期刊文献+
共找到2篇文章
< 1 >
每页显示 20 50 100
A T-Cell Model for the Biological Role of Selenium-Dependent Glutathione Peroxidase
1
作者 ALAN M. DIAMOND YASUSHI KATAOKA +3 位作者 JUDITH MURRAY duan chengying THOMAS M. FOLKST,AND PAUL. A. SANDSTROM(Department of Radiation and Cellular Oncology, University of Chicago, Chicago, IL 60637 USA Retrovirus Disease Branch, Division of Viral and Rickettsial 《Biomedical and Environmental Sciences》 SCIE CAS CSCD 1997年第2期246-252,共7页
The cytosolic form of selenium-dependent glutathione peroxidase detoxifies both hydrogen and lipid peroxides and therefore represents a major component of the cellular anti-oxidant defenses. In order to study the biol... The cytosolic form of selenium-dependent glutathione peroxidase detoxifies both hydrogen and lipid peroxides and therefore represents a major component of the cellular anti-oxidant defenses. In order to study the biological role of this enzyme, we generated an expression construct in a retroviral vector, which when introduced into immortalized human T-cells, resulted in significant increases in the activity of this important enzyme. This effect is stable over extended maintenance in culture. The anti-oxidant defenses in these same cells are also shown to be attenuated hy chemically reducing cellular glutathione levels. Collectively, the abllity to both increase and decrease the anti-oxidant defenses in human T cells results in a useful model system for the study of oxidative stress and signaling in this cell type 展开更多
关键词 RES cell A T-Cell Model for the Biological Role of Selenium-Dependent Glutathione Peroxidase HIV AIDS
下载PDF
一个Ⅰ型神经纤维瘤家系NF1基因的新突变 被引量:6
2
作者 张芹 梁玉婷 +5 位作者 高昂 段程颖 丁扬 潘宇虹 乔龙威 李红 《中华医学遗传学杂志》 CAS CSCD 2019年第2期132-135,共4页
目的 对一个Ⅰ型神经纤维瘤家系进行NF1基因突变的检测和分析,探讨其发病的分子遗传学病因。 方法 采集先证者及其父母的外周血标本,应用PCR-Sanger测序方法进行NF1基因外显子区域以及侧翼序列分析,鉴别可能存在的突变。采用Polyphen-2... 目的 对一个Ⅰ型神经纤维瘤家系进行NF1基因突变的检测和分析,探讨其发病的分子遗传学病因。 方法 采集先证者及其父母的外周血标本,应用PCR-Sanger测序方法进行NF1基因外显子区域以及侧翼序列分析,鉴别可能存在的突变。采用Polyphen-2和Provean等软件对突变进行致病性分析。 结果 先证者检测到两个突变,分别为c.702G>A(同义突变)和c.1733T>G(杂合突变),先证者父母并未检测到上述突变,在50名正常对照的NF1基因中并未发现此突变。Polyphen-2和Provean软件均预测c.1733T>G突变可能致病,突变的蛋白质在不同的物种间高度保守。 结论 NF1基因的c.1733T>C(p.Leu578Arg)突变可能是该患者的致病原因。 展开更多
关键词 Ⅰ型神经纤维瘤 NF1基因 突变
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部