全文获取类型
收费全文 | 36725篇 |
免费 | 101篇 |
国内免费 | 192篇 |
专业分类
系统科学 | 168篇 |
丛书文集 | 560篇 |
教育与普及 | 67篇 |
理论与方法论 | 139篇 |
现状及发展 | 17144篇 |
研究方法 | 1475篇 |
综合类 | 16941篇 |
自然研究 | 524篇 |
出版年
2013年 | 327篇 |
2012年 | 505篇 |
2011年 | 1023篇 |
2010年 | 225篇 |
2008年 | 629篇 |
2007年 | 708篇 |
2006年 | 687篇 |
2005年 | 650篇 |
2004年 | 666篇 |
2003年 | 629篇 |
2002年 | 621篇 |
2001年 | 1114篇 |
2000年 | 1039篇 |
1999年 | 734篇 |
1992年 | 720篇 |
1991年 | 526篇 |
1990年 | 610篇 |
1989年 | 595篇 |
1988年 | 580篇 |
1987年 | 664篇 |
1986年 | 571篇 |
1985年 | 749篇 |
1984年 | 590篇 |
1983年 | 457篇 |
1982年 | 446篇 |
1981年 | 456篇 |
1980年 | 576篇 |
1979年 | 1136篇 |
1978年 | 951篇 |
1977年 | 938篇 |
1976年 | 785篇 |
1975年 | 838篇 |
1974年 | 1047篇 |
1973年 | 978篇 |
1972年 | 1029篇 |
1971年 | 1102篇 |
1970年 | 1372篇 |
1969年 | 1087篇 |
1968年 | 1116篇 |
1967年 | 1072篇 |
1966年 | 937篇 |
1965年 | 636篇 |
1964年 | 198篇 |
1959年 | 334篇 |
1958年 | 600篇 |
1957年 | 394篇 |
1956年 | 360篇 |
1955年 | 338篇 |
1954年 | 306篇 |
1948年 | 238篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
41.
Aspirin-like drugs may block pain independently of prostaglandin synthesis inhibition 总被引:2,自引:0,他引:2
K. Brune W. S. Beck G. Geisslinger S. Menzel-Soglowek B. M. Peskar B. A. Peskar 《Cellular and molecular life sciences : CMLS》1991,47(3):257-261
Summary Using flurbiprofen, a chiral anti-inflammatory and analgesic 2-arylpropionic acid derivative, the enantiomers of which are not converted to each other (less than 5%) in rats or man, we obtained evidence that prostaglandin synthesis inhibition is primarily mediating the anti-inflammatory activity but prostaglandin synthesis independent mechanisms contribute to the analgesic effects. Thus, the S-form inhibited prostaglandin synthesis, inflammation and nociception in rats. The R-form had much less effect on prostaglandin synthesis and did not affect inflammation. It did, however, block nociception in rats almost as potently as the S-form. S-flurbiprofen, in contrast to the R-form, was clearly ulcerogenic in the gastrointestinal mucosa. These results indicate additional molecular mechanisms of analgesia and suggest the use of R-arylpropionic acids as analgesics. 相似文献
42.
43.
史济群 《华中科技大学学报(自然科学版)》1994,(3)
报道一种新颖的激光开槽、埋槽电极硅太阳电池的结构、工艺流程及其研制结果。在AM1.5,25℃,100mW/cm2的条件下,以面积为45cm3的36片硅片研制的硅太阳电池的输出参数的平均值为JSC=36.1mA/cm2,V∞=633mV,F.F.=0.798,η=18.23%,最后分析了种高性能硅太阳电池的设计特点。 相似文献
44.
FROM MANUFACTURING SCHEDULING TO SUPPLY CHAIN COORDINATION:THE CONTROL OF COMPLEXITY AND UNCERTAINTY
Peter B.LUH 《系统科学与系统工程学报(英文版)》2003,12(3):279-297
With time-based competition and rapid technology advancements, effective manufacturingscheduling and supply chain coordination are critical to quickly respond to changing marketconditions. These problems, however, are difficult in view of inherent complexity and variousuncertainties involved. Based on a series of results by the authors, decomposition and coordination byusing Lagrangian relaxation is identified in this paper as an effective way to control complexity anduncertainty.A manufacturing scheduling problem is first formulated within the job shop context withuncertain order arrivals, processing times, due dates, and part priorities as a separable optimizationproblem. A solution methodology that combines Lagrangian relaxation, stochastic dynamicprogramming, and heuristics is developed. Method improvements to effectively solve large problemsare also highlighted. To extend manufacturing scheduling within a factory to coordinate autonomicmembers across chains of suppliers, a decentralized supply chai 相似文献
45.
M. Ishibashi M. Tsuda Y. Ohizumi T. Sasaki J. Kobayashi 《Cellular and molecular life sciences : CMLS》1991,47(3):299-300
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
46.
47.
M E MacDonald A Novelletto C Lin D Tagle G Barnes G Bates S Taylor B Allitto M Altherr R Myers 《Nature genetics》1992,1(2):99-103
Analysis of 78 Huntington's disease (HD) chromosomes with multi-allele markers revealed 26 different haplotypes, suggesting a variety of independent HD mutations. The most frequent haplotype, accounting for about one third of disease chromosomes, suggests that the disease gene is between D4S182 and D4S180. However, the paucity of an expected class of chromosomes that can be related to this major haplotype by assuming single crossovers may reflect the operation of other mechanisms in creating haplotype diversity. Some of these mechanisms sustain alternative scenarios that do not require a multiple mutational origin for HD and/or its positioning between D4S182 and D4S180. 相似文献
48.
Structure of the detoxification catalyst mercuric ion reductase from Bacillus sp. strain RC607 总被引:10,自引:0,他引:10
Several hundred million tons of toxic mercurials are dispersed in the biosphere. Microbes can detoxify organo-mercurials and mercury salts through sequential action of two enzymes, organomercury lyase and mercuric ion reductase (MerA). The latter, a homodimer with homology to the FAD-dependent disulphide oxidoreductases, catalyses the reaction NADPH + Hg(II)----NADP+ + H+ + Hg(0), one of the very rare enzymic reactions with metal substrates. Human glutathione reductase serves as a reference molecule for FAD-dependent disulphide reductases and between its primary structure and that of MerA from Tn501 (Pseudomonas), Tn21 (Shigella), p1258 (Staphylococcus) and Bacillus, 25-30% of the residues have been conserved. All MerAs have a C-terminal extension about 15 residues long but have very varied N termini. Although the enzyme from Streptomyces lividans has no addition, from Pseudomonas aeruginosa Tn501 and Bacillus sp. strain RC607 it has one and two copies respectively of a domain of 80-85 residues, highly homologous to MerP, the periplasmic component of proteins encoded by the mer operon. These domains can be proteolytically cleaved off without changing the catalytic efficiency. We report here the crystal structure of MerA from the Gram-positive bacterium Bacillus sp. strain RC607. Analysis of its complexes with nicotinamide dinucleotide substrates and the inhibitor Cd(II) reveals how limited structural changes enable an enzyme to accept as substrate what used to be a dangerous inhibitor. Knowledge of the mode of mercury ligation is a prerequisite for understanding this unique detoxification mechanism. 相似文献
49.
50.
Tad M. Schmaltz 《Studies in history and philosophy of science》2003,34(4):737-762
There is considerable debate among scholars over whether Descartes allowed for genuine body–body interaction. I begin by considering Michael Della Rocca’s recent claim that Descartes accepted such interaction, and that his doctrine of the creation of the eternal truths indicates how this interaction could be acceptable to him. Though I agree that Descartes was inclined to accept real bodily causes of motion, I differ from Della Rocca in emphasizing that his ontology ultimately does not allow for them. This is not the end of the story however, since two of Descartes’s successors offered incompatible ways of developing his conflicted account of motion. I contrast the occasionalist view of Nicolas Malebranche that changes in motion derive directly from divine volitions with the non-occasionalist claim of Pierre-Sylvain Regis that such changes derive from a nature distinct from God. In light of Della Rocca’s interpretation, it is noteworthy that the issue of eternal truths is relevant to both alternative accounts. Indeed, Regis took the doctrine that such truths are created to provide crucial support for his alternative to an occasionalist account of body–body interaction. What does not help Della Rocca, however, is that Regis’s view of motion requires a fundamental revision of Descartes’s ontology. 相似文献