全文获取类型
收费全文 | 108069篇 |
免费 | 8386篇 |
国内免费 | 9023篇 |
专业分类
125478篇 |
出版年
2024年 | 240篇 |
2023年 | 1417篇 |
2022年 | 3264篇 |
2021年 | 5517篇 |
2020年 | 3781篇 |
2019年 | 4682篇 |
2018年 | 4432篇 |
2017年 | 3240篇 |
2016年 | 4595篇 |
2015年 | 6679篇 |
2014年 | 7850篇 |
2013年 | 8303篇 |
2012年 | 9980篇 |
2011年 | 8976篇 |
2010年 | 5546篇 |
2009年 | 4972篇 |
2008年 | 5710篇 |
2007年 | 5131篇 |
2006年 | 4454篇 |
2005年 | 3493篇 |
2004年 | 2968篇 |
2003年 | 2720篇 |
2002年 | 2272篇 |
2001年 | 1866篇 |
2000年 | 1694篇 |
1999年 | 1670篇 |
1998年 | 1036篇 |
1997年 | 1004篇 |
1996年 | 942篇 |
1995年 | 823篇 |
1994年 | 788篇 |
1993年 | 618篇 |
1992年 | 819篇 |
1991年 | 617篇 |
1990年 | 466篇 |
1989年 | 443篇 |
1988年 | 354篇 |
1987年 | 344篇 |
1986年 | 269篇 |
1985年 | 286篇 |
1984年 | 156篇 |
1983年 | 161篇 |
1982年 | 99篇 |
1981年 | 85篇 |
1980年 | 60篇 |
1979年 | 77篇 |
1977年 | 59篇 |
1975年 | 56篇 |
1974年 | 52篇 |
1973年 | 56篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
31.
Unpublished portions of the synthesis of a phosphinate-phosphonate diether analog of CDPdiacylglycerol are reported. The liponucleotide analog was found to be a very powerful inhibitor of platelet PI synthetase; kinetic data suggest a competitive inhibition mechanism. The structural specificity of CDPdiacylglycerol for liponucleotide-mediated biosynthetic reactions is discussed. 相似文献
32.
33.
An iso-random Bi Bi mechanism has been proposed for adenylate kinase. In this mechanism, one of the enzyme forms can bind the substrates MgATP and AMP, whereas the other form can bind the products MgADP and ADP. In a catalytic cycle, the conformational changes of the free enzyme and the ternary complexes are the rate-limiting steps. The AP(5)A inhibition equations derived from this mechanism show theoretically that AP(5)A acts as a competitive inhibitor for the forward reaction and a mixed noncompetitive inhibitor for the backward reaction. 相似文献
34.
Background
Many molecules are flexible and undergo significant shape deformation as part of their function, and yet most existing molecular shape comparison (MSC) methods treat them as rigid bodies, which may lead to incorrect shape recognition. 相似文献35.
Yi Ting Zhou Li Li Chew Sheng-cai Lin Boon Chuan Low 《Molecular biology of the cell》2010,21(18):3232-3246
The BNIP-2 and Cdc42GAP homology (BCH) domain is a novel regulator for Rho GTPases, but its impact on p50-Rho GTPase-activating protein (p50RhoGAP or Cdc42GAP) in cells remains elusive. Here we show that deletion of the BCH domain from p50RhoGAP enhanced its GAP activity and caused drastic cell rounding. Introducing constitutively active RhoA or inactivating GAP domain blocked such effect, whereas replacing the BCH domain with endosome-targeting SNX3 excluded requirement of endosomal localization in regulating the GAP activity. Substitution with homologous BCH domain from Schizosaccharomyces pombe, which does not bind mammalian RhoA, also led to complete loss of suppression. Interestingly, the p50RhoGAP BCH domain only targeted RhoA, but not Cdc42 or Rac1, and it was unable to distinguish between GDP and the GTP-bound form of RhoA. Further mutagenesis revealed a RhoA-binding motif (residues 85-120), which when deleted, significantly reduced BCH inhibition on GAP-mediated cell rounding, whereas its full suppression also required an intramolecular interaction motif (residues 169-197). Therefore, BCH domain serves as a local modulator in cis to sequester RhoA from inactivation by the adjacent GAP domain, adding to a new paradigm for regulating p50RhoGAP signaling. 相似文献
36.
J Blake D M Helmeste C H Li 《International journal of peptide and protein research》1985,25(6):575-579
Two analogs of human beta-endorphin (beta-EP) which contain cystine bridges, [Cys15-Cys26,Phe27,Gly31]-beta-EP (I) and [Cys16-Cys26,Phe27,Gly31]-beta-EP (II), were synthesized by the solid-phase method. Peptides I and II were shown to contain 2-2.5 times the opiate receptor binding activity of beta-endorphin. We also synthesized two analogs with reduced alkylated cysteine residues and these peptides, [Arg9,19,24,28,29 Cys(Cam)11,26,Phe27,Gly31] and [Arg9,19,24,28,29,Cys-(Cam)12,26,Phe27,Gly31], were shown to have approximately the same opiate receptor activity as beta-endorphin. 相似文献
37.
Wenjun Geng Jinggong Xiangyu Xiuzhen Li Zhongning Zhang Deyuan Han Yongwei Li 《Insect Science》1997,4(4):364-368
Abstract Field trials by sex pheromone of aphid to trap peach aphids Myzus persicae have been carried out in 1995 and in 1996. Suitable time and the effect of ratio of two components nepetalactone and nepetalactol to apply the lure have been observed. 相似文献
38.
39.
40.