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111.
112.
Xing GW Wu D Poles MA Horowitz A Tsuji M Ho DD Wong CH 《Bioorganic & medicinal chemistry》2005,13(8):2907-2916
Two novel hybrid molecules 3-O-sulfo-alpha/beta-galactosylceramide 3 and 4, which are derived from an immunostimulatory agent alpha-GalCer 1 and self-glycolipid ligand sulfatide 2, were designed and synthesized. Compound 3 was shown to efficiently stimulate human NKT cells to secret IL-4 and IFN-gamma, with activities similar to 1, suggesting that modification of the 3'-OH position of the galactose moiety with sulfate has no significant effect on NKT cell stimulation. As a comparison, the beta-isomer 4 has no affinity to NKT cells, which demonstrates that the alpha-glycosidic bond of galactosylceramide is crucial to the NKT cells activation. 相似文献
113.
Phospholipase C in living cells: activation, inhibition, Ca2+ requirement, and regulation of M current 总被引:5,自引:0,他引:5
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Horowitz LF Hirdes W Suh BC Hilgemann DW Mackie K Hille B 《The Journal of general physiology》2005,126(3):243-262
We have further tested the hypothesis that receptor-mediated modulation of KCNQ channels involves depletion of phosphatidylinositol 4,5-bisphosphate (PIP2) by phosphoinositide-specific phospholipase C (PLC). We used four parallel assays to characterize the agonist-induced PLC response of cells (tsA or CHO cells) expressing M1 muscarinic receptors: translocation of two fluorescent probes for membrane lipids, release of calcium from intracellular stores, and chemical measurement of acidic lipids. Occupation of M1 receptors activates PLC and consumes cellular PIP2 in less than a minute and also partially depletes mono- and unphosphorylated phosphoinositides. KCNQ current is simultaneously suppressed. Two inhibitors of PLC, U73122 and edelfosine (ET-18-OCH3), can block the muscarinic actions completely, including suppression of KCNQ current. However, U73122 also had many side effects that were attributable to alkylation of various proteins. These were mimicked or occluded by prior reaction with the alkylating agent N-ethylmaleimide and included block of pertussis toxin-sensitive G proteins and effects that resembled a weak activation of PLC or an inhibition of lipid kinases. By our functional criteria, the putative PLC activator m-3M3FBS did stimulate PLC, but with a delay and an irregular time course. It also suppressed KCNQ current. The M1 receptor-mediated activation of PLC and suppression of KCNQ current were stopped by lowering intracellular calcium well below resting levels and were slowed by not allowing intracellular calcium to rise in response to PLC activation. Thus calcium release induced by PLC activation feeds back immediately on PLC, accelerating it during muscarinic stimulation in strong positive feedback. These experiments clarify important properties of receptor-coupled PLC responses and their inhibition in the context of the living cell. In each test, the suppression of KCNQ current closely paralleled the expected fall of PIP2. The results are described by a kinetic model. 相似文献
114.
Vascular endothelial cells have impaired capacity to present immunodominant, antigenic peptides: a mechanism of cell type-specific immune escape 总被引:2,自引:0,他引:2
Kummer M Lev A Reiter Y Biedermann BC 《Journal of immunology (Baltimore, Md. : 1950)》2005,174(4):1947-1953
Vascular endothelial cells (EC) are an exposed target tissue in the course of CTL-mediated alloimmune diseases such as graft-vs-host disease (GVHD) or solid organ transplant rejection. The outcome of an interaction between CTL and target cells is determined by the amount of Ag presented and the costimulatory signals delivered by the target cells. We compared human EC with leukocytes and epithelial cells as targets for peptide-specific, MHC class I-restricted CTL clones. EC were poor targets for immunodominant CTL. Both endogenously processed antigenic proteins and exogenously added antigenic peptides are presented at 50- to 5000-fold lower levels on EC compared with any other target cell analyzed. This quantitative difference fully explained the poor CTL-mediated killing of EC. There was no evidence that lack of costimulation would contribute significantly to this cell type-specific difference in CTL activation. An HLA-A2-specific CTL clone that killed a broad selection of HLA A2-positive target cells equally well, killed EC less efficiently. Our data suggest that EC present a different Ag repertoire compared with other cell types. By this mechanism, these cells may escape an attack by effector CTL, which have been educated by professional APCs and are specific for immunodominant antigenic peptides. 相似文献
115.
Eisenberg A Biener E Charlier M Krishnan RV Djiane J Herman B Gertler A 《FEBS letters》2004,565(1-3):139-142
We generated kinase-positive and kinase-negative erbB2 tagged with YFP and the long form of leptin receptor (LEPRb) tagged with CFP. Both were as active as their untagged analogs. Both short and long isoforms of leptin receptor phosphorylated and thereby activated erbB2 upon leptin binding and enhanced MAPK activity. Our results unveil a novel route by which leptin may provoke erbB2's phosphorylation and thus enhance its oncogenic potential independently of HER family ligands or its overexpression. Using FRET technology in living cells, we found no evidence of complex formation between erbB2 and prolactin or leptin receptors, indicating that the transactivation occurs through an indirect interaction. 相似文献
116.
Horowitz JC Lee DY Waghray M Keshamouni VG Thomas PE Zhang H Cui Z Thannickal VJ 《The Journal of biological chemistry》2004,279(2):1359-1367
Transforming growth factor-beta1 (TGF-beta1) is a multifunctional cytokine involved in differentiation, growth, and survival of mesenchymal cells while inhibiting growth/survival of most other cell types. The mechanism(s) of pro-survival signaling by TGF-beta1 in mesenchymal cells is unclear. In this report, we demonstrate that TGF-beta1 protects against serum deprivation-induced apoptosis of mesenchymal cells isolated from patients with acute lung injury and of normal human fetal lung fibroblasts (IMR-90). TGF-beta receptor(s)-activated signaling in these cells involves rapid activation of the Smad and p38 MAPK pathways within minutes of TGF-beta1 treatment followed by a more delayed activation of the pro-survival phosphatidylinositol 3-kinase-protein kinase B (PKB)/Akt pathway. Pharmacological inhibition of p38 MAPK with SB203580 or expression of a p38 kinase-deficient mutant protein inhibits TGF-beta1-induced PKB/Akt phosphorylation. Conditioned medium from TGF-beta1-treated cells rapidly induces PKB/Akt activation in an SB203580- and suramin-sensitive manner, suggesting p38 MAPK-dependent production of a secreted growth factor that activates this pro-survival pathway by an autocrine/paracrine mechanism. Inhibition of the phosphatidylinositol 3-kinase-PKB/Akt pathway blocks TGF-beta1-induced resistance to apoptosis. These results demonstrate the activation of a novel TGF-beta1-activated pro-survival/anti-apoptotic signaling pathway in mesenchymal cells/fibroblasts that may explain cell-specific actions of TGF-beta1 and provide mechanistic insights into its pro-fibrotic and tumor-promoting effects. 相似文献
117.
118.
A mediterranean-type climate exists in five widely separated regions; the Mediterranean basin, parts of western North America, parts of western and southern Australia, southwestern South Africa and parts of central Chile. Streams in these regions feature seasonal disturbances of contrasting hydrology with high predictability of the timing of flooding and drying but low constancy. We would expect fish living in these streams to avoid scouring flow and breed after cessation of the flood period. The aim of the present study was to examine the adaptation of the Yarqon bleak, Acanthobrama telavivensis, an endemic cyprinid in the coastal streams of Israel, to mediterranean-type stream (mediterranean—written with a small m, is used in connection with climate or ecological region and is distinguished from Mediterranean that is used in a geographical context, referring to the Mediterranean basin.) conditions. For that we studied its reproductive strategy (age at maturity and life span, gonad activity, oocyte maturation, spawning activity and habitats, appearance of juveniles), in a major costal stream (Yarqon). Our findings show that the Yarqon bleak exhibits life history traits attuned with a mediterranean-climate hydrologic regime. It breeds in late winter and early spring, a window of opportunity between flash floods and habitat desiccation. Being a multiple spawner allows the fish to compensate for the potential loss of part of its reproductive output due to scouring flows of late floods. The ability of the Yarqon bleak to spawn on different substrate-types enables it to take advantage of different stream conditions that pertain in different years. The fish attains pre-adult size (ca. 33–42 mm) within the first year, prior to drying out of most stream reaches, and matures by the beginning of the second year (males >41; females >42 mm). The cost of these tactics is a short life span (4–5 age groups). The reproductive strategy of the Yarqon bleak falls into the category of in-channel breeding but, unlike the case suggested by a low flow recruitment model, the fish breed during the period of flood cessation, a transitional time between high and low flows, rather than at the time of low flow. Breeding at this time of the year in mediterranean-type streams puts early stages somewhat at risk of being washed away by late floods, but gains them a longer period of growth under favorable conditions. We suggest an additional positive tradeoff that should be investigated: the reduced competition with age 0 of other fish that breed later in the season. This suggested model of recruitment during the period of flood cessation seems appropriate for fish in streams with seasonal contrasting flows of high predictability but low constancy. 相似文献
119.
Effect of fatty acid chain length on suppression of ghrelin and stimulation of PYY, GLP-2 and PP secretion in healthy men 总被引:2,自引:0,他引:2
Feltrin KL Patterson M Ghatei MA Bloom SR Meyer JH Horowitz M Feinle-Bisset C 《Peptides》2006,27(7):1638-1643
We have evaluated the effects of fatty acid chain length on ghrelin, peptide YY (PYY), glucagon-like peptide-2 (GLP-2) and pancreatic polypeptide (PP) secretion and hypothesized that intraduodenal administration of dodecanoic ("C12"), but not decanoic ("C10"), acid would decrease plasma ghrelin and increase PYY, GLP-2 and PP concentrations. Plasma hormone concentrations were measured in seven healthy men during 90-min intraduodenal infusions of: (i) C12, (ii) C10 or (iii) control (rate: 2 ml/min, 0.375 kcal/min for C12/C10) and after a buffet-meal consumed following the infusion. C12 markedly suppressed plasma ghrelin and increased both PYY and GLP-2 (all P < 0.05) compared with control and C10, while C10 had no effect. Both C10 and C12 increased PP concentrations slightly (P < 0.05). We conclude that the effects of intraduodenal fatty acids on ghrelin, PYY and GLP-2 secretion are dependent on their chain length. 相似文献
120.
Pilichiewicz AN Little TJ Brennan IM Meyer JH Wishart JM Otto B Horowitz M Feinle-Bisset C 《American journal of physiology. Regulatory, integrative and comparative physiology》2006,290(3):R668-R677
Enterally administered lipid modulates antropyloroduodenal motility, gut hormone release, appetite, and energy intake. We hypothesized that these effects would be dependent on both the load, and duration, of small intestinal exposure to lipid. Eleven healthy men were studied on four occasions in a double-blind, randomized, fashion. Antropyloroduodenal motility, plasma CCK and peptide YY (PYY) concentrations, and appetite perceptions were measured during intraduodenal infusion of lipid (Intralipid) at 1) 1.33 kcal/min for 50 min, 2) 4 kcal/min for 50 min, and 3) 1.33 kcal/min for 150 min, or 4) saline for 150 min. Immediately after the infusions, energy intake was quantified. Pressure wave sequences (PWSs) were suppressed, and basal pyloric pressure, isolated pyloric pressure waves (IPPWs), plasma CCK and PYY stimulated (all P < 0.05), during the first 50 min of lipid infusion, in a load-dependent fashion. The effect of the 4 kcal/min infusion was sustained so that the suppression of antral pressure waves (PWs) and PWSs and increase in PYY remained evident after cessation of the infusion (all P < 0.05). The prolonged lipid infusion (1.33 kcal/min for 150 min) suppressed antral PWs, stimulated CCK and PYY and basal pyloric pressure (all P < 0.05), and tended to stimulate IPPWs when compared with saline throughout the entire infusion period. There was no significant effect of any of the lipid infusions on appetite or energy intake, although nausea was slightly higher (P < 0.05) with the 4 kcal/min infusion. In conclusion, both the load, and duration, of small intestinal lipid influence antropyloroduodenal motility and patterns of CCK and PYY release. 相似文献