Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Jiashen Shao"'
Publikováno v:
Chinese Medical Journal, Vol 136, Iss 6, Pp 749-751 (2023)
Externí odkaz:
https://doaj.org/article/095243fb91494888b8b4c6e162257621
Autor:
Huixin Zhang, Muoyan Xu, Jiashen Shao, Huifang Kong, Xudong Gao, Wei Zhang, Xiujuan Chang, Bin Yang, Yan Chen, Zheng Dong, Jiagan Huang, Zhen Zeng, Yongping Yang
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
BackgroundHepatocellular carcinoma (HCC) is the major cause of malignancy-related deaths worldwide, and its incidence is likely to increase in the future as life expectancy increases. Therefore, the management of elderly patients with HCC has become
Externí odkaz:
https://doaj.org/article/13507dad55484166ad04e7624e71968a
Autor:
Nan Wu, Jiashen Shao, Zhen Zhang, Shengru Wang, Ziquan Li, Sen Zhao, Yang Yang, Lian Liu, Chenxi Yu, Sen Liu, Zhengye Zhao, You Du, Yuanqiang Zhang, Lianlei Wang, Yu Zhao, Keyi Yu, Hong Zhao, Jianxiong Shen, Guixing Qiu, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, Zhihong Wu, Terry Jianguo Zhang
Publikováno v:
BMC Musculoskeletal Disorders, Vol 22, Iss 1, Pp 1-9 (2021)
Abstract Introduction Adult non-degenerative scoliosis accounts for 90% of spinal deformities in young adults. However, perioperative complications and related risk factors of long posterior instrumentation and fusion for the treatment of adult non-d
Externí odkaz:
https://doaj.org/article/f7848b01de9e4d2a96573bdb768135f3
Autor:
Jiashen Shao, Sen Zhao, Zihui Yan, Lianlei Wang, Yuanqiang Zhang, Mao Lin, Chenxi Yu, Shengru Wang, Yuchen Niu, Xiaoxin Li, Guixing Qiu, Jianguo Zhang, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, Zhihong Wu, Nan Wu
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-8 (2020)
Abstract Background Multiple epiphyseal dysplasia (MED) is a skeletal disorder characterized by delayed and irregular ossification of the epiphyses and early-onset osteoarthritis. At least 66% of the reported autosomal dominant MED (AD-MED) cases are
Externí odkaz:
https://doaj.org/article/7bf1e1b216ea4e42bd4d8cbcb3db0775
Autor:
Mei Kang, Hui Zhang, Jia Zhang, Kaifeng Huang, Jinyan Zhao, Jie Hu, Cong Lu, Jiashen Shao, Jianrong Weng, Yuemin Yang, Yan Zhuang, Xianming Xu
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
ObjectiveGestational diabetes mellitus (GDM) is a serious threat to maternal and child health. However, there isn’t a standard predictive model for the disorder in early pregnancy. This study is to investigate the association of blood indexes with
Externí odkaz:
https://doaj.org/article/b2a7508ea3004581b956df6cb5a184b6
Autor:
Chenxi Yu, Bobo Xie, Zhengye Zhao, Sen Zhao, Lian Liu, Xi Cheng, Xiaoxin Li, Bingyan Cao, Jiashen Shao, Jiajia Chen, Hengqiang Zhao, Zihui Yan, Chang Su, Yuchen Niu, Yanning Song, Liya Wei, Yi Wang, Xiaoya Ren, Lijun Fan, Beibei Zhang, Chuan Li, Baoheng Gui, Yuanqiang Zhang, Lianlei Wang, Shaoke Chen, Jianguo Zhang, Zhihong Wu, Chunxiu Gong, Xin Fan, Nan Wu
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
PurposeCongenital growth hormone deficiency (GHD) is a rare and etiologically heterogeneous disease. We aim to screen disease-causing mutations of GHD in a relatively sizable cohort and discover underlying mechanisms via a candidate gene-based mutati
Externí odkaz:
https://doaj.org/article/a76e8af7593342fb889a7a0b09459c4c
Autor:
Baoheng Gui, Chenxi Yu, Xiaoxin Li, Sen Zhao, Hengqiang Zhao, Zihui Yan, Xi Cheng, Jiachen Lin, Haiyang Zheng, Jiashen Shao, Zhengye Zhao, Lina Zhao, Yuchen Niu, Zhi Zhao, Huizi Wang, Bobo Xie, Xianda Wei, Chunrong Gui, Chuan Li, Shaoke Chen, Yi Wang, Yanning Song, Chunxiu Gong, Terry Jianguo Zhang
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
PurposeROR2, a member of the ROR family, is essential for skeletal development as a receptor of Wnt5a. The present study aims to investigate the mutational spectrum of ROR2 in children with short stature and to identify the underlying molecular mecha
Externí odkaz:
https://doaj.org/article/dedeaba4d25c45a883232970fa5d6644
Autor:
Yang Yang, Sen Zhao, Yuanqiang Zhang, Shengru Wang, Jiashen Shao, Bowen Liu, Yaqi Li, Zihui Yan, Yuchen Niu, Xiaoxin Li, Lianlei Wang, Yongyu Ye, Xisheng Weng, Zhihong Wu, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, Jianguo Zhang, Nan Wu
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)
Abstract Background Congenital scoliosis (CS) is a spinal deformity due to vertebral malformations. Although insufficiency of TBX6 dosage contributes to a substantial proportion of CS, the molecular etiology for the majority of CS remains largely unk
Externí odkaz:
https://doaj.org/article/74e5faaeafbb4c1aa0dfcd1609fc32c1
Autor:
Yang Sun, Yingfei Ma, Ping Lin, Yi-Wei Tang, Liying Yang, Yinzhong Shen, Renfan Zhang, Li Liu, Jun Cheng, Jiashen Shao, Tangkai Qi, Yan Tang, Rentian Cai, Liqian Guan, Bin Luo, Meiyan Sun, Ben Li, Zhiheng Pei, Hongzhou Lu
Publikováno v:
Emerging Microbes and Infections, Vol 5, Iss 1, Pp 1-7 (2016)
The purpose of this study was to identify fecal bacterial microbiome changes in patients with chronic human immunodeficiency virus (HIV) infection in China. Bacterial 16S rRNA genes were amplified, sequenced (454 pyrosequencing), and clustered into o
Externí odkaz:
https://doaj.org/article/0a2a02868c244827b4184be566a9ddad
Publikováno v:
International Journal of Endocrinology, Vol 2016 (2016)
Objective. To identify factors predicting the need for insulin therapy in pregnancies complicated by gestational diabetes mellitus (GDM). Methods. A total of 1352 patients with GDM diagnosed by the 75-g/2-h oral glucose tolerance test (OGTT) were enr
Externí odkaz:
https://doaj.org/article/a68f19a48e92402e9e98a2c10f0ea7d3