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The Journal of Clinical Endocrinology and Metabolism|January 19, 2022
Phenotypic Heterogeneity and Fertility Potential of Patients With 17-Hydroxylase/17,20-lyase DeficiencyYue Xu, Shutian Jiang, Zheng Yan, et al.Clinical and Translational Medicine|January 11, 2023
In-frame deletion of SMC5 related with the phenotype of primordial dwarfism, chromosomal instability and insulin resistanceWenjiao Zhu, Yuanping Shi, Changrun Zhang, et al.Endocrine|May 7, 2016
Clinical and molecular manifestation of fifteen 17OHD patients: a novel mutation and a founder effectBing Han, Liqiong Xue, Mengxia Fan, et al.Journal of Cellular Physiology|January 12, 2018
Leukotriene B4 receptor 2 regulates the proliferation, migration, and barrier integrity of bronchial epithelial cellsMin Liu, Juan Shen, Huimin Yuan, et al.Aging|July 7, 2020
Exome sequencing identifies somatic mutations in novel driver genes in non-small cell lung cancerManman Zhang, Lele Zhang, Yan Li, et al.Environmental Pollution (Barking, Essex : 1987)|November 20, 2020
Subchronic exposure to concentrated ambient PM2.5 perturbs gut and lung microbiota as well as metabolic profiles in miceZihan Ran, Yanpeng An, Ji Zhou, et al.Clinical Endocrinology|March 27, 2014
Phenotypic and molecular characteristics in eleven Chinese patients with 5α-reductase Type 2 deficiencyHui Zhu, Wei Liu, Bing Han, et al.The Journal of Steroid Biochemistry and Molecular Biology|September 26, 2022
Lessons from 17β-HSD3 deficiency: Clinical spectrum and complex molecular basis in Chinese patientsHui Zhu, Haijun Yao, Xuemeng Liu, et al.International Journal of Clinical and Experimental Medicine|January 1, 2015
Replication of association of nine susceptibility loci with Graves' disease in the Chinese Han populationWenhua Du, Cuige Liang, Fengyuan Che, et al.Nature Communications|May 29, 2015
eIF1A augments Ago2-mediated Dicer-independent miRNA biogenesis and RNA interferenceTingfang Yi, Haribabu Arthanari, Barak Akabayov, et al.Pageof 6