Area of research
Nephrology · Molecular Biology
Research interest
Research interests include Immunology, Nephropathy, Immune system, Antibody, Biology, and Glycan.
Loss of GalNAc-T14 links O-glycosylation defects to alterations in B cell homing in IgA nephropathy
Galactose-Deficient IgA1 B cells in the Circulation of IgA Nephropathy Patients Carry Preferentially Lambda Light Chains and Mucosal Homing Receptors
Leukemia Inhibitory Factor Signaling Enhances Production of Galactose-Deficient IgA1 in IgA Nephropathy
Role of Epstein-Barr Virus in Pathogenesis and Racial Distribution of IgA Nephropathy
Secretory IgA N-glycans contribute to the protection against E. coli O55 infection of germ-free piglets
Glycan Positioning Impacts HIV-1 Env Glycan-Shield Density, Function, and Recognition by Antibodies
Defining HIV-1 Envelope N-Glycan Microdomains through Site-Specific Heterogeneity Profiles
Glucocorticoids Reduce Aberrant O-Glycosylation of IgA1 in IgA Nephropathy Patients
Inhibition of STAT3 Signaling Reduces IgA1 Autoantigen Production in IgA Nephropathy
Lasioglossins LLIII affect the morphogenesis of <i>Candida albicans</i> and reduces the duration of experimental vaginal candidiasis in mice
The Origin and Activities of IgA1-Containing Immune Complexes in IgA Nephropathy
Multi-layered nanofibrous mucoadhesive films for buccal and sublingual administration of drug-delivery and vaccination nanoparticles - important step towards effective mucosal vaccines
Liposomal nanocarriers for plasminogen activators
Somatic Mutations Modulate Autoantibodies against Galactose-Deficient IgA1 in IgA Nephropathy
The Position of His-Tag in Recombinant OspC and Application of Various Adjuvants Affects the Intensity and Quality of Specific Antibody Response after Immunization of Experimental Mice
Endotoxin-minimized HIV-1 p24 fused to murine hsp70 activates dendritic cells, facilitates endocytosis and p24-specific Th1 response in mice
IgA Nephropathy and Related Diseases
Cytokines Alter IgA1 O-Glycosylation by Dysregulating C1GalT1 and ST6GalNAc-II Enzymes
Differential glycosylation of envelope gp120 is associated with differential recognition of HIV-1 by virus-specific antibodies and cell infection
Enzymatic Sialylation of IgA1 O-Glycans: Implications for Studies of IgA Nephropathy
N-Acetylgalactosaminide α2,6-sialyltransferase II is a candidate enzyme for sialylation of galactose-deficient IgA1, the key autoantigen in IgA nephropathy
HIV-1 Envelope Glycan Moieties Modulate HIV-1 Transmission
Humoral Immune Responses to <scp>HIV</scp> in the Mucosal Secretions and Sera of <scp>HIV</scp>‐Infected Women
IgA Nephropathy: Molecular Mechanisms of the Disease
Aberrant O-glycosylation and anti-glycan antibodies in an autoimmune disease IgA nephropathy and breast adenocarcinoma