首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   96篇
  免费   3篇
  国内免费   65篇
  2022年   4篇
  2021年   2篇
  2020年   3篇
  2019年   17篇
  2018年   15篇
  2017年   11篇
  2016年   2篇
  2015年   6篇
  2014年   2篇
  2013年   6篇
  2012年   4篇
  2011年   6篇
  2010年   3篇
  2009年   8篇
  2008年   6篇
  2007年   6篇
  2006年   15篇
  2005年   14篇
  2004年   4篇
  2003年   4篇
  2002年   5篇
  2001年   5篇
  2000年   5篇
  1999年   1篇
  1995年   2篇
  1994年   5篇
  1988年   1篇
  1985年   1篇
  1981年   1篇
排序方式: 共有164条查询结果,搜索用时 15 毫秒
161.
162.
Mannosyl (alpha-1,6-)-Glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase (MGAT5) is exclusively expressed in gastric carcinoma, and plays an essential role in cancer progression, but no targeted drug is available so far. The potential anti-cancer effect of Hydrogen Sulfide (H2S), has not been widely recognized. It intrigued broad interest to explore the clinical benefits of cancer therapy, with the current understanding of molecular mechanisms of H2S which remains very limited. In this study, we identify that H2S is an effective inhibitor of MGAT5, leading to reduce the expression of exclusively abnormal glycoprotein processes in gastric carcinoma. H2S specifically dissociation of karyopherin subunit alpha-2 (KPNA2) with Jun proto-oncogene (c-Jun) interaction, and blocking c-Jun nuclear translocation, and downregulation of MGAT5 expression at the level of gene and protein. Consequently, H2S impairs growth and metastasis in gastric carcinoma by targeting inhibits MGAT5 activity. In an animal tumor model study, H2S is well tolerated, inhibits gastric carcinoma growth and metastasis. Our preclinical work therefore supports that H2S acts as a novel inhibitor of MGAT5 that block tumorigenesis in gastric carcinoma. SIGNIFICANCE: This study shows that H2S can effective targeting inhibits MGAT5 activity, and demonstrates promising antitumor efficacy. These findings gain mechanistic insights into the anti-cancer capacity of H2S and may provide useful information for the clinical explorations of H2S in cancer treatment.  相似文献   
163.
The mechanistic target of rapamycin (mTOR) pathway coordinates organismal growth and homeostasis in response to growth factors, nutrients, and cellular energy stage. The pathway regulates several major cellular processes and is implicated in various pathological conditions, including hepatocellular carcinoma (HCC). This review summarizes recent advances of the mTOR pathway, highlights the potential of the mTOR pathway as a therapeutic target, and explores clinical trials targeting the mTOR pathway in HCC. Although the review focuses on the mTOR pathway involved in HCC, more comprehensive discussions (eg, developing a rational design for future trials targeting the mTOR pathway) are also applicable to other tumors.  相似文献   
164.
To characterize the urbanization pattern quantitatively,a study on the mechanisms of the landscape pattern formation could facilitate the understanding on urban landscape patterns and processes,the ecological and socioeconomic consequences of urbanization,as well as the establishment of more effective strategies for landscape management.In this study,we integrated a Geographic Information System (GIS)-based analysis on landscape pattern with an artificial neural network (ANN) to quantitatively characterize the urbanization pattern of the metropolitan area of Shanghai,China,and to establish an ANN model that could preferably simulate the responses of urban landscape pattern to the natural and socioeconomic factors such as residence area,road density,population density,urban development history and the Huangpu River as an element of economic change.Our results showed that the ANN model seems appropriate for studying the nonlinear relationship among the forcing factors of urbanization and the urban landscape patterns,which provided an effective and practical approach for further understanding the mechanisms of the landscape formation pattern and the reciprocal relationship between landscape spatial pattern and ecological process.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号