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Fang Fang
ffang24@ustc.edu.cn
English, Chinese
Anhui
University of Science and Technology of China
Basic Medical Sciences
  • 2011 - PhD in Computational and Systems Biology: National University of Singapore and Massachusetts Institute of Technology
  • Published research in Nature Cell Biology, Nature Communications, and Cell Reports
  • 2011-2014 - Stanford University School of Medicine - Postdoctoral Research
  • 2014-2019 - Montana State University - Research Scientist
  • 2019-Present - University of Science and Technology of China - Specially Appointed Professor
Transcriptional regulation and cell fate determination
Development and in vitro generation of human germ cells
Establishment of stem cell disease models
  • A PAX5-OCT4-PRDM1 developmental switch specifies human primordial germ cells, Fang F, Angulo B, Xia N, Sukhwani M, Wang Z, Carey CC, Mazurie A, Cui J, Wilkinson R, Wiedenheft B, Surani AM, Orwig KE, Reijo Pera RA, 2018
  • A distinct isoform of ZNF207 controls self-renewal and pluripotency of human embryonic stem cells in conjunction with master transcription factors, Fang F, Xia N, Angulo B, Carey J, Durruthy-Durruthy J, Sebastiano V, Bennett T, Reijo Pera RA, 2018
  • A Knock-In Reporter allows purification and characterization of mDA neurons from heterogeneous populations, Xia N, Fang F, Zhang P, Cui J, Tep-Cullison C, Hamerley T, Lee HJ, Palmer T, Bothner B, Lee HJ, Reijo Pera RA, 2017
  • Transcriptional comparison of human induced and primary midbrain dopaminergic neurons, Xia N, Zhang P, Fang F, Wang Z, Rothstein M, Augulo B, Chiang R, Taylor J, Reijo Pera RA, 2016
  • Coactivators p300/CBP regulate self-renewal in embryonic stem cells by mediating long-range chromatin structure, Fang F, Xu Y, Chen X, Ng HH, Matsudaira P, 2014
Transcriptional Regulation Cell Fate Human Germ Cells In Vitro Generation Stem Cells Disease Models Developmental Biology Reproductive Biology Cellular Biology Molecular Biology

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