|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | Knowledge-based land use/cover classification of remote sensing image in Kenli, Shandong Province, China显示文摘 | LI Jing ZHAO Gengxing YANG Peiguo | 2006 | Chinese Science Bulletin2006，51，B11： | 2 |
| 2 | The Feasibility of Total or Near-Total Bilateral Thyroidectomy for the Treatment of Bilateral Multinodular Goiter显示文摘 | Weiping Yang Tanglei Shao Jiazeng Ding Xiaotai Jin Qinyu Li Peiguo G. Chu Yun Yen Weihua Qiu | 2009 | Investigative Surgery2009，，3： | 1 |
| 3 | Increased Mortality from Delayed Diagnosisand Treatment of Obturator Hernia in Elderly Patients显示文摘 | Seewoo Varun Jin Xiaotai Yang Weiping Wang Jiayu Chu Peiguo G Yen Christina Qiu Weihua | 2012 | EN2012，，4： | 1 |
| 4 | You are what you eat: multifaceted functions of autophagy during C. elegans development显示文摘Autophagy 为降级在围住的双膜 autophagosomal 结构和它的随后的交货包含 cytosolic 内容的部分的隐遁到 lysosomes。Autophagy 活动在 Caenorhabditis elegans 开发期间在多重生物进程工作。在胚胎的 autophagy 的基础水平移开总数容易的蛋白质,父亲的线粒体和 spermatid 特定的膜的细胞器(瞬间) 。Autophagy 也由支持 phagosome 成熟贡献胚胎的 apoptotic 房间死尸的有效移动。在幼虫的开发期间, autophagy 由有选择地降级的 AIN-1 调制调停 miRNA 的基因 silencing,导致 miRNA 的 silencing 建筑群的一个部件,并且因此参予 miRNAs 控制的多重房间命运的说明。在雌雄同体 germline 的开发期间, autophagy 与核心 apoptotic 机械并列地行动执行 genotoxic 导致压力的 germline 房间死亡并且另外房间死亡 caspase 活动是什么时候,部分损害了。Autophagy 也在成年动物在变老的过程涉及类脂化合物微滴的利用。在 C 学习。elegans 在多细胞的有机体的发展提供珍贵卓见进 autophagy 的生理的功能。 | Peiguo Yang Hong Zhang | 2014 | Cell Research2014，24，1： | 1 |
| 5 | Spatial pattern of the flood disaster risk in the protected zone of the lower Yellow River embankment显示文摘 | YANG Peiguo DAI Erfu WU Shaohong KANG Xiangwu YANG Qinye XIA Fuqiang | 2006 | Chinese Science Bulletin2006，51，B11： | 1 |
| 6 | Pre-assessment on the loss and impact caused by large-scale flood disasters显示文摘 | KANG Xiangwu WU Shaohong DAI Erfu YANG Qinye LIU Ziqiang YANG Peiguo MA Xin ZHAO Ruifeng | 2006 | Chinese Science Bulletin2006，51，B11： | 1 |
| 7 | A genome-wide RNAi screen identifies genes regulating the formation of P bodies in C. elegans and their functions in NMD and RNAi显示文摘Cytoplasmic processing bodies,termed P bodies,are involved in diverse post-transcriptional processes including mRNA decay,nonsense-mediated RNA decay(NMD),RNAi,miRNA-mediated translational repression and storage of translationally silenced mRNAs.Regulation of the formation of P bodies in the context of multicellular organisms is poorly understood.Here we describe a systematic RNAi screen in C.elegans that identified 224 genes with diverse cellular functions whose inactivations result in a dramatic increase in the number of P bodies.83 of these genes form a complex functional interaction network regulating NMD.We demonstrate that NMD interfaces with many cellular processes including translation,ubiquitin-mediated protein degradation,intracellular trafficking and cytoskeleton structure.We also uncover an extensive link between translation and RNAi,with different steps in protein synthesis appearing to have distinct effects on RNAi efficiency.Moreover,the intracellular vesicular trafficking network plays an important role in the regulation of RNAi.A subset of genes enhancing P body formation also regulate the formation of stress granules in C.elegans.Our study offers insights into the cellular mechanisms that regulate the formation of P bodies and also provides a framework for system-level understanding of NMD and RNAi in the context of the development of multicellular organisms. | Yinyan Sun Peiguo Yang Yuxia Zhang Xin Bao Jun Li Wenru Hou Xiangyu Yao Jinghua Han Hong Zhang | 2011 | Protein & Cell2011，2，11： | 0 |
| 8 | The characteristics of dike-break flood in different scenarios of the lower Yellow River based on numerical simulations显示文摘更低的黄河仍然由于全球环境变化,河隧道沉积,在堤的隐藏的危险和鈥渉a nging 河鈥的相反的河政体引起的不平常的降水面对洪水的威胁吗?根据黄河的堤裂缝洪水的特征,这份报纸模仿了,在到二维的不稳定的流动模型的六种不同情形,由输入地面数据的堤裂缝洪水路由,典型历史的洪水数据和学习区域的陆地使用数据。结果显示出那:第一,洪水的路由进程将在到达更低的活动范围以后在到河的路和回来上占据另外的河;在一样的河活动范围,第二泛滥淹没北方乐队的区域在在一样的历史的洪水下面的南岸的相应地点比那大;第三,它由于在洪水平原的不同地理地点在在不同区域的洪水淹没的度是不同的;第四,洪水是深的主流的区域和流动速度是快的相对更小,但是区域非主流在洪水是浅的,流动速度是慢的的地方,相对大;并且最后,堤裂缝洪水的可能的影响区域是 141,948 km2。 | MA Xin YANG Peiguo YANG Qinye KANG Xiangwu XIA Fuqiang | 2007 | Journal of Geographical Sciences2007，17，1： | 0 |
| 9 | Research on the reservation route of the lower Yellow River显示文摘 | LIU Yanhua KANG Xiangwu WU Shaohong YANG Qinye DAI Erfu MA Xin YANG Peiguo | 2006 | Chinese Science Bulletin2006，51，B11： | 0 |
| 10 | Biomolecular phase separation in stress granule assembly and virus infection显示文摘Liquid-liquid phase separation(LLPS)has emerged as a crucial mechanism for cellular compartmentalization.One prominent example of this is the stress granule.Found in various types of cells,stress granule is a biomolecular condensate formed through phase separation.It comprises numerous RNA and RNA-binding proteins.Over the past decades,substantial knowledge has been gained about the composition and dynamics of stress granules.SGs can regulate various signaling pathways and have been associated with numerous human diseases,such as neurodegenerative diseases,cancer,and infectious diseases.The threat of viral infections continues to loom over society.Both DNA and RNA viruses depend on host cells for replication.Intriguingly,many stages of the viral life cycle are closely tied to RNA metabolism in human cells.The field of biomolecular condensates has rapidly advanced in recent times.In this context,we aim to summarize research on stress granules and their link to viral infections.Notably,stress granules triggered by viral infections behave differently from the canonical stress granules triggered by sodium arsenite(SA)and heat shock.Studying stress granules in the context of viral infections could offer a valuable platform to link viral replication processes and host anti-viral responses.A deeper understanding of these biological processes could pave the way for innovative interventions and treatments for viral infectious diseases.They could potentially bridge the gap between basic biological processes and interactions between viruses and their hosts. | Yi Liu Zhiying Yao Guiwei Lian Peiguo Yang | 2023 | Acta Biochimica et Biophysica Sinica2023，55，7： | 0 |
您所在的机构暂未开通此部分的功能，请联系管理员