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1.
以湖南安化天尖、茯砖及广西六堡3种黑茶为考察对象,研究黑茶中茶多酚的提取工艺以及抗氧化性能。针对超声波不同提取条件,采用正交试验,确定黑茶中茶多酚的最佳提取工艺条件;采用清除二苯代苦味酰自由基(DPPH)的能力和邻苯三酚自氧化体系来评价其抗氧化活性。结果表明:采用超声波热水复合浸提法提取黑茶中茶多酚的最佳提取条件为超声波提取功率250 W,提取固液比1∶25,提取温度55℃,提取时间45min,茯砖黑茶中茶多酚的提取率5.21%;同时测得茯砖黑茶具有较好的抗氧化能力,对DPPH自由基有较强的清除能力,但与维生素C(VC)相比,其抗氧化能力比VC的能力弱;其清除超氧阴离子自由基能力的IC50为0.507μg/mL。 相似文献
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AIM: To observe the effect of microRNA-19a (miR-19a) on the lipid catabolism of hepatocyte LO2, and to explore the potential mechanism. METHODS: miR-19a was over-expressed or silenced by transfection of miR-19a mimics or miR-19a inhibitor into LO2 cells, then the mRNA level of miR-19a was detected by real-time PCR. The potential target of miR-19a was found by the method of bioinformatics through internet website. The effect of miR-19a on the 3' UTR of peroxisome proliferator-activated receptor α (PPARα) was measured by dual luciferase reporter assay, and the protein level of PPARα and its 2 major downstream rate-limiting enzymes involved in lipid catabolism, acyl-coenzyme a dehydrogenase (ACADM) and carnitine palmitoyltransferase 1A (CPT1A), were detected by Western blotting. Meanwhile, the effect of miR-19a on the generation of ketone body was measured by beta-hydroxybutyric acid (β-OHB) detection assay. RESULTS: The mRNA level of miR-19a was dramatically elevated by the transfection of miR-19a mimics, and sharply decreased by the transfection of miR-19a inhibitor (P<0.05). PPARα was found as a potential target of miR-19a, and dual luciferase reporter assay and Western blotting confirmed the regulatory effect of miR-19a on the expression of PPARα, with the protein level changes of ACADM and CPT1A. miR-19a mimics down-regulated, while miR-19a inhibitor up-regulated the concentration of β-OHB in LO2 cells (P<0.05). CONCLUSION: miR-19a regulates the lipid catabolism of hepatocytes by targeting the PPARα and its 2 downstream rate-limiting enzymes. 相似文献
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变铅青链霉菌的DNA上存在着一种异常的修饰,使其在含有微量Fe~(++)的缓冲液中电泳时,双链DNA遭到降解。DNA的切割是位点特异性的。与已知修饰特征的DNA进行同步试验发现,变铅青链霉菌的这种特异性修饰与目前所发现的修饰系统(如DNA甲基化)均不相同,很可能是一种新的修饰系统。 相似文献
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AIM: To investigate the effects of transforming growth factor β1 (TGF-β1) on murine-derived dendritic cells (DC). METHODS: Murine bone marrow cells were cultured with GM-CSF and TGF-β1 to develop TGF β-DC. Then they were stimulated by lipopolysaccharide (LPS). Their phenotypes were assessed by flow cytometry (FCM). The allogeneic stimulating capacity of DC was measured by mixed lymphocyte reaction (MLR) using BrdU ELISA method. IL-12 p70 protein was detected by ELISA and the expressions of Toll like receptor 4 (TLR4) on DCs were measured by semi-quantitative RT-PCR and FCM. RESULTS: Compared to immature DC (imDC) cultured with GM-CSF alone, the expressions of CD80, CD86, I-Ab and CD40 in TGF β-DC were lower. The TGF β-DC was resistant to maturation by LPS. Maturation resistance was evident from a failure to up-regulate CMs, to stimulate larger T cell proliferation and to increase secretion of IL-12 p70. Down-regulation of TLR4 expression on TGF β-DC was also found. CONCLUSION: TGF-β1 inhibits the expression of co-stimulatory molecules on DC. It is resistant to maturation stimulus (LPS) and might be linked with TLR4 down-regulation. 相似文献
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测定了致病杆菌CB43菌株代谢物对灰葡萄病菌菌丝生长和孢子萌发的影响。结果表明:CB43代谢物对灰葡萄孢菌丝生长有较强的抑制作用,500、250、125ml/L代谢物能完全抑制菌丝的生长,并具有杀死作用。62.5ml/L的发酵液处理灰葡萄病菌菌丝72h的抑制率仍达83.35%。20ml/L的发酵液处理灰葡萄孢菌丝能引起菌丝畸形,异常分支、粗短。CB43代谢物能杀死灰葡萄孢分生孢子或抑制其萌发,500~62.5ml/L的发酵液处理16h后,孢子萌发抑制率达88.1%~97.91%。温室试验表明,CB43代谢物对黄瓜灰霉病的控制效果达84.09%,化学农药40%施佳乐的效果为72.94%。 相似文献
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以速生杨二步超低酸水解方法获得的水解液为原料,在28℃、100 r/min等发酵条件下,选择热带假丝酵母(C.2.637)和酿酒酵母(S.2.699)分别对第一步和第二步水解液进行了发酵制取燃料乙醇的研究,并考查了Ca(OH)2中和、过中和、活性炭吸附等预处理方法及菌种预适应驯化对乙醇转化率的影响。结果表明:热带假丝酵母能够更好地利用第一步水解液生成菌体,适合生产单细胞蛋白;菌种驯化后发酵速度和乙醇转化率均有提高,尤其是以酿酒酵母发酵第二步水解液,乙醇转化率由14.45%增至39.37%;Ca(OH)2过中和的方法处理后的水解液,乙醇转化率有所增加;以五碳糖为主同时含有六碳糖的速生杨第一步水解液,假丝酵母发酵产乙醇的效果好于酿酒酵母。 相似文献