全文获取类型
收费全文 | 37652篇 |
免费 | 3514篇 |
国内免费 | 23篇 |
出版年
2023年 | 157篇 |
2022年 | 308篇 |
2021年 | 847篇 |
2020年 | 460篇 |
2019年 | 626篇 |
2018年 | 718篇 |
2017年 | 592篇 |
2016年 | 1067篇 |
2015年 | 1774篇 |
2014年 | 1880篇 |
2013年 | 2217篇 |
2012年 | 2948篇 |
2011年 | 2954篇 |
2010年 | 1788篇 |
2009年 | 1515篇 |
2008年 | 2217篇 |
2007年 | 2208篇 |
2006年 | 2133篇 |
2005年 | 1871篇 |
2004年 | 1876篇 |
2003年 | 1693篇 |
2002年 | 1656篇 |
2001年 | 468篇 |
2000年 | 412篇 |
1999年 | 416篇 |
1998年 | 382篇 |
1997年 | 286篇 |
1996年 | 278篇 |
1995年 | 247篇 |
1994年 | 215篇 |
1993年 | 217篇 |
1992年 | 265篇 |
1991年 | 276篇 |
1990年 | 239篇 |
1989年 | 259篇 |
1988年 | 212篇 |
1987年 | 190篇 |
1986年 | 181篇 |
1985年 | 206篇 |
1984年 | 209篇 |
1983年 | 183篇 |
1982年 | 190篇 |
1981年 | 186篇 |
1980年 | 164篇 |
1979年 | 165篇 |
1978年 | 133篇 |
1976年 | 118篇 |
1975年 | 116篇 |
1974年 | 126篇 |
1973年 | 119篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
1.
2.
The influence of the protein matrix on the reactivity of external molecules with a species buried within the protein interior is considered in two general ways: (1) there may be structural fluctuations that allow for the diffusive penetration of the small molecules and/or (2) the external molecule may react over a distance. As a means to study the protein matrix, a reactive species within the protein can be formed by exciting tryptophan to the triplet state, and then the reaction of the triplet-state molecule with an external molecule can be monitored by a decrease in phosphorescence. In this work, the quenching ability (i.e., reactivity) was examined for H2S, CS2, and NO2- acting on tryptophan phosphorescence in parvalbumin, azurin, horse liver alcohol dehydrogenase, and alkaline phosphatase. A comparison of charged versus uncharged quenchers (H2S vs SH- and CS2 vs NO2-) reveals that the uncharged molecules are much more effective than charged species in quenching the phosphorescence of fully buried tryptophan, whereas the quenching for exposed tryptophan is relatively independent of the charge of the quencher. This is consistent with the view that uncharged triatomic molecules can penetrate the protein matrix to some extent. The energies of activation of the quenching reaction are low for the charged quenchers and higher for the uncharged CS2. A model is presented in which the quenchability of a buried tryptophan is inversely related to the distance from the surface when diffusion through the protein is the rate-limiting step.(ABSTRACT TRUNCATED AT 250 WORDS) 相似文献
3.
4.
5.
Andrew C Smith 《BMJ (Clinical research ed.)》1981,283(6306):1596-1597
6.
Denise Risch Nicholas J. Gales Jason Gedamke Lars Kindermann Douglas P. Nowacek Andrew J. Read Ursula Siebert Ilse C. Van Opzeeland Sofie M. Van Parijs Ari S. Friedlaender 《Biology letters》2014,10(4)
For decades, the bio-duck sound has been recorded in the Southern Ocean, but the animal producing it has remained a mystery. Heard mainly during austral winter in the Southern Ocean, this ubiquitous sound has been recorded in Antarctic waters and contemporaneously off the Australian west coast. Here, we present conclusive evidence that the bio-duck sound is produced by Antarctic minke whales (Balaenoptera bonaerensis). We analysed data from multi-sensor acoustic recording tags that included intense bio-duck sounds as well as singular downsweeps that have previously been attributed to this species. This finding allows the interpretation of a wealth of long-term acoustic recordings for this previously acoustically concealed species, which will improve our understanding of the distribution, abundance and behaviour of Antarctic minke whales. This is critical information for a species that inhabits a difficult to access sea-ice environment that is changing rapidly in some regions and has been the subject of contentious lethal sampling efforts and ongoing international legal action. 相似文献
7.
8.
A F Wright 《BMJ (Clinical research ed.)》1982,285(6342):609-611
9.
10.
Benjamin C. Blum Weiwei Lin Matthew L. Lawton Qian Liu Julian Kwan Isabella Turcinovic Ryan Hekman Pingzhao Hu Andrew Emili 《Molecular & cellular proteomics : MCP》2022,21(1):100189
Metabolism is recognized as an important driver of cancer progression and other complex diseases, but global metabolite profiling remains a challenge. Protein expression profiling is often a poor proxy since existing pathway enrichment models provide an incomplete mapping between the proteome and metabolism. To overcome these gaps, we introduce multiomic metabolic enrichment network analysis (MOMENTA), an integrative multiomic data analysis framework for more accurately deducing metabolic pathway changes from proteomics data alone in a gene set analysis context by leveraging protein interaction networks to extend annotated metabolic models. We apply MOMENTA to proteomic data from diverse cancer cell lines and human tumors to demonstrate its utility at revealing variation in metabolic pathway activity across cancer types, which we verify using independent metabolomics measurements. The novel metabolic networks we uncover in breast cancer and other tumors are linked to clinical outcomes, underscoring the pathophysiological relevance of the findings. 相似文献