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脂肪型脂肪酸结合蛋白(A-FABP)又称为脂肪酸结合蛋白4(FABP4)或A-FABP,是脂肪酸结合蛋白(FABPs)家族中的一员,能结合多种疏水性化合物,在脂肪和卵巢组织中分布广泛,参与脂肪酸的合成代谢,作用于卵巢组织中,对于禽类产蛋中脂肪酸的沉积会起到关键的作用,调控禽类产蛋过程中蛋的脂肪酸营养沉积,提高产蛋优良性能。该蛋白又与肌间脂肪(IMF)含量有关,保证了肉质的良好品质,这让AFABP在禽类养殖中的研究逐渐成为热点。论文就该蛋白的生理功能和在禽类中的研究进展做一介绍。 相似文献
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对液压油的分类及物理、化学性能及污染物类型做了简单介绍,主要对液压油的正确选择和使用提出了要求。 相似文献
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The aim of this study was to evaluate the combined toxicity of enrofloxacin with each of three antimicrobials (ciprofloxacin,florfenicol and sulfamethazine).MRC-5 cells were used as a cell model to simulate the damage of lung cells caused by mixed contamination of antimicrobials.Multiple concentration gradients and mixing ratios were set.CCK-8 method was used to determine the inhibition rate of cell growth caused by four antimicrobials and the inhibition rate of cell growth caused by enofloxacin mixed with three antimicrobials,respectively.Then Chou-Talalay method was used to fit the median effect plot and to calculate the combination index (CI) value.The results showed that the growth inhibition rates of MCR-5 cells caused by four single drugs went up in a step-like manner with the increase of drug concentration in the tested concentration range,among them,the growth inhibitory rate of MCR-5 cells by florfenicol was low (<4.5%).The combined toxicity of the three binary combinations showed a concentration-dependent and mixing-ratio dependence.Mixing enrofloxacin and ciprofloxacin showed synergistic toxicity (CI<1) on MRC-5 cells at high and middle concentration groups,and antagonistic toxicity (CI>1) at the very-low-concentration groups.Mixing ciprofloxacin and florfenicol mainly showed an inhibited toxicity (CI>1).Binary combination enrofloxacin and sulfamethazine might present either a synergistic joint toxicity (CI<1) or an antagonistic joint toxicity (CI>1) as the concentration and mixing ratio changing.This study showed that it was necessary to assess the combined toxicity of antimicrobials in the toxicity evaluation of antimicrobials.Using Chou-Talalay method,the joint toxicity of multiple antimicrobials could be quickly and efficiently determined at cellular level. 相似文献
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银染mRNA差异显示方法在致突变实验中的初步应用 总被引:2,自引:0,他引:2
为建立在药物致突变研究中应用银染 m RNA差异显示的方法 ,试验提取未经过 /经过环磷酰胺处理的 Balb/c小鼠肝组织的总 RNA ,并以此为模板 ,采用 d T1 2 CG、d T1 2 AG、d T1 2 GG为锚定引物 ,通过反转录、差异显示 PCR反应 ,以 6 %变性聚丙烯酰胺凝胶电泳分离差异条带 ,回收后将其再扩增。结果表明 ,RNA投入量为 3μg、镁离子浓度为 1.5~ 2 .0 mm ol/L、退火温度为 4 0℃时 ,扩增的片段条带清晰、背景低 ,差异条带明显 ,再扩增条带单一。银染 m RNA差异显示技术可成功应用于药物致突变的研究。 相似文献
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AIM: To investigate the immune depressive effect on the reactive T cells and to explore the immunologic injury mechanism of beta cells of islet in type 1 diabetes mellitus (DM-1). METHODS: pAd5/ PD-L1-GPI adenovirus vector with target gene was constructed and transfected into NIT cells which are known as a mouse insuloma cell line. The highly expressed membrane protein of PD-L1-GPI was confirmed by Western blotting. The peripheral blood non-adherence lymph leukocytes and target cells were cultured to detect lymph leukocyte proliferation and the T cell function. The level of IL-2, TNF-α and IFN-γ were detected in the cell culture fluid. RESULTS: Compared with the control group, the NIT cells modified with PD-L1-GPI inhibited the sensitized lymph leukocyte proliferation effectively and down-regulated the level of some cytokine secretions such as IL-2, IFN-γ and TNF-α (P<0.05). CONCLUSION: The islet cells expressed the PD-L1 gene inhibit the reactive responsive T cells, block up the cytotoxic effect of autoimmunity T cells, and induce the immunotolerance, which would be a value direction of the therapy of DM. 相似文献
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