MRNIP condensates promote DNA double-strand break sensing and end resection von Wang, Yun-Long, Zhao, Wan-Wen, Bai, Shao-Mei, Feng, Li-Li, Bie, Shu-Ying, Gong, Li, Wang, Fang, Wei, Ming-Biao, Feng, Wei-Xing, Pang, Xiao-Lin, Qin, Cao-Litao, Yin, Xin-Ke, Wang, Ying-Nai, Zhou, Weihua, Wahl, Daniel R., Liu, Quentin, Chen, Ming, Hung, Mien-Chie, Wan, Xiang-Bo

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PRMT1 enhances oncogenic arginine methylation of NONO in colorectal cancer von Yin, Xin-Ke, Wang, Yun-Long, Wang, Fei, Feng, Wei-Xing, Bai, Shao-Mei, Zhao, Wan-Wen, Feng, Li-Li, Wei, Ming-Biao, Qin, Cao-Litao, Wang, Fang, Chen, Zhi-Li, Yi, Hong-Jun, Huang, Yan, Xie, Pei-Yi, Kim, Taewan, Wang, Ying-Nai, Hou, Jun-Wei, Li, Chia-Wei, Liu, Quentin, Fan, Xin-Juan, Hung, Mien-Chie, Wan, Xiang-Bo

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Chromatin organizer SATB1 controls the cell identity of CD4+ CD8+ double-positive thymocytes by regulating the activity of super-enhancers von Feng, Delong, Chen, Yanhong, Dai, Ranran, Bian, Shasha, Xue, Wei, Zhu, Yongchang, Li, Zhaoqiang, Yang, Yiting, Zhang, Yan, Zhang, Jiarui, Bai, Jie, Qin, Litao, Kohwi, Yoshinori, Shi, Weili, Kohwi-Shigematsu, Terumi, Ma, Jing, Liao, Shixiu, Hao, Bingtao

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Prenatal finding of isolated ventricular septal defect: genetic association, outcomes and counseling von Chen, Xin, Zhang, Qian, Lu, Man, Feng, Qiuxia, Qin, Litao, Liao, Shixiu

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RNA sequencing revealed the multi-stage transcriptome transformations during the development of gallbladder cancer associated with chronic inflammation von Yang, Sen, Qin, Litao, Wu, Pan, Liu, Yanbing, Zhang, Yanling, Mao, Bing, Yan, Yiyang, Yan, Shuai, Tan, Feilong, Yue, Xueliang, Liu, Hongshan, Xue, Huanzhou

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Screening and identification of miR-181a-5p in oral squamous cell carcinoma and functional verification in vivo and in vitro von Xu, Guoqiang, Yang, Yiyan, Yang, Junting, Xiao, Lanfei, Wang, Xiaotang, Qin, Litao, Gao, Jiping, Xuan, Ruijing, Wu, Xiaofen, Chen, Zhaoyang, Sun, Rui, Song, Guohua

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Identification of a novel de novo mutation of SETBP1 and new findings of SETBP1 in tumorgenesis von Wang, Hongdan, Gao, Yue, Qin, Litao, Zhang, Mengting, Shi, Weili, Feng, Zhanqi, Guo, Liangjie, Zhu, Bofeng, Liao, Shixiu

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Long noncoding RNA SOX2‐OT facilitates laryngeal squamous cell carcinoma development by epigenetically inhibiting PTEN via methyltransferase EZH2 von Tai, Yong, Ji, Yuzi, Liu, Fei, Zang, Yanzi, Xu, Dingyuan, Ma, Song, Qin, Litao, Ma, Jiqing

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Experimental investigation of mononitrotoluene preparation in a continuous-flow microreactor von Yang, Anming, Yue, Jincai, Zheng, Shiqing, Yang, Xia, Kong, Lingqi, Zhou, Dongjian, Qin, Litao, Zhong, Hua

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Phase separation of Epstein-Barr virus EBNA2 protein reorganizes chromatin topology for epigenetic regulation von Yang, Yiting, Ye, Xidong, Dai, Ranran, Li, Zhaoqiang, Zhang, Yan, Xue, Wei, Zhu, Yongchang, Feng, Delong, Qin, Litao, Wang, Xin, Lei, Bo, Liao, Shixiu, Hao, Bingtao

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Identification of novel TMEM231 gene splice variants and pathological findings in a fetus with Meckel Syndrome von Zhang, Qian, Yang, Shuya, Chen, Xin, Wang, Hongdan, Li, Keyan, Zhang, Chaonan, Liao, Shixiu, Qin, Litao, Hou, Qiaofang

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Functional analysis of a novel nonsense variant c.91A>T of the TRAPPC2 gene in a Chinese family with X-linked recessive autosomal spondyloepiphyseal dysplasia tarda von Lou, Guiyu, Zhao, Yuanyin, Zhao, Huiru, Zhang, Yuwei, Hao, Bingtao, Qin, Litao, Liu, Hongyan, Liao, Shixiu

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METTL3-Mediated m6A RNA Methylation of ZBTB4 Interferes With Trophoblast Invasion and Maybe Involved in RSA von Huang, Nana, Gao, Yue, Zhang, Mengting, Guo, Liangjie, Qin, Litao, Liao, Shixiu, Wang, Hongdan

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Novel compound heterozygous mutations of the DOCK6 gene in a familial case of Adams-Oliver syndrome 2 von Wang, Zhaokun, Wang, Xin, Guiyu Lou, Litao Qin, Shasha Bian, Tang, Xia, Hongjie Zhu, Shengran Wang, Bingtao Hao, Shixiu Liao

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Functional Analysis of a Compound Heterozygous Mutation in the VPS13B Gene in a Chinese Pedigree with Cohen Syndrome von Lou, Guiyu, Ke, Yang, Zhang, Yuwei, Liangjie, Guo, Shama, Samaa Abdelmonem, Qi, Na, Qin, Litao, Liao, Shixiu, Zhao, Yuanyin

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Epicardium-Derived Tbx18 + CDCs Transplantation Improve Heart Function in Infarcted Mice von Guo, Zhenglong, Geng, Mengyuan, Qin, Litao, Hao, Bingtao, Liao, Shixiu

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Novel heterozygous mutations of the INSR gene in a familial case of Donohue syndrome von Qin, Litao, Li, Xiaobo, Hou, Qiaofang, Wang, Hongdan, Lou, Guiyu, Li, Tao, Wang, Li, Liu, Hongyan, Li, Xichuan, Liao, Shixiu

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Integrative Analysis Extracts a Core ceRNA Network of the Fetal Hippocampus With Down Syndrome von Wang, Shengran, Tang, Xia, Qin, Litao, Shi, Weili, Bian, Shasha, Wang, Zhaokun, Wang, Qingqing, Wang, Xin, Gu, Jianqin, Hao, Bingtao, Ding, Keyue, Liao, Shixiu

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A novel MIP mutation in familial congenital nuclear cataracts von Qin, Litao, Guo, Liangjie, Wang, Hongdan, Li, Tao, Lou, Guiyu, Guo, Qiannan, Hou, Qiaofang, Liu, Hongyan, Liao, Shixiu, Liu, Zhe

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Ubiquitin-induced RNF168 condensation promotes DNA double-strand break repair von Feng, Li-Li, Bie, Shu-Ying, Deng, Zhi-Heng, Bai, Shao-Mei, Shi, Jie, Qin, Cao-Litao, Liu, Huan-Lei, Li, Jia-Xu, Chen, Wan-Ying, Zhou, Jin-Ying, Jiao, Chun-Mei, Ma, Yi, Qiu, Meng-Bo, Ai, Hua-Song, Zheng, Jian, Hung, Mien-Chie, Wang, Yun-Long, Wan, Xiang-Bo, Fan, Xin-Juan

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