Hai-Bo Mei (Haibo Mei)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 8

Top Venues

Orphanet journal of rare diseases

Experimental biology and medicine (Maywood, N.J.)

Rapid communications in mass spectrometry : RCM

Journal of cellular and molecular medicine

Hunan Children's Hospital

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

Affiliation History

Hunan Children's Hospital Jan 01 2010

China

Director :: Pediatric Orthopaedics

Publications

Qian Tan, Ge Yang, Yaoxi Liu, Ting Lei, Weihua Ye, Xin Hu, Hai-Bo Mei
Retrospective Case Analysis of 104 Cases of Talipes Equinus. Journal of environmental and public health 2022 (2022)
Yaoxi Liu, Zhen Qi Qin, Yu Zheng, Jiangyan Wu, Ge Yang, Qian Tan, Guanghui Zhu, Kun Liu, Hai-Bo Mei
New insights into pathogenesis of congenital pseudarthrosis of tibia in children using periosteum proteomics analysis. Rapid communications in mass spectrometry : RCM 36 (21) (2022)
Yu Zheng, Guanghui Zhu, Yaoxi Liu, Weihua Zhao, Yongjia Yang, Zhenqing Luo, Yuyan Fu, Hai-Bo Mei, Zhengmao Hu
Case series of congenital pseudarthrosis of the tibia unfulfilling neurofibromatosis type 1 diagnosis: 21% with somatic NF1 haploinsufficiency in the periosteum. Human genetics 141 (8) (2022)
Ge Yang, Hui Yu, Yaoxi Liu, Weihua Ye, Guanghui Zhu, An Yan, Qian Tan, Hai-Bo Mei
Serum-derived exosomes from neurofibromatosis type 1 congenital tibial pseudarthrosis impaired bone by promoting osteoclastogenesis and inhibiting osteogenesis. Experimental biology and medicine (Maywood, N.J.) 246 (2) (2020)
Qian Tan, Jiang-Yan Wu, Yao-Xi Liu, Kun Liu, Jin Tang, Wei-Hua Ye, Guang-Hui Zhu, Hai-Bo Mei, Ge Yang
The neurofibromatosis type I gene promotes autophagy via mTORC1 signalling pathway to enhance new bone formation after fracture. Journal of cellular and molecular medicine 24 (19) (2020)
Yaoxi Liu, Ge Yang, Kun Liu, Jiangyan Wu, Guanghui Zhu, Jin Tang, Yu Zheng, Hai-Bo Mei
Combined surgery with 3-in-1 osteosynthesis in congenital pseudarthrosis of the tibia with intact fibula. Orphanet journal of rare diseases 15 (1) (2020)
Guanghui Zhu, Yu Zheng, Yaoxi Liu, An Yan, Zhengmao Hu, Yongjia Yang, Shiting Xiang, Liping Li, Weijian Chen, Yu Peng, Nanbert Zhong, Hai-Bo Mei
Identification and characterization of NF1 and non-NF1 congenital pseudarthrosis of the tibia based on germline NF1 variants: genetic and clinical analysis of 75 patients. Orphanet journal of rare diseases 14 (1) (2019)
Yongjia Yang, Yu Zheng, Wangming Li, Liping Li, Ming Tu, Liu Zhao, Hai-Bo Mei, Guanghui Zhu, Yimin Zhu
SMAD6 is frequently mutated in nonsyndromic radioulnar synostosis. Genetics in medicine : official journal of the American College of Medical Genetics 21 (11) (2019)

Hai-Bo Mei.css-eqlu8i{font-size:small;padding-left:4px;} (Haibo Mei)

Publication Activity (10 Years)

Top Topics

Top Venues

Hai-Bo Mei (Haibo Mei)