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   241篇
  免费   32篇
  国内免费   1篇
  2023年   1篇
  2022年   1篇
  2021年   3篇
  2020年   3篇
  2019年   4篇
  2018年   5篇
  2017年   5篇
  2016年   3篇
  2015年   7篇
  2014年   18篇
  2013年   15篇
  2012年   10篇
  2011年   17篇
  2010年   11篇
  2009年   5篇
  2008年   9篇
  2007年   13篇
  2006年   6篇
  2005年   7篇
  2004年   11篇
  2003年   4篇
  2002年   6篇
  2001年   15篇
  2000年   12篇
  1999年   18篇
  1998年   6篇
  1997年   11篇
  1996年   10篇
  1995年   8篇
  1994年   4篇
  1993年   1篇
  1992年   2篇
  1991年   3篇
  1990年   2篇
  1989年   1篇
  1988年   2篇
  1986年   2篇
  1985年   4篇
  1984年   2篇
  1983年   1篇
  1982年   2篇
  1978年   2篇
  1974年   1篇
  1971年   1篇
排序方式: 共有274条查询结果,搜索用时 125 毫秒
271.
Developing taste buds in the anterior mandibular floor of perihatching chicks were studied by high voltage electron microscopic autoradiography in order to identify proliferating gemmal cell types. Montaged profiles of 29 taste buds in five cases euthanized between embryonic day 21 and posthatching day 2 were analyzed after a single [3H]thymidine injection administered on embryonic day 16, 17 or 18. Results showed that dark cells comprised 55% of identified (n = 900 cells) and 62% of labeled (n = 568 cells) gemmal cells as compared with light, intermediate, basal or perigemmal bud cells. Dark cells had both a greater (P < 0.05) number of labeled cells and a greater amount of label (grains/nucleus) than the other four bud cell types, irrespective of injection day. The nuclear area (micron 2) of dark cells was not significantly larger (P > 0.05) than that of the other gemmal cell types and therefore cannot account for the greater amount for label in the dark cells. Interestingly, only dark cells showed a positive correlation (P < 0.003) between amount of label and nuclear area. Results suggest that, during the perihatching period of robust cell proliferation, dividing dark cells may give rise primarily, but not exclusively, to dark cell progeny.   相似文献   
272.
The major rivers of the South African ‘Lowveld’ (low-latitude savanna) suffer numerous impacts from upstream economic activities. Whereas monitoring these rivers is required to detect biodiversity losses, record pollution events and devise mitigation strategies, current monitoring programmes are inadequate. In 2009, the South African Earth Observation Network initiated an intensive long-term research programme on the Lowveld reaches of the Olifants River. Physico-chemical parameters, aquatic macroinvertebrates and fish abundances were recorded at four Lowveld sites in the Olifants River. We review six years of this programme. The results suggest deterioration in the ecological condition of the Olifants River with no discernible improvement through protected areas. Trends could not be detected. The parameters measured, sampling methods and/or sampling frequency might be responsible for the limited trends observed, or alternatively the results simply reflect stable conditions despite on-going pollution. Real time monitoring and an expansion in the parameters monitored would add value to the monitoring programme.  相似文献   
273.
274.
Myostatin maps to the interval containing the bovine mh locus   总被引:1,自引:0,他引:1  
Myostatin (GDF-8) is a member of the transforming growth factor-β superfamily and plays a role in muscle growth and development. Mice having targeted disruption of this gene display marked increases in muscle mass, a phenotype similar to the muscular hypertrophy (mh) in several cattle breeds. Physical mapping data developed from YAC clones indicate the bovine myostatin gene lies close to the centromere of bovine Chromosome (Chr) 2 (BTA2) at 2q11, indistinguishable from the cytogenetic location of the mh locus. In addition, a polymorphism in the second intron of the gene was used to show that myostatin maps within the interval previously shown to contain mh. These data suggest myostatin may be the gene causing muscular hypertrophy in cattle. Received: 19 June 1997 / Accepted: 2 July 1997  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