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1.
Julia Schwarzer Ernst Roelof Swartz Emmanuel Vreven Jos Snoeks Fenton Peter David Cotterill Bernhard Misof Ulrich Kurt Schliewen 《Proceedings. Biological sciences / The Royal Society》2012,279(1746):4389-4398
The megadiverse haplochromine cichlid radiations of the East African lakes, famous examples of explosive speciation and adaptive radiation, are according to recent studies, introgressed by different riverine lineages. This study is based on the first comprehensive mitochondrial and nuclear DNA dataset from extensive sampling of riverine haplochromine cichlids. It includes species from the lower River Congo and Angolan (River Kwanza) drainages. Reconstruction of phylogenetic hypotheses revealed the paradox of clearly discordant phylogenetic signals. Closely related mtDNA haplotypes are distributed thousands of kilometres apart and across major African watersheds, whereas some neighbouring species carry drastically divergent mtDNA haplotypes. At shallow and deep phylogenetic layers, strong signals of hybridization are attributed to the complex Late Miocene/Early Pliocene palaeohistory of African rivers. Hybridization of multiple lineages across changing watersheds shaped each of the major haplochromine radiations in lakes Tanganyika, Victoria, Malawi and the Kalahari Palaeolakes, as well as a miniature species flock in the Congo basin (River Fwa). On the basis of our results, introgression occurred not only on a spatially restricted scale, but massively over almost the whole range of the haplochromine distribution. This provides an alternative view on the origin and exceptional high diversity of this enigmatic vertebrate group. 相似文献
2.
Annette M. Bodenheimer Matthew J. Cuneo Paul D. Swartz Junhong He Hugh M. O'Neill Dean A. A. Myles Barbara R. Evans Flora Meilleur 《Acta Crystallographica. Section F, Structural Biology Communications》2014,70(6):773-776
Cel7A (previously known as cellobiohydrolase I) from Hypocrea jecorina was crystallized in two crystalline forms, neither of which have been previously reported. Both forms co‐crystallize under the same crystallization conditions. The first crystal form belonged to space group C2, with unit‐cell parameters a = 152.5, b = 44.9, c = 57.6 Å, β = 101.2°, and diffracted X‐rays to 1.5 Å resolution. The second crystal form belonged to space group P6322, with unit‐cell parameters a = b≃ 155, c≃ 138 Å, and diffracted X‐rays to 2.5 Å resolution. The crystals were obtained using full‐length Cel7A, which consists of a large 434‐residue N‐terminal catalytic domain capable of cleaving cellulose, a 27‐residue flexible linker and a small 36‐residue C‐terminal carbohydrate‐binding module (CBM). However, a preliminary analysis of the electron‐density maps suggests that the linker and CBM are disordered in both crystal forms. Complete refinement and structure analysis are currently in progress. 相似文献
3.
In vitro endothelial cell organization into capillaries is a long standing challenge of tissue engineering. We recently showed the utility of low level interstitial flow in guiding the organization of endothelial cells through a 3-D fibrin matrix-containing covalently bound vascular endothelial growth factor (VEGF). Here this synergistic phenomenon was extended to explore the effects of matrix composition on in vitro capillary morphogenesis of human blood versus lymphatic endothelial cells (BECs and LECs). Different mixtures of fibrin and collagen were used in conjunction with constant concentrations of matrix-bound VEGF and slow interstitial flow over 10 days. Interestingly, the BECs and LECs each showed a distinct preference in terms of organization for matrix composition: LECs organized the most extensively in a fibrin-only matrix, while BEC organization was optimized in the compliant collagen-containing matrices. Furthermore, the BECs and LECs produced architecturally different structures; while BECs organized in thick, branched networks containing wide lumen, the LECs were elongated into slender, overlapping networks with fine lumen. These data demonstrate the importance of the 3-D matrix composition in facilitating and coordinating BEC and LEC capillary morphogenesis, which is important for in vitro vascularization of engineered tissues. 相似文献
4.
5.
Choe MM Sporn PH Swartz MA 《American journal of physiology. Lung cellular and molecular physiology》2003,285(2):L427-L433
Recent studies have shown that mechanical forces on airway epithelial cells can induce upregulation of genes involved in airway remodeling in diseases such as asthma. However, the relevance of these responses to airway wall remodeling is still unclear since 1). mechanotransduction is highly dependent on environment (e.g., matrix and other cell types) and 2). inflammatory mediators, which strongly affect remodeling, are also present in asthma. To assess the effects of mechanical forces on the airway wall in a relevant three-dimensional inflammatory context, we have established a tissue culture model of the human airway wall that can be induced to undergo matrix remodeling. Our model contains differentiated human bronchial epithelial cells characterized by tight junctions, cilia formation, and mucus secretion atop a collagen gel embedded with human lung fibroblasts. We found that addition of activated eosinophils and the application of 50% strain to the same system increased the epithelial thickness compared with either condition alone, suggesting that mechanical strain affects airway wall remodeling synergistically with inflammation. This integrated model more closely mimics airway wall remodeling than single-cell, conditioned media, or even two-dimensional coculture systems and is relevant for examining the importance of mechanical strain on airway wall remodeling in an inflammatory environment, which may be crucial for understanding and treating pathologies such as asthma. 相似文献
6.
Subcellular location of crab poly(dA-dT) 总被引:1,自引:0,他引:1
7.
Scott?B.?NelsonEmail author Jaime?J.?Coon Courtney?J.?Duchardt Jason?D.?Fischer Samniqueka?J.?Halsey Adam?J.?Kranz Christine?M.?Parker Sarah?C.?Schneider Timothy?M.?Swartz James?R.?Miller 《Biological invasions》2017,19(5):1547-1563
Understanding how invasive plants affect biodiversity is a crucial conservation need. Numerous studies examine impacts of invasions on birds, but trends in these effects have not been synthesized. We reviewed 128 studies from North America to quantify the frequency of positive, negative, and neutral (non-significant) effects of invasive plants on avian ecology, and then evaluated support for proposed mechanisms of impacts. Our frequency-based approach enabled us to draw value from the full breadth of available literature, including articles that do not provide information necessary for meta-analyses and articles examining understudied phenomena. Total avian abundance and prevalence of individual bird species were usually unaffected by invasion, with 48.9 and 57.2% of tests showing neutral results, respectively. Avian richness decreased with invasion in 41.3% of tests. Although birds often preferred nesting in invasive vegetation (45.0% of tests), effects on nest survival were typically neutral (57.9%). Multiple metrics (e.g. body condition, fledgling survival) have received scant attention. Some of the patterns we highlight differ across ecological contexts, emphasizing the need to understand impact mechanisms. Several studies have directly linked invasion impacts to altered nest-site availability, habitat heterogeneity, and food supplies. There is mixed evidence that plant architecture impacts nest-site selection and nest predation. Our review highlights the nonuniform consequences of biological invasions. The high frequency of reported neutral effects suggests that invasions often have minimal impacts on birds, but positive and negative impacts certainly can arise. Managers considering eradicating invasive plants for avian conservation should monitor impacts locally to determine whether eradication will be beneficial. 相似文献
8.
A covalently bound photoisomerizable agonist. Comparison with reversibly bound agonists at electrophorus electroplaques
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HA Lester ME Krouse MM Nass NH Wassermann BF Erlanger 《The Journal of general physiology》1980,75(2):207-232
After disulphide bonds are reduced with dithiothreitol, trans-3- (α-bromomethyl)-3’-[α- (trimethylammonium)methyl]azobenzene (trans-QBr) alkylates a sulfhydryl group on receptors. The membrane conductance induced by this “tethered agonist” shares many properties with that induced by reversible agonists. Equilibrium conductance increases as the membrane potential is made more negative; the voltage sensitivity resembles that seen with 50 [mu]M carbachol. Voltage- jump relaxations follow an exponential time-course; the rate constants are about twice as large as those seen with 50 μM carbachol and have the same voltage and temperature sensitivity. With reversible agonists, the rate of channel opening increases with the frequency of agonist-receptor collisions: with tethered trans-Qbr, this rate depends only on intramolecular events. In comparison to the conductance induced by reversible agonists, the QBr-induced conductance is at least 10-fold less sensitive to competitive blockade by tubocurarine and roughly as sensitive to “open-channel blockade” bu QX-222. Light-flash experiments with tethered QBr resemble those with the reversible photoisomerizable agonist, 3,3’,bis-[α-(trimethylammonium)methyl]azobenzene (Bis-Q): the conductance is increased by cis {arrow} trans photoisomerizations and decreased by trans {arrow} cis photoisomerizations. As with Bis-Q, ligh-flash relaxations have the same rate constant as voltage-jump relaxations. Receptors with tethered trans isomer. By comparing the agonist-induced conductance with the cis/tans ratio, we conclude that each channel’s activation is determined by the configuration of a single tethered QBr molecule. The QBr-induced conductance shows slow decreases (time constant, several hundred milliseconds), which can be partially reversed by flashes. The similarities suggest that the same rate-limiting step governs the opening and closing of channels for both reversible and tethered agonists. Therefore, this step is probably not the initial encounter between agonist and receptor molecules. 相似文献
9.
Cell-free translation systems generally utilize high-energy phosphate compounds to regenerate the adenosine triphosphate (ATP) necessary to drive protein synthesis. This hampers the widespread use and practical implementation of this technology in a batch format due to expensive reagent costs; the accumulation of inhibitory byproducts, such as phosphate; and pH change. To address these problems, a cell-free protein synthesis system has been engineered that is capable of using pyruvate as an energy source to produce high yields of protein. The \"Cytomim\" system, synthesizes chloramphenicol acetyltransferase (CAT) for up to 6 h in a batch reaction to yield 700 microg/mL of protein. By more closely replicating the physiological conditions of the cytoplasm of Escherichia coli, the Cytomim system provides a stable energy supply for protein expression without phosphate accumulation, pH change, exogenous enzyme addition, or the need for expensive high-energy phosphate compounds. 相似文献
10.
Capturing complex 3D tissue physiology in vitro 总被引:1,自引:0,他引:1
The emergence of tissue engineering raises new possibilities for the study of complex physiological and pathophysiological processes in vitro. Many tools are now available to create 3D tissue models in vitro, but the blueprints for what to make have been slower to arrive. We discuss here some of the 'design principles' for recreating the interwoven set of biochemical and mechanical cues in the cellular microenvironment, and the methods for implementing them. We emphasize applications that involve epithelial tissues for which 3D models could explain mechanisms of disease or aid in drug development. 相似文献