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991.
992.
Araucaria trees as host plants of the longhorned beetle Huequenia livida (Coleoptera: Cerambycidae) in Argentina are reviewed. Araucaria araucana is its natural host plant in SW Argentina, but the larvae also developed in dead branches of A. angustifolia and A. bidwillii (new host plant records), when both plants were kept in the same rearing cage with the natural host plant. Pinus contorta var. murrayana, also mentioned from Argentina, may be a recently adopted secondary host. A winter and a summer generation of H. livida was documented for the first time. Huequenia livida exceeds the actual natural distribution of A. araucana following the distribution of cultivated A. araucana and Pinus trees. 相似文献
993.
CD and NMR conformational studies of a peptide encompassing the Mid Loop interface of Ship2–Sam 下载免费PDF全文
Concetta Di Natale Daniela Marasco Maurizio Pellecchia Marilisa Leone 《Biopolymers》2014,101(11):1088-1098
The lipid phosphatase Ship2 is a protein that intervenes in several diseases such as diabetes, cancer, neurodegeneration, and atherosclerosis. It is made up of a catalytic domain and several protein docking modules such as a C‐terminal Sam (Sterile alpha motif) domain. The Sam domain of Ship2 (Ship2–Sam) binds to the Sam domains of the EphA2 receptor (EphA2–Sam) and the PI3K effector protein Arap3 (Arap3–Sam). These heterotypic Sam–Sam interactions occur through formation of dimers presenting the canonical “Mid Loop/End Helix” binding mode. The central region of Ship2–Sam, spanning the C‐terminal end of α2, the α3 and α4 helices together with the α2α3 and α3α4 interhelical loops, forms the Mid Loop surface that is needed to bind partners Sam domains. A peptide encompassing most of the Ship2–Sam Mid Loop interface (Shiptide) capable of binding to both EphA2–Sam and Arap3–Sam, was previously identified. Here we investigated the conformational features of this peptide, through solution CD and NMR studies in different conditions. These studies reveal that the peptide is highly flexible in aqueous buffer, while it adopts a helical conformation in presence of 2,2,2‐trifluoroethanol. The discovered structural insights and in particular the identification of a helical motif, may lead to the design of more constrained and possibly cell permeable Shiptide analogs that could work as efficient antagonists of Ship2–Sam heterotypic interactions and embrace therapeutic applications. © 2014 Wiley Periodicals, Inc. Biopolymers 101: 1088–1098, 2014. 相似文献
994.
R. D’Anastasio J. Viciano M. Di Nicola D.T. Cesana M. Sciubba M. Del Cimmuto A. Paolucci A. Fazio L. Capasso 《HOMO》2014
Recent forensic studies have shown that the hyoid bone is a sexually dimorphic element of the human skeleton. Given the advanced techniques of collecting human remains in archeological and forensic contexts, the recovery of hyoid bones is now more frequent in skeletal samples. For that reason the authors propose a new method for estimating sex based on hyoid bodies from archeological sites. 相似文献
995.
Di Gioia D Luziatelli F Negroni A Ficca AG Fava F Ruzzi M 《Journal of biotechnology》2010,156(4):309-316
Vanillin is one of the most important flavors in the food industry and there is great interest in its production through biotechnological processes starting from natural substrates such as ferulic acid. Among bacteria, recombinant Escherichia coli strains are the most efficient vanillin producers, whereas Pseudomonas spp. strains, although possessing a broader metabolic versatility, rapidly metabolize various phenolic compounds including vanillin. In order to develop a robust Pseudomonas strain that can produce vanillin in high yields and at high productivity, the vanillin dehydrogenase (vdh)-encoding gene of Pseudomonas fluorescens BF13 strain was inactivated via targeted mutagenesis. The results demonstrated that engineered derivatives of strain BF13 accumulate vanillin if inactivation of vdh is associated with concurrent expression of structural genes for feruloyl-CoA synthetase (fcs) and hydratase/aldolase (ech) from a low-copy plasmid. The conversion of ferulic acid to vanillin was enhanced by optimization of growth conditions, growth phase and parameters of the bioconversion process. The developed strain produced up to 8.41 mM vanillin, which is the highest final titer of vanillin produced by a Pseudomonas strain to date and opens new perspectives in the use of bacterial biocatalysts for biotechnological production of vanillin from agro-industrial wastes which contain ferulic acid. 相似文献
996.
A. Palamidessi I. Testa E. Frittoli S. Barozzi M. Garrè D. Mazza P. P. Di Fiore A. Diaspro G. Scita Mario Faretta 《European biophysics journal : EBJ》2010,39(6):947-957
The dissection of the molecular circuitries at the base of cell life and the identification of their abnormal transformation
during carcinogenesis rely on the characterization of biological phenotypes generated by targeted overexpression or deletion
of gene products through genetic manipulation. Fluorescence microscopy provides a wide variety of tools to monitor cell life
with minimal perturbations. The observation of living cells requires the selection of a correct balance between temporal,
spatial and “statistical” resolution according to the process to be analyzed. In the following paper ad hoc developed optical
tools for dynamical tracking from cellular to molecular resolution will be presented. Particular emphasis will be devoted
to discuss how to exploit light–matter interaction to selectively target specific molecular species, understanding the relationships
between their intracellular compartmentalization and function. 相似文献
997.
Yeasts isolated from olive mill wastewaters from southern Italy: technological characterization and potential use for phenol removal 总被引:1,自引:0,他引:1
Milena Sinigaglia Nilde Di Benedetto Antonio Bevilacqua Maria Rosaria Corbo Angela Capece Patrizia Romano 《Applied microbiology and biotechnology》2010,87(6):2345-2354
Olive mill wastewater (OMW) samples from two traditional varieties (Peranzana and Ogliarola Garganica) of Apulian region (southern
Italy) and produced through continuous and traditional methods were microbiologically and chemically examined; thus, 104 yeasts
were isolated and selected for further analyses. The strains were identified as Candida boidinii, Pichia holstii, Pichia membranifaciens, and Saccharomyces cerevisiae and analyzed to assess their suitability to metabolize phenols. Based on phenol metabolism, 27 strains were selected and
inoculated into OMW aliquots to determine their ability to reduce phenols in vivo; then, five strains (identified with the
codes 682—C. boidinii and 625, 642, 647, and 941—P. holstii) were used as a cocktail in wastewaters for a final validation step. In this last experiment, the effects of the temperature
(10–30°C) and (NH4)2SO4 (0.0–6.0 g l−1) were studied through a central composite design approach, and the results highlighted that the cocktail was able to reduce
phenols by 40% at 10°C with 6.0 g l−1 of (NH4)2SO4 added. 相似文献
998.
999.
1000.
Jin Ming Di Jun Pang Qi Peng Sun Yan Zhang You Qiang Fang Xiao Pen Liu Jian Hua Zhou Xing Xing Ruan Xin Gao 《Molecular biology reports》2010,37(4):1849-1855
CpG-oligonucleotides (CpG-ODNs), mimicking bacterial DNA, have recently been shown to stimulate prostate cancer invasion in
vitro via Toll-like receptor 9 (TLR9). Since cyclooxygenase 2 (COX-2), frequently overexpressed in multiple tumor types including
prostate cancer, is a causal factor for tumor development, invasion and metastasis, an interesting question is raised whether
TLR9 regulates COX-2 expression in prostate cancer cells. To address this question, herein we examined COX-2 expression in
PC-3 cells stimulated with different doses and time courses of CpG-ODNs. The regulatory role of NF-κB in TLR9-mediated COX-2
expression was also investigated. CpG-ODN was found to up-regulate the expression of COX-2 in PC-3 cells in a dose- and time-dependent
manner, but have little impact on COX-1 expression. Moreover, CpG-ODN also promoted nuclear translocation and activation of
NF-κB, which appeared to be required for COX-2 induction by CpG-ODN. Overall, TLR9 up-regulates COX-2 expression in prostate
cancer cells, at least partially through the activation of NF-κB, which may be implicated in tumor invasion and metastasis. 相似文献