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Résumé Les Auteurs ont démontré que, en conditions histochimiques sur du matériel fixé au formol, les acides phosphotungstique et phosphomolybdique ont une double action: 1. une action oxydative à la charge des radicaux PAS-positifs (vic-glycols et éthyleniques) en milieu aqueux, et à la charge des radicaux aminiques en milieu anhydre; cette action entraine la transformation de ces radicaux en aldéhydes; 2. la formation d'une liaison chimique entre les aldéhydes et les molécules des acides phosphomolybdique et phosphotungstique. — La coloration du collagène, au contraire, n'est pas due ni aux radicaux aminiques ni vic-glycols et implique un mécanisme encore inconnu.
Observations about the specificity of staining of phosphotungstic and phosphomolybdic acid
Summary The authors demonstrated that phosphotungstic and phosphomolybdic acid applied to formol-fixed tissues explete two following actions: 1. An oxidative action on the PAS-positive radicals (double bonds, vic-glycols groups) if in water solution and on aminogroups if in anhydrous solution. This oxidation results in a production of aldehydic radicals 2. The formation of chemical bonds between the aldehydic new-formed groups and the molecules of phosphotungstic or phosphomolybdicacid.— However, the above mentioned mechanism of action is not applicable to the collagen staining for which a different explanation has to be supposed.相似文献
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O. de Bolòs 《Plant Ecology》1970,21(1-3):49-73
Résumé Le climat chaud et humide de la Ligurie méditerranéenne détermine la réapparition de quelques groupements végétaux connus de la Catalogne et rares ou nuls en Languedoc: Inulo-Oryzopsietum miliaceae, Cichorio-Sporoboletum poiretii, Hyparrhenietum hirto-pubescentis, Rubo-Coriarietum.Le caractère particulier de la végétation ligure a été exprimé par des groupements spéciaux: Pistacio-Rhamnetum alaterni, qui remplace le Quercetum cocciferae, groupements à Ostrya carpinifolia et à Brachypodium pinnatum des endroits frais, groupements buissonnants à Erica arborea et Genista germanica, à Rosmarinus et Genista cinerea, Asplenio-Campanuletum macrorhizae des rochers, etc.
Summary The warm and humid climate of the Mediterranean Liguria determines the reappearance of some communities, known in Catalonia, and seldom or not existing in Languedoc: Inulo-Oryzopsietum miliaceae, Cichorio-Sporoboletum poiretii, Hyparrhenietum hirto-pubescentis, Rubo-Coriarietum.The particular character of the Liguric vegetation is expressed in special communities: Pistacio-Rhamnetum alaterni, which replaces the Quercetum cocciferae, communities with Ostrya carpinifolia and with Brachypodium pinnatum in the fresh places, bushy communities with Erica arborea and Genista germanica, with Rosmarinus and Genista cinerea, Asplenio-Campanuletum macrorhizae of the rocks, and so on.
Zusammenfassung Das warme und feuchte Klima der mediterranen Ligurie bestimmt das Wiedererscheinen einiger Pflanzengesellschaften, die in Katalonien bekannt sind, aber selten oder nicht in Languedoc vorkommen: Inulo-Oryzopsietum miliaceae, Cichorio-Sporoboletum poiretii, Hyparrhenietum hirto-pubescentis, Rubo-Coriarietum.Der eigenartige Charakter der ligurischen Vegetation ist in besonderen Pflanzengesellschaften ausgedrückt: Pistacio-Rhamnetum alaterni, das das Quercetum cocciferae ersetzt, Gesellschaften mit Ostrya carpinifolia und mit Brachypodium pinnatum der frischen Standorte, Erica arborea-Genista germanica-Silikatbodengebüsche, Rosmarinus-Genista cinerea-Kalkbodengebüsche, Asplenio-Campanuletum macrorhizae der Felsen usw.相似文献
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Diamine oxidase inactivation by hydrogen peroxide 总被引:3,自引:0,他引:3
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B Mondovì G Rotilio M T Costa A Finazzi-Agrò E Chiancone R E Hansen H Beinert 《The Journal of biological chemistry》1967,242(6):1160-1167
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"Caged calcium" in Aplysia pacemaker neurons. Characterization of calcium-activated potassium and nonspecific cation currents 总被引:2,自引:0,他引:2
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We have studied calcium-activated potassium current, IK(Ca), and calcium-activated nonspecific cation current, INS(Ca), in Aplysia bursting pacemaker neurons, using photolysis of a calcium chelator (nitr-5 or nitr-7) to release "caged calcium" intracellularly. A computer model of nitr photolysis, multiple buffer equilibration, and active calcium extrusion was developed to predict volume-average and front-surface calcium concentration transients. Changes in arsenazo III absorbance were used to measure calcium concentration changes caused by nitr photolysis in microcuvettes. Our model predicted the calcium increments caused by successive flashes, and their dependence on calcium loading, nitr concentration, and light intensity. Flashes also triggered the predicted calcium concentration jumps in neurons filled with nitr-arsenazo III mixtures. In physiological experiments, calcium-activated currents were recorded under voltage clamp in response to flashes of different intensity. Both IK(Ca) and INS(Ca) depended linearly without saturation upon calcium concentration jumps of 0.1-20 microM. Peak membrane currents in neurons exposed to repeated flashes first increased and then declined much like the arsenazo III absorbance changes in vitro, which also indicates a first-order calcium activation. Each flash-evoked current rose rapidly to a peak and decayed to half in 3-12 s. Our model mimicked this behavior when it included diffusion of calcium and nitr perpendicular to the surface of the neuron facing the flashlamp. Na/Ca exchange extruding about 1 pmol of calcium per square centimeter per second per micromolar free calcium appeared to speed the decline of calcium-activated membrane currents. Over a range of different membrane potentials, IK(Ca) and INS(Ca) decayed at similar rates, indicating similar calcium stoichiometries independent of voltage. IK(Ca), but not INS(Ca), relaxes exponentially to a different level when the voltage is suddenly changed. We have estimated voltage-dependent rate constants for a one-step first-order reaction scheme of the activation of IK(Ca) by calcium. After a depolarizing pulse, INS(Ca) decays at a rate that is well predicted by a model of diffusion of calcium away from the inner membrane surface after it has entered the cell, with active extrusion by surface pumps and uptake into organelles. IK(Ca) decays somewhat faster than INS(Ca) after a depolarization, because of its voltage-dependent relaxation combined with the decay of submembrane calcium. The interplay of these two currents accounts for the calcium-dependent outward-inward tail current sequence after a depolarization, and the corresponding afterpotentials after a burst 相似文献