Xing-Hua Wang

MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy

Liang-ping Zhao, Ruo-Gu Li, X. Qiu, 2017, Clinical chemistry and laboratory medicine.

The prescriptions from Shenghui soup enhanced neurite growth and GAP-43 expression level in PC12 cells

Yue-han Song, Feng Li, Jie Ma, 2016, BMC Complementary and Alternative Medicine.

Next-generation sequencing facilitates genetic diagnosis and improves the management of patients with hearing loss in clinical practice.

Fake Li, Lihua Yu, L. Du, 2021, International journal of pediatric otorhinolaryngology.

ISL1 loss-of-function variation causes familial atrial fibrillation.

X. Qiu, Ying-Jia Xu, Yi-Qing Yang, 2020, European journal of medical genetics.

Raloxifene suppress proliferation-promoting function of estrogen in CaSKi cervical cells.

G. Lou, Jing Ma, Xiuwei Chen, 2015, International journal of clinical and experimental medicine.