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991.
Wilhelm M. Malloni Silvia De Sanctis Ana M. Tomé Elmar W. Lang Claudia E. Munte Klaus Peter Neidig Hans Robert Kalbitzer 《Journal of biomolecular NMR》2010,47(2):101-111
Strong solvent signals lead to a disappearance of weak protein signals close to the solvent resonance frequency and to base
plane variations all over the spectrum. AUREMOL-SSA provides an automated approach for solvent artifact removal from multidimensional
NMR protein spectra. Its core algorithm is based on singular spectrum analysis (SSA) in the time domain and is combined with
an automated base plane correction in the frequency domain. The performance of the method has been tested on synthetic and
experimental spectra including two-dimensional NOESY and TOCSY spectra and a three-dimensional 1H,13C-HCCH-TOCSY spectrum. It can also be applied to frequency domain spectra since an optional inverse Fourier transformation
is included in the algorithm. 相似文献
992.
993.
Cantarelli MA Pellerano RG Del Vitto LA Marchevsky EJ Camiña JM 《Phytochemical analysis : PCA》2010,21(6):550-555
Introduction – The chemometric characterisation of two plants frequently used as food and medicinal species, Achyrocline satureioides and Achyrocline venosa (Asteraceae: Gnaphalieae), was carried out based on their mineral composition. Both species, known by the common name of ‘marcelas’, are very similar in their morphological features but they have different medicinal and food properties. Objective – To develop multivariate models for the classification of A. satureiodes and A. venosa based on their mineral content. Methodology – The analytic determinations were made by means of inductively coupled plasma optical emission spectrometry from aerial parts of the plants. An internal standard was used to evaluate the accuracy in the sample treatment and the recovery of toxic elements was studied. The multivariate methods used include principal components analysis, cluster analysis and linear discriminant analysis. Results – Classification for both A. satureioides and A. venosa was successful in all cases using only four variables: aluminium, iron, magnesium and sulphur content. The concentrations of the following elements were determined: Al, As, Ba, Ca, Cd, Co, Cr, Cu, Fe, K, La, Mg, Mn, Mo, Na, Ni, P, Pb, S, Sr, Ti, V, Y and Zn. Conclusions – This method is useful to identify both species in raw material in order to detect eventual errors of selection. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
994.
Inés Infante Maria A. Morel Martha C. Ubalde Cecilia Martínez-Rosales Silvia Belvisi Susana Castro-Sowinski 《World journal of microbiology & biotechnology》2010,26(6):1047-1052
Wool is a natural animal fiber commonly used in fabrics, but requires physical and chemical processing treatment for such
applications. With the aim of developing new woollen textile products using environmentally friendly treatments, proteolytic
bacteria were isolated from raw wool samples of Merino sheep and screened for wool-degrading activity. Two isolates were identified as Bacillus megaterium L4 and Bacillus thuringiensis L11 by 16S rRNA gene sequence analysis. Both isolates grew on a minimal medium using wool-fiber or wool-fabric as sole carbon
and nitrogen sources. Bacterial growth was correlated with extracellular protease activity, and maximal protease production
was in early stationary phase. The exoprotease produced by L11 was found to be a thermo-tolerant metalloprotease stabilized
by calcium or magnesium, and had optimum activity at pH 7.0 and temperature at 40°C. During bacterial growth the wool-fiber
lost weight, but it did not show changes in diameter. When wool-fabric was used instead of wool-fiber weight loss and non-shrinking
was found. These are encouraging results for textile processing that should be useful for development of new textile products
by direct microbial processing. A potential alternative that could be suggested from our study would be to treat wool with
wool-degrading microorganisms in order to develop environmentally friendly processes. 相似文献
995.
996.
Christopher M. Harris Anna M. Ericsson Maria A. Argiriadi Claude Barberis David W. Borhani Andrew Burchat David J. Calderwood George A. Cunha Richard W. Dixon Kristine E. Frank Eric F. Johnson Joanne Kamens Silvia Kwak Biqin Li Kelly D. Mullen Denise C. Perron Lu Wang Neil Wishart Xiaoyun Wu Xiaolei Zhang Robert V. Talanian 《Bioorganic & medicinal chemistry letters》2010,20(1):334-337
We describe structure-based optimization of a series of novel 2,4-diaminopyrimidine MK2 inhibitors. Co-crystal structures (see accompanying Letter) demonstrated a unique inhibitor binding mode. Resulting inhibitors had IC50 values as low as 19 nM and moderate selectivity against a kinase panel. Compounds 15, 31a, and 31b inhibit TNFα production in peripheral human monocytes. 相似文献
997.
Highlights? AtBMI1A/B proteins prevent misexpression of embryonic traits in somatic cells ? PRC2 and AtBMI1A/B proteins maintain cells in their differentiated state ? AtBMI1A/B proteins mediate H2A monoubiquitination 相似文献
998.
999.
1000.
Gourlay LJ Sommaruga S Nardini M Sperandeo P Dehò G Polissi A Bolognesi M 《Protein science : a publication of the Protein Society》2010,19(12):2430-2439
Lipopolysaccharide (LPS) biosynthesis represents an underexploited target pathway for novel antimicrobial development to combat the emergence of multidrug‐resistant bacteria. A key player in LPS synthesis is the enzyme D ‐arabinose‐5‐phosphate isomerase (API), which catalyzes the reversible isomerization of D ‐ribulose‐5‐phosphate to D ‐arabinose‐5‐phosphate, a precursor of 3‐deoxy‐D ‐manno‐octulosonate that is an essential residue of the LPS inner core. API is composed of two main domains: an N‐terminal sugar isomerase domain (SIS) and a pair of cystathionine‐β‐synthase domains of unknown function. As the three‐dimensional structure of an enzyme is a prerequisite for the rational development of novel inhibitors, we present here the crystal structure of the SIS domain of a catalytic mutant (K59A) of E. coli D ‐arabinose‐5‐phosphate isomerase at 2.6‐Å resolution. Our structural analyses and comparisons made with other SIS domains highlight several potentially important active site residues. In particular, the crystal structure allowed us to identify a previously unpredicted His residue (H88) located at the mouth of the active site cavity as a possible catalytic residue. On the basis of such structural data, subsequently supported by biochemical and mutational experiments, we confirm the catalytic role of H88, which appears to be a generally conserved residue among two‐domain isomerases. 相似文献