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Recent Publications
Lian Liu, Linzhi Zou, Kuan Li, Hanqing Hou, Qun Hu, Shuang Liu, Jie Li, Chenmeng Song, Jiaofeng Chen, Shufeng Wang, Yangzhen Wang, Changri Li, Haibo Du, Jun-Liszt Li, Fangyi Chen, Zhigang Xu, Wenzhi Sun, Qianwen Sun, Wei Xiong?, Template-independent genome editing in the Pcdh15av-3j mouse, a model of human DFNB23 nonsyndromic deafness. Cell Reports 40, 111061.
Jie Li, Shuang Liu, Chenmeng Song, Tong Zhu, Zhikai Zhao, Wenzhi Sun, Yi Wang?, Lei Song?, Wei Xiong?, Prestin-mediated frequency selectivity does not cover ultrahigh frequencies in mice. Neuroscience Bulletin 38, 17.
Yan, Y., Tian, M., Li, M., Zhou, G., Chen, Q., Xu, M., Hu, Y., Luo, W., Guo, X., Zhang, C., Xie, H., Wu, Q. F., Xiong, W.?, Liu, S.?, and Guan, J. S.? (2022) ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder. Neuron 6273 (21) 01090-4.
Zhang, Y., Lin, G., Wang, Y.?, Xue, N., Lin, X., Du, T.?, Xiong, W.?, and Song, L.? (2021) Prestin derived OHC surface area reduction underlies age-related rescaling of frequency place coding. Hear Res, 108406.
Song, C., Li, J., Liu, S., Hou, H., Zhu, T., Chen, J., Liu, L., Jia, Y., and Xiong, W.? (2021) An L1 retrotransposon insertion induced deafness mouse model for studying the development and function of the cochlear stria vascularis. Proc Natl Acad Sci U S A 118 (40) e2107933118.
Li, J., Liu, S., Song, C., Hu, Q., Zhao, Z., Deng, T., Zou, L., Wang, S., Chen, J., Liu, L., Hou, H., Yuan, K., Zheng, H., Liu, Z., Chen, X., Sun, W., Xiao, B., and Xiong, W.? (2021) Piezo2 mediates ultrasonic hearing via cochlear outer hair cells in mice. Proc Natl Acad Sci U S A 118 (28) e2101207118.
Du, H., Zou, L., Ren, R., Li, N., Li, J., Wang, Y., Sun, J., Yang, J., Xiong, W.?, and Xu, Z.? (2020). Lack of PDZD7 long isoform disrupts ankle-link complex and causes hearing loss in mice. FASEB J 34, 1136-1149.
Wang, Y., Su, F., Wang, S., Yang, C., Tian, Y., Yuan, P., Liu, X., Xiong, W.?, and Zhang, C.? (2019) Efficient implementation of convolutional neural networks in the data processing of two-photon in vivo imaging. Bioinformatics 35, 3208-3210.
Liu, S., Wang, S., Zou, L., Li, J., Song, C., Chen, J., Hu, Q., Liu, L., Huang, P., and Xiong, W.? (2019). TMC1 is an essential component of a leak channel that modulates tonotopy and excitability of auditory hair cells in mice. Elife 8, e47441.
Hu, Q., Guo, L., Li, J., Song, C., Yu, L.?, He, D.Z.Z.?, and Xiong, W.? (2018). Deletion of Kncn Does Not Affect Kinocilium and Stereocilia Bundle Morphogenesis and Mechanotransduction in Cochlear Hair Cells. Front Mol Neurosci 11, 326.
Wang, Y.F., Li, J., Yao, X.R., Li, W., Du, H.B., Tang, M.L., Xiong, W., Chai, R.J., and Xu, Z.G. (2017). Loss of CIB2 Causes Profound Hearing Loss and Abolishes Mechanoelectrical Transduction in Mice. Front Mol Neurosci 10.
Chen, J., Zhang, X., Li, J., Song, C., Jia, Y.?, and Xiong, W.? (2016). Identification of a Novel ENU-Induced Mutation in Mouse Tbx1 Linked to Human DiGeorge Syndrome. Neural Plast 2016, 5836143.
Reviews and Books
Liu, S., Wang, S., Zou, L., and Xiong, W.? (2021) Mechanisms in cochlear hair cell mechano-electrical transduction for acquisition of sound frequency and intensity. Cell Mol Life Sci 78, 5083-5094.
Xiong, W. and Xu, Z. (2018) Mechanotransduction of the Hair Cell. Springer Singapore
Early Publications
Beurg, M., Xiong, W., Zhao, B., Müller, U., and Fettiplace, R. (2015) Subunit determination of the conductance of hair-cell mechanotransducer channels. Proc Natl Acad Sci U S A112, 1589-1594.
Xiong, W.?, T. Wagner, L. Yan, N. Grillet, and U. Müller.? (2014). Using Injectoporation to Deliver Genes to Mechanosensory Hair Cells. Nat Protoc 9, no. 10: 2438-49.
Xiong, W., Grillet, N., Elledge, H. M., Wagner, T. F.J., Zhao, B., Johnson, K. R., Kazmierczak, P. and Müller, U., “TMHS is an Integral Component of the Mechanotransduction Machinery of Cochlear Hair Cells,” Cell 151, no. 6 (2012): p. 1283-95.
Grillet, N.*, Xiong, W.*, Reynolds, A.*, Kazmierczak, P., Sato, T., Lillo, C., Dumont, R. A., Hintermann, E., Sczaniecka, A., Schwander, M., Williams, D., Kachar, B., Gillespie, P. G. and Müller, U., “Harmonin Mutations Cause Mechanotransduction Defects in Cochlear Hair Cells,” Neuron 62, no. 3 (2009): 375-387.
Schwander, M., Xiong, W., Tokita, J., Lelli, A., Elledge, H. M., Kazmierczak, P., Sczaniecka, A., Kolatkar, A., Wiltshire, T., Kuhn, P., Holt, J. R., Kachar, B., Tarantino, L. and Müller, U., “A Mouse Model for Nonsyndromic Deafness (Dfnb12) Links Hearing Loss to Defects in Tip Links of Mechanosensory Hair Cells,” Proc Natl Acad Sci U S A 106, no. 13 (2009): 5252-5257.
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