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991.
Rulon Linford Riccardo Betti Jill Dahlburg James Asay Michael Campbell Phillip Colella Jeffrey Freidberg Jeremy Goodman David Hammer Joseph Hoagland Steve Jardin John Lindl Grant Logan Keith Matzen Gerald Navratil Arthur Nobile John Sethian John Sheffield Mark Tillack Jon Weisheit 《Journal of Fusion Energy》2003,22(2):93-126
This is the final report of a panel set up by the U.S. Department of Energy (DOE) Fusion Energy Sciences Advisory Committee (FESAC) in response to a charge letter from Dr. Ray Orbach (Appendix A). In that letter, Dr. Orbach asked FESAC for an assessment of the present status of inertial fusion energy (IFE) research carried out in contributing programs. These programs include the heavy ion (HI) beam, the high average power laser (HAPL), and Z-Pinch drivers and associated technologies, including fast ignition (FI). This report, presented to FESAC on March 29, 2004, and subsequently approved by them (Appendix B), presents FESAC's response to that charge. 相似文献
992.
The majority of organic carbon in the oceans is present as dissolved organic matter (DOM); therefore understanding the distribution and dynamics of DOM is central to understanding global carbon cycles. Describing the time-space variability in colored dissolved organic matter (CDOM) has been difficult, as standard spectrophotometric methods for CDOM determination are laborious and susceptible to methodological biases. Previously, measurements of CDOM absorption in discrete water samples by use of a liquid-waveguide capillary cell (LWCC) compared favorably with measurements made with a benchtop spectrophotometer. Given this, we focused on automating the LWCC technique to improve our spatial and temporal sampling capabilities for CDOM. We found strong correlations between CDOM absorption spectra collected from discrete water samples using standard methods and selected corresponding CDOM spectra collected by the automated LWCC system. The near-continuous measurements by the LWCC system made it possible to map the temporal, spatial, and spectral variability of CDOM absorption along the ship track. 相似文献
993.
Anisotropic in-plane strain arises in quantum-well systems by design or unintentionally. We propose two methods of measuring the in-plane strain anisotropy based on the optical polarization anisotropy that arises with anisotropic in-plane strain. One method uses purely optical means to determine the strain anisotropy in quantum wells under a compressive strain that is spatially varying. A second approach, applicable to quantum wells under tensile strain or with strain that does not vary with position, requires the application of a uniaxial in-plane stress. Although the second method is experimentally more difficult, it allows analysis of systems that would otherwise be inaccessible. 相似文献
994.
Changes in surface electromyographic (EMG) amplitude during sustained, fatiguing contractions are commonly attributed to variations in muscle fiber conduction velocity (MFCV), motor unit firing rates, transmembrane action potentials and the synchronization or recruitment of motor units. However, the relative contribution of each factor remains unclear. Analytical relationships relating changes in MFCV and mean motor unit firing rates to the root mean square (RMS) and average rectified (AR) value of the surface EMG signal are derived. The relationships are then confirmed using model simulation. The simulations and analysis illustrate the different behaviors of the surface EMG RMS and AR value with changing MFCV and firing rate, as the level of motor unit superposition varies. Levels of firing rate modulation and short-term synchronization that, combined with variations in MFCV, could cause changes in EMG amplitude similar to those observed during sustained isometric contraction of the brachioradialis at 80% of maximum voluntary contraction were estimated. While it is not possible to draw conclusions about changes in neural control without further information about the underlying motor unit activation patterns, the examples presented illustrate how a combined analytical and simulation approach may provide insight into the manner in which different factors affect EMG amplitude during sustained isometric contractions. 相似文献
995.
Diffraction tomography (DT) is an inversion technique that reconstructs the refractive index distribution of a weakly scattering object. In this paper, a novel reconstruction algorithm for three-dimensional diffraction tomography employing spherical-wave sources is mathematically developed and numerically implemented. Our algorithm is numerically robust and is much more computationally efficient than the conventional filtered backpropagation algorithm. Our previously developed algorithm for DT using plane-wave sources is contained as a special case. 相似文献
996.
A scanning mobility particle sizer has been used to quantify residual particle number and mass concentrations generated by ultrasonic nebulization of deionized (DI) water stored in a variety of bottles. High variability of residual particles was found not only between different bottle types but also between different bottles of the same type. Degradation of the water quality, quantified as increased residual mass and number concentrations as a function of time, occurred to varying degrees for water stored in different bottle types. Overall, glass bottles showed the highest residual particle concentrations and exhibited the poorest stability over time. After a storage period of 3 weeks, DI water stored in Pyrex bottles showed average increases in particle mass and number densities in the aerosol of over 250% and 60%, respectively. Total dissolved impurity levels in the water increased from 110 to 290 ng mL(-1) over the 3-week period. It is hypothesized that leaching from the bottle walls increases impurity levels in the water over time. Leaching was observed for both glass and polymer bottles. Contrary to this trend, residual particle concentrations from deionized water stored in Teflon bottles showed a net decrease during the measurement period. With respect to absolute residual particle concentrations and storage stability, a Teflon bottle yielded the best performance. Total residual particle mass and number densities for Teflon were less than a factor of 15% and 1%, respectively, as compared to residual particle levels observed for the Pyrex bottle. Absolute dissolved impurity levels in the water for the Teflon bottle decreased from 7.8 to 3.7 ng mL(-1) over the 4-week period. 相似文献
997.
Sydor JR Scalf M Sideris S Mao GD Pandey Y Tan M Mariano M Moran MF Nock S Wagner P 《Analytical chemistry》2003,75(22):6163-6170
A new chip-based method to identify protein-protein interactions was developed using the guanine nucleotide exchange factor GRF2 and two interacting proteins, Ras and calmodulin, as model proteins. A generic immobilization strategy for FLAG-tagged bait proteins on a protein-repellent streptavidin chip surface was implemented by presentation of an oriented anti-FLAG antibody. A flow cell device, integrating different chip surfaces, was developed, and the interaction of immobilized GRF2 with the two analytes was verified by fluorescence assays. On-chip tryptic digest assays were then performed on the capture surface and analyzed by microLC-MS/MS. The interaction of GRF2 with calmodulin and Ras was demonstrated, and the lower limit of detection was determined. We also implemented an on-chip immunoprecipitation assay to identify GRF2-binding partners from complex protein mixtures. Cells overexpressing FLAG-GRF2 were lysed and then incubated with the anti-FLAG chip. In addition to detecting GRF2, we also identified calmodulin, demonstrating that this technique can successfully identify endogenous levels of proteins, bound to recombinant bait proteins. This chip-based method has the advantage that no subsequent gel separations of protein complexes prior to LC-MS analysis are required and is therefore amenable to miniaturized high-throughput determination of protein-protein interactions. 相似文献
998.
Keetch CA Hernánndez H Sterling A Baumert M Allen MH Robinson CV 《Analytical chemistry》2003,75(18):4937-4941
Nanoflow electrospray mass spectrometry has been applied previously to investigate noncovalent protein-protein and protein-ligand interactions. Here we evaluate a commercial microchip device for this application. We show that the microchip can be used to obtain mass spectra of the noncovalent tetramer transthyretin. The device showed a 10-fold increase in signal stability compared with a nanoflow capillary and a high level of nozzle-to-nozzle reproducibility. Binding of the natural ligand thyroxine was clearly observed, and a range of small molecules proposed as inhibitors of transthyretin amyloidosis were shown to be effective in stabilizing the tetramer. We propose that measuring the ability of small molecules to stabilize protein complexes using this automated microchip technology will enable high-throughput screening of multi-protein complexes by mass spectrometry. 相似文献
999.
Spectroscopic features of dual fluorescence/luminescence resonance energy-transfer molecular beacons 总被引:6,自引:0,他引:6
Molecular beacons have the potential to become a powerful tool in gene detection and quantification in living cells. Here we report a novel dual molecular beacons approach to reduce false-positive signals in detecting target nucleic acids in homogeneous assays. A pair of molecular beacons, each containing a fluorescence quencher and a reporter fluorophore, one with a donor and a second with an acceptor fluorophore, hybridize to adjacent regions on the same target resulting in fluorescence resonance energy transfer (FRET). The detection of a FRET signal leads to a substantially increased signal-to-background ratio compared with that seen in single molecular beacon assays and enables discrimination between fluorescence due to specific probe/target hybridization and a variety of possible false-positive events. Further, when a lanthanide chelate is used as a donor in a dual-probe assay, extremely high signal-to-background ratios can be achieved owing to the long lifetime and sharp emission peaks of the donor and the time-gated detection of acceptor fluorescence emission. These new approaches allow for the ultrasensitive detection of target molecules in a way that could be readily applied to real-time imaging of gene expression in living cells. 相似文献
1000.
Michaud AL Yurawecz MP Delmonte P Corl BA Bauman DE Brenna JT 《Analytical chemistry》2003,75(18):4925-4930
Fatty acids with conjugated double bonds have attracted great interest because of their reported potent bioactivities. However, there are currently no rapid methods for their structural characterization. We report here a convenient mass spectrometry-based strategy to establish double bond geometry by analysis of collisional dissociation products of cis/trans and trans/cis conjugated linoleic acids (CLAs), as methyl esters, and to distinguish CLAs from homoallylic (methylene-interrupted) fatty acids in a single-stage mass spectrum. A series of CLA standards with double bond positions 6,8; 7,9; 8,10; 9,11; 10,12; 11,13; 12,14; and 13,15, with all four possible geometries (cis/trans; trans/cis; cis/cis; trans/trans) were analyzed. The m/z 54 (1-methyleneimino)-1-ethenylium ion, generated by self-reaction of acetonitrile under chemical ionization conditions, reacts with unsaturated fatty acids to yield an [M + 54]+ ion, which decomposes in the single-stage mass spectrum by loss of neutral methanol to form [M + 54 - 32]+. The ratio of [M + 54]+/[M + 54 - 32]+ in the single-stage mass spectra of CLA isomers is 1 order of magnitude less than for homoallylic diene FAME. Collisional dissociation of the [M + 54]+ ion yields two diagnostic ions that contain the alpha- and omega-carbon atoms and is characteristic of double bond position in the analyte. The fragment vinylic to the trans double bond is significantly more abundant than that for the cis double bond, revealing double bond geometry. The ratio of alpha to we diagnostic ion abundances is >4.8 for cis/trans isomers, <0.5 for trans/cis isomers, and 0.7-3.2 for cis/cis and trans/trans isomers. This method provides a rapid alternative to conventional conjugated fatty acid analysis and, together with complementary elution time information provided by gas chromatography, enables rapid, positive identification of double bond position and geometry in most CLA FAME. 相似文献