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   42706篇
  免费   76篇
  国内免费   98篇
系统科学   216篇
丛书文集   909篇
教育与普及   103篇
理论与方法论   263篇
现状及发展   19492篇
研究方法   1617篇
综合类   19772篇
自然研究   508篇
  2013年   244篇
  2012年   531篇
  2011年   1063篇
  2010年   227篇
  2008年   679篇
  2007年   689篇
  2006年   756篇
  2005年   755篇
  2004年   784篇
  2003年   736篇
  2002年   729篇
  2001年   1211篇
  2000年   1106篇
  1999年   755篇
  1992年   727篇
  1991年   590篇
  1990年   637篇
  1989年   638篇
  1988年   614篇
  1987年   637篇
  1986年   662篇
  1985年   799篇
  1984年   633篇
  1983年   550篇
  1982年   492篇
  1981年   495篇
  1980年   580篇
  1979年   1352篇
  1978年   1142篇
  1977年   1163篇
  1976年   803篇
  1975年   928篇
  1974年   1326篇
  1973年   1103篇
  1972年   1153篇
  1971年   1428篇
  1970年   1851篇
  1969年   1397篇
  1968年   1324篇
  1967年   1380篇
  1966年   1165篇
  1965年   875篇
  1964年   250篇
  1959年   506篇
  1958年   780篇
  1957年   632篇
  1956年   512篇
  1955年   471篇
  1954年   519篇
  1948年   300篇
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
891.
Myelin basic protein: a multifunctional protein   总被引:1,自引:1,他引:0  
Myelin basic protein (MBP), the second most abundant protein in central nervous system myelin, is responsible for adhesion of the cytosolic surfaces of multilayered compact myelin. A member of the ‘intrinsically disordered’ or conformationally adaptable protein family, it also appears to have several other functions. It can interact with a number of polyanionic proteins including actin, tubulin, Ca2+-calmodulin, and clathrin, and negatively charged lipids, and acquires structure on binding to them. It may act as a membrane actin-binding protein, which might allow it to participate in transmission of extracellular signals to the cytoskeleton in oligodendrocytes and tight junctions in myelin. Some size isoforms of MBP are transported into the nucleus and thus they may also bind polynucleotides. Extracellular signals received by myelin or cultured oligodendrocytes cause changes in phosphorylation of MBP, suggesting that MBP is also involved in signaling. Further study of this very abundant protein will reveal how it is utilized by the oligodendrocyte and myelin for different purposes. Received 2 March 2006; received after revision 12 April 2006; accepted 16 May 2006  相似文献   
892.
Phytanic acid is a branched-chain fatty acid that accumulates in a variety of metabolic disorders. High levels of phytanic acid found in patients can exceed the millimolar range and lead to severe symptoms. Degradation of phytanic acid takes place by α-oxidation inside the peroxisome. A deficiency of its breakdown, leading to elevated levels, can result from either a general peroxisomal dysfunction or from a defect in one of the enzymes involved in α-oxidation. Research on Refsum disease, belonging to the latter group of disorders and characterized by a deficiency of the first enzyme of α-oxidation, has extended our knowledge of phytanic acid metabolism and pathology of the disease greatly over the past few decades. This review will centre on this research on phytanic acid: its origin, the mechanism by which its α-oxidation takes place, its role in human disease and the way it is produced from phytol. Received 4 October 2005; received after revision 24 February 2006; accepted 26 April 2006  相似文献   
893.
Isoprenoids are synthesized in all living organisms and are incorporated into diverse classes of end-products that participate in a multitude of cellular processes relating to cell growth, differentiation, cytoskeletal function and vesicle trafficking. In humans, the non-sterol isoprenoids, farnesyl pyrophosphate and geranylgeranyl-pyrophosphate, are synthesized via the mevalonate pathway and are covalently added to members of the small G protein superfamily. Isoprenylated proteins have key roles in membrane attachment and protein functionality, have been shown to have a central role in some cancers and are likely also to be involved in the pathogenesis and progression of atherosclerosis and Alzheimer disease. This review details current knowledge on the biosynthesis of isoprenoids, their incorporation into proteins by the process known as prenylation and the complex regulatory network that controls these proteins. An improved understanding of these processe is likely to lead to the development of novel therapies that will have important implications for human health and disease. Received 5 July 2005; received after revision 17 October 2005; accepted 22 October 2005  相似文献   
894.
Brucella has traditionally been considered a biological weapon. It was the subject of extensive offensive research in the past, and still belongs to category B pathogens on most lists. Its propensity for airborne transmission and induction of chronic debilitating disease requiring combined antibiotic regimens for treatment, its abundance around the world and its vague clinical characteristics defying rapid clinical diagnosis are some of the characteristics that apply to the pathogen's weapons potential. Yet minimal mortality, availability of treatment options, protracted inoculation period and the emergence of new, more virulent potential weapons means that its inclusion among agents of bioterrorism is nowadays mainly of historical significance. Nevertheless, in the interest of literacy and of avoiding panic, physicians and the public both should be aware of the most common zoonosis worldwide.  相似文献   
895.
896.
897.
898.
899.
900.
Nadeau JH  Topol EJ 《Nature genetics》2006,38(10):1095-1098
Recent experience with several high-profile drugs demonstrates the great challenges in developing effective and safe therapeutics. A complementary approach to the popular paradigm of disease genetics is based on inherited factors that reduce the incidence and severity of disease among individuals who are genetically predisposed to disease. We propose testing specifically for modifier genes and protective alleles among at-risk individuals and studying the efficacy of therapeutics based on the genetics of health.  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