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471.
Dr. Deborah Quaglio Laura Mangiardi Dr. Giulia Venditti Cristina Del Plato Francesca Polli Dr. Francesca Ghirga Prof. Gabriele Favero Prof. Marco Pierini Prof. Bruno Botta Prof. Franco Mazzei 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(38):8400-8406
One of the main problems in the development of immunosensors is to overcome the complexity of binding antibodies to the sensor surface. Most immobilizing methods lead to a random orientation of antibodies with a lower binding site density and immunoaffinity. In order to control the orientation of antibody immobilization, several resorc[4]arene derivatives were designed and synthesized. After the spectroscopic characterization of resorc[4]arene self-assembled monolayers (SAMs) onto gold films, the surface coverage and the orientation of insulin antibody (Ab-Ins) were assessed by a surface plasmon resonance (SPR) technique and compared with a random immobilization method. Experimental results combined with theoretical studies confirmed the dipole–dipole interaction as an important factor in antibody orientation and demonstrated the importance of the upper rim functionalization of resorcarenes. Accordingly, resorcarene 5 showed a major binding force towards Ab-Ins thanks to the H-bond interactions with the amine protein groups. Based on these findings, the resorcarene-based immunosensor is a powerful system with improved sensitivity providing new insight into sensor development. 相似文献
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473.
Electrochemical detection of nonelectroactive contaminants can be successfully faced via the use of indirect detection strategies. These strategies can provide sensitive and selective responses often coupled with portable and user-friendly analytical tools. Indirect detection strategies are usually based on the change in the signal of an electroactive probe, induced by the presence of the target molecule at a modified electrode. This critical review aims at addressing the developments in indirect electrosensing strategies for nonelectroactive contaminants in food and environmental analysis in the last few years. Emphasis is given to the strategy design, the electrode modifiers used and the feasibility of technological transfer. 相似文献
474.
Giulia Siciliano Dr. Michela Corricelli Dr. Rosa Maria Iacobazzi Prof. Fabio Canepa Dr. Daniela Comegna Prof. Elisabetta Fanizza Dr. Annarita Del Gatto Dr. Michele Saviano Prof. Valentino Laquintana Dr. Roberto Comparelli Dr. Giuseppe Mascolo Dr. Sapia Murgolo Dr. Marinella Striccoli Prof. Angela Agostiano Prof. Nunzio Denora Dr. Laura Zaccaro Prof. M. Lucia Curri Dr. Nicoletta Depalo 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(48):11048-11059
Efforts are made to perform an early and accurate detection of hepatocellular carcinoma (HCC) by simultaneous exploiting multiple clinically non-invasive imaging modalities. Original nanostructures derived from the combination of different inorganic domains can be used as efficient contrast agents in multimodal imaging. Superparamagnetic iron oxide nanoparticles (SPIONs) and Au nanoparticles (NPs) possess well-established contrasting features in magnetic resonance imaging (MRI) and X-ray computed tomography (CT), respectively. HCC can be targeted by using specific carbohydrates able to recognize asialoglycoprotein receptor 1 (ASGPR1) overexpressed in hepatocytes. Here, two different thiocarbohydrate ligands were purposely designed and alternatively conjugated to the surface of Au-speckled silica-coated SPIONs NPs, to achieve two original nanostructures that could be potentially used for dual mode targeted imaging of HCC. The results indicated that the two thiocarbohydrate decorated nanostructures possess convenient plasmonic/superparamagnetic properties, well-controlled size and morphology and good selectivity for targeting ASGPR1 receptor. 相似文献
475.
Rosario Rodil José Benito Quintana Giulia Basaglia Maria Chiara Pietrogrande Rafael Cela 《Journal of chromatography. A》2010,1217(41):6428-6435
The development and performance evaluation of an analytical method dedicated to the comprehensive determination of the most relevant antioxidants and their metabolites in aqueous environmental samples is presented. This was achieved by a miniaturised solid-phase extraction (SPE) with 10 mg Oasis HLB cartridges, which allow to achieve a concentration factor of 200, reducing organic solvent wastes (1 mL of ethyl acetate suffices for complete elution) and SPE costs and eliminating the need for solvent evaporation that otherwise compromises the recoveries of butylated hydroxytoluene (BHT) and 2,6-di-tert-butylcyclohexa-2,5-diene-1,4-dione (BHT-Q). Analytes were then determined by gas chromatography–mass spectrometry (GC–MS) after derivatisation with N-methyl-N-(tert-butyldimethylsilyl)-trifluoroacetamide (MTBSTFA) in a single run. BHT-d7 and n-propyl-paraben-d4 (PrP-d4) were used as surrogate internal standards. These surrogates allowed obtaining relative recoveries in the 80–110% range for all analytes even with complex wastewater samples and LODs at the 2–44 ng L−1 level taking into account blank issues often associated to antioxidants analysis. The method was applied to sewage and river waters, showing that the seven analytes could be detected in raw wastewater. BHT and BHT-Q were the most concentrated species in that type of sample (in the 275–871 ng L−1 range). On the other hand two metabolites of BHT, 3,5-di-tert-butyl-4-hydroxybenzaldehyde (BHT-CHO) and 3,5-di-tert-butyl-4-hydroxybenzoic acid (BHT-COOH) appeared to be the most ubiquitous species, being found in all samples in the 10–150 ng L−1 concentration range. 相似文献
476.
Antonio Ranieri Marco Borsari Stefano Casalini Giulia Di Rocco Marco Sola Carlo Augusto Bortolotti Gianantonio Battistuzzi 《Molecules (Basel, Switzerland)》2021,26(16)
Cytochrome c is a small globular protein whose main physiological role is to shuttle electrons within the mitochondrial electron transport chain. This protein has been widely investigated, especially as a paradigmatic system for understanding the fundamental aspects of biological electron transfer and protein folding. Nevertheless, cytochrome c can also be endowed with a non-native catalytic activity and be immobilized on an electrode surface for the development of third generation biosensors. Here, an overview is offered of the most significant examples of such a functional transformation, carried out by either point mutation(s) or controlled unfolding. The latter can be induced chemically or upon protein immobilization on hydrophobic self-assembled monolayers. We critically discuss the potential held by these systems as core constituents of amperometric biosensors, along with the issues that need to be addressed to optimize their applicability and response. 相似文献
477.
Giulia Cavagnari Antonio Marigonda Khai T. Nguyen Fabio S. Priuli 《Set-Valued and Variational Analysis》2018,26(3):663-691
In this paper we formulate a time-optimal control problem in the space of probability measures. The main motivation is to face situations in finite-dimensional control systems evolving deterministically where the initial position of the controlled particle is not exactly known, but can be expressed by a probability measure on \(\mathbb {R}^{d}\). We propose for this problem a generalized version of some concepts from classical control theory in finite dimensional systems (namely, target set, dynamic, minimum time function...) and formulate an Hamilton-Jacobi-Bellman equation in the space of probability measures solved by the generalized minimum time function, by extending a concept of approximate viscosity sub/superdifferential in the space of probability measures, originally introduced by Cardaliaguet-Quincampoix in Cardaliaguet and Quincampoix (Int. Game Theor. Rev. 10, 1–16, 2008). We prove also some representation results linking the classical concept to the corresponding generalized ones. The main tool used is a superposition principle, proved by Ambrosio, Gigli and Savaré in Ambrosio et al. [3], which provides a probabilistic representation of the solution of the continuity equation as a weighted superposition of absolutely continuous solutions of the characteristic system. 相似文献
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