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Journal of Autism and Developmental Disorders|November 23, 2021
Novel Variants of the SMARCA4 Gene Associated with Autistic Features Rather Than Typical Coffin-Siris Syndrome in Eight Chinese Pediatric PatientsYanyan Qian, Yuanfeng Zhou, Bingbing Wu, et al.Oncogene|June 26, 2019
Upregulation of IL-6 in CUL4B-deficient myeloid-derived suppressive cells increases the aggressiveness of cancer cellsZhiliang Xu, Linchuan Li, Yanyan Qian, et al.Journal of Cell Science|September 6, 2014
CRL4B interacts with and coordinates the SIN3A-HDAC complex to repress CDKN1A and drive cell cycle progressionQinghong Ji, Huili Hu, Fan Yang, et al.Human Molecular Genetics|February 27, 2022
mTOR pathway repressing expression of FoxO3 is a potential mechanism involved in neonatal white matter dysplasiaXiuyun Liu, Chen Dong, Kaiyi Liu, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|April 11, 2021
TRERNA1 upregulation mediated by HBx promotes sorafenib resistance and cell proliferation in HCC via targeting NRAS by sponging miR-22-3pWei Song, Chuqian Zheng, Min Liu, et al.Molecular Medicine Reports|January 21, 2022
CpG site hypomethylation at ETS1‑binding region regulates DLK1 expression in Chinese patients with Tetralogy of FallotGuixiang Tian, Lili He, Ruoyi Gu, et al.Plos Genetics|August 16, 2018
The roles of SMYD4 in epigenetic regulation of cardiac development in zebrafishDeyong Xiao, Huijun Wang, Lili Hao, et al.Human Molecular Genetics|May 31, 2015
Lack of CUL4B leads to increased abundance of GFAP-positive cells that is mediated by PTGDS in mouse brainWei Zhao, Baichun Jiang, Huili Hu, et al.Annals of Translational Medicine|July 30, 2019
The molecular epidemiology of hyperphenylalaninemia in Uygur population: incidence from newborn screening and mutational spectraYajie Su, Huijun Wang, Nuerya Rejiafu, et al.European Journal of Medical Genetics|July 9, 2018
Early onset developmental delay and epilepsy in pediatric patients with WDR45 variantsHongbo Chen, Yanyan Qian, Sha Yu, et al.Pageof 8