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711.
[目的]研究温度在考马斯亮蓝法测定蛋白质过程中的影响,为准确测定蛋白质浓度提供建议和指导.[方法]通过考马斯亮蓝法测定在不同温度和孵育时间下对已知不同浓度的牛血清蛋白的影响.[结果]在0 ~ 100 mg/ml蛋白质浓度标准曲线测定范围内,室温20℃孵育20~30 min时测定的蛋白质浓度比较稳定.同时蛋白质浓度越高,考马斯亮蓝法测定蛋白质浓度过程中对各种因素影响的抵御能力越强.[结论]采用考马斯亮蓝法测定蛋白质浓度时,环境温度、待测样品浓度以及染料与蛋白质孵育时间等是决定实验结果准确性的重要因子. 相似文献
712.
Senni K Pereira J Gueniche F Delbarre-Ladrat C Sinquin C Ratiskol J Godeau G Fischer AM Helley D Colliec-Jouault S 《Marine drugs》2011,9(9):1664-1681
The therapeutic potential of natural bioactive compounds such as polysaccharides, especially glycosaminoglycans, is now well documented, and this activity combined with natural biodiversity will allow the development of a new generation of therapeutics. Advances in our understanding of the biosynthesis, structure and function of complex glycans from mammalian origin have shown the crucial role of this class of molecules to modulate disease processes and the importance of a deeper knowledge of structure-activity relationships. Marine environment offers a tremendous biodiversity and original polysaccharides have been discovered presenting a great chemical diversity that is largely species specific. The study of the biological properties of the polysaccharides from marine eukaryotes and marine prokaryotes revealed that the polysaccharides from the marine environment could provide a valid alternative to traditional polysaccharides such as glycosaminoglycans. Marine polysaccharides present a real potential for natural product drug discovery and for the delivery of new marine derived products for therapeutic applications. 相似文献
713.
为了进一步明确大蒜绿变物质的结构及性质,该研究对绿变产物进行分离制备并探索了其相关理化活性。从绿变大蒜中提取出绿变产物,并通过AmberliteCG-50和SephadexLH-20两步纯化制备得到了蓝色素的纯化产品,其色价为76.7。对色素的理化性质进行了研究,结果表明蓝色素在酸性条件pH值7时稳定;对热处理也比较稳定,60℃以下加热处理对色素影响较小;长时间的日光照射会使蓝色素有较大的损失;一些常见的金属离子Cu2+、Zn2+、Al3+、Fe2+的存在对蓝绿色素几乎没有影响,Fe3+的存在会使色素迅速褪色。蓝色素对自由基有清除效果:质量浓度为2 mg/mL的蓝色素提取物对1,1-二苯基-2-三硝基苯肼(DPPH)清除率达到96.4%;在10 mg/mL质量浓度下,蓝色素对超氧和羟基自由基的清除率分别为96.8%和87.6%;色素提取物对自由基的清除效果低于同浓度的抗坏血酸。该研究结果对深入研究绿变色素的性质和结构奠定了初步基础。 相似文献
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716.
为了评价不同切花菊品种花瓣飞燕草素苷合成能力,以3个粉色系切花菊品种为材料,采用飞燕草素前体二氢杨梅素2 mg · mL-1溶液对花瓣进行离体添加培养,建立菊花飞燕草素苷超高效液相UPLC分析技术,并用于菊花花瓣中飞燕草素苷的鉴定。结果表明,菊花花青苷可采用0.1 mol · L-1盐酸甲醇及同体积的10%甲酸水提取,0.22 μm膜过滤。通过洗脱条件的优化可在9 min内实现飞燕草素苷与其他花青苷的分离,当飞燕草素在2.5 ~ 40 mg · L-1范围内时与色谱峰面积具有良好的线性关系,相关系数为0.997。3个粉色系菊花品种均具有催化二氢杨梅素合成飞燕草素的能力,且飞燕草素含量均在220 μg · g-1 FW以上,表明3个品种均可作为蓝色花色转基因候选品种。 相似文献
717.
Identification of wheat blue dwarf phytoplasma effectors targeting plant proliferation and defence responses
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The identification of effectors from pathogenic microbes is one of the most important subjects for elucidating infection mechanisms. Wheat blue dwarf (WBD) phytoplasma causes dwarfism, witches' broom, and yellow leaf tips in wheat plants, resulting in severe yield loss in northwestern China. In this study, 37 candidate effector proteins were transiently expressed in Nicotiana benthamiana. Plants expressing the SAP11‐like protein SWP1 exhibited typical witches' broom. Interestingly, another protein, SWP11, induced both cell death and defence responses, including H2O2 accumulation and callose deposition. Analysis by qRT‐PCR was used to show that a marker gene of the hypersensitive response, HIN1, and three pathogenesis‐related genes, PR1, PR2 and PR3, were significantly up‐regulated in leaves of N. benthamiana expressing SWP11. In addition, SWP12 and SWP21 (TENGU‐like) were shown to suppress SWP11‐, BAX‐, and/or INF1‐induced cell death. These results indicated that SWP21 has a distinct role in virulence compared with TENGU and that WBD phytoplasma possesses effectors that target plant proliferation and defence responses. The ability of these effectors to trigger or suppress plant immunity provides new insights into the phytoplasma–plant interaction. 相似文献
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719.
Ilze Irbe Juris Grinins Ingeborga Andersone Bruno Andersons 《Wood material science & engineering》2018,13(5):296-304
In this study, mould and blue stain susceptibility, capillary water uptake (CWU) and microstructural properties of two thermo-hydro-treated (THT) birch plywood products A and B were investigated. Plywood A represented a THT industrial plywood glued with a phenol formaldehyde (PF) adhesive. Plywood B represented panels from THT veneers glued with a PF film. The THT regimes were (temperature, °C/time, min): 150/10, 150/50, 160/10 and 160/50. Both THT plywood products and untreated samples were resistant to mould and blue stain growth in 1 month of exposure in laboratory and outdoor conditions. A statistically significant correlation between fungal growth in laboratory and outdoor conditions for plywood products A and B was not found (P?>?.05). Artificial weathering of both plywood products provided adverse fungal growth results compared to the natural weathering test outdoors. The fungal growth on plywood A and B samples mutually strongly correlated (P?.05) only in the outdoor test. Plywood B samples demonstrated a much lower CWU than plywood A, obviously because of microstructural changes, including densification, and type of glue used. Lower CWU of THT plywood in comparison with untreated samples did not provide clear evidence on inhibition of fungal growth. 相似文献
720.