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61.
D. maximum is a dominant species of outer reef flats in the Red Sea, reaching densities of about 22/m2 and biomass of 15.8 g dry tissue/m2 . A few individuals attached to loose rocks are found inside the breaker zone but they may have been dislodged by heavy seas from the outer reef flat. D. maximum feeds from a mucus net which is spread by wave action over the substratum. Hauling the net occurs at approximately 13 minute intervals throughout the 24 hours and lasts about two minutes. Neighbours with overlapping nets stimulate each other to haul and reduce feeding efficiency. The net is grasped by a pair of lateral jaws, tugged free of the substratum by rotation of the body and ingested by a zipper-like action of the lateral and marginal radula teeth. The robust, central and lateral teeth become worn, possibly while channelling out the substratum to accommodate new shell. Defaecation occurs about 2.4 times an hour, amounting to 10450 kcal/m2 /y. Females may brood simultaneously at least 11 egg capsules at various stages of development, which are suspended by stalks from the roof of the shell and pass through a dorsal slit in the mantle. Each capsule contains–500 embryos which develop into larvae with simple, coiled shells 0.33 mm in diameter. There is no planktonic phase. Adult shells amount to 2.5 kg/m2 on the outer reef flat, while dead shells are often occupied by blennies. Although D. maximum is not a specialized filter feeder, the highly developed ciliary mechanisms suggest that filtering may be an auxiliary feeding method. 相似文献
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64.
Barbara E. Hazlett 《CMAJ》1961,85(12):677-681
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67.
Transposon mutagenesis and complementation of the fructokinase gene in Rhizobium leguminosarum biovar trifolii 总被引:2,自引:0,他引:2
Transposon Tn5 was used to generate a fructokinase mutation in Rhizobium leguminosarum biovar trifolii BAL. The section of the genome containing Tn5 was cloned into the EcoRI site of the vector pHC79 and isolated by direct selection on medium containing kanamycin and tetracycline. Total EcoRI digestion was used to obtain a single fragment containing Tn5 and flanking DNA sequences. The flanking DNA was used as a probe to isolate an intact fructokinase gene from a pLAFR1 cosmid clone bank of the parental strain. A cosmid showing homology to the probe was tri-parentally conjugated into the fructokinase-negative strain, complementing the mutation. The complemented mutant exhibited the wild-type phenotype, with an increase in fructokinase production presumably due to multiple copies of the gene. 相似文献
68.
Behavioral economics of drug self-administration. I. Functional equivalence of response requirement and drug dose 总被引:10,自引:0,他引:10
Response requirement and dose of drug per administration are two separate factors that have been demonstrated to control drug self-administration. Recent developments in behavioral economics have shown that these two factors are in fact functionally equivalent for nondrug reinforcers, as indicated by a unit-price analysis. In this review, the unit-price notion was tested for drugs as reinforcers via a re-analysis of ten drug self-administration studies. The results of the re-analysis indicated that response requirement and reinforcer magnitude, the constituents of unit price, have functionally equivalent effects on drug consumption and that a positively decelerating demand curve is produced as unit price increases. This suggests that the behavioral-economic notion of unit price is a more parsimonious explanation of the effects of response requirement and dose in drug self-administration studies, in that it integrates and describes what was previously considered to be two distinct operations. 相似文献
69.
Summary A new culture method was used to study increases in wet and dry weight and soluble protein during normal development of the
transparent lens. Seven different media with more than ten different additives were tested for their effects on cultured lens
transparency.In vivo, rat lenses increased 53% in soluble protein content between 3 and 5.5 days of age. Only HL-1 serum-free medium containing
15 μg/ml insulin plus 1–2 ng/ml BB platelet-derived growth factor (PDGF), or 5–7 ng/ml epidermal growth factor (EGF) allowed
similar growthin vitro, during the same time period. Normal lens grwoth occurred in culture when fresh medium was delivered to lenses as a pulse
every 4–6 hours. Lenses decreased in dry weight and soluble protein content, and became opaque when the same medium was delivered
continuously. Lenses increased only 26% and 32% in soluble protein content when delivered pulses of HL-1 medium containing
BB PDGF or EGF in the absence of insulin. We suggest that pulsatile delivery of medium containing insulin and PDGF or EGF
stimulates lens growth during developmentin vitro. This pulsatile organ culture system is presented as a new approach for studying the effects of growth factors on cell proliferation,
differentiation, and receptor regulation in a developing tissue.
This work was supported by grants from EY-07031 and EY-04542 from the National Eye Institute and a grant from the Oculon Corporation.
Editor's statement This report documents an in vitro system that may mimic lens development and response to growth regulators
and hormones. The system may be useful for application to other organs and provide a foundation for cell and molecular level
analysis. 相似文献
70.
John B. Kerrison Vronique J. Arnould M. Michael Barmada Robert K. Koenekoop Barbara J. Schmeckpeper Irene H. Maumenee 《Genomics》1996,33(3):523
Congenital nystagmus is an idiopathic disorder characterized by bilateral ocular oscillations usually manifest during infancy. Vision is typically decreased due to slippage of images across the fovea. As such, visual acuity correlates with nystagmus intensity, which is the amplitude and frequency of eye movements at a given position of gaze. X-linked, autosomal dominant, and autosomal recessive pedigrees have been described, but no mapping studies have been published. We recently described a large pedigree with autosomal dominant congenital nystagmus. A genome-wide search resulted in six markers on 6p linked by two-point analysis at θ = 0 (D6S459, D6S452, D6S465, FTHP1, D6S257, D6S430). Haplotype analysis localizes the gene for autosomal dominant congenital motor nystagmus to an 18-cM region between D6S271 and D6S455. 相似文献