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961.
Emile J. M. Clerkx Hetty Blankestijn-De Vries Gerda J. Ruys Steven P. C. Groot Maarten Koornneef 《Physiologia plantarum》2004,121(3):448-461
Seeds gradually lose their viability during dry storage. The damage that occurs at the biochemical level can alter the seed physiological status and is affected by the storage conditions of the seeds. Although these environmental conditions controlling loss of viability have been investigated frequently, little information is available on the genetics of seed longevity. Using Arabidopsis mutants in defined developmental or biochemical pathways such as those affected in seed coat composition, seed dormancy, hormone function and control of oxidative stress, we tried to gain insight into the genes and mechanisms controlling viability of stored seeds. Mutations like abscisic acid insensitive3 ( abi3 ) as well as abscisic acid deficient1 ( aba1 ) show reduced longevity, which may be partially related to the seed dormancy phenotype of these mutants. Mutants with seed coat alterations, especially aberrant tests shape ( ats ), showed a stronger reduction in germination percentage after storage, indicating the importance of a 'functional' seed coat for seed longevity. A specific emphasis was placed on mutants affected in dealing with Reactive Oxygen Species (ROS). Because several pathways are involved in protection against ROS and because gene redundancy is a common feature in Arabidopsis , 'double' mutants were generated. These 'double' mutants and the corresponding single mutants were subjected to a controlled deterioration test (CDT) and a germination assay on hydrogen peroxide (H2 O2 ) after prolonged storage at two relative humidities. CDT and germination on H2 O2 affected all genotypes, although it appears that other effects like genetic background are more important than the deficiencies in the ROS scavenging pathway. Explanations for this limited effect of mutations affecting ROS scavenging are discussed. 相似文献
962.
963.
Westerterp M Boermeester MA Omloo JM Hulshof MC Vervenne WL Lutter R Out TA van Lanschot JJ 《Cancer immunology, immunotherapy : CII》2008,57(12):1837-1847
Background To compare immune responses following neoadjuvant chemoradiation therapy in combination with hyperthermia plus surgery to
those induced by surgery alone in patients with oesophageal cancer.
Methods Thirty-two patients with histopathologically proven oesophageal cancer, scheduled for potentially curative transhiatal or
transthoracic oesophagectomy with (neo, n = 20) or without (control, n = 12) neoadjuvant thermochemoradiation therapy (ThCR) were included. Peripheral blood samples were obtained before ThCR,
after 2 weeks of ThCR, 1 day before surgery, on postoperative days 1, 3, 7, and 6 weeks after surgery, for white blood cell
counts, lymphocyte subsets and T helper type 1 (Th1) and type 2 (Th2) lymphocyte responses.
Results Neo patients showed a significant decrease in granulocytes and lymphocyte subsets, and T cell cytokines after 2 weeks of ThCR.
Only CD8+ (cytotoxic) T cells recovered after ThCR to reach normal levels prior to surgery. In contrast, CD4+ T (helper) cells,
and NK- and B cells in neo patients did not recover prior to surgery (all P < 0.05). Oesophagectomy induced a significant increase in granulocytes and a decrease in lymphocytes (and subsets). Only
those subsets that had not recovered after ThCR (CD4+ T cells, NK and B cells but not CD8+ T cells), were significantly lower
(all P < 0.05) during the entire postoperative study period. Postoperatively, the stimulated cytokine production capacity of Th1
and Th2 cells, corrected for number of T cells, was not significantly different between the groups.
Conclusion Neoadjuvant thermochemoradiation for oesophageal cancer caused significant disturbances of host cellular immunity with reduced
T, NK and B cell counts, and differential recovery of cytotoxic and helper T cells leading to prolonged T cell imbalance that
extends beyond the time of surgery. The functional and anti-tumour consequences of this immunodisturbance need further investigation,
as recovery of T helper cytokine production towards surgery was less impaired than T helper cell counts. 相似文献
964.
Bmi1 regulates stem cells and proliferation and differentiation of committed cells in mammary epithelium 总被引:2,自引:0,他引:2
Pietersen AM Evers B Prasad AA Tanger E Cornelissen-Steijger P Jonkers J van Lohuizen M 《Current biology : CB》2008,18(14):1094-1099
PolycombGroup (PcG) proteins are epigenetic silencers involved in maintaining cellular identity, and their deregulation can result in cancer [1]. Mice without the PcG gene Bmi1 are runted and suffer from progressive loss of hematopoietic and neural stem cells [2-4]. Here, we assess the effects of Bmi1 on stem cells and differentiation of an epithelial tissue in vivo. We chose the mammary gland because it allows limiting dilution transplantations [5, 6] and because Bmi1 is overexpressed in breast cancer [7, 8]. Our analyses show that Bmi1 is expressed in all cells of the mouse mammary gland and is especially high in luminal cells. Loss of Bmi1 results in a severe mammary-epithelium growth defect, which can be rescued by codeletion of the Ink4a/Arf locus or pregnancy. Even though mammary stem cells are present in the absence of Bmi1, their activity is reduced, and this is only partially due to Ink4a/Arf expression. Interestingly, loss of Bmi1 causes premature lobuloalveolar differentiation, whereas overexpression of Bmi1 inhibits lobuloalveolar differentiation induced by pregnancy hormones. Because Bmi1 affects not only mammary stem cells but also more committed cells, our data warrant a more detailed analysis of the different roles of Bmi1 in breast-cancer etiology. 相似文献
965.
Tisné S Reymond M Vile D Fabre J Dauzat M Koornneef M Granier C 《Plant physiology》2008,148(2):1117-1127
Both leaf production and leaf expansion are tightly linked to cell expansion and cell division, but the functional relationships between all these variables are not clearly established. To get insight into these relationships, a quantitative genetic analysis was performed in 118 recombinant inbred lines derived from a cross between the Landsberg erecta and Antwerp accessions and was combined with a structural equation modeling approach. Main effects and epistatic interactions at the quantitative trait locus (QTL) level were detected for rosette area, rosette leaf number, leaf 6 area, epidermal cell area and number. A QTL at ERECTA marker (ER) controlled cell expansion and cell division, in interaction with two other QTLs at SNP295 and SNP21 markers. Moreover, both the screening for marker association involved in the variation of the relationships between leaf growth variables and the test of alternative functional models by structural equation modeling revealed that the allelic value at ER controlled epidermal cell area and epidermal cell number in a leaf. These effects are driven both by a whole plant mechanism associated with leaf production and by a single leaf mechanism associated with leaf expansion. The complex effects of the QTL at ER were validated in selected heterogeneous inbred families. The ERECTA gene, which is mutated in the Landsberg erecta parental line, was found to be a putative candidate responsible for these mapped effects by phenotyping mutants of this gene at the cellular level. Together, these results give insight into the complex determination of leaf epidermal cell number and area. 相似文献
966.
967.
In a companion paper (Lof et al., in Bull. Math. Biol., 2008), we describe a spatio-temporal model for insect behavior. This model includes chemical information for finding resources
and conspecifics. As a model species, we used Drosophila melanogaster, because its behavior is documented comparatively well.
We divide a population of Drosophila into three states: moving, searching, and settled. Our model describes the number of flies in each state, together with the
concentrations of food odor and aggregation pheromone, in time and in two spatial dimensions. Thus, the model consists of
5 spatio-temporal dependent variables, together with their constituting relations. Although we tried to use the simplest submodels
for the separate variables, the parameterization of the spatial model turned out to be quite difficult, even for this well-studied
species.
In the first part of this paper, we discuss the relevant results from the literature, and their possible implications for
the parameterization of our model. Here, we focus on three essential aspects of modeling insect behavior. First, there is
the fundamental discrepancy between the (lumped) measured behavioral properties (i.e., fruit fly displacements) and the (detailed)
properties of the underlying mechanisms (i.e., dispersivity, sensory perception, and state transition) that are adopted as
explanation. Detailed quantitative studies on insect behavior when reacting to infochemicals are scarce. Some information
on dispersal can be used, but quantitative data on the transition between the three states could not be found. Second, a dose-response
relation as used in human perception research is not available for the response of the insects to infochemicals; the behavioral
response relations are known mostly in a qualitative manner, and the quantitative information that is available does not depend
on infochemical concentration. We show how a commonly used Michaelis–Menten type dose-response relation (incorporating a saturation
effect) can be adapted to the use of two different but interrelated stimuli (food odors and aggregation pheromone). Although
we use all available information for its parameterization, this model is still overparameterized. Third, the spatio-temporal
dispersion of infochemicals is hard to model: Modeling turbulent dispersal on a length scale of 10 m is notoriously difficult.
Moreover, we have to reduce this inherently three-dimensional physical process to two dimensions in order to fit in the two-dimensional
model for the insects. We investigate the consequences of this dimension reduction, and we demonstrate that it seriously affects
the parameterization of the model for the infochemicals.
In the second part of this paper, we present the results of a sensitivity analysis. This sensitivity analysis can be used
in two manners: firstly, it tells us how general the simulation results are if variations in the parameters are allowed, and
secondly, we can use it to infer which parameters need more precise quantification than is available now. It turns out that
the short term outcome of our model is most sensitive to the food odor production rate and the fruit fly dispersivity. For
the other parameters, the model is quite robust.
The dependence of the model outcome with respect to the qualitative model choices cannot be investigated with a parameter
sensitivity analysis. We conclude by suggesting some experimental setups that may contribute to answering this question. 相似文献
968.
Coury F Annels N Rivollier A Olsson S Santoro A Speziani C Azocar O Flacher M Djebali S Tebib J Brytting M Egeler RM Rabourdin-Combe C Henter JI Arico M Delprat C 《Nature medicine》2008,14(1):81-87
IL-17A is a T cell-specific cytokine that is involved in chronic inflammations, such as Mycobacterium infection, Crohn's disease, rheumatoid arthritis and multiple sclerosis. Mouse models have explained the molecular basis of IL-17A production and have shown that IL-17A has a positive effect not only on granuloma formation and neurodegeneration through unknown mechanisms, but also on bone resorption through Receptor activator of NF-kappaB ligand (RANKL) induction in osteoblasts. Langerhans cell histiocytosis (LCH) is a rare disease of unknown etiology, lacking an animal model, that cumulates symptoms that are found separately in various IL-17A-related diseases, such as aggressive chronic granuloma formation, bone resorption and soft tissue lesions with occasional neurodegeneration. We examined IL-17A in the context of LCH and found that there were high serum levels of IL-17A during active LCH and unexpected IL-17A synthesis by dendritic cells (DCs), the major cell type in LCH lesions. We also found an IL-17A-dependent pathway for DC fusion, which was highly potentiated by IFN-gamma and led to giant cells expressing three major tissue-destructive enzymes: tartrate resistant acidic phosphatase and matrix metalloproteinases 9 and 12. IFN-gamma expression has been previously documented in LCH and observed in IL-17A-related diseases. Notably, serum IL-17A-dependent fusion activity correlates with LCH activity. Thus, IL-17A and IL-17A-stimulated DCs represent targets that may have clinical value in the treatment of LCH and other IL-17A-related inflammatory disorders. 相似文献
969.
Green fluorescent protein (GFP) is widely used as a marker to identify transfected cells either by fluorescence microscopy or flow cytometry. However, cell cycle analysis with propidium iodide typically employs ethanol for cell permeabilization. During this treatment, soluble GFPs generally leak out of cells, probably due to their small size. We have now significantly improved cellular retention by creating an in-frame fusion of two GFP DNA sequences, thereby generating a double-sized GFP (TwinGFP, 57 kDa). Permeabilized HeLa cells transfected with pTwinGFP showed a strong green fluorescent signal localized throughout the cells that could easily be detected by fluorescence microscopy and flow cytometry, in contrast to cells transfected with a standard single GFP construct. The experiment indicates that protein size constitutes the major determinant of the loss of fluorescence in permeabilized cells. As a proof of principle, pTwinGFP was cotransfected with the p53 tumor suppressor gene into HeLa cells, and cells transiently expressing p53 could be identified and phenotypically characterized by flow cytometry. 相似文献
970.
Worldwide, river fragmentation is primarily responsible for the decline of populations of migrating fish. In particular, anadromous
fish species, which necessarily migrate to fresh water to reproduce, are endangered since many are no longer able to reach
their natural spawning sites. In addition, pollution of rivers effectively prevents upstream or downstream movements and blocks
access to spawning grounds. This article investigates how poor water quality interferes with the life history cycle of twaite
shad Alosa fallax fallax (Lacépède, 1803), an anadromous clupeid fish, in the watershed of River Scheldt, a heavily impacted environment in West Europe.
We used two models based on known ecological and environmental information to explain past and present twaite shad distribution
within the watershed and to make inferences about a future population recovery and juvenile habitat value. We demonstrated
that historical spawning areas satisfy water quality conditions necessary to support spawning and successful development of
early life history stages of the twaite shad. However, poor water quality conditions just upstream the freshwater–saltwater
boundary still act as an effective migration barrier for upstream movement. As a consequence, spawning grounds are inaccessible
and the population is dominated by seasonal adults occurring in the lower estuarine part of the watershed. This article provides
testable and diagnostic information to the watershed management in that it identifies habitat and water quality requirements
needed to support the expected recovery of an endangered anadromous fish population.
Guest editors: S. Dufour, E. Prévost, E. Rochard & P. Williot
Fish and diadromy in Europe (ecology, management, conservation) 相似文献