Awards as PI
| Program Type | Institution | Grant Title | Award Value |
|---|---|---|---|
| Tools and Technologies III | Stanford University | A Chromatin Context Tool for Predicting iPS Lineage Predisposition and Tissue Graftability | $1,391,125 |
| Therapeutic Translational Research Projects | Stanford University | DEBCT: Genetically Corrected, Induced Pluripotent Cell-Derived Epithelial Sheets for Definitive Treatment of Dystrophic Epidermolysis Bullosa | $5,107,353 |
Total: $6,498,478.00 |
Awards as Co-PI
| Disease Team Research I | iPS Cell-Based Treatment of Dominant Dystrophic Epidermolysis Bullosa |
Publications
- Nat Genet 2018 Retinoic acid and BMP4 cooperate with p63 to alter chromatin dynamics during surface epithelial commitment. (PubMed: 30397335)
- Cell Stem Cell 2019 TFAP2C- and p63-Dependent Networks Sequentially Rearrange Chromatin Landscapes to Drive Human Epidermal Lineage Commitment. (PubMed: 30686763)