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排序方式: 共有1463条查询结果,搜索用时 14 毫秒
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In this paper, basic relationships and algorithms for numerical simulation of non-linear, self-excited vibrations in single degree-of-freedom cutting systems are presented. Non-linearities due to the tool leaving the cut, as well as interference between the cutting tool clearance face and cutting surface waviness, were taken into consideration. Examples of vibration simulation results are shown. 相似文献
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The virtual path (VP) can simplifyAtm network management by minimizing connection routing and admission costs, and by facilitating the layered control of resources. However, fully exploiting these advantages may lead to a large number of relatively low capacity virtual paths travelling on each physical link. If each VP is treated as a separate unit, as is commonly assumed, low path capacities will lead to low network utilisation. This paper carefully examines the trade-off between simplification through traffic separation and improved efficiency due to traffic consolidation. We review existing vp bandwidth assignment and control techniques, and propose a new vp tagging control method. A comparison shows that by permitting resource sharing between paths it is possible to influence significantly the trade-off between simplified network management and multiplexing gain from traffic consolidation. 相似文献
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Krzysztof Ciepliński 《Computers & Mathematics with Applications》2011,62(9):3418-3426
A mapping f:Vn?W, where V is a commutative group, W is a linear space, and n≥2 is an integer, is called multi-quadratic if it is quadratic in each variable. In this paper, we prove the generalized Hyers-Ulam stability of multi-quadratic mappings in Banach spaces and complete non-Archimedean spaces. 相似文献
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Elbieta U. Stolarczyk Weronika Strzempek Marta aszcz Andrzej Le Elbieta Menaszek Krzysztof Stolarczyk 《International journal of molecular sciences》2022,23(14)
Isoflavonoids such as genistein (GE) are well known antioxidants. The predictive biological activity of structurally new compounds such as thiogenistein (TGE)–a new analogue of GE–becomes an interesting way to design new drug candidates with promising properties. Two oxidation strategies were used to characterize TGE oxidation products: the first in solution and the second on the 2D surface of the Au electrode as a self-assembling TGE monolayer. The structure elucidation of products generated by different oxidation strategies was performed. The electrospray ionization mass spectrometry (ESI-MS) was used for identifying the product of electrochemical and hydrogen peroxide oxidation in the solution. Fourier transform infrared spectroscopy (FT-IR) with the ATR mode was used to identify a product after hydrogen peroxide treatment of TGE on the 2D surface. The density functional theory was used to support the experimental results for the estimation of antioxidant activity of TGE as well as for the molecular modeling of oxidation products. The biological studies were performed simultaneously to assess the suitability of TGE for antioxidant and antitumor properties. It was found that TGE was characterized by a high cytotoxic activity toward human breast cancer cells. The research was also carried out on mice macrophages, disclosing that TGE neutralized the production of the LPS-induced reactive oxygen species (ROS) and exhibits ABTS (2,2′-azino-bis-3-(ethylbenzothiazoline-6-sulphonic acid) radical scavenging ability. In the presented study, we identified the main oxidation products of TGE generated under different environmental conditions. The electroactive centers of TGE were identified and its oxidation mechanisms were proposed. TGE redox properties can be related to its various pharmacological activities. Our new thiolated analogue of genistein neutralizes the LPS-induced ROS production better than GE. Additionally, TGE shows a high cytotoxic activity against human breast cancer cells. The viability of MCF-7 (estrogen-positive cells) drops two times after a 72-h incubation with 12.5 μM TGE (viability 53.86%) compared to genistein (viability 94.46%). 相似文献
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Iwona Radziejewska Katarzyna Supruniuk Micha Tomczyk Wiktoria Izdebska Magorzata Borzym-Kluczyk Anna Bielawska Krzysztof Bielawski Anna Galicka 《International journal of molecular sciences》2022,23(15)
Abnormal glycosylation of cancer cells is considered a key factor of carcinogenesis related to growth, proliferation, migration and invasion of tumor cells. Many plant-based polyphenolic compounds reveal potential anti-cancer properties effecting cellular signaling systems. Herein, we assessed the effects of phenolic acid, p-coumaric acid and flavonoids such as kaempferol, astragalin or tiliroside on expression of selected cancer-related glycoforms and enzymes involved in their formation in AGS gastric cancer cells. The cells were treated with 80 and 160 µM of the compounds. RT-PCR, Western blotting and ELISA tests were performed to determine the influence of polyphenolics on analyzed factors. All the examined compounds inhibited the expression of MUC1, ST6GalNAcT2 and FUT4 mRNAs. C1GalT1, St3Gal-IV and FUT4 proteins as well as MUC1 domain, Tn and sialyl T antigen detected in cell lysates were also lowered. Both concentrations of kaempferol, astragalin and tiliroside also suppressed ppGalNAcT2 and C1GalT1 mRNAs. MUC1 cytoplasmic domain, sialyl Tn, T antigens in cell lysates and sialyl T in culture medium were inhibited only by kaempferol and tiliroside. Nuclear factor NF-κB mRNA expression decreased after treatment with both concentrations of kaempferol, astragalin and tiliroside. NF-κB protein expression was inhibited by kaempferol and tiliroside. The results indicate the rationality of application of examined polyphenolics as potential preventive agents against gastric cancer development. 相似文献
8.
Mateusz Sypniewski Zbigniew J. Krl Joanna Szyda Elbieta Kaja Magdalena Mroczek Tomasz Suchocki Adrian Lejman Maria Stpie Piotr Topolski Maciej Dbrowski Krzysztof Kotlarz Angelika Aplas Micha Wasiak Marzena Wojtaszewska Pawe Zawadzki Agnieszka Pawlak Robert Gil Paula Dobosz Joanna Stojak 《International journal of molecular sciences》2022,23(15)
Background: Severe outcomes of COVID-19 account for up to 15% of all cases. The study aims to check if any gene variants related to cardiovascular (CVD) and pulmonary diseases (PD) are correlated with a severe outcome of COVID-19 in a Polish cohort of COVID-19 patients. Methods: In this study, a subset of 747 samples from unrelated individuals collected across Poland in 2020 and 2021 was used and whole-genome sequencing was performed. Results: The GWAS analysis of SNPs and short indels located in genes related to CVD identified one variant significant in COVID-19 severe outcome in the HADHA gene, while for the PD gene panel, we found two significant variants in the DRC1 gene. In this study, both potentially protective and risk variants were identified, of which variants in the HADHA gene deserve the most attention. Conclusions: This is the first study reporting the association between the HADHA and DRC1 genetic variants and COVID-19 severe outcome based on the cohort WGS analysis. Although all the identified variants are localised in introns, they may be correlated and therefore inherited along with other risk variants, potentially causative to severe outcome of COVID-19 but not discovered yet. 相似文献
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Malgorzata Kardynska Jaroslaw Smieja Pawel Paszek Krzysztof Puszynski 《International journal of molecular sciences》2022,23(12)
Mathematical modeling of signaling pathways and regulatory networks has been supporting experimental research for some time now. Sensitivity analysis, aimed at finding model parameters whose changes yield significantly altered cellular responses, is an important part of modeling work. However, sensitivity methods are often directly transplanted from analysis of technical systems, and thus, they may not serve the purposes of analysis of biological systems. This paper presents a novel sensitivity analysis method that is particularly suited to the task of searching for potential molecular drug targets in signaling pathways. Using two sample models of pathways, p53/Mdm2 regulatory module and IFN--induced JAK/STAT signaling pathway, we show that the method leads to biologically relevant conclusions, identifying processes suitable for targeted pharmacological inhibition, represented by the reduction of kinetic parameter values. That, in turn, facilitates subsequent search for active drug components. 相似文献