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121.
Anu Vikman Sakari Sarkkola Harri Koivusalo Tapani Sallantaus Jukka Laine Niko Silvan Hannu Nousiainen Mika Nieminen 《Hydrobiologia》2010,641(1):171-183
We studied the nitrogen retention capacity of six peatland buffer areas constructed in forested catchments in southern and
central Finland. The buffers (0.1–4.9% of the total catchment area) were either undrained mires or drained peatlands rewetted
4–7 years before the present study. The N retention capacity was studied by adding ammonium nitrate (NH4NO3–N) solution into the inflow waters of the buffers once (one area) or twice (five areas) during a period of 4–6 years. Except
for the first N addition in one area, the three largest buffer areas (relative size > 1%) retained the added inorganic N almost
completely; their retention efficiencies during the year of addition were >93% for both NO3–N and NH4–N. Two of the three small buffers (relative size < 0.25%) were also able to reduce inorganic N from the through-flow waters
effectively; their retention capacities for inorganic nitrogen varied between 58 and 89%. However, one small buffer area had
a retention capacity of only <20%. The factors contributing to efficient N retention were hydrological load during N addition,
relative size of the buffer area, and its length, i.e. the distance between the inflow and outflow points. If there was any
release of the added N, it mostly occurred within a relatively short-time period (<100 days) after the treatment. The buffer
areas appeared to be efficient and long-term sinks for inorganic nitrogen because the release of N during the 2–4 years after
N addition was minor. 相似文献
122.
Pim-1 kinase promotes inactivation of the pro-apoptotic Bad protein by phosphorylating it on the Ser112 gatekeeper site 总被引:8,自引:0,他引:8
Constitutive expression of the Pim-1 kinase prolongs survival of cytokine-deprived FDCP1 cells, partly via maintenance of Bcl-2 expression. Here, we show that Pim-1 colocalizes and physically interacts with the pro-apoptotic Bad protein and phosphorylates it in vitro on serine 112, which is a gatekeeper site for its inactivation. Furthermore, wild-type Pim-1, but not a kinase-deficient mutant, enhances phosphorylation of this site in FDCP1 cells and protects cells from the pro-apoptotic effects of Bad. Our results suggest that phosphorylation of Bad by Pim-1 is one of several mechanisms via which the Pim-1 kinase can enhance Bcl-2 activity and promote cell survival. 相似文献
123.
Karvinen J Elomaa A Mäkinen ML Hakala H Mukkala VM Peuralahti J Hurskainen P Hovinen J Hemmilä I 《Analytical biochemistry》2004,325(2):317-325
Caspases are a group of cysteine proteases involved in apoptosis and inflammation. A multiparametric homogeneous assay capable of measuring activity of three different caspases in a single well of a microtiter plate is described. Different fluorescent europium, samarium, terbium, and dysprosium chelates were coupled to a caspase substrate peptide, their luminescence properties, were analyzed, and their function in a time-resolved fluorescence quenching-based caspase 3 assay was studied. Substrates for caspases 1, 2, 3, 6, and 8 and granzyme B were also synthesized and their specificities for different caspases were determined. By selecting suitable lanthanide chelates and substrates we developed a multiparametric homogeneous time-resolved fluorescence quenching-based assay for caspases 1, 3, and 6. The assay was capable of measuring the activity of both single caspases and a mixture of three caspases mixed in the same well. 相似文献
124.
Färnegårdh M Bonn T Sun S Ljunggren J Ahola H Wilhelmsson A Gustafsson JA Carlquist M 《The Journal of biological chemistry》2003,278(40):38821-38828
125.
The ninth and tenth FIII domains (FIII9-10) of human fibronectin act in synergy to promote cell adhesion via the interaction with integrin receptors. Here we describe the functional and structural properties of a set of recombinant FIII9-10 mutants containing various alanine substitutions within the key synergistic site, DRVPHSRN in FIII9, either alone or in combination with another substitution (Leu(1408) to Pro), on the opposite face of FIII9, that increases stability and the functional capacity of FIII9-10. We show that the introduction of mutations into the synergistic sequence of FIII9-10 has a negative effect on the adhesion of baby hamster kidney fibroblasts and results in reduced ability of these ligands to recognize integrin alpha(5)beta(1). Conformational stability of the FIII9 domain in the synergy site mutants is likewise reduced in comparison with native FIII9. The Leu(1408) to Pro substitution in mutant FIII9-10 proteins carrying substitutions in the synergy site results in a substantial recovery of the adhesive activity of the mutants and affinity to alpha(5)beta(1). In keeping with the enhancement of functional activity, the Leu(1408) to Pro substitution in the FIII9-10 synergy site mutants also causes a significant increase in conformational stability of FIII9. These observations imply a strong positive correlation between the biological activity and conformational stability of the assessed FIII9-10 mutants and suggest that a Leu(1408) to Pro substitution restores the biological activity of the mutants via their ability to restore their conformational stability. We conclude that domain stability may be a major determinant of the synergistic potential of FIII9. Our data underscore the value of using more than one approach in such structure-function studies and the requirement for validating the global structural integrity of protein ligands in which sequences that disrupt function have been perturbed. 相似文献
126.
Dinuclear bicyclic complexes, which have two active centers, can significantly promote the hydrolysis of the triphosphate bridge in ApppA, a 5'-cap model compound. 相似文献
127.
Four 12-mer oligodeoxyribonucleotide sequences were immobilized to uniformly sized (50 microm) polymer particles through C5-tethered thymine and N(4)-tethered cytosine bases at four different sites in each sequence. The effect of the site of immobilization on the efficiency and selectivity of hybridization of the particle-bound probes was quantified by a sandwich-type assay based on a time-resolved fluorometric measurement of an oligonucleotide probe labeled with a photoluminescent europium(III) chelate directly from the surface of a single particle. Immobilization through a base in the central part of the sequence was observed to destablize the duplex more markedly than tethering through a terminal base. The effect of a one-base mismatch on the duplex stability increased with the increasing distance from the site of immobilization. 相似文献
128.
Guimarães-Ferreira J Gewalli F David L Maltese G Heino H Lauritzen C 《Plastic and reconstructive surgery》2002,109(4):1325-31; discussion 1332
The aim of the present study was to evaluate the possibility of mobilizing calvarial bone with a fully implantable and bioresorbable device. The animal model used was the New Zealand white rabbit (n = 12). An island bone flap attached to the dura mater was created in the parietal region and amalgam markers were placed in this bone flap and in the ipsilateral frontal bone. In one group of six rabbits (group 1), a specially processed contractile 70L/30D,L polylactic acid plate, 15 x 6 x 0.6 mm, was attached to the island flap by one extremity, and to the fixed ipsilateral frontal bone by the other. In group 2 (control), no plate was added. Bone marker movement was followed with serial radiography. In group 1, there was a progressive reduction in mean marker distance over the first 48 hours, and stability thereafter. In group 2 (control), mean marker distance remained stable until the second postoperative week, after which time there was a slight increase until the end of the experimental period. At 4 weeks, the mean marker separation differed significantly between group 1 (mean, -3.62 mm; SD, 0.79 mm) and group 2 (mean, 0.34 mm; SD, 0.14 mm; p <0.001). In conclusion, a totally implantable and bioresorbable device was successfully used to mobilize calvarial bone. Polymer contractility will likely constitute the basis of a new generation of bioresorbable distractors for use in craniofacial surgery. 相似文献
129.
Kari Seppänen Reino Laatikainen Jukka T. Salonem Marjatta Kantola Simo Lötjönen Mikko Harri Llisa Nüurminen Jari Kaikkomem Kristiima Nyyssönen 《Biological trace element research》1998,65(3):197-210
The mercury-binding capacity of seleno-DL-methionine and selenium dioxide was assessed in male Wistar rats. Mercury was supplied
as fish loaves made of northern pike or rainbow trout. We used a selenium concentration of 3.4 mg/kg fish, about sixfold compared
to the equivalent quantity of mercury. Seleno-DL-methionine had a tendency to increase both methyl mercury and total mercury
in blood, although it also seemed to reduce the proportion of methyl mercury of total mercury. Selenium dioxide lowered mercury
levels by 24–29% both in the blood and in the liver of rats that were fed with northern pike. 相似文献
130.