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   8674篇
  免费   780篇
  国内免费   614篇
  2023年   105篇
  2022年   127篇
  2021年   401篇
  2020年   284篇
  2019年   334篇
  2018年   275篇
  2017年   221篇
  2016年   301篇
  2015年   511篇
  2014年   565篇
  2013年   578篇
  2012年   753篇
  2011年   717篇
  2010年   460篇
  2009年   401篇
  2008年   458篇
  2007年   467篇
  2006年   410篇
  2005年   355篇
  2004年   302篇
  2003年   300篇
  2002年   275篇
  2001年   135篇
  2000年   94篇
  1999年   91篇
  1998年   79篇
  1997年   77篇
  1996年   73篇
  1995年   69篇
  1994年   63篇
  1993年   58篇
  1992年   50篇
  1991年   33篇
  1990年   35篇
  1989年   45篇
  1988年   38篇
  1987年   22篇
  1986年   37篇
  1985年   23篇
  1984年   25篇
  1983年   27篇
  1982年   36篇
  1981年   28篇
  1980年   29篇
  1979年   30篇
  1978年   15篇
  1977年   18篇
  1973年   16篇
  1972年   17篇
  1971年   15篇
排序方式: 共有10000条查询结果,搜索用时 859 毫秒
41.
42.
43.
The incorporation of uridine into RNA in brain slices was studied. Optimal conditions for uridine incorporation were determined. The characteristics of the product suggest that de novo DNA-directcd synthesis of fairly high molecular weight material takes place. Incorporation into RNA of several areas of brain was studied. The incorporation was also studied as a function of the age of the animal. Finally, an apparent correlation was observed between the decrease in uridine incorporation with age and the increase of the enzyme uridine nucleosidase which hydrolyses uridine to uracil, a material which cannot be incorporated into RNA.  相似文献   
44.
Electron transport activity and absorbance changes associated with P700 were investigated in a mutant strain of Chlamydomonas reinhardi with impaired photosynthesis. This mutant strain, ac-8oa, cannot reduce NADP with electrons from either water or dye and ascorbate, but it has considerable Hill activity. The mutant strain shows none of the absorbance changes characteristic of P700. Although unable to carry out cyclic photosynthetic phosphorylation, ac-8oa is able to synthesize ATP when ferricyanide is provided as an electron acceptor.

These observations lead to the conclusion that a site for the coupling of photosynthetic phosphorylation with electron transport must exist between the 2 photochemical systems.

  相似文献   
45.
46.
47.
48.
49.
S100b is a calcium-binding protein that will bind to many calmodulin target molecules in a Ca2+-dependent manner. In order to study the Ca2+-dependent binding properties of S100b, its interaction with a calmodulin antagonist, trifluoperazine (TFP), was investigated using [19F]- and [1H]-NMR and UV-difference spectroscopy. It was estimated from [19F]-NMR that in the absence of Ca2+, thek 1/2 value of TFP was 130 µM, while itsk 1/2 value decreased to 28 µM in the presence of Ca2+. The addition of KCl was not antagonistic to the Ca2+-dependent interaction of TFP to S100b. The chemical exchange rate of TFP with Ca2+-bound S100b was estimated to be 9×102 sec?1. By comparison with TFP-calmodulin exchange rates, it is suggested that the TFP-binding site on S100b is structurally different from its binding sites on calmodulin. Proton NMR resonance broadening in the range 6.8–7.2 ppm, corresponding to phenylalanine nuclei of S100b, indicates that these residues may be involved in TFP binding. Addition of Ca2+ to a 1:1 mixture of S100b and TFP resulted in a red-shifted UV-difference spectrum, while no significant difference spectrum was detected when Mg2+ was added to a S100b-TFP solution. Thus, we suggest that Ca2+ induces the exposure of a hydrophobic domain on S100b containing one or more phenylalanine residues that will bind TFP but that this domain is different from the hydrophobic domain on calmodulin.  相似文献   
50.
鱼类的巨噬细胞和高等脊椎动物的一样,在吞灭入侵的病原体方面起着极其重要的作用。探索在体外长期培养巨噬细胞的方法,有助于研究巨噬细胞的机能。Braun-Nesje等虽已从硬头鳟(Salmo gairdneri)等鲑科鱼类的头肾中分离出大量的巨噬细胞,并在体外培养了3个月之久,但因细胞不分裂,无法传代。本研究改用组织块培养法和饲养层技术探索长期培养巨噬细胞的方法,并获得成功。迄今巨噬细胞已在体外培养22个月,传代48次。细胞的原代培养分为三组。前两组是单独的脾或头肾的组织培养;第三组是脾与头肾的混合组织培养。培养液是Leibovitz’s L-15,外加20%胎牛血清,100 IU/ml青霉素和100μg/ml链霉素。巨噬细胞的吞噬活力用酵母菌Candida  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