Kai Tan, PhD
Affiliations: | University of Pennsylvania, Philadelphia, PA, United States |
Area:
Computational BiologyWebsite:
https://www.med.upenn.edu/apps/faculty/index.php/g275/p8885111Google:
"Kai Tan"Parents
Sign in to add mentor| Gary Stormo | grad student | 1998-2004 | Washington University |
| Trey Ideker | post-doc | UCSD |
Children
Sign in to add trainee| Change Chen | grad student | University of Iowa Carver College of Medicine |
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Publications
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| Hsu J, Huang HT, Lee CT, et al. (2020) CHD7 and Runx1 interaction provides a braking mechanism for hematopoietic differentiation. Proceedings of the National Academy of Sciences of the United States of America |
| Gao P, Chen C, Howell ED, et al. (2020) Transcriptional regulatory network controlling the ontogeny of hematopoietic stem cells. Genes & Development |
| Zhu Q, Gao P, Tober J, et al. (2020) Developmental trajectory of pre-hematopoietic stem cell formation from endothelium. Blood |
| Chen C, Yu W, Tober J, et al. (2019) Spatial Genome Re-organization between Fetal and Adult Hematopoietic Stem Cells. Cell Reports. 29: 4200-4211.e7 |
| Packer JS, Zhu Q, Huynh C, et al. (2019) A lineage-resolved molecular atlas of embryogenesis at single-cell resolution. Science (New York, N.Y.) |
| Hu Y, Chen CH, Ding YY, et al. (2019) Optimal control nodes in disease-perturbed networks as targets for combination therapy. Nature Communications. 10: 2180 |
| Peng T, Zhu Q, Yin P, et al. (2019) SCRABBLE: single-cell RNA-seq imputation constrained by bulk RNA-seq data. Genome Biology. 20: 88 |
| Taylor DM, Aronow BJ, Tan K, et al. (2019) The Pediatric Cell Atlas: Defining the Growth Phase of Human Development at Single-Cell Resolution. Developmental Cell |
| Nicetto D, Donahue G, Jain T, et al. (2019) H3K9me3-heterochromatin loss at protein-coding genes enables developmental lineage specification. Science (New York, N.Y.) |
| Estevez B, Borst S, Jarocha DJ, et al. (2019) The Inherited Platelet Disorder of RUNX1 Haploinsufficiency (Familial Platelet Disorder with Associated Myeloid Malignancy (FPDMM)) Has a Marked Deficiency of Megakaryocyte-Biased Hematopoietic Progenitor Cells: Mechanistic Studies and Drug Correction Blood. 134: 220-220 |