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1.
Deposition of amyloid β (Aβ) fibrils in the brain is a key pathologic hallmark of Alzheimer’s disease. A class of polyphenolic biflavonoids is known to have anti-amyloidogenic effects by inhibiting aggregation of Aβ and promoting disaggregation of Aβ fibrils. In the present study, we further sought to investigate the structural basis of the Aβ disaggregating activity of biflavonoids and their interactions at the atomic level. A thioflavin T (ThT) fluorescence assay revealed that amentoflavone-type biflavonoids promote disaggregation of Aβ fibrils with varying potency due to specific structural differences. The computational analysis herein provides the first atomistic details for the mechanism of Aβ disaggregation by biflavonoids. Molecular docking analysis showed that biflavonoids preferentially bind to the aromatic-rich, partially ordered N-termini of Aβ fibril via the π–π interactions. Moreover, docking scores correlate well with the ThT EC50 values. Molecular dynamic simulations revealed that biflavonoids decrease the content of β-sheet in Aβ fibril in a structure-dependent manner. Hydrogen bond analysis further supported that the substitution of hydroxyl groups capable of hydrogen bond formation at two positions on the biflavonoid scaffold leads to significantly disaggregation of Aβ fibrils. Taken together, our data indicate that biflavonoids promote disaggregation of Aβ fibrils due to their ability to disrupt the fibril structure, suggesting biflavonoids as a lead class of compounds to develop a therapeutic agent for Alzheimer’s disease.  相似文献   
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考虑可再生能源出力、电力负荷和电价等一系列不确定性因素,提出了高比例可再生能源渗透下的多虚拟电厂日内两阶段优化调度模型。该模型通过对多虚拟电厂中运行设备小时级时间尺度和分钟级时间尺度的协调优化,达到分级消除系统中随机和扰动因素的影响,实现高比例可再生能源的安全消纳。并且在多虚拟电厂优化调度模型中,借助Markowitz均值-方差理论,提出利润函数的风险刻画,准确描述不确定性的影响。最后,通过算例分析,说明所提出模型可有效降低决策风险和不确定性因素的影响。  相似文献   
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虚拟直流发电机(VDCG)功率协调控制策略将直流电机算法嵌入到DC/DC变换器控制回路中,使其模拟直流发电机运行特性,提升直流微网直流母线电压的动态稳定性。该控制通过功率分配环实现不同容量储能装置间的功率协调分配,但已有的VDCG功率协调控制策略均采用固定励磁磁通作为虚拟电机励磁系数,当再生能源输出功率发生波动或负载发生投切时,直流母线电压会产生稳态电压偏移。为消除母线电压偏移,在详细分析VDCG功率协调控制工作机理的基础上,提出虚拟直流发电机励磁补偿控制策略,通过实时补偿VDCG励磁,消除母线电压偏移,稳定直流母线电压。构建储能装置双机并联光储直流微网仿真及实验平台,分别在再生能源功率波动和负载投切情况下对传统固定励磁磁通功率协调VDCG控制及所提VDCG励磁补偿控制策略进行对比仿真及实验验证,证明所提控制策略的正确性。  相似文献   
5.
Heparanase (Hpse) is an endo-β-D-glucuronidase capable of cleaving heparan sulfate side chains. Its upregulated expression is implicated in tumor growth, metastasis and angiogenesis, thus making it an attractive target in cancer therapeutics. Currently, a few small molecule inhibitors have been reported to inhibit Hpse, with promising oral administration and pharmacokinetic (PK) properties. In the present study, a ligand-based pharmacophore model was generated from a dataset of well-known active small molecule Hpse inhibitors which were observed to display favorable PK properties. The compounds from the InterBioScreen database of natural (69,034) and synthetic (195,469) molecules were first filtered for their drug-likeness and the pharmacophore model was used to screen the drug-like database. The compounds acquired from screening were subjected to molecular docking with Heparanase, where two molecules used in pharmacophore generation were used as reference. From the docking analysis, 33 compounds displayed higher docking scores than the reference and favorable interactions with the catalytic residues. Complex interactions were further evaluated by molecular dynamics simulations to assess their stability over a period of 50 ns. Furthermore, the binding free energies of the 33 compounds revealed 2 natural and 2 synthetic compounds, with better binding affinities than reference molecules, and were, therefore, deemed as hits. The hit compounds presented from this in silico investigation could act as potent Heparanase inhibitors and further serve as lead scaffolds to develop compounds targeting Heparanase upregulation in cancer.  相似文献   
6.
The Gli-B1-encoded γ-gliadins and non-coding γ-gliadin DNA sequences for 15 different alleles of common wheat have been compared using seven tests: electrophoretic mobility (EM) and molecular weight (MW) of the encoded major γ-gliadin, restriction fragment length polymorphism patterns (RFLPs) (three different markers), Gli-B1-γ-gliadin-pseudogene known SNP markers (Single nucleotide polymorphisms) and sequencing the pseudogene GAG56B. It was discovered that encoded γ-gliadins, with contrasting EM, had similar MWs. However, seven allelic variants (designated from I to VII) differed among them in the other six tests: I (alleles Gli-B1i, k, m, o), II (Gli-B1n, q, s), III (Gli-B1b), IV (Gli-B1e, f, g), V (Gli-B1h), VI (Gli-B1d) and VII (Gli-B1a). Allele Gli-B1c (variant VIII) was identical to the alleles from group IV in four of the tests. Some tests might show a fine difference between alleles belonging to the same variant. Our results attest in favor of the independent origin of at least seven variants at the Gli-B1 locus that might originate from deeply diverged genotypes of the donor(s) of the B genome in hexaploid wheat and therefore might be called “heteroallelic”. The donor’s particularities at the Gli-B1 locus might be conserved since that time and decisively contribute to the current high genetic diversity of common wheat.  相似文献   
7.
In this study, we investigate the immunomodulatory effects of a novel antimicrobial peptide, YD1, isolated from Kimchi, in both in vitro and in vivo models. We establish that YD1 exerts its anti-inflammatory effects via up-regulation of the Nrf2 pathway, resulting in the production of HO-1, which suppresses activation of the NF-κB pathway, including the subsequent proinflammatory cytokines IL-1β, IL-6, and TNF-α. We also found that YD1 robustly suppresses nitric oxide (NO) and prostaglandin E2 (PGE2) production by down-regulating the expression of the upstream genes, iNOS and COX-2, acting as a strong antioxidant. Collectively, YD1 exhibits vigorous anti-inflammatory and antioxidant activity, presenting it as an interesting potential therapeutic agent.  相似文献   
8.
Owing to the prohibition of cosmetic animal testing, various attempts have recently been made using skin-on-a-chip (SOC) technology as a replacement for animal testing. Previously, we reported the development of a pumpless SOC capable of drug testing with a simple drive using the principle that the medium flows along the channel by gravity when the chip is tilted using a microfluidic channel. In this study, using pumpless SOC, instead of drug testing at the single-cell level, we evaluated the efficacy of α-lipoic acid (ALA), which is known as an anti-aging substance in skin equivalents, for skin tissue and epidermal structure formation. The expression of proteins and changes in genotyping were compared and evaluated. Hematoxylin and eosin staining for histological analysis showed a difference in the activity of fibroblasts in the dermis layer with respect to the presence or absence of ALA. We observed that the epidermis layer became increasingly prominent as the culture period was extended by treatment with 10 μM ALA. The expression of epidermal structural proteins of filaggrin, involucrin, keratin 10, and collagen IV increased because of the effect of ALA. Changes in the epidermis layer were noticeable after the ALA treatment. As a result of aging, damage to the skin-barrier function and structural integrity is reduced, indicating that ALA has an anti-aging effect. We performed a gene analysis of filaggrin, involucrin, keratin 10, integrin, and collagen I genes in ALA-treated human skin equivalents, which indicated an increase in filaggrin gene expression after ALA treatment. These results indicate that pumpless SOC can be used as an in vitro skin model similar to human skin, protein and gene expression can be analyzed, and it can be used for functional drug tests of cosmetic materials in the future. This technology is expected to contribute to the development of skin disease models.  相似文献   
9.
王海宁  池卓哲 《包装工程》2021,42(12):84-90, 97
目的 为了更科学地研究和检验可穿戴产品的适合性,提出一种适合性检验方法,能够精确保留现实环境中的产品佩戴关系,并能将现实与虚拟的适合性检验研究相结合,得到合理的适合性检验结果.方法 以虚拟现实眼镜的适合性检验为例,通过高精度的三维测量技术将现实环境中的人、产品以及人—产品佩戴关系转化为三维虚拟信息,并以人—产品佩戴三维模型为参考基准对齐人和产品的虚拟模型,得到保留现实佩戴关系的人—产品佩戴模型组,再应用偏差分析法得出人—机佩戴区域的可视化适合性结果和统计数据,结合主观评价方法进一步分析产品的适合性.结论 虚实结合的产品适合性检验方法可在虚拟环境中高精度地保留现实环境中的人—产品佩戴关系,并能得到可视化的适合性检验结果,为检验和指导产品的适合性提供依据.  相似文献   
10.
自动驾驶汽车虚拟测试已成为自动驾驶或车路协同测试评价的一个重要手段,三维激光雷达数据模拟生成是自动驾驶汽车虚拟测试中的重要任务之一,目前多采用基于飞行时间原理的几何模型方法生成激光雷达三维点云数据,该方法生成点云实时性较差。布告牌是虚拟场景中常采用的树木建模方法,由于布告牌仅由两个矩形面片即八个三角形面片组成,直接采用布告牌方法生成的三维点云数据难以反映树木的真实空间信息。针对上述问题,提出了一种基于布告牌空间变换的快速树木三维点云生成方法。以布告牌的纹理图像为依据,根据纹理透明度获取树木二维平面点云分布,经二维树木点云的轮廓提取,结合树木结构的先验知识进行旋转、随机偏移和尺度变换,以更少的三角形面片数和更小的计算代价获得树木的三维点云数据。提出了一种空间直方图三维点云相似度评价方法,将三维点云空间量化为若干个子空间,获得三维点云的投影空间直方图,采用巴氏系数计算投影空间直方图相似度,以投影空间直方图加权相似度作为点云相似度评价值。实验结果表明,基于布告牌空间变换方法和几何模型方法生成的云杉等三种树木的三维点云数据的平均相似度在90%以上,且该方法生成树木点云的时间仅是几何模型法的1%,因此布告牌空间变换树木三维点云生成方法快速且准确,可以满足自动驾驶汽车虚拟测试的性能要求。  相似文献   
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