期刊文献+
共找到4篇文章
< 1 >
每页显示 20 50 100
新生隐球菌对鼠小胶质细胞细胞骨架蛋白质组的影响
1
作者 杨阳 廖万清 +5 位作者 郭秀军 林敏 王志东 徐红 陈孙孝 温海 《临床皮肤科杂志》 CAS CSCD 北大核心 2007年第4期208-211,共4页
目的:探讨新生隐球菌对鼠小胶质细胞(N9)蛋白质组的影响。方法:分别提取正常N9细胞以及与新生隐球菌(ATCC32609)作用后的N9细胞的蛋白质样品,采用双向电泳技术分离,对部分差异的蛋白质点进行基质辅助激光解吸电离飞行时间质谱分析,测定... 目的:探讨新生隐球菌对鼠小胶质细胞(N9)蛋白质组的影响。方法:分别提取正常N9细胞以及与新生隐球菌(ATCC32609)作用后的N9细胞的蛋白质样品,采用双向电泳技术分离,对部分差异的蛋白质点进行基质辅助激光解吸电离飞行时间质谱分析,测定其肽质量指纹图谱,在网上蛋白质数据库检索鉴定差异蛋白。结果:获得较好的双向电泳图像,图像分析显示:在与新生隐球菌作用前、后检测到N9细胞的蛋白质点分别是(701±29)个、(980±20)个,对表达差异的18个蛋白质点进行肽质量指纹图谱分析,经数据库检索后,鉴定出3个涉及小胶质细胞细胞骨架的蛋白质:anillin、pericentrin 2、核苷二磷酸激酶A[nucleoside diphosphate kinase A(NDP kinase A,NDPKA)]。结论:新生隐球菌对小胶质细胞的细胞骨架蛋白质造成影响,这有助于在分子水平理解隐球菌性脑膜炎的发病机制。 展开更多
关键词 新生隐球菌 小胶质细胞 细胞骨架蛋白质 蛋白质
下载PDF
反向遗传学
2
作者 罗会元 《中国生育健康杂志》 1990年第1期27-29,共3页
20世纪80年代,重组DNA技术取得了飞速的发展,人们对遗传性疾病的认识取得了突破性的进展。许多遗传病已在基因DNA水平上确定了其突变部位与性质。今后必然会发现越来越多的遗传病的突变致病基因(也就是正常基因的突变等位基因)。这必将... 20世纪80年代,重组DNA技术取得了飞速的发展,人们对遗传性疾病的认识取得了突破性的进展。许多遗传病已在基因DNA水平上确定了其突变部位与性质。今后必然会发现越来越多的遗传病的突变致病基因(也就是正常基因的突变等位基因)。这必将为遗传病的防治提供崭新的途径。 展开更多
关键词 反向遗传学 DNA 基因连锁 致病基因 遗传性疾病 常染色体易位 慢性肉芽肿病 阅读框架 细胞骨架蛋白质 细胞遗传学
下载PDF
Mechanisms and Effects on HBV Replication of the Interaction between HBV Core Protein and Cellular Filamin B 被引量:3
3
作者 Yilin Li Yishuang Sun +5 位作者 Fuyun Sun Rong Hua Chenlin Li Lang Chen Deyin Guo Jingfang Mu 《Virologica Sinica》 SCIE CAS CSCD 2018年第2期162-172,共11页
Hepatitis B virus(HBV) infection is one of the major problems that threatens global health. There have been many studies on HBV, but the relationship between HBV and host factors is largely unexplored and more studies... Hepatitis B virus(HBV) infection is one of the major problems that threatens global health. There have been many studies on HBV, but the relationship between HBV and host factors is largely unexplored and more studies are needed to clarify these interactions. Filamin B is an actin-binding protein that acts as a cytoskeleton protein, and it is involved in cell development and several signaling pathways. In this study, we showed that filamin B interacted with HBV core protein,and the interaction promoted HBV replication. The interaction between filamin B and core protein was observed in HEK293T, Huh7 and HepG2 cell lines by co-immunoprecipitation and co-localization immnofluoresence. Overexpression of filamin B increased the levels of HBV total RNAs and pre-genome RNA(pg RNA), and improved the secretion level of hepatitis B surface antigen(HBsAg) and hepatitis B e antigen(HBeAg). In contrast, filamin B knockdown inhibited HBV replication, decreased the level of HBV total RNAs and pgRNA, and reduced the secretion level of HBsAg and HBeAg. In addition, we found that filamin B and core protein may interact with each other via four blocks of argentine residues at the C-terminus of core protein. In conclusion, we identify filamin B as a novel host factor that can interact with core protein to promote HBV replication in hepatocytes. Our study provides new insights into the relationship between HBV and host factors and may provide new strategies for the treatment of HBV infection. 展开更多
关键词 Filamin B CORE HBV replication
原文传递
A novel de novo mutation of ACTG1 in two sporadic non-syndromic hearing loss cases 被引量:1
4
作者 Hongyang Wang Jing Guan +7 位作者 Lan Lan Lan Yu Linyi Xie Xu Liu Ju Yang Cui Zhao Dayong Wang Qiuju Wang 《Science China(Life Sciences)》 SCIE CAS CSCD 2018年第6期729-732,共4页
Dear Editor,Actins are a family of essential cytoskeletal proteins involved in nearly all cellular processes(Lambrechts et al.,2004).Of the six human genes that encode actins,only ACTG1and ACTB are ubiquitously expr... Dear Editor,Actins are a family of essential cytoskeletal proteins involved in nearly all cellular processes(Lambrechts et al.,2004).Of the six human genes that encode actins,only ACTG1and ACTB are ubiquitously expressed.ACTG1(OMIM#604717),which is linked to the DFNA20/26 locus,wasidentified in autosomal dominant, non-syndromic hearing loss (NSHL) cases (Baek et al., 2012; Liu et al., 2008; Park et al., 2013; Yuan et al., 2016). In addition, some ACTG1 (OMIM #614583) mutations are associated with Baraitser-Winter syndrome, which is characterized by developmental delay, facial dysmorphologies, brain malformations, colobomas, and variable hearing loss (Riviere et al., 2012). 展开更多
关键词 A novel de novo mutation of ACTG1 in two sporadic non-syndromic hearing loss cases
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部