Education
PhD., Shanghai Jiao Tong University, China, 2007
Current position
Associate Professor, Bio-X Institutes, Shanghai Jiao Tong University, China
Publications
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.