首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   7509篇
  免费   956篇
  国内免费   818篇
化学   4322篇
晶体学   76篇
力学   262篇
综合类   77篇
数学   897篇
物理学   1472篇
无线电   2177篇
  2024年   27篇
  2023年   177篇
  2022年   221篇
  2021年   281篇
  2020年   313篇
  2019年   318篇
  2018年   275篇
  2017年   298篇
  2016年   330篇
  2015年   402篇
  2014年   462篇
  2013年   664篇
  2012年   645篇
  2011年   633篇
  2010年   499篇
  2009年   526篇
  2008年   566篇
  2007年   477篇
  2006年   421篇
  2005年   314篇
  2004年   236篇
  2003年   185篇
  2002年   163篇
  2001年   107篇
  2000年   103篇
  1999年   91篇
  1998年   65篇
  1997年   52篇
  1996年   45篇
  1995年   22篇
  1994年   31篇
  1993年   29篇
  1992年   17篇
  1991年   14篇
  1990年   17篇
  1989年   17篇
  1988年   21篇
  1987年   14篇
  1986年   9篇
  1985年   17篇
  1984年   15篇
  1983年   14篇
  1982年   15篇
  1981年   11篇
  1980年   17篇
  1979年   11篇
  1978年   19篇
  1977年   15篇
  1976年   12篇
  1975年   9篇
排序方式: 共有9283条查询结果,搜索用时 144 毫秒
961.
血管瘤临床较常见,治疗手段多种,如冷冻、放射、手术及硬化剂注射等,但疗效均不甚满意。作者自1984年11月至1986年5月,用氩激光治疗血管瘤51例,随访6月至2年,疗效尚可。现报导如下:  相似文献   
962.
963.
Garwick's algorithm, for repacking LIFO lists stored in a contiguous block of memory, bases the allocation of remaining space upon both sharing and previous stack growth. A system whereby the weight applied to each method can be adjusted according to the current behavior of the stacks is discussed.We also investigate the problem of determining during memory repacking that the memory is used to saturation and the driving program should therefore be aborted. The tuning parameters studied here seem to offer no new grasp on this problem.  相似文献   
964.
13C spin–lattice relaxation times determined for the protonated carbons of carboxylic acids and methyl esters give indications of solution dimerization with the free acids. Since isopthalic and fumaric acids have two carboxyl functions they are able to polymerize in solution. Unlike the case for molecular aggregation due to weak hydrogen bonding in solution (e.g. alcohols, phenols), the 13C T1 values of mono carboxylic acids are not significantly affected by dilution to c. 10?2 M. Variable temperature T1 measurements of both the mono and dibasic acids gave activation energies for molecular reorientation of the order of 2 kcal mol?1, considerably lower than Ea for hydrogen bonded alcohols and comparable with Ea for the unassociated methyl esters of propionic and benzoic acids.  相似文献   
965.
966.
Shingyoji M  Gerion D  Pinkel D  Gray JW  Chen F 《Talanta》2005,67(3):472-478
CdSe nanocrystals, also called quantum dots (Qdots) are a novel class of fluorophores, which have a diameter of a few nanometers and possess high quantum yield, tunable emission wavelength and photostability. They are an attractive alternative to conventional fluorescent dyes. Quantum dots can be silanized to be soluble in aqueous solution under biological conditions, and thus be used in bio-detection. In this study, we established a novel Qdot-based technology platform that can perform accurate and reproducible quantification of protein concentration in a crude cell lysate background. Protein lysates have been spiked with a target protein, and a dilution series of the cell lysate with a dynamic range of three orders of magnitude has been used for this proof-of-concept study. The dilution series has been spotted in microarray format, and protein detection has been achieved with a sensitivity that is at least comparable to standard commercial assays, which are based on horseradish peroxidase (HRP)-catalyzed diaminobenzidine (DAB) chromogenesis. The data obtained through the Qdot method has shown a close linear correlation between relative fluorescence unit and relative protein concentration. The Qdot results are in almost complete agreement with data we obtained with the well-established HRP-DAB colorimetric array (R2 = 0.986). This suggests that Qdots can be used for protein quantification in microarray format, using the platform presented here.  相似文献   
967.
We present a novel means of transporting molecules in solution by applying a zero-time-average alternating motive force to the molecules, and perturbing the molecular drag coefficient synchronously with the applied force, thus causing a net drift in a direction determined by the phase of the alternating drag perturbation relative to the alternating force. We apply an electrophoretic form of the method to transport and concentrate DNA in a gel, such that all molecules migrate on average away from the nearest electrode and toward a central region. Since an electrode does not occupy this central region, this method presents the possibility of transporting and focusing DNA and other charged molecules in regions free from electrodes and the associated electrochemistry.  相似文献   
968.
In nonpolar solvents, the cyclic hexapeptide 2, which comprises alternating D-alpha-amino and D-alpha-aminoxy acids, adopts a C3-symmetric conformation with alternating eight (N--O turns)- and seven (gamma turns)-membered-ring hydrogen bonds. A series of anion-binding studies has suggested that 2 can function as an effective anion receptor that not only displays a high selectivity for chloride ions, but also the capability to extract chloride ions from aqueous solutions into organic phases.  相似文献   
969.
trans-[PtCl2(Am)(pip-pip)] x HCl complexes, where Am = ammine, methylamine and dimethylamine, react with ubiquitin to form 1:1 covalent adducts. The platinum complexes bind exclusively to Met1 of ubiquitin forming trans-[PtCl(S-Met1-Ub)(Am)(pip-pip)] adducts. These adducts are reactive towards nucleophiles and react with deoxyguanosine (dGMP) to form the ternary trans-[Pt(dGMP)(S-Met1-Ub) (Am)(pip-pip)] complex which is stable in water and even in the presence of excess glutathione (GSH). Reaction of trans-[PtCl(S-Met1-Ub)(Am)(pip-pip)] with GSH resulted in the rapid formation of the ternary complex trans-[Pt(GS)(S-Met1-Ub)(Am)(pip-pip)] which was not stable and slowly lost the platinum moiety; after 7 days the platinum moiety was completely removed and the native ubiquitin was regenerated.  相似文献   
970.
Liquid-core capsules have wide-ranging applications in the high-efficiency encapsulation and controlled release of drugs, dyes, enzymes, and other substrates. Their great utility has driven the rapid development of various preparation techniques. However, there remains no convenient technique for the preparation of submicrometer liquid-core capsules with shell thicknesses less than 100 nm. Here, we demonstrate a new interfacial free-radical polymerization approach for the straightforward preparation of liquid-core polymer capsules. Conceptually, this interfacial free-radical polymerization is analogous to the classical "nylon rope trick" wherein hydrophobic and hydrophilic monomers alternately copolymerize to constrain the polymerization at interfaces, but its free-radical mechanism allows precise control of initiation, which makes it possible to finely disperse the immiscible phases prior to polymerization.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号