全文获取类型
收费全文 | 580篇 |
免费 | 26篇 |
专业分类
林业 | 28篇 |
农学 | 4篇 |
基础科学 | 7篇 |
169篇 | |
综合类 | 53篇 |
农作物 | 18篇 |
水产渔业 | 32篇 |
畜牧兽医 | 254篇 |
园艺 | 9篇 |
植物保护 | 32篇 |
出版年
2024年 | 1篇 |
2023年 | 11篇 |
2022年 | 8篇 |
2021年 | 21篇 |
2020年 | 28篇 |
2019年 | 27篇 |
2018年 | 13篇 |
2017年 | 12篇 |
2016年 | 16篇 |
2015年 | 16篇 |
2014年 | 16篇 |
2013年 | 31篇 |
2012年 | 42篇 |
2011年 | 47篇 |
2010年 | 26篇 |
2009年 | 26篇 |
2008年 | 37篇 |
2007年 | 41篇 |
2006年 | 32篇 |
2005年 | 34篇 |
2004年 | 28篇 |
2003年 | 23篇 |
2002年 | 25篇 |
2001年 | 4篇 |
2000年 | 4篇 |
1999年 | 2篇 |
1998年 | 2篇 |
1997年 | 1篇 |
1996年 | 2篇 |
1995年 | 1篇 |
1994年 | 2篇 |
1993年 | 1篇 |
1992年 | 3篇 |
1991年 | 1篇 |
1990年 | 1篇 |
1989年 | 2篇 |
1988年 | 3篇 |
1986年 | 1篇 |
1985年 | 6篇 |
1984年 | 1篇 |
1983年 | 2篇 |
1980年 | 3篇 |
1979年 | 1篇 |
1978年 | 1篇 |
1977年 | 1篇 |
排序方式: 共有606条查询结果,搜索用时 187 毫秒
31.
Wickelgren I 《Science (New York, N.Y.)》2004,305(5681):162-163
32.
Role of histone H3 lysine 27 methylation in X inactivation 总被引:1,自引:0,他引:1
Plath K Fang J Mlynarczyk-Evans SK Cao R Worringer KA Wang H de la Cruz CC Otte AP Panning B Zhang Y 《Science (New York, N.Y.)》2003,300(5616):131-135
The Polycomb group (PcG) protein Eed is implicated in regulation of imprinted X-chromosome inactivation in extraembryonic cells but not of random X inactivation in embryonic cells. The Drosophila homolog of the Eed-Ezh2 PcG protein complex achieves gene silencing through methylation of histone H3 on lysine 27 (H3-K27), which suggests a role for H3-K27 methylation in imprinted X inactivation. Here we demonstrate that transient recruitment of the Eed-Ezh2 complex to the inactive X chromosome (Xi) occurs during initiation of X inactivation in both extraembryonic and embryonic cells and is accompanied by H3-K27 methylation. Recruitment of the complex and methylation on the Xi depend on Xist RNA but are independent of its silencing function. Together, our results suggest a role for Eed-Ezh2-mediated H3-K27 methylation during initiation of both imprinted and random X inactivation and demonstrate that H3-K27 methylation is not sufficient for silencing of the Xi. 相似文献
33.
Wickelgren I 《Science (New York, N.Y.)》2005,308(5730):1856-1858
34.
35.
36.
Prabhakar S Visel A Akiyama JA Shoukry M Lewis KD Holt A Plajzer-Frick I Morrison H Fitzpatrick DR Afzal V Pennacchio LA Rubin EM Noonan JP 《Science (New York, N.Y.)》2008,321(5894):1346-1350
Changes in gene regulation are thought to have contributed to the evolution of human development. However, in vivo evidence for uniquely human developmental regulatory function has remained elusive. In transgenic mice, a conserved noncoding sequence (HACNS1) that evolved extremely rapidly in humans acted as an enhancer of gene expression that has gained a strong limb expression domain relative to the orthologous elements from chimpanzee and rhesus macaque. This gain of function was consistent across two developmental stages in the mouse and included the presumptive anterior wrist and proximal thumb. In vivo analyses with synthetic enhancers, in which human-specific substitutions were introduced into the chimpanzee enhancer sequence or reverted in the human enhancer to the ancestral state, indicated that 13 substitutions clustered in an 81-base pair module otherwise highly constrained among terrestrial vertebrates were sufficient to confer the human-specific limb expression domain. 相似文献
37.
Richter Jana Baltruschat Helmut Kabrodt Kathrin Schellenberg Ingo 《植物病害和植物保护杂志》2011,118(3-4):109-118
Journal of Plant Diseases and Protection - The importance of herbal plants is evident in the prevalent use as flavoring ingredients in food. However, meeting the growing demand for organic grown... 相似文献
38.
SOM fractionation methods: Relevance to functional pools and to stabilization mechanisms 总被引:2,自引:0,他引:2
Margit von Lützow Ingrid Kögel-Knabner Heinz Flessa Egbert Matzner 《Soil biology & biochemistry》2007,39(9):2183-2207
Soil organic matter (SOM) consists of various functional pools that are stabilized by specific mechanisms and have certain turnover rates. For the development of mechanistic models that predict changes in SOM storage, these pools have to be quantified and characterized. In the past, numerous fractionation schemes have been developed to separate and analyse such SOM fractions. In this review, the SOM fractions obtained with such operational fractionation procedures are described in terms of their pool sizes, chemical properties, and turnover rates. The main objective of this review is to evaluate these operationally defined fractions with respect to their suitability to describe functional SOM pools that could be used to parameterize SOM turnover models. Fractionation procedures include (1) physical separation of SOM into aggregate, particle size, and density fractions and fractions according to their magnetic susceptibility, and (2) various wet chemical procedures that fractionate SOM according to solubility, hydrolysability, and resistance to oxidation or by destruction of the mineral phase. Furthermore, combinations of fractionation methods are evaluated.The active SOM pool with turnover rates <10 years may best be represented by the soil microbial biomass and the light fraction (<1.6-2 g cm−3) obtained by density fractionation (if black carbon contents are considered). Most chemical and physical fractionations as well as combinations of methods yield SOM fractions that are not homogeneous in terms of turnover rates. It has proven to be particularly difficult to isolate functional fractions that represent the passive model pools in which the majority of soil SOM is stabilized. The available fractionation methods do not correspond to specific stabilization mechanisms and hence do not describe functional SOM pools. Another problem is that comprehensive data for turnover rates and data for whole soil profiles are only now becoming available, especially for new fractionation methods. Such information as well as the use of specific markers and compound-specific isotope analysis may be important for future differentiation and evaluation of functional SOM fractions. 相似文献
39.
Ingrid M. van AarleBengt Söderström Pål Axel Olsson 《Soil biology & biochemistry》2003,35(12):1557-1564
Arbuscular mycorrhizal (AM) development in different soil types, and the influence of AM fungal hyphae on their original soil were investigated. Plantago lanceolata, which can grow in soils of a very wide pH range, was grown in two closely related limestone soils and an acid soil from rock habitats. Plants were colonised by the indigenous AM fungal community. The use of compartmented systems allowed us to compare soil with and without mycorrhizal hyphae. Root colonisation of P. lanceolata was markedly higher in the limestone soils (30-60%) than in the acid soil (5-20%), both in the original habitat and in the experimental study. Growth of extraradical AM fungal hyphae was detected in the limestone soils, but not in the acid soil, using the signature fatty acid 16:1ω5 as biomass indicator. Analysis of signature fatty acids demonstrated an increased microbial biomass in the presence of AM fungal hyphae as judged for example from an increased amount of NLFA 16:0 with 30 nmol g−1 in one of the limestone soils. Bacterial activity, but not soil phosphatase activity, was increased by around 25% in the presence of mycorrhizal hyphae in the first harvest of limestone soils. AM fungal hyphae can thus stimulate microorganisms. However, no effect of AM hyphae was observed on the soil pH or organic matter content in the limestone soils and the available P was not depleted. 相似文献
40.
Instrumental measurement of redness loss (decrease in a* value) was evaluated as a tool to follow hemoglobin (Hb)-mediated lipid oxidation in fish muscle. Two washed cod mince model systems were used (prepared at pH 6.5 and 5.5), both fortified with 15 micromol/kg of trout Hb and adjusted to pH 6.5 and 81% moisture. The rate of oxidation was varied through pH alterations (pH 6.1 and 6.9) and addition of an antioxidative cod muscle press juice. During ice storage, TBARS, painty odor, and a* values were followed. In all "oxidizing" samples, a* values correlated well with TBARS and painty odor development; r = -0.95 and -0.77, respectively. In press juice containing samples, the correlation was lower (0.55 for a vs TBARS) because there was a slight a* value decrease even in the absence of measurable lipid oxidation. a* values distinguished between "oxidizing" and stable samples within 1 day, before any lipid oxidation products could be chemically detected. It was confirmed in an aqueous phosphate buffer model system that the redness loss corresponded to a buildup of brownish met-Hb at the expense of oxy- and deoxy-Hb. The a* value data were best used as a lipid oxidation index by calculating the rate of decrease (k value) in the "initial phase" of the redness loss (before accumulation of lipid oxidation products) or in the "differentiation phase" (during the exponential raise in TBARS/painty odor). Calibration to lipid oxidation products must, however, be made for each specific sample type. Washing method, pH, Hb-type, etc., all affected both k values and absolute a* readings. Small yellowness (b*) increases also occurred along with a value losses, possibly the result of polymerized Schiff bases. 相似文献