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991.
Jaroslav Julák Vladimír Scholtz Soňa Kotúčová Olga Janoušková 《Physica medica : PM : an international journal devoted to the applications of physics to medicine and biology : official journal of the Italian Association of Biomedical Physics (AIFB)》2012,28(3):230-239
This article describes and particularly explains a new phenomenon of persistent microbicidal effect of water previously exposed to the low-temperature plasma, which cannot be attributed to the acidification only. The direct microbicidal action of plasma is well documented, being mediated by number of reactive particles with a short lifetime. However, we observed the microbicidal effect also in exposed water stored for a month, where it must be mediated by stable particles. In water and in phosphate-buffered saline, the formation of NOx and corresponding acids, H2O2 and O3 was confirmed after exposition to the low-temperature plasma generated in air by DC negative glow corona and positive streamer discharge. The time course of acidification, H2O2 and O3 formation were deremined. Except uncertain traces of HCN, SIFT-MS analysis of exposed liquids reveals no additional reactive compounds. The microbicidal effect persists almost unchanged during 4 weeks of storage, although O3 completely and H2O2 almost disappears. Staphylococcus epidermidis and Escherichia coli were inactivated within 10 min of incubation in exposed liquids, Candida albicans needs at least 1 h. The solutions prepared by artificial mixing of reactive compounds mimic the action of exposed water, but in lesser extent. The acid milieu is the main cause of the microbicidal effect, but the possibility of still unidentified additional compound remains open. 相似文献
992.
We here aim to summarise the present knowledge on zinc binding by S100 proteins. While the importance of modulation of the
function of the S100 family of EF-hand proteins by calcium is well established, a substantial proportion is also regulated
by zinc or copper. Indeed regulation by zinc in addition to calcium was suggested almost as soon as the first S100 protein
was discovered and has been confirmed for many family members by numerous experiments. For the first, “His-Zn”, group, zinc-binding
sites composed of three histidines and an aspartic acid were first proposed based on sequence comparisons and later confirmed
by structural studies. A second, “Cys-Zn”, group lacks such well-defined zinc-binding motifs and for these cysteines were
suggested as the main zinc ligands. There is no three-dimensional structure for a Cys-Zn S100 in the presence of zinc. However,
analysis of their sequences together with their X-ray structures in the absence of zinc suggests the possibility of two zinc-binding
sites: a conserved site with a degree of similarity to those of the His-Zn group and a less-defined site with a Cys interdimer-binding
motif. Some S100 protein-mediated events, such as signalling in the extracellular space, where the levels of calcium are already
high, are most unlikely to be calcium regulated. Therefore, a broader knowledge of the role of zinc in the functioning of
the S100 proteins will add significantly to the understanding how they propagate their signals. 相似文献
993.
Folia Microbiologica - The above-described method for purification of conidia of a strain ofAspergillus niger from the conidia of the parasitic fungusPenicillium purpurogenum consists in employing... 相似文献
994.
Mikhail G. Divashuk Oleg S. Alexandrov Olga V. Razumova Ilya V. Kirov Gennady I. Karlov 《PloS one》2014,9(1)
Hemp (Cannabis sativa L.) was karyotyped using by DAPI/C-banding staining to provide chromosome measurements, and by fluorescence in situ hybridization with probes for 45 rDNA (pTa71), 5S rDNA (pCT4.2), a subtelomeric repeat (CS-1) and the Arabidopsis telomere probes. The karyotype has 18 autosomes plus a sex chromosome pair (XX in female and XY in male plants). The autosomes are difficult to distinguish morphologically, but three pairs could be distinguished using the probes. The Y chromosome is larger than the autosomes, and carries a fully heterochromatic DAPI positive arm and CS-1 repeats only on the less intensely DAPI-stained, euchromatic arm. The X is the largest chromosome of all, and carries CS-1 subtelomeric repeats on both arms. The meiotic configuration of the sex bivalent locates a pseudoautosomal region of the Y chromosome at the end of the euchromatic CS-1-carrying arm. Our molecular cytogenetic study of the C. sativa sex chromosomes is a starting point for helping to make C. sativa a promising model to study sex chromosome evolution. 相似文献
995.
996.
Elisa Villa Aleksander S. Alekseev James E. Barrick Darwin R. Boardman Alexandra V. Djenchuraeva Beate Fohrer Holger Forke Natalya V. Goreva Philip H. Heckel Tatiana N. Isakova Olga Kossovaya Lance L. Lambert María-Luisa Martínez-Chacn Carlos A. Mndez Tamara I. Nemyrovska Svetlana Remizova Elias Samankassou Luis C. Snchez de Posada Katsumi Ueno Greg Wahlman David M. Work 《Palaeoworld》2009,18(2-3):114-119
Studies carried out for more than 10 years by the Task Group to establish GSSPs at the base of the Moscovian–Kasimovian and Kasimovian–Gzhelian boundaries have resulted in the proposal that the level at which the conodont species Idiognathodus simulator (Ellison, 1941) first appears be selected to mark the base of the Gzhelian Stage. This expands this eastern European chronostratigraphic unit to a global scale.I. simulator (sensu Barrick et al., 2008) has been identified so far in Midcontinent and eastern North America, the Moscow and Donets basins and southern Urals of eastern Europe, and in south-central China. Correlation of this level based on this species and other conodont species can be reinforced in some areas by ammonoid and fusulinid data. 相似文献
997.
998.
999.
Olga Dolnik Larissa Kolesnikova Sonja Welsch Thomas Strecker Gordian Schudt Stephan Becker 《PLoS pathogens》2014,10(10)
Endosomal sorting complex required for transport (ESCRT) machinery supports the efficient budding of Marburg virus (MARV) and many other enveloped viruses. Interaction between components of the ESCRT machinery and viral proteins is predominantly mediated by short tetrapeptide motifs, known as late domains. MARV contains late domain motifs in the matrix protein VP40 and in the genome-encapsidating nucleoprotein (NP). The PSAP late domain motif of NP recruits the ESCRT-I protein tumor susceptibility gene 101 (Tsg101). Here, we generated a recombinant MARV encoding NP with a mutated PSAP late domain (rMARVPSAPmut). rMARVPSAPmut was attenuated by up to one log compared with recombinant wild-type MARV (rMARVwt), formed smaller plaques and exhibited delayed virus release. Nucleocapsids in rMARVPSAPmut-infected cells were more densely packed inside viral inclusions and more abundant in the cytoplasm than in rMARVwt-infected cells. A similar phenotype was detected when MARV-infected cells were depleted of Tsg101. Live-cell imaging analyses revealed that Tsg101 accumulated in inclusions of rMARVwt-infected cells and was co-transported together with nucleocapsids. In contrast, rMARVPSAPmut nucleocapsids did not display co-localization with Tsg101, had significantly shorter transport trajectories, and migration close to the plasma membrane was severely impaired, resulting in reduced recruitment into filopodia, the major budding sites of MARV. We further show that the Tsg101 interacting protein IQGAP1, an actin cytoskeleton regulator, was recruited into inclusions and to individual nucleocapsids together with Tsg101. Moreover, IQGAP1 was detected in a contrail-like structure at the rear end of migrating nucleocapsids. Down regulation of IQGAP1 impaired release of MARV. These results indicate that the PSAP motif in NP, which enables binding to Tsg101, is important for the efficient actin-dependent transport of nucleocapsids to the sites of budding. Thus, the interaction between NP and Tsg101 supports several steps of MARV assembly before virus fission. 相似文献
1000.
Dan P. Zandberg Sandra Rollins Olga Goloubeva Robert E. Morales Ming Tan Rodney Taylor Jeffrey S. Wolf Lisa M. Schumaker Kevin J. Cullen Ann Zimrin Robert Ord Joshua E. Lubek Mohan Suntharalingam John C. Papadimitriou Dean Mann Scott E. Strome Martin J. Edelman 《Cancer immunology, immunotherapy : CII》2015,64(3):367-379