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221.
In this paper we study the monotonicity of the ratio of two hyperelliptic Abelian integrals $I_0(h)=\oint_{\Gamma_h}ydx$ and $I_1(h)=\oint_{\Gamma_h}xydx$ for which $\Gamma_h$ is a continuous family of periodic orbits of a Newtonian system with Hamiltonian function of the form $H(x,y)=\frac{1}{2}{y^2}\pm \Psi(x)$, where $\Psi$ is an arbitrary even function of degree six.  相似文献   
222.
The endoplasmic reticulum (ER) plays a multifunctional role in lipid biosynthesis, calcium storage, protein folding, and processing. Thus, maintaining ER homeostasis is essential for cellular functions. Several pathophysiological conditions and pharmacological agents are known to disrupt ER homeostasis, thereby, causing ER stress. The cells react to ER stress by initiating an adaptive signaling process called the unfolded protein response (UPR). However, the ER initiates death signaling pathways when ER stress persists. ER stress is linked to several diseases, such as cancer, obesity, and diabetes. Thus, its regulation can provide possible therapeutic targets for these. Current evidence suggests that chronic hyperglycemia and hyperlipidemia linked to type II diabetes disrupt ER homeostasis, thereby, resulting in irreversible UPR activation and cell death. Despite progress in understanding the pathophysiology of the UPR and ER stress, to date, the mechanisms of ER stress in relation to type II diabetes remain unclear. This review provides up-to-date information regarding the UPR, ER stress mechanisms, insulin dysfunction, oxidative stress, and the therapeutic potential of targeting specific ER stress pathways.  相似文献   
223.
A comparative microwave assisted and conventional synthetic strategies were applied to synthesize heterocyclic 1,3,4-oxadiazole analogues as active anti-enzymatic agents. Green synthesis of compound 1 was achieved by stirring 4-methoxybenzenesulfonyl chloride ( a ) and ethyl piperidine-4-carboxylate ( b ). Compound 1 was converted into respective hydrazide ( 2 ) by hydrazine and then into 1,3,4-oxadiazole ( 3 ) by CS2 on reflux. The electrophiles, N-alkyl/aralkyl/aryl-2-bromopropanamides ( 6a–p ) were synthesized and converted to N-alkyl/aralkyl/aryl-2-propanamide derivatives ( 7a–p ) by reaction with 3 under green chemistry. Microwave assisted method was found to be effective relative to conventional method. 13C-NMR, 1H-NMR and IR techniques were availed to corroborate structures of synthesized compounds and then subjected to screening against lipoxygenase (LOX), α-glucosidase, acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes. A number of compounds presented better potential against these enzymes. The most active compounds against LOX and α-glucosidase enzymes were subjected to molecular docking study to explore their interactions with the active sites of the enzymes.  相似文献   
224.
Cellulose - In this research work, we present a synthesis of silver and cobalt bimetal nanoparticles stabilized by a carboxymethyl cellulose biopolymer (CMC-AgCo) and its coating on a cellulose...  相似文献   
225.
Structural Chemistry - The antibiotic para-aminosalicylic acid (PAS) is decomposed into its decarboxylated product, meta-aminophenol, with a series of toxicity symptoms including hemolytic anemia....  相似文献   
226.
A carbon‐paste electrode modified with 2,7‐bis(ferrocenyl ethyl)fluoren‐9‐one and carbon nanotubes was used for the sensitive voltammetric determination of levodopa (LD). The electrochemical response characteristics of the modified electrode toward LD, uric acid (UA) and folic acid (FA) were investigated. The results showed an efficient catalytic activity of the electrode for the electrooxidation of LD, which leads to lowering its overpotential by more than 320 mV. The modified electrode exhibits an efficient electron mediating behavior together with well‐separated oxidation peaks for LD, UA and FA. Also, the modified electrode was used for determination of LD in some real samples.  相似文献   
227.
This paper deals with a new two-parameter lifetime distribution with increasing failure rate. This distribution is constructed as a distribution of a random sum of independent exponential random variables when the sample size has a zero truncated binomial distribution. Various statistical properties of the distribution are derived. We estimate the parameters by maximum likelihood and obtain the Fisher information matrix. Simulation studies show the performance of the estimators. Also, estimation of the parameters is considered in the presence of censoring. A real data set is analyzed for illustrative purposes and it is noted that the distribution is a good competitor to the gamma, Weibull, exponentiated exponential, weighted exponential and Poisson-exponential distributions for this data set.  相似文献   
228.
2-(Phenylthio)benzoates containing a remote halide function are regioselectively prepared by ‘[3+3] cyclization/homo-Michael’ reactions of 1-methoxy-1-trimethylsilyloxy-3-phenylthio-1,3-butadienes with 1,1-diacylcyclopropanes.  相似文献   
229.
A novel deamination of 2-alkyl/aryl 3-amino-4(3H)-quinazolinones series using aqueous KMnO4 under thermal condition and microwave irradiation is described. Compared to thermal condition, significantly higher yields in much shorter times were observed for reactions under microwave irradiation. A plausible mechanism has been proposed for the oxidative water-promoted deamination.  相似文献   
230.
The electrocatalytic reduction of nitrite has been studied by poly(ortho‐toluidine) films modified carbon paste electrode (P‐OT/MCPE). Cyclic voltammetry and chronoamperometry techniques were used to investigate the suitability of poly(ortho‐toluidine) as a mediator for the electrocatalytic nitrite reduction in aqueous solution with various pH. Results showed that pH 0.00 is the most suitable for this purpose. In the optimum pH, the reduction of nitrite occurs at a potential about 600 mV more positive than unmodified carbon paste electrode. The catalytic reaction rate constant, (kh), was calculated 8.68×102 M?1 s?1 by the data of chronoamperometry. The catalytic reduction peak current was linearly dependent on the nitrite concentration and the linearity range obtained was 5.00×10?4 M–1.90×10?2 M. Detection limit has been found to be 3.38×10?4 M (2σ). This method has been successfully employed for quantification of nitrite in real sample.  相似文献   
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