期刊文献+
共找到32篇文章
< 1 2 >
每页显示 20 50 100
草莓乙烯受体Ers1基因反义植物表达载体构建
1
作者 唐霞 刘思思 马俊莲 《安徽农业科学》 CAS 2012年第7期3899-3900,共2页
[目的]构建草莓Ers1基因反义植物表达载体,为探明该基因的功能以及采用生物技术方法改良草莓品种奠定基础。[方法]根据已克隆的草莓乙烯受体Ers1基因序列及表达载体pBI121上的酶切位点设计1对带限制性内切酶位点的特异性引物,以Ers1基... [目的]构建草莓Ers1基因反义植物表达载体,为探明该基因的功能以及采用生物技术方法改良草莓品种奠定基础。[方法]根据已克隆的草莓乙烯受体Ers1基因序列及表达载体pBI121上的酶切位点设计1对带限制性内切酶位点的特异性引物,以Ers1基因的测序质粒为模板,PCR扩增到草莓Ers1基因片段,克隆片段及载体经双酶切消化后,回收产物定向连接,将克隆片段反向补插入到植物表达载体pBI121的35S和gusA之间,构建成该基因的反义植物表达载体。[结果]经酶切鉴定,成功构建了草莓Ers1基因反义植物表达载体。[结论]该研究为进一步探讨Ers1基因功能及利用生物技术方法调控果实成熟衰老进程,从而改善草莓果实的贮运性能奠定基础。 展开更多
关键词 草莓 乙烯受体ers1 植物表达载体
下载PDF
全明星草莓乙烯受体Ers1基因克隆及序列分析 被引量:1
2
作者 刘思思 马俊莲 +2 位作者 唐霞 张子德 宋春丽 《华北农学报》 CSCD 北大核心 2011年第5期46-49,共4页
克隆了与草莓成熟有关的乙烯受体Ers1基因片段,为进一步研究Ers1基因功能并通过基因技术改善草莓贮运性能奠定基础。以全明星草莓成熟果实中分离得到基因组DNA为模板,经PCR扩增到一条约700 bp的特异片段,将该片段克隆到PEGM-T easy vec... 克隆了与草莓成熟有关的乙烯受体Ers1基因片段,为进一步研究Ers1基因功能并通过基因技术改善草莓贮运性能奠定基础。以全明星草莓成熟果实中分离得到基因组DNA为模板,经PCR扩增到一条约700 bp的特异片段,将该片段克隆到PEGM-T easy vector上经测序分析,基因全长667 bp,编号222个氨基酸。序列分析结果表明,该序列与Chandler-Ers1的cDNA序列同源性99%,氨基酸序列同源性98%。 展开更多
关键词 草莓 乙烯受体ers1 基因克隆 序列分析
下载PDF
文心兰OnERS1全长基因克隆及表达分析 被引量:10
3
作者 田晓岩 杨翠萍 +5 位作者 胡进 闫冰玉 巩笑笑 庄玉粉 潘英文 刘进平 《分子植物育种》 CAS CSCD 北大核心 2017年第4期1265-1272,共8页
为了了解乙烯信号受体在文心兰切花衰老中的作用,利用RACE技术克隆了文心兰乙烯受体基因OnERS1(Gen Bank登录号为KP410729)。生物信息学分析表明,OnERS1基因编码631个氨基酸,分子量为70 773.7,等电点为6.82,是跨膜蛋白,与其它植物的ETR... 为了了解乙烯信号受体在文心兰切花衰老中的作用,利用RACE技术克隆了文心兰乙烯受体基因OnERS1(Gen Bank登录号为KP410729)。生物信息学分析表明,OnERS1基因编码631个氨基酸,分子量为70 773.7,等电点为6.82,是跨膜蛋白,与其它植物的ETR乙烯受体蛋白的相似性在74%~99%之间,属ETR1类乙烯受体。基因表达分析结果表明,OnERS1基因在根和蕊柱中表达量最高,在叶片、侧瓣和花萼中次之,在茎和唇瓣中表达量最低;文心兰切花衰老期间OnERS1基因的表达量在第0~6 d持续增加,第6 d后突然下降,第8 d后下降到一个极低的水平。与此同时,花器官中的乙烯释放从第8 d之前缓慢上升,第8~10 d急剧升高。OnERS1基因的时空表达特异性表达说明它可能与花衰老有关。 展开更多
关键词 文心兰 乙烯受体 ETR1 ers1 基因克隆 荧光定量PCR
原文传递
加拿大豌豆品种(系)抗白粉病表型和基因型鉴定 被引量:8
4
作者 付海宁 孙素丽 +2 位作者 朱振东 段灿星 杨晓明 《植物遗传资源学报》 CAS CSCD 北大核心 2014年第5期1028-1033,共6页
对36个引自加拿大的豌豆品种(系)进行抗白粉病表型和标记基因型鉴定,明确了豌豆品种Cooper和Tara白粉病抗性等位基因。苗期接种了2个不同地理来源的豌豆白粉病菌分离物,32个品种(系)对2个分离物均表现为免疫;品系MP1818-2对云南白粉菌... 对36个引自加拿大的豌豆品种(系)进行抗白粉病表型和标记基因型鉴定,明确了豌豆品种Cooper和Tara白粉病抗性等位基因。苗期接种了2个不同地理来源的豌豆白粉病菌分离物,32个品种(系)对2个分离物均表现为免疫;品系MP1818-2对云南白粉菌分离物EPYN免疫,但对北京分离物EPBJ感病;其余3个品种对2个分离物均感病。4个与豌豆抗白粉病基因er1连锁的SCAR标记将36个豌豆品种(系)区分为5个标记基因型。与野生型PsMLO1基因序列比较发现,豌豆品种Cooper和Tara的PsMLO1候选基因均在680 bp处发生C变G的单核苷酸突变。 展开更多
关键词 豌豆 白粉病 抗病性 标记基因型 er1
下载PDF
异补骨脂素对光老化HDF细胞ER/TGF-β_1/Smads信号通路的调控效应研究 被引量:6
5
作者 顾婷 徐占玲 +4 位作者 朴成玉 刘爽 高海娜 吴修红 张宁 《中药材》 CAS 北大核心 2017年第7期1683-1686,共4页
目的:研究异补骨脂素对光老化人真皮成纤维(HDF)细胞ER/TGF-β_1/Smads信号通路的调控效应。方法:建立长波紫外线(UVA)损伤HDF模型,给予不同浓度异补骨脂素和通路阻断剂进行干预,MTT法检测细胞增殖率,Western blotting和Real Time-PCR... 目的:研究异补骨脂素对光老化人真皮成纤维(HDF)细胞ER/TGF-β_1/Smads信号通路的调控效应。方法:建立长波紫外线(UVA)损伤HDF模型,给予不同浓度异补骨脂素和通路阻断剂进行干预,MTT法检测细胞增殖率,Western blotting和Real Time-PCR法检测各组细胞内信号转导分子(Smad3)、转化生长因子(TGF-β_1)、Ⅰ型胶原(COL1A1)蛋白和对应mRNA的表达。结果:与正常对照组比较,模型组增殖率及Smad3、TGF-β_1、COL1A1蛋白和mRNA表达均显著降低(P<0.01);与模型组比较,各给药组增殖率和Smad3、TGF-β_1、COL1A1蛋白及mRNA表达均显著升高(P<0.01);与异补骨脂素高浓度组比较,TGF-β_1、Smad3、ER三个阻断剂组相对应的TGF-β_1、Smad3和COL1A1蛋白及相应mRNA表达均显著降低(P<0.01)。结论:异补骨脂素能增加HDF细胞TGF-β_1、Smad3、COL1A1蛋白及mRNA表达,对光老化HDF细胞胶原合成有促进作用;但这种作用能被TGF-β_1、Smad3和ER阻断剂所抑制,推测异补骨脂素促进胶原合成的作用机制与ER/TGF-β_1/Smads信号通路有关。 展开更多
关键词 异补骨脂素 光老化HDF细胞 ER/TGF-β1/Smads信号通路
下载PDF
ER110S-1焊丝拉拔过程中退火工艺及机理探讨 被引量:4
6
作者 喻兰英 罗宏 罗昌森 《热加工工艺》 CSCD 北大核心 2010年第16期168-171,共4页
用差热分析法确定了ER110S-1焊丝的相变点,通过扫描电镜观察分析了断口的形貌特征。进行多种再结晶退火和等温球化退火,用金相显微镜观察金相组织,测定维氏硬度和晶粒度,从而确定最佳球化退火工艺。研究表明:ER110S-1焊丝最佳球化退火... 用差热分析法确定了ER110S-1焊丝的相变点,通过扫描电镜观察分析了断口的形貌特征。进行多种再结晶退火和等温球化退火,用金相显微镜观察金相组织,测定维氏硬度和晶粒度,从而确定最佳球化退火工艺。研究表明:ER110S-1焊丝最佳球化退火工艺为660℃保温12 h,随炉冷至380℃空冷;ER110S-1焊丝进行再结晶退火的球化效果优于等温球化退火;ER110S-1焊丝预拉拔产生的塑性变形可以促进再结晶退火的球化率。 展开更多
关键词 ER110S-1焊丝 拉拔 再结晶退火 等温球化退火 球化机理
下载PDF
稻瘟病菌(Magnaporthe grisea)诱导的水稻早期反应基因ER1的5’端cDNA片段克隆及序列分析 被引量:2
7
作者 周建明 朱群 白永延 《植物生理学报(0257-4829)》 CSCD 1999年第4期413-416,共4页
The 5’ end cDNA fragment(ER1’) of early responsive gene(ER1) of rice(Oryza sativa L. subsp. japonica No.4) induced by blast fungus M. grisea has been isolated and sequenced (606 bp) by 5’RACE technique(Fig. 2). DNA... The 5’ end cDNA fragment(ER1’) of early responsive gene(ER1) of rice(Oryza sativa L. subsp. japonica No.4) induced by blast fungus M. grisea has been isolated and sequenced (606 bp) by 5’RACE technique(Fig. 2). DNA sequence analysis showed that ER1’ (606 bp) can encode 134 amino acids and there are 309 bp nucleotides located at the 3’ end of the untranslated region of mRNA of ER1 gene(Fig. 3). The 89 bp overlapping fragment was found between the 5’ end of ER1 cDNA fragment and the 3’ end of ER1’(Fig. 3). The partial identities of amino acid sequence deduced from ER1’ with an unknown protein(gene accession number AC002409) of Arabidopsis thaliana was 82%(Fig. 4). 展开更多
关键词 水稻 稻瘟病菌 ER1基因 5'cDNA片段 5’RACE
下载PDF
PGRMC1在激素治疗中促进乳腺癌细胞增殖的机制研究 被引量:1
8
作者 赵越 阮祥燕 +2 位作者 谷牧青 许新 程姣姣 《中国癌症防治杂志》 CAS 2022年第4期378-384,共7页
目的探讨孕激素受体膜组分1(progesterone receptor membrane components 1,PGRMC1)在激素治疗中促进乳腺癌细胞增殖的作用机制。方法雌激素受体(estrogen receptor,ER)阳性的乳腺癌MCF7细胞经雌孕激素处理后,用过表达PGRMC1、敲降ER抑... 目的探讨孕激素受体膜组分1(progesterone receptor membrane components 1,PGRMC1)在激素治疗中促进乳腺癌细胞增殖的作用机制。方法雌激素受体(estrogen receptor,ER)阳性的乳腺癌MCF7细胞经雌孕激素处理后,用过表达PGRMC1、敲降ER抑制因子PHB1(shPHB1⁃1和shPHB1⁃2)及其相应阴性对照的慢病毒液进行感染。采用免疫共沉淀联合质谱分析及GST pull⁃down实验检测PGRMC1与PHB复合体(PHB1和PHB2)的相互作用,免疫印迹法和RT⁃qPCR检测PHB1、PHB2和PGRMC1的表达情况,CCK⁃8和EDU实验检测细胞的增殖能力,流式细胞术检测细胞周期情况,RT⁃qPCR检测ER信号通路下游靶基因THBS1、CXCL12和GREB1的表达情况。结果免疫共沉淀联合质谱分析发现,PHB1和PHB2均存在于PGRMC1的免疫共沉淀组分中;GST pull⁃down鉴定体外条件下PGRMC1与PHB复合体存在直接相互作用。与相应对照组相比,过表达PGRMC1和下调PHB1的乳腺癌细胞增殖速度均明显加快(均P<0.05),S期和G2/M期阳性细胞比例均明显增加(均P<0.05),且能够显著促进ER信号通路下游靶基因THBS1、CXCL12和GREB1的表达(均P<0.01)。PGRMC1过表达后MCF7细胞中PHB1与ER的相互作用减弱。下调PHB1后再过表达PGRMC1的细胞周期中,S期和G2/M期阳性细胞比例与单独下调PHB1相比无明显变化(均P>0.05)。结论PGRMC1可能通过与PHB复合体结合,并解除后者对ER信号通路的抑制作用,从而促进ER信号通路的活化和下游靶基因的表达,加速激素刺激条件下乳腺癌细胞的恶性增殖。 展开更多
关键词 乳腺癌 孕激素受体膜组分1 雌激素受体 ER抑制因子1 ER抑制因子2
下载PDF
双酚A对雄性斑马鱼的内分泌干扰效应
9
作者 魏华 任周 +2 位作者 曹娜 陈阿琴 陶贤继 《上海农业学报》 CSCD 北大核心 2012年第4期6-10,共5页
为了探讨双酚A(BPA)内分泌干扰效应,研究了BPA对斑马鱼肝脏雌激素受体(Esr1 mRNA)、芳基烃水解酶受体(AhR2 mRNA)以及卵黄蛋白原(VTG1 mRNA)表达的影响。结果表明:BPA暴露12 h后,Esr1 mRNA和VTG1显著提高(P<0.05)。BPA暴露24 h后,Esr... 为了探讨双酚A(BPA)内分泌干扰效应,研究了BPA对斑马鱼肝脏雌激素受体(Esr1 mRNA)、芳基烃水解酶受体(AhR2 mRNA)以及卵黄蛋白原(VTG1 mRNA)表达的影响。结果表明:BPA暴露12 h后,Esr1 mRNA和VTG1显著提高(P<0.05)。BPA暴露24 h后,Esr1 mRNA和VTG1 mRNA相对表达量依1日保持相当高的水平(P<0.05)。暴露48 h后,Esr1 mRNA的相对表达量继续升高。暴露72 h后,Esr1 mRNA和VTG1 mRNA相对表达量低于暴露12、24 h和48 h。暴露48 h后,AhR2相对表达量为0 h的3.22倍。暴露过程中,Esr1 mRNA和VTG1 mRNA相对表达量变化一致。BPA对雄性斑马鱼的Esr1 mRNA和VTG1mRNA诱导能力较强,但对AhR2诱导能力较弱。表明BPA对斑马鱼的内分泌干扰作用存在多途径过程。 展开更多
关键词 斑马鱼 双酚A Esr1(ERα) AhR2 VTG
下载PDF
冷却速率对Mg_(97)Er_2Zn_1合金凝固组织和力学性能的影响
10
作者 张晋涛 吁艳林 《铸造技术》 CAS 北大核心 2013年第12期1627-1630,共4页
采用光学显微镜、X射线衍射、压缩及硬度试验,研究了不同冷却速率对Mg97Er2Zn1合金铸态组织和力学性能的影响。结果表明,在15~113℃/s的冷却速率范围,Mg97Er2Zn1合金的初生相呈树枝晶状,随着冷却速率增加,树枝晶逐渐细化,二次枝晶间距变... 采用光学显微镜、X射线衍射、压缩及硬度试验,研究了不同冷却速率对Mg97Er2Zn1合金铸态组织和力学性能的影响。结果表明,在15~113℃/s的冷却速率范围,Mg97Er2Zn1合金的初生相呈树枝晶状,随着冷却速率增加,树枝晶逐渐细化,二次枝晶间距变小,合金的晶粒形貌由粗大的树枝状转变成细小的针状。第二相由非连续网状分布变成了连续网状分布再变成细条状分布。冷却速率的变化对Mg97Er2Zn1合金中的第二相的组成没有太大影响,合金中的第二相依然由X-Mg12Er1Zn1相和(Mg,Zn)xEr相组成。Mg97Er2Zn1合金的力学性能随着冷却速率的提高而增加。 展开更多
关键词 Mg97Er2Zn1合金 冷却速率 凝固组织 力学性能
下载PDF
Er/M/1排队系统的忙期
11
作者 孙荣恒 《重庆大学学报(自然科学版)》 EI CAS CSCD 1998年第5期75-78,共4页
设θ为Er/M/1排队系统的忙期,M为在一个忙期中服务完的顾客数。给出了θ的LST和M的PGF以及θ、M的前两阶矩。
关键词 Er/M/1系统 忙期 顾客数 服务系统 排队系统
下载PDF
松脂醇二葡萄糖苷对光老化HDF细胞ER/TGF-β1/Smads信号通路的调控机制 被引量:3
12
作者 高海娜 蔡周权 +2 位作者 林莺 文霞 孙慧峰 《中国医药生物技术》 2018年第5期426-431,共6页
目的从分子生物学水平探讨杜仲中松脂醇二葡萄糖苷(PDG)对光老化人真皮成纤维细胞(HDF)ER/TGF-β1/Smads信号通路的调控机制。方法建立以长波紫外线模型损伤HDF细胞。给予不同浓度PDG和通路阻断剂进行干预,用MTT检测细胞增殖率,Real tim... 目的从分子生物学水平探讨杜仲中松脂醇二葡萄糖苷(PDG)对光老化人真皮成纤维细胞(HDF)ER/TGF-β1/Smads信号通路的调控机制。方法建立以长波紫外线模型损伤HDF细胞。给予不同浓度PDG和通路阻断剂进行干预,用MTT检测细胞增殖率,Real time-PCR和Western blot法检测各组细胞内含有的信号转化生长因子(TGF-β1)、转导分子(Smad3)、I型胶原(COL1A1)对应mRNA和蛋白的表达。结果与空白组比较,模型组增殖率及TGF-β1、Smad3、COL1A1 mRNA和蛋白表达均显著降低(P <0.01);与模型组比较,各给药组增殖率和TGF-β1、Smad3、COL1A1mRNA和蛋白表达均显著升高(P<0.01);与PDG高浓度组比较,TGF-β1、Smad3、ER三个阻断剂组相对应的TGF-β1、Smad3和COL1A1相应mRNA和蛋白表达均显著降低(P <0.01)。结论 PDG能增加HDF细胞TGF-β1、Smad3、COL1A1对应mRNA和蛋白表达,对光老化HDF细胞胶原合成有促进作用;但这种作用能被TGF-β1、Smad3和ER阻断剂所抑制, PDG促进胶原合成的作用机制可能与ER/TGF-β1/Smads信号通路有关。 展开更多
关键词 松脂醇二葡萄糖苷 人真皮成纤维细胞 植物雌激素 ER/TGF-β1/Smads信号通路
下载PDF
Aberrant DNA-PKcs and ERGIC1 expression may be involved in initiation of gastric cancer 被引量:4
13
作者 Fu-rong Wang Yu-cai Wei +4 位作者 Zhi-jian Han Wen-ting He Xiao-ying Guan Hao Chen Yu-min Li 《World Journal of Gastroenterology》 SCIE CAS 2017年第33期6119-6127,共9页
AIM to investigate the molecular mechanisms of gastric carcinogenesis.METHODS We used label-free quantification technology integrated with liquid chromatography-tandem mass spectrometry(Lc-m S/m S) analysis to identif... AIM to investigate the molecular mechanisms of gastric carcinogenesis.METHODS We used label-free quantification technology integrated with liquid chromatography-tandem mass spectrometry(Lc-m S/m S) analysis to identify differentially expressed proteins in 160 specimens of normal gastric mucosa,gastric mucosa with mild dysplasia,moderate dysplasia,severe dysplasia,and early mucosal gastric cancer(Gc) collected at the Second Hospital of Lanzhou University from 2010 to 2015. Immunohistochemistry was used to verify the differentially expressed proteins detected by Lc-m S/m S.RESULTS With a threshold of a 1.2-fold change and a P-value< 0.05 between mild dysplasia,moderate dysplasia,severe dysplasia or early mucosal Gc and matched normal gastric mucosa tissues,proteomic analysis identified 365 significantly differentially expressed proteins. Er GIc1 expression decreased,while DNAPKcs expression increased gradually along with different stages of Gc initiation based on the tendency of fold change. the expression patterns of Er GIc1 and DNA-PKcs revealed by immunohistochemistry were consistent with the Lc-m S/m S results.CONCLUSION the results suggest that aberrant Er GIc1 and DNAPKcs expression may be involved in Gc initiation. 展开更多
关键词 DNA-PKCS Er GIc1 DYSPLASIA PROTEOMICS Gastric cancer
下载PDF
Resistance to powdery mildew in the pea cultivar Xucai 1 is conferred by the gene er1 被引量:2
14
作者 Suli Sun Zhongyi Wang +3 位作者 Haining Fu Canxing Duan Xiaoming Wang Zhendong Zhu 《The Crop Journal》 SCIE CAS CSCD 2015年第6期489-499,共11页
Powdery mildew, caused by Erysiphe pisi D.C., is a major constraint to pea production worldwide. The pea cultivar Xucai 1 has shown high resistance to E. pisi under greenhouse and field conditions. The objectives of t... Powdery mildew, caused by Erysiphe pisi D.C., is a major constraint to pea production worldwide. The pea cultivar Xucai 1 has shown high resistance to E. pisi under greenhouse and field conditions. The objectives of this study were to identify and characterize genes conferring resistance to powdery mildew in Xucai 1. Three crosses, Qizhen 76 × Xucai 1,Bawan 6 × Xucai 1, and Xucai 1 × Bawan 6, were made to generate populations for genetic analysis. The resistance to E. pisi and segregation ratios in the F_1, F_2, and F_(2:3)populations suggested a single recessive gene conferring the resistance of Xucai 1. Bulked segregant analysis was used to map the resistance gene using two F2 populations. The resistance gene was close to markers AD60 and c5 DNAmet on linkage group VI with genetic distances of9.9 c M and 15.4 c M in the Xucai 1 × Bawan 6 F_2 population and 8.7 c M and 8.1 c M in the Qizhen 76 × Xucai 1 F_2 population, respectively, suggesting that the resistance gene was an er1 allele. This hypothesis was confirmed by comparison of the c DNA sequences of the Ps MLO1 gene between the parents and the Ps MLO1 wild type. Three distinct types of transcripts in Xucai 1, characterized by a 129-bp deletion and 155- and 220-bp insertions,were detected, consistent with the structure of the er1-2 allele. We concluded that resistance in Xucai 1 was conferred by er1-2 and that its linked markers will be useful in pea breeding programs. 展开更多
关键词 ERYSIPHE pisi er1-2 PEA Powdery MILDEW Xucai1
下载PDF
Two major er1 alleles confer powdery mildew resistance in three pea cultivars bred in Yunnan Province, China
15
作者 Suli Sun Yuhua He +2 位作者 Cheng Dai Canxing Duan Zhendong Zhu 《The Crop Journal》 SCIE CAS CSCD 2016年第5期353-359,共7页
Powdery mildew, caused by Erysiphe pisi D.C., is an important disease of pea(Pisum sativum L.).The use of cultivars carrying powdery mildew resistance alleles at the er1 locus is the most effective and economical mean... Powdery mildew, caused by Erysiphe pisi D.C., is an important disease of pea(Pisum sativum L.).The use of cultivars carrying powdery mildew resistance alleles at the er1 locus is the most effective and economical means of controlling this disease. The objectives of this study were to screen Chinese elite pea cultivars for resistance to E. pisi and to identify the responsible gene at the er1 locus. Among the 37 pea cultivars tested, three(Yunwan 8, Yunwan 21, and Yunwan 23) were immune to E. pisi infection in phenotypic evaluations. The full-length cD NA sequences of the er1 candidate gene, PsM LO1, from the three resistant cultivars and control plants were analyzed. Comparison of the cD NA sequences of 10 clones revealed differences among the powdery mildew-resistant cultivars, susceptible controls, and wild-type cultivar Sprinter. The observed resistance in Yunwan 8 plants resulted from a point mutation(C → G) at position 680 of PsM LO1 that introduced a stop codon, leading to premature termination of protein synthesis. The responsible resistance allele was identified as er1–1. Powdery mildew resistance in Yunwan 21 and Yunwan 23 plants was caused by identical insertions or deletions in PsM LO1. Three distinct PsM LO1 transcripts were observed in Yunwan 21 and Yunwan 23 plants. These transcripts were characterized by a129-bp deletion and 155- and 220-bp insertions, respectively. The responsible resistance allele was identified as er1–2. We have characterized two important er1 alleles in three E. pisi-resistant pea cultivars bred in Yunnan Province, China. These cultivars represent important genetic resources for the breeding of powdery mildew-resistant pea cultivars. 展开更多
关键词 Erysiphe pisi er1 PEA Powdery mildew Yunnan Province
下载PDF
Improvement in the calculation of anti-Stokes energy transfer and experimental justification based on Er_(0.01)Yb_xY_(1 0.01 x)VO_4 crystal
16
作者 陈晓波 卢建 +5 位作者 张蕴芝 徐小灵 冯宝华 王策 Gregory J. Salamo 杨国建 《Chinese Physics B》 SCIE EI CAS CSCD 2010年第9期604-611,共8页
The improvement on the calculation of anti-Stokes energy transfer rate is studied in the present work. The additional proportion coefficient between Stokes and anti-Stokes light intensities of quantum Raman scattering... The improvement on the calculation of anti-Stokes energy transfer rate is studied in the present work. The additional proportion coefficient between Stokes and anti-Stokes light intensities of quantum Raman scattering theory as compared with the classical Raman theory is introduced to successfully describe the anti-Stokes energy transfer. The theoretical formula for the improvement on the calculation of anti-Stokes energy transfer rate is derived for the first time in this study. The correctness of introducing coefficient exp{△E/kT} from well-known Raman scatter theory is demonstrated also. Moreover, the experimental lifetime measurement in Er0.01YbxY1-0.01-xVO4 crystal is performed to justify the validity of our important improvement in the original phonon-assisted energy transfer theory for the first time. 展开更多
关键词 improvement of anti-Stokes energy transfer Raman scattering quantum and classical theory Er0.01YbxY1-0.01-xVO4 crystal
下载PDF
温度/过程控制器
17
《电子产品世界》 2004年第04B期38-38,共1页
关键词 Omron公司 响应时间 E5AR1/4DIN E5ER1/8DIN 温度/过程控制器
下载PDF
ER50-G与ER55-Ni1在不同温度下的应用
18
作者 胡杰超 《金属加工(热加工)》 2018年第4期36-37,共2页
通过焊接工艺评定试验,确定焊丝的选用,并制定合理的焊接方法、焊接参数,保证焊接质量,实现了产品在不同生存温度下两种焊丝的应用,为我公司提供了相关的技术支撑。
关键词 焊接工艺 ER50—G ER55-Ni1 3.0WM机组 底座
下载PDF
Roles of endoplasmic reticulum stress and apoptosis signaling pathways in gynecologic tumor cells:A systematic review 被引量:2
19
作者 Kangsheng Liu Weimin Fang +1 位作者 Erhu Sun Yajun Chen 《Oncology and Translational Medicine》 2017年第3期131-135,共5页
Efficient functioning of the endoplasmic reticulum(ER) is very important for most cellular activities, such as protein folding and modification. The ER closely interacts with other organelles, including the Golgi body... Efficient functioning of the endoplasmic reticulum(ER) is very important for most cellular activities, such as protein folding and modification. The ER closely interacts with other organelles, including the Golgi body, endosome, membrane, and mitochondria, providing lipids and proteins for the repair of these organelles. ER stress can be induced by various abnormal materials in the cell. ER stress is a compensatory intracellular environment disorder that occurs during areaction. ER can sense the stress and respond to it through translational attenuation, upregulation of the genes for ER chaperones and related proteins, and degradation of unfolded proteins by a quality-control system, but excessive ER activation can cause cell death. The Pubmed and Web of Science databases were searched for full-text articles, and the terms "endoplasmic reticulum stress/unfolded protein response/gynecologic tumor cell apoptosis" were used as key words. Thirty-five studies of ER stress and unfolded protein response published from 2000 to 2016 were analyzed. Stress triggers apoptosis through a variety of signaling pathways. Increasing evidence has shown that the ER plays an important role in tumor cell diseases. The present review discusses the molecular mechanisms underlying unfolded protein response and its ability to promote survival and proliferation in gynecologic tumor cells. 展开更多
关键词 endoplasmic reticulum(ER) unfolded protein response(UPR) inositol-requiring-JNK(IRE1-JNK) caspase CCAAT-enhancer-binding protein homologous protein(CHOP) gynecologic tumor cell
下载PDF
Ethanol extract of Cyathulae Radix inhibits osteoclast differentiation and bone loss 被引量:1
20
作者 SHI Liying REN Liuyi +7 位作者 LI Jinping LIU Xin LU Jingjing JIA Lujuan XIE Baoping TANG Siyuan LIU Wei ZHANG Jie 《Chinese Journal of Natural Medicines》 SCIE CAS CSCD 2024年第3期212-223,共12页
Cyathulae Radix,a traditional Chinese medicine and a common vegetable,boasts a history spanning millennia.It enhances bone density,boosts metabolism,and effectively alleviates osteoporosis-induced pain.Despite its his... Cyathulae Radix,a traditional Chinese medicine and a common vegetable,boasts a history spanning millennia.It enhances bone density,boosts metabolism,and effectively alleviates osteoporosis-induced pain.Despite its historical use,the molecular mechanisms behind Cyathulae Radix’s impact on osteoporosis remain unexplored.In this study,we investigated the effects and mechanisms of Cyathulae Radix ethanol extract(CEE)in inhibiting osteoporosis and osteoclastogenesis.Eight-week-old female mice underwent ovariectomy and were treated with CEE for eight weeks.Micro-computed tomography(micro-CT)assessed histomorphometric parameters,bone tissue staining observed distal femur histomorphology,and three-point bending tests evaluated tibia mechanical properties.Enzyme-linked immunosorbent assay(ELISA)measured serum estradiol(E2),receptor activator for nuclear factor B ligand(RANKL),and osteoprotegerin(OPG)levels.Osteoclastogenesis-related markers were analyzed via Western blotting(WB)and quantitative real-time polymerase chain reaction(qRT-PCR).Additionally,CEE effects on RANKL-induced osteoclast formation and bone resorption were investigated in vitro using tartrate-resistant acid phosphatase(TRAP)staining,qRT-PCR,and WB assay.Compared with the ovariectomy(OVX)group,CEE treatment enhanced trabecular bone density,maximal load-bearing capacity,and various histomorphometric parameters.Serum E2 and OPG levels significantly increased,while Receptor activator of nuclear factor-κB(RANK)decreased in the CEE group.CEE downregulated matrix metallopeptidase 9(MMP-9),Cathepsin K(CTSK),and TRAP gene and protein expression.In bone marrow macrophages(BMMs),CEE reduced mature osteoclasts,bone resorption pit areas,and MMP-9,CTSK,and TRAP expression during osteoclast differentiation.Compared with DMSO treatment,CEE markedly inhibited RANK,TNF receptor associated factor 6(TRAF6),Proto-oncogene c-Fos(c-Fos),Nuclear factor of activated T-cells cytoplasmic 1(NFATc1)expressions,and Extracellular regulated protein kinases(ERK),c-Jun N-terminal kinase(JNK),NF-kappa B-p65(p65)phosphorylation in osteoclasts.In conclusion,CEE significantly inhibits OVX-induced osteoporosis and RANKL-induced osteoclastogenesis,potentially through modulating the Estrogen Receptor(ER)/RANK/NFATc1 signaling pathway. 展开更多
关键词 OSTEOPOROSIS OSTEOCLAST BMMs Cyathulae Radix RANKL ER/RANK/NFATc1 signaling pathway
原文传递
上一页 1 2 下一页 到第
使用帮助 返回顶部