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181.
The birefringence of MBBA, determined from the channeled spectra, decreases when the wavelength increases, showing a normal dispersion. The changes induced by an external electrostatic field acting perpendicular on the nematic director in the birefringence values were evidenced. The birefringence increases with the electrostatic field intensity which enhances the preferential alignment by the big values of the electric dipole moments induced parallel to the long MBBA molecule. The main refractive indices were interferometrically measured for three visible monochromatic radiations and the birefringence values were concordant with those estimated from the channeled spectra. The main molecular polarizabilities were estimated.  相似文献   
182.
The prompt component at intermediate velocity of light charged particles is investigated. An improved coalescence model coupled to the intra-nuclear cascade code ISABEL is used to obtain light complex particle energy spectra and multiplicities as a function of impact parameter. The results are compared with experimental data from the 36Ar + 58Ni experiment at 95 MeV/nucleon, performed with the INDRA 4π detection system. The calculated prompt component is found to rather well reproduce proton spectra. For complex light charged particles the calculated components well populate the high energy part of spectra. Prompt emission can therefore explain the large transverse energies experimentally observed at mid-rapidity. Received: 27 July 2000 / Accepted: 20 November 2000  相似文献   
183.
High spin states of 101Rh have been populated using the reaction 70Zn+36S at 130 MeV. γ-rays were detected with the EUROGAM2 array. New high-spin bands have been observed in this nucleus up to 45/2, 57/2 and 65/2+ states. They have been interpreted using the Nilsson-Strutinsky cranking formalism as terminating configurations. Two of the bands were observed up to the predicted terminating states which are built up from g9/2 protons as well as d5/2, g7/2 and h11/2 neutrons relative to a 90Zr core. Received: 30 October 1998  相似文献   
184.
We consider the family of fibres of a polynomial function f on a smooth noncompact algebraic real surface and we characterise the regular fibres of f which are atypical due to their asymptotic behaviour at infinity. We compare to the similar problem in the complex case. Received: 5 May 1998 / Revised version: 20 March 1999  相似文献   
185.
In this Letter we develop a general procedure leading from a Mourre-type estimation for a given self-adjoint operator H to a Hardy-type weighted inequality. We use this method in order to prove exponential decay for eigenvectors of a large class of perturbations of operators of convolution with bounded analytic functions.  相似文献   
186.
In this paper we consider the 3D real-valued Maxwell-Bloch equations with a parametric control given by \(\dot {x}=y+az+byz,\dot {y}=xz,\dot {z}=-xy\) (\(a,b\in \mathbb {R}\)). We give two Lie-Poisson structures of this system that are related with well-known Lie algebras. Moreover, we construct infinitely many Hamilton-Poisson realizations of this system. We also analyze the stability of the equilibrium points, as well as the existence of periodic orbits. In addition, we emphasize some connections between the energy-Casimir mapping of the considered system and the above-mentioned dynamical elements.  相似文献   
187.
In this paper we introduce and study the concept of subgroup commutativity degree of a finite group G. This quantity measures the probability of two random subgroups of G commuting. Explicit formulas are obtained for some particular classes of finite groups.  相似文献   
188.
Let f : 2N+ be a polymatroid (an integer‐valued non‐decreasing submodular set function with f(??) = 0). We call S ? N a base if f(S) = f(N). We consider the problem of finding a maximum number of disjoint bases; we denote by m* be this base packing number. A simple upper bound on m* is given by k* = max{k : ΣiεNfA(i) ≥ kfA(N),?A ? N} where fA(S) = f(AS) ‐ f(A). This upper bound is a natural generalization of the bound for matroids where it is known that m* = k*. For polymatroids, we prove that m* ≥ (1 ? o(1))k*/lnf(N) and give a randomized polynomial time algorithm to find (1 ? o(1))k*/lnf(N) disjoint bases, assuming an oracle for f. We also derandomize the algorithm using minwise independent permutations and give a deterministic algorithm that finds (1 ? ε)k*/lnf(N) disjoint bases. The bound we obtain is almost tight because it is known there are polymatroids for which m* < (1 + o(1))k*/lnf(N). Moreover it is known that unless NP ? DTIME(nlog log n), for any ε > 0, there is no polynomial time algorithm to obtain a (1 + ε)/lnf(N)‐approximation to m*. Our result generalizes and unifies two results in the literature. © 2009 Wiley Periodicals, Inc. Random Struct. Alg., 2009  相似文献   
189.
Recent studies have revealed the existence of liver cancer stem cells (CSCs). Therefore, there is an urgent need for new and effective treatment strategies specific to liver CSCs. In this work, the poly(d,l-lactide-coglycolide) nanoparticles containing paclitaxel were prepared by emulsification-solvent evaporation method. The nanoparticles decorated with anti-CD133 antibody, termed targeted nanoparticles, were prepared by carbodiimide chemistry for liver CSCs. The physicochemical characteristics of the nanoparticles (i.e., encapsulation efficiency, particle size distribution, morphology, and in vitro release) were investigated. Cellular uptake and accumulation in tumor tissue of nanoparticles were observed. To assess anti-tumor activity of nanoparticles in vitro and in vivo, cell survival assay and tumor regression study were carried out using liver cancer cell lines (Huh7 and HepG2) and their xenografts. Particle size of targeted nanoparticles was 429.26 ± 41.53 nm with zeta potential of ?11.2 mV. Targeted nanoparticles possessed spherical morphology and high encapsulation efficiency (87.53 ± 5.9 %). The accumulation of targeted nanoparticles depends on dual effects of passive and active targeting. Drug-loaded nanoparticles showed cytotoxicity on the tumor cells in vitro and in vivo. Targeted nanoparticles resulted in significant improvement in therapeutic response through selectively eliminating CD133 positive subpopulation. These results suggested that the novel nanoparticles could be a promising candidate with excellent therapeutic efficacy for targeting liver CSCs.  相似文献   
190.
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