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991.
The epidermal growth factor-seven transmembrane (EGF-TM7) receptor CD97 is required for neutrophil migration and host defense 总被引:4,自引:0,他引:4
Leemans JC te Velde AA Florquin S Bennink RJ de Bruin K van Lier RA van der Poll T Hamann J 《Journal of immunology (Baltimore, Md. : 1950)》2004,172(2):1125-1131
The epidermal growth factor-seven transmembrane (EGF-TM7) family is a group of seven-span transmembrane receptors predominantly expressed by cells of the immune system. Family members CD97, EGF module-containing mucin-like receptor (EMR) 1, EMR2, EMR3, EMR4, and EGF-TM7-latrophilin-related protein are characterized by an extended extracellular region with a variable number of N-terminal EGF-like domains. EGF-TM7 receptors bind cellular ligands as demonstrated by the interaction of CD97 with decay accelerating factor (CD55) and dermatan sulfate. Investigating the effect of newly generated mAb on the migration of neutrophilic granulocytes, we here report for the first time in vivo data on the function of CD97. In dextran sulfate sodium-induced experimental colitis, we show that homing of adoptively transferred neutrophils to the colon was significantly delayed when cells were preincubated with CD97 mAb. The consequences of this defect in neutrophil migration for host defense are demonstrated in a murine model of Streptococcus pneumoniae-induced pneumonia. Mice treated with CD97 mAb to EGF domain 1 (1B2) and EGF domain 3 (1C5) displayed a reduced granulocytic inflammatory infiltrate at 20 h after inoculation. This was associated with a significantly enhanced outgrowth of bacteria in the lungs at 44 h and a strongly diminished survival. Together, these findings indicate an essential role for CD97 in the migration of neutrophils. 相似文献
992.
Jouke P. Kardolus Herman J. van Eck Ronald G. van den Berg 《Plant Systematics and Evolution》1998,210(1-2):87-103
Using the AFLP technique highly informative DNA fingerprints were generated from 19 taxa ofSolanum sect.Petota (potatoes) and three taxa ofSolanum sect.Lycopersicum (tomatoes). Both phenetic and cladistic analyses were conducted from the individual genotypic level to the species level. An AFLP fingerprint, using a combination of suitable AFLP primers, generated 12 to 71 scorable fragments per genotype which was sufficient for taxonomic interpretation. The classifications based on the molecular markers were generally in agreement with current taxonomic opinions. Unexpectedly,S. microdontum was associated with ser.Megistacroloba rather than with ser.Tuberosa, andS. demissum (ser.Demissa) and species of ser.Acaulia appeared closely affiliated. AFLP is an efficient and reliable technique to generate biosystematic data and therefore a promising tool for evolutionary studies. 相似文献
993.
Krook J; Vreugdenhil D; Dijkema C; van der Plas L 《Journal of experimental botany》1998,49(329):1917-1924
Cells were grown in batch culture on a mixture of 50 mM glucose and
fructose as the carbon source; either the glucose or the fructose was
[1-13C]-labelled. In order to investigate the uptake
and conversion of glucose and fructose during long-term labelling
experiments in cell suspensions of Daucus carota L.,
samples were taken every 2 d during a 2 week culture period and sucrose and
starch were assayed by means of HPLC and 13C-nuclear
magnetic resonance. The fructose moieties of sucrose had a lower labelling
percentage than the glucose moieties. Oxidative pentose phosphate pathway
activity in the cytosol is suggested to be responsible for this loss of
label of especially C-1 carbons. A combination of oxidative pentose
phosphate pathway activity, a relatively high activity of pathway to
sucrose synthesis and a slow equilibration between glucose-6-phosphate and
fructose-6-phosphate could explain these results. Starch contained glucose
units with a much lower labelling percentage than glucose moieties of
sucrose: it was concluded that a second, plastid-localized, oxidative
pentose phosphate pathway was responsible for removal of C-1 carbons of the
glucosyl units used for synthesis of starch. Redistribution of label from
[1-13C]-hexoses to
[6-13C]-hexoses also occurred: 18-45% of the label
was found at the C-6 carbons. This is a consequence of cycling between
hexose phosphates and those phosphates in the cytosol catalysed by PFP. The
results indicate that independent (oxidative pentose phosphate pathway
mediated) sugar converting cycles exist in the cytosol and
plastid.Key words: Daucus carotaL., cell suspensions,
carbon-13 nuclear magnetic resonance, 13C-NMR,
carbohydrate cycling, oxidative pentose phosphate pathway, plastid.
相似文献
994.
G.J.H. Buisman C.T.W. van Helteren G.F.H. Kramer J.W. Veldsink J.T.P Derksen F.P. Cuperus 《Biotechnology letters》1998,20(2):131-136
Of seven lipases used to esterify functionalized phenols and fatty acids to synthesize lipophilic antioxidants, that from Candida antarctica lipase B (CAL-B) had the highest catalytic activity. Esterification yields of benzoic acid derivatives catalyzed by CAL-B are below 2% after 7 days. In contrast, relatively high yields were obstained for the esterification of (poly)phenols bearing primary hydroxy groups and aliphatic acids (85% yield within 15 hours). Crude products were purified and used as lipophilic antioxidants in sunflower oil. 相似文献
995.
J. A. Wilmer S. R. Abrams J. P. F. G. Helsper L. H. W. van der Plas 《Journal of Plant Growth Regulation》1998,17(1):19-23
Modification of the structure of abscisic acid (ABA) has been reported to result in modification of its physiologic activity.
In this study we tested the effect of removing methyl groups from the ring and of chirality of ABA on activity in microspore-derived
embryos of oilseed rape (Brassica napus L.). The natural (+)-ABA molecule induced growth inhibition and an increase in the amount of erucic acid accumulated in the
oil at medium concentrations less than 1 μm. (−)-ABA showed similar effects. Removing the 7′-methyl group resulted in a dramatic decrease in activity: (+)-7′-demethyl-ABA
retained some activity as a growth inhibitor; a 10–100 μm concentration of this compound was needed for a response, and (−)-7′-demethyl-ABA was almost completely inactive. Similar
effects were observed with regard to elongase activity, which catalyzes erucic acid biosynthesis from oleic acid. Removal
of the 8′- and 9′-methyl groups resulted in a more complex response. These compounds all showed intermediate activity; for
growth inhibition, the presence of the 9′-methyl was the more important determinant, whereas chirality dominated the response
on erucic acid accumulation, with the (+)-enantiomers being more active.
Received July 25, 1997; accepted October 31, 1997 相似文献
996.
MARGRIET van ASCH PETER H. van TIENDEREN † LEONARD J. M. HOLLEMAN MARCEL E. VISSER 《Global Change Biology》2007,13(8):1596-1604
Climate change has led to an advance in phenology in many species. Synchrony in phenology between different species within a food chain may be disrupted if an increase in temperature affects the phenology of the different species differently, as is the case in the winter moth egg hatch–oak bud burst system. Operophtera brumata (winter moth) egg hatch date has advanced more than Quercus robur (pedunculate oak) bud burst date over the past two decades. Disrupted synchrony will lead to selection, and a response in phenology to this selection may lead to species genetically adapting to their changing environment. However, a prerequisite for such genetic change is that there is sufficient genetic variation and severe enough fitness consequences. So far, examples of observed genetic change have been few. Using a half-sib design, we demonstrate here that O. brumata egg-hatching reaction norm is heritable, and that genetic variation exists. Fitness consequences of even a few days difference between egg hatch and tree bud opening are severe, as we experimentally determined. Estimates of genetic variation and of fitness were then combined with a climate scenario to predict the rate and the amount of change in the eggs' response to temperature. We predict a rapid response to selection, leading to a restoration of synchrony of egg hatch with Q. robur bud opening. This study shows that in this case there is a clear potential to adapt – rapidly – to environmental change. The current observed asynchrony is therefore not due to a lack of genetic variation and at present it is unclear what is constraining O. brumata to adapt. This kind of model may be particularly useful in gaining insight in the predicted amount and rate of change due to environmental changes, given a certain genetic variation and selection pressure. 相似文献
997.
A RNA Interference Screen Identifies the Protein Phosphatase 2A Subunit PR55γ as a Stress-Sensitive Inhibitor of c-SRC 下载免费PDF全文
Pieter J. A Eichhorn Menno P Creyghton Kevin Wilhelmsen Hans van Dam Ren Bernards 《PLoS genetics》2007,3(12)
Protein Phosphatase type 2A (PP2A) represents a family of holoenzyme complexes with diverse biological activities. Specific holoenzyme complexes are thought to be deregulated during oncogenic transformation and oncogene-induced signaling. Since most studies on the role of this phosphatase family have relied on the use of generic PP2A inhibitors, the contribution of individual PP2A holoenzyme complexes in PP2A-controlled signaling pathways is largely unclear. To gain insight into this, we have constructed a set of shRNA vectors targeting the individual PP2A regulatory subunits for suppression by RNA interference. Here, we identify PR55γ and PR55δ as inhibitors of c-Jun NH2-terminal kinase (JNK) activation by UV irradiation. We show that PR55γ binds c-SRC and modulates the phosphorylation of serine 12 of c-SRC, a residue we demonstrate to be required for JNK activation by c-SRC. We also find that the physical interaction between PR55γ and c-SRC is sensitive to UV irradiation. Our data reveal a novel mechanism of c-SRC regulation whereby in response to stress c-SRC activity is regulated, at least in part, through loss of the interaction with its inhibitor, PR55γ. 相似文献
998.
Endocytic down-regulation of ErbB2 is stimulated by cleavage of its C-terminus 总被引:1,自引:0,他引:1 下载免费PDF全文
Lerdrup M Bruun S Grandal MV Roepstorff K Kristensen MM Hommelgaard AM van Deurs B 《Molecular biology of the cell》2007,18(9):3656-3666
High ErbB2 levels are associated with cancer, and impaired endocytosis of ErbB2 could contribute to its overexpression. Therefore, knowledge about the mechanisms underlying endocytic down-regulation of ErbB2 is warranted. The C-terminus of ErbB2 can be cleaved after various stimuli, and after inhibition of HSP90 with geldanamycin this cleavage is accompanied by proteasome-dependent endocytosis of ErbB2. However, it is unknown whether C-terminal cleavage is linked to endocytosis. To study ErbB2 cleavage and endocytic trafficking, we fused yellow fluorescent protein (YFP) and cyan fluorescent protein (CFP) to the N- and C-terminus of ErbB2, respectively (YFP-ErbB2-CFP). After geldanamycin stimulation YFP-ErbB2-CFP became cleaved in nonapoptotic cells in a proteasome-dependent manner, and a markedly larger relative amount of cleaved YFP-ErbB2-CFP was observed in early endosomes than in the plasma membrane. Furthermore, cleavage took place at the plasma membrane, and cleaved ErbB2 was internalized and degraded far more efficiently than full-length ErbB2. Concordantly, a C-terminally truncated ErbB2 was also readily endocytosed and degraded in lysosomes compared with full-length ErbB2. Altogether, we suggest that geldanamycin leads to C-terminal cleavage of ErbB2, which releases the receptor from a retention mechanism and causes endocytosis and lysosomal degradation of ErbB2. 相似文献
999.
Okon EB Chung AW Zhang H Laher I van Breemen C 《Canadian journal of physiology and pharmacology》2007,85(5):562-567
Diabetes mellitus impairs endothelial function, which can be considered as the hallmark in the development of cardiovascular diseases. Hyperglycemia, hyperinsulinemia, and hyperlipidemia are believed to contribute to endothelial dysfunction. In the present study, we investigated the possible links among these plasma metabolic markers and endothelial function in a mouse model during the development of type 2 diabetes. C57BL/6J-Lepob/ob mice at 8, 12, and 16 weeks were used to study endothelial function during the establishment of type 2 diabetes. Endothelial function was accessed in vitro in the thoracic aorta by measuring acetylcholine (ACh)-stimulated vasodilatation. Blood plasma was obtained for the measurements of glucose, insulin, triglycerides, and cholesterol levels. Correlation and multiple regression analysis revealed strong negative associations between the ACh responsiveness and the plasma levels of glucose, insulin, and lipid profiles at the age of 8 weeks. Associations were observed at neither older age nor in C57BL/6J mice. In conclusion, the increase in plasma levels of glucose, insulin, and lipids is associated with the impairment of the endothelial function during the early stage of the development of type 2 diabetes. The loss of correlation at an older age suggests multifactorial regulation of endothelial function and cardiovascular complications at later stages of the disease. 相似文献
1000.
Chung S Verheij MM Hesseling P van Vugt RW Buell M Belluzzi JD Geyer MA Martens GJ Civelli O 《PloS one》2011,6(7):e19286
Deficits in sensorimotor gating measured by prepulse inhibition (PPI) of the startle have been known as characteristics of patients with schizophrenia and related neuropsychiatric disorders. PPI disruption is thought to rely on the activity of the mesocorticolimbic dopaminergic system and is inhibited by most antipsychotic drugs. These drugs however act also at the nigrostriatal dopaminergic pathway and exert adverse locomotor responses. Finding a way to inhibit the mesocorticolimbic- without affecting the nigrostriatal-dopaminergic pathway may thus be beneficial to antipsychotic therapies. The melanin-concentrating hormone (MCH) system has been shown to modulate dopamine-related responses. Its receptor (MCH1R) is expressed at high levels in the mesocorticolimbic and not in the nigrostriatal dopaminergic pathways. Interestingly a genomic linkage study revealed significant associations between schizophrenia and markers located in the MCH1R gene locus. We hypothesize that the MCH system can selectively modulate the behavior associated with the mesocorticolimbic dopamine pathway. Using mice, we found that central administration of MCH potentiates apomorphine-induced PPI deficits. Using congenic rat lines that differ in their responses to PPI, we found that the rats that are susceptible to apomorphine (APO-SUS rats) and exhibit PPI deficits display higher MCH mRNA expression in the lateral hypothalamic region and that blocking the MCH system reverses their PPI deficits. On the other hand, in mice and rats, activation or inactivation of the MCH system does not affect stereotyped behaviors, dopamine-related responses that depend on the activity of the nigrostriatal pathway. Furthermore MCH does not affect dizocilpine-induced PPI deficit, a glutamate related response. Thus, our data present the MCH system as a regulator of sensorimotor gating, and provide a new rationale to understand the etiologies of schizophrenia and related psychiatric disorders. 相似文献