Kai Yang

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 6

Top Topics

Left Ventricular

Tyrosine Kinase

Top Venues

Molecular genetics & genomic medicine

Cell death discovery

This page only lists publications with an associated author ORCID identifier.

Publications

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
Functional assessment of a novel biallelic MYH3 variation causing CPSKF1B (contractures, pterygia, and spondylocarpotarsal fusion syndrome1B). Molecular genetics & genomic medicine 12 (3) (2024)
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
Functional assessment of a novel biallelic MYH3 variation causing CPSKF1B (contractures, pterygia, and spondylocarpotarsal fusion syndrome1B). Molecular genetics & genomic medicine 12 (3) (2024)
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
Assessment of a novel variation in DHODH gene causing Miller syndrome: The first report in Chinese population. Molecular genetics & genomic medicine (2023)
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
NTRK1 knockdown induces mouse cognitive impairment and hippocampal neuronal damage through mitophagy suppression via inactivating the AMPK/ULK1/FUNDC1 pathway. Cell death discovery 9 (1) (2023)
Li-Min Cui, Jian-Ye Jiang, Ning-Ning Hu, Hong-En Zou, Bao-Zhen Zhao, Cong-Ying Han, Kai Yang, Yi-Peng Wang, Huan-Xia Xing
Whole exome sequencing identified a novel compound heterozygous variation in COL7A1 gene causing dystrophic epidermolysis bullosa. Molecular genetics & genomic medicine 10 (5) (2022)
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
Prenatal Cases Reflect the Complexity of the COL1A1/2 Associated Osteogenesis Imperfecta. Genes 13 (9) (2022)