Zobrazeno 1 - 10
of 127
pro vyhledávání: '"Wei‐bo Xia"'
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:
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
Publikováno v:
eLife, Vol 12 (2023)
Plastin 3 (PLS3), a protein involved in formation of filamentous actin (F-actin) bundles, is important in human bone health. Recent studies identify PLS3 as a novel bone regulator and PLS3 mutations can lead to a rare monogenic early-onset osteoporos
Externí odkaz:
https://doaj.org/article/4b44a117e1c14a5eab38051ce4b1a4f9
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
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:
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:
Chinese Medical Journal, Vol 134, Iss 15, Pp 1869-1871 (2021)
Externí odkaz:
https://doaj.org/article/3c2c5237c23d4ca2bfd93aa86f0b2cfa
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
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-9 (2019)
Abstract Background Primary hypertrophic osteoarthropathy (PHO) is a rare disease related to HPGD and SLCO2A1 gene mutation. Gastrointestinal involvement of PHO is even rarer with unknown pathogenesis. Clinical features of GI complication in PHO mimi
Externí odkaz:
https://doaj.org/article/5bcbdbbb0b73481d9dd506d955900b4d
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