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   3335篇
  免费   241篇
  3576篇
  2023年   18篇
  2022年   27篇
  2021年   42篇
  2020年   41篇
  2019年   44篇
  2018年   53篇
  2017年   45篇
  2016年   103篇
  2015年   142篇
  2014年   158篇
  2013年   171篇
  2012年   259篇
  2011年   210篇
  2010年   151篇
  2009年   111篇
  2008年   178篇
  2007年   180篇
  2006年   170篇
  2005年   167篇
  2004年   165篇
  2003年   154篇
  2002年   158篇
  2001年   60篇
  2000年   44篇
  1999年   32篇
  1998年   59篇
  1997年   39篇
  1996年   30篇
  1995年   37篇
  1994年   31篇
  1993年   30篇
  1992年   38篇
  1991年   21篇
  1990年   24篇
  1989年   18篇
  1988年   24篇
  1987年   27篇
  1986年   22篇
  1985年   15篇
  1984年   15篇
  1982年   11篇
  1981年   23篇
  1980年   17篇
  1979年   14篇
  1978年   19篇
  1977年   12篇
  1976年   11篇
  1974年   11篇
  1973年   10篇
  1972年   12篇
排序方式: 共有3576条查询结果,搜索用时 15 毫秒
111.
Marianne Stahl 《Planta》1949,37(1):103-148
Ohne ZusammenfassungMit 27 Textabbildungen.  相似文献   
112.
113.
114.
The Cytotoxic Necrotizing Factor 1 (CNF1) is a protein toxin which is a major virulence factor of pathogenic Escherichia coli strains. Here, we identified the Lutheran (Lu) adhesion glycoprotein/basal cell adhesion molecule (BCAM) as cellular receptor for CNF1 by co-precipitation of cell surface molecules with tagged toxin. The CNF1-Lu/BCAM interaction was verified by direct protein-protein interaction analysis and competition studies. These studies revealed amino acids 720 to 1014 of CNF1 as the binding site for Lu/BCAM. We suggest two cell interaction sites in CNF1: first the N-terminus, which binds to p37LRP as postulated before. Binding of CNF1 to p37LRP seems to be crucial for the toxin''s action. However, it is not sufficient for the binding of CNF1 to the cell surface. A region directly adjacent to the catalytic domain is a high affinity interaction site for Lu/BCAM. We found Lu/BCAM to be essential for the binding of CNF1 to cells. Cells deficient in Lu/BCAM but expressing p37LRP could not bind labeled CNF1. Therefore, we conclude that LRP and Lu/BCAM are both required for toxin action but with different functions.  相似文献   
115.
Ohne ZusammenfassungMit 42 Textabbildungen.  相似文献   
116.
Ohne ZusammenfassungDissertation der Naturwissenschaftlichen Fakultät der Universität Frankfurt am Main.  相似文献   
117.
118.
Investigatory behavior with novel, inanimate objects by two groups of four juvenile greater bushbabies (Otolemur garnettii) was examined in the laboratory. Substantial investigatory behavior was shown by all subjects. In the first study, subjects showed interest in a wide variety of nonfood stimulus objects. In the second, subjects displayed sustained interest in and investigation of non-food stimulus objects over three sessions. Bushbabies showed preferences for larger, more manipulable objects and variations in total contact over days. Individual differences were observed in the duration and types of contact with objects. These observations contradict earlier reports that prosimians show little interest in inanimate, non-food objects.  相似文献   
119.
Bacterial genomes are a huge reservoir of genes encoding J-domain protein co-chaperones that recruit the molecular chaperone DnaK to assist protein substrates involved in survival, adaptation, or fitness. The atc operon of the aquatic mesophilic bacterium Shewanella oneidensis encodes the proteins AtcJ, AtcA, AtcB, and AtcC, and all of them, except AtcA, are required for growth at low temperatures. AtcJ is a short J-domain protein that interacts with DnaK, but also with AtcC through its 21 amino acid C-terminal domain. This interaction network is critical for cold growth. Here, we show that AtcJ represents a subfamily of short J-domain proteins that (i) are found in several environmental, mostly aquatic, β- or ɣ-proteobacteria and (ii) contain a conserved PX7W motif in their C-terminal extension. Using a combination of NMR, biochemical and genetic approaches, we show that the hydrophobic nature of the tryptophan of the S. oneidensis AtcJ PX7W motif determines the strong AtcJ–AtcC interaction essential for cold growth. The AtcJ homologues are encoded by operons containing at least the S. oneidensis atcA, atcB, and atcC homologues. These findings suggest a conserved network of DnaK and Atc proteins necessary for low-temperature growth and, given the variation in the atc operons, possibly for other biological functions.  相似文献   
120.
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