Mei Li (M Li)

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 14

Top Topics

Postmenopausal Women

Bone Regeneration

Top Venues

Molecular genetics & genomic medicine

Journal of endocrinological investigation

The Journal of clinical endocrinology and metabolism

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

Publications

Jing Hu, Bingna Zhou, Xiaoyun Lin, Qian Zhang, Feifei Guan, Lei Sun, Jiayi Liu, Ou Wang, Yan Jiang, Wei-Bo Xia, Xiaoping Xing, Mei Li
Impaired bone strength and bone microstructure in a novel early-onset osteoporotic rat model with a clinically relevant PLS3 mutation. eLife 12 (2023)
Jing Hu, Bingna Zhou, Xiaoyun Lin, Qian Zhang, Feifei Guan, Lei Sun, Jiayi Liu, Ou Wang, Yan Jiang, Wei-Bo Xia, Xiaoping Xing, Mei Li
Impaired bone strength and bone microstructure in a novel early-onset osteoporotic rat model with a clinically relevant PLS3 mutation. eLife 12 (2023)
Jing Hu, Bingna Zhou, Xiaoyun Lin, Qian Zhang, Feifei Guan, Lei Sun, Jiayi Liu, Ou Wang, Yan Jiang, Wei-Bo Xia, Xiaoping Xing, Mei Li
Impaired bone strength and bone microstructure in a novel early-onset osteoporotic rat model with a clinically relevant PLS3 mutation. eLife 12 (2023)
Jing Hu, Bingna Zhou, Xiaoyun Lin, Qian Zhang, Feifei Guan, Lei Sun, Jiayi Liu, Ou Wang, Yan Jiang, Wei-Bo Xia, Xiaoping Xing, Mei Li
Impaired bone strength and bone microstructure in a novel early-onset osteoporotic rat model with a clinically relevant PLS3 mutation. eLife 12 (2023)
Jing Hu, Bingna Zhou, Xiaoyun Lin, Qian Zhang, Feifei Guan, Lei Sun, Jiayi Liu, Ou Wang, Yan Jiang, Wei-Bo Xia, Xiaoping Xing, Mei Li
Impaired bone strength and bone microstructure in a novel early-onset osteoporotic rat model with a clinically relevant PLS3 mutation. eLife 12 (2023)
Jing Hu, Bingna Zhou, Xiaoyun Lin, Qian Zhang, Feifei Guan, Lei Sun, Jiayi Liu, Ou Wang, Yan Jiang, Wei-Bo Xia, Xiaoping Xing, Mei Li
Impaired bone strength and bone microstructure in a novel early-onset osteoporotic rat model with a clinically relevant PLS3 mutation. eLife 12 (2023)
Jing Hu, Bingna Zhou, Xiaoyun Lin, Qian Zhang, Feifei Guan, Lei Sun, Jiayi Liu, Ou Wang, Yan Jiang, Wei-Bo Xia, Xiaoping Xing, Mei Li
Impaired bone strength and bone microstructure in a novel early-onset osteoporotic rat model with a clinically relevant PLS3 mutation. eLife 12 (2023)
W-B Zheng, J Hu, L Sun, J-Y Liu, Q Zhang, O Wang, Y Jiang, W-B Xia, X-P Xing, Mei Li
Correlation of lipocalin 2 and glycolipid metabolism and body composition in a large cohort of children with osteogenesis imperfecta. Journal of endocrinological investigation (2023)
Jing Hu, Bingna Zhou, Xiaoyun Lin, Qian Zhang, Feifei Guan, Lei Sun, Jiayi Liu, Ou Wang, Yan Jiang, Wei-Bo Xia, Xiaoping Xing, Mei Li
Impaired bone strength and bone microstructure in a novel early-onset osteoporotic rat model with a clinically relevant PLS3 mutation. eLife 12 (2023)
Jing Hu, Bingna Zhou, Xiaoyun Lin, Qian Zhang, Feifei Guan, Lei Sun, Jiayi Liu, Ou Wang, Yan Jiang, Wei-Bo Xia, Xiaoping Xing, Mei Li
Impaired bone strength and bone microstructure in a novel early-onset osteoporotic rat model with a clinically relevant PLS3 mutation. eLife 12 (2023)
Lei Sun, Jing Hu, Jiayi Liu, Qian Zhang, Ou Wang, Yan Jiang, Weibo Xia, Xiaoping Xing, Mei Li
Relationship of Pathogenic Mutations and Responses to Zoledronic Acid in a Cohort of Osteogenesis Imperfecta Children. The Journal of clinical endocrinology and metabolism 107 (9) (2022)
Jing Hu, Lu-Jiao Li, Wen-Bin Zheng, Di-Chen Zhao, Ou Wang, Yan Jiang, Xiao-Ping Xing, Mei Li, Weibo Xia
A novel mutation in PLS3 causes extremely rare X-linked osteogenesis imperfecta. Molecular genetics & genomic medicine 8 (12) (2020)
Wen-Bin Zheng, Lu-Jiao Li, Di-Chen Zhao, Ou Wang, Yan Jiang, Wei-Bo Xia, Xiao-Ping Xing, Mei Li
Novel variants in COL2A1 causing rare spondyloepiphyseal dysplasia congenita. Molecular genetics & genomic medicine 8 (3) (2020)
Lujiao Li, Dichen Zhao, Wenbin Zheng, Ou Wang, Yan Jiang, Weibo Xia, Xiaoping Xing, Mei Li
A novel missense mutation in P4HB causes mild osteogenesis imperfecta. Bioscience reports 39 (4) (2019)