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   969篇
  免费   27篇
  国内免费   7篇
化学   681篇
晶体学   3篇
力学   21篇
数学   154篇
物理学   144篇
  2023年   7篇
  2022年   33篇
  2021年   42篇
  2020年   29篇
  2019年   27篇
  2018年   13篇
  2017年   14篇
  2016年   43篇
  2015年   20篇
  2014年   45篇
  2013年   67篇
  2012年   60篇
  2011年   87篇
  2010年   50篇
  2009年   37篇
  2008年   48篇
  2007年   55篇
  2006年   47篇
  2005年   43篇
  2004年   41篇
  2003年   23篇
  2002年   26篇
  2001年   13篇
  2000年   7篇
  1999年   6篇
  1998年   6篇
  1997年   3篇
  1996年   7篇
  1995年   4篇
  1994年   3篇
  1991年   3篇
  1984年   2篇
  1983年   2篇
  1981年   3篇
  1980年   2篇
  1977年   5篇
  1939年   2篇
  1937年   5篇
  1936年   4篇
  1935年   2篇
  1934年   9篇
  1933年   6篇
  1932年   4篇
  1931年   4篇
  1930年   2篇
  1929年   5篇
  1912年   3篇
  1911年   2篇
  1906年   3篇
  1905年   2篇
排序方式: 共有1003条查询结果,搜索用时 15 毫秒
121.
Ohne Zusammenfassung  相似文献   
122.
123.
In the present study, the potential of lead and cadmium removal by the extracellular polymeric substances (EPS) produced from Parachlorella kessleri and Chlorella vulgaris were investigated. Carbohydrates were the dominant components of EPS from both analyzed species. The contents of reducing sugars, uronic acids, and amino acids were higher in EPS synthesized by C. vulgaris than in EPS from P. kessleri. The analysis of the monosaccharide composition showed the presence of rhamnose, mannose and galactose in the EPS obtained from both species. The ICP-OES (inductively coupled plasma optical emission spectrometry) analyses demonstrated that C. vulgaris EPS showed higher sorption capacity in comparison to P. kessleri EPS. The sorption capacity of C. vulgaris EPS increased with the increase in the amount of metal ions. P. kessleri EPS had a maximum sorption capacity in the presence of 100 mg/L of metal ions. The FTIR analysis demonstrated that the carboxyl, hydroxyl, and carbonyl groups of EPS play a key role in the interactions with metal ions. The present study showed C. vulgaris EPS can be used as a biosorbent in bioremediation processes due to its biochemical composition, the presence of significant amounts of negatively charged uronic acids, and higher sorption capacity.  相似文献   
124.
Dyslipidemias are one of the risk factors for cardiovascular diseases, the leading cause of death and hospitalization worldwide. One way to control cholesterol levels is to control the exogenous cholesterol intake in the body. Natural polyphenolic compounds, namely theaflavins from plant extracts such as black tea, showed the ability to inhibit the formation of the micellar structure, essential for the absorption of cholesterol in the intestine. There are several methodologies to determine this effect, many of which are expensive and time-consuming. Due to these facts, the main purposes of this work were to optimize an inexpensive colorimetric method to study, in vitro, the micellar solubility of cholesterol and applied it to plant extracts. In this work, Cymbopogon citratus leaf extracts, its phenolic fractions, and flavonoids were evaluated. The non-delipidified infusion (CcI) obtained a maximum percentage of micelle destruction of 59.22% for a concentration of 50 μg/mL and the delipidified infusion (CcdI) obtained a maximum percentage of micelle destruction of 58.01% for a concentration of 200 μg/mL. In the case of the fraction of phenolic acids (CcPAs), 23.85% of maximum micellar destruction was recorded for the concentration of 100 μg/mL, while for the fraction of flavonoids (CcF), the micellar destruction was 92.74% at 1 μg/mL, and for the tannin fraction (CcT) of 99.45% at 25 μg/mL. Luteolin presented a percentage of micelle destruction of 94.83% in the concentration of 1 ng/mL, followed by luteolin-7-O-glucoside with 93.71% and luteo-lin-6-C-glucoside with 91.26% at the concentrations of 25 ng/mL and 50 ng/mL, respectively. These results suggest the capability of polyphenols from Cymbopogon citratus to prevent the cholesterol absorption in the gut by micellar destruction, and its contribution for cholesterol-lowering activity.  相似文献   
125.
126.
127.
128.
129.
130.
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