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   1502篇
  免费   57篇
  国内免费   15篇
化学   965篇
晶体学   3篇
力学   34篇
数学   304篇
物理学   268篇
  2023年   9篇
  2022年   16篇
  2021年   28篇
  2020年   38篇
  2019年   34篇
  2018年   21篇
  2017年   28篇
  2016年   63篇
  2015年   47篇
  2014年   49篇
  2013年   92篇
  2012年   101篇
  2011年   122篇
  2010年   87篇
  2009年   65篇
  2008年   84篇
  2007年   76篇
  2006年   49篇
  2005年   68篇
  2004年   59篇
  2003年   48篇
  2002年   51篇
  2001年   35篇
  2000年   24篇
  1999年   23篇
  1998年   26篇
  1997年   17篇
  1996年   23篇
  1995年   17篇
  1994年   14篇
  1993年   10篇
  1992年   8篇
  1990年   5篇
  1989年   4篇
  1988年   4篇
  1987年   4篇
  1986年   4篇
  1985年   8篇
  1984年   9篇
  1983年   6篇
  1982年   9篇
  1981年   11篇
  1980年   8篇
  1978年   8篇
  1977年   4篇
  1976年   6篇
  1975年   8篇
  1974年   6篇
  1973年   7篇
  1972年   7篇
排序方式: 共有1574条查询结果,搜索用时 15 毫秒
11.
Ultraviolet light can be used to immobilize biomolecules onto thiol reactive surfaces in order to, e.g., make biosensors. The mechanism involves light-induced formation of free, reactive thiol groups in disulphide containing molecules. This technology allows for the creation of arrays of biomolecules with a high degree of reproducibility, circumventing the need for often expensive nano/micro-dispensing technologies. The ultimate size of the immobilized spots is defined by the focal area of the UV beam. Light-induced immobilization has the added benefit that the immobilized molecules will be spatially oriented and covalently bound to the surface. In this paper, we demonstrate the utility of a sensor array created with the new sensor technology when integrated into a microfluidic system. Protein arrays made using light-induced immobilization showed successful antigen/antibody binding in a flow cell allowing the visualisation of real time binding and enzyme activity. This new technology is ideal for the creation of protein/DNA microarrays, can replace present micro-dispensing arraying technologies and is ideal as a molecular imprinting technology.  相似文献   
12.
The structure and properties of optimal networks depend on the cost functional being minimized and on constraints to which the minimization is subject. We show here two different formulations that lead to identical results: minimizing the dissipation rate of an electrical network under a global constraint is equivalent to the minimization of a power-law cost function introduced by Banavar et al. [Phys. Rev. Lett. 84, 4745 (2000)10.1103/PhysRevLett.84.4745]. An explicit scaling relation between the currents and the corresponding conductances is derived, proving the potential flow nature of the latter. Varying a unique parameter, the topology of the optimized networks shows a transition from a tree topology to a very redundant structure with loops; the transition corresponds to a discontinuity in the slope of the power dissipation.  相似文献   
13.
Cortical lesions have recently been a focus of multiple sclerosis (MS) MR research. In this study, we present a white matter signal attenuating sequence optimized for cortical lesion detection at 7 T. The feasibility of white matter attenuation (WHAT) for cortical lesion detection was determined by scanning eight patients (four relapsing/remitting MS, four secondary progressive MS) at 7 T. WHAT showed excellent gray matter-white matter contrast, and cortical lesions were hyperintense to the surrounding cortical gray matter, The sequence was then optimized for cortical lesion detection by determining the set of sequence parameters that produced the best gray matter-cortical lesion contrast in a 10-min scan. Despite the B1 inhomogeneities common at ultra-high field strengths, WHAT with an adiabatic inversion pulse showed good cortical lesion detection and would be a valuable component of clinical MS imaging protocols.  相似文献   
14.
Taking into account effects of late energy injection, we examine big bang nucleosynthesis (BBN) constraints on axino dark matter scenarios with long-lived charged sleptons. We calculate 4-body slepton decays into the axino, a lepton, and a quark–antiquark pair since they govern late hadronic energy injection and associated BBN constraints. For supersymmetric hadronic axion models, we present the obtained hadronic BBN constraints and show that they can be more restrictive than the ones associated with catalyzed BBN via slepton-bound-state formation. From the BBN constraints on hadronic and electromagnetic energy release, we find new upper limits on the Peccei–Quinn scale.  相似文献   
15.
16.
17.
In the presence of scalar (J) and residual dipolar (D) couplings, the transfer efficiency of homonuclear Hartmann-Hahn and COSY-type mixing depends on the ratio D/J and on the mixing sequence. This dependence is analyzed theoretically and the results are confirmed experimentally. At least two different mixing sequences are required to yield good transfer efficiencies for all ratios D/J. In contrast to COSY-type experiments, homonuclear Hartmann-Hahn sequences can provide efficient transfer even if the sum of D and J is zero, i.e., if the coupling vanishes in the weak coupling limit.  相似文献   
18.
19.
Steering a quantum harmonic oscillator state along cyclic trajectories leads to a path-dependent geometric phase. Here we describe its experimental observation in an electronic harmonic oscillator. We use a superconducting qubit as a nonlinear probe of the phase, which is otherwise unobservable due to the linearity of the oscillator. We show that the geometric phase is, for a variety of cyclic paths, proportional to the area enclosed in the quadrature plane. At the transition to the nonadiabatic regime, we study corrections to the phase and dephasing of the qubit caused by qubit-resonator entanglement. In particular, we identify parameters for which this dephasing mechanism is negligible even in the nonadiabatic regime. The demonstrated controllability makes our system a versatile tool to study geometric phases in open quantum systems and to investigate their potential for quantum information processing.  相似文献   
20.
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