首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   827篇
  免费   34篇
  国内免费   66篇
林业   39篇
农学   66篇
基础科学   26篇
  40篇
综合类   285篇
农作物   82篇
水产渔业   43篇
畜牧兽医   217篇
园艺   100篇
植物保护   29篇
  2024年   1篇
  2023年   10篇
  2022年   25篇
  2021年   27篇
  2020年   29篇
  2019年   34篇
  2018年   19篇
  2017年   32篇
  2016年   61篇
  2015年   38篇
  2014年   51篇
  2013年   61篇
  2012年   54篇
  2011年   73篇
  2010年   54篇
  2009年   43篇
  2008年   48篇
  2007年   55篇
  2006年   36篇
  2005年   31篇
  2004年   28篇
  2003年   25篇
  2002年   17篇
  2001年   10篇
  2000年   16篇
  1999年   8篇
  1998年   7篇
  1997年   7篇
  1996年   6篇
  1995年   3篇
  1994年   2篇
  1993年   1篇
  1992年   2篇
  1990年   1篇
  1989年   2篇
  1988年   1篇
  1987年   3篇
  1984年   1篇
  1975年   1篇
  1973年   1篇
  1962年   1篇
  1956年   1篇
  1955年   1篇
排序方式: 共有927条查询结果,搜索用时 296 毫秒
51.
桑树杂交组合桂桑优12的育成   总被引:3,自引:1,他引:2  
应用遗传互补和杂种优势原理 ,育成桑树新品种 (杂交组合 )桂桑优 12。其F1群体整齐、发条数多、枝高节密、叶大叶厚、耐剪伐、再生能力强、发芽较早、收造较晚、产叶量较高、叶质较优、繁育较易 ,适宜常规栽培以及加速生丰产和省力化养蚕栽培。与对照沙 2×伦 10 9相比 ,每公顷桑叶产量增产 11 36 % ,桑叶养蚕万头蚕产茧层量增加 4 4 2 % ,10 0kg桑叶产茧量增产 3 18% ,每公顷桑园产茧量增产 19 6 3%。  相似文献   
52.
AIM: To investigate the effect of uric acid on the maturation and the biological function of murine bone-marrow derived dendritic cells (BMDCs) in vitro.METHODS: BMDCs were cultured with GM-CSF, IL-4, LPS and uric acid. Cell phenotypes were analyzed by flow cytometry. MTT was used to detect the effect of uric acid on the function of BMDCs in stimulating the proliferation of T cells. IL-12 released by BMDCs was also detected. RESULTS: BMDCs were cultured and identified. Uric acid at concentrations of 200 mg/L and 400 mg/L increased the expression of the molecules (CD11c, CD83, CD86, IA/IE) on BMDCs surface and the IL-12 level in the culture supernatants (P<0.05), promoted the proliferation of T cells at the T: DC rate 5∶1, 10∶1, 20∶1 (P<0.05). However, uric acid at concentration of 70 mg/L had no effect on above molecule expression (P>0.05), no effect on T cell proliferation with BMDCs (P>0.05) was observed. CONCLUSION: Uric acid promotes the differentiation, maturation, the expression of co-stimulatory molecules, the IL-12 production in BMDCs and enhances the ability of BMDCs to stimulate the proliferation of T cell in a specical dose range.  相似文献   
53.
AIM: To investigate the immunological function of sodium butyrate-induced immature dendritic cells in vitro.METHODS: The human monocyte-derived dendritic cells were induced in the presence of human granulocyte macrophage-colony stimulating factor(GM-CSF) and interleukin-4 (IL-4), combined with sodium butyrate. The immunological function of sodium butyrate-induced dendritic cells was detected by the FCM, endocytic activity, T cells stimulatory proliferation capacity, and interleukin-12 (IL-12) production.RESULTS: Sodium butyrate could down-regulate the major histocompatibility complex(MHC) class II and costimulatory molecules of dendritic cells, increase the endocytic activity, induce a stage of T-cell anergey, and inhibit the T helper cell type 1-skewing factor IL-12 production. CONCLUSION: Sodium butyrate inhibits the maturation of dendritic cells and induces production of immature dendritic cells, which may help to explore the machenism of its epigenitic modification.  相似文献   
54.
55.
AIM: In order to study the effect of endogenous interferon system and Th1 response modes on hepatitis B virus infection, the 2′, 5′ oligoadenylate synthetase (2-5OAS), IL-2 and IL-12 were selected as the research parameters. METHODS: The activity of 2-5OAS in peripheral blood mononeuclear cells was determined by sensitive radioenzymatic assay. IL-2 and IL-12 were determined by ELISA. RESULTS: Compared to normal control, the 2-5OAS, IL-2 or IL-12 were not significantly changed (P>0.05) in the asymptomatic HBsAg carricer group. The 2-5OAS, IL-2 and IL-12 were significantly up-regulated (P<0.01) in the group of acute hepatitis, but in the groups of chronic hepatitis, liver cirrhosis and hepatocellular carcinoma, the 2-5OAS, IL-2, IL-12 were significantly down-regulated (P<0.05). Moreover, with the progression of patient′s conditions and with the complications of liver cirrhosis and hepatocellular carcinoma, the 2-5OAS, IL-2 and IL-12 decreased progressively, the 2-5OAS, IL-2, IL-12 were the lowest in guoups of liver cirrhosis and hepatocellular carcinoma (vs each groups of chronic hepatitis, P<0.05). CONCLUSION: The endogenous interferon system and Th1 response are significantly alterable in the different period of hepatitis B virus infection and among the different clinical types. The cellular immunity plays an important role in recovery from HBV infection.  相似文献   
56.
冀豆12遗传背景导入系蛋白、脂肪含量分布特征   总被引:2,自引:0,他引:2  
以高蛋白品种冀豆12为受体亲本,不同来源、不同蛋白脂肪含量的大豆种质资源为供体亲本,构建了28个组合BC2F1后代群体,分析冀豆12遗传背景导入系后代蛋白、脂肪含量分布特征。结果表明,28个后代群体均有蛋白含量超高亲个体,超高亲个体比例介于4.0%~68.2%之间,超高亲比例≥40%的组合有18个,占64.3%,BC2F1后代群体蛋白含量以超高亲和偏高亲类型组合为主。而脂肪含量分布特征恰相反,BC2F1后代群体脂肪含量以超低亲和偏低亲类型组合为主,超高亲个体比例介于0~67.4%,超高亲个体比例≥40%的组合有7个,占25.0%,9个组合无超高亲后代。表明以冀豆12为遗传背景通过有限回交易选育高蛋白含量品种,而不易选育高脂肪含量品种。本研究结果为利用冀豆12培育高蛋白品种提供了依据。  相似文献   
57.
对淬火前的热挤压棒用不同的冷拉拔量进行拉拔,结果表明;冷拉拔量对棒材的组织和性能有不同的影响.当变形量达到10%时,经淬火后的棒材其组织是均匀的细晶组织.  相似文献   
58.
【目的】试验旨在探究circRNA-Zfp609调节C2C12成肌细胞增殖和分化的潜在分子机制。【方法】利用RT-PCR和测序分析小鼠骨骼肌组织和C2C12成肌细胞中circRNA-Zfp609的表达,实时荧光定量PCR检测小鼠心脏、肝脏、脾脏、肺脏、肾脏、胃、小肠、骨骼肌组织及增殖12、24、36、48 h和分化0、1、3、5 d的C2C12成肌细胞中circRNA-Zfp609的相对表达量;实时荧光定量PCR检测分化0、1、3、5 d的C2C12成肌细胞中肌细胞生成素(MyoG)和肌球蛋白重链(MyHC)的相对表达量。用circRNA-Zfp609的干扰表达载体(siRNA)干扰细胞,通过CCK-8测定siRNA对C2C12成肌细胞增殖率的影响;用实时荧光定量PCR检测siRNA干扰对circRNA-Zfp609、MyoG和MyHC相对表达量的影响。通过TargetScan 7.0和miRDB软件预测circRNA-Zfp609上与肌肉分化相关的miRNA位点,将筛选的miRNAs的过表达载体转染HEK293T细胞,利用双荧光素酶报告试验验证circRNA-Zfp609与miRNA的互作关系。根据miRNAs对circRNA-Zfp609的互作,构建circRNA-Zfp609的野生型和突变型载体并转染HEK293T细胞,利用双荧光素酶报告试验验证circRNA-Zfp609对miRNA的靶向关系。【结果】PCR和测序结果表明,小鼠骨骼肌中可表达circRNA-Zfp609;circRNA-Zfp609在小鼠骨骼肌中表达水平最高,在其他组织中的表达量由高到低依次是肾脏、肺脏、心脏、肝脏、胃、脾脏和小肠。与12 h相比,在C2C12成肌细胞增殖的36和48 h circRNA-Zfp609的相对表达量显著增加(P<0.05);与分化第0天相比,在C2C12成肌细胞分化的第1、3和5天circRNA-Zfp609的相对表达量均显著增加(P<0.05),MyoG、MyHC的相对表达量均极显著增加(P<0.01)。与NC组相比,siRNA组C2C12成肌细胞的增殖率和circRNA-Zfp609相对表达量均极显著降低(P<0.01),MyoG和MyHC的相对表达量显著降低(P<0.05)。circRNA-Zfp609上有miR-150-5p、miR-327、miR-344g-3p和miR-615-5p 4种与肌肉分化相关的miRNAs。circRNA-Zfp609与miR-615-5p的吸附能力最强,具有靶向结合作用。circRNA-Zfp609可以作为分子海绵与调控肌肉分化相关的miR-615-5p相互作用。【结论】circRNA-Zfp609在小鼠的组织中广泛表达,在骨骼肌中表达水平最高;circRNA-Zfp609在C2C12成肌细胞增殖和分化的不同时期差异表达,circRNA-Zfp609上有4个与肌肉分化相关的miRNAs,其中miR-615-5p与circRNA-Zfp609具有靶向关系。本研究结果可为与家畜骨骼肌生长发育相关的研究提供参考。  相似文献   
59.
This article presents a validation of a method, proposed in Podlaski (2003), for estimating the degree of tree damage. This method belongs to a group of small-area methods. To estimate the degree of tree damage in individual P3 sub-blocks of the SINUS system of information on the natural environment, a classification based on the degree of defoliation was used. Spatial distribution of the degree of tree damage was estimated through unrestricted simple random sampling. The maximum total estimation error for proportions of fir and beech with a damage degree of zero, and also with second and third degrees jointly, reached a maximum of 35.6% for fir, and 33.8% for beech. P3 sub-blocks characterised by the highest proportion of the healthiest trees (at least 15% being undamaged trees) occurred in patches in the case of fir, and in larger, compact areas in the case of beech. Because spatial diversification in the health of fir, and to a smaller degree in the case of beech, occurs at small scales, small-area methods for estimating tree condition are necessary. An analogous scheme, combining small-area with large-area methods (utilising sub-blocks of the network of large-area systems in a small-area inventory, and establishing a common database), could be used on a wider scale; for example, by supplementing the program of estimating tree health carried out by the United Nations Economic Commission for Europe (Lorenz et al. 2002) with local inventories.  相似文献   
60.
刚果12号桉施肥效应研究   总被引:2,自引:1,他引:2  
在贫瘠低丘上对刚果12号桉进行不同肥料配合和不同用量的施肥试验,结果表明NPK,NK,NP和PK配合施用的能极显著地促进刚果12号桉的生长,5年生时蓄积比对照分别增加19.40,18.45,16.40,15.05m^3/hm^2,N,P,K肥单施的蓄积比对照纷别增加5.30,5.25,4.80m^3/hm^2肥料的配合施用极显著地优于N,P,K单施,材积的增长量随施肥量的增加而增加。  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号