Peng Wang

PINK1 p.K520RfsX3 mutation identified in a Chinese family with early-onset Parkinson’s disease

Chengyuan Song, H. Deng, Yiming Liu, 2018, Neuroscience Letters.

The genetics of Parkinson disease

Peng Wang, Hao Deng, Joseph Jankovic, 2018, Ageing Research Reviews.

Identifying a BRCA2 c.5722_5723del mutation in a Han-Chinese family with breast cancer

Xiaorong Li, H. Deng, Shaihong Zhu, 2019, Bioscience reports.

Down‐regulation of Notch receptor signaling pathway induces caspase‐dependent and caspase‐independent apoptosis in lung squamous cell carcinoma cells

Jian-hua Zhou, J. Wen, Peng Wang, 2012, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.

[Expression of FGF-2 and osteopontin in non-small cell lung cancer].

Hongzheng Ren, Jian-hua Zhou, Haiying Jiang, 2009, Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences.

Hemizygous F8 p.G201E mutation identified in a Chinese family with haemophilia A

H. Deng, S. Deng, Han Chen, 2019, Journal of the Chinese Medical Association : JCMA.

Increased Expression of Prohibitin and its Relationship with Poor Prognosis in Esophageal Squamous Cell Carcinoma

Jin-sheng Wang, G-Q Pan, Hong-Zheng Ren, 2010, Pathology & Oncology Research.

PINK1 p.K520RfsX3 mutation identified in a Chinese family with early-onset Parkinson’s disease

Chengyuan Song, H. Deng, Yiming Liu, 2018, Neuroscience Letters.