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压水堆启动前需要进行物理启动试验,其中调临界是相对耗时的一部分。采用次临界条件下的试验,可以省去调临界的步骤,提高物理启动试验的安全性和适用性,加速物理启动试验的进程,提高压水堆的负荷因子。目前,次临界反应性测量受限于测量信号较弱,背景噪声强,误差较大,难以满足商用压水堆的工程应用要求。本文基于源倍增方法,利用空间重要性修正因子和信号线性修正提高次临界反应性测量的精度,成功地在核电厂首循环上实现了次临界反应性测量的蒙特卡罗方法计算,取得了较好的计算精度与效果。 相似文献
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公用配电变压器并列运行的可行性分析及应用 总被引:1,自引:0,他引:1
城市10 kV公用配电线路的线损普遍较高,其中公用配电变压器本身的损耗占线损的很大比例.城市届民的用电负荷随季节和天气的变化而发生较大变化,城市公用配电变压器在一年中约有半年时间负荷达不到额定负荷的50%.因此,根据实际情况制定方案,就近将2台配电变压器并列运行,视负荷情况投切其中的一台变压器,以达到节能、降损的目的. 相似文献
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Zhi He Li Zheng Qiqi Chen Sen Xiong Zhide He Jiaxiang Hu Zhijun Ma Qian Zhang Jiayang He Lijuan Ye Liang He Jie Luo Xiaobin Gu Mingwang Zhang Ziting Tang Yuanyuan Jiao Yong Pu Jinxin Xiong Kuo Gao Bolin Lai Shiyong Yang Deying Yang Taiming Yan 《International journal of molecular sciences》2022,23(23)
Bmpr2 plays a central role in the regulation of reproductive development in mammals, but its role during ovarian development in fish is still unclear. To ascertain the function of bmpr2 in ovarian development in the ricefield eel, we isolated and characterized the bmpr2 cDNA sequence; the localization of Bmpr2 protein was determined by immunohistochemical staining; and the expression patterns of bmpr2 in ovarian tissue incubated with FSH and hCG in vitro were analyzed. The full-length bmpr2 cDNA was 3311 bp, with 1061 amino acids encoded. Compared to other tissues, bmpr2 was abundantly expressed in the ovary and highly expressed in the early yolk accumulation (EV) stages of the ovary. In addition, a positive signal for Bmpr2 was detected in the cytoplasm of oocytes in primary growth (PG) and EV stages. In vitro, the expression level of gdf9, the ligand of bmpr2, in the 10 ng/mL FSH treatment group was significantly higher after incubation for 4 h than after incubation for different durations. However, bmpr2 expression in the 10 ng/mL FSH treatment group at 2 h, 4 h and 10 h was significantly lower. Importantly, the expression level of bmpr2 and gdf9 in the 100 IU/mL hCG group had similar changes that were significantly decreased at 4 h and 10 h. In summary, Bmpr2 might play a pivotal role in ovarian growth in the ricefield eel, and these results provide a better understanding of the function of bmpr2 in ovarian development and the basic data for further exploration of the regulatory mechanism of gdf9 in oocyte development. 相似文献
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Yi Zhao Eliud Morales Dvila Xue Li Beiyu Tang Ariana I. Rabinowitsch Jose Manuel Perez-Aguilar Carl P. Blobel 《International journal of molecular sciences》2022,23(21)
The metalloprotease ADAM17 is a key regulator of the TNFα, IL-6R and EGFR signaling pathways. The maturation and function of ADAM17 is controlled by the seven-membrane-spanning proteins iRhoms1 and 2. The functional properties of the ADAM17/iRhom1 and ADAM17/iRhom2 complexes differ, in that stimulated shedding of most ADAM17 substrates tested to date can be supported by iRhom2, whereas iRhom1 can only support stimulated shedding of very few ADAM17 substrates, such as TGFα. The first transmembrane domain (TMD1) of iRhom2 and the sole TMD of ADAM17 are important for the stimulated shedding of ADAM17 substrates by iRhom2. However, little is currently known about how the iRhoms interact with different substrates to control their stimulated shedding by ADAM17. To provide new insights into this topic, we tested how various chimeras between iRhom1 and iRhom2 affect the stimulated processing of the EGFR-ligands TGFα (iRhom1- or 2-dependent) and EREG (iRhom2-selective) by ADAM17. This uncovered an important role for the TMD7 of the iRhoms in determining their substrate selectivity. Computational methods utilized to characterize the iRhom1/2/substrate interactions suggest that the substrate selectivity is determined, at least in part, by a distinct accessibility of the substrate cleavage site to stimulated ADAM17. These studies not only provide new insights into why the substrate selectivity of stimulated iRhom2/ADAM17 differs from that of iRhom1/ADAM17, but also suggest new approaches for targeting the release of specific ADAM17 substrates. 相似文献
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Xiamei Kang Xiao Zhou Yanting Tang Zhijie Jiang Jiaqi Chen Muhammad Mohsin Min Yue 《International journal of molecular sciences》2022,23(17)
Salmonella enterica, serovar Gallinarum, biovar Pullorum, is an avian-specific pathogen which has caused considerable economic losses to the poultry industry worldwide. Two-component systems (TCSs) play an essential role in obtaining nutrients, detecting the presence of neighboring bacteria and regulating the expression of virulence factors. The genome analysis of S. Pullorum strain S06004 suggesting the carriage of 22 pairs of TCSs, which belong to five families named CitB, OmpR, NarL, Chemotaxis and LuxR. In the CitB family, three pairs of TCSs, namely CitA-CitB, DcuS-DcuR and DpiB-DpiA, remain unaddressed in S. Pullorum. To systematically investigate the function of the CitB family in S. Pullorum, four mutants, ΔcitAB (abbreviated as Δcit), ΔdcuSR (Δdcu), ΔdpiBA (Δdpi) and ΔcitABΔdcuSRΔdpiBA (Δ3), were made using the CRISPR/Cas9 system. The results demonstrated that the CitB family did not affect the growth of bacteria, the results of biochemical tests, invasion and proliferation in chicken macrophage HD-11 cells and the expression of fimbrial protein. But the mutants showed thicker biofilm formation, higher resistance to antimicrobial agents, enhanced tolerance to inhibition by egg albumen and increased virulence in chicken embryos. Moreover, the deletion of Dpi TCS was detrimental to survival after exposure to hyperosmotic and oxidative environments, as well as the long-term colonization of the small intestine of chickens. Collectively, we provided new knowledge regarding the possible role of the CitB family involved in the pathogenic processes of S. Pullorum. 相似文献