Zhaohui Ye, Ph.D.
Affiliations: | 2009 | Johns Hopkins University, Baltimore, MD |
Area:
Cell Biology, Molecular BiologyGoogle:
"Zhaohui Ye"Parents
Sign in to add mentor| Linzhao Cheng | grad student | 2009 | Johns Hopkins | |
| (Developing a human pluripotent stem cell model for hematopoiesis and blood disorders.) | ||||
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Publications
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| Kamaldinov T, Zhang L, Wang L, et al. (2023) Generation of induced pluripotent stem cell lines from helper and cytotoxic T cells of healthy individuals. Stem Cell Research. 69: 103113 |
| Wang L, Ye Z, Jang YY. (2021) Convergence of human pluripotent stem cell, organoid, and genome editing technologies. Experimental Biology and Medicine (Maywood, N.J.). 1535370220985808 |
| McGrath E, Shin H, Zhang L, et al. (2019) Targeting specificity of APOBEC-based cytosine base editor in human iPSCs determined by whole genome sequencing. Nature Communications. 10: 5353 |
| Chaudhari P, Tian L, Ye Z, et al. (2019) Human-relevant preclinical in vitro models for studying hepatobiliary development and liver diseases using induced pluripotent stem cells. Experimental Biology and Medicine (Maywood, N.J.). 1535370219834895 |
| Chaudhari P, Tian L, Kim A, et al. (2018) Transient c-Src suppression during endodermal commitment of human iPSCs results in abnormal profibrotic cholangiocyte-like cells. Stem Cells (Dayton, Ohio) |
| Tian L, Ye Z, Kafka K, et al. (2018) Biliary Atresia Relevant Human iPSCs Recapitulate Key Disease Features in a Dish. Journal of Pediatric Gastroenterology and Nutrition |
| Cai L, Bai H, Mahairaki V, et al. (2017) A Universal Approach to Correct Various HBB Gene Mutations in Human Stem Cells for Gene Therapy of Beta-Thalassemia and Sickle Cell Disease. Stem Cells Translational Medicine |
| Tian L, Eldridge L, Chaudhari P, et al. (2017) Derivation of a disease-specific human induced pluripotent stem cell line from a biliary atresia patient. Stem Cell Research. 24: 25-28 |
| Yuan X, Li Z, Baines AC, et al. (2017) A hypomorphic PIGA gene mutation causes severe defects in neuron development and susceptibility to complement-mediated toxicity in a human iPSC model. Plos One. 12: e0174074 |
| Liu S, Ye Z, Gao Y, et al. (2017) Generation of human iPSCs from an essential thrombocythemia patient carrying a V501L mutation in the MPL gene. Stem Cell Research. 18: 57-59 |