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   1101篇
  免费   109篇
  国内免费   1篇
  2023年   4篇
  2022年   5篇
  2021年   19篇
  2020年   14篇
  2019年   15篇
  2018年   17篇
  2017年   16篇
  2016年   38篇
  2015年   65篇
  2014年   61篇
  2013年   70篇
  2012年   98篇
  2011年   82篇
  2010年   49篇
  2009年   41篇
  2008年   73篇
  2007年   77篇
  2006年   44篇
  2005年   49篇
  2004年   61篇
  2003年   52篇
  2002年   34篇
  2001年   13篇
  2000年   8篇
  1999年   25篇
  1998年   6篇
  1997年   12篇
  1996年   5篇
  1993年   4篇
  1992年   8篇
  1991年   4篇
  1990年   7篇
  1989年   8篇
  1988年   10篇
  1987年   4篇
  1986年   4篇
  1984年   4篇
  1982年   9篇
  1981年   4篇
  1980年   4篇
  1978年   7篇
  1977年   3篇
  1974年   5篇
  1973年   3篇
  1969年   3篇
  1968年   6篇
  1967年   6篇
  1962年   6篇
  1960年   5篇
  1958年   3篇
排序方式: 共有1211条查询结果,搜索用时 15 毫秒
1.
Traditional gene targeting methods in mice are complex and time consuming, especially when conditional deletion methods are required. Here, we describe a novel technique for assessing gene function by injection of modified antisense morpholino oligonucleotides (MOs) into the heart of mid-gestation mouse embryos. After allowing MOs to circulate through the embryonic vasculature, target tissues were explanted, cultured and analysed for expression of key markers. We established proof-of-principle by partially phenocopying known gene knockout phenotypes in the fetal gonads (Stra8, Sox9) and pancreas (Sox9). We also generated a novel double knockdown of Gli1 and Gli2, revealing defects in Leydig cell differentiation in the fetal testis. Finally, we gained insight into the roles of Adamts19 and Ctrb1, genes of unknown function in sex determination and gonadal development. These studies reveal the utility of this method as a means of first-pass analysis of gene function during organogenesis before committing to detailed genetic analysis.  相似文献   
2.
Evolutionary analyses of population translocations (experimental or accidental) have been important in demonstrating speed of evolution because they subject organisms to abrupt environmental changes that create an episode of selection. However, the strength of selection in such studies is rarely measured, limiting our understanding of the evolutionary process. This contrasts with long-term, mark–recapture studies of unmanipulated populations that measure selection directly, yet rarely reveal evolutionary change. Here, we present a study of experimental evolution of male colour in Trinidadian guppies where we tracked both evolutionary change and individual-based measures of selection. Guppies were translocated from a predator-rich to a low-predation environment within the same stream system. We used a combination of common garden experiments and monthly sampling of individuals to measure the phenotypic and genetic divergence of male coloration between ancestral and derived fish. Results show rapid evolutionary increases in orange coloration in both populations (1 year or three generations), replicating the results of previous studies. Unlike previous studies, we linked this evolution to an individual-based analysis of selection. By quantifying individual reproductive success and survival, we show, for the first time, that males with more orange and black pigment have higher reproductive success, but males with more black pigment also have higher risk of mortality. The net effect of selection is thus an advantage of orange but not black coloration, as reflected in the evolutionary response. This highlights the importance of considering all components of fitness when understanding the evolution of sexually selected traits in the wild.  相似文献   
3.
4.
5.
6.
7.
The Pubishers wish to apologise for the inadvertent mis-spellingof Charles J. Wysocki and other errors in the above article,which should be corrected as follows. On Page 471, Table I, the first Number in the second columnshould read 2:6. On page 477, Table II, the results under d-limonene should readas below. On page 481, the NIH grant number to CJW is DC00298.  相似文献   
8.
9.
10.
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