Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Di-Chen Zhao"'
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:
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
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
Autor:
Wen‐bin Zheng, Lu‐jiao Li, Di‐chen Zhao, Ou Wang, Yan Jiang, Wei‐bo Xia, Xiao‐ping Xing, Mei Li
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Abstract Background Spondyloepiphyseal dysplasia congenita (SEDC) is an extremely rare inherited chondrodysplasia characterized by abnormal epiphyses, short stature, and flattened vertebral bodies. We investigate the phenotypes and the disease‐asso
Externí odkaz:
https://doaj.org/article/ff8940886cf643a5858599f670ac7e65
Autor:
Jiayi Liu, Ou Wang, Lei Sun, Di‐chen Zhao, Weibo Xia, Yan Jiang, Wenbing Zheng, Bingna Zhou, Hu Jing, Mei Li, Xiaoping Xing
Publikováno v:
Endocrine. 74:270-280
The increased social and economic burdens make osteoporosis in men an emerging public health issue. However, the quality of life among men with osteoporosis is still unclear. This systematic review and meta-analysis aimed to evaluate the health-relat
Publikováno v:
Molecular Medicine Reports
Autoimmune polyendocrine syndrome type 1 (APS-1) is a rare inherited autoimmune disease, characterized by a classic triad, including chronic mucocutaneous candidiasis, primary adrenocortical insufficiency and hypoparathyroidism. The present study inv
Publikováno v:
Bone. 127:164-171
Vertebral compression fracture (VCF) is a common and severe complication of osteogenesis imperfecta (OI). We prospectively observe the changes of vertebral shape during zoledronic acid (ZOL) treatment and assess influence factors of VCF in OI childre
Autor:
Yan Jiang, Wen‐bin Zheng, Mei Li, Jing Hu, Ou Wang, Lu‐jiao Li, Xiao-ping Xing, Di‐chen Zhao, Wei-bo Xia
Publikováno v:
Bone Reports, Vol 13, Iss, Pp 100616-(2020)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
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–phenotype cha
Autor:
Yan Jiang, Mei Li, Xiaoping Xing, Wen‐bin Zheng, Di‐chen Zhao, Lu-jiao Li, Ou Wang, Weibo Xia
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Background Spondyloepiphyseal dysplasia congenita (SEDC) is an extremely rare inherited chondrodysplasia characterized by abnormal epiphyses, short stature, and flattened vertebral bodies. We investigate the phenotypes and the disease‐associated va