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Hereditas|June 2, 2021
Somatic frameshift mutation in PIK3CA causes CLOVES syndrome by provoking PI3K/AKT/mTOR pathwayWei Yan, Bin Zhang, Huijun Wang, et al.Biochemical and Biophysical Research Communications|February 5, 2013
A new Nav1.7 mutation in an erythromelalgia patientMark Estacion, Yang Yang, Sulayman D Dib-Hajj, et al.Marine Pollution Bulletin|September 2, 2023
Understanding the efficiency of "political attention and governance action" on marine waste discharge in the coastal provinces in ChinaChao YangThe Journal of Investigative Dermatology|March 6, 2021
Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular KeratinocytesZhongya Song, Xi Chen, Qian Zhao, et al.Experimental Dermatology|February 22, 2023
Biallelic mutations in LSS in autosomal-recessive mutilating palmoplantar keratodermaShengru Zhou, Xingyuan Jiang, Yuhao Zhu, et al.Biochemical and Biophysical Research Communications|October 6, 2009
Erythromelalgia mutation L823R shifts activation and inactivation of threshold sodium channel Nav1.7 to hyperpolarized potentialsAngelika Lampert, Sulayman D Dib-Hajj, Emmanuella M Eastman, et al.The Journal of Investigative Dermatology|January 23, 2022
KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes AlopeciaJun Cui, Qian Zhao, Zhongya Song, et al.Asian Journal of Andrology|August 27, 2013
The miRNA let-7a1 inhibits the expression of insulin-like growth factor 1 receptor (IGF1R) in prostate cancer PC-3 cellsLi-Na Wang, Wei-Wen Chen, Ju Zhang, et al.Pageof 731