Jing Ma

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 14

Top Topics

Congenital Heart Disease

Cell Proliferation

Top Venues

Journal of cellular and molecular medicine

Clinical and translational medicine

Disease markers

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

Publications

Bowen Zhang, Yongchang Zhu, Zhen Zhang, Feizhen Wu, Xiaojing Ma, Wei Sheng, Ranran Dai, Zhenglong Guo, Weili Yan, Lili Hao, Guoying Huang, Duan Ma, Bingtao Hao, Jing Ma
SMC3 contributes to heart development by regulating super-enhancer associated genes. Experimental & molecular medicine (2024)
Huanqiang Zhao, Yu Xiong, Zixiang Zhou, Qixin Xu, Yang Zi, Xiujie Zheng, Shiguo Chen, Xirong Xiao, Lili Gong, Huangfang Xu, Lidong Liu, Huiqing Lu, Yutong Cui, Shuyi Shao, Jin Zhang, Jing Ma, Qiongjie Zhou, Duan Ma, Xiaotian Li
A hidden proteome encoded by circRNAs in human placentas: Implications for uncovering preeclampsia pathogenesis. Clinical and translational medicine 14 (7) (2024)
Run Yang, Yaoyao Fu, Chenlong Li, Yin Chen, Aijuan He, Xin Jiang, Jing Ma, Tianyu Zhang
Profiling of Long Non-Coding RNAs in Auricular Cartilage of Patients with Isolated Microtia. Genetic testing and molecular biomarkers 28 (2) (2024)
Huanqiang Zhao, Yu Xiong, Zixiang Zhou, Qixin Xu, Yang Zi, Xiujie Zheng, Shiguo Chen, Xirong Xiao, Lili Gong, Huangfang Xu, Lidong Liu, Huiqing Lu, Yutong Cui, Shuyi Shao, Jin Zhang, Jing Ma, Qiongjie Zhou, Duan Ma, Xiaotian Li
A hidden proteome encoded by circRNAs in human placentas: Implications for uncovering preeclampsia pathogenesis. Clinical and translational medicine 14 (7) (2024)
Lili Hao, Jing Ma, Feizhen Wu, Xiaojing Ma, Maoxiang Qian, Wei Sheng, Tizhen Yan, Ning Tang, Xin Jiang, Bowen Zhang, Deyong Xiao, Yanyan Qian, Jin Zhang, Nan Jiang, Wenhao Zhou, Weicheng Chen, Duan Ma, Guoying Huang
WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation. Clinical and translational medicine 12 (7) (2022)
Yuexin Xu, Xiaogang Bao, Xiaoyun Chen, Peixuan Wu, Shiyu Chen, Bowen Zhang, Jing Ma, Guohua Xu, Duan Ma
STARD3NL inhibits the osteogenic differentiation by inactivating the Wnt/β-catenin pathway via binding to Annexin A2 in osteoporosis. Journal of cellular and molecular medicine 26 (5) (2022)
Jing Ma, Yu Zhang, Zijun Yan, Peixuan Wu, Chenlong Li, Run Yang, Xinyu Lu, Xin Chen, Aijuan He, Yaoyao Fu, Duan Ma, Weidong Tian, Tianyu Zhang
Single-cell transcriptomics reveals pathogenic dysregulation of previously unrecognised chondral stem/progenitor cells in children with microtia. Clinical and translational medicine 12 (2) (2022)
Mujie Ye, Runnan Gao, Shiyu Chen, Meng Wei, Jing Wang, Bowen Zhang, Suwen Wu, Yuexin Xu, Peixuan Wu, Xin Chen, Jing Ma, Duan Ma, Kuiran Dong
Downregulation of MEG3 and upregulation of EZH2 cooperatively promote neuroblastoma progression. Journal of cellular and molecular medicine 26 (8) (2022)
Shiyu Chen, Hao Li, Jicui Zheng, Lili Hao, Tianrui Jing, Peixuan Wu, Bowen Zhang, Duan Ma, Jing Zhang, Jing Ma
Expression Profiles of Exosomal MicroRNAs Derived from Cerebrospinal Fluid in Patients with Congenital Hydrocephalus Determined by MicroRNA Sequencing. Disease markers 2022 (2022)
Jing Ma, Shiyu Chen, Lili Hao, Wei Sheng, WeiCheng Chen, Xiaojing Ma, Bowen Zhang, Duan Ma, Guoying Huang
Hypermethylation-mediated down-regulation of lncRNA TBX5-AS1:2 in Tetralogy of Fallot inhibits cell proliferation by reducing TBX5 expression. Journal of cellular and molecular medicine 24 (11) (2020)
Tianrui Jing, Jing Ma, Huanqiang Zhao, Jin Zhang, Nan Jiang, Duan Ma
MAST1 modulates neuronal differentiation and cell cycle exit via P27 in neuroblastoma cells. FEBS open bio 10 (6) (2020)
Wenjun Xia, Jiongjiong Hu, Jing Ma, Jianbo Huang, Tianrui Jing, Lisha Deng, Jin Zhang, Nan Jiang, Duan Ma, Zhaoxin Ma
Mutations in TOP2B cause autosomal-dominant hereditary hearing loss via inhibition of the PI3K-Akt signalling pathway. FEBS letters 593 (15) (2019)
Wenjun Xia, Jiongjiong Hu, Jing Ma, Jianbo Huang, Xu Wang, Nan Jiang, Jin Zhang, Zhaoxin Ma, Duan Ma
Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss. Clinical genetics 96 (4) (2019)
Lili Hao, Shanshan Li, Duan Ma, Shiyu Chen, Bowen Zhang, Deyong Xiao, Jin Zhang, Nan Jiang, Shayi Jiang, Jing Ma
Two novel ANK1 loss-of-function mutations in Chinese families with hereditary spherocytosis. Journal of cellular and molecular medicine 23 (6) (2019)