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   416393篇
  免费   53180篇
  国内免费   196篇
  469769篇
  2018年   3556篇
  2016年   4626篇
  2015年   6598篇
  2014年   7617篇
  2013年   11022篇
  2012年   12231篇
  2011年   12579篇
  2010年   8450篇
  2009年   7876篇
  2008年   11104篇
  2007年   11467篇
  2006年   10662篇
  2005年   10283篇
  2004年   9932篇
  2003年   9910篇
  2002年   9530篇
  2001年   19725篇
  2000年   19935篇
  1999年   15734篇
  1998年   5477篇
  1997年   6037篇
  1996年   5741篇
  1995年   5361篇
  1994年   5255篇
  1993年   5383篇
  1992年   13353篇
  1991年   13181篇
  1990年   12564篇
  1989年   12366篇
  1988年   11279篇
  1987年   10925篇
  1986年   10209篇
  1985年   10159篇
  1984年   8502篇
  1983年   7339篇
  1982年   5642篇
  1981年   5023篇
  1980年   4845篇
  1979年   7997篇
  1978年   6397篇
  1977年   5822篇
  1976年   5488篇
  1975年   6028篇
  1974年   6220篇
  1973年   6150篇
  1972年   5551篇
  1971年   5106篇
  1970年   4258篇
  1969年   4101篇
  1968年   3674篇
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
961.
962.
963.
964.
This study was designed to assess the changes in fiber-type distribution of the extensor digitorum longus (EDL) muscle of the mouse during the first 21 days of age following neonatal sciatic neurectomy. Denervated and normal muscles were compared at 7, 14, and 21 days of age and the normal EDL was also studied at 1 day of age. Frozen sections of the EDL were treated histochemically to detect NADH-tetrazolium reductase and myosin ATPase reactions. Quantitative assessment included measurements of cross-sectional areas and fiber counting. Denervation resulted in muscle atrophy which was due primarily to a decrease in individual fiber area as opposed to fiber loss. Histochemical maturation of the EDL was severely affected by neonatal denervation during the first three postnatal weeks. By 21 days, two extrafusal fiber types which were both oxidative could be distinguished. One type was highly atrophied and resembled an immature fiber exhibiting myosin ATPase staining at both acid and alkaline preincubation conditions, whereas another type was less atrophied and showed myosin ATPase staining resembling fast-twitch (type IIA) fibers. These findings emphasize the importance of an intact nerve supply in determining the phenotypic expression of skeletal muscle, and point to the early postnatal period as a critical stage in fiber type differentiation.  相似文献   
965.
966.
967.
968.
Cycling virgin female rats were treated with clomiphene citrate (CC) during dioestrus of the reproductive cycle. Animals were sacrificed 2 days after the initial injection and their vaginal tissue was examined by scanning electron microscopy. Animals treated with one dose of CC had an epithelium consistent with a prolonged dioestrus. Treatment with CC for 2 days induced changes in the epithelium that had no resemblance to any normal hormonally controlled event in the vagina. It was found that CC had effects consistent with progesterone alone as well as effects unique to this superovulatory drug.  相似文献   
969.
970.
Earlier work demonstrated that the activity of liver phosphofructokinase (PFK-L2) and immunoreactive PFK-L2 were decreased in diabetic rats and increased to normal or super-normal amounts following insulin treatment (Dunaway, G.A., and Weber, G., (1974) Arch. Biochem. Biophys. 162, 629-637). This report indicates that the decrease in levels of PFK-L2 in diabetic rats is a result of an accelerated degradation rate while the synthetic rate remains nearly normal. Following insulin treatment, the rate of PFK-L2 synthesis is enhanced 2-fold, whereas the rate of degradation appears to be greatly diminished. An inverse relationship is shown to exist between the PFK-L2 levels and the rates of PFK-L2 degradation, suggesting that the levels of PFK-L2 are primarily regulated by degradation rate. In addition, the levels of the PFK-L2 peptide stabilizing factor are inversely proportional to rates of PFK-L2 degradation. These results indicate that insulin mediates the rate of degradation of PFK-L2 by controlling the level of the peptide stabilizing factor.  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