Chad Cowan
Affiliations: | Harvard University, Cambridge, MA, United States |
Area:
Diabetes, Coronary artery diseaseWebsite:
https://hscrb.harvard.edu/res-fl-cowanGoogle:
"Chad Cowan"Children
Sign in to add trainee| Robert Schinzel | grad student | Harvard | |
| Leonardo M.R. Ferreira | grad student | 2012-2016 | Harvard |
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Publications
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| Pope BD, Warren CR, Dahl MO, et al. (2020) Fattening chips: hypertrophy, feeding, and fasting of human white adipocytes . Lab On a Chip |
| Kanchan K, Iyer K, Yanek LR, et al. (2020) Genomic integrity of human induced pluripotent stem cells across nine studies in the NHLBI NextGen program. Stem Cell Research. 46: 101803 |
| Meissner TB, Cowan CA. (2020) More Bang for Your Buck: “Off-The-Shelf” Solutions for Cell Replacement Therapy Stemjournal. 2: 1-5 |
| Han X, Wang M, Duan S, et al. (2019) Generation of hypoimmunogenic human pluripotent stem cells. Proceedings of the National Academy of Sciences of the United States of America |
| Rossmann MP, Hoi K, Chan V, et al. (2019) Transcriptional Regulation of Coenzyme Q Biosynthesis By TIF1γ Drives Erythropoiesis Blood. 134: 152-152 |
| Odorico J, Markmann J, Melton D, et al. (2018) Report of the Key Opinion Leaders Meeting on Stem Cell-Derived Beta Cells. Transplantation |
| Warren CR, O'Sullivan JF, Friesen M, et al. (2017) Induced Pluripotent Stem Cell Differentiation Enables Functional Validation of GWAS Variants in Metabolic Disease. Cell Stem Cell. 20: 547-557.e7 |
| Lin MI, Paik E, Mishra B, et al. (2017) CRISPR/Cas9 Genome Editing to Treat Sickle Cell Disease and B-Thalassemia: Re-Creating Genetic Variants to Upregulate Fetal Hemoglobin Appear Well-Tolerated, Effective and Durable. Blood. 130: 284-284 |
| Naylor RW, McGhee CN, Cowan CA, et al. (2016) Derivation of Corneal Keratocyte-Like Cells from Human Induced Pluripotent Stem Cells. Plos One. 11: e0165464 |
| Peters DT, Henderson CA, Warren CR, et al. (2016) Asialoglycoprotein receptor 1 is a specific cell-surface marker for isolating hepatocytes derived from human pluripotent stem cells. Development (Cambridge, England). 143: 1475-81 |