ASSOCIATION OF COL1A1 SP1 AND FOK-I VDR GENETIC POLYMORPHISMS IN YOUNG MALE IDIOPATHIC OSTEOPOROSIS

机译：年轻男性特发性骨质疏松症中COL1A1 SP1和Fok-I VDR遗传多态性的关联

代理获取

本网站仅为用户提供外文OA文献查询和代理获取服务，本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文，但由于OA文献来源多样且变更频繁，仍可能出现获取不到、文献不完整或与标题不符等情况，如果获取不到我们将提供退款服务。请知悉。

页面导航

摘要
著录项
相似文献
相关主题

摘要

IntroductionPrimary osteoporosis during childhood and adolescence represents an uncommon condition, and secondary forms are more likely to manifest at this age due to chronic disease and adverse effects of medical treatment.

机译：前言在儿童和青少年时期，原发性骨质疏松症是一种罕见的疾病，由于慢性疾病和药物治疗的不良影响，在该年龄更容易出现继发性骨质疏松。

著录项

期刊名称 Acta Endocrinologica (Bucharest)
作者
S.C. Man; M. Chiriac; M.S. Militaru; A.P. Trifa; M. Goia-Socol; C.E. Georgescu;
展开▼
作者单位

展开▼
年(卷),期 2017(13),2
年度 2017
页码 224–227
总页数 4
原文格式 PDF
正文语种
中图分类
关键词
gene polymorphisms Sp1 binding site vitamin D receptor type I collagen idiopathic osteoporosis juvenile osteoporosis;

机译：基因多态性;Sp1结合位点;维生素D受体;I型胶原蛋白;特发性骨质疏松症;青少年骨质疏松症;

相似文献

外文文献
中文文献
专利

1. ASSOCIATION OF COL1A1 SP1 AND FOK-I VDR GENETIC POLYMORPHISMS IN YOUNG MALE IDIOPATHIC OSTEOPOROSIS [J] . Man S. C., Chiriac M., Militaru M. S., Acta endocrinologica: the international journal of the Romanian Society of Endocrinology . 2017,第2期

机译：Col1a1和Fok-i vdr遗传多态性在年轻男性特发性骨质疏松症中的关联
2. Association of otosclerosis with Sp1 binding site polymorphism in COL1A1 gene: evidence for a shared genetic etiology with osteoporosis. [J] . McKenna MJ, Nguyen Huynh AT, Kristiansen AG Otology and neurotology: official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology . 2004,第4期

机译：耳硬化症与COL1A1基因Sp1结合位点多态性的关联：骨质疏松症的共同遗传病因的证据。
3. A novel, non-functional, COL1A1 polymorphism is not associated with lumbar disk disease in young male Greek subjects unlike that of the Sp1 site [J] . Thalia Bei, Constantinos Tilkeridis, Stavros Garantziotis, Hormones: International Journal of Endocrinology and Metabolism . 2008,第3期

机译：与Sp1位点不同，新型的，非功能性的COL1A1多态性与年轻的希腊男性受试者的腰椎间盘疾病无关
4. Association between Vitamin D receptor (VDR) polymorphisms and matrix metalloproteinase-9 (MMP-9) in female workers of lead battery plants [C] . Wei-Te Wu, Chin-Ching Wu, Yu-Jen Lin, Annual conference of the International Society of Exposure Science . 2014

机译：铅蓄电池工厂女工体内维生素D受体（VDR）多态性与基质金属蛋白酶9（MMP-9）的关联
5. The role of matrix metalloproteinases in atherosclerosis in the young: Genetic association studies and functional analyses of promoter polymorphisms. [D] . Yoon, Sungpil. 2001

机译：基质金属蛋白酶在年轻人的动脉粥样硬化中的作用：遗传关联研究和启动子多态性的功能分析。
6. A novel non-functional COL1A1 polymorphism is not associated with lumbar disk disease in young male Greek subjects unlike that of the Sp1 site [O] . Thalia Bei, Constantinos Tilkeridis, Stavros Garantziotis, -1

机译：与Sp1位点不同新型的非功能性的COL1A1多态性与年轻的希腊男性受试者的腰椎盘疾病无关
7. Association Between Polymorphisms of VDR, COL1A1, and LCT Genes and Bone Mineral Density in Belarusian Women With Severe Postmenopausal Osteoporosis [O] . Pavel Marozik, Irma Mosse, Vidmantas Alekna, 2013

机译：白俄罗斯骨疏松症的白俄罗斯妇女的VDR，COL1A1和LCT基因和骨密度的多态性之间的关联

ASSOCIATION OF COL1A1 SP1 AND FOK-I VDR GENETIC POLYMORPHISMS IN YOUNG MALE IDIOPATHIC OSTEOPOROSIS

摘要

著录项

相似文献

相关主题

期刊订阅