首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   1195篇
  免费   15篇
  国内免费   4篇
电工技术   29篇
综合类   1篇
化学工业   223篇
金属工艺   51篇
机械仪表   35篇
建筑科学   11篇
能源动力   35篇
轻工业   87篇
水利工程   12篇
石油天然气   1篇
武器工业   1篇
无线电   123篇
一般工业技术   189篇
冶金工业   352篇
原子能技术   18篇
自动化技术   46篇
  2023年   3篇
  2022年   12篇
  2021年   14篇
  2020年   5篇
  2019年   8篇
  2018年   11篇
  2017年   4篇
  2016年   12篇
  2015年   9篇
  2014年   18篇
  2013年   42篇
  2012年   41篇
  2011年   55篇
  2010年   39篇
  2009年   43篇
  2008年   51篇
  2007年   41篇
  2006年   26篇
  2005年   34篇
  2004年   24篇
  2003年   30篇
  2002年   35篇
  2001年   26篇
  2000年   28篇
  1999年   31篇
  1998年   119篇
  1997年   82篇
  1996年   57篇
  1995年   38篇
  1994年   25篇
  1993年   35篇
  1992年   19篇
  1991年   21篇
  1990年   13篇
  1989年   23篇
  1988年   15篇
  1987年   13篇
  1986年   13篇
  1985年   17篇
  1984年   14篇
  1983年   3篇
  1982年   4篇
  1981年   7篇
  1980年   8篇
  1979年   3篇
  1978年   5篇
  1977年   8篇
  1976年   11篇
  1974年   5篇
  1967年   2篇
排序方式: 共有1214条查询结果,搜索用时 15 毫秒
991.
Nukacin ISK-1 is a lantibiotic produced by Staphylococcus warneri ISK-1. The gene cluster of nukacin ISK-1 consists of at least nukAMTFEG, ORF1 and ORF7. In this study, we demonstrated the heterologous production of nukacin ISK-1 in Lactococcus lactis by the artificial polycistronic expression of nukAMTFEG-ORF7 under the control of the nisin-controlled expression (NICE) system. Consequently, the recombinant L. lactis showed antimicrobial activity. Mass analysis clarified the presence of nukacin ISK-1 produced in the culture supernatant. These results suggested that the recombinant L. lactis produced nukacin ISK-1 heterologously. Inactivation of nukA, -M or -T resulted in the complete loss of the nukacin ISK-1 production phenotype. This finding suggested that nukAMT are indispensably associated with the biosynthesis of nukacin ISK-1. To our knowledge, this is the first report of the heterologous production of lantibiotic using the NICE system.  相似文献   
992.
Molecular chaperone DnaK of halophilic Tetragenococcus halophilus JCM5888 was characterized under salinity conditions both in vitro and in vivo. The dnaK gene was cloned into an expression vector and transformed into Escherichia coli. The DnaK protein obtained from the recombinant E. coli showed a significantly higher refolding activity of denatured lactate dehydrogenase than that from non-halophilic Lactococcus lactis under NaCl concentrations higher than 1 M. E. coli without the overexpression of DnaK exhibited a growth profile with a prolonged lag phase and suppressed maximum cell density in Luria-Bertani medium containing 5% (0.86 M) NaCl. On the contrary, the overexpression of T. halophilus DnaK greatly shortened this prolonged lag phase with no effect on maximum growth, while that of L. lactis DnaK decreased maximum growth. The amount of protein aggregates was increased by salt stress in the E. coli cells, while this aggregation was greatly suppressed by the overexpression of T, halophilus DnaK. These results suggest that heterologous overexpression of T. halophilus DnaK, via its chaperone activity, promotes salinity adaptation of E. coli.  相似文献   
993.
Perfluorinated compounds in the Cape Fear Drainage Basin in North Carolina   总被引:4,自引:0,他引:4  
Concern over perfluorinated organic compounds (PFCs), e.g., perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA), is due to a number of recent studies which show that the PFCs are persistent, bioaccumulative, and toxic in animals. Despite sustained interest in this topic, little information is available concerning the environmental distributions of the compounds. In this study, a new method was developed for the analysis of 10 target PFCs and its performance was examined in a systematic evaluation of surface water in the Cape Fear River Basin in North Carolina. One hundred samples from 80 different locations were collected during the spring of 2006. Detectable levels of the target PFCs were found in all samples, and were comparable to values reported previously, with maximum PFOS at 132 ng/L, PFOA at 287 ng/L, perfluorononanoic acid (C9) at 194 ng/L, and perfluoroheptanoic acid (C7) at 329 ng/L. In general, the lowest concentrations of the PFCs were found in the smallest tributaries while the highest levels were found in middle reaches of the Drainage Basin. Variability of PFC concentrations suggests a series of source inputs throughout the Basin. Seventeen sample sites (22%) had PFOS concentrations greater than 43 ng/L, a conservative safe water concentration estimated to be protective of avian life. In addition, a total of 26 sites (32%) had PFOA concentrations above 40 ng/L.  相似文献   
994.
995.
Facile orientation of boron nitride (BN) with high anisotropy in epoxy resin-based nanocomposite films was performed in a polyepoxide matrix using a nanosecond-pulse electric field to generate a high electric flux. Control of the BN anisotropy was achieved in the polymer without damaging the composite films or requiring surface modification of the BN. The degree of BN orientation perpendicular to the nanocomposite film plane, which was parallel to the electric flux, could be controlled by applying the nanosecond pulse for different lengths of time before cross-linking. The resulting composite films with oriented BN nanosheets manifested improved thermal diffusivity compared to a composite prepared without orientation.  相似文献   
996.
997.
Reactions of metallurgical-grade silicon (MG-Si) with gaseous hydrogen bromide (HBr) has been monitored by means of online gas chromatography in a flow reactor system. The formation of tri-bromosilane started to occur at 380 °C, accompanied by the consumption of HBr. The conversion of HBr into bromosilanes increased with an increase in reaction temperature and reached a maximum at 440 °C. An increase of the HBr concentration in a HBr-N2 mixed gas led to an increase in the consumption of MG-Si, while it reduced the selectivity of the tri-bromosilane formation. An increase in total flow rate of the reaction gas caused a dramatic decrease in the HBr conversion and enhanced the selectivity of the tri-bromosilane formation. The rate constant for overall bromination reaction at 400 °C was measured to be 0.46 s−1. Concentrations of impurities in the product were much less than those in MG-Si. Moreover, kerf loss silicon was subjected to the bromination reaction under the optimized conditions.  相似文献   
998.
Objective: The hepatic metabolism of six compounds newly synthesized as retinoid X receptor agonists was characterized in rat and human liver microsomes to examine the relationship between their hepatic metabolism profiles and side chain structures, considering the interspecies difference.

Materials and methods: The compounds used have a 6-[N-ethyl-N-(3-alkoxy-4-isopropylphenyl)amino]nicotinic or 6-[N-ethyl-N-(4-alkoxy-3-isopropylphenyl)amino]nicotinic acid skeleton, in which the isopropoxy, isobutoxy or cyclopropylmethoxy group is employed for the alkoxy group. These compounds were incubated with the microsomes, and their Michaelis--Menten parameters were determined. The incubation study was also performed with various cytochrome P450 (CYP) inhibitors to examine their susceptibilities to the inhibitors. In addition, a molecular docking simulation was conducted to assess the compound’s spatial configuration with the CYP isoform when necessary.

Results: The Michaelis--Menten parameters determined are comparable between rats and humans for the compounds having 3-isobutoxy, 4-isobutoxy, 4-isopropoxy and 4-cyclopropylmethoxy groups. However, it was indicated that all compounds except that having the 3-isobutoxy group are metabolized in a different manner between rats and humans. That is, the extent of the contribution of each CYP isozyme is different between those two species. A molecular docking simulation showed that the spatial configuration of the compound to be associated with CYP2D6 markedly changes depending on whether the isobutoxy group is situated at the 3- or 4-position.

Conclusion: A slight difference in the side chain structures markedly alters the compound’s metabolic profile, which amplifies the interspecies difference regarding the profile, increasing the difficulty in characterizing the profile in humans with the structural-property relationship and interspecies extrapolation.  相似文献   

999.
We expand the range of applications of a tuning fork probe (TFP) in frequency-modulation atomic force microscopy (FM-AFM) by attaching a long metal tip at a certain angle. By the combined flexure of the metal tip and the tuning fork prong, this TFP can change the direction of the detectable force by switching the resonance frequency, which has not been realized with conventional TFPs with short tips. The oscillatory behavior of the tip apex of the TFP is predicted by computer simulations and is experimentally confirmed with scanning electron microscope. FM-AFM operations using this TFP are performed in various environments, i.e., in ultrahigh vacuum, air, and water. FM-AFM images obtained at an atomic step of highly oriented pyrolytic graphite in air show a clear difference depending on the excitation frequency. It is also revealed that the higher order flexural modes of this TFP are advantageous for FM-AFM in water due to the reduction in the degree of hydrodynamic damping.  相似文献   
1000.
The exo-electron emission behaviour from Ti, W, Mo, Fe, Al, Ni, Cd, Zn and Pb metals was investigated during and after being cut in O2 and N2 gases at a gas pressure of 3 × 10−2 Pa and in a vacuum of 4 × 10−4 Pa. The results showed that the emission behaviour of electrons during and after cutting depends on the combination of metal and the surrounding gas species. The emission intensity of electrons while cutting various metals in O2 gas increased sharply with an increase in the negative value of the heat cf formation, ΔHf of the oxide. The emission intensity in N2 was also higher at higher negative values of ΔHf of the metal nitride. Electron emission intensity from the cut metal surface is concluded to be a function of the heat of formation of reaction products of the metal surface with the surrounding gas.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号