全文获取类型
收费全文 | 1907篇 |
免费 | 156篇 |
出版年
2024年 | 2篇 |
2023年 | 16篇 |
2022年 | 25篇 |
2021年 | 49篇 |
2020年 | 30篇 |
2019年 | 37篇 |
2018年 | 56篇 |
2017年 | 37篇 |
2016年 | 67篇 |
2015年 | 110篇 |
2014年 | 114篇 |
2013年 | 141篇 |
2012年 | 163篇 |
2011年 | 147篇 |
2010年 | 107篇 |
2009年 | 83篇 |
2008年 | 114篇 |
2007年 | 107篇 |
2006年 | 103篇 |
2005年 | 94篇 |
2004年 | 76篇 |
2003年 | 77篇 |
2002年 | 75篇 |
2001年 | 19篇 |
2000年 | 9篇 |
1999年 | 15篇 |
1998年 | 25篇 |
1997年 | 13篇 |
1996年 | 16篇 |
1995年 | 13篇 |
1994年 | 9篇 |
1993年 | 10篇 |
1992年 | 7篇 |
1991年 | 10篇 |
1990年 | 7篇 |
1989年 | 8篇 |
1988年 | 8篇 |
1987年 | 3篇 |
1986年 | 5篇 |
1985年 | 9篇 |
1984年 | 14篇 |
1983年 | 3篇 |
1982年 | 8篇 |
1981年 | 4篇 |
1980年 | 6篇 |
1979年 | 3篇 |
1972年 | 2篇 |
1968年 | 1篇 |
1967年 | 2篇 |
1956年 | 1篇 |
排序方式: 共有2063条查询结果,搜索用时 15 毫秒
31.
32.
The sources of reinfestation of a treated apiary byVarroa jacobsoni Oud. were studied in Friuli (North-Eastern Italy), in an area with a high density of colonies. Ten colonies, initiallyVarroa-free, were treated with Apistan or Bayvarol strips and mites killed by these treatments were counted twice a week for 1 year. Five hives were provided with drone excluders, to avoid the entrance of drones from other apiaries. Nectar and honeydew flow were monitored.The reinfestation rate was low during spring, varied between 1.6–13.7 mites/day/colony during June, July and first week of August, and rose impressively during September and October (up to a mean of 75.6 mites/day/colony); it was relatively high when nectar flow was scarce. The presence of drone excluders did not help to limit the number of mites imported: drones did not seem to be the main cause of reinfestation. The coincidence between the increase in the reinfestation rate and the scarcity of nectar flow and the massive importation of mites, observed especially in September and October, suggest that reinfestation was mainly caused by robbing of infested colonies (mostly feral swarms) by the bees of treated colonies.Research carried out with the financial contribution of C.E.C. (Grant RAB/1989/066). 相似文献
33.
Steroidogenesis in isolated adrenocortical cells. Correlation with receptor-bound adenosine 3′:5′-cyclic monophosphate 下载免费PDF全文
Ernesto J. Podesta Alfred Milani Hans Steffen Robert Neher 《The Biochemical journal》1979,180(2):355-363
Because several groups have recently questioned a mediating role for cyclic AMP in adrenocortical steroidogenesis, we analysed the problem in more detail by measuring three different cyclic AMP pools in cells isolated from decapsulated rat adrenals. Extra-cellular, total intracellular and bound intracellular cyclic AMP were determined by radioimmunoassay in comparison with corticosterone production induced by low corticotropin concentrations. The increase in extracellular and total intracellular cyclic AMP with low corticotropin concentrations was dependent on the presence of a phosphodiesterase inhibitor and short incubation times. Bound intracellular cyclic AMP was less dependent on these two parameters. In unstimulated cells cyclic AMP bound to its receptor represents only a small fraction of the total intracellular cyclic AMP. After stimulation by a concentration of corticotropin around the threshold for corticosterone production, an increase in bound cyclic AMP was observed which correlated very well with steroidogenesis both temporally and with respect to corticotropin concentration. This finding was complemented by measuring a concomitant decrease in free receptor sites. Full occupancy of the receptors was not necessary for maximal steroidogenesis. Binding kinetics of cyclic [(3)H]AMP in concentrations equivalent to the intracellular cyclic AMP concentration suggest the presence of at least three different intracellular cyclic AMP pools. These observations are in agreement with a possible role for cyclic AMP as a mediator of acute steroidogenesis induced by low corticotropin concentrations. 相似文献
34.
Bonacchi A Taddei ML Petrai I Efsen E Defranco R Nosi D Torcia M Rosini P Formigli L Rombouts K Zecchi S Milani S Pinzani M Laffi G Marra F 《Histology and histopathology》2008,23(3):327-340
The liver represents a site of expression of neurotrophins and their receptors. We have characterized the expression and intracellular localization of the nerve growth factor (NGF) receptor, Trk-A, in liver cells in vivo and in vitro. In both normal and fibrotic liver tissue, Trk-A immunostaining was present in different cell types, including parenchymal cells and cells of the inflammatory infiltrate. In hepatocytes and activated stellate cells (HSC), Trk-A showed a predominant nuclear localization, both in the presence and absence of injury. In cultured HSC, Trk-A was found to be functional, because exposure of the cells to recombinant NGF resulted in stimulation of cell migration and activation of intracellular signaling pathways, including Ras-ERK and PI3K/Akt. Remarkably, in cultured HSC, Trk-A staining was found constitutively in the nucleus. In these cells, Trk-A could be stained only by antibodies directed against the intracellular domain but not by those recognizing the extracellular portion of Trk-A suggesting that the intracellular portion of the receptor is the major determinant of nuclear Trk-A staining. In contrast to HSC, freshly isolated hepatocytes did not show any nuclear localization of the intracellular portion of Trk-A. In pheocromocytoma cells, nuclear staining for Trk-A was not present in conditions of serum deprivation, but could be induced by exposure to NGF or to a mixture of soluble mediators. We conclude that nuclear localization of the intracellular domain of Trk-A is observed constitutively in liver cells such as HSC, while in other cell types it could be induced in response to soluble factors. 相似文献
35.
Rachael G Dean Leanne C Balding Riccardo Candido Wendy C Burns Zemin Cao Stephen M Twigg Louise M Burrell 《The journal of histochemistry and cytochemistry》2005,53(10):1245-1256
The temporal and spatial expression of transforming growth factor (TGF)-beta(1) and connective tissue growth factor (CTGF) was assessed in the left ventricle of a myocardial infarction (MI) model of injury with and without angiotensin-converting enzyme (ACE) inhibition. Coronary artery ligated rats were killed 1, 3, 7, 28, and 180 days after MI. TGF-beta(1), CTGF, and procollagen alpha1(I) mRNA were localized by in situ hybridization, and TGF-beta(1) and CTGF protein levels by immunohistochemistry. Collagen protein was measured using picrosirius red staining. In a separate group, rats were treated for 6 months with an ACE inhibitor. There were temporal and regional differences in the expression of TGF-beta(1), CTGF, and collagen after MI. Procollagen alpha1(I) mRNA expression increased in the border zone and scar peaking 1 week after MI, whereas collagen protein increased in all areas of the heart over the 180 days. Expression of TGF-beta(1) mRNA and protein showed major increases in the border zone and scar peaking 1 week after MI. The major increases in CTGF mRNA and protein occurred in the viable myocardium at 180 days after MI. Long-term ACE inhibition reduced left ventricular mass and decreased fibrosis in the viable myocardium, but had no effect on cardiac TGF-beta(1) or CTGF. TGF-beta(1) is involved in the initial, acute phase of inflammation and repair after MI, whereas CTGF is involved in the ongoing fibrosis of the heart. The antifibrotic benefits of captopril are not mediated through a reduction in CTGF. 相似文献
36.
Giovanni Spagna Riccardo N. Barbagallo Rosa Palmeri Cristina Restuccia Paolo Giudici 《Enzyme and microbial technology》2002,31(7):1030-1035
Three hundred sixty-one yeast strains (80 of which ascribable to Saccharomyces cerevisiae) were isolated from Sicilian musts and wines with the purpose of looking for β-glucosidase (βG, EC 3.2.1.21) activity. Of these, the AL 41 strain had highest endogenous βG activity and was identified as belonging to the species S. cerevisiae by biochemical and molecular methods. This enzyme was subsequently characterized. It had optimum effect at pH 3.5–4.0, whilst optimum temperature was 20 °C, compatible with typical wine-cellar conditions; it was not inhibited by ethanol, at concentrations of 12–14%, or fructose and glucose. The βG was also characterised in terms of the kinetic parameters Km (2.55 mM) and Vmax (1.71 U mg−1 of protein). Finally, it remained stable for at least 35 days in model solutions of must and wine. 相似文献
37.
Multiple stressors on biotic interactions: how climate change and alien species interact to affect pollination 总被引:1,自引:0,他引:1
Oliver Schweiger Jacobus C. Biesmeijer Riccardo Bommarco Thomas Hickler Philip E. Hulme Stefan Klotz Ingolf Kühn Mari Moora Anders Nielsen Ralf Ohlemüller Theodora Petanidou Simon G. Potts Petr Pyšek Jane C. Stout Martin T. Sykes Thomas Tscheulin Montserrat Vilà Gian‐Reto Walther Catrin Westphal Marten Winter Martin Zobel Josef Settele 《Biological reviews of the Cambridge Philosophical Society》2010,85(4):777-795
Global change may substantially affect biodiversity and ecosystem functioning but little is known about its effects on essential biotic interactions. Since different environmental drivers rarely act in isolation it is important to consider interactive effects. Here, we focus on how two key drivers of anthropogenic environmental change, climate change and the introduction of alien species, affect plant–pollinator interactions. Based on a literature survey we identify climatically sensitive aspects of species interactions, assess potential effects of climate change on these mechanisms, and derive hypotheses that may form the basis of future research. We find that both climate change and alien species will ultimately lead to the creation of novel communities. In these communities certain interactions may no longer occur while there will also be potential for the emergence of new relationships. Alien species can both partly compensate for the often negative effects of climate change but also amplify them in some cases. Since potential positive effects are often restricted to generalist interactions among species, climate change and alien species in combination can result in significant threats to more specialist interactions involving native species. 相似文献
38.
Donini S Percudani R Credali A Montanini B Sartori A Peracchi A 《Biochemical and biophysical research communications》2006,350(4):922-928
The genomes of several vertebrates contain two genes encoding proteins highly similar to threonine synthase (TS), even though the biosynthesis of l-threonine (l-Thr) is not known to occur in these animals. We report a bioinformatic analysis of the two TS-like genes, the recombinant expression of one murine TS homolog (mTSH2) and its initial biochemical characterization. Recombinant mTSH2 contained bound pyridoxal-5'-phosphate (PLP), but did not synthesize l-Thr. The enzyme did, however, bind O-phospho-homoserine (PHS; the actual TS substrate) and degraded it to alpha-ketobutyrate, phosphate, and ammonia-a known side reaction of microbial TSs. mTSH2 also degraded O-phospho-threonine (PThr) to alpha-ketobutyrate, showing that it can act as a catabolic phospho-lyase on both gamma- and beta-phosphorylated substrates. These findings suggest an unusual evolutionary origin for mTSH2, whereby an original TS enzyme became 'recycled' into a phospho-lyase upon dismissal, in metazoa, of the l-Thr biosynthetic pathway. 相似文献
39.
Fraaije MW Kamerbeek NM Heidekamp AJ Fortin R Janssen DB 《The Journal of biological chemistry》2004,279(5):3354-3360
EtaA is a newly identified FAD-containing monooxygenase that is responsible for activation of several thioamide prodrugs in Mycobacterium tuberculosis. It was found that purified EtaA displays a remarkably low activity with the antitubercular prodrug ethionamide. Hinted by the presence of a Baeyer-Villiger monooxygenase sequence motif in the EtaA sequence, we have been able to identify a large number of novel EtaA substrates. It was discovered that the enzyme converts a wide range of ketones to the corresponding esters or lactones via a Baeyer-Villiger reaction, indicating that EtaA represents a Baeyer-Villiger monooxygenase. With the exception of aromatic ketones (phenylacetone and benzylacetone), long-chain ketones (e.g. 2-hexanone and 2-dodecanone) also are converted. EtaA is also able to catalyze enantioselective sulfoxidation of methyl-p-tolylsulfide. Conversion of all of the identified substrates is relatively slow with typical k(cat) values of around 0.02 s(-1). The best substrate identified so far is phenylacetone (K(m) = 61 microM, k(cat) = 0.017 s(-1)). Redox monitoring of the flavin cofactor during turnover of phenylacetone indicates that a step in the reductive half-reaction is limiting the rate of catalysis. Intriguingly, EtaA activity could be increased by one order of magnitude by adding bovine serum albumin. This reactivity and substrate acceptance-profiling study provides valuable information concerning this newly identified prodrug activator from M. tuberculosis. 相似文献
40.