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991.
以噻吩-2-甲醛为原料,与磷酰基乙酸三乙酯在氢化钠存在下反应制备3-(2-噻吩)丙烯酸乙酯,后通过水解制备3-(2-噻吩)丙烯酸,总收率78.5%,纯度98.6%,可制备121 g每批。考察了原料滴加速度、物料摩尔比、溶剂用量、柱层析硅胶用量对化合物2合成的影响,确定了最佳条件为:滴加速度8 m L/min、噻吩-2-甲醛与膦酰基乙酸三乙酯摩尔比为1:1.2,溶剂1.6 L,柱层析用硅胶与粗产物重量比为1:15,该步反应收率92.3%,水解后产物经重结晶获得纯品,收率85%。产物结构通过质谱、核磁鉴定正确。 相似文献
992.
993.
Ah-Young Kwon Ju-Yeon Jeong Hyun Park Sohyun Hwang Gwangil Kim Haeyoun Kang Jin-Hyung Heo Hye Jin Lee Tae-Heon Kim Hee Jung An 《International journal of molecular sciences》2022,23(10)
Alteration in expression of miRNAs can cause various malignant changes and the metastatic process. Our aim was to identify the miRNAs involved in cervical squamous cell carcinoma (SqCC) and metastasis, and to test their utility as indicators of metastasis and survival. Using microarray technology, we performed miRNA expression profiling on primary cervical SqCC tissue (n = 6) compared with normal control (NC) tissue and compared SqCC that had (SqC-M; n = 3) and had not (SqC-NM; n = 3) metastasized. Four miRNAs were selected for validation by qRT-PCR on 29 SqC-NM and 27 SqC-M samples, and nine metastatic lesions (ML-SqC), from a total of 56 patients. Correlation of miRNA expression and clinicopathological parameters was analyzed to evaluate the clinical impact of candidate miRNAs. We found 40 miRNAs differentially altered in cervical SqCC tissue: 21 miRNAs were upregulated and 19 were downregulated (≥2-fold, p < 0.05). Eight were differentially altered in SqC-M compared with SqC-NM samples: four were upregulated (miR-494, miR-92a-3p, miR-205-5p, and miR-221-3p), and four were downregulated (miR-574-3p, miR-4769-3p, miR-1281, and miR-1825) (≥1.5-fold, p < 0.05). MiR-22-3p might be a metastamiR, which was gradually further downregulated in SqC-NM > SqC-M > ML-SqC. Downregulation of miR-30e-5p significantly correlated with high stage, lymph node metastasis, and low survival rate, suggesting an independent poor prognostic factor. 相似文献
994.
MicroRNA-331-3p Suppresses Cervical Cancer Cell Proliferation and E6/E7 Expression by Targeting NRP2
Tomomi Fujii Keiji Shimada Aya Asano Yoshihiro Tatsumi Naoko Yamaguchi Masaharu Yamazaki Noboru Konishi 《International journal of molecular sciences》2016,17(8)
Aberrant expression of microRNAs (miRNAs) is involved in the development and progression of various types of cancers. In this study, we investigated the role of miR-331-3p in cell proliferation and the expression of keratinocyte differentiation markers of uterine cervical cancer cells. Moreover, we evaluated whether neuropilin 2 (NRP2) are putative target molecules that regulate the human papillomavirus (HPV) related oncoproteins E6 and E7. Cell proliferation in the human cervical cancer cell lines SKG-II, HCS-2, and HeLa was assessed using the 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt (MTS) assay. Cellular apoptosis was measured using the TdT-mediated dUTP nick end labeling (TUNEL) and Annexin V assays. Quantitative RT-PCR was used to measure the messenger RNA (mRNA) expression of the NRP2, E6, E7, p63, and involucrin (IVL) genes. A functional assay for cell growth was performed using cell cycle analyses. Overexpression of miR-331-3p inhibited cell proliferation, and induced G2/M phase arrest and apoptosis in SKG-II, HCS-2 and HeLa cells. The luciferase reporter assay of the NRP2 3′-untranslated region revealed the direct regulation of NRP2 by miR-331-3p. Gene expression analyses using quantitative RT-PCR in SKG-II, HCS-2, and HeLa cells overexpressing miR-331-3p or suppressing NRP2 revealed down-regulation of E6, E7, and p63 mRNA and up-regulation of IVL mRNA. Moreover, miR-331-3p overexpression was suppressed NRP2 expression in protein level. We showed that miR-331-3p and NRP2 were key effectors of cell proliferation by regulating the cell cycle, apoptosis. NRP-2 also regulates the expression of E6/E7 and keratinocyte differentiation markers. Our findings suggest that miR-331-3p has an important role in regulating cervical cancer cell proliferation, and that miR-331-3p may contribute to keratinocyte differentiation through NRP2 suppression. miR-331-3p and NRP2 may contribute to anti-cancer effects. 相似文献
995.
Gabriel Rinnerthaler Hubert Hackl Simon Peter Gampenrieder Frank Hamacher Clemens Hufnagl Cornelia Hauser-Kronberger Franz Zehentmayr Gerd Fastner Felix Sedlmayer Brigitte Mlineritsch Richard Greil 《International journal of molecular sciences》2016,17(2)
For quantitative microRNA analyses in formalin-fixed paraffin-embedded (FFPE) tissue, expression levels have to be normalized to endogenous controls. To investigate the most stably-expressed microRNAs in breast cancer and its surrounding tissue, we used tumor samples from primary tumors and from metastatic sites. MiRNA profiling using TaqMan® Array Human MicroRNA Cards, enabling quantification of 754 unique human miRNAs, was performed in FFPE specimens from 58 patients with metastatic breast cancer. Forty-two (72%) samples were collected from primary tumors and 16 (28%) from metastases. In a cross-platform analysis of a validation cohort of 32 FFPE samples from patients with early breast cancer genome-wide microRNA expression analysis using SurePrintG3 miRNA (8 × 60 K)® microarrays from Agilent® was performed. Eleven microRNAs could be detected in all samples analyzed. Based on NormFinder and geNorm stability values and the high correlation (rho ≥ 0.8) with the median of all measured microRNAs, miR-16-5p, miR-29a-3p, miR-126-3p, and miR-222-3p are suitable single gene housekeeper candidates. In the cross-platform validation, 29 human microRNAs were strongly expressed (mean log2-intensity > 10) and 21 of these microRNAs including miR-16-5p and miR-29a-3p were also stably expressed (CV < 5%). Thus, miR-16-5p and miR-29a-3p are both strong housekeeper candidates. Their Normfinder stability values calculated across the primary tumor and metastases subgroup indicate that miR-29a-3p can be considered as the strongest housekeeper in a cohort with mainly samples from primary tumors, whereas miR-16-5p might perform better in a metastatic sample enriched cohort. 相似文献
996.
以(NH4) 2S2O8溶液为浸渍溶液,采用溶胶-凝胶法制备了添加稀土Sm元素的固体酸催化剂S2O82-/SnO2-Fe2O3-Sm2O3,采用FT-IR、XRD、TG-DTA等分析方法对催化剂进行表征.将催化剂应用于乙酸正丁酯的合成反应,考察了铁锡元素摩尔比、浸渍液浓度、焙烧温度、焙烧时间和稀土含量等条件对固体酸催化性能的影响,得到催化剂的最佳制备条件为:铁锡元素摩尔比为1∶4,(NH4)2S2O8浸渍液浓度为2.0 mol/L,焙烧温度为500℃,焙烧时间为2.5h,添加稀土氧化钐含量为3%,乙酸正丁酯的酯化率最高达98%以上.添加稀土Sm元素的催化剂稳定性能良好,再生实验表明催化剂结焦及S2O2-基团的流失是催化剂失活的主要原因. 相似文献
997.
998.
In the present work, transparent and anti-fogging AlPO4-5 films were prepared on glass substrates using a novel developed process. The process entails a simple in-situ sol–gel followed by vapor phase transport. The in-situ sol–gel process was implemented by coating the precursor sols for the synthesis of AlPO4-5 on the glass substrates successively using the spin-coating method. The films and powders scribed from the films were characterized by X-Ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscope (SEM), atomic force microscope (AFM), X-ray photoelectron spectroscopy and transmission electron microscope (TEM). The unique films were composed of oblique oriented nano-flake AlPO4-5 crystals with the thickness of about 20 nm. The formation of nano-flake crystals can be ascribed to the high concentration of the precursors, resulting in the formation of a supersaturation system. The obtained films showed high antifogging performance due to the superhydrophilicity with a water contact angle of lower than 1.0°. The silicone oil contact angle was also low about 8.2°. In addition, heteroatom-substituted AlPO4-5 films showing different colors can be obtained easily by simply adding transition metal ions in the phosphate acid solution during the preparation that can extend the application of the method for different coating demand. 相似文献
999.
李小坚 《北方工业大学学报》1993,5(3):40-46
本文基于2人2级stackelberg鼓励性对策下的广义平衡解的定义,引出决策可行区和可接受区的概念,推出广义平衡解存在的充分必要条件,并拓广到多人多级情形.总结和应用等价原则对多级递阶系统进行简约,在适当条件下,可将多级决策系统简化成单人决策问题.通过探讨广义平衡解的决策过程,揭示嵌套信息结构下可接受区的反嵌套关系,从而有助于理解和应用带鼓励性对策的多级递阶决策方法. 相似文献
1000.
讨论了用惯性基准法进行轨道参数实时检测的算法,并对车载轨向实时检测装置的实现作了简要介绍. 相似文献