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91.
Laterally nanostructured vesicles, polygonal bilayer sheets, and segmented wormlike micelles 总被引:1,自引:0,他引:1
We report the formation of vesicles with a laterally nanostructured membrane by self-assembly of "miktoarm" star terpolymers, that is, macromolecules with three chemically distinct arms. The lateral structure consists of approximately hexagonally packed fluorocarbon channels with 4.1 nm radii, immersed in a continuous, two-dimensional hydrocarbon bilayer. We also show that the assembly of these vesicles proceeds via metastable polygonal, faceted bilayer sheets. 相似文献
92.
A design for an adaptive three-port electronic circulator is presented. The circuit has particular use in telephone work and this model can provide isolation when the terminating load varies over the range200 Omega - 1 kOmega . The whole circuit is realizable in microelectronic form. 相似文献
93.
94.
James P. Lodge 《Aerosol science and technology》2013,47(4):459-468
The aspiration of large particles (18–30.5 μm) in the human nose was studied to determine the inhalation efficiency as a function of particle size, and to evaluate the upper size cutoff for inhalable particles in still air. Under these conditions, the ability of a particle to be inhaled is dependent on the inhalation velocity entering the nose and the particle terminal settling velocity. Nasal inhalation of radiolabeled pollen and wood dust aerosols was measured in four subjects at normal resting breathing rates. The efficiency of nasal aspiration was found to decrease as the square of the particle size. The upper size cutoff for inhalability was estimated to be approximately 39 μm in still air. 相似文献
95.
B Devadas SK Freeman CA McWherter NS Kishore JK Lodge E Jackson-Machelski JI Gordon JA Sikorski 《Canadian Metallurgical Quarterly》1998,41(6):996-1000
A new class of biologically active nonpeptidic inhibitors of Candida albicans NMT has been synthesized starting from the octapeptide ALYASKLS-NH2 (2). The synthetic strategy entailed the preparation of novel protected Ser-Lys mimics 9 and 12 from (S)- or (R)-3-iodotyrosine and then grafting key enzyme recognition elements in a stepwise manner. Like 2, compounds 16, 17, and 18 are competitive Candida NMT inhibitors that bind to the peptide recognition site of the enzyme. Moreover, 16-18 have an affinity comparable to that of 2 even though they are devoid of peptide bonds. In contrast to 2, these nonpeptidic inhibitors exhibit antifungal activity. 相似文献
96.
In cats anaesthetised with pentobarbitone, the effect of inhibitors of the in vitro cellular uptake of GABA were tested on the responses of single central neurones to GABA and other depressant amino acids. (4)- AND (-)-nepecotic acid, (4)-2,4-diaminobutyric acid (DABA) and 2,2-dimethyl-beta-alanine, enhanced the action of GABA on spinal, cerebellar and cerebral cortical neurones. In the spinal cord DABA, and to a less estent (-)-nipecotic acid, enhanced the action of beta-alanine, whereas the actions of glycine and taurine were unaffected by DABA and reduced by (-)-nipecotic acid. In the cerebellum and cerebral cortex, these two substances enhanced the action of GABA, usually to a greater extent than that of beta-alanine and taurine, although this specificity was not marked. The GABA-mediated basket cell inhibition of Purkinje cells in the cerebellum was unaffected by DABA and (-)-nipecotic acid, and neither substance appears suitable for determining the role of uptake processes in the inactivation of synapitcally released GABA. Quantitatively these in vivo results agree more closely with recent vitro uptake studies in cat tissue than the previously published data on rat cerebral cortex and dorsal root ganglia, and the observations provide further evidence for the importance of cellular uptake in maintaining low extraneuronal concentrations of inhibitory amino acid transmitters. 相似文献
97.
Mass-spectrometric techniques were applied to elucidate the mechanism by which polymers release condensation nuclei during pyrolysis. 相似文献
98.
99.
The recent proof that man-made chlorofluorocarbons (CFCs) are seriously damaging the ozone layer and the suggestion that they may contribute to the global warming phenomenon, has led to the development of international regulatory controls through the Montreal Protocol. The expected tightening of these controls sill inevitably result in the virtual disappearance of these solvents over the next few years. In the face of rapidly decreasing availability and increasing unit price therefore, many industries are taking a hard look at alternative materials for a range of applications. Here, the authors provide a background to the harmful effects of the CFCs against which the electronics industry has to make important decisions regarding their replacements 相似文献
100.
SM Fitzjohn ZA Bortolotto MJ Palmer AJ Doherty PL Ornstein DD Schoepp AE Kingston D Lodge GL Collingridge 《Canadian Metallurgical Quarterly》1998,37(12):1445-1458
Understanding the roles of metabotropic glutamate (mGlu) receptors has been severely hampered by the lack of potent antagonists. LY341495 (2S-2-amino-2-(1S,2S-2-carboxycyclopropyl-1-yl)-3-(xanth-9-y l)propanoic acid) has been shown to block group II mGlu receptors in low nanomolar concentrations (Kingston, A.E., Ornstein, P.L., Wright, R.A., Johnson, B.G., Mayne, N.G., Burnett, J.P., Belagaje, R., Wu, S., Schoepp, D.D., 1998. LY341495 is a nanomolar potent and selective antagonist at group II metabotropic glutamate receptors. Neuropharmacology 37, 1-12) but can be used in higher concentrations to block all hippocampal mGlu receptors, identified so far by molecular cloning (mGlu1-5,7,8). Here we have further characterised the mGlu receptor antagonist activity of LY341495 and have used this compound to investigate roles of mGlu receptors in hippocampal long-term potentiation (LTP) and long-term depression (LTD). LY341495 competitively antagonised DHPG-stimulated PI hydrolysis in AV12-664 cells expressing either human mGlu1 or mGlu5 receptors with Ki-values of 7.0 and 7.6 microM, respectively. When tested against 10 microM L-glutamate-stimulated Ca2+ mobilisation in rat mGlu5 expressing CHO cells, it produced substantial or complete block at a concentration of 100 microM. In rat hippocampal slices, LY341495 eliminated 30 microM DHPG-stimulated PI hydrolysis and 100 microM (1S,3R)-ACPD-inhibition of forskolin-stimulated cAMP formation at concentrations of 100 and 0.03 microM, respectively. In area CA1, it antagonised DHPG-mediated potentiation of NMDA-induced depolarisations and DHPG-induced long-lasting depression of AMPA receptor-mediated synaptic transmission. LY341495 also blocked NMDA receptor-independent depotentiation and setting of a molecular switch involved in the induction of LTP; effects which have previously been shown to be blocked by the mGlu receptor antagonist (S)-MCPG. These effects may therefore be due to activation of cloned mGlu receptors. In contrast, LY341495 did not affect NMDA receptor-dependent homosynaptic LTD; an effect which may therefore be independent of cloned mGlu receptors. Finally, LY341495 failed to antagonise NMDA receptor-dependent LTP and, in area CA3, NMDA receptor-independent, mossy fibre LTP. Since in the same inputs these forms of LTP were blocked by (S)-MCPG, a novel type of mGlu receptor may be involved in their induction. 相似文献