骨量和肌肉双变量复杂性状与11个候选基因68个SNP和单倍型的核心家系连锁和群体关联分析

81170803
2011
H0712.骨转换、骨代谢异常及钙磷代谢异常
章振林
面上项目
教授
上海交通大学
55万元
核心家系;骨密度;肌肉量;风险基因型;遗传变异
2012-01-01到2015-12-31
  • 中英文摘要
  • 结题摘要
  • 结题报告
  • 项目成果
  • 项目参与人
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序号 标题 类型 作者
1 Establishing Reference Intervals for Bone Turnover Markers in the Healthy Shanghai Population and the Relationship with Bone Mineral Density in Postmenopausal Women 期刊论文 Zhang, Hao|Yue, Hua|Gu, Jie-Mei|Zhang, Zhen-Lin|
2 血清硬骨素水平和基因多态性与中国绝经后妇女骨密度和骨转换指标的关系 期刊论文 章振林|
3 Association of single nucleotide polymorphism Rs2236518 in PRDM16 gene with BMI in Chinese males 期刊论文 Hu, Yun-qiu|Li, Miao|Liu, Yu-juan|Zhang, Zhen-lin|
4 Lean Mass Predicts Hip Geometry and Bone Mineral Density in Chinese Men and Women and Age Comparisons of Body Composition. 期刊论文 Hu Yun-Qiu|Fu Wen-Zhen|Li Miao|Zhang Zhen-Lin|
5 Association of ALOX15 gene polymorphisms with obesity-related phenotypes in Chinese nuclear families with male offspring 期刊论文 Li, Miao|Liu, Yu-juan|Fu, Wen-zhen|Zhang, Zhen-lin|
6 Associations of Serum Sclerostin and Polymorphisms in the SOST Gene With Bone Mineral Density and Markers of Bone Metabolism in Postmenopausal Chinese Women 期刊论文 Li, Miao|Liu, Yu-juan|Zheng, Hui|Zhang, Zhen-lin|
7 Contribution of Myostatin gene polymorphisms to normal variation in lean mass, fat mass and peak BMD in Chinese male offspring 期刊论文 Li, Miao|Liu, Yu-juan|Wu, Song-hua|Zhang, Zhen-lin|
8 SOST基因多态性在中国女性中与骨代谢指标的关系 会议论文
9 Susceptibility genes for osteoporotic fracture in postmenopausal Chinese women. 期刊论文 Fu, Wen-Zhen|Yue, Hua|Ke, Yao-Hua|Zhang, Zhen-Lin|
10 Associations of polymorphisms in the SOST gene and bone mineral density in postmenopausal Chinese Women 期刊论文 Hu, Yun-Qiu|Li, Miao|Fu, Wen-Zhen|Zhang, Zhen-Lin|
11 A novel mutation in the SLCO2A1 gene in a Chinese family with primary hypertrophic osteoarthropathy 期刊论文 He, Jin-Wei|Fu, Wen-Zhen|Zhang, Chang-Qing|Zhang, Zhen-Lin|
12 Association of ALOX12 and ALOX15 gene polymorphisms with age at menarche and natural menopause in Chinese women. 期刊论文 Li Miao|Fu Wen-Zhen|Liu Yu-Juan|Zhang Zhen-Lin|
13 Identification of one novel mutation in the C-propeptide of COL2A1 in a Chinese family with spondyloperipheral dysplasia 期刊论文 He, Jin-Wei|Fu, Wen-Zhen|Zhang, Chang-Qing|Zhang, Zhen-Lin|
14 A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family 期刊论文 Hu, Yun-Qiu|Li, Miao|Fu, Wen-Zhen|Zhang, Zhen-Lin|
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