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61.
62.
Fernande D. Rochon Robert Melanson Jean-Pierre Macquet Francine Belanger-Gariepy Andre L. Beauchamp 《Inorganica chimica acta》1985,108(1):17-21
The structure of the complex [Pt(trans-1,2-di- aminocyclohexane) (acetate)2]·H2O has been determined by X-ray diffraction. This racemic compound is orthorhombic, space group Aba2, a = 20.813(9), b = 7.926(5), c = 17.296(8) Å, Z = 8. The structure was refined on 1214 nonzero Cu Kα reflections to R = 0.028. The square planar environment of Pt includes the amino groups of the diamine in cis positions and oxygens from two monodentate acetates. The PtN and PtO distances average 2.00(3) and 2.02(3) Å, respectively. The bite of the diamine ligand imposes a NPtN angle of 85(1)°, whereas the small OPtO angle of 85(1)° probably results from packing effects. The average plane through the puckered cyclohexyl ring makes an angle of 19° with the PtN2O2 plane. The molecules are stacked by pairs along the b axis. The two molecules of each pair are 180° apart about the stacking axis, and form altogether four NH···O hydrogen bonds. 相似文献
63.
64.
Common generalized vitiligo is an acquired depigmenting disorder characterized by a chronic and progressive loss of melanocytes from the epidermis and follicular reservoir. However, the mechanism of melanocyte disappearance has never been clearly understood, and the intervention of cellular and humoral autoimmune phenomena as primary events remains unproven. In this review, is discussed the data supporting the major theories of vitiligo, namely melanocyte destruction (autoimmune, neural and impaired redox status) and melanocyte inhibition or defective adhesion. Based on recent morphologic findings in vivo supporting a chronic detachment and transepidermal loss of melanocytes in common generalized vitiligo, a new theory is suggested proposing melanocytorrhagy as the primary defect underlying melanocyte loss, integrating most of the possible triggering/precipitating/enhancing effects of other known factors. 相似文献
65.
Modelling the attack success of planktonic predators: patterns and mechanisms of prey size selectivity 总被引:1,自引:0,他引:1
Caparroy Philippe; Thygesen Uffe Hogsbro; Visser Andre W. 《Journal of plankton research》2000,22(10):1871
A mathematical model of the attack success of planktonic predators(fish larvae and carnivorous copepods) is proposed. Based ona geometric representation of attack events, the model considershow the escape reaction characteristics (speed and direction)of copepod prey affect their probability of being captured.By combining the attack success model with previously publishedhydrodynamic models of predator and prey perception, we examinehow predator foraging behaviour and prey perceptive abilityaffect the size spectra of encountered and captured copepodprey. We examine food size spectra of (i) a rheotactic cruisingpredator, (ii) a suspension-feeding hovering copepod and (iii)a larval fish. For rheotactic predators such as carnivorouscopepods, a central assumption of the model is that attack istriggered by prey escape reaction, which in turn depends onthe deformation rate of the fluid created by the predator. Themodel demonstrates that within a species of copepod prey, theability of larger stages to react at a greater distance fromthe predator results in increased strike distance and, hence,lower capture probability. For hovering copepods, the vorticityfield associated with the feeding current also acts in modifyingthe prey escape direction. The model demonstrates that the reorientationof the prey escape path towards the centre of the feeding current'sflow field results in increased attack success of the predator.Finally, the model examines how variability in the kineticsof approach affects the strike distance of larval fish. In caseswhere observational data are available, model predictions closelyfit observations. 相似文献
66.
Tissue-based quantitative proteome analysis of human hepatocellular carcinoma using tandem mass tags
Dominik Andre Megger Kristin Rosowski Maike Ahrens Thilo Bracht Martin Eisenacher Jörg F. Schlaak 《Biomarkers》2017,22(2):113-122
Context and objective: Human hepatocellular carcinoma (HCC) is a severe malignant disease, and accurate and reliable diagnostic markers are still needed. This study was aimed for the discovery of novel marker candidates by quantitative proteomics.
Methods and results: Proteomic differences between HCC and nontumorous liver tissue were studied by mass spectrometry. Among several significantly upregulated proteins, translocator protein 18 (TSPO) and Ras-related protein Rab-1A (RAB1A) were selected for verification by immunohistochemistry in an independent cohort. For RAB1A, a high accuracy for the discrimination of HCC and nontumorous liver tissue was observed.
Conclusion: RAB1A was verified to be a potent biomarker candidate for HCC. 相似文献
67.
68.
The plasma concentrations of testosterone, androstenedione,5-androstene-3β, 17β-diol, 5α-dihydrotestosterone and 17β-hydroxy-androgens have been measured in normal women and in patients with idiopathic hirsutism. The mean levels of all the compounds studied were higher in the group of patients with hirsutism than in the controls and apart from dihydrotestosterone, this difference was statistically significant. The correlation between the plasma levels of the various steroids was examined. In the normal subjects, testosterone and androstenedione levels were well correlated, but in the hirsute patients, the correlation is poor. It is suggested that this is related to altered binding of testosterone to plasma proteins in these patients. No one of the steroid levels measured was consistently abnormal in hirsutism, but in 40% of the patients, plasma androstenedione levels were above the normal range. 相似文献
69.
Drosophila melanogaster acetylcholinesterase: Identification and expression of two mutations responsible for cold- and heat-sensitive phenotypes 总被引:2,自引:0,他引:2
Annick Mutero Jean-Marc Bride Madeleine Pralavorio Didier Fournier 《Molecular & general genetics : MGG》1994,243(6):699-705
Ace
IJ29 and Ac
IJ40 are cold- and heat-sensitive variants of the gene coding for acetylcholinesterase in Drosophila melanogaster. In the homozygous condition, these mutations are lethal when animals are raised at restrictive temperatures, i.e., below 23° C for Ace
IJ29 or above 25° C for Ace
IJ40. The coding regions of the gene in these mutants were sequenced and mutations changing Ser374 to Phe in Ace
IJ29 and Pro75 to Leu in Ace
IJ40 were found. Acetylcholinesterases bearing these mutations were expressed in Xenopus oocytes and we found that these mutations decrease the secretion rate of the protein most probably by affecting its folding. This phenomenon is exacerbated at restrictive temperatures decreasing the amount of secreted acetylcholinesterase below the lethality threshold. In parallel, the substitution of the conserved Asp248 by an Asn residue completely inhibits the activity of the enzyme and its secretion, preventing the correct folding of the protein in a non-conditional manner. 相似文献
70.
Cutting edge: TLR9 and TLR2 signaling together account for MyD88-dependent control of parasitemia in Trypanosoma cruzi infection 总被引:4,自引:0,他引:4
Bafica A Santiago HC Goldszmid R Ropert C Gazzinelli RT Sher A 《Journal of immunology (Baltimore, Md. : 1950)》2006,177(6):3515-3519
Activation of innate immune cells by Trypanosoma cruzi-derived molecules such as GPI anchors and DNA induces proinflammatory cytokine production and host defense mechanisms. In this study, we demonstrate that DNA from T. cruzi stimulates cytokine production by APCs in a TLR9-dependent manner and synergizes with parasite-derived GPI anchor, a TLR2 agonist, in the induction of cytokines by macrophages. Compared with wild-type animals, T. cruzi-infected Tlr9(-/-) mice displayed elevated parasitemia and decreased survival. Strikingly, infected Tlr2(-/-)Tlr9(-/-) mice developed a parasitemia equivalent to animals lacking MyD88, an essential signaling molecule for most TLR, but did not show the acute mortality displayed by MyD88(-/-) animals. The enhanced susceptibility of Tlr9(-/-) and Tlr2(-/-)Tlr9(-/-) mice was associated with decreased in vivo IL-12/IFN-gamma responses. Our results reveal that TLR2 and TLR9 cooperate in the control of parasite replication and that TLR9 has a primary role in the MyD88-dependent induction of IL-12/IFN-gamma synthesis during infection with T. cruzi. 相似文献