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   665篇
  免费   126篇
  791篇
  2022年   5篇
  2021年   7篇
  2016年   6篇
  2015年   15篇
  2014年   16篇
  2013年   25篇
  2012年   24篇
  2011年   29篇
  2010年   18篇
  2009年   14篇
  2008年   23篇
  2007年   15篇
  2006年   28篇
  2005年   27篇
  2004年   21篇
  2003年   26篇
  2002年   25篇
  2001年   32篇
  2000年   27篇
  1999年   16篇
  1998年   14篇
  1997年   14篇
  1996年   13篇
  1995年   10篇
  1994年   11篇
  1992年   15篇
  1991年   27篇
  1990年   19篇
  1989年   21篇
  1988年   16篇
  1987年   14篇
  1986年   9篇
  1985年   15篇
  1984年   9篇
  1983年   7篇
  1982年   14篇
  1981年   8篇
  1980年   7篇
  1979年   9篇
  1978年   10篇
  1976年   9篇
  1975年   9篇
  1974年   6篇
  1973年   11篇
  1972年   10篇
  1971年   8篇
  1970年   7篇
  1969年   8篇
  1968年   5篇
  1934年   5篇
排序方式: 共有791条查询结果,搜索用时 0 毫秒
591.
592.
593.
594.
595.
Coomassie brilliant blue and Ponceau red have traditionally been used to stain electroblotted proteins, since they are compatible with existing N-terminal and internal protein microsequencing as well as with immunoblotting procedures. With recent improvements in sequencing and immunoblotting technology, detection of significantly smaller amounts of protein has become necessary. Metal complexes were evaluated as alternatives to conventional stains. Electroblotted proteins were detected by blocking nonspecific sites with polyvinylpyrrolidone-40 followed by incubation in metal chelate solutions at acidic pH values. Two of the most promising metal chelate stains were the Ferrozine/ferrous complex and the ferrocyanide/ferric complex. Both stained a wide variety of proteins and peptides quantitatively. Dot blots and 1D and 2D electroblots were successfully stained using iron chelates. When these two stains were utilized in combination, they were of equivalent sensitivity to colloidal gold stain. The reversibility of the metal chelate stains was substantiated by incubating stained membranes at neutral to basic pH in the presence of 20 mM ethylenediaminetetraacetic acid to rapidly elute the complexes from the bound proteins. The chelate stains were determined to be fully compatible with immunoblotting, N-terminal, and in situ internal protein microsequencing.  相似文献   
596.
597.

Background  

The persistence of cooperative relationships is an evolutionary paradox; selection should favor those individuals that exploit their partners (cheating), resulting in the breakdown of cooperation over evolutionary time. Our current understanding of the evolutionary stability of mutualisms (cooperation between species) is strongly shaped by the view that they are often maintained by partners having mechanisms to avoid or retaliate against exploitation by cheaters. In contrast, we empirically and theoretically examine how additional symbionts, specifically specialized parasites, potentially influence the stability of bipartite mutualistic associations. In our empirical work we focus on the obligate mutualism between fungus-growing ants and the fungi they cultivate for food. This mutualism is exploited by specialized microfungal parasites (genus Escovopsis) that infect the ant's fungal gardens. Using sub-colonies of fungus-growing ants, we investigate the interactions between the fungus garden parasite and cooperative and experimentally-enforced uncooperative ("cheating") pairs of ants and fungi. To further examine if parasites have the potential to help stabilize some mutualisms we conduct Iterative Prisoner's Dilemma (IPD) simulations, a common framework for predicting the outcomes of cooperative/non-cooperative interactions, which incorporate parasitism as an additional factor.  相似文献   
598.
599.
600.
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