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排序方式: 共有247条查询结果,搜索用时 15 毫秒
241.
Yun Y Shanov V Tu Y Subramaniam S Schulz MJ 《The journal of physical chemistry. B》2006,110(47):23920-23925
Highly aligned arrays of multiwalled carbon nanotube (MWCNT) on layered Si substrates have been synthesized by chemical vapor deposition (CVD). The effect of the substrate design and the process parameters on the growth mechanism were studied. Adding water vapor to the reaction gas mixture of hydrogen and ethylene enhanced the growth which led to synthesis of longer CNT arrays with high density. Environmental scanning electron microscopy (ESEM), energy-dispersive spectroscopy (EDS), and atomic force microscopy (AFM) were used to analyze the CNT morphology and composition. Quadrupole mass spectroscopy (QMS) provided in-situ information on the gas spices within the reaction zone. On the basis of results, we verified the top growth mechanism and evaluated the reason of decline and stoppage of the CNT growth after extended period of deposition. Multilayered Si substrates with a top film of Al2O3, having appropriate roughness, provide favorable conditions to form catalyst islands with uniform distribution and size. Using water-assisted CVD process and optimized substrate design, our group succeeded to grow vertically aligned, patterned MWCNT up to 4-mm long. The arrays were of high purity and weak adhesion which allowed to be peeled off easily from the substrate. 相似文献
242.
Rozkiewicz DI Kraan Y Werten MW de Wolf FA Subramaniam V Ravoo BJ Reinhoudt DN 《Chemistry (Weinheim an der Bergstrasse, Germany)》2006,12(24):6290-6297
We describe a straightforward approach to the covalent immobilization of cytophilic proteins by microcontact printing, which can be used to pattern cells on substrates. Cytophilic proteins are printed in micropatterns on reactive self-assembled monolayers by using imine chemistry. An aldehyde-terminated monolayer on glass or on gold was obtained by the reaction between an amino-terminated monolayer and terephthaldialdehyde. The aldehyde monolayer was employed as a substrate for the direct microcontact printing of bioengineered, collagen-like proteins by using an oxidized poly(dimethylsiloxane) (PDMS) stamp. After immobilization of the proteins into adhesive "islands", the remaining areas were blocked with amino-poly(ethylene glycol), which forms a layer that is resistant to cell adhesion. Human malignant carcinoma (HeLa) cells were seeded and incubated onto the patterned substrate. It was found that these cells adhere to and spread selectively on the protein islands, and avoid the poly(ethylene glycol) (PEG) zones. These findings illustrate the importance of microcontact printing as a method for positioning proteins at surfaces and demonstrate the scope of controlled surface chemistry to direct cell adhesion. 相似文献
243.
Subramaniam D Libisch F Li Y Pauly C Geringer V Reiter R Mashoff T Liebmann M Burgdörfer J Busse C Michely T Mazzarello R Pratzer M Morgenstern M 《Physical review letters》2012,108(4):046801
Using low-temperature scanning tunneling spectroscopy, we map the local density of states of graphene quantum dots supported on Ir(111). Because of a band gap in the projected Ir band structure around the graphene K point, the electronic properties of the QDs are dominantly graphenelike. Indeed, we compare the results favorably with tight binding calculations on the honeycomb lattice based on parameters derived from density functional theory. We find that the interaction with the substrate near the edge of the island gradually opens a gap in the Dirac cone, which implies soft-wall confinement. Interestingly, this confinement results in highly symmetric wave functions. Further influences of the substrate are given by the known moiré potential and a 10% penetration of an Ir surface resonance into the graphene layer. 相似文献
244.
The age of information (AoI) is now well established as a metric that measures the freshness of information delivered to a receiver from a source that generates status updates. This paper is motivated by the inherent value of packets arising in many cyber-physical applications (e.g., due to precision of the information content or an alarm message). In contrast to AoI, which considers all packets are of equal importance or value, we consider status update systems with update packets carrying values as well as their generated time stamps. A status update packet has a random initial value at the source and a deterministic deadline after which its value vanishes (called ultimate staleness). In our model, the value of a packet either remains constant until the deadline or decreases in time (even after reception) starting from its generation to the deadline when it vanishes. We consider two metrics for the value of information (VoI) at the receiver: sum VoI is the sum of the current values of all packets held by the receiver, whereas packet VoI is the value of a packet at the instant it is delivered to the receiver. We investigate various queuing disciplines under potential dependence between value and service time and provide closed form expressions for both average sum VoI and packet VoI at the receiver. Numerical results illustrate the average VoI for different scenarios and relations between average sum VoI and average packet VoI. 相似文献
245.
Daniela Goncalves Monteiro Gautam Rishi Declan M. Gorman Guillaume Burnet Randy Aliyanto K. Johan Rosengren David M. Frazer V. Nathan Subramaniam Richard J. Clark 《Molecules (Basel, Switzerland)》2022,27(19)
The protein HFE (homeostatic iron regulator) is a key regulator of iron metabolism, and mutations in HFE underlie the most frequent form of hereditary haemochromatosis (HH-type I). Studies have shown that HFE interacts with transferrin receptor 1 (TFR1), a homodimeric type II transmembrane glycoprotein that is responsible for the cellular uptake of iron via iron-loaded transferrin (holo-transferrin) binding. It has been hypothesised that the HFE/TFR1 interaction serves as a sensor to the level of iron-loaded transferrin in circulation by means of a competition mechanism between HFE and iron-loaded transferrin association with TFR1. To investigate this, a series of peptides based on the helical binding interface between HFE and TFR1 were generated and shown to significantly interfere with the HFE/TFR1 interaction in an in vitro proximity ligation assay. The helical conformation of one of these peptides, corresponding to the α1 and α2 helices of HFE, was stabilised by the introduction of sidechain lactam “staples”, but this did not result in an increase in the ability of the peptide to disrupt the HFE/TFR1 interaction. These peptides inhibitors of the protein–protein interaction between HFE and TFR1 are potentially useful tools for the analysis of the functional role of HFE in the regulation of hepcidin expression. 相似文献
246.
247.