全文获取类型
收费全文 | 4564篇 |
免费 | 36篇 |
国内免费 | 56篇 |
专业分类
系统科学 | 94篇 |
丛书文集 | 178篇 |
教育与普及 | 194篇 |
理论与方法论 | 17篇 |
现状及发展 | 395篇 |
研究方法 | 555篇 |
综合类 | 3219篇 |
自然研究 | 4篇 |
出版年
2023年 | 17篇 |
2022年 | 22篇 |
2019年 | 20篇 |
2018年 | 23篇 |
2017年 | 16篇 |
2016年 | 16篇 |
2015年 | 17篇 |
2014年 | 45篇 |
2013年 | 29篇 |
2012年 | 319篇 |
2011年 | 346篇 |
2010年 | 102篇 |
2009年 | 60篇 |
2008年 | 352篇 |
2007年 | 339篇 |
2006年 | 321篇 |
2005年 | 346篇 |
2004年 | 310篇 |
2003年 | 261篇 |
2002年 | 246篇 |
2001年 | 179篇 |
2000年 | 239篇 |
1999年 | 93篇 |
1998年 | 28篇 |
1997年 | 19篇 |
1996年 | 26篇 |
1995年 | 22篇 |
1994年 | 25篇 |
1993年 | 24篇 |
1992年 | 20篇 |
1991年 | 23篇 |
1990年 | 21篇 |
1989年 | 25篇 |
1988年 | 21篇 |
1987年 | 26篇 |
1986年 | 20篇 |
1985年 | 22篇 |
1984年 | 27篇 |
1983年 | 14篇 |
1982年 | 26篇 |
1981年 | 22篇 |
1979年 | 15篇 |
1970年 | 18篇 |
1959年 | 52篇 |
1958年 | 109篇 |
1957年 | 57篇 |
1956年 | 62篇 |
1955年 | 50篇 |
1954年 | 63篇 |
1948年 | 23篇 |
排序方式: 共有4656条查询结果,搜索用时 507 毫秒
71.
72.
73.
74.
75.
m·K1∪T(1,2,n)及其补图的匹配刻画 总被引:1,自引:1,他引:0
申世昌 《河南师范大学学报(自然科学版)》2011,39(5):13-15
研究了图的匹配刻画问题,利用匹配根的信息,根据匹配多项式的性质,给出了m·K1∪ T(1,2,n)及其补图匹配刻画的充分必要条件是n≠1,2,5,9. 相似文献
76.
Latency and ongoing replication have both been proposed to explain the drug-insensitive human immunodeficiency virus (HIV) reservoir maintained during antiretroviral therapy. Here we explore a novel mechanism for ongoing HIV replication in the face of antiretroviral drugs. We propose a model whereby multiple infections per cell lead to reduced sensitivity to drugs without requiring drug-resistant mutations, and experimentally validate the model using multiple infections per cell by cell-free HIV in the presence of the drug tenofovir. We then examine the drug sensitivity of cell-to-cell spread of HIV, a mode of HIV transmission that can lead to multiple infection events per target cell. Infections originating from cell-free virus decrease strongly in the presence of antiretrovirals tenofovir and efavirenz whereas infections involving cell-to-cell spread are markedly less sensitive to the drugs. The reduction in sensitivity is sufficient to keep multiple rounds of infection from terminating in the presence of drugs. We examine replication from cell-to-cell spread in the presence of clinical drug concentrations using a stochastic infection model and find that replication is intermittent, without substantial accumulation of mutations. If cell-to-cell spread has the same properties in vivo, it may have adverse consequences for the immune system, lead to therapy failure in individuals with risk factors, and potentially contribute to viral persistence and hence be a barrier to curing HIV infection. 相似文献
77.
Cryptic variation is caused by the robustness of phenotypes to mutations. Cryptic variation has no effect on phenotypes in a given genetic or environmental background, but it can have effects after mutations or environmental change. Because evolutionary adaptation by natural selection requires phenotypic variation, phenotypically revealed cryptic genetic variation may facilitate evolutionary adaptation. This is possible if the cryptic variation happens to be pre-adapted, or "exapted", to a new environment, and is thus advantageous once revealed. However, this facilitating role for cryptic variation has not been proven, partly because most pertinent work focuses on complex phenotypes of whole organisms whose genetic basis is incompletely understood. Here we show that populations of RNA enzymes with accumulated cryptic variation adapt more rapidly to a new substrate than a population without cryptic variation. A detailed analysis of our evolving RNA populations in genotype space shows that cryptic variation allows a population to explore new genotypes that become adaptive only in a new environment. Our observations show that cryptic variation contains new genotypes pre-adapted to a changed environment. Our results highlight the positive role that robustness and epistasis can have in adaptive evolution. 相似文献
78.
79.
Phosphorus cycle: A broken biogeochemical cycle 总被引:8,自引:0,他引:8
80.
Cederwall B Moradi FG Bäck T Johnson A Blomqvist J Clément E de France G Wadsworth R Andgren K Lagergren K Dijon A Jaworski G Liotta R Qi C Nyakó BM Nyberg J Palacz M Al-Azri H Algora A de Angelis G Ataç A Bhattacharyya S Brock T Brown JR Davies P Di Nitto A Dombrádi Z Gadea A Gál J Hadinia B Johnston-Theasby F Joshi P Juhász K Julin R Jungclaus A Kalinka G Kara SO Khaplanov A Kownacki J La Rana G Lenzi SM Molnár J Moro R Napoli DR Singh BS Persson A Recchia F Sandzelius M Scheurer JN Sletten G 《Nature》2011,469(7328):68-71
Shell structure and magic numbers in atomic nuclei were generally explained by pioneering work that introduced a strong spin-orbit interaction to the nuclear shell model potential. However, knowledge of nuclear forces and the mechanisms governing the structure of nuclei, in particular far from stability, is still incomplete. In nuclei with equal neutron and proton numbers (N = Z), enhanced correlations arise between neutrons and protons (two distinct types of fermions) that occupy orbitals with the same quantum numbers. Such correlations have been predicted to favour an unusual type of nuclear superfluidity, termed isoscalar neutron-proton pairing, in addition to normal isovector pairing. Despite many experimental efforts, these predictions have not been confirmed. Here we report the experimental observation of excited states in the N = Z = 46 nucleus (92)Pd. Gamma rays emitted following the (58)Ni((36)Ar,2n)(92)Pd fusion-evaporation reaction were identified using a combination of state-of-the-art high-resolution γ-ray, charged-particle and neutron detector systems. Our results reveal evidence for a spin-aligned, isoscalar neutron-proton coupling scheme, different from the previous prediction. We suggest that this coupling scheme replaces normal superfluidity (characterized by seniority coupling) in the ground and low-lying excited states of the heaviest N = Z nuclei. Such strong, isoscalar neutron-proton correlations would have a considerable impact on the nuclear level structure and possibly influence the dynamics of rapid proton capture in stellar nucleosynthesis. 相似文献