全文获取类型
收费全文 | 3176篇 |
免费 | 544篇 |
国内免费 | 478篇 |
专业分类
化学 | 2336篇 |
晶体学 | 33篇 |
力学 | 225篇 |
综合类 | 45篇 |
数学 | 317篇 |
物理学 | 1242篇 |
出版年
2024年 | 8篇 |
2023年 | 56篇 |
2022年 | 112篇 |
2021年 | 106篇 |
2020年 | 139篇 |
2019年 | 104篇 |
2018年 | 116篇 |
2017年 | 117篇 |
2016年 | 146篇 |
2015年 | 131篇 |
2014年 | 181篇 |
2013年 | 222篇 |
2012年 | 222篇 |
2011年 | 301篇 |
2010年 | 206篇 |
2009年 | 211篇 |
2008年 | 216篇 |
2007年 | 198篇 |
2006年 | 173篇 |
2005年 | 124篇 |
2004年 | 109篇 |
2003年 | 85篇 |
2002年 | 78篇 |
2001年 | 69篇 |
2000年 | 60篇 |
1999年 | 76篇 |
1998年 | 66篇 |
1997年 | 51篇 |
1996年 | 48篇 |
1995年 | 51篇 |
1994年 | 52篇 |
1993年 | 48篇 |
1992年 | 48篇 |
1991年 | 38篇 |
1990年 | 41篇 |
1989年 | 32篇 |
1988年 | 25篇 |
1987年 | 32篇 |
1986年 | 23篇 |
1985年 | 13篇 |
1984年 | 8篇 |
1983年 | 11篇 |
1982年 | 12篇 |
1981年 | 5篇 |
1980年 | 7篇 |
1979年 | 5篇 |
1977年 | 3篇 |
1976年 | 2篇 |
1975年 | 2篇 |
1957年 | 4篇 |
排序方式: 共有4198条查询结果,搜索用时 15 毫秒
151.
V. Cozan A. Butuc A. Stoleru M. Rusu Yushan Ni Mengxian Ding 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(12):899-906
Abstract New copolyether sulfones containing 2,5-bis(4-oxo-benzylidene)-cyclopentanone moieties were prepared in the conventional literature manner by condensing the dipotassium salts of 2,5-bis(4-hydroxyphenzyl- idene)cyclopentanone (I) and 2, 2-bis(4-hydroxyphenyl)propane (Bisphenol A, III) with 4,4′-dichlorodiphenyl sulfone (II), or by condensing the dipotassium salts of I with chlorine-terminated Bisphenol A-4,4′-di-chlorodiphenylsulfone copolymers (V). The resulting copolyether sulfones were confirmed by IR, viscometry, DSC measurements, thermooptical (TOA), and thermogravimetric analysis (TGA). 相似文献
152.
Liyong Chen Mingzu Zhang Zhuang Liu Zixu Gu Yingfeng Tu Peihong Ni 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(11):862-871
A biocompatible complex has been prepared as gene carrier via electrostatic interaction, which is composed of a polycation, that is, poly[(dimethylamino)ethyl methacrylate] end-capped with cholesterol moiety (Chol-PDMAEMA30), along with a polyanion named poly(aspartic acid)-grafted-poly(ethylene glycol) (PASP-g-PEG). The complexes have less cytotoxicity compared to the case of alone Chol-PDMAEMA30 or branched polyethylenimine (PEI) system. In the present study, biocompatible complexes have been prepared as gene carrier via electrostatic interaction, which is composed of a polycation, that is, poly[(dimethylamino)ethyl methacrylate] end-capped with cholesterol moiety (Chol-PDMAEMA30), along with a polyanion named poly(aspartic acid)-grafted-poly(ethylene glycol) (PASP-g-PEG). We first synthesized polysuccinimide (PSI) via condensation polymerization of aspartic acid, and then used PEG-NH2 to react with the partial pentacyclic rings of PSI to yield a kind of graft copolymer polysuccinimide-grafted-poly(ethylene glycol) (PSI-g-PEG). After hydrolysis of the residual succinimide units, a new biodegradable and biocompatible graft copolymer PASP-g-PEG was prepared successfully. Chol-PDMAEMA30 was synthesized via oxyanion-initiated polymerization, as reported in our previous literature. We investigated the interactions between every pair among calf thymus DNA, Chol-PDMAEMA30, and PASP-g-PEG by agarose gel retardation assay. The results indicate that the prepared complexes could completely bind DNA and may become more stable during systemic circulation. The complexes have less cytotoxicity compared to the case of alone Chol-PDMAEMA30 or branched polyethylenimine (PEI) system. Furthermore, the physicochemical properties of the complexes were also investigated by zeta potential, transmission electron microscopy (TEM) and dynamic light scattering (DLS) measurements. These biodegradable and biocompatible polymeric carriers have potential applications in gene delivery. 相似文献
153.
154.
155.
156.
Lingjuan Xiong Rong Wang Chen Liang Fangqi Cao Yulan Rao Xin Wang Libo Zeng Chunfang Ni Haiying Ye Yurong Zhang 《Analytical and bioanalytical chemistry》2013,405(30):9805-9816
Ecgonine is suggested to be a promising marker of cocaine (COC) ingestion. A combined mass spectrometry (MS) and tandem MS (MS/MS) method was developed to simultaneously determine ecgonine and seven other metabolites of cocaine in human urine and whole blood with ultra-high-pressure liquid chromatography coupled with quadrupole time-of-flight mass spectrometry. The compounds were extracted from as little as 100 μL of sample by solid-phase extraction with a 96-well μElution solid-phase extraction plate. The protonated molecules or fragment ions at accurate mass acquired in MS mode were used to quantify specific analytes, following by dedicated MS/MS identification. The assay was linear in the range from 5 to 50-100 ng/mL for urine samples, except for ecgonine methyl ester (10-200 ng/mL) and ecgonine (40-400 ng/mL), and was linear from 1-2 to 50 ng/mL for whole blood samples, except for ecgonine methyl ester (20-1,000 ng/mL) and ecgonine (40-2,000 ng/mL). The correlation coefficients were all greater than 0.99. The limits of detection ranged from 0.2 to 16 ng/mL, and the lower limits of quantification ranged from 1 to 40 ng/mL. The repeatability and intermediate precision were 18.1 % or less. The accuracy was in the range from 80.0 to 122.9 %, process efficiencies were in the range from 8.6 to 177.4 %, matrix effects were in the range from 28.7 to 171.0 %, and extraction recoveries were in the range from 41.0 to 114.3 %, except for ecgonine (12.8 % and 9.3 % at low and high concentrations, respectively). This method was highly sensitive in comparison with previously published methods. The validated method was successfully applied to the analysis of real samples derived from forensic cases, and the results verified that, on the basis of data from four positive samples, ecgonine is a promising marker of cocaine ingestion. Figure
Procedure for the determination of ecgonine and seven other cocaine metabolites in human urine and whole blood using a combined mass spectrometry and tandem MS method aIer the solid‐phase extraction of the anaytes 相似文献
157.
Irene C. Perez Caroline Le Guiner Weiyi Ni Jennifer Lyles Philippe Moullier Richard O. Snyder 《Analytical and bioanalytical chemistry》2013,405(30):9641-9653
Athletes who illicitly use drugs to enhance their athletic performance are at risk of being banned from sports competitions. Consequently, some athletes may seek new doping methods that they expect to be capable of circumventing detection. With advances in gene transfer vector design and therapeutic gene transfer, and demonstrations of safety and therapeutic benefit in humans, there is an increased probability of the pursuit of gene doping by athletes. In anticipation of the potential for gene doping, assays have been established to directly detect complementary DNA of genes that are top candidates for use in doping, as well as vector control elements. The development of molecular assays that are capable of exposing gene doping in sports can serve as a deterrent and may also identify athletes who have illicitly used gene transfer for performance enhancement. PCR-based methods to detect foreign DNA with high reliability, sensitivity, and specificity include TaqMan real-time PCR, nested PCR, and internal threshold control PCR. 相似文献
158.
Maria Lorna A. De Leoz Shuai Wu John S. Strum Milady R. Niñonuevo Stephanie C. Gaerlan Majid Mirmiran J. Bruce German David A. Mills Carlito B. Lebrilla Mark A. Underwood 《Analytical and bioanalytical chemistry》2013,405(12):4089-4105
Human milk oligosaccharides (HMOs), though non-nutritive to the infant, shape the intestinal microbiota and protect against pathogens during early growth and development. Infant formulas with added galacto-oligosaccharides have been developed to mimic the beneficial effects of HMOs. Premature infants have an immature immune system and a leaky gut and are thus highly susceptible to opportunistic infections. A method employing nanoflow liquid chromatography time-of-flight mass spectrometry (MS) is presented to simultaneously identify and quantify HMOs in the feces and urine of infants, of which 75 HMOs have previously been fully structurally elucidated. Matrix-assisted laser desorption/ionization Fourier transform ion cyclotron resonance MS was employed for high-resolution and rapid compositional profiling. To demonstrate this novel method, samples from mother–infant dyads as well as samples from infants receiving infant formula fortified with dietary galacto-oligosaccharides or probiotic bifidobacteria were analyzed. Ingested oligosaccharides are demonstrated in high abundance in the infant feces and urine. While the method was developed to examine specimens from preterm infants, it is of general utility and can be used to monitor oligosaccharide consumption and utilization in term infants, children, and adults. This method may therefore provide diagnostic and therapeutic opportunities. Figure
Quantification of human milk oligosacchairdes in the milk, feces, and urine of a mother-infant dyad by MALDI FT-ICR (spectra) and nano-LC MS (pie charts) 相似文献
159.
Der‐Lii M. Tzou Lin‐Kai Ni Mei‐Man Chen Min‐Chuan Chiou Li‐Chou Chen Shan‐Te Hsu Kuo‐Lung Ku Chien‐Chung Cheng 《中国化学会会志》2013,60(9):1107-1112
Solid‐state Nuclear Magnetic Resonance (ss‐NMR) 13C single‐pulse excitation spectroscopy in combination with the magic‐angle spinning (MAS) technique was applied to a series of Phalaenopsis tissues, including the leaf, sheath, stem, and root, at different growth and spiking periods. Compared with{1H}/13C cross‐polarization MAS spectra, the 13C single‐pulse excitation MAS spectra displayed very distinct spectral patterns, recognizable as fingerprints of the tissues studied. 1Here, we demonstrate that solid‐state 13C single‐pulse excitation NMR spectroscopy provides a direct and robust analytical tool for studying the various tissues of Phalaenopsis in different growth and spiking induction periods. 相似文献
160.
Mao Chen Ting Zhao Zhong‐Xin Zhu Chao Niu Dan‐dan Ruan Mao‐Wei Ni Xuan Zhou Li‐Tai Jin 《Electrophoresis》2013,34(24):3277-3286
An improved Stains‐All (ISA) staining method for phosphoproteins in SDS‐PAGE was described. Down to 0.5–1 ng phosphoproteins (α‐casein, β‐casein, or phosvitin) can be successfully selectively detected by ISA stain, which is approximately 120‐fold higher than that of original Stains‐All stain, but is similar to that of commonly used Pro‐Q Diamond stain. Furthermore, unlike the original Stains‐All protocol that was time consuming and light unstable, ISA stain could be completed within 60 min without resorting to protect the gels from light during the whole staining procedure. According to the results, it is concluded that ISA stain is a rapid, sensitive, specific, and economic staining method for a broad application to the research of phosphoproteins. 相似文献