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101.
102.
The possible conformations of sialic acid were analysed using semi-empirical potential functions. The solid state conformation has approx. 0.2 kcal/mol higher energy than the minimum energy conformation. These studies suggest that in solution sialic acid may exist preponderantly in two different conformations which differ in the orientation of the terminal hydroxymethyl group of glycerol side-chain. The present model is consistent with 1H- and 13C-NMR data, but differs from the earlier models. 相似文献
103.
Kinji Endo Yōko Umeyama Junko Nakajima Hiroyasu Kawai 《Bioscience, biotechnology, and biochemistry》2013,77(7):1545-1551
Three kinds of nuclease preparations, each of which having both endonuclease activity that formed 5′-mononucleotides and 3′-nucleotidase activity, were separated and partially purified from Shii-take, Lentinus edodes. Both enzyme activities of each preparation showed a similar thermostability and electrophoretic mobility on Polyacrylamide gel, and a competitive relationship was observed between RNA and 3′-AMP in their enzyme reactions. From these results, it is concluded that both enzyme activities of these three preparations reside in a single protein, respectively. They resemble one another in substrate specificity, cleavage pattern of RNA and thermostability, but are distinguishable from one another by molecular weight, electrophoretic mobility and optimum pH for degradation of RNA. 相似文献
104.
The isolation of the germacradienolide isabelin from Zexmenia valerii is reported. In contrast to isabelin, the closely related lactones deoxymikanolide and scandenolide exist in solution in one conformation only, which is similar to that of dihvdromikanolide in the solid state. The C-3 stereochemistry of scandenolide is revised. 相似文献
105.
Sustainable intensification of crop residue exploitation for bioenergy: Opportunities and challenges
Ioanna Mouratiadou Tommaso Stella Thomas Gaiser Birka Wicke Claas Nendel Frank Ewert Floor van der Hilst 《Global Change Biology Bioenergy》2020,12(1):71-89
Crop residue exploitation for bioenergy can play an important role in climate change mitigation without jeopardizing food security, but it may be constrained by impacts on soil organic carbon (SOC) stocks, and market, logistic and conversion challenges. We explore opportunities to increase bioenergy potentials from residues while reducing environmental impacts, in line with sustainable intensification. Using the case study of North Rhine‐Westphalia in Germany, we employ a spatiotemporally explicit approach combined with stakeholder interviews. First, the interviews identify agronomic and environmental impacts due to the potential reduction in SOC as the most critical challenge associated with enhanced crop residue exploitation. Market and technological challenges and competition with other residue uses are also identified as significant barriers. Second, with the use of agroecosystem modelling and estimations of bioenergy potentials and greenhouse gas emissions till mid‐century, we evaluate the ability of agricultural management to tackle the identified agronomic and environmental challenges. Integrated site‐specific management based on (a) humus balancing, (b) optimized fertilization and (c) winter soil cover performs better than our reference scenario with respect to all investigated variables. At the regional level, we estimate (a) a 5% increase in technical residue potentials and displaced emissions from substituting fossil fuels by bioethanol, (b) an 8% decrease in SOC losses and associated emissions, (c) an 18% decrease in nitrous oxide emissions, (d) a 37% decrease in mineral fertilizer requirements and emissions from their production and (e) a 16% decrease in nitrate leaching. Results are spatially variable and, despite improvements induced by management, limited amounts of crop residues are exploitable for bioenergy in areas prone to SOC decline. In order to sustainably intensify crop residue exploitation for bioenergy and reconcile climate change mitigation with other sustainability objectives, such as those on soil and water quality, residue management needs to be designed in an integrated and site‐specific manner. 相似文献
106.
107.
微生物残体在土壤有机质的形成和稳定过程中发挥着重要作用,但湿地开垦对土壤微生物残体积累特征的影响尚不清楚。本研究以三江平原小叶章湿地为对象,采集原始自然湿地和开垦改种豆科作物后不同耕作年限(5年、10年和25年)的土壤,以氨基糖为微生物残体的标识物,探讨湿地开垦对土壤微生物残体积累特征的影响。结果表明: 自然湿地开垦为农田后显著降低了土壤中氨基糖的含量,且随着开垦年限的增加,氨基糖的损失比例也增加。与自然湿地相比,开垦25年后土壤中的氨基葡萄糖、氨基半乳糖和胞壁酸含量分别下降38.0%、38.1%和35.9%,且在开垦最初5年中细菌来源的胞壁酸下降速率(25.8%)远高于真菌来源的氨基葡萄糖(14.9%),说明短期内湿地开垦对细菌的影响较真菌更加迅速。湿地开垦为农田5、15和25年后,土壤氨基糖总量分别下降21.1%、34.0%和38.0%;同时,氨基糖总量占土壤有机质的比例也受到湿地开垦的显著影响,由自然湿地中的4.8%降至开垦25年后的4.4%。这说明长期湿地开垦加速了土壤有机质中微生物来源有机组分的分解转化,进而改变土壤有机质的组成。这些变化将影响湿地生态系统中土壤有机质的长期稳定和功能演变。 相似文献
108.
Jesús Jiménez-Barbero Juan L. Asensio G. Cuevas A. Canales M. C. Fernández-Alonso F. Javier Cañada 《Biocatalysis and Biotransformation》2013,31(1-2):13-22
This review focuses, in a non-exhaustive manner, on the essential structural and conformational features of protein–carbohydrate interactions and on some applications of NMR spectroscopy to deal with this topic from different levels of complexity. 相似文献
109.
Daniel Baranowski Bozenna Golankiewicz Wojciech Folkman Mariusz Popenda 《Nucleosides, nucleotides & nucleic acids》2013,32(10):707-719
GRAPHICAL ABSTRACT We synthesized a new 2-methyl derivative of wyosine using a multistep procedure starting from guanosine. We examined different synthetic paths and optimized the conditions for each step. Based on MD calculations and analysis of the 3 J HH and J C1′H1′ of the ribose moiety, we discovered that the sugar part adopted conformation specific for the East region rarely occurring in solution. This unusual conformational preference is probably due to steric repulsions between the methyl group at position 2 and the 5′-CH2OH group. We observed that N-glycosidic bond stability weakened 14-fold upon the introduction of the methyl group in position 2 compared with wyosine. 相似文献
110.
Manju Rajeswaran Thamarapu Srikrishnan 《Nucleosides, nucleotides & nucleic acids》2013,32(10-11):1113-1126
The pyrimidine nucleoside, 1-β-D-ribofuranosyl pyridine-2-one-5-carboxamide, is an anti inflammatory agent used in the treatment of adjuvant-induced arthritis. It is the 2-one isomer of 1-β-D-ribofuranosyl pyridine-4-one 5-carboxamide, an unusual nucleoside isolated from the urine of patients with chronic myelogenic leukemia and an important cancer marker. Crystals of 1-β-D-ribofuranosyl pyridine-2-one-5-carboxamide are monoclinic, space group C2, with the cell dimensions a = 31.7920(13), b = 4.6872 (3), c = 16.1838(11), β = 93.071(3)°, V = 2408.2(2) Å3, Dcalc = 1.496 mg/m3 and Z = 8 (two molecules in the asymmetric unit). The structure was obtained by the application of direct methods to diffractometric data and refined to a final R value of 0.050 for 1669 reflections with I ≥ 3σ. The nucleoside exhibits an anti conformation across the glycosidic bond (χCN = ?15.5°, ?18.9°), a C3 ′- endo C2 ′ -exo [3 2T] ribose pucker and g+ across the C(4 ′)-C(5 ′) exocyclic bond. The amino group of the carboxamide group is distal from the 2-one and lacks the intramolecular hydrogen bonding found in the related 2-one molecule. Nuclear magnetic resonance studies shows also an anti conformation across the glycosidic bond but the solution conformation of the furanose ring is not the same as that found in the solid state. 相似文献