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31.
Y. A. Zulueta J. A. Dawson Y. Leyet F. Guerrero J. Anglada‐Rivera M. T. Nguyen 《physica status solidi b》2016,253(2):345-350
32.
Marco P. Monopoli Cláudia Sá e Cunha Miguel Prudêncio Eulália Pereira Iseult Lynch Kenneth A. Dawson Ricardo Franco 《Particle & Particle Systems Characterization》2016,33(12):906-915
Conjugates formed by antibody adsorption to gold nanoparticles (AuNP) have found extensive utilization in immunoassays due to the high surface area and interesting optical and electronic properties of the nanomaterials. Nevertheless, the mechanism of formation of antibody‐AuNP conjugates and their antigen binding characteristics have not been sufficiently explored in terms of specificity and consequent clinical applicability. Dynamic light scattering and related techniques have been successfully employed to detect antigen binding to antibody‐AuNP complexes. Here, a range of different techniques from the bionanotechnology realm have been applied to obtain a detailed picture of a competitive immunoassay for malaria antigen detection, based on fluorescence‐quenching by AuNPs. Both agarose gel electrophoresis and differential centrifugal sedimentation (DCS) analyses provide binding constants in the same order of magnitude, for antibody binding to AuNP and for antigen binding to antibody‐AuNP conjugates. Both techniques are also able to reveal inhibition of antigen binding in the presence of a major blood plasma protein, transferrin (via competitive binding). DCS is further used to show inhibition of the binding of the antigen in the presence of human plasma, a realistic testing condition, of high relevance to the implementation of immunoassays at the clinical level. 相似文献
33.
William M. Dawson Freddie J. O. Martin Guto G. Rhys Kathryn L. Shelley R. Leo Brady Derek N. Woolfson 《Chemical science》2021,12(20):6923
The rational design of linear peptides that assemble controllably and predictably in water is challenging. Short sequences must encode unique target structures and avoid alternative states. However, the non-covalent forces that stabilize and discriminate between states are weak. Nonetheless, for α-helical coiled-coil assemblies considerable progress has been made in rational de novo design. In these, sequence repeats of nominally hydrophobic (h) and polar (p) residues, hpphppp, direct the assembly of amphipathic helices into dimeric to tetrameric bundles. Expanding this pattern to hpphhph can produce larger α-helical barrels. Here, we show that pentameric to nonameric barrels are accessed by varying the residue at one of the h sites. In peptides with four L/I–K–E–I–A–x–Z repeats, decreasing the size of Z from threonine to serine to alanine to glycine gives progressively larger oligomers. X-ray crystal structures of the resulting α-helical barrels rationalize this: side chains at Z point directly into the helical interfaces, and smaller residues allow closer helix contacts and larger assemblies.Systematic de novo design of peptides that form α-helical barrels with functionalisable central channels with a range of internal diameters. 相似文献
34.
35.
Bonnett PE Carpenter KJ Dawson S Davey RJ 《Chemical communications (Cambridge, England)》2003,(6):698-699
In many situations the process of crystallisation from solution is known to occur via metastable crystalline states (polymorphs or solvates). Here we present what we believe to be a novel example of small molecule crystallisation in which the initial separation of a solute rich liquid phase precedes the crystallisation event. We believe this occurs because a submerged liquid-liquid phase boundary is accessible within the metastable zone of the crystal nucleation process. 相似文献
36.
The substrate specificity of 4-oxalocrotonate tautomerase (4-OT) is characterized by electrostatic interactions between positively charged arginine (Arg) side chains on the enzyme and the dianionic substrate, 4-oxalocrotonate. To generate specific hydrogen-bonding interactions with a monoanionic substrate analogue, we have introduced a urea functional group into the active site by replacing arginine side chains with isosteric citrulline (Cit) residues. This design was based on the complementarity between the urea functionality of citrulline and the uncharged amide function of the substrate, as opposed to the guanidinium-carboxylate electrostatic interaction between the wild-type enzyme and the natural substrate. Indeed, the synthetic (Arg39Cit)4-OT analogue catalyzed the tautomerization of the non-natural monoamide-monoacid substrate while it was a poor catalyst for the natural diacid substrate. The specificity of (Arg39Cit)4-OT for the monoamide-monoacid substrate relative to that of the diacid substrate was found to be 740-fold greater than that of the wild-type enzyme for tautomerization of the non-natural substrate as compared with the natural one. The role of electrostatic interactions in the tautomerization of the monoamide-monoacid substrate was probed in detail with several other Arg to Cit analogues of this enzyme. This study has demonstrated that chemical manipulation of the functional groups within the active site of an enzyme can modify its catalytic activity and substrate specificity in a predictable way, suggesting that the incorporation of noncoded amino acids into proteins has great promise for the development of new enzymatic mechanisms and new binding interactions. 相似文献
37.
Saskia Biskup Darren J Moore Alexis Rea Bettina Lorenz-Deperieux Candice E Coombes Valina L Dawson Ted M Dawson Andrew B West 《BMC neuroscience》2007,8(1):102
Background
Mutations within the leucine-rich repeat kinase 2 (LRRK2) gene account for a significant proportion of autosomal-dominant and some late-onset sporadic Parkinson's disease. Elucidation of LRRK2 protein function in health and disease provides an opportunity for deciphering molecular pathways important in neurodegeneration. In mammals, LRRK1 and LRRK2 protein comprise a unique family encoding a GTPase domain that controls intrinsic kinase activity. The expression profiles of the murine LRRK proteins have not been fully described and insufficiently characterized antibodies have produced conflicting results in the literature. 相似文献38.
39.
A model is presented to describe the propagation of positive corona streamers in the low field region of a non-uniform field gap in atmospheric air. It has been assumed that the growth is a property solely of the streamer tip, uninfluenced by the channel conductivity. Calculations from the model indicate that the criterion for propagation of a streamer in zero external field is that the number of ions in the tip be 108 and the radius about 3×10?3 cm. It is proposed that the streamer ceases to propagate as a result of the loss of energy of the tip due to the formation of ion pairs in the channel. The results of previous experimental observations of streamers are compared with calculations derived from the model, and a prediction from the model of the lifetime of streamers after voltage removal is discussed. 相似文献
40.
The general question of the properties of light, neutral colored spin-zero particles in QCD is examined. Models with spontaneous breaking of QCD at very large distances, such as that of DeRújula, Giles, and Jaffe and the SO(3) scheme of Slansky, Goldman, and Shaw, require such light colored Higgs scalars. These scalars will form color-singlet hadronic bound states at short distances and estimates are given of bound state masses, decay widths, and production rates in processes such as ψ → γ + X within the MIT bag model. The resulting states are expected in the mass neighborhood ~1.5 GeV and should resemble glueballs. 相似文献