• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Matrix metalloproteinase-9 genotypes and haplotypes are associated with multiple sclerosis and with the degree of disability of the disease.

作者信息

Fernandes Karla S S, Brum Doralina Guimaraes, Sandrim Valeria Cristina, Guerreiro Carlos Tostes, Barreira Amilton Antunes, Tanus-Santos José Eduardo

机构信息

Department of Pharmacology, Medicine and Rehabilitation of the Locomotor Apparatus, Medical School of Ribeirão Preto, University of São Paulo, 14049-900, Ribeirão Preto, SP, Brazil.

出版信息

J Neuroimmunol. 2009 Sep 29;214(1-2):128-31. doi: 10.1016/j.jneuroim.2009.07.004. Epub 2009 Jul 24.

DOI:10.1016/j.jneuroim.2009.07.004
PMID:19631393
Abstract

Multiple sclerosis (MS) is an autoimmune disease causing severe neurological disability. This study was carried out in order to determine whether the MMP-9 C(-1562)T and (CA)(13-25) polymorphisms are associated with MS. A total of 165 patients (92 whites/73 mulattos) and 191 controls (96 whites/95 mulattos) were enrolled in the study. While no difference in C(-1562)T polymorphism was observed between MS and healthy subjects, (CA)(n) genotypes and alleles were associated with MS. Moreover, the haplotypes are not associated with MS but seem to be relevant to the clinical status of MS. Thus the (CA)(n) polymorphism may contribute to MS susceptibility, but C(-1562)T and (CA)(n) haplotypes may modulate disease severity.

摘要

相似文献

1
Matrix metalloproteinase-9 genotypes and haplotypes are associated with multiple sclerosis and with the degree of disability of the disease.
J Neuroimmunol. 2009 Sep 29;214(1-2):128-31. doi: 10.1016/j.jneuroim.2009.07.004. Epub 2009 Jul 24.
2
Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study.单核苷酸多态性在 MMP-9 基因与易感性发展多发性硬化症的意大利病例对照研究。
J Neuroimmunol. 2010 Aug 25;225(1-2):175-9. doi: 10.1016/j.jneuroim.2010.04.016. Epub 2010 May 14.
3
Matrix metalloproteinase-9 and matrix metalloproteinase-2 gene polymorphisms in multiple sclerosis.多发性硬化症中基质金属蛋白酶-9和基质金属蛋白酶-2基因多态性
J Neuroimmunol. 2008 Dec 15;205(1-2):105-9. doi: 10.1016/j.jneuroim.2008.08.007. Epub 2008 Oct 5.
4
Matrix metalloproteinase-9 -1562 C/T gene polymorphism in Serbian patients with multiple sclerosis.
J Neuroimmunol. 2007 Sep;189(1-2):147-50. doi: 10.1016/j.jneuroim.2007.06.022. Epub 2007 Jul 25.
5
Association of MMP1, MMP3, MMP9, and MMP12 polymorphisms with risk and clinical course of multiple sclerosis in a Polish population.波兰人群中基质金属蛋白酶1、基质金属蛋白酶3、基质金属蛋白酶9和基质金属蛋白酶12基因多态性与多发性硬化症风险及临床病程的关联
J Neuroimmunol. 2009 Sep 29;214(1-2):113-7. doi: 10.1016/j.jneuroim.2009.06.014. Epub 2009 Jul 22.
6
The interleukin 23 receptor gene in multiple sclerosis: a case-control study.多发性硬化症中的白细胞介素23受体基因:一项病例对照研究。
J Neuroimmunol. 2008 Feb;194(1-2):173-80. doi: 10.1016/j.jneuroim.2007.11.011.
7
APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers.APOE ε变异与多发性硬化易感性及疾病严重程度:一些答案
Neurology. 2006 May 9;66(9):1373-83. doi: 10.1212/01.wnl.0000210531.19498.3f.
8
CCR5-Delta32 genetic polymorphism associated with benign clinical course and magnetic resonance imaging findings in Brazilian patients with multiple sclerosis.CCR5-Delta32基因多态性与巴西多发性硬化症患者的良性临床病程及磁共振成像结果相关。
Int J Mol Med. 2007 Sep;20(3):337-44.
9
Matrix metalloproteinase-9 and matrix metalloproteinase-2 as biomarkers of various courses in multiple sclerosis.基质金属蛋白酶-9和基质金属蛋白酶-2作为多发性硬化症不同病程的生物标志物。
Mult Scler. 2009 Mar;15(3):316-22. doi: 10.1177/1352458508099482. Epub 2009 Jan 19.
10
Association between the -1562 C/T polymorphism of matrix metalloproteinase-9 gene and lumbar disc disease in the young adult population in North China.华北年轻成年人群中基质金属蛋白酶-9基因-1562 C/T多态性与腰椎间盘疾病的关联
Connect Tissue Res. 2009;50(3):181-5. doi: 10.1080/03008200802585630.

引用本文的文献

1
Does the functional polymorphism-1562C/T of MMP-9 gene influence brain disorders?基质金属蛋白酶-9(MMP-9)基因的功能性多态性-1562C/T是否会影响脑部疾病?
Front Cell Neurosci. 2023 May 3;17:1110967. doi: 10.3389/fncel.2023.1110967. eCollection 2023.
2
Association of the matrix metalloproteinases (MMPs) family gene polymorphisms and the risk of coronavirus disease 2019 (COVID-19); implications of contribution for development of neurological symptoms in the COVID-19 patients.基质金属蛋白酶(MMPs)家族基因多态性与 2019 年冠状病毒病(COVID-19)风险的关联;对 COVID-19 患者神经系统症状发展的贡献意义。
Mol Biol Rep. 2023 Jan;50(1):173-183. doi: 10.1007/s11033-022-07907-y. Epub 2022 Nov 1.
3
Matrix metalloproteinases (MMPs) family gene polymorphisms and the risk of multiple sclerosis: systematic review and meta-analysis.
基质金属蛋白酶(MMPs)家族基因多态性与多发性硬化症的风险:系统评价和荟萃分析。
BMC Neurol. 2020 May 29;20(1):218. doi: 10.1186/s12883-020-01804-2.
4
Association Study between Functional Polymorphisms of Gene Promoter and Multiple Sclerosis Susceptibility in an Iranian Population.伊朗人群中基因启动子功能多态性与多发性硬化易感性的关联研究。
Iran J Public Health. 2019 Sep;48(9):1697-1703.
5
Matrix Metalloproteinases in Non-Neoplastic Disorders.非肿瘤性疾病中的基质金属蛋白酶
Int J Mol Sci. 2016 Jul 21;17(7):1178. doi: 10.3390/ijms17071178.
6
Therapeutic potential of matrix metalloproteinases in Duchenne muscular dystrophy.基质金属蛋白酶在杜氏肌营养不良症中的治疗潜力。
Front Cell Dev Biol. 2014 Apr 1;2:11. doi: 10.3389/fcell.2014.00011. eCollection 2014.
7
The significance of matrix metalloproteinases in the immunopathogenesis and treatment of multiple sclerosis.基质金属蛋白酶在多发性硬化症免疫发病机制及治疗中的意义
Sultan Qaboos Univ Med J. 2014 Feb;14(1):e13-25. doi: 10.12816/0003332. Epub 2014 Jan 27.
8
Matrix metalloproteinases, synaptic injury, and multiple sclerosis.基质金属蛋白酶、突触损伤与多发性硬化症。
Front Psychiatry. 2010 Oct 5;1:130. doi: 10.3389/fpsyt.2010.00130. eCollection 2010.