Investigation of a Novel LRP6 Variant Causing Autosomal-Dominant Tooth Agenesis by Yan-xia Huang, Chun-yan Gao, Chun-yan Zheng, Xu Chen, You-sheng Yan, Yong-qing Sun, Xing-yue Dong, Kai Yang, Dong-liang Zhang

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Assessment of a novel variation in DHODH gene causing Miller syndrome: The first report in Chinese population by Kai Yang, Li‐Man Fu, Xiao‐Yang Chu, Jing Zhang, Wen‐Qi Chen, You‐Sheng Yan, Yi‐Peng Wang, Dong‐Liang Zhang, Cheng‐Hong Yin, Qing Guo

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Investigation of a Novel NTRK1 Variation Causing Congenital Insensitivity to Pain With Anhidrosis by Kai Yang, Yi-Cheng Xu, Hua-Ying Hu, Ya-Zhou Li, Qian Li, Ying-Yi Luan, Yan Liu, Yong-Qing Sun, Zhan-Ke Feng, You-Sheng Yan, Cheng-Hong Yin

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Functional assessment of a novel biallelic MYH3 variation causing CPSKF1B (contractures, pterygia, and spondylocarpotarsal fusion syndrome1B) by Qing‐bing He, Cai‐hong Wu, Dong‐lan Sun, Jia‐yu Yuan, Hua‐ying Hu, Kai Yang, Wen‐qi Chen, You‐sheng Yan, Guang‐yue Yin, Jing Zhang, Ya‐zhou Li

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Prenatal Cases Reflect the Complexity of the <i>COL1A1/2</i> Associated Osteogenesis Imperfecta by Kai Yang, Yan Liu, Jue Wu, Jing Zhang, Hua-ying Hu, You-sheng Yan, Wen-qi Chen, Shu-fa Yang, Li-juan Sun, Yong-qing Sun, Qing-qing Wu, Cheng-hong Yin

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SGMS1 facilitates osteogenic differentiation of MSCs and strengthens osteogenesis-angiogenesis coupling by modulating Cer/PP2A/Akt pathway by Kai Yang, Ying-yi Luan, Shan Wang, You-sheng Yan, Yi-peng Wang, Jue Wu, Yong-qing Sun, Jing Zhang, Wen-qi Chen, Yu-lan Xiang, Ze-lu Li, Dong-liang Zhang, Cheng-hong Yin

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NTRK1 knockdown induces mouse cognitive impairment and hippocampal neuronal damage through mitophagy suppression via inactivating the AMPK/ULK1/FUNDC1 pathway by Kai Yang, Jue Wu, Shang Li, Shan Wang, Jing Zhang, Yi-peng Wang, You-sheng Yan, Hua-ying Hu, Ming-fang Xiong, Chao-bo Bai, Yong-qing Sun, Wen-qi Chen, Yang Zeng, Jun-liang Yuan, Cheng-hong Yin

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