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Indexes optimization of outburst forecast while a rock cross-cut coal is uncovered by pulsed water jet 下载免费PDF全文
To obtain the best outburst prediction index of rock cross-cut coal uncovering slotted by pulsed water jet,the effects of the rigidity coefficient’s measured value and the initial velocity of gas diffusion to the integrative indexes D and K are analyzed based on the dynamic evolution of coal crake field under water jet. Thus the integrative indexes D and K are excluded. A grey relation model of outburst prediction indexes(K1,S and P)from 7 coal mine’ rock cross-cut coal uncovering in Chongqing,Sichuan and Henan is set up. And the grey relation degrees of the 3 prediction indexes to outburst hazard are calculated by using grey relational analysis method. The results show that the outburst hazard can be more accurately reflected by the cuttings desorption index K1 when a cross-cut coal uncovering slotted by pulsed water jet,and it should be considered as the best outburst prediction index. 相似文献
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为了研究铁皮石斛最佳的组织培养方法,本试验以铁皮石斛带节茎段作为外植体,探寻铁皮石斛的最佳基本培养基,最优消毒时间,以及不同浓度的NAA和6-BA对腋芽诱导、丛芽增殖、生根壮苗的影响.结果表明:以铁皮石斛带节茎段作外植体时,最佳的基本培养基是1/2MS培养基,在1‰HgCl2中浸泡消毒的最优时间为10 min;诱导腋芽时以1/2MS+10 g·L-1蔗糖+0.6 mg·L-1 NAA+1.5 mg·L-16-BA为最佳培养基;诱导丛芽增殖的最佳培养基为1/2MS+0.6 mg·L-1 NAA+1.5 mg·L-16-BA;诱导生根的最佳培养基为1/2MS+0.5 mg·L-1 IBA+0.9 mg·L-1 NAA. 相似文献
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嵌合O型口蹄疫病毒多表位基因猪细小病毒VLPs载体疫苗的构建 总被引:3,自引:0,他引:3
综合运用生物信息学和分子生物学技术,模拟PPV VP2蛋白表面不同Loop区插入O型FMDV VP1蛋白上多表位基因(VP1:21~40、141~160和200~213残基)空间构象,并在VP2 N端引入通用型辅助性T淋巴细胞表位(PADRE),人工合成嵌合基因并克隆到杆状病毒转移载体pFastBac HTA中,转化E.coli DH10Bac感受态细胞,经三抗筛选,获得重组杆状病毒表达质粒rBac-FMDV VP1∶PPV VP2,用脂质体法转染Sf9细胞。对rBac-FMDVVP1∶PPV VP2感染的Sf9细胞,用间接免疫荧光试验(IFA)检测,具有特异性荧光;用Western-blotting分析,在64 000处出现一条特异蛋白条带;电镜观察,重组VP2蛋白能够自主组装成病毒样颗粒。红细胞凝集试验证实,表达的嵌合蛋白PPV∶VP2-FMDV∶VP1具有与全病毒类似的血凝活性。 相似文献
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从农户的发展能力、经济能力和社交能力3方面选取16个指标,运用组合赋权法确定指标权重,构建农户可持续生计评价指标体系,并基于此评估农业电商扶贫的成效。结合文献与实地调研获取的湖北省252份农户(含贫困户与脱贫户)调查数据,先对农户的可持续生计进行测度,然后运用OLS、2SLS、LIML、IVGMM和IV-Tobit共5种回归方法对农业电商扶贫中影响农户可持续生计的因素进行分析,并采用ISM模型分析论证了各影响因素的关联性质和层次结构。结果显示:样本农户的可持续生计水平一般,发展能力和经济能力相对较高,社交能力相对较弱,但这3种能力均未达到中等水平,有待提高。是否参与农业电商、亲戚中有无村干部、公共服务、政府支持和产业基础在农业电商扶贫中对农户的可持续生计具有显著(P<0.1)影响。是否参与农业电商和亲戚中有无村干部是表层直接影响因素,政府支持和产业基础是中层间接影响因素,公共服务是底层因素。因素之间的逻辑层次结构可用“单驱动、双路径”来概括。 相似文献
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AIM To construct the mouse embryonic stem cell (ESC) line with stable pancreatic and duodenal homeobox 1 (Pdx1 ) expression by Tet-On system, which may lay a foundation for further research on the differentiation of Pdx1+ definitive endoderm cells into pancreatic cells. METHODS The Pdx1 -overexpressing lentiviral vector with green fluorescent protein marker and puromycin resistance was constructed by Tet-On system and was used to infect the mouse ESC. The cells were divided into 3 groups: blank control group (ESC group), empty lentivirus control group (PDX1- ESC group) and Pdx1 lentivirus transfection group (PDX1+ ESC group). Flow cytometry was used to detect the transfected cells after screening by doxycycline (DOX). The function of Tet-On system and the expression of Pdx1 gene were detected. The transfected cells in PDX1- ESC group and PDX1+ ESC group were sorted by flow cytometry, and constructed ESC line with stable expression of Pdx1 and negative control ESC line were verified. RESULTS (1) The positive rates of transfected cells in PDX1- ESC group and PDX1+ ESC group were 90.72% and 94.01% after screening by DOX, respectively. The positive rates of transfected cells in PDX1- ESC group and PDX1+ ESC group was 97.84% and 98.13% after sorting by flow cytometry, respectively. (2) With DOX, green fluorescence was observed in PDX1- ESC group and PDX1+ ESC group. The mRNA and protein expression of Pdx1 was significantly increased in PDX1+ ESC group (P <0.05). Without DOX, no green fluorescence was observed in the cells of the 3 groups, and no significant difference in the mRNA and protein expression of Pdx1 was observed (P >0.05). (3) After 3 months of cryopreservation, the cell lines still survived in resuscitation culture and were regulated by DOX. CONCLUSION Using Tet-On system, the mouse ESC line with inducible Pdx1 expression were successfully established and could be used as an effective cell model to research the differentiation of Pdx1+ definitive endoderm cells into pancreatic cells. 相似文献