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161.
Conjugation morphology of Zygogonium ericetorum (Zygnematophyceae,Charophyta) from a high alpine habitat 下载免费PDF全文
Rosalina Stancheva Klaus Herburger Robert G. Sheath Andreas Holzinger 《Journal of phycology》2016,52(1):131-134
Reproductive characteristics are important for defining taxonomic groups of filamentous Zygnematophyceae, but they have not been fully observed in the genus Zygogonium. Specimens of Z. ericetorum previously studied and used to clarify the generic concept lacked fertile material, which was obtained recently. This study illustrates for the first time, using color light microscopic and fluorescence images, a consequent conjugation stage in Z. ericetorum, including completely developed zygospores and purple cytoplasmic residue content left outside the zygospores, similar to aplanospore formation. Structures confirmed earlier reports and provided new observation informative regarding phylogenetically relevant reproductive characters of Z. ericetorum. 相似文献
162.
Lisa Borkner Andrew Kaiser Willeke van de Kasteele Reinhard Andreesen Andreas Mackensen John B. Haanen Ton N. Schumacher Christian Blank 《Cancer immunology, immunotherapy : CII》2010,59(8):1173-1183
Adoptive cell transfer (ACT), either using rapidly expanded tumor infiltrating lymphocytes or T-cell receptor transduced peripheral
blood lymphocytes, can be considered one of the most promising approaches in cancer immunotherapy. ACT results in the repopulation
of the host with high frequencies of tumor-specific T cells; however, optimal function of these cells within the tumor micro-environment
is required to reach long-term tumor clearance. We and others have shown that ongoing anti-tumor immune responses can be impaired
by the expression of ligands, such as PD-L1 (B7-H1) on tumor cells. Such inhibitory molecules can affect T cells at the effector
phase via their receptor PD-1. PD-L1/PD-1 interaction has indeed been shown crucial in inducing T-cell anergy and maintaining
peripheral tolerance. In order to maximize anti-tumor responses, antibodies that target the PD-1/PD-L1 axis are currently
in phase I/II trials. Alternatively, a more refined approach could be the selective targeting of PD-1 in tumor-specific T
cells to obtain long-term resistance against PD-1-mediated inhibition. We addressed whether this goal could be achieved by
means of retroviral siRNA delivery. Effective siRNA sequences resulting in the reduction of surface PD-1 expression led to
improved murine as well as human T-cell immune functions in response to PD-L1 expressing melanoma cells. These data suggest
that blockade of PD-1-mediated T-cell inhibition through siRNA forms a promising approach to achieve long-lasting enhancement
of tumor-specific T-cell function in adoptive T-cell therapy protocols. 相似文献
163.
Traditional cultivation-based methods to quantify microbial abundance are not suitable for analyses of microbial communities
in environmental or medical samples, which consist mainly of uncultured microorganisms. Recently, different cultivation-independent
quantification approaches have been developed to overcome this problem. Some of these techniques use specific fluorescence
markers, for example ribosomal ribonucleic acid targeted oligonucleotide probes, to label the respective target organisms.
Subsequently, the detected cells are visualized by fluorescence microscopy and are quantified by direct visual cell counting
or by digital image analysis. This article provides an overview of these methods and some of their applications with emphasis
on (semi-)automated image analysis solutions. 相似文献
164.
Günther Klonner Johannes Wessely Andreas Gattringer Dietmar Moser Iwona Dullinger Karl Hülber Sabine B. Rumpf Svenja Block Oliver Bossdorf Marta Carboni Luisa Conti Wayne Dawson Emily Haeuser Martin Hermy Tamara Münkemüller Madalin Parepa Wilfried Thuiller Sebastiaan Van der Veken Kris Verheyen Mark van Kleunen Franz Essl Stefan Dullinger 《Ecography》2019,42(9):1548-1557
Climate warming is supposed to enlarge the area climatically suitable to the naturalization of alien garden plants in temperate regions. However, the effects of a changing climate on the spread of naturalized ornamentals have not been evaluated by spatially and temporarily explicit range modelling at larger scales so far. Here, we assess how climate change and the frequency of cultivation interactively determine the spread of 15 ornamental plants over the 21st century in Europe. We coupled species distribution modelling with simulations of demography and dispersal to predict range dynamics of these species in annual steps across a 250 × 250 m raster of the study area. Models were run under four scenarios of climate warming and six levels of cultivation intensity. Cultivation frequency was implemented as size of the area used for planting a species. Although the area climatically suitable to the 15 species increases, on average, the area predicted to be occupied by them in 2090 shrinks under two of the three climate change scenarios. This contradiction obviously arises from dispersal limitations that were pronounced although we assumed that cultivation is spatially adapting to the changing climate. Cultivation frequency had a much stronger effect on species spread than climate change, and this effect was non‐linear. The area occupied increased sharply from low to moderate levels of cultivation intensity, but levelled off afterwards. Our simulations suggest that climate warming will not necessarily foster the spread of alien garden plants in Europe over the next decades. However, climatically suitable areas do increase and hence an invasion debt is likely accumulating. Restricting cultivation of species can be effective in preventing species spread, irrespective of how the climate develops. However, for being successful, they depend on high levels of compliance to keep propagule pressure at a low level. 相似文献
165.
Tetanus neurotoxin and botulinum neurotoxins are the causative agents of tetanus and botulism. They block the release of neurotransmitters from synaptic vesicles in susceptible animals and man and act in nanogram quantities because of their ability to specifically attack motoneurons. They developed an ingenious strategy to enter neurons. This involves a concentration step via complex polysialo gangliosides at the plasma membrane and the uptake and ride in recycling synaptic vesicles initiated by binding to a specific protein receptor. Finally, the neurotoxins shut down the synaptic vesicle cycle, which they had misused before to enter their target cells, via specific cleavage of protein core components of the cellular membrane fusion machinery. The uptake of four out of seven known botulinum neurotoxins into synaptic vesicles has been demonstrated to rely on binding to intravesicular segments of the synaptic vesicle proteins synaptotagmin or synaptic vesicle protein 2. This review summarizes the present knowledge about the cell receptor molecules and the mode of toxin-receptor interaction that enables the toxins' sophisticated access to their site of action. 相似文献
166.
167.
Loy A Schulz C Lücker S Schöpfer-Wendels A Stoecker K Baranyi C Lehner A Wagner M 《Applied and environmental microbiology》2005,71(3):1373-1386
For simultaneous identification of members of the betaproteobacterial order "Rhodocyclales" in environmental samples, a 16S rRNA gene-targeted oligonucleotide microarray (RHC-PhyloChip) consisting of 79 probes was developed. Probe design was based on phylogenetic analysis of available 16S rRNA sequences from all cultured and as yet uncultured members of the "Rhodocyclales." The multiple nested probe set was evaluated for microarray hybridization with 16S rRNA gene PCR amplicons from 29 reference organisms. Subsequently, the RHC-PhyloChip was successfully used for cultivation-independent "Rhodocyclales" diversity analysis in activated sludge from an industrial wastewater treatment plant. The implementation of a newly designed "Rhodocyclales"-selective PCR amplification system prior to microarray hybridization greatly enhanced the sensitivity of the RHC-PhyloChip and thus enabled the detection of "Rhodocyclales" populations with relative abundances of less than 1% of all bacteria (as determined by fluorescence in situ hybridization) in the activated sludge. The presence of as yet uncultured Zoogloea-, Ferribacterium/Dechloromonas-, and Sterolibacterium-related bacteria in the industrial activated sludge, as indicated by the RHC-PhyloChip analysis, was confirmed by retrieval of their 16S rRNA gene sequences and subsequent phylogenetic analysis, demonstrating the suitability of the RHC-PhyloChip as a novel monitoring tool for environmental microbiology. 相似文献
168.
169.
Gene expression of myogenic factors and phenotype-specific markers in electrically stimulated muscle of paraplegics. 总被引:2,自引:0,他引:2
170.
The ESCRT-III subunit hVps24 is required for degradation but not silencing of the epidermal growth factor receptor 下载免费PDF全文
Bache KG Stuffers S Malerød L Slagsvold T Raiborg C Lechardeur D Wälchli S Lukacs GL Brech A Stenmark H 《Molecular biology of the cell》2006,17(6):2513-2523
The endosomal sorting complexes required for transport, ESCRT-I, -II, and -III, are thought to mediate the biogenesis of multivesicular endosomes (MVEs) and endosomal sorting of ubiquitinated membrane proteins. Here, we have compared the importance of the ESCRT-I subunit tumor susceptibility gene 101 (Tsg101) and the ESCRT-III subunit hVps24/CHMP3 for endosomal functions and receptor signaling. Like Tsg101, endogenous hVps24 localized mainly to late endosomes. Depletion of hVps24 by siRNA showed that this ESCRT subunit, like Tsg101, is important for degradation of the epidermal growth factor (EGF) receptor (EGFR) and for transport of the receptor from early endosomes to lysosomes. Surprisingly, however, whereas depletion of Tsg101 caused sustained EGF activation of the mitogen-activated protein kinase pathway, depletion of hVps24 had no such effect. Moreover, depletion of Tsg101 but not of hVps24 caused a major fraction of internalized EGF to accumulate in nonacidified endosomes. Electron microscopy of hVps24-depleted cells showed an accumulation of EGFRs in MVEs that were significantly smaller than those in control cells, probably because of an impaired fusion with lyso-bisphosphatidic acid-positive late endosomes/lysosomes. Together, our results reveal functional differences between ESCRT-I and ESCRT-III in degradative protein trafficking and indicate that degradation of the EGFR is not required for termination of its signaling. 相似文献