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171.
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Eliška Rejmánková 《Folia Geobotanica》1973,8(1):1-13
Seasonal changes in the growth rate of duckweeds—Lemna minor L. andL. gibba L. associated in the communityLemnetum gibbae (W. Koch 1954)Miyawaki etTx. 1960—were investigated at the Podzámecký fishpond at Pr?honice near Praha, during the growing season of 1969. Initial and final dry weight values (W 1 andW 2) of selected samples of the duckweed community were assessed at weekly intervals. The relative growth rate (RGR) was calculated from the dry weight increments, and correlated with water temperature, mean air temperature and sunshine duration. A linear regression equation was fitted to describe the dependence ofRGR on these factors. 相似文献
173.
Genetic Location in Escherichia coli K-12 of the Ultraviolet-Sensitive Mutation uvrD3 总被引:3,自引:1,他引:2 下载免费PDF全文
Eli C. Siegel 《Journal of bacteriology》1970,104(1):604-605
A host cell reactivation-negative mutation, uvrD3, in Escherichia coli K-12 is located between ilv and metE. 相似文献
174.
The paper summarizes the results of the palaeoecological study of one profile of the Bláto mire, situated in southeastern Bohemia (Czechoslovakia). The authors evaluate their finds and endeavour to present a phytocenological picture of the composition and succession of peatforming communities from the Alleröd Period onwards. 相似文献
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Benjamin Y. Klein Hannah Ben-Bassat Eli Breuer Vered Solomon Gershon Golomb 《Journal of cellular biochemistry》1998,68(2):186-194
Bisphosphonates (BPs) are inhibitors of bone resorption and soft tissue calcification. The biological effects of the BPs in calcium-related disorders are attributed mainly to their incorporation in bone, enabling direct interaction with osteoclasts and/or osteoblasts through a variety of biochemical pathways. Structural differences account for the considerable differences in the pharmacological activity of BPs. We compared the effects of two structurally different compounds, alendronate and 2-(3′-dimethylaminopyrazinio)ethylidene-1,1-bisphosphonic acid betaine (VS-6), in an osteoprogenitor differentiation system. The BPs were examined in a bone marrow stromal-cell culture system, which normally results in osteoprogenitor differentiation. The drugs were present in the cultures from days 2 to 11 of osteogenic stimulation, a period estimated as being comparable to the end of proliferation and the matrix-maturation stages. We found that the two different BPs have opposing effects on specific alkaline phosphatase (ALP) activity, on stromal-cell proliferation, and on cell-mediated mineralization. These BPs differentially interact with cell-associated phosphohydrolysis, particularly at a concentration of 10−2 of ALP Km, in which alendronate inhibits whereas VS-6 did not inhibit phosphatase activity. VS-6 treatment resulted in similar and significantly increased mineralization at 10 and 1 μM drug concentrations, respectively. In contrast, mineralization was similar to control, and significantly decreased at 10 and 1 μM drug concentrations, respectively, under alendronate treatment. J. Cell. Biochem. 68:186–194, 1998. © 1998 Wiley-Liss, Inc. 相似文献
178.
Joseph Tillotson Magdalena Kedzior Larissa Guimarães Alison B. Ross Tara L. Peters Andrew J. Ambrose Cody J. Schmidlin Donna D. Zhang Letícia V. Costa-Lotufo Abimael D. Rodríguez Jonathan H. Schatz Eli Chapman 《Bioorganic & medicinal chemistry letters》2017,27(17):4082-4085
Activation of translation initiation is a common trait of cancer cells. Formation of the heterotrimeric eukaryotic initiation factor F (eIF4F) complex is the rate-limiting step in 5′ m7GpppN cap-dependent translation. This trimeric complex includes the eIF4E cap binding protein, the eIF4G scaffolding protein, and the DEAD box RNA helicase eIF4A. eIF4A is an ATP-dependent helicase and because it is the only enzyme in the eIF4F complex, it has been shown to be a potential therapeutic target for a variety of malignancies. To this end, we have used a simple ATPase biochemical screen to survey several hundred marine and terrestrial derived natural products. Herein, we report the discovery of two natural products from marine sources, elisabatin A (1) and allolaurinterol (2), which show low µM inhibition of eIF4A ATPase activity. Enzymological analyses revealed 1 and 2 to be ATP-competitive, and cellular evaluations showed reasonable cytotoxicity against A549 (lung cancer) and MDA-MA-468 (breast cancer) cell lines. However, only compound 2 showed potent inhibition of helicase activity congruent with its ATPase inhibitory activity. 相似文献
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Lenka?Macková Petr?Vít ?uba??uri?ová Pavol?Eliá?Jr Tomá??UrfusEmail author 《Plant Systematics and Evolution》2017,303(4):481-495
Prunus fruticosa is a rare shrub occurring in Eurasian thermophilous forest-steppe alliances. The species frequently hybridizes with cultivated Prunus species in Europe (allochthonous tetraploid P. cerasus and partly indigenous diploid P. avium). Propidium iodide flow cytometry, distance-based morphometrics, elliptic Fourier analysis and embryology were employed to evaluate the extent of hybridization in six Slovak populations. Flow cytometric analyses revealed three ploidy levels: diploid (P. avium), triploid (P. × mohacsyana) and tetraploid (P. fruticosa, P. × eminens and P. cerasus). In addition, P. fruticosa and P. cerasus, at the tetraploid level, were found to differ in absolute genome size. An embryological evaluation suggested the existence of a triploid block in P. × mohacsyana and significant potential for hybridization among tetraploid taxa (indicated also by a continuous distribution of genome size data and further mirrored by morphometrics). Although hybrids significantly differ in ploidy level and embryological characteristics, they are almost indistinguishable using morphological characters. Hybridization with P. cerasus thus turns out to be a significant threat to wild populations of P. fruticosa compared to the relatively weak influence of P. avium. 相似文献