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111.
Lee Taylor Adrian W. Midgley Bryna Chrismas Angela R. Hilman Leigh A. Madden Rebecca V. Vince Lars R. McNaughton 《Amino acids》2011,40(2):393-401
Heat shock protein 72 (HSP72) performs vital roles within the body at rest and during periods of stress. In vitro, research
demonstrates HSP72 induction in response to hypoxia. Recently, in vivo, an acute hypoxic exposure (75 min at 2,980 m) was
sufficient to induce significant increases in monocyte expressed HSP72 (mHSP72) and a marker of oxidative stress in healthy human subjects. The purpose of the current study was to identify the impact
of 10 consecutive days of hypoxic exposures (75 min at 2,980 m) on mHSP72 and erythropoietin (EPO) expression, markers of oxidative stress, and maximal oxygen consumption in graded incremental aerobic
exercise. Eight male subjects were exposed to daily normobaric hypoxic exposures for 75 min at 2,980 m for 10 consecutive
days, commencing and ceasing at 0930 and 1045, respectively. This stressor was sufficient to induce significant increases
in mHSP72, which was significantly elevated from day 2 of the hypoxic exposures until 48 h post-final exposure. Notably, this increase
had an initial rapid (30% day on day compared to baseline) and final slow phase (16% day on day compared to baseline) of expression.
The authors postulate that 7-day hypoxic exposure in this manner would be sufficient to induce near maximum hypoxia-mediated
basal mHSP72 expression. Elevated levels of mHSP72 are associated with acquired thermotolerance and provide cross tolerance to non-related stressors in vivo, the protocol used
here may provide a useful tool for elevating mHSP72 in vivo. Aside from these major findings, significant transient daily elevations were seen in a marker of oxidative stress,
alongside sustained increases in EPO expression. However, no physiologically significant changes were seen in maximal oxygen
consumption or time to exhaustion. 相似文献
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The enantioselectivity and enantiomeric separation of five racemic piperidine-2,6-dione compounds, on the cellulose tris(3,5-dimethylphenyl carbamate) chiral stationary phase Chiralcel OD-CSP were investigated under the same chromatographic conditions. This class of drugs includes glutethimide, aminoglutethimide, cyclohexylaminoglutethimide, pyridoglutethimide, and phenglutarimide. The results revealed that chiral recognition and the binding sites of these drugs on the Chiralcel OD column are similar, regardless of the absolute configuration of the individual enantiomers. A possible chiral recognition mechanism(s) for this class of drugs and the CSP is presented. © 1994 Wiley-Liss, Inc. 相似文献
115.
Calum X. Cunningham Vince Scoleri Christopher N. Johnson Leon A. Barmuta Menna E. Jones 《Ecography》2019,42(12):2157-2168
Top predators cause avoidance behaviours in competitors and prey, which can lead to niche partitioning and facilitate coexistence. We investigate changes in partitioning of the temporal niche in a mammalian community in response to both the rapid decline in abundance of a top predator and its rapid increase, produced by two concurrent natural experiments: 1) the severe decline of the Tasmanian devil due to a transmissible cancer, and 2) the introduction of Tasmanian devils to an island, with subsequent population increase. We focus on devils, two mesopredators and three prey species, allowing us to examine niche partitioning in the context of intra‐ and inter‐specific competition, and predator–prey interactions. The most consistent shift in temporal activity occurred in devils themselves, which were active earlier in the night at high densities, presumably because of heightened intraspecific competition. When devils were rare, their closest competitor, the spotted‐tailed quoll, increased activity in the early part of the night, resulting in increased overlap with the devil's temporal niche and suggesting release from interference competition. The invasive feral cat, another mesopredator, did not shift its temporal activity in response to either decreasing or increasing devil densities. Shifts in temporal activity of the major prey species of devils were stronger in response to rising than to falling devil densities. We infer that the costs associated with not avoiding predators when their density is rising (i.e. death) are higher than the costs of continuing to adopt avoidance behaviours as predator densities fall (i.e. loss of foraging opportunity), so rising predator densities may trigger more rapid shifts. The rapid changes in devil abundance provide a unique framework to test how the non‐lethal effects of top predators affect community‐wide partitioning of temporal niches, revealing that this top predator has an important but varied influence on the diel activity of other species. 相似文献
116.
Anna M Soltyk C Roger MacKenzie Vince M Wolski Tomoko Hirama Pavel I Kitov David R Bundle James L Brunton 《The Journal of biological chemistry》2002,277(7):5351-5359
Escherichia coli verotoxin, also known as Shiga-like toxin, binds to eukaryotic cell membranes via the glycolipid Gb(3) receptors which present the P(k) trisaccharide Galalpha(1-4)Galbeta(1-4)Glcbeta. Crystallographic studies have identified three P(k) trisaccharide (P(k)-glycoside) binding sites per verotoxin 1B subunit (VT1B) monomer while NMR studies have identified binding of P(k)-glycoside only at site 2. To understand the basis for this difference, we studied binding of wild type VT1B and VT1B mutants, defective at one or more of the three sites, to P(k)-glycoside and pentavalent P(k) trisaccharide (pentaSTARFISH) in solution and Gb(3) presented on liposomal membranes using surface plasmon resonance. Site 2 was the key site in terms of free trisaccharide binding since mutants altered at sites 1 and 3 bound this ligand with wild type affinity. However, effective binding of the pentaSTARFISH molecule also required a functional site 3, suggesting that site 3 promotes pentavalent binding of linked trisaccharides at site 1 and site 2. Optimal binding to membrane-associated Gb(3) involved all three sites. Binding of all single site mutants to liposomal Gb(3) was weaker than wild type VT1B binding. Site 3 mutants behaved as if they had reduced ability to enter into high avidity interactions with Gb(3) in the membrane context. Double mutants at site 1/site 3 and site 2/site 3 were completely inactive in terms of binding to liposomal Gb(3,) even though the site 1/site 3 mutant bound trisaccharide with almost wild type affinity. Thus site 2 alone is not sufficient to confer high avidity binding to membrane-localized Gb(3). Cytotoxic activity paralleled membrane glycolipid binding. Our data show that the interaction of verotoxin with the Gb(3) trisaccharide is highly context dependent and that a membrane environment is required for biologically relevant studies of the interaction. 相似文献
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Richard Langlois C.C. Lee Charles R. Cantor Robert Vince Sidney Pestka 《Journal of molecular biology》1976,106(2):297-313
The distance between the erythromycin binding site on the 50 S Escherichia coli ribosome and protein L7 has been measured by singlet-singlet energy transfer. A non-covalently bound erythromycin derivative, fluoroscein isothiocyanate erythromycylamine, was used as the acceptor. This derivative can be completely displaced from ribosomes by erythromycin, suggesting that they have the same binding site. 1,5-Iodoacetylethylenediamine naptholsulfonate-labeled protein L7 served as the fluorescent donor. It was reconstituted with salt/ethanol-washed 50 S cores. This readdition was accompanied by total recovery of elongation factor G-dependent GTPase activity. This suggests that the protein modification does not significantly perturb 50 S function or structure. Energy transfer measurements by both static and lifetime techniques were in good agreement. After consideration of various errors that enter the measurements and calculations, the L7-erythromycin distance is estimated to be 70 ± 10 Å. This long distance is interesting, since both sites may be involved in translocation.The fluorescent derivative of erythromycin was also used to study binding kinetics to the 50 S and 70 S ribosomes. Binding is a simple second-order step and proceeds about 11 times faster on the 70 S particle. Exchange of the fluorescent derivative with excess erythromycin is limited by the dissociation rate, and this is four times faster on the 70 S particle. These results suggest that the erythromycin site is more accessible on the 70 S particle, and may be an indication of conformational changes in the 50 S ribosome upon combination with the 30 S ribosome. 相似文献
119.
Collection and study of the freshwater red alga, Boldia, from 10 previously unreported habitats disclosed specimens not assignable to either of the two established species. Boldia angustata Deason and Nichols is reduced to synonomy with the earlier described B. erythrosiphon Herndon because of significant overlap between the specific characteristics. Boldia erythrosiphon Herndon emend Howard and Parker is a pleomorphic alga with a more widespread distribution than previously recorded. It is perennial, alternating between an erect saccate frond and prostrate filaments, and both phases are linked by a basal holdfast of pseudoparenchymatous or filamentous construction. Sexual reproduction was not observed; however, asexual reproduction resulted from monospores released by mature fronds, which then germinated to produce basal structures, and through the initiation of erect uniseriate filaments eventually formed new fronds. Absolute growth requirements were not determined; however, similarities in habitats, specifically the abundance of other red algal genera and a predominance of manganese in both snail and rock substrates of Boldia, suggest an interaction of stream temperature, chemistry, substrate, and photoperiod as limiting the distribution of Boldia erythrosiphon. 相似文献
120.