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71.
A Multivalent Ligand for the Mannose‐6‐Phosphate Receptor for Endolysosomal Targeting of an Activity‐Based Probe
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Dr. Sascha Hoogendoorn Dr. Gijs H. M. van Puijvelde Prof. Dr. Johan Kuiper Prof. Dr. Gijs A. van der Marel Prof. Dr. Herman S. Overkleeft 《Angewandte Chemie (International ed. in English)》2014,53(41):10975-10978
The ubiquitously expressed mannose‐6‐phosphate receptors (MPRs) are a promising class of receptors for targeted compound delivery into the endolysosomal compartments of a variety of cell types. The development of a synthetic, multivalent, mannose‐6‐phosphate (M6P) glycopeptide‐based MPR ligand is described. The conjugation of this ligand to fluorescent DCG‐04, an activity‐based probe for cysteine cathepsins, enabled fluorescent readout of its receptor‐targeting properties. The resulting M6P‐cluster–BODIPY–DCG‐04 probe was shown to efficiently label cathepsins in cell lysates as well as in live cells. Furthermore, the introduction of the 6‐O‐phosphates leads to a completely altered uptake profile in COS and dendritic cells compared to a mannose‐containing ligand. Competition with mannose‐6‐phosphate abolished all uptake of the probe in COS cells, and we conclude that the mannose‐6‐phosphate cluster targets the MPR and ensures the targeted delivery of cargo bound to the cluster into the endolysosomal pathway. 相似文献
72.
73.
Jan Claereboudt Magda Claeys Herman Geise Renaat Gijbels Akos Vertes 《Journal of the American Society for Mass Spectrometry》1993,4(10):798-812
The use of laser microprobe mass spectrometry (LMMS) for the structural characterization of thermolabile quaternary phosphonium salts has been evaluated. A comparison has been made between LM mass spectra obtained by direct analysis of “neat” organic salts and the corresponding “matrix-assisted” LM mass spectra. Main limitations of LMMS for the direct analysis of neat organic salts (i.e., no matrix) result from (1) formation of artifact ions that originate from thermal degradation and surface recombination reactions and (2) poor shot-to-shot reproducibility of the spectra. Dilution of the organic salts in a suitable, UV-absorbing matrix (e.g., nicotinic acid) significantly enhances the quality of the LM mass spectra. Improvements are: (1) an increase of the ion yield of preformed cations, (2) reduction or elimination of thermal decomposition and other deleterious surface reactions, and (3) a much better shot-to-shot spectral reproducibility. An interesting analytical feature is that these LM mass spectra, which contain only a few matrix peaks, can be obtained for subnanogram amounts of sample. The results also show that triphenylphosphonium salts with polycyclic aromatic substituents can be used as “molecular thermometers” to probe both the temperatures experienced by the sample molecules during the laser-induced desorption ionization process and the internal energies of the desorbed ion species. In this way, quaternary phosphonium salts can be used for evaluating whether improvements have been achieved by applying different sample treatments. Comparison of four different matrices (i.e., nicotinic acid, ammonium chloride, glycerol, and 3-nitrobenzylalcohol) indicates that the effectiveness of a matrix to reduce thermal degradation and to decrease the internal energies of the ions depends on the UV-absorption characteristics and the volatilization/sublimation temperature of the matrix material. 相似文献
74.
Jan A. Herman Kazimiera Herman Terry B. McMahon 《Journal of the American Society for Mass Spectrometry》1991,2(3):220-225
Fourier transform ion cyclotron resonance mass spectrometry has been used to measure the reaction rates for ions derived from methylamine with dimethylamine or trimethylamine. The use of the selective ion ejection technique greatly simplifies the elucidation of the ion-molecule reaction channels. The rate constants for proton transfer from protonated metwlamine, CH3NH 3 + (m/z 32), to dimethylamine and trimethylamine are 16.1 ± 1.6 × 10?10 and 9.3 ± 0.9 × 10?10 cm3 molec?1s?1, respectively. The rate constants for charge transfer from methylamine molecular ion, CH3NH 2 + (m/z 31), to dimethylamine and trimethylamine are 9.3 ± 1.8 x 10?10 and 15.0 ± 5 × 10?10 cm3molec?1s?1, respectively. 相似文献
75.
Herman Bachelard Peter Morris Andrew Taylor Nicola Thatcher 《Magnetic resonance imaging》1995,13(8):1223-1226
We are applying multi-nuclear high-field (500 MHz) MR spectroscopy of metabolising whole tissue preparations of the mammalian brain to studies on individual components of convulsions, which include prolonged depolarization, metabolic deprivation, and the effects of excitotoxins. The responses of glial cells and neurones can be partially distinguished by following labelling patterns of metabolic intermediates from 13C-labelled glucose or acetate (which enters only glial cells). This approach clearly confirmed our earlier indications that the metabolic response to depolarization (40 mM extracellular K+) occurs essentially in glial cells. Some evidence for metabolic shuttling between glia and neurones was obtained from the changes in C3/C4 ratios of glutamate and glutamine, and the C2/C3 of GABA. Mechanisms for metabolic support of neurones by glia may be of importance in neuronal protection under such metabolic stress as occurs in epilepsy. Changes in free intracellular divalent cations ([Ca2+]i and [Zn2+]i) were monitored using the 19F-MRS indicator, 5FBAPTA. Large increases in [Ca2+]i and decreases in PCr were produced by excitotoxins (glutamate and NMDA), depolarization or ischaemia, but intracellular Zn2+ appeared only after exposure to the excitotoxins. The NMDA receptor blocker, MK801, removed all of the responses to NMDA, but only prevented the appearance of Zn2+ observed with glutamate. These results indicate that the damage caused to neurones by such insults as convulsions is not due simply to the presence of excessive excitotoxic glutamate. 相似文献
76.
A major difficulty in the study of large-scale complex systems involving human decision-making with non-linear collective effects is that of obtaining pertinent data at the desired level of detail. A controlled experiment involving real commuters in a hypothetical computer simulated traffic system is described as an alternative approach of conducting observational studies to support the modelling of such complex dynamic interactive decision systems. An overview of the principal characteristics of the traffic system's evolution obtained in this experiment is presented. Also illustrated are the features of a proposed behavioral framework where users are viewed as boundedly rational seekers of a satisfactory choice outcome. 相似文献
77.
Fabrication of strong long-period gratings in hydrogen-free fibers with 157-nm F2-laser radiation 总被引:2,自引:0,他引:2
Long-period gratings were fabricated in standard telecommunication fiber (Corning SMF-28) by use of what is believed to be record short-wavelength light from a 157-nm F(2) laser. Strong loss peaks were formed without the need for enhancement techniques such as hydrogen loading. The magnitude of the attenuation peak was sensitive to the single-pulse laser fluence, decreasing with increasing pulse fluence as a result of nonuniform 157-nm laser interaction with both the fiber cladding and core. The long-period fiber gratings have good wavelength stability (Dlambda~7 nm) under thermal annealing at 150 degrees C. 相似文献
78.
We introduce the inverted prefix tries (a variation of suffix tries) as a convenient formalism for stating and proving properties of the Ehrenfeucht–Mycielski sequence [A. Ehrenfeucht, J. Mycielski, A pseudorandom sequence—how random is it? American Mathematical Monthly 99 (1992) 373-375]. We also prove an upper bound on the position in the sequence by which all strings of a given length will have appeared; our bound is given by the Ackermann function, which, in light of experimental data, may be a gross over-estimate. Still, it is the best explicitly known upper bound at the moment. Finally, we show how to compute the next bit in the sequence in a constant number of operations. 相似文献
79.
MaxwellD. Cummings Jimmy Lindberg Tse‐I Lin Herman deKock Oliver Lenz Elisabet Lilja Sara Fellnder Vera Baraznenok Susanne Nystrm Magnus Nilsson Lotta Vrang Michael Edlund sa Rosenquist Bertil Samuelsson Pierre Raboisson Kenneth Simmen 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2010,122(9):1552-1552