Zhaohui Ye, Ph.D.

2009 Johns Hopkins University, Baltimore, MD 
Cell Biology, Molecular Biology
"Zhaohui Ye"


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Linzhao Cheng grad student 2009 Johns Hopkins
 (Developing a human pluripotent stem cell model for hematopoiesis and blood disorders.)
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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
Jang YY, Ye Z. (2016) Gene correction in patient-specific iPSCs for therapy development and disease modeling. Human Genetics
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