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   42652篇
  免费   3568篇
  国内免费   3850篇
  2024年   111篇
  2023年   596篇
  2022年   1308篇
  2021年   2051篇
  2020年   1439篇
  2019年   1866篇
  2018年   1773篇
  2017年   1332篇
  2016年   1852篇
  2015年   2747篇
  2014年   3182篇
  2013年   3385篇
  2012年   3946篇
  2011年   3529篇
  2010年   2255篇
  2009年   1968篇
  2008年   2362篇
  2007年   2079篇
  2006年   1838篇
  2005年   1550篇
  2004年   1287篇
  2003年   1109篇
  2002年   912篇
  2001年   719篇
  2000年   589篇
  1999年   581篇
  1998年   366篇
  1997年   360篇
  1996年   325篇
  1995年   263篇
  1994年   276篇
  1993年   188篇
  1992年   274篇
  1991年   241篇
  1990年   197篇
  1989年   150篇
  1988年   111篇
  1987年   137篇
  1986年   128篇
  1985年   94篇
  1984年   83篇
  1983年   58篇
  1982年   54篇
  1981年   45篇
  1980年   31篇
  1979年   47篇
  1978年   25篇
  1977年   29篇
  1976年   24篇
  1975年   28篇
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
1.
2.
Recently we have studied thermodynamics of membrane-mediated β-amyloid formation in equilibrium experiments using penetratin-lipid mixtures. The results showed that penetratin bound to the membrane interface in the α-helical conformation when the peptide/lipid (P/L) ratios were below a lipid-dependent critical value P/L. When P/L reached P/L, small β-aggregates emerged, which served as the nuclei for large β-aggregates. Here we studied the corresponding kinetic process to understand the potential barriers for the membrane-mediated β-amyloid formation. We performed kinetic experiments using giant unilamellar vesicles made of 7:3 DOPC/DOPG. The observed time behavior of individual giant unilamellar vesicles, although complex, exhibited the physical effects seen in equilibrium experiments. Most interestingly, a potential barrier appeared to block penetratin from translocating across the bilayer. As a result, the kinetic value for the critical threshold P/L is roughly one-half of the value measured in equilibrium where peptides bind symmetrically on both sides of lipid bilayers. We also investigated the similarity and differences between the charged and neutral lipids in their interactions with penetratin. We reached an important conclusion that the bound states of peptides in lipid bilayers are largely independent of the charge on the lipid headgroups.  相似文献   
3.
4.
A recombinant cell line (NIH3T3:pLtkSN) was made by infecting parental cells (NIH3T3) with a recombinant retrovirus (pLtkSN) encoding herpes simplex virus thymidine kinase (HSVtk) gene. The cells expressing HSVtk (NIH3T3:pLtkSN) grew 2.3 times more than the parental cells (NIH3T3) in Dulbecco's Modified Eagles Media containing 10% (v/v) horse serum. The NIH3T3:pLtkSN cells also showed a significant enhancement in the maximal cell concentration and the specific growth rate even at 2.5% serum concentration. The specific O2 uptake rate of NIH3T3 was 2.1 times greater than that of NIH3T3:pLtkSN. Under both O2-limited and O2-unlimited conditions, it appears that HSVtk plays an important role in enhancing the growth characteristics of animal cells.  相似文献   
5.
6.
7.
Described here is a three-day protocol that directly yields DNA sequence after isolating and PCR amplifying genomic DNA from a small sample of frozen nasopharyngeal carcinoma tissue embedded in optimal cutting temperature (OCT) compound. The method is consistently successful, reproducible and will facilitate the rapid analysis of DNA sequence from very small samples.  相似文献   
8.
  相似文献   
9.
Using the reconstituted Ca-ATPase vesicles as a model system, we demonstrated that the presence of 1,2-dioleoyl-sn-glycerol (diolein) in the membrane introduces a pronounced enhancement in the Ca-transport function of Ca-ATPase, while the 1,2-dipalmitoyl-sn-glycerol (dipalmitin) does not. We also found by both 31P NMR and freeze-fraction electron microscopy that diolein destabilized lipid bilayers to a greater extent than did dipalmitin. We conclude that the tendency of diacylglycerols to destabilize the phospholipid bilayer is related to their capacity to enhance the activity of the membrane calcium pump.  相似文献   
10.
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