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   4368篇
  免费   26篇
  国内免费   62篇
系统科学   24篇
丛书文集   83篇
教育与普及   64篇
理论与方法论   5篇
现状及发展   1975篇
研究方法   202篇
综合类   2091篇
自然研究   12篇
  2012年   59篇
  2011年   86篇
  2010年   38篇
  2009年   104篇
  2008年   88篇
  2007年   116篇
  2006年   72篇
  2005年   118篇
  2004年   130篇
  2003年   84篇
  2002年   83篇
  2001年   220篇
  2000年   193篇
  1999年   141篇
  1998年   32篇
  1997年   28篇
  1996年   21篇
  1995年   30篇
  1992年   100篇
  1991年   90篇
  1990年   92篇
  1989年   70篇
  1988年   78篇
  1987年   80篇
  1986年   60篇
  1985年   98篇
  1984年   81篇
  1983年   62篇
  1982年   65篇
  1981年   59篇
  1980年   75篇
  1979年   146篇
  1978年   134篇
  1977年   110篇
  1976年   80篇
  1975年   73篇
  1974年   98篇
  1973年   103篇
  1972年   89篇
  1971年   111篇
  1970年   100篇
  1969年   96篇
  1968年   95篇
  1967年   87篇
  1966年   86篇
  1965年   58篇
  1959年   24篇
  1958年   41篇
  1957年   32篇
  1956年   29篇
排序方式: 共有4456条查询结果,搜索用时 15 毫秒
11.
Summary A new bromotyrosine-derived alkaloid with antileukemic activity, purealidin A (5), has been isolated from the Okinawan marine spongePsammaplysilla purea and its chemical structure elucidated on the basis of the spectroscopic data.  相似文献   
12.
Alzheimer’s disease (AD) is a neurodegenerative disorder associated with cognitive and behavioral dysfunction and is the leading cause of dementia in the elderly. Several studies have implicated molecular and cellular signaling cascades involving the serine-threonine kinase, glycogen synthase kinase β(GSK-3β) in the pathogenesis of AD. GSK-3β may play an important role in the formation of neurofibrillary tangles and senile plaques, the two classical pathological hallmarks of AD. In this review, we discuss the interaction between GSK-3β and several key molecules involved in AD, including the presenilins, amyloid precursor protein, tau, and β-amyloid. We identify the signal transduction pathways involved in the pathogenesis of AD, including Wnt, Notch, and the PI3 kinase/Akt pathway. These may be potential therapeutic targets in AD. Received 19 December 2005; received after revision 24 January 2006; accepted 6 February 2006  相似文献   
13.
Progress on nuclear liquid gas phase transition (LGPT) or critical behavior has been simply reviewed and some signals of LGPT in heavy ion collisions, especially in NIMROD data, are focused. These signals include the power-law charge distribution, the largest fluctuation of the fragment observables, the nuclear Zipf law, caloric curve and critical exponent analysis etc.  相似文献   
14.
1 Results Rare earth doped waveguide amplifiers and devices have been demonstrated in silica, crystal and other glass hosts. These rare earth doped optical waveguide devices are based on inorganic materials. Many processing steps are required and can lead to long fabrication time and low yield.Polymer materials offer many distinct properties compared to inorganic materials, such as ease of fabrication, low production costs, simple processing steps, and compatibility with micro-fabrication technologies. ...  相似文献   
15.
The fraction of pyruvate dehydrogenase complex (PDC) in the active form is reduced by the activities of dedicated PD kinase isozymes (PDK1, PDK2, PDK3 and PDK4). Via binding to the inner lipoyl domain (L2) of the dihydrolipoyl acetyltransferase (E2 60mer), PDK rapidly access their E2-bound PD substrate. The E2-enhanced activity of the widely distributed PDK2 is limited by dissociation of ADP from its C-terminal catalytic domain, and this is further slowed by pyruvate binding to the N-terminal regulatory (R) domain. Via the reverse of the PDC reaction, NADH and acetyl-CoA reductively acetylate lipoyl group of L2, which binds to the R domain and stimulates PDK2 activity by speeding up ADP dissociation. Activation of PDC by synthetic PDK inhibitors binding at the pyruvate or lipoyl binding sites decreased damage during heart ischemia and lowered blood glucose in insulin-resistant animals. PDC activation also triggers apoptosis in cancer cells that selectively convert glucose to lactate. Received 25 August 2006; received after revision 20 November 2006; accepted 20 December 2006  相似文献   
16.
17.
1 Results Strongly disordered metals with the high chemical and catalytic activity are often called as skeletal metals.Usually for their preparation the metallides of d-metal (which afterwards will be left in the “skeleton“) and chemically active component(s) are firstly synthesized.Then the last one(s) is (are) removed by the leaching with aqueous solutions of alkalis or carbonates.However,this method sometime fails,first of all,for the reactions,which should be realized in non-aqueous conditions.In th...  相似文献   
18.
1 Results The photosynthetic bacterial reaction center (RC) is a membrane protein complex.The RC is composed of three protein subunits and redox components such as bacteriochlorophylls, bacteriopheophytins,and quinones.The RC performs the photochemical electron transfer from the bacteriochlorophyll dimer through a series of electron donor and acceptor molecules to a secondary quinone,QB.QB accepts electrons from a primary quinone,QA,in two sequential electron transfer reactions.The second electron trans...  相似文献   
19.
Protein-protein interaction analyses have uncovered a ciliary and basal body protein network that, when disrupted, can result in nephronophthisis (NPHP), Leber congenital amaurosis, Senior-L?ken syndrome (SLSN) or Joubert syndrome (JBTS). However, details of the molecular mechanisms underlying these disorders remain poorly understood. RPGRIP1-like protein (RPGRIP1L) is a homolog of RPGRIP1 (RPGR-interacting protein 1), a ciliary protein defective in Leber congenital amaurosis. We show that RPGRIP1L interacts with nephrocystin-4 and that mutations in the gene encoding nephrocystin-4 (NPHP4) that are known to cause SLSN disrupt this interaction. RPGRIP1L is ubiquitously expressed, and its protein product localizes to basal bodies. Therefore, we analyzed RPGRIP1L as a candidate gene for JBTS and identified loss-of-function mutations in three families with typical JBTS, including the characteristic mid-hindbrain malformation. This work identifies RPGRIP1L as a gene responsible for JBTS and establishes a central role for cilia and basal bodies in the pathophysiology of this disorder.  相似文献   
20.
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