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51.
Eleven flavonol glycosides and two anthocyanins, only one of which was previously identified, were isolated from the flower petals of okra, Hibiscus esculentus L. On the basis of chromatographic, spectral, and degradative evidence, the following structural assignments were made: quercetin 4′-glucoside, quercetin 7-glucoside, quercetin 5-glucoside, quercetin 3-diglucoside, quercetin 4′-diglucoside, quercetin 3-triglucoside, quercetin 5-rhamnoglucoside, gossypetin 8-glucoside, gossypetin 8-rhamnoglucoside, gossypetin 3-glucosido-8-rhamnoglucoside, cyanidin 4′-glucoside, and cyanidin 3-glucosido-4′ glucoside. Some evidence was obtained of a pentahy-droxy, monomethoxy-flavone glycoside. The total flavonoid content in the red portion of the petal was 0.48% of fresh weight; that in the white portion was 2.51%. The two anthocyanins comprised 28.5% of the flavonoid content of the red flower but only a trace of the content of the white. 相似文献
52.
53.
Summary The plant-infection technique for the estimation of rhizobia, in which small-seeded hosts are grown on agar within test-tubes, is applicable to soils with a moderate rhizobial population (in the order of at least 100/g). Account might have to be taken of skips (less diluted: negative, when more diluted are positive) likely to result, at least in part, from unfavourable conditions for rhizobial survival, multiplication or nodulation. Because of such effects, a sparse population (in the order of (10/g) may not be detected even without dilution (1 g soil per plant tube). Localisation of rhizobia in the soil is likely to be important in determining contact with the plant roots in the dilution count and in sampling from the field. Difficulties with sparsely populated soils can be partly overcome by carefully conducted direct sowings of sterilised seed, preferably in the confines of cores, either left in the field or brought back to the glasshouse. 相似文献
54.
Howard K. Thompson Jr. Robert H. Peter Henry D. McIntosh 《Bulletin of mathematical biology》1966,28(2):167-179
Previously proposed formulae for the quantitative estimation of bidirectional shunts across ventricular septal defects require
determination of the oxygen contents of mixed venous, pulmonary artery, pulmonary venous, and aortic blood. Because these
formulae do not take into account the mixing of oxygenated with unoxygenated blood within the ventricles, their use must result
in underestimation of shunt flows in each direction. A mathematical model for a ventricular defect is examined, in which it
is assumed that mixing of blood occurs in each of six sites in the venae cavae or right atrium, right ventricle, pulmonary
artery, left atrium, left ventricle, and aorta. A total of fourteen streams of blood can flow from one to another of these
mixing sites. As long as complete mixing occurs in the six specified mixing sites, any degree of mixing or non-mixing of the
various streams is permitted. From the equations characterizing the model, formulae are derived in which the shunt flow in
each direction is expressed in terms of the oxygen contents in the six mixing sites and the fractions of blood which enter
the shunt from either side without prior mixing in a ventricular mixing site. The previously reported formulae, which apply
when no ventricular mixing is allowed to occur, lead to theoretical minimum values for the shunt flows in each direction.
At the opposite extreme where all the shunting blood is required to mix in a ventricle before entering the shunt, formulae
for maximum possible shunt flows are also obtained. The absolute values for the left-to-right and right-to-left shunt flows,
which must lie somewhere between the theoretical maximum and minimum values, cannot be computed from blood gas data alone.
This work was supported in part by grant HE-07563 from the National Heart Institute of the National Institutes of Health and
grants-in-aid from the American and North Carolina Heart Associations and the Life Insurance Medical Research Fund.
Work completed during tenure as U.S.P.H.S. post-doctoral fellow. 相似文献
55.
Evidence on the Basis of the Centromere Effect in the Large Autosomes of Drosophila Melanogaster 总被引:1,自引:1,他引:0 下载免费PDF全文
Peter E. Thompson 《Genetics》1964,49(5):761-769
56.
A novel succinyl dipeptide stimulates directed cell migration by modulating protein kinase C activity 总被引:1,自引:0,他引:1
R N Mascardo W Thompson M A Gallo T C Chambers G Eilon 《Journal of cellular physiology》1990,142(2):401-409
In determining the mechanism of the chemokinetic action of the thiol protease inhibitor, E-64, in endothelial cell monolayers subjected to wounding, we synthesized succinyl-leucyl-agmatine (SLA), an analogue of E-64 that lacked the epoxy group and protease inhibitory effect. We observed that this analogue retained its chemokinetic effect on wounded endothelial cells. Its stimulatory action on endothelial cell polarization response to wounding was rapid and associated with directed cell migration. Furthermore, its effect on cellular polarization was blocked by protein kinase C (PKC) inhibitors and mimicked by pharmacologic agents that stimulated PKC activity. To determine if SLA's chemokinetic action was mediated by protein kinase C activation, we compared the effects of SLA and the tumor promoter phorbol myristate acetate (PMA) on the translocation of PKC activity in endothelial cells. We observed that both SLA and PMA induced the translocation of PKC activity from the cytosolic to the particulate fraction of the cells. We also observed that both SLA and PMA induced the phosphorylation of two proteins (Mr 23.4 and 36.5 kDa) in intact 32P-labeled cells. Thus, SLA stimulates the endothelial cell locomotor response to wounding by stimulating PKC activity. 相似文献
57.
Fusion protein-based epitope mapping of phytochrome. Precise identification of an evolutionarily conserved domain 总被引:1,自引:0,他引:1
L K Thompson L H Pratt M M Cordonnier S Kadwell J L Darlix L Crossland 《The Journal of biological chemistry》1989,264(21):12426-12431
Fusion proteins are used to define with precision an evolutionarily conserved domain on the carboxyl-terminal portion of the chromoprotein phytochrome. Simultaneously, assignments of two other epitopes are made with significantly greater precision, while the location of a fourth is confirmed. The epitope-mapping method that is described here is systematic, using complementary, overlapping nested sets of fusion proteins of predefined sequence rather than randomly generated peptides. Moreover, in contrast to previous methods, this approach yields rigorous and unambiguous assignments because it relies solely upon the ability of an antibody to detect a given polypeptide. A cDNA fragment encoding phytochrome amino acids 464-1129, which is its carboxyl terminus, was identified in lambda gt11 and subcloned in frame into the lacZ alpha sequence of pUC18. Four nested sets of subclones in pUC18 were created by digestion with selected restriction endonucleases and with the exonuclease Bal31. Fusion proteins were analyzed by immunoblotting following sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The epitope for monoclonal antibody Oat-13 was confirmed to be between residues 551 and 617, while the epitopes for Oat-8 and Oat-28 were narrowed to 624-686 and 624-747, respectively. The epitope recognized by Pea-25, Pea-2, and Oat-15 was resolved unequivocally to a sequence of only seven residues (residues 765-771): N-Pro-Ile-Phe-Gly-Ala-Asp-Glu-C. 相似文献
58.
Biomphalaria glabrata infected with Schistosoma mansoni and maintained on an artificial diet of Spirulina alga displayed reduced growth during the 5 wk following patency. Food consumption per unit snail weight was unaffected. Infected snails also failed to lay eggs. No difference in percentage of assimilation was observed between control and infected individuals, but infected snails had significantly decreased gross conversion efficiencies. The effects of infection on nutrition of B. glabrata were similar to those observed in nutrient-deprived snails fed diets containing low Spirulina levels. Nutrient deprivation, however, did not alter conversion efficiency. 相似文献
59.
Graham W. Burton Keith U. Ingold Kevin H. Cheeseman Trevor F. Slater 《Free radical research》1990,11(1):99-107
-Tocopherol, a superior chain-breaking, peroxyl radical-trapping antioxidant and the most active component of vitamin E, is elevated in liver tumor cells, contributing to their greater resistance towards lipid peroxidation compared to cells from normal tissues. Also, in regenerating rat liver the level of vitamin E has been found to fluctuate in phase with the rate of cell division. In order to study the biokinetcis and mechanisms of the distribution of vitamin E in organs and within tissues of animals, deuterated forms of -tocopherol have been synthesized and their uptake into blood and tissues has been measured by gas chromatography-mass spectrometry. Measurement of the competitive uptake from a mixture of the RRR-and SRR--tocopherol stereoisomers labelled with different amounts of deuterium shows that the liver exerts a strong preference for secretion of the natural (RRR) stereoisomer into the plasma. It is suggested that a tocopherol-binding protein plays a key role in this process. 相似文献
60.
Aerosolization of recombinant SLPI to augment antineutrophil elastase protection of pulmonary epithelium 总被引:6,自引:0,他引:6
Vogelmeier C.; Buhl R.; Hoyt R. F.; Wilson E.; Fells G. A.; Hubbard R. C.; Schnebli H. P.; Thompson R. C.; Crystal R. G. 《Journal of applied physiology》1990,69(5):1843-1848
In a variety of lung diseases the respiratory epithelial surface must contend with an increased burden of neutrophil elastase (NE). One candidate for augmenting epithelial anti-NE protection is the secretory leukoprotease inhibitor (SLPI). In vitro evaluation demonstrated that 96 +/- 1% of the recombinant SLPI (rSLPI) molecules were capable of inhibiting NE, with an association rate constant of 7.1 +/- 0.1 X 10(6) M-1.s-1. Evaluation of rSLPI after in vitro and in vivo aerosolization showed that aerosolization did not alter rSLPI. Aerosolization of a single dose of 50 mg rSLPI to sheep resulted in a fourfold increase of the anti-NE capacity in epithelial lining fluid (ELF) at 3 h, with a half-life in ELF of 12 h. After aerosolization some rSLPI appeared in lung lymph. Simultaneous aerosolization of rSLPI and recombinant alpha 1-antitrypsin (rAAT) demonstrated a molar ratio of the concentration in lymph to the concentration in ELF 3 h after the aerosol eightfold higher for rAAT than for rSLPI. Overall, these observations demonstrate that it is feasible to use aerosolized rSLPI to directly augment the anti-NE capacity of the lung, particularly on the pulmonary epithelial surface. 相似文献