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51.
In vitro, 4-amino-6-trichloroethenyl-1,3-benzenedisulfonamide, a potent fasciolicide, causes a potent concentration-dependent inhibition of glucose uptake by mature Fasciola hepatica. In F. hepatica treated with the disulfonamide and then fed [U-14C]glucose, there was a 60% inhibition of glucose utilization and a corresponding inhibition of acetate and propionate formation. Treated fluke parasites possessed much lower levels of adenosine triphosphate, phosphoenolpyruvate, glucose 6-phosphate, and fructose 6-phosphate than untreated parasites and contained higher levels of glycerol and the free sugars fructose and mannose. Direct measurement of the effect of the disulfonamide on the glycolytic enzymes of F. hepatica demonstrated that 3-phosphoglycerate kinase (EC 2.7.2.3) and phosphoglyceromutase (EC 2.7.5.3) were inhibited. It is therefore suggested that the fasciolicidal activity of 4-amino-6-trichloroethenyl-1, 3-benzenedisulfonamide is due to inhibition of the enzymes 3-phosphoglycerate kinase and phosphoglyceromutase which effectively blocks the Embden-Myerhof glycolytic pathway. 相似文献
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It has been shown in an earlier paper that chicks that were housed and trained in pairs demonstrated a greater resistance to extinction of the neonatal approach response than did chicks that were housed and trained in isolation. The purpose of the present study was to attempt to replicate these results and to determine whether housing or training is the more important factor in generating the previous finding. Eighty-three, white Leghorn chicks were tested in an experiment employing a 2 × 2 factorial design comparing social vs isolate housing and social vs isolate imprinting training on resistance to extinction of a socially-reinforced running response. The data were consistent with the earlier findings and also revealed that the housing condition is more important in producing subsequent social searching than is the training condition. 相似文献
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Contribution of crop model structure,parameters and climate projections to uncertainty in climate change impact assessments 总被引:2,自引:0,他引:2
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Fulu Tao Reimund P. Rötter Taru Palosuo Carlos Gregorio Hernández Díaz‐Ambrona M. Inés Mínguez Mikhail A. Semenov Kurt Christian Kersebaum Claas Nendel Xenia Specka Holger Hoffmann Frank Ewert Anaelle Dambreville Pierre Martre Lucía Rodríguez Margarita Ruiz‐Ramos Thomas Gaiser Jukka G. Höhn Tapio Salo Roberto Ferrise Marco Bindi Davide Cammarano Alan H. Schulman 《Global Change Biology》2018,24(3):1291-1307
Climate change impact assessments are plagued with uncertainties from many sources, such as climate projections or the inadequacies in structure and parameters of the impact model. Previous studies tried to account for the uncertainty from one or two of these. Here, we developed a triple‐ensemble probabilistic assessment using seven crop models, multiple sets of model parameters and eight contrasting climate projections together to comprehensively account for uncertainties from these three important sources. We demonstrated the approach in assessing climate change impact on barley growth and yield at Jokioinen, Finland in the Boreal climatic zone and Lleida, Spain in the Mediterranean climatic zone, for the 2050s. We further quantified and compared the contribution of crop model structure, crop model parameters and climate projections to the total variance of ensemble output using Analysis of Variance (ANOVA). Based on the triple‐ensemble probabilistic assessment, the median of simulated yield change was ?4% and +16%, and the probability of decreasing yield was 63% and 31% in the 2050s, at Jokioinen and Lleida, respectively, relative to 1981–2010. The contribution of crop model structure to the total variance of ensemble output was larger than that from downscaled climate projections and model parameters. The relative contribution of crop model parameters and downscaled climate projections to the total variance of ensemble output varied greatly among the seven crop models and between the two sites. The contribution of downscaled climate projections was on average larger than that of crop model parameters. This information on the uncertainty from different sources can be quite useful for model users to decide where to put the most effort when preparing or choosing models or parameters for impact analyses. We concluded that the triple‐ensemble probabilistic approach that accounts for the uncertainties from multiple important sources provide more comprehensive information for quantifying uncertainties in climate change impact assessments as compared to the conventional approaches that are deterministic or only account for the uncertainties from one or two of the uncertainty sources. 相似文献
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R. Kalendar T. Grob M. Regina A. Suoniemi A. Schulman 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》1999,98(5):704-711
The BARE-1 retrotransposon is an active, dispersed, and highly abundant component of the genome of barley (Hordeum vulgare) and other species in its genus. Like all retrotransposons of its kind, BARE-1 is bounded by long terminal repeats (LTRs). We have developed two amplification-based marker methods based on the position
of given LTRs within the genome. The IRAP (Inter-Retrotransposon Amplified Polymorphism) markers are generated by the proximity of two LTRs using outward-facing primers annealing to LTR target sequences.
In REMAP (REtrotransposon-Microsatellite Amplified Polymorphism), amplification between LTRs proximal to simple sequence repeats such as constitute microsatellites produces markers.
The methods can distinguish between barley varieties and produce fingerprint patterns for species across the genus. The patterns
indicate that although the BARE-1 family of retrotransposons is disperse, these elements are locally clustered or nested and often found near tandem arrays
of a simple sequence repeat.
Received: 30 June 1998 / Accepted: 21 August 1998 相似文献
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Retrotransposon BARE-1 and Its Role in Genome Evolution in the Genus Hordeum. 总被引:11,自引:0,他引:11
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CM Vicient A Suoniemi K Anamthawat-Jnsson J Tanskanen A Beharav E Nevo AH Schulman 《The Plant cell》1999,11(9):1769-1784