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991.
Joseph R. Coelho Charles W. Holliday Jon M. Hastings Elizabeth Maty Meghan Swigart Angela Mendell 《Journal of thermal biology》2007
(1) Male western cicada killers (Sphecius grandis) had elevated, apparently regulated, thorax temperatures during territorial patrolling. (2) Abdomen temperature increased steeply with increasing ambient temperature, approaching thorax temperature when ambient temperature exceeded 35 °C. (3) Both indirect evidence and heating experiments demonstrated the apparent ability to shunt heat from thorax to abdomen. (4) Dead, dry wasps reached lethal temperatures when placed in full sunlight on the bare ground, and substantially lower temperatures on plants. (5) The percentage of males perching was extremely low, occurring primarily during early morning hours. Most perching occurred on plants, and very little on the ground. (6) In contrast to what has been reported for eastern cicada killers (Sphecius speciosus), S. grandis males did not appear to use sophisticated behaviors to regulate body temperature during territorial defense, relying primarily on physiological mechanisms. (7) This strategy may be more appropriate for S. grandis in the hotter, drier environment of the lowland Chihuahuan desert. 相似文献
992.
Nitroxyl (HNO) has received recent and significant interest due to its novel and potentially important pharmacology. However, the chemical/biochemical mechanism(s) responsible for its biological activity remain to be established. Some of the most important biological targets for HNO are thiols and thiol proteins. Consistent with this, it was recently reported that HNO inhibits the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH), a protein with a catalytically important cysteine thiol at its active site. Interestingly, it was reported that intracellular GAPDH inhibition occurred without significantly altering the cellular thiol redox status of glutathione. Herein, the nature of this reaction specificity was examined. HNO is found to irreversibly inhibit GAPDH in a manner that can be protected against by one of its substrates, glyceraldehyde-3-phosphate (G-3-P). These results are consistent with the idea that HNO has the ability to react with and oxidize a variety of intracellular thiols and the ease or facility of cellular re-reduction of the thiol targets can determine the target specificity. 相似文献
993.
A Wetland Change Model has been developed to identify the vulnerability of coastal wetlands at broad spatial (regional to
global (mean spatial resolution of 85 km)) and temporal scales (modelling period of 100 years). The model provides a dynamic
and integrated assessment of wetland loss, and a means of estimating the transitions between different vegetated wetland types
and open water under a range of scenarios of sea-level rise and changes in accommodation space from human intervention. This
paper is an overview of key issues raised in the process of quantifying broad-scale vulnerabilities of coastal wetlands to
forcing from sea-level rise discussing controlling factors of tidal range, sediment availability and accommodation space,
identification of response lags and defining the threshold for wetland loss and transition. 相似文献
994.
995.
Contribution of the FtsQ transmembrane segment to localization to the cell division site 总被引:1,自引:0,他引:1
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Scheffers DJ Robichon C Haan GJ den Blaauwen T Koningstein G van Bloois E Beckwith J Luirink J 《Journal of bacteriology》2007,189(20):7273-7280
The Escherichia coli cell division protein FtsQ is a central component of the divisome. FtsQ is a bitopic membrane protein with a large C-terminal periplasmic domain. In this work we investigated the role of the transmembrane segment (TMS) that anchors FtsQ in the cytoplasmic membrane. A set of TMS mutants was made and analyzed for the ability to complement an ftsQ mutant. Study of the various steps involved in FtsQ biogenesis revealed that one mutant (L29/32R;V38P) failed to functionally insert into the membrane, whereas another mutant (L29/32R) was correctly assembled and interacted with FtsB and FtsL but failed to localize efficiently to the cell division site. Our results indicate that the FtsQ TMS plays a role in FtsQ localization to the division site. 相似文献
996.
Mechanisms of acrolein-induced myocardial dysfunction: implications for environmental and endogenous aldehyde exposure 总被引:1,自引:0,他引:1
Luo J Hill BG Gu Y Cai J Srivastava S Bhatnagar A Prabhu SD 《American journal of physiology. Heart and circulatory physiology》2007,293(6):H3673-H3684
Aldehydes are ubiquitous pollutants generated during the combustion of organic materials and are present in air, water, and food. Several aldehydes are also endogenous products of lipid peroxidation and by-products of drug metabolism. Despite well-documented high reactivity of unsaturated aldehydes, little is known regarding their cardiovascular effects and their role in cardiac pathology. Accordingly, we examined the myocardial effects of the model unsaturated aldehyde acrolein. In closed-chest mice, intravenous acrolein (0.5 mg/kg) induced rapid but reversible left ventricular dilatation and dysfunction. In mouse myocytes, micromolar acrolein acutely depressed myofilament Ca(2+) responsiveness without altering catecholamine sensitivity, similar to the phenotype of stunned myocardium. Immunoblotting revealed increased acrolein-protein adducts and protein-carbonyls in both acrolein-exposed myocardium (1.8-fold increase, P < 0.002) and myocytes (6.4-fold increase, P < 0.02). Both the contractile dysfunction and adduct formation were markedly attenuated by pretreatment with the thiol donor N-acetylcysteine (5 mM). Two-dimensional gel electrophoresis and mass-assisted laser desorption/ionization time-of-flight mass spectrometry analysis revealed two groups of adducted proteins, sarcomeric/cytoskeletal proteins (cardiac alpha-actin, desmin, myosin light polypeptide 3) and energy metabolism proteins (mitochondrial creatine kinase-2, ATP synthase), indicating site-specific protein modification that was confirmed by immunohistochemical colocalization. We conclude that direct exposure to acrolein induces selective myofilament impairment, which may be, in part, related to the modification of proteins involved in myocardial contraction and energy metabolism. Myocardial dysfunction induced by acrolein and related aldehydes may be symptomatic of toxicological states associated with ambient or occupational exposures or drug toxicity. Moreover, aldehydes such as acrolein may mediate cardiac dysfunction in pathologies characterized by high-oxidative stress. 相似文献
997.
998.
Studying multisite binary and ternary protein interactions by global analysis of isothermal titration calorimetry data in SEDPHAT: application to adaptor protein complexes in cell signaling
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Houtman JC Brown PH Bowden B Yamaguchi H Appella E Samelson LE Schuck P 《Protein science : a publication of the Protein Society》2007,16(1):30-42
Multisite interactions and the formation of ternary or higher-order protein complexes are ubiquitous features of protein interactions. Cooperativity between different ligands is a hallmark for information transfer, and is frequently critical for the biological function. We describe a new computational platform for the global analysis of isothermal titration calorimetry (ITC) data for the study of binary and ternary multisite interactions, implemented as part of the public domain multimethod analysis software SEDPHAT. The global analysis of titrations performed in different orientations was explored, and the potential for unraveling cooperativity parameters in multisite interactions was assessed in theory and experiment. To demonstrate the practical potential and limitations of global analyses of ITC titrations for the study of cooperative multiprotein interactions, we have examined the interactions of three proteins that are critical for signal transduction after T-cell activation, LAT, Grb2, and Sos1. We have shown previously that multivalent interactions between these three molecules promote the assembly of large multiprotein complexes important for T-cell receptor activation. By global analysis of the heats of binding observed in sets of ITC injections in different orientations, which allowed us to follow the formation of binary and ternary complexes, we observed negative and positive cooperativity that may be important to control the pathway of assembly and disassembly of adaptor protein particles. 相似文献
999.
The molecular genetic basis of adaptive variation is of fundamental importance for evolutionary dynamics, but is still poorly known. Only in very few cases has the relationship between genetic variation at the molecular level, phenotype and function been established in natural populations. We examined the functional significance and genetic basis of a polymorphism in production of leaf hairs, trichomes, in the perennial herb Arabidopsis lyrata. Earlier studies suggested that trichome production is subject to divergent selection. Here we show that the production of trichomes is correlated with reduced damage from insect herbivores in natural populations, and using statistical methods developed for medical genetics we document an association between loss of trichome production and mutations in the regulatory gene GLABROUS1. Sequence data suggest that independent mutations in this regulatory gene have provided the basis for parallel evolution of reduced resistance to insect herbivores in different populations of A. lyrata and in the closely related Arabidopsis thaliana. The results show that candidate genes identified in model organisms provide a valuable starting point for analysis of the genetic basis of phenotypic variation in natural populations. 相似文献
1000.
Inhibition of choline transport by redox-active cholinomimetic bis-catechol reagents 总被引:1,自引:0,他引:1
Cai S Mukherjee J Tillekeratne LM Hudson RA Kirchhoff JR 《Bioorganic & medicinal chemistry》2007,15(22):7042-7047
Both N,N'-(2,3-dihydroxybenzyl)-N,N,N',N'-tetramethyl-1,6-hexanediamine dibromide (DTH, 6) and N,N'-(2,3-dihydroxybenzyl)-N,N,N',N'-tetramethyl-1,10-decanediamine dibromide (DTD, 7), which are symmetrical bis-catechol substituted hexamethonium and decamethonium analogues, respectively, were found to inhibit high-affinity choline transport in mouse brain synaptosomes. Inhibitory properties were evaluated using an extraordinarily sensitive capillary electrophoresis method employing electrochemical detection at an enzyme-modified microelectrode. Dose-response curves were generated for each inhibitor and IC(50) values were determined to be 76 microM for 6 and 21 microM for 7. Lineweaver-Burk analysis revealed that both molecules inhibit high-affinity choline uptake by a mixed inhibition mechanism. The K(I) values for 6 and 7 were determined to be 73+/-1 and 31+/-2 microM, respectively. The inhibition properties were further compared to a series of mono-catechol analogues, 3-[(trimethylammonio)methyl]catechol (1), N,N-dimethylepinephrine (4) and 6-hydroxy-N,N-dimethylepinephrine (5), as well as the well-characterized hemicholinium inhibitors, hemicholinium-15 (HC-15, 8) and hemicholinum-3 (HC-3, 9). 相似文献