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專(zhuān)家人才
- 姓名： 馮波
- 性別： 女
- 職稱(chēng)： 副教授
- 學(xué)歷： 博士
- 電話(huà)：
- 傳真：
- 電子郵件:
- 通訊地址 廣州市黃埔區開(kāi)源大道190號
Academic qualifications:
2002.1 – 2006.10 Ph.D. Temasek LifeSciences Laboratory, National University of Singapore
1993.9 – 1996.7 M.Sc. Nankai University, China
1989.9 – 1993.7 B.Sc. Nankai University, China
Present academic position:
2017.7 – Associate Professor, School of Biomedical Sciences, Faculty of Medicine, The Chinese University of Hong Kong
2021.8 – Deputy Chief of Developmental and Regenerative Biology Program, School of Biomedical Sciences, Faculty of Medicine, CUHK.
2018.2 – Deputy Director, CUHK-GIBH Joint Laboratory on Stem Cell and Regenerative Medicine
Previous academic positions held:
2010.11 – 2017.7 Assistant Professor, School of Biomedical Sciences, Faculty of Medicine, The Chinese University of Hong Kong
2007.1 – 2010.11 Postdoctoral Fellow & Research Associate, Genome Institute of Singapore, Singapore
1999.3 – 2006.12 Junior Research Fellow, Temasek LifeSciences Laboratory, Singapore
1996.7 – 1999.2 Tutor, Tianjin Normal University, China
簡(jiǎn)歷：
研究領(lǐng)域：
承擔科研項目情況：
社會(huì )任職：
獲獎及榮譽(yù)：
Section A (5 representative publications in recent 5 years)
1. Chen L, Hong M, Luan C, Gao H, Ru G, Guo X, Zhang D, Zhang S, Li C, Wu J, Randolph PB, Sousa AA, Qu C, Zhu Y, Guan Y, Wang L, Liu M, Feng B, Song G, Liu DR & Li D. Adenine transversion editors enable precise, efficient A？T-to-C？G base editing in mammalian cells and embryos. Nat Biotechnol Epub. Jun15 (2023).
2. He X*, Zhang Z*, Xue J, Wang Y, Zhang S, Wei J, Zhang C, Wang J, Urip BA, Ngan CC, Sun J, Li Y, Lu Z, Zhao H, Pei D, Li CK, Feng B#. Low-dose AAV-CRISPR-mediated liver-specific knock-in restored hemostasis in neonatal hemophilia B mice with subtle antibody response. Nat Comm 13:7275. (2022).
3. He X, Urip BA, Zhang Z, Ngan CC, Feng B#. Evolving AAV-delivered therapeutics towards ultimate cures. J Mol Med. 99(5):593-617 (2021).
4. Wang J, Zhang C, Feng B#, The rapidly advancing Class 2 CRISPR-Cas technologies: a customizable toolbox for molecular manipulations. J Cell Mol Med. 24:3256-3270 (2020)
5. Zhang C, He X, Kwok YK, Wang F, Xue Y, Zhao H, Suen KW, Wang CC, Ren J, Chen GG, Lai BS, Li J, Xia Y, Chan AM, Chan WY#, Feng B#, Homology-independent multiallelic disruption via CRISPR/Cas9-based knock-in yields distinct functional outcomes in human cells. BMC Biology 16:151 (2018).
Section B (5 representative publications beyond recent 5 years)
1. He X, Tan C, Wang F, Wang Y, Zhou R, Cui D, You W, Zhao H, Ren J & Feng B#. Knock-in of large reporter genes in human cells via CRISPR/Cas9-induced homology-dependent and independent DNA repair, Nucleic Acids Res 44(9):e85 (2016).
2. Hu J, Lei Y, Wong WK, Liu S, Lee KC, He X, You W, Zhou R, Guo JT, Chen X, Peng X, Sun H, Huang H, Zhao H & Feng B#, Direct activation of human and mouse Oct4 genes using engineered TALE and Cas9 transcription factors, Nucleic Acids Res 42(7):4375-90 (2014).
3. Chia NY, Chan YS, Feng B*, Lu X, Orlov YL, Moreau D, Kumer P, Yang L, Jiang J, Lau MS, Huss M, Soh BS, Kraus P, Li P, Lufkin T, Lim B, Clarke ND, Bard F & Ng HH, A genome-wide RNAi screen reveals determinants of human ES cell identity. Nature 468: 316–20 (2010). (*Co-first authors)
4. Feng B, Ng JH, Heng JC, Ng HH., Molecules that promote or enhance reprogramming of somatic cells to induced pluripotent stem cells, Cell Stem Cell 4, 301-12 (2009).
5. Feng B, Jian, J, Kraus P, Ng JH, Heng JC, Chan YS, Yaw LP, Zhang W, Loh YH, Han J, Vega VB, Cacheux-Rataboul V, Lim B, Lufkin T & Ng HH, Reprogramming of fibroblasts into induced pluripotent stem cells with orphan nuclear receptor Esrrb. Nat Cell Biol 11:197-203 (2009).