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   501076篇
  免费   59931篇
  国内免费   306篇
  2018年   4542篇
  2017年   4161篇
  2016年   6625篇
  2015年   10213篇
  2014年   11333篇
  2013年   15737篇
  2012年   18417篇
  2011年   18574篇
  2010年   12260篇
  2009年   11250篇
  2008年   16130篇
  2007年   16647篇
  2006年   15186篇
  2005年   15009篇
  2004年   14736篇
  2003年   14013篇
  2002年   13494篇
  2001年   22264篇
  2000年   22230篇
  1999年   18044篇
  1998年   6971篇
  1997年   7009篇
  1996年   6840篇
  1995年   6224篇
  1994年   6265篇
  1993年   6098篇
  1992年   14128篇
  1991年   13373篇
  1990年   12976篇
  1989年   12848篇
  1988年   11526篇
  1987年   11087篇
  1986年   10175篇
  1985年   10013篇
  1984年   8597篇
  1983年   7412篇
  1982年   5939篇
  1981年   5374篇
  1980年   4974篇
  1979年   7904篇
  1978年   6179篇
  1977年   5679篇
  1976年   5271篇
  1975年   5561篇
  1974年   6019篇
  1973年   5850篇
  1972年   5211篇
  1971年   4843篇
  1970年   4044篇
  1969年   3955篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
81.
Synaptonemal complexes and meiosis in myxomycetes   总被引:4,自引:0,他引:4  
Synaptonemal complexes (SC) have been observed in spores 18–24 hr past cleavage in natural fruitings of Physarum cinereum, P. bogoriense, Hemitrichia stipitata, Tubifera ferruginosa, and Arcyria incarnata. Laboratory fruitings of Arcyria cinerea, Stemonitis herbatica, and a homothallic isolate of Physarum pusillum also have SC's present in spores during the same postcleavage period. The presence of these paired chromosomes of meiotic prophase in spores of species collected in nature and in a diversity of taxa suggests that the usual position of meiosis in Myxomycetes is inside the postcleavage spore. Criteria are proposed for evaluating the validity of the SC as an indicator of meiosis.  相似文献   
82.
83.
The cell surface of the parasitic protozoan Leishmania mexicana is coated by glycosylphosphatidylinositol (GPI)-anchored glycoproteins, a GPI-anchored lipophosphoglycan and a class of free GPI glycolipids. To investigate whether the anchor or free GPIs are required for parasite growth we cloned the L.mexicana gene for dolichol-phosphate-mannose synthase (DPMS) and attempted to create DPMS knockout mutants by targeted gene deletion. DPMS catalyzes the formation of dolichol-phosphate mannose, the sugar donor for all mannose additions in the biosynthesis of both the anchor and free GPIs, except for a alpha1-3-linked mannose residue that is added exclusively to the free GPIs and lipophosphoglycan anchor precursors. The requirement for dolichol-phosphate-mannose in other glycosylation pathways in L.mexicana is minimal. Deletion of both alleles of the DPMS gene (lmdpms) consistently resulted in amplification of the lmdpms chromosomal locus unless the promastigotes were first transfected with an episomal copy of lmdpms, indicating that lmdpms, and possibly GPI biosynthesis, is essential for parasite growth. As evidence presented in this and previous studies indicates that neither GPI-anchored glycoproteins nor lipophosphoglycan are required for growth of cultured parasites, it is possible that the abundant and functionally uncharacterized free GPIs are essential membrane components.  相似文献   
84.
85.
86.
STACE, C. A. & JARVIS, C. E., 1985. TypiHcation of Linnaean taxa of annual Poaceae: Poeae related to Vulpia and Desmazeria. The status and typification of 15 Linnaean species of annual grasses related to Vulpia and Desmazeria are discussed. Of these 15, eight are represented by holotypes or lectotypes in LINN, two by lectotypes in Herb. A. van Royen (L), and one by a neotype in LINN. One (Festuca marina) is based on a pre-Linnaean polynomial and is represented by a lectotype in Herb. Sloane (BM); one (Cynosurus durus) has no known type specimens and we have chosen a Barrelier (1714) illustration as lectotype; one (Nardus aristatus) is an illegitimate name change for Nardus incurvus Gouan, for which we have selected a Scheuchzer (1719) illustration as lectotype; and finally Festuca incrassala appeared on a cancelled page of Species Plantarum and has no nomenclatural standing.  相似文献   
87.
88.
89.
90.
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