Area of research
Sensory Systems · Molecular Biology
Research interest
Research interests include Cell biology, Biology, ORAI1, Enamel paint, Chemistry, and Reprogramming.
Mitochondrial dysfunction promotes the transition of precursor to terminally exhausted T cells through HIF-1α-mediated glycolytic reprogramming
The glucose transporter GLUT3 controls T helper 17 cell responses through glycolytic-epigenetic reprogramming
Tissue resident and follicular Treg cell differentiation is regulated by CRAC channels
Differential regulation of Ca <sup>2+</sup> influx by ORAI channels mediates enamel mineralization
Evidence That Calcium Entry Into Calcium-Transporting Dental Enamel Cells Is Regulated by Cholecystokinin, Acetylcholine and ATP
Altered Ca2+ signaling in enamelopathies
Store-Operated Ca2+ Entry Controls Clonal Expansion of T Cells through Metabolic Reprogramming
ORAI2 modulates store-operated calcium entry and T cell-mediated immunity
Role of Dysregulated Cytokine Signaling and Bacterial Triggers in the Pathogenesis of Cutaneous T-Cell Lymphoma
Store-operated Ca2+ entry controls ameloblast cell function and enamel development
Store-Operated Ca 2+ Entry in Follicular T Cells Controls Humoral Immune Responses and Autoimmunity
Store-operated Ca2+ entry regulates Ca2+-activated chloride channels and eccrine sweat gland function
Ca<sup>2+</sup> transport and signalling in enamel cells
Dental enamel cells express functional SOCE channels