We apply the nanopatterned 2D hPSC-CM monolayer for understanding cardiac electrical and mechanical couplings; micropatterned single hPSC-cardiomyocyte for modeling familial cardiomyopathies, micropatterned cardiac microfiber for hPSC-CM maturation in calcium handling and T-tubule formation; micropatterned 3D cardiovascular organoid for modeling heart development, drug-induced and environment-caused birth defects, and congenital heart diseases.
We apply various interventions for assisting cardiovascular repair, such as acellular therapy with microRNA (miRNA), nanoparticle and injectable hydrogel for improving cardiac function; NIR-II small molecule with high quantum yield and sensitivity for in vivo stem cell tracking and quantification in long term; and 3D bioprinting for cardiovascular remuscularization and revascularization.
We apply soft lithography, 3D printing, and macro/microfluidics for biofabricating biomedical microdevices for better understanding the developments of cardiovascular pathophysiology.
iPSC and disease modeling
Genome editing and CRISPR/Cas9 technology
Genome and next-generation sequencing
Cardiovascular Health and treatment
Cardiac biomechanics and modeling
Hypertrophic cardiomyopathy and transgenic mouse model
Funding Information
American Heart Association Research Programs
NIH Grants & Funding Due Dates
NSF-Engineering of Biomedical System
Genome/transcriptome search
Druggable target help
scRNA-Seq
Tabula MurisSapiens
iPSC-CM RNA-seq
iPSC-CMs vs. fetal vs. adult heart LV
Cardiac Secretome Credit to Lam lab @ UDel
Heart Development