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   520篇
  免费   27篇
  2022年   3篇
  2021年   9篇
  2020年   4篇
  2019年   8篇
  2018年   9篇
  2017年   8篇
  2016年   16篇
  2015年   16篇
  2014年   21篇
  2013年   28篇
  2012年   46篇
  2011年   31篇
  2010年   22篇
  2009年   17篇
  2008年   31篇
  2007年   32篇
  2006年   24篇
  2005年   28篇
  2004年   25篇
  2003年   16篇
  2002年   22篇
  2001年   13篇
  2000年   11篇
  1999年   8篇
  1998年   6篇
  1997年   3篇
  1995年   2篇
  1994年   2篇
  1993年   9篇
  1992年   11篇
  1991年   8篇
  1990年   5篇
  1989年   3篇
  1988年   7篇
  1987年   3篇
  1986年   2篇
  1985年   4篇
  1978年   2篇
  1977年   2篇
  1974年   3篇
  1972年   2篇
  1970年   2篇
  1969年   2篇
  1967年   2篇
  1966年   2篇
  1964年   2篇
  1935年   1篇
  1932年   1篇
  1931年   1篇
  1927年   1篇
排序方式: 共有547条查询结果,搜索用时 203 毫秒
541.
Summary Acids like hydrogen fluoride, hydrazoic and fluoroacetic have been shown to prevent the germination of ascospores of N. tetrasperma when dormant spores are treated. On the other hand, propionate, cysteine and others are ineffective when used in this way. When activated ascospores were treated, much lower concentrations of the acids were sufficient to poison the spores. As in other systems, these substances are most effective at a pH below their pKa.The kinetics of uptake of fluoride by dormant ascospores were studied and shown to be very different from those reported for cations. However, P32 was not absorbed by dormant ascospores, even at pH 1.5.Respiratory inhibition by azide and fluoroacetate occurred immediately after the spores were activated, but in the case of 5-nitro-2-furfuryl methyl ether no effect was observed until just before germination occurred.These results suggest that a permeability barrier exists in the dormant ascospore which disappears upon germination. Moreover, the dormant spore seems to be permeable to acids of small size but impermeable to those possessing more than 3 methylene groups or of equivalent size.This work was made possible by a grant from the Michigan-Memorial Phoenix Project of the University of Michigan to whom the authors would like to express their gratitude.  相似文献   
542.
In the Frasier syndrome there is an association between XY gonadal dysgenesis and chronic renal failure. Owing to an observed sex reversal, the Y chromosomes of two girls with this syndrome have been analyzed. Using molecular-biology techniques, no major alterations of the known sex-determining area of the Y chromosome were found. Furthermore, the sequence did not reveal impairment of the recently described testis-determining factor SRY. These data suggest that in the Frasier syndrome, XY sex reversal and renal failure could be the result of either faulty gene(s) located downstream in the sex differentiation pathway during embryogenesis, or impaired SRY regulation. Preliminary results on the Wilms' tumor suppressor gene WT1, a candidate for acting downstream to SRY, are also provided.  相似文献   
543.
544.
545.
546.
547.
Summary The presence of prolactin-like neuropeptides was demonstrated immunocytochemically in the brain and affiliated neuroendocrine structures of the insect Leucophaea maderae. Use of the unlabelled peroxidase-antiperoxidase method of Sternberger revealed a rather widespread and differential distribution of reaction products resembling human (hPRL) and ovine (oPRL) prolactin. Tests with antirat PRL antibody were negative. The specificity of the antibodies used was established by liquid-phase absorptions and confirmed in tissue control systems. In L. maderae, anti-oPRL identifies part of an oPRL-like molecule different from human and rat PRL. Anti-hPRL reveals part of a human and ovine PRL-like molecule different from rat prolactin. These results indicate the occurrence, in the nervous tissue of one insect species, of at least two types of prolactin-like molecules.Supported in part by SNF grants 11-5082 and 11-6652 (G.N.H.) and NIH Grant NS 22344-02 (B.S.). The authors are indebted to Mrs. Bente Hershøj for skillful technical assistance  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