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91.
Purpose
The purpose was to compare T2* relaxation times and proton density fat-fraction (PDFF) values between brown (BAT) and white (WAT) adipose tissue in lean and ob/ob mice.Materials and Methods
A group of lean male mice (n=6) and two groups of ob/ob male mice placed on similar 4-week (n=6) and 8-week (n=8) ad libitum diets were utilized. The animals were imaged at 3 T using a T2*-corrected chemical-shift-based water–fat magnetic resonance imaging (MRI) method that provides simultaneous estimation of T2* and PDFF on a voxel-wise basis. Regions of interest were drawn within the interscapular BAT and gonadal WAT depots on co-registered T2* and PDFF maps. Measurements were assessed using analysis of variance, Bonferroni-adjusted t test for multigroup comparisons and the Tukey post hoc test.Results
Significant differences (P<.01) in BAT T2* and PDFF were observed between the lean and ob/ob groups. The ob/ob animals exhibited longer BAT T2* and greater PDFF than lean animals. However, only BAT PDFF was significantly different (P<.01) between the two ob/ob groups. When comparing BAT to WAT within each group, T2* and PDFF values were consistently lower in BAT than WAT (P<.01). The difference was most prominent in the lean animals. In both ob/ob groups, BAT exhibited very WAT-like appearances and properties on the MRI images.Conclusion
T2* and PDFF are lower in BAT than WAT. This is likely due to variations in tissue composition. The values were consistently lower in lean mice than in ob/ob mice, suggestive of the former's greater demand for BAT thermogenesis and reflective of leptin hormone deficiencies and diminished BAT metabolic activity in the latter. 相似文献92.
Many physical phenomena are modeled by nonclassical hyperbolic boundary value problems with nonlocal boundary conditions. In this paper, the problem of solving the one-dimensional wave equation subject to given initial and non-local boundary conditions is considered. These non-local conditions arise mainly when the data on the boundary cannot be measured directly. Several finite difference methods with low order have been proposed in other papers for the numerical solution of this one dimensional non-classic boundary value problem. Here, we derive a new family of efficient three-level algorithms with higher order to solve the wave equation and also use a Simpson formula with higher order to approximate the integral conditions. Additionally, the fourth-order formula is also adapted to nonlinear equations, in particular to the well-known nonlinear Klein–Gordon equations which many physical problems can be modeled with. Numerical results are presented and are compared with some existing methods showing the efficiency of the new algorithms. 相似文献
93.
Ningsih Z Hossain MA Wade JD Clayton AH Gee ML 《Langmuir : the ACS journal of surfaces and colloids》2012,28(4):2217-2224
The mechanism of interaction between a model antimicrobial peptide and phospholipid unilamellar vesicle membranes was studied using fluorescence spectroscopy, fluorescence lifetime measurements, and light scattering. The peptide, a mellitin mutant, was labeled at position K14 with the polarity-sensitive probe AlexaFluor 430. The kinetics of the interaction of this derivative with various concentrations of 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC) vesicles was examined. Our work unveiled two novel aspects of peptide-lipid interactions. First, the AB plot or phasor analysis of the fluorescence lifetime studies revealed at least three different peptide states, the population of which depended on the lipid to peptide (L:P) concentration ratio. Second, complex fluorescence kinetics were observed over extended time-scales from 30 s to 2 h. The extended kinetics was only observed at particular lipid concentrations (L:P ratios 20:1 and 10:1) and not at others (30, 40, 50 and 100:1 L:P ratio). Analysis of the complex kinetics revealed several intermediates. We assign these to distinct states of the peptide formed during helix insertion into the vesicle membrane that are intermediate to lytic pore formation. 相似文献
94.
The intramolecular dipolar cycloaddition of an azide with an alkyne has provided a useful entry into triazole fused tricyclic heterocycles containing both the triazole ring and the oxazolidin-2-one ring system. The requisite azido-alkynes have been prepared via a two-step sequence from fused ring aziridines. A series of 6-12 membered rings containing both the oxazolidinone and triazole rings have been prepared. These ring systems have been designed as conformationally restrained analogs of RNA-binding oxazolidinones. 相似文献
95.
Two-dimensional π-systems are of current interest in the design of functional organic molecules, exhibiting unique behavior for applications in organic electronics, single-molecule devices, and sensing. Here we describe the synthesis and characterization of "push-pull macrocycles": electron-rich and electron-poor moieties linked by a pair of (matched) conjugated bridges. We have developed a two-component macrocyclization strategy that allows these structures to be synthesized with efficiencies comparable to acyclic donor-bridge-acceptor systems. Compounds with both cross-conjugated (m-phenylene) and linearly conjugated (2,5-thiophene) bridges have been prepared. As expected, the compounds undergo excitation to locally excited states followed by fluorescence from charge-transfer states. The m-phenylene-based systems exhibit slower charge-recombination rates presumably due to reduced electronic coupling through the cross-conjugated bridges. Interestingly, pairing the linearly conjugated 2,5-thiophene bridges also slows charge recombination. DFT calculations of frontier molecular orbitals show that the direct HOMO-LUMO transition is polarized orthogonal to the axis of charge transfer for these symmetrical macrocyclic architectures, reducing the electronic coupling. We believe the push-pull macrocycle design may be useful in engineering functional frontier molecular orbital symmetries. 相似文献
96.
97.
Thermospray high-performance liquid chromatography-mass spectrometry was used to confirm the identity of five bulk anticancer drugs, and in some cases, to identify drug impurities. Analysis resulted in both molecular weight and structural (fragment ions) information obtained from the full scan spectra of as little as 50 ng of each drug. The technique was also used to evaluate the chromatographic specificity of corresponding ultraviolet or refractive index high-performance liquid chromatographic detection in the presence of drug degradation products. 相似文献
98.
D. P. E. Dickson N. M. K. Reid S. Mann V. J. Wade R. J. Ward T. J. Peters 《Hyperfine Interactions》1989,45(1-4):223-231
Mössbauer spectroscopy has shown that the iron-containing cores of the biological iron storage material haemosiderin produced under normal and various pathological conditions are significantly different in their magnetic properties. The differences have been correlated with information on the particle size, morphology, crystallinity and mineral form of the haemosiderin cores obtained by complementary electron microscopy and electron diffraction studies. These results have important implications for the use of Mössbauer spectroscopy in determining the properties of small particle magnetic systems and also considerable relevance for the improved understanding and treatment of iron overload disease. 相似文献
99.
Iron Mössbauer spectroscopy has provided evidence for the presence in deep-sea smoker vents of superparamagnetic material, which is correlated with anaerobic bacteria found to thrive there. The finding of superparamagnetic terrestrial vent material suggests that prospecting for such material on Mars may be a way to locate sites with micropaleontological potential. 相似文献
100.