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71.
Seok-Zun Song Kyung-Tae Kang LeRoy B. Beasley Nung-Sing Sze 《Linear algebra and its applications》2008,429(1):209-223
An m×n matrix A over a semiring is called regular if there is an n×m matrix G over such that AGA=A. We study the problem of characterizing those linear operators T on the matrices over a semiring such that T(X) is regular if and only if X is. Complete characterizations are obtained for many semirings including the Boolean algebra, the nonnegative reals, the nonnegative integers and the fuzzy scalars. 相似文献
72.
In a recent paper, Neumann and Sze considered for an n × n nonnegative matrix A, the minimization and maximization of ρ(A + S), the spectral radius of (A + S), as S ranges over all the doubly stochastic matrices. They showed that both extremal values are always attained at an n × n permutation matrix. As a permutation matrix is a particular case of a normal matrix whose spectral radius is 1, we consider here, for positive matrices A such that (A + N) is a nonnegative matrix, for all normal matrices N whose spectral radius is 1, the minimization and maximization problems of ρ(A + N) as N ranges over all such matrices. We show that the extremal values always occur at an n × n real unitary matrix. We compare our results with a less recent work of Han, Neumann, and Tastsomeros in which the maximum value of ρ(A + X) over all n × n real matrices X of Frobenius norm was sought. 相似文献
73.
Matrix-assisted laser desorption/ionization-mass spectrometry (MALDI-MS) is rarely used for the analysis of small molecules (< 700 Da) because the low m/z signal is overwhelmed by a high background of matrix ions. We have developed a solution to this problem that employs a novel polymer composite which is formed by covalently cross-linking alpha-cyano-4-hydroxycinnamic acid (HCCA) to SU-8 photoresist via cationic photo-polymerization. Since the HCCA molecules are immobilized, background noise resulting from the matrix ions is significantly reduced or eliminated. Moreover, owing to the hydrophobic surface of the polymer film, the sample spots shrink during solvent evaporation and thus the analytes can be concentrated. As a result, this polymer composite improves detection sensitivity and extends the analyzable species to the low-mass region. The covalent incorporation of HCCA with SU-8 was validated with reflectance FTIR spectroscopy, and the polymer surface was characterized with scanning electron microscopy (SEM). Using MRFA, a small peptide as a standard, 8 mg of HCCA per mL of SU-8 photoresist was found to yield the highest sensitivity and the lowest background noise. Analytes such as peptides or small organic molecules were further examined on this composite surface and no analyte degradation was observed. In a trial of peptide mass fingerprinting of cytochrome c on the composite substrate, the inclusion of low m/z tryptic peptides in the database search dramatically improved the protein identification probability score. 相似文献
74.
Electroanalysis of Natural Compounds as Copper Chelating Agents for Alzheimer’s Disease Therapy
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Vinci Wing Sze Hung Lucas Paines Bressan Kanghoon Seo Kagan Kerman 《Electroanalysis》2015,27(11):2670-2678
The development of therapeutic compounds that can attenuate the toxicity exerted by the accumulation of metal ions has been an area of intensive research in neurodegenerative diseases. In this report, an electrochemical method was developed to determine the Cu(II)‐chelating ability of polyphenols that were implicated in Alzheimer’s disease (AD). The results suggested the strength of flavonoids to chelate Cu(II) as epigallocatechin‐3‐gallate (EGCG)>resveratrol>clioquinol>baicalein~scyllo‐inositol. Furthermore, the number of hydroxyl groups was found to play a role to lower Cu(II) oxidation signal using differential pulse voltammetry. 相似文献
75.
The inverse mean first passage time problem is given a positive matrix M∈Rn,n, then when does there exist an n-state discrete-time homogeneous ergodic Markov chain C, whose mean first passage matrix is M? The inverse M-matrix problem is given a nonnegative matrix A, then when is A an inverse of an M-matrix. The main thrust of this paper is to show that the existence of a solution to one of the problems can be characterized by the existence of a solution to the other. In so doing we extend earlier results of Tetali and Fiedler. 相似文献
76.
Chen X Fung YM Chan WY Wong PS Yeung HS Chan TW 《Journal of the American Society for Mass Spectrometry》2011,22(12):2232-2245
Electron capture dissociation (ECD) of model peptides adducted with first row divalent transition metal ions, including Mn2+, Fe2+, Co2+, Ni2+, Cu2+, and Zn2+, were investigated. Model peptides with general sequence of ZGGGXGGGZ were used as probes to unveil the ECD mechanism of
metalated peptides, where X is either V or W; and Z is either R or N. Peptides metalated with different divalent transition
metal ions were found to generate different ECD tandem mass spectra. ECD spectra of peptides metalated by Mn2+ and Zn2+ were similar to those generated by ECD of peptides adducted with alkaline earth metal ions. Series of c-/z-type fragment ions with and without metal ions were observed. ECD of Fe2+, Co2+, and Ni2+ adducted peptides yielded abundant metalated a-/y-type fragment ions; whereas ECD of Cu2+ adducted peptides generated predominantly metalated b-/y-type fragment ions. From the present experimental results, it was postulated that electronic configuration of metal ions
is an important factor in determining the ECD behavior of the metalated peptides. Due presumably to the stability of the electronic
configuration, metal ions with fully-filled (i.e., Zn2+) and half filled (i.e., Mn2+) d-orbitals might not capture the incoming electron. Dissociation of the metal ions adducted peptides would proceed through
the usual ECD channel(s) via “hot-hydrogen” or “superbase” intermediates, to form series of c-/z
•- fragments. For other transition metal ions studied, reduction of the metal ions might occur preferentially. The energy liberated
by the metal ion reduction would provide enough internal energy to generate the “slow-heating” type of fragment ions, i.e.,
metalated a-/y- fragments and metalated b-/y- fragments. 相似文献
77.
Chen X Chan WY Wong PS Yeung HS Chan TW 《Journal of the American Society for Mass Spectrometry》2011,22(2):233-244
Peptides adducted with different divalent Group IIB metal ions (Zn2+, Cd2+, and Hg2+) were found to give very different ECD mass spectra. ECD of Zn2+ adducted peptides gave series of c-/z-type fragment ions with and without metal ions. ECD of Cd2+ and Hg2+ adducted model peptides gave mostly a-type fragment ions with M+• and fragment ions corresponding to losses of neutral side chain from M+•. No detectable a-ions could be observed in ECD spectra of Zn2+ adducted peptides. We rationalized the present findings by invoking both proton-electron recombination and metal-ion reduction
processes. As previously postulated, divalent metal-ions adducted peptides could adopt several forms, including (a) [M + Cat]2+, (b) [(M + Cat – H) + H]2+, and (c) [(M + Cat – 2H) + 2H]2+. The relative population of these precursor ions depends largely on the acidity of the metal–ion peptide complexes. Peptides
adducted with divalent metal-ions of small ionic radii (i.e., Zn2+) would form predominantly species (b) and (c); whereas peptides adducted with metal ions of larger ionic radii (i.e., Hg2+) would adopt predominantly species (a). Species (b) and (c) are believed to be essential for proton-electron recombination
process to give c-/z-type fragments via the labile ketylamino radical intermediates. Species (c) is particularly important for the formation of
non-metalated c-/z-type fragments. Without any mobile protons, species (a) are believed to undergo metal ion reduction and subsequently induce
spontaneous electron transfer from the peptide moiety to the charge-reduced metal ions. Depending on the exothermicity of
the electron transfer reaction, the peptide radical cations might be formed with substantial internal energy and might undergo
further dissociation to give structural related fragment ions. 相似文献
78.
A clickable, affinity-based probe (AfBP), which was modified from staurosporine (a natural product kinase inhibitor), has been synthesized and used in situ for activity-based proteome profiling of potential cellular targets of staurosporine in HepG2 cancer cells. 相似文献
79.
Ryu G Huang J Hofmann O Walshe CA Sze JY McClean GD Mosley A Rattle SJ deMello JC deMello AJ Bradley DD 《Lab on a chip》2011,11(9):1664-1670
We demonstrate a compact, low cost and practical fluorescence detection system for lab-on-a-chip applications. The system comprises a commercially available InGaN light emitting diode (501 nm) as light source, an organic or silicon photodiode detector, absorptive dye coated colour filters and linear and reflective polarisers. An injection moulded polystyrene microfluidic chip is used as the platform for fluorescence immunoassays for cardiac markers myoglobin and CK-MB. The optical limit of detection (LOD) is measured using a TransFluoSphere? suspension at 5.6 × 10(4) beads μl(-1) which can be equated to ~3 nM fluorescein equivalent concentration. The LOD for the human plasma immunoassays is measured as 1.5 ng ml(-1) for both myoglobin and CK-MB. 相似文献
80.