Zobrazeno 1 - 10
of 160
pro vyhledávání: '"Wen-zhen Fu"'
Autor:
Xin-Yi Wei, Jing Zhang, Yin Zhang, Wen-Zhen Fu, Long-Gen Zhong, Yi-Duo Pan, Jian Sun, Xiao-Ping Liao, Ya-Hong Liu, Yu-Feng Zhou
Publikováno v:
BMC Veterinary Research, Vol 20, Iss 1, Pp 1-10 (2024)
Abstract Background Gamithromycin is an effective therapy for bovine and swine respiratory diseases but not utilized for rabbits. Given its potent activity against respiratory pathogens, we sought to determine the pharmacokinetic profiles, antimicrob
Externí odkaz:
https://doaj.org/article/3a69c9b27e6f4fc3b6824eaf8a80213e
Autor:
Su-qin Shi, Shan-shan Li, Xiao-ya Zhang, Zhe Wei, Wen-zhen Fu, Jin-wei He, Yun-qiu Hu, Miao Li, Li-li Zheng, Zhen-lin Zhang
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
ObjectiveThe current study was conducted to determine whether peak bone mineral density (BMD) and obesity phenotypes are associated with certain LGR4 gene polymorphisms found in Chinese nuclear families with female children.MethodsA total of 22 singl
Externí odkaz:
https://doaj.org/article/a75257226dfe4004bd70a18eb2828f98
Publikováno v:
Acta Pharmacol Sin
Plastin 3 (PLS3) has been identified as a candidate gene for bone fragility in the Rotterdam study (RS) population. So far, however, whether PLS3 polymorphisms are genetic risk factors for osteoporosis in Asian population remains unclear. In order to
Autor:
Hua Yue, Jin-bo Yu, Jin-wei He, Zeng Zhang, Wen-zhen Fu, Hao Zhang, Chun Wang, Wei-wei Hu, Jie-mei Gu, Yun-qiu Hu, Miao Li, Yu-juan Liu, Zhen-Lin Zhang
Publikováno v:
PLoS ONE, Vol 9, Iss 5, p e97830 (2014)
OBJECTIVE: X-linked dominant hypophosphatemia (XLH) is the most prevalent form of inherited rickets/osteomalacia in humans. The aim of this study was to identify PHEX gene mutations and describe the clinical features observed in 6 unrelated Chinese f
Externí odkaz:
https://doaj.org/article/c70bf2d1b2364494a226c7820a99d9b2
Autor:
Yi-Ming, Guo, Jian-Hao, Cheng, Hao, Zhang, Jin-Wei, He, Hua, Yue, Wei-Wei, Hu, Jie-Mei, Gu, Yun-Qiu, Hu, Wen-Zhen, Fu, Chun, Wang, Zhen-Lin, Zhang
Publikováno v:
Genes; Volume 13; Issue 3; Pages: 439
Purposes: In order to investigate the association between serum periostin levels and the variation of its encoding gene POSTN and the prevalence of vertebral fractures and bone mineral density (BMD) in Chinese postmenopausal women, an association stu
Autor:
Wei-Wei Hu, Zeng Zhang, Jin-Wei He, Wen-Zhen Fu, Chun Wang, Hao Zhang, Hua Yue, Jie-Mei Gu, Zhen-Lin Zhang
Publikováno v:
International Journal of Endocrinology, Vol 2013 (2013)
The reference ranges of bone turnover markers (BTMs) were important during the treatment of osteoporosis, and the associations with bone mineral density (BMD) were controversial. The aim of this study was to establish the reference ranges of N-termin
Externí odkaz:
https://doaj.org/article/64012d24f64c4dc382f2ccc57b713142
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e72337 (2013)
Osteogenesis imperfecta (OI) type V is an autosomal-dominant disease characterized by calcification of the forearm interosseous membrane, radial head dislocation, a subphyseal metaphyseal radiodense line, and hyperplastic callus formation. The causat
Externí odkaz:
https://doaj.org/article/b39915c82670471f9356da86fa20f980
Autor:
Han-Kui Lu, Zeng Zhang, Yao-Hua Ke, Jin-Wei He, Wen-Zhen Fu, Chang-Qing Zhang, Zhen-Lin Zhang
Publikováno v:
PLoS ONE, Vol 7, Iss 11, p e47264 (2012)
There is a lack of large-scale studies on vitamin D status and its relationship to parathyroid hormone (PTH) and bone turnover markers in adults living in Shanghai. The objectives were to determine the prevalence of vitamin D insufficiency in Shangha
Externí odkaz:
https://doaj.org/article/8474da838ed44546a7fea78596fd9090
Whole-Exome Sequencing Identifies Novel Recurrent Somatic Mutations in Sporadic Parathyroid Adenomas
Publikováno v:
Endocrinology. 159:3061-3068
Primary hyperparathyroidism is commonly caused by excess production of parathyroid hormone from sporadic parathyroid adenomas. However, the genetic architecture of sporadic primary hyperparathyroidism remains largely uncharacterized, especially in th
Autor:
Li Li, Shoukui Xiang, Yu-juan Liu, Luyue Qi, Zhen-Lin Zhang, Jin-Wei He, Wen-Zhen Fu, Yun-qiu Hu
Publikováno v:
Acta Biochimica et Biophysica Sinica. 51:341-343