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   12016篇
  免费   24篇
  国内免费   45篇
系统科学   35篇
丛书文集   80篇
教育与普及   30篇
理论与方法论   43篇
现状及发展   5143篇
研究方法   589篇
综合类   5997篇
自然研究   168篇
  2013年   102篇
  2012年   215篇
  2011年   365篇
  2010年   88篇
  2009年   59篇
  2008年   205篇
  2007年   240篇
  2006年   211篇
  2005年   239篇
  2004年   219篇
  2003年   217篇
  2002年   206篇
  2001年   379篇
  2000年   365篇
  1999年   263篇
  1992年   232篇
  1991年   181篇
  1990年   205篇
  1989年   190篇
  1988年   201篇
  1987年   205篇
  1986年   161篇
  1985年   248篇
  1984年   170篇
  1983年   149篇
  1982年   166篇
  1981年   135篇
  1980年   170篇
  1979年   385篇
  1978年   291篇
  1977年   288篇
  1976年   250篇
  1975年   288篇
  1974年   308篇
  1973年   308篇
  1972年   344篇
  1971年   344篇
  1970年   428篇
  1969年   361篇
  1968年   382篇
  1967年   351篇
  1966年   320篇
  1965年   203篇
  1959年   107篇
  1958年   204篇
  1957年   137篇
  1956年   122篇
  1955年   105篇
  1954年   81篇
  1948年   83篇
排序方式: 共有10000条查询结果,搜索用时 259 毫秒
41.
tRNase Z: the end is not in sight   总被引:1,自引:0,他引:1  
Although the enzyme tRNase Z has only recently been isolated, a plethora of data has already been acquired concerning the enzyme. tRNase Z is the endonuclease that catalyzes the removal of the tRNA 3′ trailer, yielding the mature tRNA 3′ end ready for CCA addition and aminoacylation. Another substrate cleaved by tRNase Z is the small chromogenic phosphodiester bis(p-nitrophenyl)phosphate (bpNPP), which is the smallest tRNase Z substrate known so far. Hitherto the biological function as tRNA 3′-end processing enzyme has been shown only in one prokaryotic and one eukaryotic organism, respectively. This review summarizes the present information concerning the two tRNase Z substrates pre-tRNA and bpNPP, as well as the metal requirements of tRNase Z enzymes. Received 29 March 2007; received after revision 15 May 2007; accepted 21 May 2007  相似文献   
42.
Glycolysis is an evolutionary conserved metabolic pathway that provides small amounts of energy in the form of ATP when compared to other pathways such as oxidative phosphorylation or fatty acid oxidation. The ATP levels inside metabolically active cells are not constant and the local ATP level will depend on the site of production as well as the respective rates of ATP production, diffusion and consumption. Membrane ion transporters (pumps, exchangers and channels) are located at sites distal to the major sources of ATP formation (the mitochondria). We review evidence that the glycolytic complex is associated with membranes; both at the plasmalemma and with membranes of the endo/sarcoplasmic reticular network. We examine the evidence for the concept that many of the ion transporters are regulated preferentially by the glycolytic process. These include the Na+/K+-ATPase, the H+-ATPase, various types of Ca2+-ATPases, the Na+/H+ exchanger, the ATP-sensitive K+ channel, cation channels, Na+ channels, Ca2+ channels and other channels involved in intracellular Ca2+ homeostasis. Regulation of these pumps, exchangers and ion channels by the glycolytic process has important consequences in a variety of physiological and pathophysiological processes, and a better understanding of this mode of regulation may have important consequences for developing future strategies in combating disease and developing novel therapeutic approaches. Received 20 July 2007; received after revision 30 July 2007; accepted 17 August 2007  相似文献   
43.
44.
45.
1 Results Classic oxidants require rigorous control of the experimental conditions added with the problem of lack of selectivity. Catalysis by transition metals with environmentally safe oxidants provides synthetic routes to minimize pollution by giving environmental benign by-products. Fe (Ⅵ) is a powerful and a selective oxidant with Fe(Ⅲ) as a by-product, while hydrogen peroxide is clean with water as the only by-product. Separation of sodium or potassium ferrates requires tedious processes. Associat...  相似文献   
46.
The association of variants in complement factors H and B with age-related macular degeneration has led to more intense genetic and functional analysis of the complement pathway. We identify a nonsynonymous coding change in complement factor 3 that is strongly associated with risk of age-related macular degeneration in a large case-control sample.  相似文献   
47.
48.
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