Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Yao-Hua Ke"'
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
Autor:
Chun Wang, Yi-Ming Hu, Jin-Wei He, Jie-Mei Gu, Hao Zhang, Wei-Wei Hu, Hua Yue, Gao Gao, Wen-Jin Xiao, Jin-Bo Yu, Yao-Hua Ke, Yun-Qiu Hu, Miao Li, Yu-Juan Liu, Wen-Zhen Fu, Ying Ren, Zhen-Lin Zhang
Publikováno v:
PLoS ONE, Vol 6, Iss 12, p e28874 (2011)
Low density lipoprotein receptor-related protein 2 gene (LRP2) is located next to the genomic region showing suggestive linkage with both hip and wrist bone mineral density (BMD) phenotypes. LRP2 knockout mice showed severe vitamin D deficiency and b
Externí odkaz:
https://doaj.org/article/107eb2dc8fd14aceb7f1e93aeb512133
Autor:
Yao-Hua Ke, 柯耀華
95
The automatic generation fuzzy neural network (AGFNN) controller with supervisory control for permanent magnet linear synchronous motor (PMLSM) is proposed in this thesis. It comprises an AGFNN controller, which has ability of neuron automati
The automatic generation fuzzy neural network (AGFNN) controller with supervisory control for permanent magnet linear synchronous motor (PMLSM) is proposed in this thesis. It comprises an AGFNN controller, which has ability of neuron automati
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/krz768
Autor:
Wen-Zhen Fu, Changqing Zhang, Zhen-Lin Zhang, Yao-Hua Ke, Jin-Wei He, Zeng Zhang, Min-fang Tao
Publikováno v:
Acta Pharmacologica Sinica. 34:1070-1074
To assess associations of the serum level of 25-hydroxyvitamin D with insulin resistance and β-cell function in a healthy Chinese female population. This cross-sectional study included 1382 female participants free of type 2 diabetes who were recrui
Autor:
Hao Zhang, Jin-Wei He, Yun-qiu Hu, Wei-Wei Hu, Chun Wang, Jie-Mei Gu, Zhen-Lin Zhang, Yu-juan Liu, Yao-Hua Ke, Hua Yue, Wen-Zhen Fu, Miao Li
Publikováno v:
Acta Pharmacologica Sinica. 34:710-716
PRD1-BF-1-RIZ1 homologous domain containing protein-16 (PRDM16) is a cell-autonomous transcriptional component that stimulates the development of brown fat cells. The aim of this study was to investigate the contribution of genetic variants of PRDM16
Autor:
Miao Li, Wei-Wei Hu, Zhen-Lin Zhang, Jie-Mei Gu, Jin-Wei He, Zeng Zhang, Wen-Zhen Fu, Yu-juan Liu, Hao Zhang, Chun Wang, Yao-Hua Ke, Hua Yue, Yun-qiu Hu
Publikováno v:
Bone. 52:9-16
Introduction Inclusion-body myopathy (IBM) with Paget's disease of bone (PDB) and frontotemporal dementia (FTD), designated as IBMPFD, is a rare, autosomal dominant disorder (MIM 605382 ). IBMPFD is caused by mutations in the gene that encode valosin
Autor:
Jie-Mei Gu, Chun Wang, Hao Zhang, Weibo Xia, Yu-juan Liu, Jin-Wei He, Yun-qiu Hu, Wei-Wei Hu, Hua Yue, Yao-Hua Ke, Zhen-Lin Zhang, Wen-Zhen Fu, Zeng Zhang, Miao Li
Publikováno v:
The American Journal of Human Genetics. 90:125-132
By using whole-exome sequencing, we identified a homozygous guanine-to-adenine transition at the invariant -1 position of the acceptor site of intron 1 (c.97-1GA) in solute carrier organic anion transporter family member 2A1 (SLCO2A1), which encodes
Publikováno v:
Archives of Medical Research. 43:21-30
Background and Aims Hypophosphatasia is a genetic disorder characterized by defective bone and tooth mineralization and a deficiency of serum and bone alkaline phosphatase activity. To date, few studies have identified gene mutations in Chinese patie
Publikováno v:
Nephrology. 17:20-25
Aim: Lowe syndrome is a rare, multisystem, X-linked disorder characterized by anomalies affecting the eyes, the nervous system and the kidneys. The objective of this study was to identify and characterize the clinical manifestations of mutations of t
Autor:
Congrong Wang, Hao Zhang, Jie-Mei Gu, Yao-Hua Ke, Jin-Bo Yu, Yuan Liu, Hua Yue, Jin-Wei He, Zhijian Zhang, Wen-Zhen Fu, Maolan Li, Wei-Wei Hu, Gao Gao, Wen-jin Xiao, Yun-qiu Hu
Publikováno v:
Osteoporosis International. 23:1889-1897
Association between ten single-nucleotide polymorphisms (SNPs) in the human ALOX12 and ALOX15 genes and variations in peak bone mineral density (BMD) in a large sample of Chinese nuclear families with female offspring using the quantitative transmiss