Dejun Li

发表

Mutational analysis of the androgen receptor gene in two Chinese families with complete androgen insensitivity syndrome

Song Wang, Haikun Xu, W. An, 2016, Experimental and therapeutic medicine.

Identification of a novel frameshift mutation of the EXT2 gene in a family with multiple osteochondroma

Peng Xia, Haikun Xu, Qingyang Shi, 2015, Oncology letters.

Gonadectomy In Conditions Affecting Sex Development - A Registry-Based Cohort Study.

K. Lachlan, S. Poyrazoglu, F. Darendeliler, 2021, European journal of endocrinology.

Complete androgen insensitivity syndrome caused by c.1769-1G > C mutation and activation of a cryptic splice acceptor site in the androgen receptor gene

Song Wang, N. Cacalano, Peng Xia, 2018, Steroids.

Treatment Adherence to Injectable Treatments in Pediatric Growth Hormone Deficiency Compared With Injectable Treatments in Other Chronic Pediatric Conditions: A Systematic Literature Review

M. Maghnie, B. Miller, R. Gomez, 2022, Frontiers in Endocrinology.

Cytogenetic and molecular characterization of an oligoasthenozoospermia male carrier of an unbalanced Y;22 translocation

Xuan Wang, Hongguo Zhang, Ruizhi Liu, 2019, Medicine.

Proteomic Discovery and Array-Based Validation of Biomarkers from Urinary Exosome by Supramolecular Probe.

W. Tao, Lianghai Hu, Muhammad Mujahid Ali, 2023, Journal of proteome research.

Polymyxin B in Patients With Renal Impairment: Is It Necessary to Adjust Dose?

Genquan Yan, Ruifang Nie, B. Leng, 2022, Frontiers in Pharmacology.

Glycoproteomic Analysis of Urinary Extracellular Vesicles for Biomarkers of Hepatocellular Carcinoma

Lianghai Hu, Shuyue Wang, Dejun Li, 2023, Molecules.