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41.
42.
Aquatic mosses are important primary producers in High-Arctic lakes, but little information is available on their contribution to the overall production in these lakes. In order to predict effects of climate change on whole-lake ecosystem characteristics, more knowledge is needed on the role of moss in primary production, the extent of nutrient limitation of moss primary production and whether moss serves as food resource for secondary producers. In this study, we conducted an in situ growth experiment of an aquatic moss in a High-Arctic lake in NE Greenland and used these data to determine annual net production of this moss in the whole lake. We also measured tissue-N and tissue-P in order to assess nutrient limitation of moss production, measured in situ decomposition rates by litter bag experiments over 1 year and assessed the role of moss as food source by analysing stable isotope 15N and 13C of relevant organism groups in the lake. Net primary production of moss was 1.3 gC m?2 year?1 and constituted 23 % of the total benthic primary production and 18 % of the total lake primary production. Stoichiometric assessments suggested N and P limitation of moss growth. On average, 15 % of the standing biomass was decomposed per year. Our results also indicate that moss is not directly used as food resource by herbivores, but the most abundant herbivore, Lepidurus arcticus, is feeding on the epiphytic biofilm on the moss. Moss biomass is instead incorporated into the microbial decomposer pathway. All together, the study shows that moss plays an important ecological role as primary producer in High-Arctic lakes and functions as substrate for periphytic biofilm that serves as food resource for important herbivore invertebrates. 相似文献
43.
Ursø B Ilondo MM Holst PA Christoffersen CT Ouwens M Giorgetti S Van Obberghen E Naor D Tornqvist H De Meyts P 《Cellular signalling》2003,15(4):385-394
Insulin and growth hormone (GH) induce mitogenic and metabolic signals in cells, GH either directly or indirectly via IGF-I production. We have studied a spontaneous murine T-cell lymphoma (LB cells) devoid of IGF-1 receptors in which proliferation is maintained by insulin [Int. J. Cancer 50 (1992) 80], and show that GH is more potent than insulin, with both GH and insulin dose-response curves for thymidine incorporation being bell-shaped. Binding showed somatogenic rather than lactogenic GH receptors. Insulin stimulated phosphorylation of the insulin receptor and of a 160-kDa protein, identified as the IRS-4 protein. This phosphorylated IRS-4 associated with PI3-kinase, which was activated along with the downstream p70(S6) kinase, whereas the Ras-MAPK pathway was not. Using selective inhibitors, the PI3-kinase, but not p70(S6) kinase or MEK, was found to be involved in insulin-stimulated DNA synthesis. GH induced tyrosine phosphorylation of IRS-4 and nuclear translocation of STAT5. The LB cells constitute a new model for studying GH and insulin signalling without interference of IGF-1 receptors. 相似文献
44.
45.
Rosie A. Fisher Charles D. Koven William R. L. Anderegg Bradley O. Christoffersen Michael C. Dietze Caroline E. Farrior Jennifer A. Holm George C. Hurtt Ryan G. Knox Peter J. Lawrence Jeremy W. Lichstein Marcos Longo Ashley M. Matheny David Medvigy Helene C. Muller‐Landau Thomas L. Powell Shawn P. Serbin Hisashi Sato Jacquelyn K. Shuman Benjamin Smith Anna T. Trugman Toni Viskari Hans Verbeeck Ensheng Weng Chonggang Xu Xiangtao Xu Tao Zhang Paul R. Moorcroft 《Global Change Biology》2018,24(1):35-54
Numerous current efforts seek to improve the representation of ecosystem ecology and vegetation demographic processes within Earth System Models (ESMs). These developments are widely viewed as an important step in developing greater realism in predictions of future ecosystem states and fluxes. Increased realism, however, leads to increased model complexity, with new features raising a suite of ecological questions that require empirical constraints. Here, we review the developments that permit the representation of plant demographics in ESMs, and identify issues raised by these developments that highlight important gaps in ecological understanding. These issues inevitably translate into uncertainty in model projections but also allow models to be applied to new processes and questions concerning the dynamics of real‐world ecosystems. We argue that stronger and more innovative connections to data, across the range of scales considered, are required to address these gaps in understanding. The development of first‐generation land surface models as a unifying framework for ecophysiological understanding stimulated much research into plant physiological traits and gas exchange. Constraining predictions at ecologically relevant spatial and temporal scales will require a similar investment of effort and intensified inter‐disciplinary communication. 相似文献
46.
G H Thoresen T E Sand M Refsnes O F Dajani T K Guren I P Gladhaug A Killi T Christoffersen 《Journal of cellular physiology》1990,144(3):523-530
Although several lines of evidence implicate cyclic AMP in the humoral control of liver growth, its precise role is still not clear. To explore further the role of cyclic AMP in hepatocyte proliferation, we have examined the effects of glucagon and other cyclic AMP-elevating agents on the DNA synthesis in primary cultures of adult rat hepatocytes, with particular focus on the temporal aspects. The cells were cultured in a serum-free, defined medium and treated with epidermal growth factor (EGF), insulin, and dexamethasone. Exposure of the hepatocytes to low concentrations (10 pM-1 nM) of glucagon in the early stages of culturing (usually within 6 h from plating) enhanced the initial rate of S phase entry without affecting the lag time from the plating to the onset of DNA synthesis, whereas higher concentrations inhibited it. In contrast, glucagon addition at later stages (24-45 h after plating) produced only the inhibition. Thus, if glucagon was added at a time when there was a continuous EGF/insulin-induced recruitment of cells to S phase, the rate of G1-S transition was markedly decreased within 1-3 h. This inhibitory effect occurred at low glucagon concentrations (ID50 less than 1 nM) and was mimicked by cholera toxin, forskolin, isobutyl methylxanthine, and 8-bromo cyclic AMP. The results indicate that cyclic AMP has dual effects on hepatocyte proliferation with a stimulatory modulation early in the prereplicative period (G0 or early G1), and a marked inhibition exerted immediately before the transition from G1 to S phase. 相似文献
47.
Jette Junge Kirsten D Bentsen Per Christoffersen Marianne Orholm Thorkild I A S?rensen Thomas Horn 《BMJ (Clinical research ed.)》1988,296(6637):1629-1630
In a study of 142 male alcohol abusers without evidence of cirrhosis the presence of intralobular fibronectin in the liver was investigated in relation to the subsequent development of the disease. All 142 initial biopsy samples showed preserved architecture. During a follow up period of 10-13 years 23 patients (16%) developed cirrhosis. Twelve of 110 patients with normal or slightly increased amounts of parenchymal fibronectin in the initial biopsy specimen developed cirrhosis, whereas eight out of 27 patients with moderately increased amounts and three out of five with significantly increased amounts later developed the disease (p<0·005).Semiquantitative assessment of the amount of parenchymal fibronectin at an early stage of alcoholic liver disease is of definite predictive value for the development of cirrhosis. 相似文献
48.
Monica Aasrum G. Hege Thoresen Thoralf Christoffersen Ingvild J. Brusevold 《Journal of cell communication and signaling》2018,12(4):699-707
Whereas the p38 MAP kinase has largely been associated with anti-proliferative functions, several observations have indicated that it may also have positive effects on proliferation. In hepatocytes, we have found that p38 has opposing effects on DNA synthesis when activated by EGF and HGF. Here we have studied the function of p38 in EGF- and HGF-induced DNA synthesis in the two pancreatic carcinoma cell lines AsPC-1 and Panc-1. In Panc-1 cells, the MEK inhibitor PD98059 reduced EGF- and HGF-induced DNA synthesis, while the p38 inhibitor SB203580 strongly increased the basal DNA synthesis and reduced expression of the cyclin-dependent kinase inhibitor (CDKI) p21. In contrast, in AsPC-1 cells, EGF- and HGF-induced DNA synthesis was not significantly reduced by PD98059 but was inhibited by SB203580. Treatment with SB203580 amplified the sustained ERK phosphorylation induced by these growth factors and caused a marked upregulation of the expression of p21, which could be blocked by PD98059. These results suggest that while DNA synthesis in Panc-1 cells is enhanced by ERK and strongly suppressed by p38, in AsPC-1 cells, p38 exerts a pro-mitogenic effect through MEK/ERK-dependent downregulation of p21. Thus, p38 may have suppressive or stimulatory effects on proliferation depending on the cell type, due to differential cross-talk between the p38 and MEK/ERK pathways. 相似文献
49.
Magne Refsnes Olav F. Dajani Dagny Sandnes G. Hege Thoresen John-Arne Rttingen Jens-Gustav Iversen Thoralf Christoffersen 《Journal of cellular physiology》1995,164(3):465-473
While many observations indicate that prostaglandins may act as positive regulators of hepatocyte proliferation, the underlying mechanisms are not known. We have examined some of the signal pathways in the growth response induced by prostaglandins in hepatocytes, with particular focus on adenylyl cyclase and phosphoinositide-specific phospholipase C. Adult rat hepatocytes were cultured as primary monolayers in serum-free medium in the presence of EGF and insulin. PGE2 or PGF2α (added 0-3 h after plating) enhanced the incorporation of [3H]-thymidine into DNA (measured at 50 h); at 100 γM the stimulation was about threefold. PGI2 and PGD2 also showed significant but smaller stimulatory effects. No significant increase in the level of cyclic AMP (cAMP) was detected in response to any of the prostaglandins. Low concentrations of glucagon (0.1-10 nM), a potent activator of hepatic adenylyl cyclase, or 8-bromo-cAMP (0.1-10 γM) enhanced the DNA synthesis. When 8-bromo-cAMP was used in maximally effective concentrations, no further stimulation was obtained by combining it with glucagon, whereas the effects of PGE2 and 8-bromo-cAMP were completely additive. All the prostaglandins also showed additivity with the effect of glucagon on the DNA synthesis. PGE2, PGF2α, PGI2, and PGD2 increased intracellular inositol-1,4,5-trisphosphate (InsP3), with a relative order of efficacy roughly corresponding to their activity as stimulators of DNA synthesis. Increases in cytosolic free Ca2+, as measured in single cells, were elicited in a majority of the hepatocytes by all these prostaglandins at 1 γM. Supramaximal concentrations of vasopressin, a strong activator of phospholipase C in hepatocytes, acted additively with PGE2 on the DNA synthesis. Pretreatment of the hepatocytes with a concentration of pertussis toxin that prevented the inhibitory effect of PGE2 on glucagon-induced cAMP accumulation did not abolish the ability of PGE2 to stimulate the DNA synthesis. The results do not support a role for adenylyl cyclase activation in the stimulatory effect of prostaglandins on hepatocyte growth. While the data are compatible with an involvement of phosphoinositide-specific phospholipase C in the growth-promoting effect of prostaglandins in cultured rat hepatocytes, they suggest this may not be the sole mechanism. © 1995 Wiley-Liss, Inc. 相似文献
50.
Marcel Prothmann Florian von Knobelsdorff-Brenkenhoff Agnieszka T?pper Matthias A. Dieringer Etham Shahid Andreas Graessl Jan Rieger Darius Lysiak C. Thalhammer Till Huelnhagen Peter Kellman Thoralf Niendorf Jeanette Schulz-Menger 《PloS one》2016,11(2)