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971.
The trans-Golgi network (TGN) is one of the main, if not the main, sorting stations in the process of intracellular protein trafficking.
It is therefore of central importance to understand how the key players in the TGN-based sorting and delivery process, the
post-Golgi carriers (PGCs), form and function. Over the last few years, modern morphological approaches have generated new
insights into the questions of PGC biogenesis, structure and dynamics. Here, we present a view by which the “lifecycle” of
a PGC consists of several distinct stages: the formation of TGN tubular export domains (where different cargoes are segregated
from each other and from the Golgi enzymes); the docking of these tubular domains onto molecular motors and their extrusion
towards the cell periphery along microtubules; the fission of the forming PGC from the donor membrane; and the delivery of
the newly formed PGC to its specific acceptor organelle. It is now important to add the many molecular machineries that have
been described as operating at the TGN to this “morphofunctional map” of the TGN export process. 相似文献
972.
Alexander P. Tulloch 《Phytochemistry》1978,17(9):1613-1615
Leaf wax of a glaucous variety of Poa ampla contains hydrocarbons (5%, C23–C35), esters (9%, C36–C56), free acids (3%, C16–C34), free alcohols (6%, mainly C26); hentriacontane-14,16-dione (14%), 5-oxohentriacontane-14,16-dione (1%); hydroxy β-diketones (56%) and unidentified material (6%). The hydroxy β-diketones, which are more abundant in this wax than in others, were shown by 13C NMR to consist of 4-hydroxy (15%), 5-hydroxy (70%) and 6-hydroxy (15%) hentriacontane-14,16-diones. 相似文献
973.
Effects of chronic food restriction and treatments with leptin or ghrelin on different reproductive parameters of male rats 总被引:1,自引:0,他引:1
Sirotkin AV Chrenková M Nitrayová S Patras P Darlak K Valenzuela F Pinilla L Tena-Sempere M 《Peptides》2008,29(8):1362-1368
The existence of a close relationship between energy status and reproductive function is well-documented, especially in females, but its underlying mechanisms remain to be fully unfolded. This study aimed to examine the effects of restriction of daily calorie intake, as well as chronic treatments with the metabolic hormones leptin and ghrelin, on the secretion of different reproductive hormones, namely pituitary gonadotropins and prolactin, as well as testosterone, in male rats. Restriction (50%) in daily food intake for 20 days significantly reduced body weight as well as plasma PRL and T levels, without affecting basal LH and FSH concentrations and testicular weight. Chronic administration of leptin to rats fed ad libitum increased plasma PRL levels and decreased circulating T, while it did not alter other hormonal parameters under analysis. In contrast, in rats subjected to 50% calorie restriction, leptin administration increased plasma T levels and reduced testis weight. Conversely, ghrelin failed to induce major hormonal changes but tended to increase testicular weight in fed animals, while repeated ghrelin injections in food-restricted males dramatically decreased plasma LH and T concentrations and reduced testis weight. In sum, we document herein the isolated and combined effects of metabolic stress (50% food restriction) and leptin or ghrelin treatments on several reproductive hormones in adult male rats. Overall, our results further stress the impact and complex way of action of different metabolic cues, such as energy status and key hormones, in reproductive function also in the male. 相似文献
974.
A novel inhibitor of cyclin-Cdk activity detected in transforming growth factor beta-arrested epithelial cells. 总被引:17,自引:5,他引:17 下载免费PDF全文
J M Slingerland L Hengst C H Pan D Alexander M R Stampfer S I Reed 《Molecular and cellular biology》1994,14(6):3683-3694
Transforming growth factor beta (TGF-beta) is a potent inhibitor of epithelial cell growth. Cyclins E and A in association with Cdk2 have been shown to play a role in the G1-to-S phase transition in mammalian cells. We have studied the effects of TGF-beta-mediated growth arrest on G1/S cyclins E and A. Inhibition of cyclin A-associated kinase by TGF-beta is primarily due to a decrease in cyclin A mRNA and protein. By contrast, while TGF-beta inhibits accumulation of cyclin E mRNA, the reduction in cyclin E protein is minimal. Instead, we find that the activation of cyclin E-associated kinase that normally accompanies the G1-to-S phase transition is inhibited. A novel inhibitor of cyclin-Cdk complexes was detected in TGF-beta-treated cell lysates. Inhibition is mediated by a heat-stable protein that targets both Cdk2 and Cdc2 kinases. In G0-arrested cells, a similar inhibitor of Cdk2 kinase was detected. These data suggest the existence of an inhibitor of cyclin-dependent kinases induced under different conditions to mediate antiproliferative responses. 相似文献
975.
Densities of Vibrio vulnificus in the intestines of fish from the U.S. Gulf Coast. 总被引:3,自引:4,他引:3 下载免费PDF全文
Densities of Vibrio vulnificus in the intestinal contents of various finfish, oysters, and crabs and in sediment and waters of the U.S. Gulf Coast were determined by the most probable number procedure. Species were identified by enzyme immunoassay. During the winter, densities of V. vulnificus were low, and the organism was isolated more frequently from sheepshead fish than from sediment and seawater. From April to October, V. vulnificus densities were considerably higher (2 to 5 logs) in estuarine fish than in surrounding water, sediment, or nearby oysters and crustacea. Highest densities were found in the intestinal contents of certain bottom-feeding fish (10(8)/100 g), particularly those that consume mollusks and crustaceans. Densities of V. vulnificus in fish that feed primarily on plankton and other finfish were similar to those in oysters, sediment, and crabs (10(5)/100 g). V. vulnificus was found infrequently in offshore fish. The presence of high densities of V. vulnificus in the intestines of common estuarine fish may have both ecological (growth and transport) and public health (food and wound infections) implications. 相似文献
976.
Alexander Kieneke Wilko H. Ahlrichs Pedro Martínez Arbizu Thomas Bartolomaeus 《Zoomorphology》2008,127(1):1-20
In an attempt to obtain detailed information on the entire protonephridial system in Gastrotricha, we have studied the protonephridial
ultrastructure of two paucitubulatan species, Xenotrichula carolinensis syltensis and Chaetonotus maximus by means of complete sets of ultrathin sections. In spite of some differences in detail, the morphology of protonephridia
in both examined species shows a common pattern: Both species have one pair of protonephridia that consist of a bicellular
terminal organ, a voluminous, aciliar canal cell and an adjacent, aciliar nephridiopore cell. The terminal organ consists
of two monociliar terminal cells each with a distal cytoplasmic lobe. These lobes interdigitate and surround cilia and microvilli
of the terminal cells. Where both lobes interdigitate, a meandering cleft is formed that is covered by the filtration barrier.
We here term the entire structure composite filter. The elongated, in some regions convoluted protonephridial lumen opens
distally to the outside via a permanent nephridiopore. A comparison with the protonephridia of other species of the Gastrotricha
allows hypothesising the following autapomorphies of the Paucitubulata: The bicellular terminal organ with a composite filter,
the convoluted distal canal cell lumen and the absence of cilia, ciliary basal structures and microvilli within the canal
cell. Moreover, this comparative survey could confirm important characteristics of the protonephridial system assumed for
the ground pattern of Gastrotricha like, for example, the single terminal cell with one cilium surrounded by eight microvilli. 相似文献
977.
The influence of the local anesthetic lidocaine on electrostatic properties of a lipid membrane bilayer was studied by molecular dynamics simulations. The electrostatic dipole potential, charge densities, and orientations of the headgroup angle have been examined in the presence of different amounts of charged or uncharged forms of lidocaine. Important changes in the membrane properties caused by the presence of both forms of lidocaine are presented and discussed. Our simulations have shown that both charged and uncharged lidocaine cause almost the same increase in the electrostatic potential in the middle of the membrane, although for different reasons. The increase, ∼90 mV for 9 mol % of lidocaine and 220 mV for 28 mol % of lidocaine, is of a size that may affect the functioning of voltage-gated ion channels. 相似文献
978.
A procedure is presented for refinement of a homology model of E. coli tRNAVal, originally based on the X-ray structure of yeast tRNAPhe, using experimental residual dipolar coupling (RDC) and small angle X-ray scattering (SAXS) data. A spherical sampling algorithm
is described for refinement against SAXS data that does not require a globbic approximation, which is particularly important
for nucleic acids where such approximations are less appropriate. Substantially higher speed of the algorithm also makes its
application favorable for proteins. In addition to the SAXS data, the structure refinement employed a sparse set of NMR data
consisting of 24 imino N–HN RDCs measured with Pf1 phage alignment, and 20 imino N–HN RDCs obtained from magnetic field dependent alignment of tRNAVal. The refinement strategy aims to largely retain the local geometry of the 58% identical tRNAPhe by ensuring that the atomic coordinates for short, overlapping segments of the ribose-phosphate backbone and the conserved
base pairs remain close to those of the starting model. Local coordinate restraints are enforced using the non-crystallographic
symmetry (NCS) term in the XPLOR-NIH or CNS software package, while still permitting modest movements of adjacent segments.
The RDCs mainly drive the relative orientation of the helical arms, whereas the SAXS restraints ensure an overall molecular
shape compatible with experimental scattering data. The resulting structure exhibits good cross-validation statistics (jack-knifed
Q
free = 14% for the Pf1 RDCs, compared to 25% for the starting model) and exhibits a larger angle between the two helical arms
than observed in the X-ray structure of tRNAPhe, in agreement with previous NMR-based tRNAVal models.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
979.
Baranova IN Kurlander R Bocharov AV Vishnyakova TG Chen Z Remaley AT Csako G Patterson AP Eggerman TL 《Journal of immunology (Baltimore, Md. : 1950)》2008,181(10):7147-7156
Scavenger receptor CD36 mediates Staphylococcus aureus phagocytosis and initiates TLR2/6 signaling. We analyzed the role of CD36 in the uptake and TLR-independent signaling of various bacterium, including Escherichia coli, Klebsiella pneumoniae, Salmonella typhimurium, S. aureus, and Enterococcus faecalis. Expression of human CD36 in HeLa cells increased the uptake of both gram-positive and gram-negative bacteria compared with the control mock-transfected cells. Bacterial adhesion was associated with pathogen phagocytosis. Upon CD36 transfection, HEK293 cells, which demonstrate no TLR2/4 expression, acquired LPS responsiveness as assessed by IL-8 production. The cells demonstrated a marked 5- to 15-fold increase in cytokine release upon exposure to gram-negative bacteria, while the increase was much smaller (1.5- to 3-fold) with gram-positive bacteria and lipoteichoic acid. CD36 down-regulation utilizing CD36 small interfering RNA reduced cytokine release by 40-50% in human fibroblasts induced by both gram-negative and gram-positive bacteria as well as LPS. Of all MAPK signaling cascade inhibitors tested, only the inhibitor of JNK, a stress-activated protein kinase, potently blocked E. coli/LPS-stimulated cytokine production. NF-kappaB inhibitors were ineffective, indicating direct TLR-independent signaling. JNK activation was confirmed by Western blot analyses of phosphorylated JKN1/2 products. Synthetic amphipathic peptides with an alpha-helical motif were shown to be efficient inhibitors of E. coli- and LPS-induced IL-8 secretion as well as JNK1/2 activation/phosphorylation in CD36-overexpressing cells. These results indicate that CD36 functions as a phagocytic receptor for a variety of bacteria and mediates signaling induced by gram-negative bacteria and LPS via a JNK-mediated signaling pathway in a TLR2/4-independent manner. 相似文献
980.
The agr quorum-sensing system of Staphylococcus aureus modulates the expression of virulence factors in response to autoinducing peptides (AIPs). Recent studies have suggested a role for the agr system in S. aureus biofilm development, as agr mutants exhibit a high propensity to form biofilms, and cells dispersing from a biofilm have been observed displaying an active agr system. Here, we report that repression of agr is necessary to form a biofilm and that reactivation of agr in established biofilms through AIP addition or glucose depletion triggers detachment. Inhibitory AIP molecules did not induce detachment and an agr mutant was non-responsive, indicating a dependence on a functional, active agr system for dispersal. Biofilm detachment occurred in multiple S. aureus strains possessing divergent agr systems, suggesting it is a general S. aureus phenomenon. Importantly, detachment also restored sensitivity of the dispersed cells to the antibiotic rifampicin. Proteinase K inhibited biofilm formation and dispersed established biofilms, suggesting agr-mediated detachment occurred in an ica-independent manner. Consistent with a protease-mediated mechanism, increased levels of serine proteases were detected in detaching biofilm effluents, and the serine protease inhibitor PMSF reduced the degree of agr-mediated detachment. Through genetic analysis, a double mutant in the agr-regulated Aur metalloprotease and the SplABCDEF serine proteases displayed minimal extracellular protease activity, improved biofilm formation, and a strongly attenuated detachment phenotype. These findings indicate that induction of the agr system in established S. aureus biofilms detaches cells and demonstrate that the dispersal mechanism requires extracellular protease activity. 相似文献