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111.
Toshinobu?TokumotoEmail author Ayami?Kondo Junko?Miwa Ryo?Horiguchi Mika?Tokumoto Yoshitaka?Nagahama Noriyuki?Okida Katsutoshi?Ishikawa 《BMC biochemistry》2003,4(1):6
Background
During Xenopusoocyte maturation, the amount of a 48 kDa protein detected in the 26S proteasome fraction (p48) decreased markedly during oocyte maturation to the low levels seen in unfertilized eggs. The results indicate that the interaction of at least one protein with the 26S proteasome changes during oocyte maturation and early development. An alteration in proteasome function may be important for the regulation of developmental events, such as the rapid cell cycle, in the early embryo. In this study, we identified p48. 相似文献112.
Takanori Shibata Ai Kawachi Mika Ogawa Yusuke Kuwata Kyoji Tsuchikama Kohei Endo 《Tetrahedron》2007,63(52):12853-12859
A chiral rhodium complex catalyzed an enantioselective [2+2+2] cycloaddition of unsymmetrical diynes with norbornene, and tetracyclic products were obtained in good to excellent ee. The cycloaddition of a symmetrical diyne with styrene derivatives as coupling partners gave bicyclic products in good ee. 相似文献
113.
Elin Nilsen Janne Puputti Mika Lindén Jean le Bell Mikael Perander Mari-Ann Einarsrud 《Journal of Sol-Gel Science and Technology》2003,26(1-3):1239-1242
A new low cost inorganic binder system for large volume products like fiber insulation, building materials, etc. has been developed based on sol-gel technology. The precursor for the binder system is an amorphous mineral raw material containing silica as the major component. The sol was prepared by dissolving the amorphous mineral material in formic acid and the mineral was dissolved in a few hours dependent on the molarity of the formic acid. The sol stability was dependent on the solids content and the pH. The gel formation was studied using light scattering and NMR. The results show a growing particle size of particles mainly consisting of silica while the other cations were dissolved in the pore liquid. During the drying of the wet gels, salts of these cations were crystallized in the pores and further decomposed during heating. The derived binder shows good wetting properties to mineral fiber surfaces and a good strength of paper-binder composites. The new binder system applicable to approximately 800°C has a great potential as a substitute for some traditional organic systems. 相似文献
114.
Compain S Schlemmer D Levi M Pruvost A Goujard C Grassi J Benech H 《Journal of mass spectrometry : JMS》2005,40(1):9-18
Besides liquid chromatographic (LC)/UV methods adapted to therapeutic drug monitoring, there is still a need for more powerful techniques that can be used for pharmacological research and clinical purposes. We developed an LC method coupled with tandem mass spectrometry (MS/MS) to separate, detect and quantify with high sensitivity the nucleoside analogues used in multitherapies (zidovudine, stavudine, zalcitabine, didanosine, lamivudine and abacavir) in plasma and in the intracellular medium. We worked on two essential issues: (i) the need to use two ionization modes in order to achieve the best sensitivity, which leads to the optimization of the chromatographic separation of drugs detected in the positive ionization mode and drugs detected in the negative ionization mode, and (ii) the need to optimize the extraction step in order to enhance sample recovery. The peripheral blood mononuclear cells were lysed in Tris buffer-MeOH. A clean-up procedure was performed by solid-phase extraction only for plasma samples. The LC separation was carried out on a Zorbax Stable Bond C(18) column followed by MS/MS analysis after electrospray ionization in either the negative or positive mode. The positive ionization mode was applied at the beginning of the run to detect zalcitabine and lamivudine, then the ionization mode was changed to negative for the detection of didanosine, stavudine, internal standard and zidovudine. The calibration range for all the analytes was 0.5-200 ng ml(-1). The recoveries were between 64 and 90%, with coefficients of variation (CVs) lower than 15%. The inaccuracy (bias) was +/-15% with CVs always lower than 12%. The analytes were stable at room temperature and in the extraction solvent for at least 24 h, after storage at -80 degrees C for 3 months, after three freeze-thaw cycles and in the injection solvent after 48 h at 4 degrees C. Together with the measurement of intracellular triphosphorylated metabolites thanks to the powerful plasma and intracellular assay method for intact drugs, it is possible to describe the behaviour of nucleoside analogues against HIV through plasma pharmacokinetics, cell membrane diffusion including drug transport involvement, and also the intracellular metabolism. 相似文献
115.
116.
Khriachtchev L Macoas E Pettersson M Rasanen M 《Journal of the American Chemical Society》2002,124(37):10994-10995
The trans and cis forms of formic acid (HCOOH) in solid argon favor essentially different photodissociation (193 nm) products, H2O + CO and H2 + CO2, respectively. The branching ratio of these channels differs between the two conformers by a factor of >10. The observed selective photodissociation features conformational memory when the transition state of a molecule is reached before torsional randomization. These data demonstrate that the photodissociation products can be efficiently steered with selective narrow-band infrared radiation promoting rotational isomerism, which makes a strong case of optically controlled chemical reactions 相似文献
117.
Smått JH Spliethoff B Rosenholm JB Lindén M 《Chemical communications (Cambridge, England)》2004,(19):2188-2189
Nanocrystalline cobalt oxide, Co(3)O(4), monoliths exhibiting hierarchical bimoidal porosity have been prepared by nanocasting of porous silica monoliths. 相似文献
118.
Christen M Hünenberger PH Bakowies D Baron R Bürgi R Geerke DP Heinz TN Kastenholz MA Kräutler V Oostenbrink C Peter C Trzesniak D van Gunsteren WF 《Journal of computational chemistry》2005,26(16):1719-1751
We present the latest version of the Groningen Molecular Simulation program package, GROMOS05. It has been developed for the dynamical modelling of (bio)molecules using the methods of molecular dynamics, stochastic dynamics, and energy minimization. An overview of GROMOS05 is given, highlighting features not present in the last major release, GROMOS96. The organization of the program package is outlined and the included analysis package GROMOS++ is described. Finally, some applications illustrating the various available functionalities are presented. 相似文献
119.
Eiji Tanahashi Katsutoshi Murase Mika Shibuya Yumie Igarashi Hideharu Ishida Akira Hasegawa 《Journal of carbohydrate chemistry》2013,32(6):831-858
Abstract A systematic synthesis of sulfatide (I) and novel sulfatide analogs (II-VI) carrying 2-(tetradecyl)hexadecyl group as a ceramide substitute is described. The 3-O-, 4-O- and 3,4-di-O-levulinoyl derivatives of galactopyranosyl trichloroacetimidates (1, 12, and 13) were coupled with (2S,3R,4E)-3-O-acetyl-2-octadecanamido-4-octadecene-1,3-diol or 2-(tetradecyl)hexadecan-1-ol. The resulting glycolipids (2, 4, 14, and 15) were each transformed, by selective removal of the levulinoyl group(s), and successive sulfation and de-O-acylation, into the 3-sulfates (I, II), 4-sulfate (III), and 3,4-disulfate (IV). The 6-sulfate (V) was prepared from 2-(tetradecyl)hexadecyl β-D-galactopyranoside (21) via the 6-O-t-butyldimethylsilyl derivative, while the 3′-sulfate of 2-(tetradecyl)hexadecyl β-D-lactoside (VI) was synthesized from 2-(trimethylsilyl)ethyl 3′-O-benzyl-β-D-lactoside (26). The structures of the sulfated glycolipids (I-VI) were characterized by ion-spray MS, MS/MS, and 1H NMR spectrometry. 相似文献
120.
A. L. Chaney S. L. Phansalkar P. Reiss J. Proszt J. Mika L. W. Winkler N. G. Heatley K. Linderstrøm-Lane H. Hoher K. Schwarz Fr. L. Hahn G. Roeder A. G. Rütgerswerken E. P. White A. A. Benedetti-Pichler Z. Ja. Rabinowitsch und M. W. Osolina 《Fresenius' Journal of Analytical Chemistry》1944,127(1):36-42
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