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   325252篇
  免费   21938篇
  国内免费   61篇
  347251篇
  2021年   2738篇
  2020年   2236篇
  2019年   2549篇
  2018年   5496篇
  2017年   5202篇
  2016年   6727篇
  2015年   7719篇
  2014年   9034篇
  2013年   12589篇
  2012年   15081篇
  2011年   15157篇
  2010年   10209篇
  2009年   8212篇
  2008年   13004篇
  2007年   13297篇
  2006年   12512篇
  2005年   11648篇
  2004年   11454篇
  2003年   10865篇
  2002年   10459篇
  2001年   11299篇
  2000年   10925篇
  1999年   8686篇
  1998年   2868篇
  1997年   2554篇
  1996年   2350篇
  1995年   2190篇
  1992年   6666篇
  1991年   6784篇
  1990年   6634篇
  1989年   6520篇
  1988年   6060篇
  1987年   5605篇
  1986年   5130篇
  1985年   5412篇
  1984年   4353篇
  1983年   3578篇
  1982年   2431篇
  1979年   3913篇
  1978年   3010篇
  1977年   2764篇
  1976年   2706篇
  1975年   3242篇
  1974年   3552篇
  1973年   3524篇
  1972年   3071篇
  1971年   2931篇
  1970年   2513篇
  1969年   2436篇
  1968年   2294篇
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
61.
Indirect evidence has suggested that the Msh2-Msh6 mispair-binding complex undergoes conformational changes upon binding of ATP and mispairs, resulting in the formation of Msh2-Msh6 sliding clamps and licensing the formation of Msh2-Msh6-Mlh1-Pms1 ternary complexes. Here, we have studied eight mutant Msh2-Msh6 complexes with defective responses to nucleotide binding and/or mispair binding and used them to study the conformational changes required for sliding clamp formation and ternary complex assembly. ATP binding to the Msh6 nucleotide-binding site results in a conformational change that allows binding of ATP to the Msh2 nucleotide-binding site, although ATP binding to the two nucleotide-binding sites appears to be uncoupled in some mutant complexes. The formation of Msh2-Msh6-Mlh1-Pms1 ternary complexes requires ATP binding to only the Msh6 nucleotide-binding site, whereas the formation of Msh2-Msh6 sliding clamps requires ATP binding to both the Msh2 and Msh6 nucleotide-binding sites. In addition, the properties of the different mutant complexes suggest that distinct conformational states mediated by communication between the Msh2 and Msh6 nucleotide-binding sites are required for the formation of ternary complexes and sliding clamps.  相似文献   
62.
63.
64.
65.
66.
67.
An easy, reproducible and fast procedure to isolate DNA from cotton leaves is described. The addition of 0.5 M glucose in the extraction buffer avoids browning by polyphenolic compounds and improves the quality of DNA for molecular analysis. The DNA yield ranged between 150–400 mg per gram of fresh tissue. The DNA was suitable for digestion by restriction enzymes and amplificatiion by Taq DNA polymerase.  相似文献   
68.
Intrastriatal corticotrophin-releasing hormone (CRH) was shown to induce a decrease in the plasma tectosterone concentration. Besides, the 6-OHDA pre-treatment completely prevented the suppression of plasma testosterone in response to intrastriatal CRH administration. The findings suggest that the striatum is involved in the extrahypothalamic regulation of the gonadal endocrine function.  相似文献   
69.
The development of the fin and limb buds involves a balance of centrifugal (active) and centripetal (passive) mechanical forces, the first of which acts to move the walls of these structures away from each other and the second of which holds them together. When the volume of the mesodermal core increases, the generated force meets with the resistance of the basal membrane, and as a result, the limb bud has a tendency to acquire a cylindrical shape. Collagen fibers, individual mesenchymal cells, and their groups hold together the dorsal and the ventral wall of the limb bud, prevent the movement of these walls away from each other, and in this way direct bud growth along the proximodistal and the anteroposterior axes. The balance of the forces which stretch the ectodermal layer and those which constrain it has also been observed in the development of other body parts.  相似文献   
70.
In this paper we quantify and characterize the expression of recombinant beta-lactoglobulin (rBLG) in prokaryote and eukaryote cells. In Escherichia coli we used the pET26 vector, which permits the secretion of rBLG in periplasm. We studied the expression of rBLG in COS-7 cells and in vivo in mouse tibialis muscle. The expression of rBLG was measured by two immunoassays specific, respectively, for BLG in its native and denatured conformation. We observed that rBLG was essentially expressed in a denatured form in E. coli even in the periplasm, whereas rBLG in eukaryote cells was found in its native conformation.  相似文献   
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