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991.
Marianne Borloo Koen Augustyns Alexander Belyaev Ingrid de Meester Anne-Marie Lambeir Filip Goossens Willy Bollaert Padinchare Rajan Simon Scharpé Achiel Haemers 《Letters in Peptide Science》1995,2(3-4):198-202
Summary A series of azaproline dipeptides with various N-substituents were synthesized as possible active-site-directed inhibitors of two proline-specific serine proteases, dipeptidyl peptidase IV and prolyl oligopeptidase. Compounds with semicarbazide, carbazate, acylhydrazine and sulphonylhydrazine structures were tested. Some compounds show moderate activity, i.e., in the millimolar range. 相似文献
992.
The mechanism of the aniline hydroxylase activity of methaemoglobin in a monooxygenase system consisting of NADH as electron donor, riboflavin, FAD, FMN or methylene blue as electron carrier and methaemoglobin as the terminal oxidase has been studied. Hydrogen peroxide is produced from oxygen in a methaemoglobin-independent process. 4-Aminophenol is subsequently produced peroxidatively by an NADH-dependent process; NADH prevents a further oxidation of 4-aminophenol in the presence of haemoglobin. In the absence of electron carrier, NADH slowly reduces haemoglobin and then oxyhaemoglobin reacts with aniline to give 4-aminophenol. In the absence of electron donor and electron carrier, oxyhaemoglobin and aniline give rise to the reversible production of 4-aminophenol. 相似文献
993.
Phosphofructokinase (EC 2.7.1.11) from rabbit liver was purified to homogeneity. Preincubation of enzyme results in nonlinearity
of enzyme activity with enzyme concentration. Therefore K0.5 of enzyme for fructose 6 phosphate in the absence or presence of fructose 2,6 bisphosphate or polyethylene glycol or in the
presence of both was determined at physiological concentrations of its various effectors by taking the initial rate obtained
by adding the enzyme last. They decrease the K0.5 value from 4.1 mM to about 0.2mM. The K0.5 of enzyme for fructose 2,6 bisphosphate was also determined under the above conditions. It is about 4.3ΜM. Transient kinetics of phosphofructokinase at varying concentrations of enzyme in the presence of fructose 2,6 bisphosphate
or polyethylene glycol or in the presence of both were studied. It was found that although they decrease t1/2
i.e. the time to reach half the maximal steady rate by about 5–8 fold, it was about constant at varying concentrations of the
enzyme. These results indicate that fructose 2,6 bisphosphate and polyethylene glycol decrease K0.5 of the enzyme for fructose 6 phosphate not by associating the enzyme to higher aggregates, but by a different mechanism. 相似文献
994.
Structure and properties of pectin gels in plant cell walls 总被引:20,自引:4,他引:16
MICHAEL C. JARVIS 《Plant, cell & environment》1984,7(3):153-164
Abstract This review deals with recent advances in the structural characterization of pectins and the gels which they form, in relation to auxin-induced extension growth, the ripening of fruit, and cellular recognition. Pectins are block polysaccharides. Heavily branched, largely methyl-esterified blocks alternate with unbranched blocks of varying degrees of esterification. The unbranched, non-esterified blocks can aggregate through calcium binding to form the junction zones that hold a gel together. The aggregates are of two, or possibly four, chains at low calcium levels, and larger with excess calcium. The fall in wall pH during auxin-induced growth activates glycanase enzymes. These may attack some components of the pectic fraction, as well as xyloglucans. Pectin-bound calcium ions may be displaced but this probably has little effect on gel strength. Pectins may be cross-linked by diferulate esters when growth stops. The softening of ripe fruit is due to loss of cohesion in the pectin gel. In apples this results from replacement of the pectins by more esterified forms. In many other fruits it results from depolymerization by polygalacturonases, assisted by pectinesterases, so that the remaining segments are too short for effective calcium binding. Pectins have a further role in the recognition reactions between plant cells and some of their bacterial and fungal pathogens. 相似文献
995.
James S. Clegg 《Cell biochemistry and biophysics》1984,6(3):153-169
Cysts of the crustaceanArtemia are a useful model for studies on intracellular water because they are capable of essentially complete and reversible desiccation.
We have used a variety of techniques on this system, the present work being an attempt to estimate the density of intracellular
water (ρw). The density of individual cysts was evaluated from sedimentation velocity. Heptane displacement methods were used to determine
the volume of a known mass of cysts, from which the density was calculated. The two methods produce comparable results. It
was shown that the densities and water contents of large masses of cysts accurately reflect those of individual cysts. Cyst
densities (ρc) were determined over the entire range of water content from 0 to 0.63 weight fraction of water (W
f), and temperature dependence was measured for 0.61W
f over 2–41°C. The following refer to 25°C. No marked change was detected in ρc until the water content exceeded 0.15W
f, at which ρc decreased as a linear function of Wf to maximum water content. However, the cyst does not behave ideally in the sense that
the densities of the nonaqueous components and added water are not additive as a function ofW
f. The partial specific volume of water in cysts at maximum hydration was estimated to be 3% larger than that of pure water.
These observations are compared with density measurements on other systems, and with previous findings on the physical properties
of water in this system. 相似文献
996.
F. A. Popp W. Nagl K. H. Li W. Scholz O. Weingärtner R. Wolf 《Cell biochemistry and biophysics》1984,6(1):33-52
The phenomenon of ultraweak photon emission from living systems was further investigated in order to elucidate the physical
properties of this radiation and its possible source. We obtained evidence that the light has a high degree of coherence because
of (1) its photon count statistics, (2) its spectral distribution, (3) its decay behavior after exposure to light illumination,
and (4) its transparency through optically thick materials. Moroever, DNA is apparently at least an important source, since
conformational changes induced with ethidium bromide in vivo are clearly reflected by changes of the photon emission of cells.
The physical properties of the radiation are described, taking DNA as an exciplex laser system, where a stable state can be
reached far from thermal equilibrium at threshold. 相似文献
997.
998.
Vsevolod A. Tverdislov Salam El Karadaghi Doris J. Bucher Juri A. Zakomirdin Igor G. Kharitonenkov 《生物化学与生物物理学报:生物膜》1984,778(2):276-280
The dependence of the surface potential difference (ΔU), transversal elasticity module (E1) and membrane conductivity (G0) on the concentrations of the antiviral drugs, rimantadine and amantadine was studied in the planar bilayer lipid membrane system. The method used was based on independent measurements of the second and third harmonics of the membrane capacitance current. The binding constants of bilayer lipid membranes obtained from the drug adsorption isotherms were 2.1 · 105 M?1 and 1.3 · 104 M?1 for rimantadine and amantadine, respectively. The changes in G0 took place only after drug adsorption saturation had been achieved. The influence of rimantadine and amantadine on the interaction of bilayer lipid membranes with matrix protein from influenza virus was also investigated. The presence of 70 μg/ml rimantadine in the bathing solution resulted in an increase in the concentration of M-protein at which the adsorption and conductance changes were observed. The effects of amantadine were similar to those of rimantadine but required a higher critical concentration of amantadine. The results obtained suggest that the antiviral properties of rimantadine and amantadine may be related to the interaction of these drugs with the cell membrane, which can affect virus penetration into the cell as well as maturation of the viral particle at the cell membrane. 相似文献
999.
The rate of electron transfer through Photosystem I (reduced 2,6-dichlorophenol indophenol (DCIPH2 → methylviologen) in a low-salt thylakoid suspension is inhibited by Mg2+ both under light-limited and the light-saturated conditions, the magnitude of inhibition being the same. The 2,6-dichlorophenol indophenol (DCIP) concentration dependence of the light-saturated rate in the presence and in the absence of Mg2+ shows that the overall rate constant of the photoreaction is not altered by Mg2+. With N,N,N′,N′-tetramethyl-p-phenylenediamine or 2,3,5,6-tetramethylphenylenediamine as electron donor only the light-limited rate, not the light-saturated rate, is inhibited by Mg2+ and the magnitude of inhibition is the same as with DCIP as donor. The results are interpreted in terms of heterogeneous Photosystem I, consisting of two types, PS I-A and PS I-B, where PS I-A is involved in cation-regulation of excitation energy distribution and becomes unavailable for DCIPH2 → methyl viologen photoelectron transfer in the presence of Mg2+. 相似文献
1000.
Hans C.P. Matthijs Eva M.E. Ludérus Huub J.M. Löffler Marijke J.C. Scholts Ruud Kraayenhof 《BBA》1984,766(1):29-37
The oxidation of NADPH and NADH was studied in the light and in the dark using sonically derived membrane vesicles and osmotically shocked spheroplasts. These two types of cell-free membrane preparations mostly differ in that the cell and thylakoid membranes are scrambled in the former type and that they are more or less separated in the latter type of preparations. In the light, using both kinds of preparations, each of NADPH and NADH donates electrons via the plastoquinone-cytochrome redox complex (Qbc redox complex) to the thylakoid membrane-bound cytochrome c-553 preoxidized by a light flash and to methylviologen via Photosystem I. NADPH donates electrons to the thylakoid membrane via a weakly rotenone-sensitive dehydrogenase to a site that is situated beyond the 3(3′,4′-dichlorophenyl)-1,1-dimethylurea sensitive site and before plastoquinone. Ferredoxin and easily soluble cytoplasmic proteins are presumably not involved in light-mediated NADPH oxidation. Inhibitors of electron transfer at the Qbc redox complex as the dinitrophenylether of 2-iodo-4-nitrothymol, 2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone and 2-n-heptyl-4-hydroxy-quinone-N-oxide are effective, but antimycin A and KCN are not. The oxidation of NADH showed comparable sensitivity to these inhibitors. However, the oxidation of NADH is antimycin-A-sensitive regardless of the kind of membrane preparation used, indicating that in this case electrons are donated to a different site on the thylakoid membrane. In the dark, NADPH and NADH donate electrons at sites that behave similar to those of light-mediated oxidation, indicating that the initial steps of electron transfer are situated at the thylakoid membranes. However, NADPH oxidation is in some cases not sensitive to inhibitors active at the Qbc redox complex. It is concluded that O2 reduction takes place at two different sites, one partly developed in vitro, situated near the rotenone-sensitive NADPH dehydrogenase, and another, highly KCN-sensitive one, situated beyond the Qbc redox complex and used in vivo. The terminal oxygen-reducing step of NADPH and NADH oxidation in the dark showed a preparation-dependent sensitivity for KCN, more than 80% inhibition in sonically derived membrane vesicles and less than 30% inhibition in osmotically shocked spheroplasts. From this result we tentatively conclude that the highly KCN-sensitive oxidase is not necessarily located at the thylakoid membrane and could be located at the cytoplasmic membrane. 相似文献