廖新化，男，教授。中国细胞生物学协会会员，中国实验动物协会英文期刊Animal Models and Experimental Medicine（AMEM）编委。
邮箱 liao_xinhua@hotmail.com
教育与工作经历
1996/9 - 2000/5，兰州大学，生物学学士
2000/9 - 2005/7，中科院生物化学与细胞生物学研究所，生物化学与分子生物 学博士
2005/12 - 2010/12，美国国立卫生研究院，糖尿病、消化道疾病及肾病研究所，细胞与发育生物学部，访问****/博士后
2010/12 - 2013/12，美国贝勒医学院，干细胞与再生医学研究中心，博士后
2014/2 – 2017/10，福建医科大学，转化医学研究院/基础医学院，闽江********
2017/10 – 至今， 上海大学，生命科学学院，教授
主要研究领域
皮肤和毛囊干细胞维持、激活和再生的原理
皮肤和毛发相关疾病治疗关键技术的研究
肿瘤干细胞调控的原理和相关药物的开发
代表性研究成果
1. Liao, X.H., Buggey, J., and Kimmel, A.R. (2010). Chemotactic activation of Dictyostelium AGC-family kinases AKT and PKBR1 requires separate but coordinated functions of PDK1 and TORC2. Journal of Cell Science 123, 983-992 (被 Faculty 1000推介) .
2. Liao, X.H.#, Meena, N.P., Southall, N., Liu, L., Swaroop, M., Zhang, A.L., Xiang, J.J., Parent, C.A., Zheng, W., and Kimmel, A. R. (2016) A High-Throughput, Multi-Cell Phenotype Assay for the Identification of Novel Inhibitors of Chemotaxis/Migration. Scientific Reports, 9;6:22273 (#co-corresponding author). (受Current Protocol in Cell Biology邀请撰写其中的实验方法，并由编辑在Advanced Science News撰写专评进行媒体推介).
3. Liao, X.H., Buggey, J., Lee, Y.K., and Kimmel, A.R. (2013). Chemoattractant stimulation of TORC2 is regulated by receptor/G protein-targeted inhibitory mechanisms that function upstream and independently of an essential GEF/Ras activation pathway in Dictyostelium. Molecular Biology of the Cell 24, 2146-2155.
近五年代表性论文
1. Wei, J.P., Gong, Y., Zhong, H.B., Wang, H.T. and Liao, X.H#. ( 2020) EGFL6 expression in hair follicle central isthmus is dependent on the presence of terminal Schwann cells. Experimental dermatology （发现皮肤神经和上皮细胞的互作关系）
2. Liao, X.H*., Zhang, A.L.*, Zheng, M. *, Li, M.Q., Chen, C.P., Xu, H.J., Chu, Q.S., Yang, D.Y., Lu, W.X., Tsai, T.F., Liu, H.K., Zhou, X.Z., Lu, K.P. (2017) Chemical or genetic Pin1 inhibition exerts potent anticancer activity against hepatocellular carcinoma by blocking multiple cancer-driving pathways, Scientific Reports, 6;7:43639.
3. Jiang, L.C., Wang, L., Chen, C.P., M.Q., L., and Liao, X.H.# (2017). Lgr6 is dispensable for epidermal cell proliferation and wound repair. Experimental Dermatology, 26(2):105-107.
4. Liao, X.H., and Nguyen, H. (2014). Epidermal expression of Lgr6 is dependent on nerve endings and Schwann cells. Experimental Dermatology. 23(3):195-8.
5. Wang J.C.*, Liao, X.H.*, Zheng M., Yang D.Y., Liu H.K. Zhou X.Z. and Lu K.P. (2017) The roles of prolyl isomerase Pin1 in cancer-related viral and bacterial infections, Current Molecular Medicine, 16(9):793-802 (co-first author).