Relationship Between Polymorphism of Thrombin-Activatable Fibrinolysis Inhibitor Gene +1040C/T and a Cohort of Chinese Women With Recurrent Spontaneous Abortion von Fang, Ping, Cai, Decheng, Du, Lijun, Shen, Fei, Zhang, Chengfang, Li, Meijuan

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Simulation on thermal characteristics of high-speed motorized spindle von Chen, Bin, Guan, Xin, Cai, Decheng, Li, Haolin

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Separation Promoted by Molecular Recognition of a Core Engineered Macromolecular Nanocapsule von Wan, Decheng, Pu, Hongting, Cai, Xiangyu

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Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with Hemoglobinopathies von Shang, Xuan, Peng, Zhiyu, Ye, Yuhua, Asan, Zhang, Xinhua, Chen, Yan, Zhu, Baosheng, Cai, Wangwei, Chen, Shaoke, Cai, Ren, Guo, Xiaoling, Zhang, Chonglin, Zhou, Yuqiu, Huang, Shuodan, Liu, Yanhui, Chen, Biyan, Yan, Shanhuo, Chen, Yajun, Ding, Hongmei, Yin, Xiaolin, Wu, Liusong, He, Jing, Huang, Dongai, He, Sheng, Yan, Tizhen, Fan, Xin, Zhou, Yuehong, Wei, Xiaofeng, Zhao, Sumin, Cai, Decheng, Guo, Fengyu, Zhang, Qianqian, Li, Yun, Zhang, Xuelian, Lu, Haorong, Huang, Huajie, Guo, Junfu, Zhu, Fei, Yuan, Yuan, Zhang, Li, Liu, Na, Li, Zhiming, Jiang, Hui, Zhang, Qiang, Zhang, Yijia, Juhari, Wan Khairunnisa Wan, Hanafi, Sarifah, Zhou, Wanjun, Xiong, Fu, Yang, Huanming, Wang, Jian, Zilfalil, Bin Alwi, Qi, Ming, Yang, Yaping, Yin, Ye, Mao, Mao, Xu, Xiangmin

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Mechanism Investigation of Tagetes patula L. against Chronic Nonbacterial Prostatitis by Metabolomics and Network Pharmacology von Liu, Xueying, Ran, Xiaoku, Riaz, Muhammad, Kuang, Haixue, Dou, Deqiang, Cai, Decheng

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Unusual survival of a twin with homozygous α0-thalassemia due to chimerism von Pang, Dejian, Shang, Xuan, Cai, Decheng, Yang, Fang, Lu, Huijie, Cheng, Yi, Wei, Xiaofeng, He, Fei, Xu, Xiangmin

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Whole exome sequencing identifies an AMBN missense mutation causing severe autosomal-dominant amelogenesis imperfecta and dentin disorders von Lu, Ting, Li, Meiyi, Xu, Xiangmin, Xiong, Jun, Huang, Cheng, Zhang, Xuelian, Hu, Aiqin, Peng, Ling, Cai, Decheng, Zhang, Leitao, Wu, Buling, Xiong, Fu

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Evaluation of plasma D-dimer for the diagnosis in Chinese patients with hepatocellular carcinoma: A meta-analysis von Fang, Ping, Du, Lijun, Cai, Decheng

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A tetranucleotide deletion in the ANK1 gene causes hereditary spherocytosis; a case of misdiagnosis von Zhu, Fei, Liang, Min, Xu, Linlin, Peng, Zhiyong, Cai, Decheng, Wei, Xiaofeng, Lin, Li, Shang, Xuan

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Chemical Constituents of Tagetes patula and Their Neuroprotecting Action von Liu, Linlin, Luo, Simin, Yu, Miao, Metwaly, Ahmed M., Ran, Xiaoku, Ma, Chunyan, Dou, Deqiang, Cai, Decheng

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APC c.4621CT variant causing Gardner's syndrome in a Han Chinese family may be inherited through maternal mosaicism von Cai, Decheng, He, Fei, Xu, Xiangmin, Xiong, Fu, Zhang, Leitao

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Akt phosphorylation and kinase activity are down-regulated during hibernation in the 13-lined ground squirrel von Cai, Decheng, McCarron, Richard M, Yu, Erik Z, Li, Yingyue, Hallenbeck, John

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A novel 223 kb deletion in the beta‐globin gene cluster was identified in a Chinese thalassemia major patient von Zhu, Fei, Wei, Xiaofeng, Cai, Decheng, Pang, Dejian, Zhong, Jianmei, Liang, Min, Zuo, Yangjin, Xu, Xiangmin, Shang, Xuan

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APC c.4621C>T variant causing Gardner's syndrome in a Han Chinese family may be inherited through maternal mosaicism von Cai, Decheng, He, Fei, Xu, Xiangmin, Xiong, Fu, Zhang, Leitao

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Development and Application of Portable Reflectometric Spectroscopy Combined with Solid-Phase Extraction for Determination of Potassium in Flue-Cured Tobacco Leaves von Cai, Kai, Gao, Weichang, Li, Xiang, Lin, Yechun, Li, Decheng, Quan, Wenxuan, Zhao, Ruijuan, Ren, Xueliang

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Mechanisms for Increased Levels of Phosphorylation of Elongation Factor-2 during Hibernation in Ground Squirrels von Chen, Yun, Matsushita, Masayuki, Nairn, Angus C, Damuni, Zahi, Cai, Decheng, Frerichs, Kai U, Hallenbeck, John M

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A case report of heterozygous TINF2 gene mutation associated with pulmonary fibrosis in a patient with dyskeratosis congenita von Du, Hongchun, Guo, Yubiao, Ma, Di, Tang, Kejing, Cai, Decheng, Luo, Yifeng, Xie, Canmao

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Thalassaemia intermedia caused by coinheritance of a β‐thalassaemia mutation and a de novo duplication of α‐globin genes in the paternal allele von Pang, Dejian, Shang, Xuan, Cai, Decheng, Zhu, Fei, Cheng, Yi, Zhong, Jianmei, Yi, Sheng, Zhang, Qianqian, Xu, Xiangmin

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VPS4B deficiency causes early embryonic lethality and induces signal transduction disorders of cell endocytosis von Chen, Danna, He, Fei, Lu, Ting, Huang, Jin, Li, Meiyi, Cai, Decheng, Huang, Cheng, Chen, Dong, Xiong, Fu

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Cloning and characterization of a forkhead transcription factor gene, FoxO1a, from thirteen-lined ground squirrel von Cai, Decheng, McCarron, Richard M., Hallenbeck, John

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