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   112570篇
  免费   1892篇
  国内免费   1263篇
  115725篇
  2023年   161篇
  2022年   330篇
  2021年   525篇
  2020年   357篇
  2019年   438篇
  2018年   12256篇
  2017年   11014篇
  2016年   8021篇
  2015年   1629篇
  2014年   1335篇
  2013年   1655篇
  2012年   5768篇
  2011年   14174篇
  2010年   12793篇
  2009年   8896篇
  2008年   10800篇
  2007年   12319篇
  2006年   1198篇
  2005年   1375篇
  2004年   1759篇
  2003年   1789篇
  2002年   1508篇
  2001年   672篇
  2000年   545篇
  1999年   387篇
  1998年   211篇
  1997年   185篇
  1996年   128篇
  1995年   109篇
  1994年   138篇
  1993年   130篇
  1992年   222篇
  1991年   215篇
  1990年   172篇
  1989年   186篇
  1988年   158篇
  1987年   145篇
  1986年   122篇
  1985年   128篇
  1984年   96篇
  1983年   112篇
  1982年   76篇
  1981年   58篇
  1979年   69篇
  1977年   84篇
  1976年   63篇
  1975年   59篇
  1974年   71篇
  1972年   274篇
  1971年   321篇
排序方式: 共有10000条查询结果,搜索用时 20 毫秒
101.
A hypothesis has been developed to relate stringent control in bacteria to a set of interactions involved in the regulation of growth of transformed and untransformed mammalian cells.  相似文献   
102.
Kimball and Wilson1 reported that the arabinose analogue of cytidine (ara-C) inhibited DNA polymerase in a crude extract prepared from Ehrlich ascites cells. Furth and Cohen2 observed cytosine arabinoside triphosphate (ara-CTP) inhibited DNA polymerase in extracts from either calf thymus or bovine lymphosarcoma tissue, although these investigators3 had already found no effect of ara-CTP on DNA polymerase from Escherichia coli. The inhibition in both of these cases could be substantially reversed by dCTP; but incorporation of the arabinose nucleotide (ara-CMP) into DNA could not be unequivocally demonstrated. Graham and Whitmore4 reported the incorporation of ara-C into DNA in vivo and the inhibition of a DNA polymerase from L cells by ara-CTP. They found that ara-CMP was initially incorporated into small DNA strands but subsequently appeared in long strands. Momparler5 has presented evidence that, in vitro, ara-C incorporation was limited to the 3′-hydroxyl end of DNA chains. Such incorporation might be expected to block further chain elongation but this expectation was not supported by the evidence presented by Graham and Whitmore.  相似文献   
103.
JACOB and Fuerst1,2 demonstrated the presence of a bacteriolytic enzyme (λ-endolysin) in the induced cultures of lysogenic Escherichia coli K12 (λ). The enzyme was later identified as the product of gene R; of phage λ3 which is involved in bacterial lysis at the end of a latent period. The enzyme is apt to form spheroplast-like structures in E. coli2 and one would therefore expect its substrate to be murein.  相似文献   
104.
105.
106.
107.
108.
Alterations affecting the epidermal growth factor/transforming growth factor alpha-responsive mitogenic pathway are frequently detected in malignancies. In particular, the epidermal growth factor receptor has been found overexpressed in a number of human tumors. Production and secretion of transforming growth factor type alpha has also been shown in several tumor cells but not in their normal counterparts. In this review we describe the establishment of in vitro model systems to study the transforming potential of these molecules and summarize our current understanding of the mechanisms involved in transformation by genes encoding a growth factor and a growth factor receptor.  相似文献   
109.
Univariate and multivariate statistical analyses have been performed on 19 morphometric variables of adult male specimens belonging to three genetically identified species within Pseudoterranova decipiens (Nematoda: Ascaridida) parasitic in the digestive tract of seals. Two morphometric keys are proposed for the identification of the three species. One key, which uses two variables, determines a frequency of error of 3.8% (3/79). The second key, which uses two canonical discriminant functions based on seven variables previously selected with a stepwise procedure, gives 100% (76/76) accurate classification.  相似文献   
110.
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