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   292027篇
  免费   34301篇
  国内免费   148篇
  2018年   2400篇
  2016年   3085篇
  2015年   4036篇
  2014年   4917篇
  2013年   6734篇
  2012年   7699篇
  2011年   7910篇
  2010年   5202篇
  2009年   5033篇
  2008年   7147篇
  2007年   7320篇
  2006年   7205篇
  2005年   6923篇
  2004年   6786篇
  2003年   6617篇
  2002年   6456篇
  2001年   17243篇
  2000年   17427篇
  1999年   13250篇
  1998年   3763篇
  1997年   4032篇
  1996年   3739篇
  1995年   3486篇
  1994年   3462篇
  1993年   3541篇
  1992年   10387篇
  1991年   10315篇
  1990年   9802篇
  1989年   9635篇
  1988年   8989篇
  1987年   8355篇
  1986年   7554篇
  1985年   7406篇
  1984年   5821篇
  1983年   5070篇
  1982年   3611篇
  1981年   3178篇
  1980年   3028篇
  1979年   5348篇
  1978年   4112篇
  1977年   3747篇
  1976年   3295篇
  1975年   3775篇
  1974年   3946篇
  1973年   3888篇
  1972年   3419篇
  1971年   3182篇
  1970年   2822篇
  1969年   2739篇
  1968年   2411篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
991.
992.
The effects of N,N'-dicyclohexylcarbodiimide (DCCD) and various ionophores on light-induced 22Na+-transport were studied in right-side-out membrane vesicles from Halobacterium halobium R1M1. The light-induced Na+ efflux was inhibited at the same DCCD concentration (greater than 40 nmol/mg protein) as required for inhibition of the Na+-dependent membrane potential (delta phi) formation. This supports our previous indication that the DCCD-sensitive, Na+-dependent transformation of pH-gradient (delta pH) into delta phi is mediated by Na+/H+-antiporter (Murakami, N. and Konishi, T. (1985) J. Biochem. 98, 897-907). FCCP or a combination of valinomycin and triphenyltin (TPT) inhibits the light-induced Na+ efflux in accordance with the notion of protonmotive force (delta mu H+)-driven antiporter. However, a marked lag in initiation of the Na+ efflux occurred in the presence of valinomycin, TPMP+, or a small amount of FCCP, suggesting that a gating step is involved in the Na+ efflux. On the other hand, the delta pH-dissipating ionophore TPT did not cause the lag. A simultaneous determination of delta phi, delta pH, and Na+ efflux rate at the initial stage of illumination revealed that the antiporter is gated by delta phi rather than delta mu H+.  相似文献   
993.
The in vitro action of hydro-alcoholic extracts of plants from Ivory Coast pharmacopoeia was analyzed on cultured rat pituitary cells. Cells were treated for 24 hours with various doses of extracts and then stimulated for 4 hours with 10(-8) M LHRH. Extracts from Afrormosia laxiflora, Cola nitida, Pterocarpus erinaceus and Tetrapleura tetraptera inhibit the LHRH-induced release of LH. On the contrary, extract from Combretodendron africanum stimulates the basal release of LH and this increase is added to the LHRH-induced release. Therefore, the natural substances contained in these plants may in vitro exert a regulation of the gonadotropin release.  相似文献   
994.
A peroxidase-anti-peroxidase (PAP) method using polyclonal anti-PR antibodies was used to localize progesterone receptor (PR) electron microscopically in the chick oviduct. The immunoreaction precipitate indicating PR was localized inside the nuclei of epithelial, glandular and stromal cells. In the estrogen withdrawn oviduct cytoplasmic immunoreaction precipitate was not seen. Inside the nucleus unoccupied PR was localized mainly like the heterochromatin. As visualized by the PAP technique, the localization of PR was not systematically changed after progesterone administration. In conclusion, we suggest that progesterone receptor in the chick oviduct is an intranuclear protein.  相似文献   
995.
The survival of Chinese hamster cell V79-4 after hyperthermic treatment (42 degrees C, 40 minutes) in the exponential growth phase considerably increases with the duration of holding them in the growth medium at 37 degrees C before hypertonic salt treatment (1.5 M NaCl, 15 minutes). The experimental data are interpreted as a recovery of mammalian cells from thermal lesions, whose lethal action manifests itself at high salt concentrations.  相似文献   
996.
997.
998.
999.
1000.
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