Zobrazeno 1 - 10
of 106
pro vyhledávání: '"Xiao‐ping Xing"'
Autor:
Di-chen Zhao, Xiao-yun Lin, Jing Hu, Bing-na Zhou, Qian Zhang, Ou Wang, Yan Jiang, Wei-bo Xia, Xiao-ping Xing, Mei Li
Publikováno v:
BMC Musculoskeletal Disorders, Vol 24, Iss 1, Pp 1-10 (2023)
Abstract Introduction Osteoporosis leads to more serious consequences in men than in women, but less is known about its impacts on health-related quality of life (HRQoL) of men, and whether the anti-osteoporosis treatment can improve HRQoL of men wit
Externí odkaz:
https://doaj.org/article/96e989bae47c440b83b7b1a4ef3e5170
Autor:
Bing-na Zhou, Qian Zhang, Xiao-yun Lin, Jing Hu, Di-chen Zhao, Yan Jiang, Xiao-ping Xing, Mei Li
Publikováno v:
BMC Musculoskeletal Disorders, Vol 23, Iss 1, Pp 1-11 (2022)
Abstract Background The reduction in androgen level gives rise to a decrease in bone mineral density (BMD) and muscle strength, but the exact mechanisms are unclear. We investigated the roles of novel cytokines of sclerostin and irisin on bone and mu
Externí odkaz:
https://doaj.org/article/ec896b77b2dd40c5bf82cf9faa3238e9
Autor:
Jia-Jia Wang, Yi Yang, Ya-Bing Wang, An Song, Yan Jiang, Mei Li, Wei-Bo Xia, Yan-Ping Liu, Ou Wang, Xiao-Ping Xing
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
ObjectivesPseudohypoparathyroidism (PHP) is a rare disease, especially when combined with pregnancy. We aimed to explore the changes in serum calcium/parathyroid hormone (PTH) level and medical treatment in a case series of PHP during pregnancy and t
Externí odkaz:
https://doaj.org/article/f43aaab5c4fc4a9284db4a65c7ae0034
Autor:
Wen-bin Zheng, Jing Hu, Di-Chen Zhao, Bing-Na Zhou, Ou Wang, Yan Jiang, Wei-Bo Xia, Xiao-ping Xing, Mei Li
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
ObjectiveOsteoblasts are discovered to secrete hormones with endocrine effects on metabolism, and osteocalcin (OC) is the most abundant non-collagenous protein in bone. We investigate the relationship between serum OC levels and glycolipid metabolism
Externí odkaz:
https://doaj.org/article/5b6044928d3240b488f22c24cce7fcba
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-8 (2021)
Abstract Background Autoimmune polyendocrine syndrome type 1 (APS1) is a hereditary disease caused by mutations in the AIRE gene with both endocrine and non-endocrine organ involvement. The existing data from China are limited, and this study aims to
Externí odkaz:
https://doaj.org/article/8e2843f7f5044490be3151e623109a10
Autor:
Yan Jiang, Xiang Li, Li Huo, Yong Liu, Wei Lyu, Lian Zhou, Wei Yu, Huan-Wen Wu, Xiao-Ping Xing, Mei Li, Ou Wang, Yue Chi, Rui-Zhi Jiajue, Yu Pei, Jian-Min Liu, Jian-Ming Ba, Qiao Zhang, Zhi-Feng Sheng, Zhen-Lin Zhang, Jia-Jun Zhao, Salvatore Minisola, Wei-Bo Xia, Li-Shao Guo, on behalf of Chinese Society of Osteoporosis and Bone Mineral Research and Chinese Society of Endocrinology
Publikováno v:
Chinese Medical Journal, Vol 134, Iss 11, Pp 1264-1266 (2021)
Externí odkaz:
https://doaj.org/article/aa26dbc31e834453b3ea9f2b26ba5283
Autor:
Da Zhang, Lin Lu, Hui-Juan Zhu, Yu Xiao, Xian-Lin Han, Shun-Da Du, Hua-Dan Xue, Qing-Xing Liu, Zhao-Hui Zhu, Ming-Ming Hu, Xiao Zhai, Xiao-Ping Xing, Zhao-Lin Lu
Publikováno v:
International Journal of Endocrinology, Vol 2022 (2022)
Objectives. To analyze and summarize the effect of SSA treatment on EAS due to p-NETs (EAS-p-NETs). Methods. Thirteen patients with EAS-p-NETs treated with SSAs at our center or described in the literature were included in this study. Clinical charac
Externí odkaz:
https://doaj.org/article/4af07185acd04753a2f2bd4e3874a349
Autor:
Lu Yuan, Ruo-xi Liao, Yuan-yuan Lin, Yan Jiang, Ou Wang, Mei Li, Xiao-ping Xing, Qian-qian Pang, Evelyn Hsieh, Wei-bo Xia
Publikováno v:
Journal of Orthopaedic Translation, Vol 18, Iss , Pp 109-118 (2019)
Background: Primary hypertrophic osteoarthropathy (PHO) is a rare disease involving joint, bone and skin. Two underlying genes responsible for this disease—hydroxyprostaglandin dehydrogenase (HPGD) and solute carrier organic anion transporter famil
Externí odkaz:
https://doaj.org/article/073fb1f07c134ccbb21748f30e5f5363
Autor:
Lu-Jiao Li, Fang Lyu, Yu-Wen Song, Ou Wang, Yan Jiang, Wei-Bo Xia, Xiao-Ping Xing, Mei Li, Xin Chen
Publikováno v:
Chinese Medical Journal, Vol 132, Iss 2, Pp 145-153 (2019)
Abstract. Background:. Osteogenesis imperfecta (OI), a heritable bone fragility disorder, is mainly caused by mutations in COL1A1 gene encoding α1 chain of type I collagen. This study aimed to investigate the COL1A1 mutation spectrum and quantitativ
Externí odkaz:
https://doaj.org/article/12a69068ecfc4001ba1ae6c743729241
Autor:
Jing Hu, Lu‐jiao Li, Wen‐bin Zheng, Di‐chen Zhao, Ou Wang, Yan Jiang, Xiao‐ping Xing, Mei Li, Weibo Xia
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 12, Pp n/a-n/a (2020)
Abstract Background Osteogenesis imperfecta (OI) is a phenotypically and genetically heterogeneous bone disease characterized by bone fragility and recurrent fractures. X‐linked inherited OI with mutation in PLS3 is so rare that its genotype–phen
Externí odkaz:
https://doaj.org/article/efb8c0809faa4565b3ab112bcb672bdb