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   36881篇
  免费   3184篇
  国内免费   19篇
  2023年   105篇
  2022年   283篇
  2021年   628篇
  2020年   388篇
  2019年   504篇
  2018年   648篇
  2017年   557篇
  2016年   961篇
  2015年   1645篇
  2014年   1763篇
  2013年   2157篇
  2012年   2920篇
  2011年   2956篇
  2010年   1843篇
  2009年   1736篇
  2008年   2450篇
  2007年   2488篇
  2006年   2335篇
  2005年   2158篇
  2004年   2123篇
  2003年   1971篇
  2002年   1919篇
  2001年   419篇
  2000年   285篇
  1999年   419篇
  1998年   487篇
  1997年   352篇
  1996年   317篇
  1995年   280篇
  1994年   245篇
  1993年   262篇
  1992年   241篇
  1991年   181篇
  1990年   169篇
  1989年   175篇
  1988年   145篇
  1987年   130篇
  1986年   103篇
  1985年   145篇
  1984年   164篇
  1983年   114篇
  1982年   132篇
  1981年   118篇
  1980年   98篇
  1979年   61篇
  1978年   78篇
  1977年   70篇
  1976年   43篇
  1974年   37篇
  1973年   40篇
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
31.
32.
33.
The Le Quesne test of character compatibility uses pairwise comparisons of characters to detect homoplasy in phylogenetic character data. If a pair of characters fails this test we can conclude that a minimum of a single extra step is required by the pair of characters. The rationale of the Le Quesne test is extended to comparisons of triplets of characters. The triplet homoplasy test can reveal that that there is a minimum of four extra steps across a triplet of characters and thus that there are at least two extra steps associated with one of the characters. The triplet homoplasy test can thus detect higher orders of homoplasy than can be detected by the pairwise Le Quesne test. The possibility of quartet and other higher-order homoplasy tests is discussed. The utility of higher-order homoplasy tests is discussed. It is suggested higher-order homoplasy tests have potential uses analogous to the uses of the Le Quesne test, particularly with respect to data exploration.  相似文献   
34.
35.
36.

Background  

NOL7 is a candidate tumor suppressor that localizes to a chromosomal region 6p23. This locus is frequently lost in a number of malignancies, and consistent loss of NOL7 through loss of heterozygosity and decreased mRNA and protein expression has been observed in tumors and cell lines. Reintroduction of NOL7 into cells resulted in significant suppression of in vivo tumor growth and modulation of the angiogenic phenotype. Further, NOL7 was observed to localize to the nucleus and nucleolus of cells. However, the mechanisms regulating its subcellular localization have not been elucidated.  相似文献   
37.
38.
39.
Comparative mapping studies of X-linked genes in mammals have provided insights into the evolution of the X chromosome. Many reptiles including the American alligator, Alligator mississippiensis, do not appear to possess heteromorphic sex chromosomes, and sex is determined by the incubation temperature of the egg during embryonic development. Mapping of homologues of mammalian X-linked genes in reptiles could lead to a greater understanding of the evolution of vertebrate sex chromosomes. One of the genes used in the mammalian mapping studies was ZFX, an X-linked copy of the human ZFY gene which was originally isolated as a candidate for the mammalian testis-determining factor (TDF). ZFX is X-linked in eutherians, but maps to two autosomal locations in marsupials and monotremes, close to other genes associated with the eutherian X. The alligator homologue of the ZFY/ZFX genes, Zfc, has been isolated and described previously. A detailed karyotype of A. mississippiensis is presented, together with chromosomal in situ hybridisation data localising the Zfc gene to chromosome 3. Further chromosomal mapping studies using eutherian X-linked genes may reveal conserved chromosomal regions in the alligator that have become part of the eutherian X chromosome during evolution.  相似文献   
40.
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