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[会议论文] 作者:hao zhang,jin-wei he,zhen-lin zhang,
来源:第六届国际骨质疏松及骨矿盐疾病学术会议 年份:2012
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Association between frizzled-related protein gene polymorphisms and peak bmd variation in chinese nu
[会议论文] 作者:Gao Gao,Zhen-Lin Zhang,Jin-Wei He,
来源:第六届国际骨矿研究学术会议暨第八届国际骨质疏松研讨会 年份:2008
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Association between polymorphisms of clerostin domaincontaining protein 1 (SOSTDC1) gene and peak BM
[会议论文] 作者:Jin-Wei He,Hua Yue,Zhen-Lin Zhang,
来源:第六届国际骨矿研究学术会议暨第八届国际骨质疏松研讨会 年份:2008
Objective:To investigate the association of Clerostin domaincontaining protein 1(SOSTDC1) gene polymorphisms and peak bone mineral density (BMD)in Chinese women and men.Methods:We performed to genotyp...
[会议论文] 作者:Hua Yue,Zhen-lin Zhang,Jin-wei He,
来源:第六届国际骨矿研究学术会议暨第八届国际骨质疏松研讨会 年份:2008
Objective To characterize the clinical manifestations and features of photography of Progressive Pseudorheumatoid Dysplasia (PPD)(OMIM 208230) and screen the mutations of the disease causing WISP3,and...
,Novel mutations of TCIRG1 cause a malignant and mild phenotype of autosomal recessive osteopetrosis
[期刊论文] 作者:Xiao-ya ZHANG,Jin-wei HE,Wen-zhen FU,Chun WANG,Zhen-lin ZHANG,
来源:中国药理学报(英文版) 年份:2017
Human autosomal recessive osteopetrosis (ARO),also known as infantile malignant osteopetrosis,is a rare genetic bone disorder that often causes death.Mutations...
[期刊论文] 作者:Yao-hua KE,Hua YUE,Jin-wei HE,Yu-juan LIU,Zhen-lin ZHANG,
来源:中国药理学报(英文版) 年份:2009
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[会议论文] 作者:Zeng Zhang,Jin-Wei He,Wen-Zhen Fu,Zhen-Lin Zhang,Chang-Qing Zhang,
来源:第九届中国南方骨质疏松论坛暨江西省骨质疏松学术会 年份:2013
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Mutational survey of the PHEX gene in 10 unrelated Chinese families with X-linked hypophosphatemic r
[会议论文] 作者:Hua Yue,Jin-Bo Yu,Jia Xu,Jin-Wei He,Zhen-Lin Zhang,
来源:第六届国际骨质疏松及骨矿盐疾病学术会议 年份:2012
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Identification of five novel mutations in the SLCO2A1 gene in four unrelated Chinese families with p
[会议论文] 作者:Zeng Zhang,Jin-Wei He,Wen-Zhen Fu,Chang-Qing Zhang,Zhen-Lin Zhang,
来源:第六届国际骨质疏松及骨矿盐疾病学术会议 年份:2012
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Identification of one recurrent mutation in the TRAPPC2 gene in a large Chinese family with spondylo
[会议论文] 作者:Zeng Zhang,Jin-Wei He,Wen-Zhen Fu,Chang-Qing Zhang,Zhen-Lin Zhang,
来源:第六届国际骨质疏松及骨矿盐疾病学术会议 年份:2012
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Identification of one novel mutation in the EVC2 gene in a Chinese family with Ellis-van Creveld syn
[会议论文] 作者:Zeng Zhang,Jin-Wei He,Wen-Zhen Fu,Chang-Qing Zhang,Zhen-Lin Zhang,
来源:第六届国际骨质疏松及骨矿盐疾病学术会议 年份:2012
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Mutational survey of the PHEX gene in 10 unrelated Chinese families with X-linked hypophosphatemic r
[会议论文] 作者:Hua Yue,Jin-Bo Yu,Jia Xu,Jin-Wei He,Zhen-Lin Zhang,
来源:第六届国际骨质疏松及骨矿盐疾病学术会议 年份:2012
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Serum 25-hydroxyvitamin D is associated with insulin resistance and beta cell function in Chinese po
[会议论文] 作者:Zeng Zhang,Jin-Wei He,Wen-Zhen Fu,Chang-Qing Zhang,Zhen-Lin Zhang,
来源:第六届国际骨质疏松及骨矿盐疾病学术会议 年份:2012
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[会议论文] 作者:Hui Zheng,Chong Shao,Jin-wei He,Wen-zhen Fu,Zhen-lin Zhang,
来源:中华医学会第七次全国骨质疏松和骨矿盐疾病学术会议 年份:2013
Objective Progressive diaphyseal dysplasia (PDD) or Camurati-Engelmann disease is a rare autosomal dominant progressive diaphyseal dysplasia caused by mutations in the transforming growth factor-β 1 (...
[会议论文] 作者:Zeng Zhang,Jin-Wei He,Wen-Zhen Fu,Chang-Qing Zhang,Zhen-Lin Zhang,
来源:第六届国际骨质疏松及骨矿盐疾病学术会议 年份:2012
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[会议论文] 作者:Zeng Zhang,Jin-Wei He,Wen-Zhen Fu,Chang-Qing Zhang,Zhen-Lin Zhang,
来源:第九届中国南方骨质疏松论坛暨江西省骨质疏松学术会 年份:2013
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Mutational survey of the PHEX gene In 10 unrelated Chinese families with X-linked hypophosphatemic r
[会议论文] 作者:hua yue,Jin-Bo Yu,Jia Xu,Jin-Wei He,Zhen-Lin Zhang,
来源:中华医学会第十一次全国内分泌学学术会议 年份:2012
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,Genetic variants in the PLS3 gene are associated with osteoporotic fractures in postmenopausal Chin
[期刊论文] 作者:Chong Shao,Yi-wen Wang,Jin-wei He,Wen-zhen Fu,Chun Wang,Zhen-lin Zhang,
来源:中国药理学报(英文版) 年份:2019
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...
The A242T mutation in the low-density lipoprotein receptor-related protein 5 gene in one Chinese fam
[会议论文] 作者:Chun Wang,Jin-Wei He,Yun-Qiu Hu,Miao Li,Yu-Juan Liu,Zhen-Lin Zhang,
来源:第六届国际骨质疏松及骨矿盐疾病学术会议 年份:2012
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[期刊论文] 作者:Zhen-lin ZHANG,Yue-juan QIN,Jin-wei HE,Qi-ren HUANG,Miao LI,Yun-qiu HU,Yu-juan LIU,
来源:中国药理学报(英文版) 年份:2005
Aim: To investigate the possible association of Q89R, N740N and A1330V polymorphisms in low-density lipoprotein receptor-related protein 5 (LRP5) gene with bone...
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