您的位置: 专家智库 > >

国家自然科学基金(30571725)

作品数:7 被引量:15H指数:2
相关作者:吕社民朱文华孟列素刘越王慧莲更多>>
相关机构:西安交通大学更多>>
发文基金:国家自然科学基金教育部留学回国人员科研启动基金更多>>
相关领域:医药卫生生物学更多>>

文献类型

  • 7篇中文期刊文章

领域

  • 6篇医药卫生
  • 1篇生物学

主题

  • 4篇基因
  • 3篇类风湿
  • 3篇类风湿关节炎
  • 3篇关节炎
  • 3篇风湿
  • 3篇风湿关节炎
  • 2篇动物
  • 2篇动物模型
  • 2篇性疾病
  • 2篇易感基因
  • 2篇免疫
  • 2篇克隆
  • 2篇关节
  • 2篇复杂性疾病
  • 1篇单核
  • 1篇单核苷酸
  • 1篇单核苷酸多态
  • 1篇单核苷酸多态...
  • 1篇单体型
  • 1篇多态

机构

  • 5篇西安交通大学

作者

  • 5篇吕社民
  • 1篇刘越
  • 1篇韩燕
  • 1篇孟列素
  • 1篇朱文华
  • 1篇杨旭东
  • 1篇钟波
  • 1篇宁启兰
  • 1篇张富军
  • 1篇王慧莲

传媒

  • 2篇西安交通大学...
  • 2篇Journa...
  • 1篇浙江大学学报...
  • 1篇生命的化学
  • 1篇中华风湿病学...

年份

  • 1篇2011
  • 2篇2009
  • 2篇2008
  • 2篇2006
7 条 记 录,以下是 1-7
排序方式:
用动物模型定位、克隆复杂性疾病的易感基因:以类风湿关节炎动物模型为范例(续前)被引量:1
2006年
吕社民
关键词:复杂性疾病关节炎易感基因动物模型
Toll样受体与类风湿关节炎被引量:2
2008年
Toll样受体(toll like receptor,TLR)是一类重要模式识别受体(pattern recognition receptor,PRR),参与识别多种非特异性的、保守的微生物组分以及相应内源性配体。它们不仅在天然免疫中具有重要作用.也是联系天然免疫与特异性免疫的桥梁,从多个方面影响特异性免疫应答,因此在包括类风湿关节炎(rheumatoid arthritis,RA)在内的慢性免疫性炎症疾病的发生发展中扮演着重要角色。本文将综述近年来TLR最新的研究进展,并探讨其与RA的关系。
孟列素朱文华吕社民
关键词:TOLL样受体类风湿关节炎特异性免疫应答模式识别受体天然免疫内源性配体
Methotrexate ameliorates pristane-induced arthritis by decreasing IFN-γ and IL-17A expressions被引量:1
2011年
Objective: This study was carried out to test the effects of methotrexate (MTX) and black seed oil (BSO) on pristane-induced arthritis (PIA) in rats.Methods: Inbred dark agouti (DA) rats were induced by a single subcutaneous injection of pristane,and then treated with MTX or BSO.Arthritis severity was evaluated macroscopically and microscopically.Plasma nitric oxide (NO) concentration was determined by the Griess method and cytokine mRNA expression in the spleen was detected by the real-time reverse transcription-polymerase chain reaction (RT-PCR).Results: The clinical arthritis severity was decreased after MTX treatment,while the BSO groups did not show significant changes compared with the disease group.The plasma NO level of the MTX group was significantly decreased compared with the disease group,but the BSO groups showed no difference from the disease group in plasma NO levels.The interferon-γ (IFN-γ) and interleukin-17A (IL-17A) mRNA expressions in the spleens were significantly decreased in the MTX group,but only showed a declining trend in the BSO groups compared with the disease group.Neither MTX nor BSO had an effect on the mRNA expressions of IL-4,transforming growth factor β (TGF-β),and tumor necrosis factor-α (TNF-α) in the spleen.Conclusions: MTX,but not BSO,can reduce the arthritis severity and decrease the mRNA expressions of IFN-γ and IL-17A in pristane-induced arthritis of rats.
Wei-kun HOULie-su MENGFang ZHENGYu-rong WENWen-hua ZHUCong-shan JIANGXiao-jing HEYan ZHOUShe-min LU
Relationships between endothelial nitric oxide synthase gene polymorphisms and osteoporosis in postmenopausal women被引量:6
2009年
Objective:To investigate the relationships between endothelial nitric oxide synthases(eNOS) G894T and 27 bpvariable number tandem repeat(VNTR) gene polymorphisms and osteoporosis in the postmenopausal women of Chinese Han nationality.Methods:In the present study,281 postmenopausal women from Xi'an urban area in West China were recruited,and divided into osteoporosis,osteopenia,and normal groups according to the diagnostic criteria of osteoporosis proposed by World Health Organization(WHO).The bone mineral density(BMD) values of lumbar vertebrae and left hips were determined by QDR-2000 dual energy X-ray absorptiometry.Blood samples were tested for plasma biochemical indicators including testosterone,estradiol,calcitonin,osteocalcin,and procollagen type I amino-terminal propeptide by enzyme-linked immunosorbent assay(ELISA),tartrate-resistant acid phosphatase by spectrophotometric method,and the content of nitric oxide by Griess method.Genome DNA was extracted from whole blood,and G894T polymorphism of eNOS gene was analyzed by using polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP) method and 27 bp-VNTR polymorphism of eNOS gene was genotyped by PCR method.Then the relationships between genotypes and biochemical indicators,genotypes and osteoporosis,and haplotypes and osteoporosis were analyzed.Results:The average BMD values of the femoral neck,ward's triangle and lumbar vertebrae 1~4(L1~L4) in the subjects with T/T genotype in eNOS G894T locus were significantly higher than those in the subjects with G/T and G/G genotypes(P<0.05).The average BMD of the femoral neck in the subjects with a/a genotype of eNOS 27 bp-VNTR locus was evidently higher than that in the subjects with b/b genotype(P<0.05).The plasma testosterone and os-teocalcin concentrations in the subjects of eNOS G894T G/T genotype were evidently higher than those in the subjects of other genotypes(P<0.05);the plasma estradiol concentration in the subjects of eNOS 27 bp-VNTR a/a genotype was obviously higher than that in
Shun-zhi LIUHong YANWei-kun HOUPeng XUJuan TIANLi-fang TIANBo-feng ZHUJie MAShe-min LU
关键词:绝经
利用抑制性消减杂交技术筛选大鼠哮喘相关基因
2009年
目的:利用哮喘大鼠模型筛选与哮喘发病相关的差异性表达基因。方法:采用抑制性消减杂交技术,以哮喘大鼠肺组织总RNA为检验子,对照大鼠肺组织总RNA为驱赶子,将消减杂交获得的DNA片断与pGEM-T Easy Vector连接,构建cDNA文库后,转化大肠杆菌DH5α,筛选阳性克隆。将获得的阳性克隆插入片段进行测序分析,测序结果与GenBank数据库中cDNA和EST序列进行相似性比对,获得差异性表达基因的信息。结果:扩增消减cDNA文库获得300余个白色克隆,随即挑选36个测序,除去重复序列,结果中含有已知的基因4个,ESTs 2个及与任何序列无同源性的新基因片段3个。结论:成功构建了哮喘大鼠肺脏差异性表达基因的正向消减cDNA文库,筛选出数个与哮喘相关的差异表达基因。
钟波王慧莲Muhammad Shahzad宁启兰韩燕杨旭东张富军吕社民
关键词:抑制性消减杂交CDNA文库
单核苷酸多态性影响基因功能的机制被引量:2
2008年
单核苷酸多态性(single nucleotide polymorphism,SNP),最早是作为一种基因组作图的遗传标记,随着研究的进一步深入,发现SNP本身也可影响基因功能。非同义cSNP由于其改变编码的氨基酸,对基因功能的影响容易理解。其他类型的SNP,由于不改变所编码的氨基酸,以前不为研究者所重视。但近来,尤其是分子机制方面的研究表明,同义cSNP可通过改变mRNA的二级结构、翻译速度等影响基因功能的发挥;内含子区SNP可通过改变剪接位点的活性来影响基因功能;调控区的rSNP则可通过影响启动子元件来调节基因的功能。此外,一个基因内若干相关联的SNP位点可通过形成不同的单体型,影响mRNA二级结构的稳定性,进而调节基因功能。
刘越吕社民
关键词:单核苷酸多态性基因功能分子机制单体型
用动物模型定位、克隆复杂性疾病的易感基因:以类风湿关节炎动物模型为范例被引量:3
2006年
基于复杂性疾病的临床异质性,或称表型异质性;遗传异质性,或称位点异质性;多基因的微效作用;异位显性(epistasis);拟表型(phenocopy);环境因素的作用等特点,鉴定复杂性疾病的易感基因是一种艰巨有时难以完成的任务。近交系动物遗传背景清晰,动物实验可控制环境因素的干扰,以及转基因动物在研究基因功能中独特的作用,应用动物模型为筛选鉴定人类复杂性疾病的易感基因提供了不可替代的工具。以大鼠类风湿关节炎模型为例,定位克隆易感基因步骤包括:①选择亲代近交系,建立关节炎模型;②分离育种,连锁分析、确定数量性状位点(QTLs);③建立Congenic系、窄化QTL区域;④位置克隆基因;⑤易感基因的功能验证。我们应用这一策略从朴日斯烷(Pristane)诱导的关节炎大鼠模型中已筛选出十余个控制关节炎发生发展的非MHC基因位点,在此基础上克隆的Pia4基因被鉴定为是中性粒细胞胞浆因子1(Ncf1)。说明该研究策略是完全可行的,并且可能发现新的功能基因或已知基因的新功能。
吕社民
关键词:复杂性疾病关节炎易感基因动物模型
共1页<1>
聚类工具0