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   338905篇
  免费   39928篇
  国内免费   206篇
  2016年   3840篇
  2015年   5190篇
  2014年   5977篇
  2013年   8903篇
  2012年   11016篇
  2011年   11278篇
  2010年   7199篇
  2009年   6266篇
  2008年   9988篇
  2007年   10307篇
  2006年   9722篇
  2005年   9437篇
  2004年   9114篇
  2003年   9082篇
  2002年   8738篇
  2001年   12467篇
  2000年   12738篇
  1999年   10081篇
  1998年   4053篇
  1997年   4134篇
  1996年   4196篇
  1995年   3886篇
  1994年   3885篇
  1993年   3855篇
  1992年   8589篇
  1991年   8350篇
  1990年   8113篇
  1989年   8028篇
  1988年   7565篇
  1987年   7495篇
  1986年   6946篇
  1985年   7135篇
  1984年   6111篇
  1983年   5491篇
  1982年   4441篇
  1981年   4299篇
  1980年   3892篇
  1979年   6252篇
  1978年   4968篇
  1977年   4722篇
  1976年   4510篇
  1975年   4871篇
  1974年   5317篇
  1973年   5211篇
  1972年   4775篇
  1971年   4328篇
  1970年   3828篇
  1969年   3837篇
  1968年   3424篇
  1967年   2947篇
排序方式: 共有10000条查询结果,搜索用时 62 毫秒
191.
The structure of the viral RNA in alfalfa mosaic virus (AlMV) was investigated by means of 31P-nuclear magnetic resonance (NMR). It was found that the 31P-NMR line width of AlMV Top a particles is significantly smaller than that of the larger Bottom particles. At low temperatures, the totational correlation time of the 31P nuclei essentially equals the tumbling rate of the virus particle, indicating that the RNA is contained rigidly inside the virion. At more elevated temperatures, the NMR line width sharpens more than expected on the basis of viscosity changes and the RNA exhibits internal mobility. The occurrence of internal mobility is paralleled by an increased internal mobility of the N-terminal part of the coat protein, as could be observed by 1H-NMR spectroscopy. The influence of EDTA on the 31P-NMR line width appeared to be negligible, which is in agreement with the idea that AlMV does not 'swell' like several other RNA-containing plant viruses.  相似文献   
192.
193.
194.
195.
196.
Summary The iliofibularis muscle ofXenopus laevis is reported to contain five types of fibres which have different force—velocity relationships. Ten fibres of each type were selected on the basis of succinate dehydrogenase activity, cross-sectional area and location in the muscle, in order to assess the validity of the fibre type classification.Maximum calcium-stimulated myofibrillar ATPase activity (V max) and apparent Michaelis constant (K m) for ATP were determined for these 50 fibres from serial sections. The values obtained varied according to the type of fibre. Type 1 had the highest and type 5 the lowest values forK m andV max.In a separate experiment, single freeze-dried fibres were used to determine the relationship between their ATP content and apparentK m for ATP. There was a tendency for high ATP concentrations in fibres with highK m values.When myofibrillar ATPase activity was related to the maximum velocity of shortening of the five fibre types, a significant correlation was found. It is concluded that calcium-stimulated myofibrillar ATPase histochemistry allows an estimate of the maximum shortening velocity of muscle fibres fromXenopus laevis.  相似文献   
197.
198.
Albert's method, of staining diphtheria cultures consists of staining a fixed smear for one minute (some laboratories stain for five minutes) with a solution containing toluidine blue and malachite (or methyl) green, washing with water, and applying Albert's iodine for one minute. This procedure is discussed and criticized, and in addition the mechanism of the stain is elucidated. Also, the procedure which involves staining a fixed smear for one minute with Loeffler's alkaline methylene blue solution is discussed and criticized.

To overcome the objections to the above staining methods, a different method is proposed. This consists of staining a fixed smear with an acid solution of toluidine blue, washing with water, applying Albert's iodine for one minute, washing with water, and finally applying a safranin solution for 15-20 seconds. The theoretical basis for this method is presented.  相似文献   
199.
200.
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