of Coxsackie Virus A10.
Structural and functional analysis of protective antibodies targeting the threefold plateau of enterovirus 71.
Glutathione facilitates enterovirus assembly by binding at a druggable pocket.
Symmetrical arrangement of positively charged residues around the 5-fold axes of SAT type foot-and-mouth disease virus enhances cell culture of field viruses.
Unexpected mode of engagement between enterovirus 71 and its receptor SCARB2.