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951.
Michel De Wilde Teresa Cabezón Raimundo Villarroel Albert Herzog Alex Bollen 《Molecular & general genetics : MGG》1975,142(1):19-33
Summary Two spontaneous mutants of Escherichia coli strain KMBL-146 selected for resistance to the aminoglycoside antibiotic neamine show severe restriction of amber suppressors in vivo. Purified ribosomes from the mutant strains exhibit low neamine-induced misreading in vitro and a decreased affinity for the related antibiotic streptomycin.Biochemical analysis shows that the mutants each have two modified 30S ribosomal proteins, S12 and S5. In agreement with these results, genetic analysis shows that two mutations are present, neither of which confers resistance to neamine by itself; the mutation located in gene rpxL (the structural gene for protein S12) confers streptomycin dependence but this dependence is suppressed in the presence of the second mutation, located in gene rpxE (the structural gene for protein S5). 相似文献
952.
H. M. Canelas F. B. De Jorge W. C. Pereira J. Sallum 《Journal of neurochemistry》1968,15(12):1455-1461
Abstract— Twenty-nine autopsy specimens of intracerebral tumours (nine astrocytomata, ten medulloblastomata and ten glioblastomata multiforme), as well as samples of peritumoral and apparently normal brain tissue, have been studied for Na, K, P, Ca, Mg, Cu, and S contents.
The tumour tissue, irrespective of the histological characteristics, as compared to the 'normal' and perineoplastic tissues, showed higher concentration of Ca, Mg, Cu and S. The peritumoral tissue, regardless of the tumour type, showed a higher concentration of Cu than the 'normal' control brain.
The more malignant glioblatomata and medulloblastomata. The Cu levels did not show a significant diference. 相似文献
The tumour tissue, irrespective of the histological characteristics, as compared to the 'normal' and perineoplastic tissues, showed higher concentration of Ca, Mg, Cu and S. The peritumoral tissue, regardless of the tumour type, showed a higher concentration of Cu than the 'normal' control brain.
The more malignant glioblatomata and medulloblastomata. The Cu levels did not show a significant diference. 相似文献
953.
954.
Darin A. Croft Jennifer M. H. Chick Federico Anaya 《Journal of Mammalian Evolution》2011,18(4):245-268
The rodents of the middle Miocene fauna of Quebrada Honda Bolivia are described. The most abundant rodent is the chinchillid Prolagostomus sp. More precise identification of this species will require revision of early to middle Miocene lagostomines, taking into account variation in modern populations. The next most common rodents are the tiny octodontoid Acarechimys, sp. nov.?, and the caviid Guiomys unica. The Acarechimys species may be unique to Quebrada Honda, but verification awaits revision of this geographically and temporally widespread genus. Guiomys unica is a recently described species otherwise known only from two Patagonian localities, El Petiso and Río Chico. Two rodents are unique to Quebrada Honda. Mesoprocta hypsodus, gen. et sp. nov., is a dasyproctid distinguished by its very hypsodont, cement-covered cheek teeth. Quebradahondomys potosiensis, gen. et sp. nov., is an adelphomyine echimyid distinguished by the less oblique lophids of its trilophodont cheek teeth, among other features. The rodents of Quebrada Honda are more similar to those of Patagonia than those of northern South America, paralleling patterns seen in other mammal groups from this fauna. 相似文献
955.
Daniele De Simone Lorella D’Amico Daniela Bressanin Emma Motta Tiziana Annesi 《Mycological Progress》2011,10(3):301-306
Thirteen isolates of Inonotus rickii/Ptychogaster cubensis, from different geographic provenances, were analyzed by sequencing ITS1, ITS 2 and 5,8S ribosomal RNA region. A phylogenetic
tree, also including sequences available in Genbank database, showed that the strains enclosed in this study fall into two
well-separated groups, one formed by isolates from Florida (USA) and the other one by isolates from Europe, Argentina and
China. Differences were also highlighted on the growth rate of mycelial cultures at different temperatures. In fact, although
the tested isolates generally attained the best growth at 30°C, isolates from Europe seem well adapted to higher temperatures
and went on growing at 40°C whilst the growth of isolates from Florida significantly decreased at 35°C. Since the teleomorph
I. rickii was never detected in Florida, and in this study noticeable differences were detected by analysis of ITS region, the existence
of two possible distinct species, not discriminated solely on the basis of morphological characters, could be suggested. 相似文献
956.
The cystine/glutamate exchanger (antiporter xc−) is a membrane transporter involved in the uptake of cystine, the rate-limiting amino acid in the synthesis of glutathione.
Recent studies suggest that the antiporter plays a role in the slow oxidative excitotoxity and in the pathological effects
of β-N-oxalylamino-l-alanine, the molecule responsible for neurolathyrism, a neurotoxic upper motor neuron disease. The mouse cystine/glutamate
exchanger has been cloned and showed to be composed of two distinct proteins, one of which being a novel protein, named xCT,
of 502 amino acids and 12 putative trans-membrane domains. We have generated and purified a polyclonal antibody to mouse xCT
and studied its expression in rat brain and in different cultured cells (astrocytes, fibroblasts and neurons) using Western
blot and immunocytochemical techniques. Expression of xCT was also studied in rat brain and muscle at different developmental
stages. Parallel experiments were carried out with antibodies to the heavy chain of 4F2 surface antigen, the non-specific
subunit of the antiporter xc−. xCT antibody detected in all cell and tissue extracts a specific band of about 40 kDa. Subcellular fractionation demonstrated
that xCT is concentrated mainly in the microsomal-mitochondrial fraction, in accord with its structure as transmembrane protein.
Immunocytochemical analysis showed a strong staining in all cells examined, included neurons. Furthermore, both xCT and the
heavy chain of 4F2 surface antigen increased in the brain during development, reaching the highest expression in adulthood.
The study of the expression and developmental profile of xCT represents a first step towards a better characterization of
its biochemical properties and function, which in turn may help to understand the relative contribution of the xc− antiporter in the pathogenesis of certain neurodegenerative diseases. 相似文献
957.
Helen Michels Susanne Lildal Amsinck Erik Jeppesen Luc De Meester 《Hydrobiologia》2007,594(1):117-129
In shallow temperate lakes, zooplankton populations may exhibit diel horizontal migration (DHM) and move towards macrophytes
during the day to avoid fish. Using a natural Daphnia magna population, we undertook an experimental investigation aimed to describe the genetic variation for DHM and to study whether
an adaptive micro-evolutionary response occurred to changes in macrophyte coverage and fish predation pressure through time.
Twenty-seven D. magna clones were hatched from ephippia in the sediment of shallow Lake Ring, Denmark. This lake was eutrophied during the 20th
century and was subject to restoration measures in the 1970s. The DHM behaviour of the clones was observed both in the presence
and absence of fish kairomone. Significant interclonal variation in DHM behaviour occurred in both treatments. To study the
micro-evolutionary response of the Lake Ring D. magna population, two approaches were used. First, we compared the DHM behaviour of clones derived from ephippia collected at different
depths. A comparison was conducted between clones resurrected from the period of eutrophication (1960–1980) and from the period
of recovery (1986–2000). A significant treatment (presence and absence of fish kairomone) × period interaction effect was
identified, suggesting a significant micro-evolutionary response for DHM behaviour. The D. magna clones exhibited a significantly stronger horizontal migration response during the period of eutrophication than in the recovery
phase. Second, clonal means, representing the influence of the genotype on the trait, were correlated with environmental conditions
(macrophyte cover, fish predation pressure and Secchi depth). The results of this analysis also suggest that a micro-evolutionary
response by Daphnia has occurred in reaction to changes in fish predation pressure. In periods with high fish predation pressure, Daphnia migrated more strongly towards the plants.
Guest editor: Piet Spaak
Cladocera: Proceedings of the 7th International Symposium on Cladocera 相似文献
958.
Oxidative DNA damage is one of the most common threats to genome stability and DNA repair enzymes provide protection from the effects of oxidized DNA bases. In mammalian cells, base excision repair (BER) mediated by the OGG1 and MYH DNA glycosylases prevents the accumulation of 8-oxoguanine (8-oxoG) in DNA. When steady-state levels of DNA 8-oxoG were measured in myh(-/-) and myh(-/-)/ogg1(-/-) mice, an age-dependent accumulation of the oxidized purine was found in lung and small intestine of doubly defective myh(-/-)/ogg1(-/-) mice. Since there is an increased incidence of lung and small intestinal cancer in myh(-/-)/ogg1(-/-) mice, these findings are consistent with a causal role for unrepaired oxidized DNA bases in cancer development. We previously presented in vitro evidence that mismatch repair (MMR) participates in the repair of oxidative DNA damage and msh2(-/-) mouse embryo fibroblasts also have increased steady state levels of DNA 8-oxoG. To investigate whether DNA 8-oxoG also accumulates in vivo, basal levels were measured in several organs of 4-month-old msh2(-/-) mice and their wild-type counterparts. Msh2(-/-) mice had significantly increased levels of DNA 8-oxoG in spleen, heart, liver, lung, kidney and possibly small intestine but not in bone marrow, thymus or brain. The tissue-specificity of DNA 8-oxoG accumulation in msh2(-/-) and other DNA repair defective mice suggests that DNA protection of different organs is mediated by different combinations of repair pathways. 相似文献
959.
Han SK Federico S Grillo A Giaquinta G Herzog W 《Biomechanics and modeling in mechanobiology》2007,6(3):139-150
The integrity of articular cartilage depends on the proper functioning and mechanical stimulation of chondrocytes, the cells
that synthesize extracellular matrix and maintain tissue health. The biosynthetic activity of chondrocytes is influenced by
genetic factors, environmental influences, extracellular matrix composition, and mechanical factors. The mechanical environment
of chondrocytes is believed to be an important determinant for joint health, and chondrocyte deformation in response to mechanical
loading is speculated to be an important regulator of metabolic activity. In previous studies of chondrocyte deformation,
articular cartilage was described as a biphasic material consisting of a homogeneous, isotropic, linearly elastic solid phase,
and an inviscid fluid phase. However, articular cartilage is known to be anisotropic and inhomogeneous across its depth. Therefore,
isotropic and homogeneous models cannot make appropriate predictions for tissue and cell stresses and strains. Here, we modelled
articular cartilage as a transversely isotropic, inhomogeneous (TI) material in which the anisotropy and inhomogeneity arose
naturally from the microstructure of the depth-dependent collagen fibril orientation and volumetric fraction, as well as the
chondrocyte shape and volumetric fraction. The purpose of this study was to analyse the deformation behaviour of chondrocytes
using the TI model of articular cartilage. In order to evaluate our model against experimental results, we simulated indentation
and unconfined compression tests for nominal compressions of 15%. Chondrocyte deformations were analysed as a function of
location within the tissue. The TI model predicted a non-uniform behaviour across tissue depth: in indentation testing, cell
height decreased by 43% in the superficial zone and between 11 and 29% in the deep zone. In unconfined compression testing,
cell height decreased by 32% in the superficial zone, 25% in the middle, and 18% in the deep zones. This predicted non-uniformity
is in agreement with experimental studies. The novelty of this study is the use of a cartilage material model accounting for
the intrinsic inhomogeneity and anisotropy of cartilage caused by its microstructure. 相似文献
960.
de Barros CM Andrade LR Allodi S Viskov C Mourier PA Cavalcante MC Straus AH Takahashi HK Pomin VH Carvalho VF Martins MA Pavão MS 《The Journal of biological chemistry》2007,282(3):1615-1626
The hemolymph of ascidians (Chordata-Tunicata) contains different types of hemocytes embedded in a liquid plasma. In the present study, heparin and a sulfated heteropolysaccharide were purified from the hemolymph of the ascidian Styela plicata. The heteropolysaccharide occurs free in the plasma, is composed of glucose ( approximately 60%) and galactose ( approximately 40%), and is highly sulfated. Heparin, on the other hand, occurs in the hemocytes, and high performance liquid chromatography of the products formed by degradation with specific lyases revealed that it is composed mainly by the disaccharides DeltaUA(2SO(4))-1-->4-beta-d-GlcN(SO(4)) (39.7%) and DeltaUA(2SO(4))-1-->4-beta-d-GlcN(SO(4))(6SO(4)) (38.2%). Small amounts of the 3-O-sulfated disaccharides DeltaUA(2SO(4))-1-->4-beta-d-GlcN(SO(4))(3SO(4)) (9.8%) and DeltaUA(2SO(4))-1-->4-beta-d-GlcN(SO(4))(3SO(4))(6SO(4)) (3.8%) were also detected. These 3-O-sulfated disaccharides were demonstrated to be essential for the binding of the hemocyte heparin to antithrombin III. Electron microscopy techniques were used to characterize the ultrastructure of the hemocytes and to localize heparin and histamine in these cells. At least five cell types were recognized and classified as univacuolated and multivacuolated cells, amebocytes, hemoblasts, and granulocytes. Immunocytochemistry showed that heparin and histamine co-localize in intracellular granules of only one type of hemocyte, the granulocyte. These results show for the first time that in ascidians, a sulfated galactoglucan circulates free in the plasma, and heparin occurs as an intracellular product of a circulating basophil-like cell. 相似文献