Rapid syntheses of N-fused heterocycles via acyl-transfer in heteroaryl ketones von Ye, Dan, Lu, Hong, He, Yi, Zheng, Zhaojing, Wu, Jinghao, Wei, Hao

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Anti-Obesity and Gut Microbiota Modulation Effect of Secoiridoid-Enriched Extract from Fraxinus mandshurica Seeds on High-Fat Diet-Fed Mice von Guo, Sen, Zhao, Haoan, Ma, Zhongxiao, Zhang, Shanshan, Li, Mingrou, Zheng, Zhaojing, Ren, Xiameng, Ho, Chi-Tang, Bai, Naisheng

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Nickel‐Catalyzed Directed Benzylation of Ortho C−H Bonds in Aromatic Amides through C−H/C−N Cleavage von Li, Jiawei, Zheng, Zhaojing, Xiao, Tiantian, Xu, Peng‐Fei, Wei, Hao

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A novel missense mutation of TNNI2 in a Chinese family cause distal arthrogryposis type 1 von Wang, Bo, Zheng, Zhaojing, Wang, Zhigang, Zhang, Xiaoqing, Yang, Haiou, Cai, Haiqing, Fu, Qihua

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Screening for coding variants in FTO and SH2B1 genes in Chinese patients with obesity von Zheng, Zhaojing, Hong, Li, Huang, Xiaodong, Yang, Peirong, Li, Juan, Ding, Yu, Yao, Ru-En, Geng, Juan, Shen, Yongnian, Shen, Yiping, Fu, Qihua, Yu, Yongguo

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Nitrogen atom insertion into arenols to access benzazepines von He, Yi, Wang, Juanjuan, Zhu, Tongtong, Zheng, Zhaojing, Wei, Hao

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Brønsted Acid‐Catalyzed Markovnikov Hydroarylation of Arylcyclobutene: A Route to gem‐Diaryl‐Substituted Cyclobutanes von Wang, Xiuhong, Sun, Zhening, Wang, Juanjuan, Zheng, Zhaojing, Lu, Hong, Wei, Hao

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A non-covalent binding strategy for the stabilization of fish collagen triple helices to promote its applications von Sun, Zhening, Ge, Yihao, Cai, Xinhui, Liu, Qian, Yang, Zhiwei, Chen, Xi, Zheng, Zhaojing

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Three novel missense mutations in the filamin B gene are associated with isolated congenital talipes equinovarus von Yang, Haiou, Zheng, Zhaojing, Cai, Haiqing, Li, Huimin, Ye, Xingchen, Zhang, Xiaoqing, Wang, Zhigang, Fu, Qihua

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Molecular diagnostics for congenital heart disease: a narrative review of the current technologies and applications von Zu, Bailing, Zheng, Zhaojing, Fu, Qihua

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Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield von Geng, Juan, Picker, Jonathan, Zheng, Zhaojing, Zhang, Xiaoqing, Wang, Jian, Hisama, Fuki, Brown, David W, Mullen, Mary P, Harris, David, Stoler, Joan, Seman, Ann, Miller, David T, Fu, Qihua, Roberts, Amy E, Shen, Yiping

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Toll-like receptor 6 V327M polymorphism is associated with an increased risk of Klebsiella pneumoniae infection von Yang, Haiou, Zhang, Xiaoqing, Geng, Juan, Zheng, Zhaojing, Fu, Qihua

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A novel GJA1 mutation identified by whole exome sequencing in a Chinese family with autosomal dominant syndactyly von You, Guolin, Cai, Haiqing, Jiang, Limin, Zheng, Zhaojing, Wang, Bo, Fu, Qihua, Wang, Jing

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Rare Copy Number Variations Might Not be Involved in the Molecular Pathogenesis of PA–IVS in an Unselected Chinese Cohort von He, Xiaomin, Zhang, Xiaoqing, Jing, Hui, Zhang, Xiaoyang, Gao, Manchen, Chen, Huiwen, Geng, Juan, Zheng, Zhaojing, Fu, Qihua, Zhu, Zhongqun, Zheng, Jinghao

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A New Subtype of Multiple Synostoses Syndrome Is Caused by a Mutation in GDF6 That Decreases Its Sensitivity to Noggin and Enhances Its Potency as a BMP Signal von Wang, Jian, Yu, Tingting, Wang, Zhigang, Ohte, Satoshi, Yao, Ru‐en, Zheng, Zhaojing, Geng, Juan, Cai, Haiqing, Ge, Yihua, Li, Yuchan, Xu, Yunlan, Zhang, Qinghua, Gusella, James F, Fu, Qihua, Pregizer, Steven, Rosen, Vicki, Shen, Yiping

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Molecular defects identified by whole exome sequencing in a child with Fanconi anemia von Zheng, Zhaojing, Geng, Juan, Yao, Ru-en, Li, Caihua, Ying, Daming, Shen, Yongnian, Ying, Lei, Yu, Yongguo, Fu, Qihua

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A unique combination of 17pter trisomy and 21qter monosomy in a boy with developmental delay, severe intellectual disability, growth retardation and dysmorphisms von Zheng, Zhaojing, Yao, Ru-en, Geng, Juan, Jin, Xingming, Shen, Yongnian, Ying, Daming, Fu, Qihua, Yu, Yongguo

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Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield von Geng, Juan, Picker, Jonathan, Zheng, Zhaojing, Zhang, Xiaoqing, Wang, Jian, Hisama, Fuki, Brown, David W, Mullen, Mary P, Harris, David, Stoler, Joan, Seman, Ann, Miller, David T, Fu, Qihua, Roberts, Amy E, Shen, Yiping

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Identification of LDLR mutations in two Chinese pedigrees with familial hypercholesterolemia von Yao, Ru-en, Wang, Jian, Geng, Juan, Zheng, Zhaojing, Yu, Tingting, Yu, Yongguo, Fu, Qihua

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Elevated NKT cell levels in adults with severe chronic immune thrombocytopenia von XU, RUILONG, ZHENG, ZHAOJING, MA, YONGJUN, HU, YINGPING, ZHUANG, SHUNHONG, WEI, BIN, LU, JIANXING

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