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291.
Beate Kuhnt 《Informatik-Spektrum》1997,20(1):29-32
Eingegangen am 29.07.1996, in überarbeiteter Form am 11.12.1996 相似文献
292.
Petr P. KhlyabichAuthor Vitae Beate BurkhartAuthor VitaeAndrey E. RudenkoAuthor Vitae Barry C. Thompson 《Polymer》2013
Polymer–fullerene bulk heterojunction (BHJ) solar cells have consistently been at the forefront of the growing field of organic photovoltaics (OPV). The enduring vision of OPV is the promise of combining a simple, low-cost approach with an efficient, flexible, lightweight platform. While efficiencies have improved remarkably over the last decade through advances in device design, mechanistic understanding, and evolving chemical structural motifs, steps forward have often been tied to a loss of simplicity and a deviation from the central vision of OPV. Within the context of active layer optimization, our focus is to target high efficiency while maintaining simplicity in polymer design and active layer processing. To highlight this strategy, this feature article focuses on our work on random poly(3-hexylthiophene) (P3HT) analogs and their application in binary and ternary blend polymer–fullerene solar cells. These random conjugated polymers are conceptually based on combining simple monomers strategically to influence polymer properties as opposed to the synthesis of highly tailored and synthetically complex monomers. The ternary blend approach further exemplifies the focus on device simplicity by targeting efficiencies that are competitive with complex tandem solar cells, but within the confines of a single active-layer processing step. These research directions are described within the broader context of recent progress in the field of polymer–fullerene BHJ solar cells. 相似文献
293.
Murdoch TB Fu H MacFarlane S Sydora BC Fedorak RN Slupsky CM 《Analytical chemistry》2008,80(14):5524-5531
Inflammatory bowel disease (IBD) is a chronic debilitating disorder that is thought to have both genetic and environmental contributors. Commensal microflora have been shown to play a key part in the disease process. Metabolomics, the study of large numbers of small molecule metabolites, has demonstrated that disease and/or changes in gut microbial composition modulate mammalian urine metabolite fingerprints. The aim of this project was to associate the development of IBD with specific changes in a mouse urinary metabolic fingerprint. Interleukin-10 (IL-10) gene-deficient mice were raised alongside age-matched 129/SvEv controls in conventional housing. Urine samples (22 h) were collected at ages 4, 6, 8, 12, 16, and 20 weeks. Metabolite concentrations were derived from analysis of nuclear magnetic resonance spectra, and both multivariate and two-way analysis of variance (ANOVA) statistical techniques were applied to the resulting data. Principal component analysis and partial least-squares-discriminant analysis of urine derived from the control and IL-10 gene-deficient mice revealed that while both groups initially had similar metabolic profiles, they diverged substantially with the onset of IBD as assessed through external phenotypic changes. Several metabolites, including trimethylamine (TMA) and fucose, changed dramatically in the IL-10 gene-deficient mice following 8 weeks of age, concomitant with the known timeline for development of severe histological injury. This study illustrates that metabolomics is effective at distinguishing IBD using urinary metabolite profiles. 相似文献
294.
Pagel K Seri T von Berlepsch H Griebel J Kirmse R Böttcher C Koksch B 《Chembiochem : a European journal of chemical biology》2008,9(4):531-536
The common feature of proteins involved in many neurodegenerative diseases is their ability to adopt at least two different stable conformations. The conformational transition that shifts the equilibrium from the functional, mostly partially alpha-helical structure, to the beta-sheet rich amyloid can be triggered by numerous factors, such as mutations in the primary structure or changes in the environment. We present a set of model peptides that, without changes in their primary structure, react in a predictable fashion in the presence of transition metal ions by adopting different conformations and aggregate morphologies. These de novo designed peptides strictly follow the characteristic heptad repeat of the alpha-helical coiled-coil structural motif. Furthermore, domains that favor beta-sheet formation have been incorporated to make the system prone to amyloid formation. As a third feature, histidine residues create sensitivity towards the presence of transition metal ions. CD spectroscopy, ThT fluorescence experiments, and transmission electron microscopy were used to characterize peptide conformation and aggregate morphology in the presence of Cu2+ and Zn2+. Furthermore, the binding geometry within peptide-Cu2+ complexes was characterized by electron paramagnetic resonance spectroscopy. 相似文献
295.
296.
Relaxin acts as a pregnancy-specific signal in feline species, but specific information about protein structure and binding is essential for the improvement of pregnancy diagnosis in endangered feline species, like the Iberian lynx. To generate a felid-specific relaxin antibody, the DNA and protein sequences of lynx and cat were determined and peptides were chosen for antibody generation. In addition, relaxin and relaxin receptor (RXFP1) mRNA expressions were measured in uteri and ovaries of pregnant domestic cats and lynx placentae. Using real-time PCR and immunohistochemistry, it was established that feline placenta is the main source of relaxin during pregnancy. In other tested tissues, relaxin mRNA expression was weak. The RXFP1 mRNA expression was found mainly in cat uterine tissue and feline placentae. It was assumed that these tissues were main targets for relaxin. In the ovary, relaxin immunostaining was associated with blood vessels, signifying its role in vascularization. 相似文献
297.
Jrg Lange Werner Rack Aneta Kurpiela Felicitas Rdel Beate Hrnel‐Metzger 《Stahlbau》2010,79(10):720-728
Der folgende Beitrag gibt einen Überblick über den Stahlleichtbau mit Verbundelementen. Im Vordergrund stehen hierbei Bauteile mit Blechdicken < 3 mm, die im Verbund mit OSB‐ oder Gipskartonplatten wirken. Durch die Verbundwirkung ergeben sich nennenswerte Verbesserungen der Tragfähigkeit und der Gebrauchstauglichkeit sowie der bauphysikalischen Eigenschaften. Weiterhin werden Sandwichelemente behandelt. Lightweight steel construction with composite elements. This paper contains an overview of lightweight steel structures acting compositely with other materials. Primarily members with wall thicknesses below 3 mm are covered. They act together with OSB‐ or gypsum‐boards. This leads to a significant improvement of the ultimate load as well as of the serviceability and building physics aspects. Furthermore sandwich panels are discussed. 相似文献
298.
For the production of spliced veneers the veneers are coated with thin cellulose fleece or special paper layers, and thereby
thin composites are generated. This article describes the mechanical properties of such a composite material consisting of
0.35 mm beech (Fagus sylvatica L.) veneer and a 0.12 mm cellulose fleece bonded with a PVAc adhesive. 相似文献
299.
Linda Waldherr Maria Seitanidou Marie Jakešová Verena Handl Sophie Honeder Marta Nowakowska Tamara Tomin Meysam Karami Rad Tony Schmidt Joachim Distl Ruth Birner-Gruenberger Gord von Campe Ute Schäfer Magnus Berggren Beate Rinner Martin Asslaber Nassim Ghaffari-Tabrizi-Wizsy Silke Patz Daniel T. Simon Rainer Schindl 《Advanced Materials Technologies》2021,6(5):2001302
Successful treatment of glioblastoma multiforme (GBM), the most lethal tumor of the brain, is presently hampered by (i) the limits of safe surgical resection and (ii) “shielding” of residual tumor cells from promising chemotherapeutic drugs such as Gemcitabine (Gem) by the blood brain barrier (BBB). Here, the vastly greater GBM cell-killing potency of Gem compared to the gold standard temozolomide is confirmed, moreover, it shows neuronal cells to be at least 104-fold less sensitive to Gem than GBM cells. The study also demonstrates the potential of an electronically-driven organic ion pump (“GemIP”) to achieve controlled, targeted Gem delivery to GBM cells. Thus, GemIP-mediated Gem delivery is confirmed to be temporally and electrically controllable with pmol min−1 precision and electric addressing is linked to the efficient killing of GBM cell monolayers. Most strikingly, GemIP-mediated GEM delivery leads to the overt disintegration of targeted GBM tumor spheroids. Electrically-driven chemotherapy, here exemplified, has the potential to radically improve the efficacy of GBM adjuvant chemotherapy by enabling exquisitely-targeted and controllable delivery of drugs irrespective of whether these can cross the BBB. 相似文献
300.
Xin Fan Yang Gao Fan Yang Jian Liang Low Lei Wang Beate Paulus Yi Wang Andrej Trampuz Chong Cheng Rainer Haag 《Advanced functional materials》2023,33(33):2301986
Diabetic ulcers induced by multidrug-resistant (MDR) bacteria have severely endangered diabetic populations. These ulcers are very challenging to treat because the local high glucose concentration can both promote bacterial growth and limit the immune system's bactericidal action. Herein, a glucose oxidase-peroxidase (GOx-POD) dual-enzyme mimetic (DEM) bionanocatalyst, Au@CuBCats is synthesized to simultaneously control glucose concentration and bacteria in diabetic ulcers. Specifically, the AuNPs can serve as GOx mimics and catalyze the oxidation of glucose for the formation of H2O2; the H2O2 can then be further catalytically converted into OH via the POD-mimetic copper single atoms. Notably, the unique copper single atoms coordinated by one oxygen and two nitrogen atoms (CuN2O1) exhibit better POD catalytic performance than natural peroxidase. Further DFT calculations are conducted to study the catalytic mechanism and reveal the advantage of this CuN2O1 structure as compared to other copper single-atom sites. Both in vitro and in vivo experiments confirm the outstanding antibacterial therapeutic efficacy of the DEM bionanocatalyst. This new bionanocatalyst will provide essential insights for the next generation of antibiotic-free strategies for combating MDR bacterial diabetic ulcers, and also offer inspiration for designing bionanocatalytic cascading medicines. 相似文献