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   29727篇
  免费   89篇
  国内免费   161篇
系统科学   158篇
丛书文集   501篇
教育与普及   42篇
理论与方法论   125篇
现状及发展   13901篇
研究方法   1311篇
综合类   13508篇
自然研究   431篇
  2013年   285篇
  2012年   436篇
  2011年   858篇
  2010年   190篇
  2008年   555篇
  2007年   597篇
  2006年   603篇
  2005年   572篇
  2004年   568篇
  2003年   525篇
  2002年   527篇
  2001年   953篇
  2000年   882篇
  1999年   626篇
  1992年   598篇
  1991年   426篇
  1990年   493篇
  1989年   499篇
  1988年   466篇
  1987年   553篇
  1986年   478篇
  1985年   602篇
  1984年   489篇
  1983年   371篇
  1982年   342篇
  1981年   377篇
  1980年   470篇
  1979年   911篇
  1978年   771篇
  1977年   749篇
  1976年   620篇
  1975年   634篇
  1974年   857篇
  1973年   774篇
  1972年   795篇
  1971年   853篇
  1970年   1084篇
  1969年   829篇
  1968年   841篇
  1967年   819篇
  1966年   699篇
  1965年   491篇
  1964年   168篇
  1959年   252篇
  1958年   443篇
  1957年   295篇
  1956年   259篇
  1955年   249篇
  1954年   247篇
  1948年   166篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
41.
Several hundred million tons of toxic mercurials are dispersed in the biosphere. Microbes can detoxify organo-mercurials and mercury salts through sequential action of two enzymes, organomercury lyase and mercuric ion reductase (MerA). The latter, a homodimer with homology to the FAD-dependent disulphide oxidoreductases, catalyses the reaction NADPH + Hg(II)----NADP+ + H+ + Hg(0), one of the very rare enzymic reactions with metal substrates. Human glutathione reductase serves as a reference molecule for FAD-dependent disulphide reductases and between its primary structure and that of MerA from Tn501 (Pseudomonas), Tn21 (Shigella), p1258 (Staphylococcus) and Bacillus, 25-30% of the residues have been conserved. All MerAs have a C-terminal extension about 15 residues long but have very varied N termini. Although the enzyme from Streptomyces lividans has no addition, from Pseudomonas aeruginosa Tn501 and Bacillus sp. strain RC607 it has one and two copies respectively of a domain of 80-85 residues, highly homologous to MerP, the periplasmic component of proteins encoded by the mer operon. These domains can be proteolytically cleaved off without changing the catalytic efficiency. We report here the crystal structure of MerA from the Gram-positive bacterium Bacillus sp. strain RC607. Analysis of its complexes with nicotinamide dinucleotide substrates and the inhibitor Cd(II) reveals how limited structural changes enable an enzyme to accept as substrate what used to be a dangerous inhibitor. Knowledge of the mode of mercury ligation is a prerequisite for understanding this unique detoxification mechanism.  相似文献   
42.
43.
There is considerable debate among scholars over whether Descartes allowed for genuine body–body interaction. I begin by considering Michael Della Rocca’s recent claim that Descartes accepted such interaction, and that his doctrine of the creation of the eternal truths indicates how this interaction could be acceptable to him. Though I agree that Descartes was inclined to accept real bodily causes of motion, I differ from Della Rocca in emphasizing that his ontology ultimately does not allow for them. This is not the end of the story however, since two of Descartes’s successors offered incompatible ways of developing his conflicted account of motion. I contrast the occasionalist view of Nicolas Malebranche that changes in motion derive directly from divine volitions with the non-occasionalist claim of Pierre-Sylvain Regis that such changes derive from a nature distinct from God. In light of Della Rocca’s interpretation, it is noteworthy that the issue of eternal truths is relevant to both alternative accounts. Indeed, Regis took the doctrine that such truths are created to provide crucial support for his alternative to an occasionalist account of body–body interaction. What does not help Della Rocca, however, is that Regis’s view of motion requires a fundamental revision of Descartes’s ontology.  相似文献   
44.
45.
46.
47.
48.
Seaweed culture     
WALKER FT  SMITH MM 《Nature》1948,162(4105):31
  相似文献   
49.
50.
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