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991.
992.
口蹄疫病毒P1基因在大肠杆菌中的高效表达及其生物活性的初步分析 总被引:8,自引:0,他引:8
将口蹄疫病毒 (FMDV)结构蛋白基因P1的完整cDNA序列插入原核表达性载体pGEX KG中 ,使P1基因与GST融合 ,获得融合表达质粒pKG P1,转化E .coliBL21 (DE3) ,经IPTG诱导 ,SDS PADE结果表明GST P1融合蛋白获得高效表达 ,Western blot检测证实表达的融合蛋白具有免疫学活性 ,表达产物主要存在于细菌裂解液上清中。进一步采用GST纯化试剂盒纯化P1蛋白并作为诊断抗原 ,建立了P1 ELISA诊断方法 ,与FMD间接血凝 (IHA)检测方法平行检测 86 4份血清样品 ,总的符合率达87%。 相似文献
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One of the largest environmental assessment programs in the United States was initiated in the early 1990s to determine the chemical characteristics of soil located within the planned alignment for the Central Artery (I-93) / Tunnel (I-90) (CA/T) Project in Boston, Massachusetts. The primary purpose of the program was to support management of the handling and disposal of over 17 million cubic yards of soil to be excavated during construction of the CA/T Project. As part of this work, more than 8,000 soil samples were collected from more than 2,600 soil borings and analyzed for a range of chemical contaminants, including volatile organic compounds, acid/base neutral compounds, total petroleum hydrocarbons, polychlorinated biphenyls, and heavy metals. The soils encountered during the investigations exhibited properties influenced by numerous anthropogenic activities. These activities, such as vehicular emissions, historic industrial/manufacturing operations, and waterfront filling with both building rubble and dredge spoils from Boston Harbor, resulted in soils primarily contaminated with petroleum hydrocarbons and metals. As a result of this program, an extensive database of the chemical constituents present in urban soils in downtown Boston was developed. These results were primarily used to delineate the limits of contaminated areas affecting the planned construction. In addition, the database has been used by the Project to support various soil management activities, as well as by the regulatory community in developing guidelines and criteria governing the management of contaminated soils in Massachusetts. This paper focuses on the various applications of this database throughout the course of the Project, and with the additional aim of stimulating potential future applications by both the regulatory and scientific communities. 相似文献
996.
Xiao-Qian Zhao Jian-Fei Hu and Jun Yu * Beijing Institute of Genomics Chinese Academy of Sciences Beijing China Graduate School ofChinese Academy of Sciences Beijing China College of Life Sciences Peking University Beijing China James D.Watson Institute of Genome Sciences Zhejiang University Hangzhou China. 《基因组蛋白质组与生物信息学报(英文版)》2006,4(4):203-211
DNA polymerase III is one of the five eubacterial DNA polymerases that is re-sponsible for the replication of DNA duplex. Among the ten subunits of the DNApolymerase III core enzyme, the alpha subunit catalyzes the reaction for polymer-izing both DNA strands. In this study, we extracted genomic sequences of thealpha subunit from 159 sequenced eubacterial genomes, and carried out sequence-based phylogenetic and structural analyses. We found that all eubacterial genomeshave one or more alpha subunits, which form either homodimers or heterodimers.Phylogenetic and domain structural analyses as well as copy number variations ofthe alpha subunit in each bacterium indicate the classification of alpha subunit intofour basic groups: polC, dnaE1, dnaE2, and dnaE3. This classification is of essencein genome composition analysis. We also consolidated the naming convention toavoid further confusion in gene annotations. 相似文献
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低温对水稻类囊体膜蛋白磷酸化及光合机构光能分配的影响 总被引:8,自引:0,他引:8
研究了低温胁迫对水稻类囊体膜蛋白磷酸化和光能分配的影响。类囊体膜蛋白组分的SDS-PAGE和免疫印迹分析结果显示,低温弱光条件下光系统Ⅱ(PSⅡ)功能蛋白的稳态水平均有所降低。低温(77K)荧光分析表明,低温处理后类囊体膜光能吸收明显下降,而且FPSⅡ/FPSⅠ的比值均较对照组下降,表明低温弱光条件下有更多的激发能被分配到PSⅠ。低温处理同时还改变了类囊体膜蛋白磷酸化水平,捕光天线LHCⅡ蛋白中lhcb1的磷酸化水平明显降低,lhcb2的磷酸化水平增加,进一步证实lhcb2向PSⅠ移动,改变光能分配。PSⅡ反应中心D1、D2蛋白和核心天线CP43的磷酸化水平增高,有利于PSⅡ二聚体的稳定。 相似文献
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