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AIM To investigate the effects of cytochrome P450 (CYP450) epoxygenase/epoxyeicosatrienoic acid (EET) pathway on insulin resistance in obese mice, and to explore the possible mechanisms. METHODS High-fat diet-induced obesity model was established in C57BL/6Cnc mice, and the obese mice were randomly divided into 3 groups, including obesity group (treated with saline; n=10), EET group (treated with 11,12-EET; n=10) and EET inhibitor 14,15-epoxyeicosa-5(Z)-enoic acid (EEZE) group (n=10). Normal C57BL/6Cnc mice (n=10) treated with saline served as control. Protein expression of CYP2J2 (one of CYP450 epoxygenases) and hypoxia-inducible factor-1α (HIF-1α) was measured by Western blot. Vessel-like structure was detected by immunofluorescence staining. The serum levels of insulin, tumor necrosis factor-α (TNF-α), interleukin (IL)-1β, IL-6 and monocyte chemoattractant protein-1 (MCP-1) were measured by ELISA. RESULTS In obese mice, homeostasis model assessment of insulin resistance (HOMA-IR) values were increased, the protein level of CYP2J2 was reduced, and the protein level of HIF-1α was increased in adipose tissues as compared with the controls (P<0.05). The serum levels of MCP-1, IL-1β, IL-6 and TNF-α were also significantly increased in obese mice (P<0.05). After treatment with 11, 12-EET, the HOMA-IR values were decreased compared with vehicle-treated obese mice, HIF-1α expression levels were decreased in the adipose tissue, and the serum levels of MCP-1, IL-1β, IL-6 and TNF-α were reduced (P<0.05). Immunohistochemical results of adipose tissue from vehicle-treated obese mice showed a marked decrease in vessel-like structures (CD31-positive) compared with normal control mice (P<0.05). EET treatment significantly increased the newly formed vessel-like structures in the visceral adipose tissues of obese mice as compared with vehicle-treated obese mice (P<0.05). CONCLUSION High-fat diet-induced obesity and insulin resistance are closely related to the CYP450 pathway. Exogenous EETs effectively decrease obesity-induced insulin resistance possibly through pro-angiogenesis and attenuation of hypoxia and inflammation.  相似文献   
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洱源丛枝瑚杀虫活性成分研究   总被引:1,自引:0,他引:1  
洱源丛枝瑚(Ramaria eryuanensis)石油醚萃取物经过柱层析得到单体化合物B8,该化合物对小菜蛾3龄幼虫72 h的LC50为3.375 7 mg/mL。经FAB-MS、1HNMR、13CNMR及DEPT等波谱鉴定,并与文献值对照,确定其为麦角甾-7,22-二烯-3β,5α,6β-三醇。  相似文献   
4.
为探究马传染性贫血病毒(EIAV)附属蛋白Rev负调控Tripartite motif-containing protein 5α(TRIM5α)介导的AP-1信号通路的机制,本研究将pEIAV-Rev-HA和pcDNA3.1质粒分别与含TRIM5α基因的质粒及pGL3-AP-1-Luc(AP-1报告质粒)共转染HEK 293T细胞,采用荧光素酶试验检测Rev对TRIM5α激活的AP-1信号通路的影响;将pEIAV-Rev-HA和pcDNA3.1质粒分别与含TAK1、TAB2、P38和c-Jun基因的质粒及pGL3-AP-1-Luc共转染HEK 293T细胞,采用荧光素酶试验检测Rev对TRIM5α下游转导分子(TAK1、TAB2、P38、c-Jun)激活的AP-1信号通路的影响;将pEIAV-Rev-HA和pcDNA3.1质粒分别与含TAK1、TAB2、P38基因的质粒共转染HEK293T细胞,利用western blot试验分别检测TAK1、TAB2、P38的表达水平;将pEIAV-Rev-HA和pcDNA3.1质粒分别与含P38基因的质粒共转染HEK 293T细胞后加入蛋白酶体抑制剂MG132,利用western blot检测P38蛋白的表达情况。结果显示,共转染EIAV-Rev-HA实验组中TRIM5α对AP-1的激活倍数为0.4,而共转染pcDNA3.1对照组中相应的激活倍数为26.0;共转染pEIAV-Rev-HA实验组中,TAK1、TAB2、P38和c-Jun对AP-1信号通路的激活倍数分别为7.7、0.1、0.6、9.8,而共转染pcDNA3.1对照组中对AP-1信号通路的激活倍数分别为60.0、1.5、6.3、12.0;转染pEIAV-Rev-HA+pP38-Flag组与转染pcDNA3.1+pP38-Flag组相比,前者P38蛋白的表达量显著降低;加入蛋白酶体抑制剂组则恢复了P38蛋白的表达。上述结果表明,EIAV Rev显著下调eqTRIM5α及其下游转导分子TAK1、TAB2、P38激活的AP-1信号通路,但不显著下调c-Jun激活的AP-1信号通路;EIAV Rev通过蛋白酶体途径降解P38蛋白的表达而抑制eqTRIM5α激活的AP-1信号通路。本研究结果为理解EIAV与宿主蛋白相互作用提供参考依据。  相似文献   
5.
α-溶血素在金黄葡萄球菌的致病过程中发挥着不可或缺的作用。本研究采用最小抑茵浓度测定、茵液上清溶血活性以及α-溶血素含量测定、荧光定量PCR及细胞毒性的测定等相关试验验证了橙皮素对金黄葡萄球菌α-溶血素表达的影响。结果显示,无抗茵活性的橙皮素在较低质量浓度下即可抑制金黄葡萄球菌α-溶血素的表达及其编码基因的转录,是-种潜在的以毒力因子为靶标的前导化合物,并可进一步开发用于抗金黄葡萄球茵感染。  相似文献   
6.
为研究鸡α-干扰素对罗曼雏鸡免疫功能的影响,将60羽健康1日龄罗曼雏鸡随机分为2组,即对照组、试验组。试验组鸡于1日龄胸肌注射鸡-α干扰素,0.5 mL/羽;对照组鸡同期每羽注射生理盐水0.5 mL。试验开始后,于第4 d、8 d、12 d、16 d、20 d对鸡进行翅下静脉采血,并于20日龄剖杀摘取免疫器官。研究表明,鸡注射α-干扰素后,其外周血液ANAE+T淋巴细胞百分率和鸡脾相对湿重显著高于对照组,鸡α-干扰素在一定范围内可提高雏鸡免疫功能。  相似文献   
7.
运用矩阵分析方法,讨论了非奇异H-矩阵的判定问题,得到两个非奇异H-矩阵新的判定准则,并以数值例子说明判定方法的有效性.  相似文献   
8.
本研究旨在探讨牦牛不同部位皮肤内血管和神经的分布情况,及检测低氧诱导因子-1α(HIF-1α)在不同部位皮肤上的定位及相对表达量,探究牦牛皮肤对高原低氧环境的适应机制。采用HE、Masson’s三色和Verhoeff VG染色法,对成年牦牛皮肤内血管和神经结构进行观察与分析;采用免疫组织化学、实时荧光定量PCR和蛋白免疫印迹法,对HIF-1α的mRNA和蛋白在成年牦牛皮肤组织中表达与分布进行研究。结果表明,颈部血管与神经密度最高,前臂部和小腿部次之,跖部最低,部位间差异显著(P<0.05)。HIF-1α主要表达在表皮层、毛囊的上皮根鞘、皮脂腺、汗腺、血管、神经;颈部、前臂部和小腿部强阳性表达,跖部阳性表达。HIF-1α mRNA的相对表达量跖部明显低于其他部位(P<0.05),其他三个部位两两比较差异不显著(P>0.05)。HIF-1α蛋白相对表达量颈部最高,跖部最低,差异显著(P<0.05)。研究结果提示,成年牦牛不同部位皮肤内不同血管和神经形态结构相似,密度从颈部到前肢再到后肢差异显著。HIF-1α的差异性表达进一步说明皮肤在牦牛适应低氧环境中发挥作用。  相似文献   
9.
One of the most important processes determining the proper course of gestation and its physiological termination in cows is the adhesion of epithelial cells allowing for direct contact of maternal and foetal parts of the placenta. Throughout pregnancy, placental cells are under strict hormonal control, which among others regulates the concentration and activity of specific proteins participating in the extracellular matrix remodelling of foetal membranes. The aim of the study was to evaluate the influence of progesterone and prostaglandin F on the adhesion of epithelial cells at early-mid pregnancy in cows. Additionally, the impact of selected hormones on anti-adhesive properties of decorin was evaluated. Caruncular epithelial cells were isolated from healthy cows during pregnancy, immediately after slaughter. Primary cell cultures derived from the 2nd and 4th month of gestation were used in the experiments. The viability of cells was assessed by MTT assay. The adhesion of cells to fibronectin was measured spectrophotometrically. The activity of metalloproteinases was confirmed by the metalloproteinase assay. Progesterone (10–5 and 10–7 mol/L) and prostaglandin F (10–4, 10–5 and 10–7 mol/L) increased the viability of bovine caruncular epithelial cells in the 2nd month of pregnancy. The treatment with prostaglandin F significantly reduced the number of adherent cells from the 2nd month of gestation at the doses of 10–4 and 10–5 mol/L. Both progesterone and prostaglandin F were shown to have an effect of decorin resulting in both a decrease in metalloproteinase activity and an increase in adhesion of cells to fibronectin.  相似文献   
10.
紫外辐照对产α-ALDC枯草芽孢杆菌的诱变效应   总被引:1,自引:0,他引:1  
采用紫外诱变(波长260nm,功率15w)对一株产α-乙酰乳酸脱羧酶的枯草芽孢杆菌(Bacillus subtilis)BS059菌株进行诱变处理。结果表明,在紫外辐照时间为50s时,诱变效果较好。从正突变菌株中反复筛选,得到两株产酶量较高的菌株BS059-15和BS059-22,比原出发菌株的酶活分别提高了107.62%和162.25%。经过连续传代试验,证明其遗传性状稳定,为可遗传变异。  相似文献   
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