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1.
Katsunori Hatakeyama Shota Yuzawa Kaoru Tonosaki Yoshihito Takahata Satoru Matsumoto 《Breeding Science》2022,72(2):115
Clubroot resistance (CR) is an important trait in Chinese cabbage breeding worldwide. Although Crr1a, the gene responsible for clubroot-resistance, has been cloned and shown to encode the NLR protein, its allelic variation and molecular function remain unknown. Here, we investigated the sequence variation and function of three Crr1a alleles cloned from six CR F1 cultivars of Chinese cabbage. Gain-of-function analysis revealed that Crr1aKinami90_a isolated from the cv. ‘Kinami 90’ conferred clubroot resistance as observed for Crr1aG004. Because two susceptible alleles commonly lacked 172 amino acids in the C-terminal region, we investigated clubroot resistance in transgenic Arabidopsis harboring the chimeric Crr1a, in which 172 amino acids of the functional alleles were fused to the susceptible alleles. The fusion of the C-terminal region to the susceptible alleles restored resistance, indicating that their susceptibility was caused by the lack of the C-terminus. We developed DNA markers to detect the two functional Crr1a alleles, and demonstrated that the functional Crr1a alleles were frequently found in European fodder turnips, whereas they were rarely introduced into Japanese CR cultivars of Chinese cabbage. These results would contribute to CR breeding via marker-assisted selection and help our understanding of the molecular mechanisms underlying clubroot resistance. 相似文献
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为了研究轴伸贯流泵在不同流量工况下的压力脉动特性,应用计算流体动力学软件对泵内流场进行数值计算,揭示不同流量工况下泵内压力脉动的变化规律,并利用真机进行压力脉动测试以验证数值计算方法的可靠性.结果表明:机组各监测面的压力脉动都具有一定的周期性,转轮处波峰和波谷与转轮叶片数相关,压力脉动主频为叶频;前导叶进口截面压力脉动... 相似文献
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通过分析4个完成测序和注释的植物基因组,系统地分离鉴定了97个水稻、玉米、高粱和拟南芥的CCT结构域基因,并对相应蛋白质的结构和基因之间的系统演化关系进行了分析。结果表明:CCT结构域基因的蛋白质结构和特性在不同物种之间具有广泛的变异;不同基因组中CCT结构域基因通过染色体复制扩展了基因家族成员。根据其CCT结构域分为4组,其中1个亚组集中了绝大部分的禾本科CCT结构域基因,该亚组基因可能特异参与了禾本科作物开花时间的调控。基因家族成员的扩展,蛋白质结构的改变以及基因表达模式的变异共同导致了CCT结构域基因家族成员在物种间和物种内的功能分化。 相似文献
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总结了林业应用系统本体构建的基本方法,介绍了本体知识模型的构建思路,以期为本体技术的推广应用提供参考。 相似文献
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In order to analyze the antigenicity of porcine Japanese encephalitis virus (JEV) E protein domain Ⅲ, which was expressed by pET-28a vector with His-tag and purified through Ni-NTA, the BALB/c mice were immunized with the purified protein.We identified the antigenicity of domain Ⅲ of E protein and the anti-mice and anti-porcine JEV E Ⅲ protein specific antibody titers by SDS-PAGE, Western blotting, indirect ELISA and IFA.SDS-PAGE results showed the expressed target protein existed mainly in the form of inclusion body.Western blotting, ELISA test results showed that the protein had good reactivity with anti-serum.The mice immunized with the purified JEV E Ⅲ protein generated 1×105 anti-JEV E Ⅲ protein specific antibody titers by ELISA, and the porcine immunized with the porcine JEV generated 5.1×104 anti-JEV specific antibody titers.The IFA results showed that JEV E Ⅲ protein anti-serum could identify JEV antigen.The above results showed that the recombinant JEV E Ⅲ had good antigenicity.These results provided important basis for development of diagnostic antigen for JEV. 相似文献
7.
Many factors affect the propagation of ultra high frequency(UHF) signals caused by partial discharge(PD) on the waveforms and energy of signals in transformer.To investigate the relationshi Pof factors and UHF signals,simulation model of transformer for PD study are established.UHF signals in simulation model of transformer caused by PD are calculated using finite difference time domain method.By means of amplitude and cumulative energy plot of simulation signals,and combing the measured result,the following factors:distance between PD source and detection position,different metallic conductor position around detection position and iron core and winding are researched,which contribute to comprehend the propagation characteristic of UHF signals and detect UHF signals accurately. 相似文献
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AIM: To investigate the effect of F-box domain on the regulation of MCF-7 cell proliferation by FBXO39 protein. METHODS: The effect of F-box domain on the localization of FBXO39 protein in the MCF-7 cells was investigated. MCF-7 cell cDNA library was used as the template resource. The full-length cDNA sequence of FBXO39 was amplified by PCR method and subcloned into eukaryotic expression vector pEGFP-C2. The pEGFP-FBXO39ΔF (F-box domain deletion mutation) plasmid was successfully constructed with the template resource of pEGFP-FBXO39 plasmid. The recombinant plasmids were transfected into the MCF-7 cells, and then the expression of FBXO39 and FBXO39ΔF were determined by Western blot. The cellular localization of FBXO39 and FBXO39ΔF were observed by confocal microscopy. The localization of endogenous FBXO39 in the MCF-7 cells was detected by immunofluorescence staining. In addition, MTT and EdU assays were used to measure the cell proliferation, flow cytometry was used to measure the cell cycle distribution, and immunohistochemical staining was used to observe the expression of FBXO39 in the breast cancer and para-carcinoma tissues. RESULTS: The eukaryotic expression vector pEGFP-FBXO39 and pEGFP-FBXO39ΔF were constructed successfully. F-box domain had no effect on the cell localization of FBXO39. FBXO39 promoted MCF-7 cell proliferation but FBXO39ΔF did not. FBXO39 was highly expressed in the breast cancer tissues. CONCLUSION: F-box domain had no effect on the cellular localization of FBXO39 protein. However, it plays an important role in the biological function of FBXO39. FBXO39 may be related to breast cancer tumorigenesis. 相似文献