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991.
Xiang Wang Yanhui Peng Jeremy W. Singer Anania Fessehaie Stephen L. Krebs Rajeev Arora 《Plant science》2009,177(6):607-617
Leaves of overwintering evergreen rhododendrons are typically exposed to freezing temperatures and high light during winters which can potentially result in photon flux exceeding that required for photochemistry. This excess energy, if not dissipated as heat or fluorescence, may cause photooxidative damage to PSII. The goal of this study is to compare the photoprotection strategies during seasonal cold acclimation (CA) in two Rhododendron species (R. catawbiense Michx. and R. ponticum L.) that are divergent in their leaf freezing tolerance and thermonastic behaviour (temperature-induced leaf movement). R. catawbiense exhibits thermonasty while R. ponticum does not. Differences in leaf freezing tolerance (LT50), photosynthesis, photoinhibition, early light-induced proteins (ELIPs) gene expression, and accumulation of antioxidant metabolites and enzymes during seasonal CA were investigated. During seasonal CA, maximum photosynthetic rate (Pmax) and maximum quantum efficiency of PSII (Fv/Fm) were significantly down-regulated. Compared with R. catawbiense, R. ponticum showed less photoinhibition and higher overall accumulation (in magnitude) of antioxidant systems while R. catawbiense exhibited more efficient up-regulation of ELIP expression and antioxidant system (i.e., greater efficiency of increasing this pool in winter months relative to the summer levels). The two species respond differently to winter conditions and have evolved strategies to avoid, reduce and/or tolerate photooxidative stress in winter. These include down-regulation of photosynthesis and up-regulation of ELIPs and antioxidant systems, together with specialized leaf anatomy and thermonasty behaviour. 相似文献
992.
During pregnancy, VEGF (vascular endothelial growth factor) regulates in part endothelial angiogenesis and vasodilation. In the present study we examine the relative roles of VEGFRs (VEGF receptors) and associated signalling pathways mediating the effects of VEGF(165) on eNOS (endothelial nitric oxide synthase) activation. Despite equal expression levels of VEGFR-1 and VEGFR-2 in UAECs (uterine artery endothelial cells) from NP (non-pregnant) and P (pregnant) sheep, VEGF(165) activates eNOS at a greater level in P- compared with NP-UAEC, independently of Akt activation. The selective VEGFR-1 agonist PlGF (placental growth factor)-1 elicits only a modest activation of eNOS in P-UAECs compared with VEGF(165), whereas the VEGFR-2 kinase inhibitor blocks VEGF(165)-stimulated eNOS activation, suggesting VEGF(165) predominantly activates eNOS via VEGFR-2. Although VEGF(165) also activates ERK (extracellular-signal-regulated kinase)-1/2, this is not necessary for eNOS activation since U0126 blocks ERK-1/2 phosphorylation, but not eNOS activation, and the VEGFR-2 kinase inhibitor inhibits eNOS activation, but not ERK-1/2 phosphorylation. Furthermore, the inability of PlGF to activate ERK-1/2 and the ability of the VEGFR-2 selective agonist VEGF-E to activate ERK-1/2 and eNOS suggests again that both eNOS and ERK-1/2 activation occur predominantly via VEGFR-2. The lack of VEGF(165)-stimulated Akt phosphorylation is consistent with a lack of robust phosphorylation of Ser(1179)-eNOS. Although VEGF(165)-stimulated eNOS phosphorylation is observed at Ser(617) and Ser(635), pregnancy does not significantly alter this response. Our finding that VEGF(165) activation of eNOS is completely inhibited by wortmannin but not LY294002 implies a downstream kinase, possibly a wortmannin-selective PI3K (phosphoinositide 3-kinase), is acting between the VEGFR-2 and eNOS independently of Akt. 相似文献
993.
Genetically-diverse parasite infections are common in nature, however what mechanisms influence parasite load are still under debate. Rauch et al. found consistently lower parasite loads in genetically-mixed infections compared to uniform infections. Using the additive partition of Loreau and Hector they demonstrated that this lower parasite load was due to negative complementarity effects, but they only found weak selection effects. Complementarity effects arise from differentiation among genotypes that accrue equally to all genotypes, while selection effects arise from unexpectedly high performance of certain genotypes in mixed infections. However, selection effects might arise either because genotypes with certain traits perform unexpectedly well in mixed infections at the expense of other genotypes ('dominance effects', DEs), or because genotypes with certain traits perform unexpectedly well, but not at the expense of others genotypes ('trait dependent complementarity effects', TDCEs). Here, we reanalyze the data of Rauch et al. using the tripartite partition of Fox to separate DEs, TDCEs and trait-independent complementarity effects (TICEs, corresponding to the complementarity effect of Loreau and Hector). We found significantly negative TDCEs that contribute strongly to the low parasite loads in mixed infections. We suggest novel, testable hypotheses to explain negative TDCEs. Ours is the first study to demonstrate consistently-strong TDCEs, which are rare in studies of the productivity of plant mixtures. Our results highlight the importance of testing for TDCEs, rather than assuming them to be small. We discuss the interpretation and value of the tripartite partition as an analytical tool complementary to more mechanistic approaches. 相似文献
994.
Crucifers (Brassicaceae, Cruciferae) are a large family comprisingsome 338 genera and c. 3,700 species. The family includes importantcrops as well as several model species in various fields ofplant research. This paper reports new genome size (GS) datafor more than 100 cruciferous species in addition to previouslypublished C-values (the DNA amount in the unreplicated gameticnuclei) to give a data set comprising 185 Brassicaceae taxa,including all but 1 of the 25 tribes currently recognized. Evolutionof GS was analyzed within a phylogenetic framework based ongene trees built from five data sets (matK, chs, adh, trnLF,and ITS). Despite the 16.2-fold variation across the family,most Brassicaceae species are characterized by very small genomeswith a mean 1C-value of 0.63 pg. The ancestral genome size (ancGS)for Brassicaceae was reconstructed as anc1C = 0.50 pg. Approximately50% of crucifer taxa analyzed showed a decrease in GS comparedwith the ancGS. The remaining species showed an increase inGS although this was generally moderate, with significant increasesin C-value found only in the tribes Anchonieae and Physarieae.Using statistical approaches to analyze GS, evolutionary gainsor losses in GS were seen to have accumulated disproportionatelyfaster within longer branches. However, we also found that GShas not changed substantially through time and most likely evolvespassively (i.e., a tempo that cannot be distinguished betweenneutral evolution and weak forms of selection). The data revealan apparent paradox between the narrow range of small GSs overlong evolutionary time periods despite evidence of dynamic genomicprocesses that have the potential to lead to genome obesity(e.g., transposable element amplification and polyploidy). Toresolve this, it is suggested that mechanisms to suppress amplificationand to eliminate amplified DNA must be active in Brassicaceaealthough their control and mode of operation are still poorlyunderstood. 相似文献
995.
The principal bottleneck in protein structure prediction is the refinement of models from lower accuracies to the resolution observed by experiment. We developed a novel constraints‐based refinement method that identifies a high number of accurate input constraints from initial models and rebuilds them using restrained torsion angle dynamics (rTAD). We previously created a Bayesian statistics‐based residue‐specific all‐atom probability discriminatory function (RAPDF) to discriminate native‐like models by measuring the probability of accuracy for atom type distances within a given model. Here, we exploit RAPDF to score (i.e., filter) constraints from initial predictions that may or may not be close to a native‐like state, obtain consensus of top scoring constraints amongst five initial models, and compile sets with no redundant residue pair constraints. We find that this method consistently produces a large and highly accurate set of distance constraints from which to build refinement models. We further optimize the balance between accuracy and coverage of constraints by producing multiple structure sets using different constraint distance cutoffs, and note that the cutoff governs spatially near versus distant effects in model generation. This complete procedure of deriving distance constraints for rTAD simulations improves the quality of initial predictions significantly in all cases evaluated by us. Our procedure represents a significant step in solving the protein structure prediction and refinement problem, by enabling the use of consensus constraints, RAPDF, and rTAD for protein structure modeling and refinement. Proteins 2009. © 2009 Wiley‐Liss, Inc. 相似文献
996.
Greg A. Knock Vladimir A. Snetkov Yasin Shaifta Michelle Connolly Svetlana Drndarski Anthony Noah Ghazaleh E. Pourmahram Silke Becker Philip I. Aaronson Jeremy P.T. Ward 《Free radical biology & medicine》2009,46(5):633-642
Reactive oxygen species play a key role in vascular disease, pulmonary hypertension, and hypoxic pulmonary vasoconstriction. We investigated contractile responses, intracellular Ca2+ ([Ca2+]i), Rho-kinase translocation, and phosphorylation of the regulatory subunit of myosin phosphatase (MYPT-1) and of myosin light chain (MLC20) in response to LY83583, a generator of superoxide anion, in small intrapulmonary arteries (IPA) of rat. LY83583 caused concentration-dependent constrictions in IPA and greatly enhanced submaximal PGF2α-mediated preconstriction. In small femoral or mesenteric arteries of rat, LY83583 alone was without effect, but it relaxed a PGF2α-mediated preconstriction. Constrictions in IPA were inhibited by superoxide dismutase and tempol, but not catalase, and were endothelium and guanylate cyclase independent. Constrictions were also inhibited by the Rho-kinase inhibitor Y27632 and the Src-family kinase inhibitor SU6656. LY83583 did not raise [Ca2+]i, but caused a Y27632-sensitive constriction in α-toxin-permeabilized IPA. LY83583 triggered translocation of Rho-kinase from the nucleus to the cytosol in pulmonary artery smooth muscle cells and enhanced phosphorylation of MYPT-1 at Thr-855 and of MLC20 at Ser-19 in IPA. This enhancement was inhibited by superoxide dismutase and abolished by Y27632. Hydrogen peroxide did not activate Rho-kinase. We conclude that in rat small pulmonary artery, superoxide triggers Rho-kinase-mediated Ca2+ sensitization and vasoconstriction independent of hydrogen peroxide. 相似文献
997.
998.
Peter I. Dosa Sonja Strah-Pleynet Honnappa Jayakumar Martin Casper Marc Decaire Yifeng Xiong Juerg Lehmann Karoline Choi Katie Elwell Amy Wong Robert R. Webb John W. Adams Juan Ramirez Jeremy G. Richman William Thomsen Graeme Semple Bradley R. Teegarden 《Bioorganic & medicinal chemistry letters》2009,19(18):5486-5489
Potent 5-HT2A inverse-agonists containing phenyl-pyrazole ureas with an amino side chain were identified. Optimization of this series resulted in selective compounds that proved effective in modulating 5HT-induced amplification of ADP-stimulated human platelet aggregation. 相似文献
999.
Dan M. Berger Nancy Torres Minu Dutia Dennis Powell Greg Ciszewski Ariamala Gopalsamy Jeremy I. Levin Kyung-Hee Kim Weixin Xu James Wilhelm YongBo Hu Karen Collins Larry Feldberg Steven Kim Eileen Frommer Donald Wojciechowicz Robert Mallon 《Bioorganic & medicinal chemistry letters》2009,19(23):6519-6523
As part of our research effort to discover B-Raf kinase inhibitors, we prepared a series of C-3 substituted N-(3-(pyrazolo[1,5-a]pyrimidin-7-yl)phenyl)-3-(trifluoromethyl)benzamides. X-ray crystallography studies revealed that one of the more potent inhibitors (10n) bound to B-Raf kinase without forming a hinge-binding hydrogen bond. With basic amine residues appended to C-3 aryl residues, cellular activity and solubility were enhanced over previously described compounds of this class. 相似文献
1000.
Philip J. Skinner Peter J. Webb Carleton R Sage Huong T. Dang Cameron C. Pride Ruoping Chen Susan Y. Tamura Jeremy G. Richman Daniel T. Connolly Graeme Semple 《Bioorganic & medicinal chemistry letters》2009,19(15):4207-4209
A series of 5-N,N-disubstituted-5-aminopyrazole-3-carboxylic acids were prepared and found to act as highly potent and selective agonists of the G-Protein Coupled Receptor (GPCR) GPR109b, a low affinity receptor for niacin and some aromatic d-amino acids. Little activity was observed at the highly homologous higher affinity niacin receptor, GPR109a. 相似文献