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151.
Kerth G Petrov B Conti A Anastasov D Weishaar M Gazaryan S Jaquiéry J König B Perrin N Bruyndonckx N 《Molecular ecology》2008,17(10):2368-2381
Investigating macro-geographical genetic structures of animal populations is crucial to reconstruct population histories and to identify significant units for conservation. This approach may also provide information about the intraspecific flexibility of social systems. We investigated the history and current structure of a large number of populations in the communally breeding Bechstein's bat ( Myotis bechsteinii ). Our aim was to understand which factors shape the species' social system over a large ecological and geographical range. Using sequence data from one coding and one noncoding mitochondrial DNA region, we identified the Balkan Peninsula as the main and probably only glacial refugium of the species in Europe. Sequence data also suggest the presence of a cryptic taxon in the Caucasus and Anatolia. In a second step, we used seven autosomal and two mitochondrial microsatellite loci to compare population structures inside and outside of the Balkan glacial refugium. Central European and Balkan populations both were more strongly differentiated for mitochondrial DNA than for nuclear DNA, had higher genetic diversities and lower levels of relatedness at swarming (mating) sites than in maternity (breeding) colonies, and showed more differentiation between colonies than between swarming sites. All these suggest that populations are shaped by strong female philopatry, male dispersal, and outbreeding throughout their European range. We conclude that Bechstein's bats have a stable social system that is independent from the postglacial history and location of the populations. Our findings have implications for the understanding of the benefits of sociality in female Bechstein's bats and for the conservation of this endangered species. 相似文献
152.
Multiple conformations of E. coli Hsp90 in solution: insights into the conformational dynamics of Hsp90 总被引:1,自引:0,他引:1
Krukenberg KA Förster F Rice LM Sali A Agard DA 《Structure (London, England : 1993)》2008,16(5):755-765
Hsp90, an essential eukaryotic chaperone, depends upon its intrinsic ATPase activity for function. Crystal structures of the bacterial Hsp90 homolog, HtpG, and the yeast Hsp90 reveal large domain rearrangements between the nucleotide-free and the nucleotide-bound forms. We used small-angle X-ray scattering and recently developed molecular modeling methods to characterize the solution structure of HtpG and demonstrate how it differs from known Hsp90 conformations. In addition to this HtpG conformation, we demonstrate that under physiologically relevant conditions, multiple conformations coexist in equilibrium. In solution, nucleotide-free HtpG adopts a more extended conformation than observed in the crystal, and upon the addition of AMPPNP, HtpG is in equilibrium between this open state and a closed state that is in good agreement with the yeast AMPPNP crystal structure. These studies provide a unique view of Hsp90 conformational dynamics and provide a model for the role of nucleotide in effecting conformational change. 相似文献
153.
Structure of the mammalian 80S ribosome at 8.7 A resolution 总被引:1,自引:0,他引:1
Chandramouli P Topf M Ménétret JF Eswar N Cannone JJ Gutell RR Sali A Akey CW 《Structure (London, England : 1993)》2008,16(4):535-548
In this paper, we present a structure of the mammalian ribosome determined at approximately 8.7 A resolution by electron cryomicroscopy and single-particle methods. A model of the ribosome was created by docking homology models of subunit rRNAs and conserved proteins into the density map. We then modeled expansion segments in the subunit rRNAs and found unclaimed density for approximately 20 proteins. In general, many conserved proteins and novel proteins interact with expansion segments to form an integrated framework that may stabilize the mature ribosome. Our structure provides a snapshot of the mammalian ribosome at the beginning of translation and lends support to current models in which large movements of the small subunit and L1 stalk occur during tRNA translocation. Finally, details are presented for intersubunit bridges that are specific to the eukaryotic ribosome. We suggest that these bridges may help reset the conformation of the ribosome to prepare for the next cycle of chain elongation. 相似文献
154.
Andrej Vilfan 《Biophysical journal》2009,97(4):1130-1137
We present a model study of gliding assays in which actin filaments are moved by nonprocessive myosin motors. We show that even if the power stroke of the motor protein has no lateral component, the filaments will rotate around their axis while moving over the surface. Notably, the handedness of this twirling motion is opposite from that of the actin filament structure. It stems from the fact that the gliding actin filament has target zones, where its subunits point toward the surface and are therefore more accessible for myosin heads. Each myosin head has a higher binding probability before it reaches the center of the target zone than afterwards, which results in a left-handed twirling. We present a stochastic simulation and an approximative analytical solution. The calculated pitch of the twirling motion depends on the filament velocity (ATP concentration). It reaches ∼400 nm for low speeds and increases with higher speeds. 相似文献
155.
Viktor Demko Andrej Pavlovič Danka Valková L’udmila Slováková Bernhard Grimm Ján Hudák 《Planta》2009,230(1):165-176
Light-independent chlorophyll (Chl) biosynthesis is a prerequisite for the assembly of photosynthetic pigment–protein complexes
in the dark. Dark-grown Larix decidua Mill. seedlings synthesize Chl only in the early developmental stages and their Chl level rapidly declines during the subsequent
development. Our analysis of the key regulatory steps in Chl biosynthesis revealed that etiolation of initially green dark-grown
larch cotyledons is connected with decreasing content of glutamyl-tRNA reductase and reduced 5-aminolevulinic acid synthesizing
capacity. The level of the Chl precursor protochlorophyllide also declined in the developing larch cotyledons. Although the
genes chlL, chlN and chlB encoding subunits of the light-independent protochlorophyllide oxidoreductase were constitutively expressed in the larch
seedlings, the accumulation of the ChlB subunit was developmentally regulated and ChlB content decreased in the fully developed
cotyledons. The efficiency of chlB RNA-editing was also reduced in the mature dark-grown larch seedlings. In contrast to larch, dark-grown seedlings of Picea abies (L.) Karst. accumulate Chl throughout their whole development and show a different control of ChlB expression. Analysis of
the plastid ultrastructure, photosynthetic proteins by Western blotting and photosynthetic parameters by gas exchange and
Chl fluorescence measurements provide additional experimental proofs for differences between dark and light Chl biosynthesis
in spruce and larch seedlings. 相似文献
156.
Daniela Leite Fabrino Christopher K.E. Bleck Elsa Anes Andrej Hasilik Rossana C.N. Melo Michael Niederweis Gareth Griffiths Maximiliano Gabriel Gutierrez 《Microbes and infection / Institut Pasteur》2009,11(10-11):868-875
Non-pathogenic mycobacteria such us Mycobacterium smegmatis reside in macrophages within phagosomes that fuse with late endocytic/lysosomal compartments. This sequential fusion process is required for the killing of non-pathogenic mycobacteria by macrophages. Porins are proteins that allow the influx of hydrophilic molecules across the mycobacterial outer membrane. Deletion of the porins MspA, MspC and MspD significantly increased survival of M. smegmatis in J774 macrophages. However, the mechanism underlying this observation is unknown. Internalization of wild-type M. smegmatis (SMR5) and the porin triple mutant (ML16) by macrophages was identical indicating that the viability of the porin mutant in vivo was enhanced. This was not due to effects on phagosome trafficking since fusion of phagosomes containing the mutant with late endocytic compartments was unaffected. Moreover, in ML16-infected macrophages, the generation of nitric oxide (NO) was similar to the wild type-infected cells. However, ML16 was significantly more resistant to the effects of NO in vitro compared to SMR5. Our data provide evidence that porins render mycobacteria vulnerable to killing by reactive nitrogen intermediates within phagosomes probably by facilitating uptake of NO across the mycobacterial outer membrane. 相似文献
157.
Libusha Kelly Ursula Pieper Narayanan Eswar Franklin A. Hays Min Li Zygy Roe-Zurz Deanna L. Kroetz Kathleen M. Giacomini Robert M. Stroud Andrej Sali 《Journal of structural and functional genomics》2009,10(4):269-280
Membrane proteins serve as cellular gatekeepers, regulators, and sensors. Prior studies have explored the functional breadth
and evolution of proteins and families of particular interest, such as the diversity of transport-associated membrane protein
families in prokaryotes and eukaryotes, the composition of integral membrane proteins, and family classification of all human
G-protein coupled receptors. However, a comprehensive analysis of the content and evolutionary associations between membrane
proteins and families in a diverse set of genomes is lacking. Here, a membrane protein annotation pipeline was developed to
define the integral membrane genome and associations between 21,379 proteins from 34 genomes; most, but not all of these proteins
belong to 598 defined families. The pipeline was used to provide target input for a structural genomics project that successfully
cloned, expressed, and purified 61 of our first 96 selected targets in yeast. Furthermore, the methodology was applied (1)
to explore the evolutionary history of the substrate-binding transmembrane domains of the human ABC transporter superfamily,
(2) to identify the multidrug resistance-associated membrane proteins in whole genomes, and (3) to identify putative new membrane
protein families. 相似文献
158.
159.
Juergen Graessler Dominik Schwudke Peter E. H. Schwarz Ronny Herzog Andrej Shevchenko Stefan R. Bornstein 《PloS one》2009,4(7)
Background
Dyslipoproteinemia, obesity and insulin resistance are integrative constituents of the metabolic syndrome and are major risk factors for hypertension. The objective of this study was to determine whether hypertension specifically affects the plasma lipidome independently and differently from the effects induced by obesity and insulin resistance.Methodology/Principal Findings
We screened the plasma lipidome of 19 men with hypertension and 51 normotensive male controls by top-down shotgun profiling on a LTQ Orbitrap hybrid mass spectrometer. The analysis encompassed 95 lipid species of 10 major lipid classes. Obesity resulted in generally higher lipid load in blood plasma, while the content of tri- and diacylglycerols increased dramatically. Insulin resistance, defined by HOMA-IR >3.5 and controlled for BMI, had little effect on the plasma lipidome. Importantly, we observed that in blood plasma of hypertensive individuals the overall content of ether lipids decreased. Ether phosphatidylcholines and ether phosphatidylethanolamines, that comprise arachidonic (20∶4) and docosapentaenoic (22∶5) fatty acid moieties, were specifically diminished. The content of free cholesterol also decreased, although conventional clinical lipid homeostasis indices remained unaffected.Conclusions/Significance
Top-down shotgun lipidomics demonstrated that hypertension is accompanied by specific reduction of the content of ether lipids and free cholesterol that occurred independently of lipidomic alterations induced by obesity and insulin resistance. These results may form the basis for novel preventive and dietary strategies alleviating the severity of hypertension. 相似文献160.
Li Ding Maciej Paszkowski-Rogacz Anja Nitzsche Mikolaj Michal Slabicki Anne-Kristin Heninger Ingrid de Vries Ralf Kittler Magno Junqueira Andrej Shevchenko Herbert Schulz Norbert Hubner Michael Xavier Doss Agapios Sachinidis Juergen Hescheler Roberto Iacone Konstantinos Anastassiadis A. Francis Stewart M. Teresa Pisabarro Antonio Caldarelli Ina Poser Frank Buchholz 《Cell Stem Cell》2009,4(5):403-415