Gabsang Lee

Recruit of porcine oocytes excluded from nuclear transfer program for the production of embryos following parthenogenetic activation.

Production of nuclear transfer-derived piglets using porcine fetal fibroblasts transfected with the enhanced green fluorescent protein.

Hematopoietic cells.

Isolation and directed differentiation of neural crest stem cells derived from human embryonic stem cells.

Osteogenic potential of embryonic stem cells in tooth sockets.

High-throughput screening assay for the identification of compounds regulating self-renewal and differentiation in human embryonic stem cells.

Modelling pathogenesis and treatment of familial dysautonomia using patient-specific iPSCs.

Induced pluripotent stem cell technology for the study of human disease.

Expansion and maintenance of human embryonic stem cell-derived endothelial cells by TGFbeta inhibition is Id1 dependent.

Derivation of neural crest cells from human pluripotent stem cells.

Efficient derivation of functional floor plate tissue from human embryonic stem cells.

Genomic safe harbors permit high β-globin transgene expression in thalassemia induced pluripotent stem cells.

miR-371-3 expression predicts neural differentiation propensity in human pluripotent stem cells.

Modelling familial dysautonomia in human induced pluripotent stem cells.

Evaluation of developmental toxicants and signaling pathways in a functional test based on the migration of human neural crest cells.

Combined small-molecule inhibition accelerates developmental timing and converts human pluripotent stem cells into nociceptors.

Large-scale screening using familial dysautonomia induced pluripotent stem cells identifies compounds that rescue IKBKAP expression.

Modeling neural crest induction, melanocyte specification, and disease-related pigmentation defects in hESCs and patient-specific iPSCs.

Candidate ALS therapeutics motor toward "in vitro clinical trials".

Dual-SMAD Inhibition/WNT Activation-Based Methods to Induce Neural Crest and Derivatives from Human Pluripotent Stem Cells.