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Molecular Cell|September 24, 2019
Histone Modifications Regulate Chromatin Compartmentalization by Contributing to a Phase Separation MechanismLiang Wang, Yifei Gao, Xiangdong Zheng, et al.
The EMBO Journal|January 7, 2021
Crystal structure of bacterial cytotoxic necrotizing factor CNFY reveals molecular building blocks for intoxicationPaweena Chaoprasid, Peer Lukat, Sabrina Mühlen, et al.
Neurobiology of Disease|September 7, 2024
Dynamic cerebellar and sensorimotor network compensation in tremor-dominated Parkinson's diseaseBo Shen, Qun Yao, Wei Li, et al.
Oncogene|August 20, 2024
Alternative splicing of ALDOA confers tamoxifen resistance in breast cancerShiyi Yu, Rui Wu, Yue Si, et al.
CNS Neuroscience & Therapeutics|November 10, 2024
Static and Dynamic Functional Network Connectivity in Parkinson's Disease Patients With Postural Instability and Gait DisorderBo Shen, Qun Yao, Yixuan Zhang, et al.
Journal of Medical Genetics|January 1, 2020
Increased TBX6 gene dosages induce congenital cervical vertebral malformations in humans and miceXiaojun Ren, Nan Yang, Nan Wu, et al.
Human Molecular Genetics|October 12, 2018
TBX6 compound inheritance leads to congenital vertebral malformations in humans and miceNan Yang, Nan Wu, Ling Zhang, et al.
Kidney International|May 26, 2020
Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndromeNan Yang, Nan Wu, Shuangshuang Dong, et al.
American Journal of Human Genetics|January 12, 2021
Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndromeNa Chen, Sen Zhao, Angad Jolly, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 15, 2019
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage modelJiaqi Liu, Nan Wu, , et al.
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