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231.
Structural insights into the molecular organization of the S-layer from Clostridium difficile 总被引:1,自引:1,他引:0
Robert P. Fagan David Albesa-Jové Omar Qazi Dmitri I. Svergun Katherine A. Brown Neil F. Fairweather 《Molecular microbiology》2009,71(5):1308-1322
Clostridium difficile expresses a surface layer (S-layer) which coats the surface of the bacterium and acts as an adhesin facilitating interaction of the bacterium with host enteric cells. The S-layer contains a high-molecular-weight S-layer protein (HMW SLP) and its low-molecular-weight partner protein (LMW SLP). We show that these proteins form a tightly associated non-covalent complex, the H/L complex, and we identify the regions of both proteins responsible for complex formation. The 2.4 Å X-ray crystal structure of a truncated derivative of the LMW SLP reveals two domains. Domain 1 has a two-layer sandwich architecture while domain 2, predicted to orientate towards the external environment, contains a novel fold. Small-angle X-ray scattering analysis of the H/L complex shows an elongated molecule, with the two SLPs arranged 'end-to-end' interacting with each other through a small contact area. Alignment of LMW SLPs, which exhibit high sequence diversity, reveals a core of conserved residues that could reflect functional conservation, while allowing for immune evasion through sequence variation. These structures are the first described for the S-layer of a bacterial pathogen, and provide insights into the assembly and biogenesis of the S-layer. 相似文献
232.
Olga Krysko Peter Vandenabeele Dmitri V. Krysko Claus Bachert 《Apoptosis : an international journal on programmed cell death》2010,15(9):1137-1146
Phagocytosis of dying cells is a complex and dynamic process coordinated by the interaction of many surface molecules, adaptors,
and chemotactic molecules, and it is controlled at multiple levels. This well regulated clearance process is of utmost importance
for the development and homeostasis of organisms because defective or inefficient phagocytosis may contribute to human pathologies.
In this review we discuss recent advances in the knowledge of the molecular interactions involved in recognition and clearance
of apoptotic cells and how derangement of these processes can contribute to the pathogenesis of chronic airway diseases such
as chronic obstructive pulmonary disease, cystic fibrosis and asthma. We will briefly consider how different types of macrophages
are implicated in chronic airway diseases. Finally, we will address possible therapeutic strategies, such as the use of macrolide
antibiotics and statins, for modulating apoptotic cell clearance. 相似文献
233.
234.
M. A. Dzhaubermezov N. V. Ekomasova S. S. Litvinov R. I. Khusainova V. L. Akhmetova N. V. Balinova E. K. Khusnutdinova 《Russian Journal of Genetics》2017,53(10):1152-1158
The genetic diversity in two ethnic groups of the central part of the North Caucasus (Balkars and Karachays) using 50 diallelic loci in the non-recombining region of the Y chromosome was analyzed. For the first time, an analysis of distribution of frequencies of Y-chromosome haplogroups in Balkars considering different subethnic groups (Baksans, Chegems, Kholams, Bezengiyevs, and Malkars) was conducted. The major Y-chromosome haplogroups in the studied groups of Balkars and Karachays were G2a-P16 and R1a- Z2123. In addition, for a better understanding of genetic relationship between the male lineages in the studied populations and other populations of the Caucasus, we performed an analysis of R1a-M198 subhaplogroups in 22 populations of this region. The principal component analysis demonstrated that a greater difference was observed between Kholams and the other Balkar subgroups. According to the F st analysis, Chegems, for which the prevalence of haplogroup R1b-M478 (32.2%) was reported, demonstrated the maximum difference from the other subpopulations of Balkars and Karachays. 相似文献
235.
236.
Julia Litvinov Anna E. V. Hagström Yubitza Lopez Meenu Adhikari Katerina Kourentzi Ulrich Strych Federico A. Monzon William Foster Philip T. Cagle Richard C. Willson 《Biotechnology letters》2014,36(9):1863-1868
We report a novel, modular approach to immuno-detection based on antibody recognition and PCR read-out that employs antibody-conjugated bacteriophage and easily-manipulated non-pathogenic viruses as affinity agents. Our platform employs phage genetically tagged for in vivo biotinylation during phage maturation that can easily be linked, through avidin, to any biotinylated affinity agent, including full-length antibodies, peptides, lectins or aptamers. The presence of analyte is reported with high sensitivity through real-time PCR. This approach avoids the need to clone antibody-encoding DNA fragments, allows the use of full-length, high affinity antibodies and, by having DNA reporters naturally encapsulated inside the bacteriophage, greatly reduces nonspecific binding of DNA. We validate the efficacy of this new approach through the detection of Vascular Endothelial Growth Factor, a known angiogenic cancer biomarker protein, at attomolar concentrations in bronchoalveolar lavage fluid. 相似文献
237.
Alan O. Bergland Emily L. Behrman Katherine R. O'Brien Paul S. Schmidt Dmitri A. Petrov 《PLoS genetics》2014,10(11)
In many species, genomic data have revealed pervasive adaptive evolution indicated by the fixation of beneficial alleles. However, when selection pressures are highly variable along a species'' range or through time adaptive alleles may persist at intermediate frequencies for long periods. So called “balanced polymorphisms” have long been understood to be an important component of standing genetic variation, yet direct evidence of the strength of balancing selection and the stability and prevalence of balanced polymorphisms has remained elusive. We hypothesized that environmental fluctuations among seasons in a North American orchard would impose temporally variable selection on Drosophila melanogaster that would drive repeatable adaptive oscillations at balanced polymorphisms. We identified hundreds of polymorphisms whose frequency oscillates among seasons and argue that these loci are subject to strong, temporally variable selection. We show that these polymorphisms respond to acute and persistent changes in climate and are associated in predictable ways with seasonally variable phenotypes. In addition, our results suggest that adaptively oscillating polymorphisms are likely millions of years old, with some possibly predating the divergence between D. melanogaster and D. simulans. Taken together, our results are consistent with a model of balancing selection wherein rapid temporal fluctuations in climate over generational time promotes adaptive genetic diversity at loci underlying polygenic variation in fitness related phenotypes. 相似文献
238.
One‐Step Template‐Free Synthesis of Highly Porous Boron Nitride Microsponges for Hydrogen Storage 下载免费PDF全文
Highly porous, sponge‐like boron nitride materials, namely microsponges (BNMSs), with ultrahigh surface areas up to 1900 m2 g‐1, are prepared by a facile, one‐step, template‐free reaction of boric acid and dicyanamide. Detailed analysis confirms the increase of the interlayer (0002) distances compared to standard graphitic BN and reveals special dislocation structures in the BNMSs. The resulting textural parameters such as the Brunauer‐Emmett‐Teller (BET) specific surface areas and pore volumes are easily tunable over a wide range by adjusting the synthesis temperature or composition of the precursors. It is demonstrated that these microporous materials (with pore widths of 1.0 nm) display comparatively high and reversible H2 sorption capacities from 1.65 to 2.57 wt% at 1 MPa and –196 °C on a material basis. 相似文献
239.
Ribosome‐associated pentatricopeptide repeat proteins function as translational activators in mitochondria of trypanosomes 下载免费PDF全文
Inna Aphasizheva Dmitri A. Maslov Yu Qian Lan Huang Qi Wang Catherine E. Costello Ruslan Aphasizhev 《Molecular microbiology》2016,99(6):1043-1058
Mitochondrial ribosomes of Trypanosoma brucei are composed of 9S and 12S rRNAs, eubacterial‐type ribosomal proteins, polypeptides lacking discernible motifs and approximately 20 pentatricopeptide repeat (PPR) RNA binding proteins. Several PPRs also populate the polyadenylation complex; among these, KPAF1 and KPAF2 function as general mRNA 3′ adenylation/uridylation factors. The A/U‐tail enables mRNA binding to the small ribosomal subunit and is essential for translation. The presence of A/U‐tail also correlates with requirement for translation of certain mRNAs in mammalian and insect parasite stages. Here, we inquired whether additional PPRs activate translation of individual mRNAs. Proteomic analysis identified KRIPP1 and KRIPP8 as components of the small ribosomal subunit in mammalian and insect forms, but also revealed their association with the polyadenylation complex in the latter. RNAi knockdowns demonstrated essential functions of KRIPP1 and KRIPP8 in the actively respiring insect stage, but not in the mammalian stage. In the KRIPP1 knockdown, A/U‐tailed mRNA encoding cytochrome c oxidase subunit 1 declined concomitantly with the de novo synthesis of this subunit whereas polyadenylation and translation of cyb mRNA were unaffected. In contrast, the KRIPP8 knockdown inhibited A/U‐tailing and translation of both CO1 and cyb mRNAs. Our findings indicate that ribosome‐associated PPRs may selectively activate mRNAs for translation. 相似文献
240.
Guixin Shi Wenjin Cui Michael Benchimol Yu-Tsueng Liu Robert F. Mattrey Rajesh Mukthavaram Santosh Kesari Sadik C. Esener Dmitri Simberg 《PloS one》2013,8(3)
Circulating tumor cells (CTCs) are exfoliated at various stages of cancer, and could provide invaluable information for the diagnosis and prognosis of cancers. There is an urgent need for the development of cost-efficient and scalable technologies for rare CTC enrichment from blood. Here we report a novel method for isolation of rare tumor cells from excess of blood cells using gas-filled buoyant immuno-microbubbles (MBs). MBs were prepared by emulsification of perfluorocarbon gas in phospholipids and decorated with anti-epithelial cell adhesion molecule (EpCAM) antibody. EpCAM-targeted MBs efficiently (85%) and rapidly (within 15 minutes) bound to various epithelial tumor cells suspended in cell medium. EpCAM-targeted MBs efficiently (88%) isolated frequent tumor cells that were spiked at 100,000 cells/ml into plasma-depleted blood. Anti-EpCAM MBs efficiently (>77%) isolated rare mouse breast 4T1, human prostate PC-3 and pancreatic cancer BxPC-3 cells spiked into 1, 3 and 7 ml (respectively) of plasma-depleted blood. Using EpCAM targeted MBs CTCs from metastatic cancer patients were isolated, suggesting that this technique could be developed into a valuable clinical tool for isolation, enumeration and analysis of rare cells. 相似文献