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81.
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83.
Cloning and sequencing of IS1086, an Alcaligenes eutrophus insertion element related to IS30 and IS4351. 下载免费PDF全文
Q Dong A Sadouk D van der Lelie S Taghavi A Ferhat J M Nuyten B Borremans M Mergeay A Toussaint 《Journal of bacteriology》1992,174(24):8133-8138
A new insertion sequence (IS), designated IS1086, was isolated from Alcaligenes eutrophus CH34 by being trapped in plasmid pJV240, which contains the Bacillus subtilis sacB and sacR genes. The 1,106-bp IS1086 element contains partially matched (22 of 28 bp) terminal-inverted repeats and a long open reading frame. Hybridization data suggest the presence of one copy of IS1086 in the strain CH34 heavy-metal resistance plasmid pMOL28 and at least two copies in its chromosome. Analysis of the IS1086 nucleotide sequence revealed striking homology with two other IS elements, IS30 and IS4351, suggesting that they are three close members in a family of phylogenetically related insertion sequences. One open reading frame of the Spiroplasma citri phage SpV1-R8A2 B was also found to be related to this IS family but to a lesser extent. Comparison of the G+C contents of IS30 and IS1086 revealed that they conform to their respective hosts (46 versus 50% for IS30 and Escherichia coli and 64.5% for IS1086 and A. eutrophus). The pressure on the AT/GC ratio led to a very different codon usage in these two closely related IS elements. Results suggesting that IS1086 transposition might be activated by some forms of stress are discussed. 相似文献
84.
An axisymmetric deformation of a viscoelastic sphere bounded by a prestressed elastic thin shell in response to external pressure is studied by a finite element method. The research is motivated by the need for understanding the passive behavior of human leukocytes (white blood cells) and interpreting extensive experimental data in terms of the mechanical properties. The cell at rest is modeled as a sphere consisting of a cortical prestressed shell with incompressible Maxwell fluid interior. A large-strain deformation theory is developed based on the proposed model. General non-linear, large strain constitutive relations for the cortical shell are derived by neglecting the bending stiffness. A representation of the constitutive equations in the form of an integral of strain history for the incompressible Maxwell interior is used in the formulation of numerical scheme. A finite element program is developed, in which a sliding boundary condition is imposed on all contact surfaces. The mathematical model developed is applied to evaluate experimental data of pipette tests and observations of blood flow. 相似文献
85.
L A Guarino W Dong B Xu D R Broussard R W Davis D L Jarvis 《Journal of virology》1992,66(12):7113-7120
The PstI K fragment of Autographa californica nuclear polyhedrosis virus (AcMNPV) encodes a protein with a molecular weight of 31,000. To define the role of this protein (pp31) in virus infection further, it was overexpressed in bacteria and used to produce polyclonal antiserum. Radioimmunoprecipitation analysis indicated that pp31 was synthesized during both the early and late phases of virus infection, consistent with previous analyses indicating that the gene was regulated by tandem early and late promoters. Metabolic labeling of cells with carrier-free phosphate indicated that pp31 was phosphorylated. Biochemical fractionation experiments showed that pp31 was localized in the nucleus and that it was more stably associated with the nucleus at later times of infection. Immunoblot analysis of subnuclear fractions indicated that pp31 was associated predominantly with the chromatin and nuclear matrix fractions. Immunofluorescence experiments confirmed that the pp31 protein was localized in the nucleus. Nuclear staining was relatively uniform early but was more centrally nuclear later in infection. Immunoelectron microscopy indicated that the pp31 protein was a component of virogenic stroma. Southwestern (DNA-protein) blot analysis demonstrated that pp31 is a DNA-binding protein. These findings suggest a possible role for pp31 in the virus life cycle. 相似文献
86.
F M Dong L L Wang C M Wang J P Cheng Z Q He Z J Sheng R Q Shen 《Applied and environmental microbiology》1992,58(8):2531-2535
Two genes of the meta pathway of phenol degradation were cloned from a phenol-utilizing strain of Bacillus stearothermophilus and were mapped by subcloning and by use of a Tn5 insertion mutation. They code for phenol hydroxylase and catechol 2,3-dioxygenase, respectively. The gene encoding catechol 2,3-dioxygenase, which is more thermostable than catechol 2,3-dioxygenase encoded by the other gene, shares rather limited homology with that from Pseudomonas putida. 相似文献
87.
The F9 cell is a mouse embryonal teratocarcinoma which can be induced to differentiate into visceral endoderm by treatment with retinoic acid (RA). Treatment with RA in conventional studies was carried out in the constant presence of RA. Here we demonstrate that treatment with RA can be as short as 3 hrs to induce differentiation of F9 cells. Morphology, alpha-fetoprotein gene activity, and temporal patterns of F9 cell differentiation are the same with both short- and long-term treatment with RA. 相似文献
88.
Dong Jae Lee Jin A Lee Dae-Han Chae Hwi-Seo Jang Young-Joon Choi Dalsoo Kim 《Mycobiology》2022,50(5):382
White mold (or Sclerotinia stem rot), caused by Sclerotinia species, is a major air, soil, or seed-transmitted disease affecting numerous crops and wild plants. Microscopic or culture-based methods currently available for their detection and identification are time-consuming, laborious, and often erroneous. Therefore, we developed a multiplex quantitative PCR (qPCR) assay for the discrimination, detection, and quantification of DNA collected from each of the three economically relevant Sclerotinia species, namely, S. sclerotiorum, S. minor, and S. nivalis. TaqMan primer/probe combinations specific for each Sclerotinia species were designed based on the gene sequences encoding aspartyl protease. High specificity and sensitivity of each probe were confirmed for sclerotium and soil samples, as well as pure cultures, using simplex and multiplex qPCRs. This multiplex assay could be helpful in detecting and quantifying specific species of Sclerotinia, and therefore, may be valuable for disease diagnosis, forecasting, and management. 相似文献
89.
草地贪夜蛾幼虫在玉米和小麦上的取食和生长发育特性比较 总被引:1,自引:0,他引:1
【目的】评估草地贪夜蛾Spodoptera frugiperda转移至小麦上为害和暴发的风险。【方法】采用室内饲养观察与调查统计的方法,测定和比较了23℃下草地贪夜蛾在玉米和小麦上的取食和生长发育特性及种群生命表参数。【结果】草地贪夜蛾在小麦上可以完成世代,其3龄后幼虫取食小麦的取食量及体重指标显著地高于同处理后时间在玉米上取食的;而食物利用效率、幼虫存活率、幼虫发育历期、卵孵化率均显著低于取食玉米的。取食玉米和取食小麦的草地贪夜蛾的平均蛹重、产卵前期、单雌产卵量等指标间无显著差异。另外,生命表参数比较结果表明,取食玉米和取食小麦的草地贪夜蛾的平均世代周期(T)、内禀增长率(rm)和周限增长率(λ)间均无显著差异,取食玉米的草地贪夜蛾的净增殖率(R0)为303.55±2.04,显著高于取食小麦的。【结论】草地贪夜蛾取食小麦时,生长发育速度快,能够完成世代生活史,但其食物利用效率、种群繁殖能力等却均低于取食玉米时,说明草地贪夜蛾更适宜在玉米上取食为害,存在转移至小麦为害的风险,但考虑到虫源、自然温度等条件,草地贪夜蛾在小麦上暴发的风险较小。本研... 相似文献
90.
20世纪90年代以来中国生态空间演化的时空格局和梯度效应 总被引:3,自引:0,他引:3
改革开放以来中国经济和城市化的快速发展促使生产和生活空间挤占大量生态空间,系统认识和评估我国生态空间演化的宏观格局和过程对于生态文明建设具有重要的理论和现实意义。为揭示全国生态空间变化的时空过程,在对生态空间内涵进行界定的基础上,结合全国尺度时序土地利用数据构建生态空间分类体系,并评估1990—2015年中国生态空间演化特征。结果表明:1990—2015年中国生态用地面积持续减少,主要向半生态用地转变,发生在重要的粮食生产区域及周边;半生态用地面积波动明显,前期主要表现为不断扩张,后期大量转换为弱生态用地,发生在主要城市群地区;弱生态用地持续扩张,与城镇化进程不断加速相关。中国生态空间演变过程表现出一定的区域差异和梯度效应,不同区域生态空间变化发生的拐点时间有所不同,呈现"自东向西、由南到北"的3级梯度特征,区域生态空间状况与经济发展战略及生态空间管控具有较强的相关性。本研究对于国家生态空间管控近远期战略方案制订具有一定启示,建议处于不同梯度的各地区应基于区域生态空间演化所处阶段和不同驱动机制,确定分区域生态空间安全红线目标和生态空间管控方案。 相似文献