首页> 外国专利> ASSOCIATION OF PLXNA2 POLYMORPHISMS WITH VERTEBRAL FRACTURE RISK AND BONE MINERAL DENSITY

ASSOCIATION OF PLXNA2 POLYMORPHISMS WITH VERTEBRAL FRACTURE RISK AND BONE MINERAL DENSITY

机译:PLXNA2多态性与椎骨骨折风险和骨矿物质密度的关联

摘要

PLXNA2 (plexin A2) gene pleiomorphism, itself and vertebral fracture risk and bone density (BMD), it is arranged to predict the genetic predisposition of osteoporosis and the sensibility of the osteoporosis to a theme, so that gene pleiomorphism is used as the useful mark for the associated fracture of osteoporosis and there. A PLXNA2 gene pleiomorphisms of a for predict be to the sensibility of osteoporosis+14G ,+183429C T or haplocype Block1-ht2, wherein it is the danger that G associated with vertebral fracture risks it that+14th bases, which are G and+799th bases,; Or it is associated with the BMD of entire femur, rotor, femoral shaft and ward's triangle by+799G a ,+135391G a or+190531G C. For predicting the priming paint for not containing SEQ ID to the sleeve piece of the sensibility of osteoporosis: 1 pair of SEQ ID not: 70 for not screening the series jump of PLXNA2 gene pleiomorphisms and the priming paint and probe of SEQ ID: 71 pairs of SEQ IDs not: 114 be genotyping.
机译:PLXNA2(plexin A2)基因多态性,自身以及椎骨骨折风险和骨密度(BMD)的安排可预测骨质疏松症的遗传易感性和骨质疏松症对主题的敏感性,因此将基因多态性用作有用的标记并伴有骨质疏松的相关骨折。的PLXNA2基因多态性可预测为骨质疏松症+ 14G>,+ 183429C> T或单倍体Block1-ht2的敏感性,其中与椎骨骨折相关的G可能会威胁到+14个碱基,即G和+799基础,;或者它与整个股骨,转子,股骨干和病房三角形的BMD相关联,为+ 799G> a,+ 135391G> a或+ 190531G>C。用于预测底漆的套筒上不含SEQ ID的底漆骨质疏松症的敏感性:1对SEQ ID not:70,用于不筛选PLXNA2基因多态性的系列跳跃,而SEQ ID:71对的引物和探针的引物和探针则不进行基因分型。

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