Education

PhD., Shanghai Jiao Tong University, China, 2007

Current position

Associate Professor, Bio-X Institutes, Shanghai Jiao Tong University, China

Publications

1. Khan, R. I., Wang, Y., Afrin, S., Wang, B., Liu, Y., Zhang, X., Chen, L., Zhang, W., He, L. and Ma, G. (2016). Transcriptional regulator PrqR plays a negative role in glucose metabolism and oxidative stress acclimation in Synechocystis sp. PCC 6803. Sci Rep 6: 32507.
2. Wang, Y., Li, C., Khan, M. R., Wang, Y., Ruan, Y., Zhao, B., Zhang, B., Ma, X., Zhang, K., Zhao, X., Ye, G., Guo, X., Feng, G., He, L. and Ma, G. (2016). An Engineered Rare Codon Device for Optimization of Metabolic Pathways. Sci Rep 6: 20608.
3. Wu, H., Wang, Y., Wang, Y., Cao, X., Wu, Y., Meng, Z., Su, Q., Wang, Z., Yang, S., Xu, W., Liu, S., Cheng, P., Wu, J., Khan, M. R., He, L. and Ma, G. (2014). Quantitatively relating gene expression to light intensity via the serial connection of blue light sensor and CRISPRi. ACS Synth Biol 3(12): 979-982.
4. Zhu, X., Huang, S., Zhang, L., Wu, Y., Chen, Y., Tao, Y., Wang, Y., He, S., Shen, S., Wu, J., Li, B., Guo, X., He, L. and Ma, G. (2014). Constitutive activation of ectodermal beta-catenin induces ectopic outgrowths at various positions in mouse embryo and affects abdominal ventral body wall closure. PLoS One 9(3): e92092.
5. Zhu, X., Wu, Y., Huang, S., Chen, Y., Tao, Y., Wang, Y., He, S., Shen, S., Wu, J., Guo, X., Li, B., He, L. and Ma, G. (2014). Overexpression of Wnt5a in mouse epidermis causes no psoriasis phenotype but an impairment of hair follicle anagen development. Exp Dermatol 23(12): 926-928.
6. Huang, S., Zhu, X., Liu, Y., Tao, Y., Feng, G., He, L., Guo, X. and Ma, G. (2012). Wls is expressed in the epidermis and regulates embryonic hair follicle induction in mice. PLoS One 7(9): e45904.
7. Ma, G., Li, L., Hu, Y., Chau, J. F., Au, B. J., Jia, D., Liu, H., Yeh, J., He, L., Hao, A. and Li, B. (2012). Atypical Atm-p53 genetic interaction in osteogenesis is mediated by Smad1 signaling. J Mol Cell Biol 4(2): 118-120.
8. Ma, G., Yu, J., Xiao, Y., Chan, D., Gao, B., Hu, J., He, Y., Guo, S., Zhou, J., Zhang, L., Gao, L., Zhang, W., Kang, Y., Cheah, K. S., Feng, G., Guo, X., Wang, Y., Zhou, C. Z. and He, L. (2011). Indian hedgehog mutations causing brachydactyly type A1 impair Hedgehog signal transduction at multiple levels. Cell Res 21(9): 1343-1357.
9. Gao, B., Hu, J., Stricker, S., Cheung, M., Ma, G., Law, K. F., Witte, F., Briscoe, J., Mundlos, S., He, L., Cheah, K. S. and Chan, D. (2009). A mutation in Ihh that causes digit abnormalities alters its signalling capacity and range. Nature 458(7242): 1196-1200.
10. Ma, G., He, Z., Fang, W., Tang, W., Huang, K., Li, Z., He, G., Xu, Y., Feng, G., Zheng, T., Zhou, J., He, L. and Shi, Y. (2008). The Ser9Gly polymorphism of the dopamine D3 receptor gene and risk of schizophrenia: an association study and a large meta-analysis. Schizophr Res 101(1-3): 26-35.