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Robarge MJ Bom DC Tumey LN Varga N Gleason E Silver D Song J Murphy SM Ekema G Doucette C Hanniford D Palmer M Pawlowski G Danzig J Loftus M Hunady K Sherf BA Mays RW Stricker-Krongrad A Brunden KR Harrington JJ Bennani YL 《Bioorganic & medicinal chemistry letters》2005,15(6):1749-1753
The chemoattractant receptor-homologous molecule expressed on T(H)2 cells (CRTH-2), also found on eosinophils and basophils, is a prostaglandin D2 receptor involved in the recruitment of these cell types during an inflammatory response. In this report, we describe the synthesis and optimization of a ramatroban isostere that is a selective and potent antagonist of CRTH-2 which may be useful in the treatment of certain diseases. 相似文献
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Haijun Liu Hao Zhang Jeremy D. King Nathan R. Wolf Mindy Prado Michael L. Gross Robert E. Blankenship 《BBA》2014
The orange carotenoid protein (OCP), a member of the family of blue light photoactive proteins, is required for efficient photoprotection in many cyanobacteria. Photoexcitation of the carotenoid in the OCP results in structural changes within the chromophore and the protein to give an active red form of OCP that is required for phycobilisome binding and consequent fluorescence quenching. We characterized the light-dependent structural changes by mass spectrometry-based carboxyl footprinting and found that an α helix in the N-terminal extension of OCP plays a key role in this photoactivation process. Although this helix is located on and associates with the outside of the β-sheet core in the C-terminal domain of OCP in the dark, photoinduced changes in the domain structure disrupt this interaction. We propose that this mechanism couples light-dependent carotenoid conformational changes to global protein conformational dynamics in favor of functional phycobilisome binding, and is an essential part of the OCP photocycle. 相似文献
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Nathan S. Little John J. Riggins Tor P. Schultz Andrew J. Londo Michael D. Ulyshen 《Journal of Insect Behavior》2012,25(2):197-206
Surprisingly little research has been conducted to investigate interactions between subterranean termites and bark beetles.
Facilitative interactions between these organisms could easily alter stand dynamics and impact wood utilization strategies.
A series of American Wood Protection Association Standard E1-09 “choice tests” were carried out to determine the feeding preference
of Reticulitermes flavipes Kollar (Isoptera: Rhinotermitidae) for blue-stained sapwood and sapwood impregnated with various bark beetle pheromones.
Reticulitermes flavipes exhibited a feeding preference for both air-dried and kiln-dried blue-stained sapwood, unstained sapwood treated with frontalin,
and air-dried blue-stained sapwood treated with a 0.02% solution of both frontalin and endo-brevicomin. The implications of these results are far reaching, with particular relevance to forest health, ecology, and utilization. 相似文献
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Shahab SW Matyunina LV Mezencev R Walker LD Bowen NJ Benigno BB McDonald JF 《PloS one》2011,6(7):e22508
MicroRNAs (miRNAs) are short (~22 nucleotides) regulatory RNAs that can modulate gene expression and are aberrantly expressed in many diseases including cancer. Previous studies have shown that miRNAs inhibit the translation and facilitate the degradation of their targeted messenger RNAs (mRNAs) making them attractive candidates for use in cancer therapy. However, the potential clinical utility of miRNAs in cancer therapy rests heavily upon our ability to understand and accurately predict the consequences of fluctuations in levels of miRNAs within the context of complex tumor cells. To evaluate the predictive power of current models, levels of miRNAs and their targeted mRNAs were measured in laser captured micro-dissected (LCM) ovarian cancer epithelial cells (CEPI) and compared with levels present in ovarian surface epithelial cells (OSE). We found that the predicted inverse correlation between changes in levels of miRNAs and levels of their mRNA targets held for only ~11% of predicted target mRNAs. We demonstrate that this low inverse correlation between changes in levels of miRNAs and their target mRNAs in vivo is not merely an artifact of inaccurate miRNA target predictions but the likely consequence of indirect cellular processes that modulate the regulatory effects of miRNAs in vivo. Our findings underscore the complexities of miRNA-mediated regulation in vivo and the necessity of understanding the basis of these complexities in cancer cells before the therapeutic potential of miRNAs can be fully realized. 相似文献
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