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   479251篇
  免费   47851篇
  国内免费   266篇
  2018年   9467篇
  2017年   9179篇
  2016年   9235篇
  2015年   7751篇
  2014年   8657篇
  2013年   12170篇
  2012年   15305篇
  2011年   19789篇
  2010年   14687篇
  2009年   13853篇
  2008年   17519篇
  2007年   19284篇
  2006年   12179篇
  2005年   12398篇
  2004年   12036篇
  2003年   11517篇
  2002年   11239篇
  2001年   17558篇
  2000年   17698篇
  1999年   13959篇
  1998年   5069篇
  1997年   5321篇
  1996年   4946篇
  1995年   4627篇
  1994年   4487篇
  1993年   4560篇
  1992年   11631篇
  1991年   11561篇
  1990年   11291篇
  1989年   10922篇
  1988年   10487篇
  1987年   10086篇
  1986年   9360篇
  1985年   9232篇
  1984年   7758篇
  1983年   6716篇
  1982年   5179篇
  1981年   4618篇
  1980年   4469篇
  1979年   7422篇
  1978年   5859篇
  1977年   5394篇
  1976年   5201篇
  1975年   5604篇
  1974年   6301篇
  1973年   6170篇
  1972年   6265篇
  1971年   5665篇
  1970年   4641篇
  1969年   4576篇
排序方式: 共有10000条查询结果,搜索用时 171 毫秒
51.
52.
53.
54.
55.
An agar-degrading marine bacterium identified as a Microscilla species was isolated from coastal California marine sediment. This organism harbored a single 101-kb circular DNA plasmid designated pSD15. The complete nucleotide sequence of pSD15 was obtained, and sequence analysis indicated a number of genes putatively encoding a variety of enzymes involved in polysaccharide utilization. The most striking feature was the occurrence of five putative agarase genes. Loss of the plasmid, which occurred at a surprisingly high frequency, was associated with loss of agarase activity, supporting the sequence analysis results.  相似文献   
56.
Expression of the glycoprotein clusterin is markedly increased following tissue injury. One function of clusterin is to promote cell interactions which are perturbed in these pathologic settings. Clusterin causes cell aggregation and adhesion in vitro yet the molecular mechanism for this effect is not known. In order to identify the active site(s) of clusterin, 34 peptides, each 15 amino acid residues in length, were synthesized from hydrophilic regions of human clusterin. When studied individually, none of the peptides caused aggregation of LLC-PK1 cells, a porcine renal epithelial cell line. However, two out of the 34 peptides inhibited clusterin-induced cell aggregation in a dose-dependent manner. Scrambled versions of these two 'active' peptides did not inhibit cell aggregation. Seven peptides promoted cell adhesion. In conclusion, these findings provide evidence for novel amino acid sequences mediating clusterin-induced renal cell interactions.  相似文献   
57.
58.
Self-consistent steady-state axisymmetric configurations of a plasma envelope with a uniform anisotropic conductivity around a rotating magnetized spherical body are considered. A set of electrodynamic and magnetohydrodynamic equations is analyzed under the assumption that the mass velocity of a moving weakly ionized plasma has only the azimuthal component. The equations describing the profile of the angular frequency of the rotating plasma envelope, the magnetic field, the conduction currents, and the plasma density distribution are solved in the limit of a strong anisotropy of the conductivity of a weakly ionized gas. The applicability of the results obtained to a qualitative interpretation of the phenomena occurring in the plasmaspheres of magnetized planets is discussed.  相似文献   
59.
The operating and storage stability of a receptor element of an amperometric biosensor based on thePseudomonas rathonis strain T capable of degrading surfactants was tested. Microbial cells were immobilized by incorporation in gels (agar, agarose, and calcium-alginate), polyvinyl alcohol membrane, adhesion to Chromatographic paper GF/A, or by cross-linking induced by glutaric aldehyde. Incorporation of microbial cells in agar gel provides long-standing conservation of their activity and viability during measurements of high concentrations of surfactants and allows the receptor element of the biosensor to be rapidly recovered after measurements.  相似文献   
60.
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