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91.
92.
Christelle Boileau Johanne Martel-Pelletier Judith Caron Philippe Msika Georges B Guillou Caroline Baudouin Jean-Pierre Pelletier 《Arthritis research & therapy》2009,11(2):R41-9
Introduction
The aims of this study were, first, to investigate the in vivo effects of treatment with avocado/soybean unsaponifiables on the development of osteoarthritic structural changes in the anterior cruciate ligament dog model and, second, to explore their mode of action. 相似文献93.
94.
F. L. Laksmana P. J. A. Hartman Kok H. Vromans H. W. Frijlink K. Van der Voort Maarschalk 《AAPS PharmSciTech》2009,10(3):732-742
Next to the coating formulation, process conditions play important roles in determining coating quality. This study aims to
develop an operational window that separates layering from agglomeration regimes and, furthermore, the one that leads to the
best coating quality in a fluidized bed coater. The bed relative humidity and the droplet size of the coating aerosol were
predicted using a set of engineering models. The coating quality was characterized using a quantitative image analysis method,
which measures the coating thickness distribution, the total porosity, and the pore size in the coating. The layering regime
can be achieved by performing the coating process at a certain excess of the viscous Stokes number (ΔSt
v). This excess is dependent on the given bed relative humidity and droplet size. The higher the bed relative humidity, the
higher is the ΔSt
v required to keep the process in the layering regime. Further, it is shown that using bed relative humidity and droplet size
alone is not enough to obtain constant coating quality. The changes in bed relative humidity and droplet size have been identified
to correlate to the fractional area of particles sprayed per unit of time. This parameter can effectively serve as an additional
parameter to be considered for a better control on the coating quality. High coating quality is shown to be achieved by performing
the process close to saturation and spraying droplets small enough to obtain high spraying rate, but not too small to cause
incomplete coverage of the core particles. 相似文献
95.
Christopher A. Emerling Hieu T. Huynh Minh A. Nguyen Robert W. Meredith Mark S. Springer 《Proceedings. Biological sciences / The Royal Society》2015,282(1819)
Retinal opsin photopigments initiate mammalian vision when stimulated by light. Most mammals possess a short wavelength-sensitive opsin 1 (SWS1) pigment that is primarily sensitive to either ultraviolet or violet light, leading to variation in colour perception across species. Despite knowledge of both ultraviolet- and violet-sensitive SWS1 classes in mammals for 25 years, the adaptive significance of this variation has not been subjected to hypothesis testing, resulting in minimal understanding of the basis for mammalian SWS1 spectral tuning evolution. Here, we gathered data on SWS1 for 403 mammal species, including novel SWS1 sequences for 97 species. Ancestral sequence reconstructions suggest that the most recent common ancestor of Theria possessed an ultraviolet SWS1 pigment, and that violet-sensitive pigments evolved at least 12 times in mammalian history. We also observed that ultraviolet pigments, previously considered to be a rarity, are common in mammals. We then used phylogenetic comparative methods to test the hypotheses that the evolution of violet-sensitive SWS1 is associated with increased light exposure, extended longevity and longer eye length. We discovered that diurnal mammals and species with longer eyes are more likely to have violet-sensitive pigments and less likely to possess UV-sensitive pigments. We hypothesize that (i) as mammals evolved larger body sizes, they evolved longer eyes, which limited transmittance of ultraviolet light to the retina due to an increase in Rayleigh scattering, and (ii) as mammals began to invade diurnal temporal niches, they evolved lenses with low UV transmittance to reduce chromatic aberration and/or photo-oxidative damage. 相似文献
96.
C. A. Kreikemeier T. B. Engle K. L. Lucot S. D. Kachman T. E. Burkey D. C. Ciobanu 《Animal genetics》2015,46(2):205-208
Tumor necrosis factor alpha (TNF‐α) is a pro‐inflammatory cytokine with a role in activating adaptive immunity to viral infections. By inhibiting the capacity of plasmacytoid dendritic cells to produce interferon‐α and TNF‐α, porcine circovirus 2 (PCV2) limits the maturation of myeloid dendritic cells and impairs their ability to recognize viral and bacterial antigens. Previously, we reported QTL for viremia and immune response in PCV2‐infected pigs. In this study, we analyzed phenotypic and genetic relationships between TNF‐α protein levels, a potential indicator of predisposition to PCV2 co‐infection, and PCV2 susceptibility. Following experimental challenge with PCV2b, TNF‐α reached the peak at 21 days post‐infection (dpi), at which time a difference was observed between pigs that expressed extreme variation in viremia and growth (P < 0.10). A genome‐wide association study (n = 297) revealed that genotypes of 56 433 SNPs explained 73.9% of the variation in TNF‐α at 21 dpi. Major SNPs were identified on SSC8, SSC10 and SSC14. Haplotypes based on SNPs from a SSC8 (9 Mb) 1‐Mb window were associated with variation in TNF‐α (P < 0.02), IgG (P = 0.05) and IgM (P < 0.13) levels at 21 dpi. Potential overlap of regulatory mechanisms was supported by the correlations between genomic prediction values of TNF‐α and PCV2 antibodies (21 dpi, r > 0.22), viremia (14–21 dpi, P > 0.29) and viral load (r = 0.31, P < 0.0001). Characterization of the QTL regions uncovered genes that could influence variation in TNF‐α levels as well as T‐ and B‐cell development, which can affect disease susceptibility. 相似文献
97.
98.
Daw-Yang Hwang Stefan Kohl Xueping Fan Asaf Vivante Stefanie Chan Gabriel C. Dworschak Julian Schulz Albertien M. van Eerde Alina C. Hilger Heon Yung Gee Tracie Pennimpede Bernhard G. Herrmann Glenn van de Hoek Kirsten Y. Renkema Christoph Schell Tobias B. Huber Heiko M. Reutter Neveen A. Soliman Natasa Stajic Radovan Bogdanovic Elijah O. Kehinde Richard P. Lifton Velibor Tasic Weining Lu Friedhelm Hildebrandt 《Human genetics》2015,134(8):905-916
99.
100.