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151.
152.
153.
G. Bánó L. Szalai K. Kutasi P. Hartmann Z. Donkó K. Rózsa Á. Kiss T.M. Adamowicz 《Applied physics. B, Lasers and optics》2000,70(4):521-525
Single-mode operation at the Au-II 690-nm transition was obtained in a segmented hollow-cathode discharge laser without the
use of any additional frequency-selective device. The pressure of the helium buffer gas, which is responsible for the significant
homogeneous broadening of the laser line, was varied between 10 and 20 mbar. The discharge was excited with rectangular current
pulses (up to 3 A) six times exceeding the threshold value. The time dependence of the laser output during the 1-ms-long discharge
pulses is explained on the basis of the temperature and pressure changes in the tube. The highest small-signal gain at optimal
discharge conditions was 11%m−1.
Received: 1 July 1999 / Revised version: 4 November 1999 / Published online: 23 February 2000 相似文献
154.
155.
We consider a system formulation for Sturm–Liouville operators with formally self-adjoint boundary conditions on a graph. An M-matrix associated with the boundary value problem is defined and related to the matrix Prüfer angle associated with the system boundary value problem, and consequently with the boundary value problem on the graph. Asymptotics for the M-matrix are obtained as the eigenparameter tends to negative infinity. We show that the boundary conditions may be recovered, up to a unitary equivalence, from the M-matrix and that the M-matrix is a Herglotz function. This is the first in a series of papers devoted to the reconstruction of the Sturm–Liouville problem on a graph from its M-matrix. 相似文献
156.
E. Hartmann 《Fresenius' Journal of Analytical Chemistry》1989,335(8):954-959
Summary Frequently different concepts are designated by the terms limit of detection, limit of determination and limit of quantification in the chemical literature. The statistical models used for the definitions can be classified as to their primary purpose: to estimate concentrations or to test hypotheses. In addition a further classification with respect to the control of the local or the multiple type-I error can be carried out.For characterizing an analytical method, an analytical system or a series of analyses the application of a statistical test is appropiate. However, the attempt to control the probability of the multiple type-I error should not be made in this context in order to avoid an unreasonably high probability of the type-II error, which consists of overlooking the presence of some substance of interest. 相似文献
157.
158.
F.J. Hartmann 《Hyperfine Interactions》1999,119(1-4):175-184
The experiments on metastable antiprotonic helium atoms are reviewed.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
159.
Non-contact protein microarray fabrication using a procedure based on liquid bridge formation 总被引:1,自引:1,他引:0
Michael Hartmann Johan Sjödahl Mårten Stjernström Johan Redeby Thomas Joos Johan Roeraade 《Analytical and bioanalytical chemistry》2009,393(2):591-598
Contemporary microarrayers of contact or non-contact format used in protein microarray fabrication still suffer from a number
of problems, e.g. generation of satellite spots, inhomogeneous spots, misplaced or even absent spots, and sample carryover.
In this paper, a new concept of non-contact sample deposition that reduces such problems is introduced. To show the potential
and robustness of this pressure-assisted deposition technique, different sample solutions known to cause severe problems or
to be even impossible to print with conventional microarrayers were accurately printed. The samples included 200 mg mL–1 human serum albumin, highly concentrated sticky cell adhesion proteins, pure high-salt cell-lysis buffer, pure DMSO, and
a suspension of 5-μm polystyrene beads. Additionally, a water-immiscible liquid fluorocarbon, which was shown not to affect
the functionality of the capture molecules, was employed as a lid to reduce evaporation during microarray printing. The fluorocarbon
liquid lid was shown to circumvent hydrolysis of water-sensitive activated surfaces during long-term deposition procedures. 相似文献
160.
Peter Max Gehrig Bernd Roschitzki Dorothea Rutishauser Sonja Reiland Ralph Schlapbach 《Rapid communications in mass spectrometry : RCM》2009,23(10):1435-1445
In order to investigate gas‐phase fragmentation reactions of phosphorylated peptide ions, matrix‐assisted laser desorption/ionization (MALDI) and electrospray ionization (ESI) tandem mass (MS/MS) spectra were recorded from synthetic phosphopeptides and from phosphopeptides isolated from natural sources. MALDI‐TOF/TOF (TOF: time‐of‐flight) spectra of synthetic arginine‐containing phosphopeptides revealed a significant increase of y ions resulting from bond cleavages on the C‐terminal side of phosphothreonine or phosphoserine. The same effect was found in ESI‐MS/MS spectra recorded from the singly charged but not from the doubly charged ions of these phosphopeptides. ESI‐MS/MS spectra of doubly charged phosphopeptides containing two arginine residues support the following general fragmentation rule: Increased amide bond cleavage on the C‐terminal side of phosphorylated serines or threonines mainly occurs in peptide ions which do not contain mobile protons. In MALDI‐TOF/TOF spectra of phosphopeptides displaying N‐terminal fragment ions, abundant b–H3PO4 ions resulting from the enhanced dissociation of the pSer/pThr–X bond were detected (X denotes amino acids). Cleavages at phosphoamino acids were found to be particularly predominant in spectra of phosphopeptides containing pSer/pThr–Pro bonds. A quantitative evaluation of a larger set of MALDI‐TOF/TOF spectra recorded from phosphopeptides indicated that phosphoserine residues in arginine‐containing peptides increase the signal intensities of the respective y ions by almost a factor of 3. A less pronounced cleavage‐enhancing effect was observed in some lysine‐containing phosphopeptides without arginine. The proposed peptide fragmentation pathways involve a nucleophilic attack by phosphate oxygen on the carbon center of the peptide backbone amide, which eventually leads to cleavage of the amide bond. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献