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排序方式: 共有1507条查询结果,搜索用时 31 毫秒
41.
Almerinda Di Benedetto Paola Russo Roberto Sanchirico Valeria Di Sarli 《American Institute of Chemical Engineers》2015,61(5):1572-1580
A Computational Fluid Dynamics (CFD) model was developed with the aim at simulating the turbulent flow field and associated dust dispersion in an agitated spherical explosion vessel. Simulations were performed in the presence of two counter‐rotating fans and also after having switched‐off the fans. Numerical results have shown that the dust mainly accumulates at the center of the sphere in the space left by the four vortices formed. After the switch‐off of the fans, the dust particles start filling the empty volumes inside the sphere, reaching a quite uniform distribution (with concentration equal to the nominal value) and simultaneously ensuring a controlled value of turbulent kinetic energy. © 2015 American Institute of Chemical Engineers AIChE J, 61: 1572–1580, 2015 相似文献
42.
Target Hopping as a Useful Tool for the Identification of Novel EphA2 Protein–Protein Antagonists 下载免费PDF全文
Dr. Daniele Pala Dr. Simonetta Russo Dr. Riccardo Castelli Dr. Iftiin Hassan‐Mohamed Dr. Carmine Giorgio Dr. Alessio Lodola 《ChemMedChem》2014,9(1):67-72
Lithocholic acid (LCA), a physiological ligand for the nuclear receptor FXR and the G‐protein‐coupled receptor TGR5, has been recently described as an antagonist of the EphA2 receptor, a key member of the ephrin signalling system involved in tumour growth. Given the ability of LCA to recognize FXR, TGR5, and EphA2 receptors, we hypothesized that the structural requirements for a small molecule to bind each of these receptors might be similar. We therefore selected a set of commercially available FXR or TGR5 ligands and tested them for their ability to inhibit EphA2 by targeting the EphA2‐ephrin‐A1 interface. Among the selected compounds, the stilbene carboxylic acid GW4064 was identified as an effective antagonist of EphA2, being able to block EphA2 activation in prostate carcinoma cells, in the micromolar range. This finding proposes the “target hopping” approach as a new effective strategy to discover new protein–protein interaction inhibitors. 相似文献
43.
Paola Savoia Tommaso Deboli Alberto Previgliano Paolo Broganelli 《International journal of molecular sciences》2015,16(10):23300-23317
Basal cell carcinoma (BCC) is the most common cancer in individuals with fair skin type (I–II) and steadily increasing in incidence (70% of skin malignancy). It is locally invasive but metastasis is usually very rare, with an estimated incidence of 0.0028%–0.55%. Conventional therapy is surgery, especially for the H region of the face and infiltrative lesions; in case of inoperable tumors, radiotherapy is a valid option. Recently, topical photodynamic therapy (PDT) has become an effective treatment in the management of superficial and small nodular BCC. PDT is a minimally invasive procedure that involves the administration of a photo-sensibilizing agent followed by irradiation at a pre-defined wavelength; this determines the creation of reactive oxygen species that specifically destroy target cells. The only major side effect is pain, reported by some patients during the irradiation. The high cure rate and excellent cosmetic outcome requires considering this possibility for the management of patients with both sporadic and hereditary BCC. In this article, an extensive review of the recent literature was made, in order to clarify the role of PDT as a possible alternative therapeutic option in the treatment of BCC. 相似文献
44.
Pietro Russo Giorgio Simeoli Domenico Acierno Valentina Lopresto 《Polymer Composites》2015,36(11):2022-2029
Polyolefin‐based composite laminates reinforced with jute fabric were prepared by compression molding and investigated in terms of flexural properties and impact behavior. The use of a virgin polypropylene as the matrix was compared with two polyolefin matrices coming from discarded car bumpers and selected packaging wastes, respectively, and mainly constituted by mixtures of polyethylene and polypropylene resins. The influence of a coupling agent (maleated polypropylene) was always considered in order to improve the interfacial adhesion and, consequently, the composite strength. The effect of this coupling agent, clearly dependent on the amount of polypropylene phase in the overall mixture, was found to be satisfactory only in the case of virgin polypropylene‐based systems. These latter, in presence of maleated polypropylene, have shown higher flexural parameters, lower propagation energy and higher breaking impact load with respect to uncompatibilized ones. Results were supported by morphological observations of impact surfaces, always highlighting a poor adhesion at the reinforcement–matrix interface except in compatibilized virgin polypropylene‐based laminates. POLYM. COMPOS., 36:2022–2029, 2015. © 2014 Society of Plastics Engineer 相似文献
45.
Pietro Altimari Erasmo Mancusi Lucia Russo Silvestro Crescitelli 《American Institute of Chemical Engineers》2012,58(3):899-913
Networks of N identical catalytic reactors with periodically switched inlet and outlet sections are studied for first‐order irreversible exothermic reactions. Switching strategies with inlet and outlet sections periodically jumping a fixed number ns of reactors are considered and the mechanisms governing the formation of traveling temperature wave‐trains are analyzed as ns and N are varied. To this aim, a geometric approach to the analysis of the network energy balance is developed. Based on this approach, infinite domains of traveling temperature wave‐trains are predicted for any ns and N. Analytical approximations are derived for the stability limits and the spatiotemporal patterns of these regimes. Stability boundaries predicted analytically include for any solution the largest part of the stability region computed by numerical simulation. Moreover, good agreement is found between the structure of the spatiotemporal patterns computed numerically and that predicted based on the proposed approach. © 2011 American Institute of Chemical Engineers AIChE J, 2012 相似文献
46.
Wai Ling Cheung-Lee Madison E. Parry Dr. Chuhan Zong Alexis Jaramillo Cartagena Prof. Seth A. Darst Prof. Nancy D. Connell Dr. Riccardo Russo Prof. A. James Link 《Chembiochem : a European journal of chemical biology》2020,21(9):1335-1340
We report the heterologous expression, structure, and antimicrobial activity of a lasso peptide, ubonodin, encoded in the genome of Burkholderia ubonensis. The topology of ubonodin is unprecedented amongst lasso peptides, with 18 of its 28 amino acids found in the mechanically bonded loop segment. Ubonodin inhibits RNA polymerase in vitro and has potent antimicrobial activity against several pathogenic members of the Burkholderia genus, most notably B. cepacia and B. multivorans, causative agents of lung infections in cystic fibrosis patients. 相似文献
47.
Piyush Modak Willis Hammond Michael Jaffe Malavika Nadig Richard Russo 《应用聚合物科学杂志》2020,137(11):48454
Natural polysaccharides like chitosan and dextran have garnered considerable interest in biomedical applications due to their biocompatibility, biodegradability, and nontoxicity. Nonetheless, the development of a reproducible class of medical devices from these materials is challenging and has had limited success. Chitosan and dextran are inherently variable and synthesis using these materials is prone to inconsistencies. In this study, we put forward a robust product development regimen that allows these natural materials to be developed into a reproducible class of biomaterials. First, an array of validated characterization methods (Proton Nuclear Magnetic Resonance, titrations, Ultraviolet spectroscopy, Size Exclusion Chromatography—Multi-Angle Light Scattering, Size Exclusion Chromatography—Refractive Index, and proprietary methods) were developed that allowed rigorous specifications to be set for unprocessed chitosan and dextran, chitosan and dextran intermediates, and chemically modified materials—acrylated chitosan (aCHN) and oxidized dextran (oDEX). Second, a robust and reproducible synthesis scheme involving various in-process controls was developed to chemically modify the unprocessed polysaccharides. Third, purification methods to remove byproducts and low-molecular-weight impurities for both aCHN and oDEX were developed. The study presents a viable strategy for converting variable, natural materials into a reproducible class of biomaterials that can be applied in various biomedical applications. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48454. 相似文献
48.
G Doronzo M Viretto I Russo L Mattiello G Anfossi M Trovati 《International journal of molecular sciences》2012,13(8):9478-9488
Type 1 diabetes is characterized by insulin deficiency, type 2 by both insulin deficiency and insulin resistance: in both conditions, hyperglycaemia is accompanied by an increased cardiovascular risk, due to increased atherosclerotic plaque formation/instabilization and impaired collateral vessel formation. An important factor in these phenomena is the Vascular Endothelial Growth Factor (VEGF), a molecule produced also by Vascular Smooth Muscle Cells (VSMC). We aimed at evaluating the role of high glucose on VEGF-A(164) synthesis and secretion in VSMC from lean insulin-sensitive and obese insulin-resistant Zucker rats (LZR and OZR). In cultured aortic VSMC from LZR and OZR incubated for 24 h with d-glucose (5.5, 15 and 25 mM) or with the osmotic controls l-glucose and mannitol, we measured VEGF-A(164) synthesis (western, blotting) and secretion (western blotting and ELISA). We observed that: (i) d-glucose dose-dependently increases VEGF-A(164) synthesis and secretion in VSMC from LZR and OZR (n = 6, ANOVA p = 0.002-0.0001); (ii) all the effects of 15 and 25 mM d-glucose are attenuated in VSMC from OZR vs. LZR (p = 0.0001); (iii) l-glucose and mannitol reproduce the VEGF-A(164) modulation induced by d-glucose in VSMC from both LZR and OZR. Thus, glucose increases via an osmotic mechanism VEGF synthesis and secretion in VSMC, an effect attenuated in the presence of insulin resistance. 相似文献
49.
Russo Krauss I Sica F Mattia CA Merlino A 《International journal of molecular sciences》2012,13(3):3782-3800
Serum albumin is one of the most widely studied proteins. It is the most abundant protein in plasma with a typical concentration of 5 g/100 mL and the principal transporter of fatty acids in plasma. While the crystal structures of human serum albumin (HSA) free and in complex with fatty acids, hemin, and local anesthetics have been characterized, no crystallographic models are available on bovine serum albumin (BSA), presumably because of the poor diffraction power of existing hexagonal BSA crystals. Here, the crystallization and diffraction data of a new BSA crystal form, obtained by the hanging drop method using MPEG 5K as precipitating agent, are presented. The crystals belong to space group C2, with unit-cell parameters a = 216.45 Å, b = 44.72 Å, c = 140.18 Å, β = 114.5°. Dehydration was found to increase the diffraction limit of BSA crystals from ~8 Å to 3.2 Å, probably by improving the packing of protein molecules in the crystal lattice. These results, together with a survey of more than 60 successful cases of protein crystal dehydration, confirm that it can be a useful procedure to be used in initial screening as a method of improving the diffraction limits of existing crystals. 相似文献
50.
Dr. Tommaso Felicetti Prof. Giuseppe Manfroni Prof. Violetta Cecchetti Dr. Rolando Cannalire 《ChemMedChem》2020,15(24):2391-2419
Infections by flaviviruses, such as Dengue, West Nile, Yellow Fever and Zika viruses, represent a growing risk for global health. There are vaccines only for few flaviviruses while no effective treatments are available. Flaviviruses share epidemiological, structural, and ecologic features and often different viruses can co-infect the same host. Therefore, the identification of broad-spectrum inhibitors is highly desirable either for known flaviviruses or for viruses that likely will emerge in the future. Strategies targeting both virus and host factors have been pursued to identify broad-spectrum antiflaviviral agents. In this review, we describe the most promising and best characterized targets and their relative broad-spectrum inhibitors, identified by drug repurposing/libraries screenings and by focused medicinal chemistry campaigns. Finally, we discuss about future strategies to identify new broad-spectrum antiflavivirus agents. 相似文献