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41.
Vaccine approaches against AIDS have focused on inducing cellular immune responses, since many studies revealed the role of T cell responses in the control of human immunodeficiency virus or simian immunodeficiency virus (SIV) infections. The experimental infection of rhesus macaques with SIV or chimeric SHIV is routinely used as a model for AIDS. In such models, DNA immunization is a tool to elicit specific T cell responses and to study their protective efficacy. DNA immunogenicity in primates depends on parameters such as level of antigen expression, choice of the antigen among SIV proteins, use of fusion proteins, route of immunization, and addition of adjuvants. Recent results suggest that priming with DNA and boosting with attenuated recombinant viral vectors, each expressing corresponding SIV antigens, leads to improved specific immunity and, in some cases, affords protection against pathogenic challenge. After preclinical evaluations, DNA has entered clinical trials for a therapeutic or prophylactic gene-based AIDS vaccine.  相似文献   
42.
The studies reviewed here evaluated the role cellular immune system components play in control of brucellosis by conducting comparative studies with brucella-resistant C57BL/10 or C57BL/6 mice and susceptible BALB/c mice. We have shown by both in vitro and in vivo studies that activation of macrophages with interferon-gamma (IFN-γ) is an important factor for control of infection with B. abortus in the mouse model and that the mechanism of anti-brucella activity largely involved reactive oxygen intermediates. Differences in control of the organism by resistant and susceptible mice was not related to inherent differences in the ability of their macrophages to control infection either with or without IFN-γ activation nor was it attributable to NK cells since we found no role for them in control of brucellosis in either mouse strain. However, relative resistance to brucellosis did correlate with increased production of IFN-γ by CD4 T cells during the first weeks after infection while IL-10 contributed to susceptibility in BALB/c mice. Moreover, by 3 weeks post-infection splenocytes from the susceptible BALB/c mice failed to produce IFN-γ and relied on TNF- as well as CD8 T cells to control infection until the end of the plateau phase around 6 weeks post-infection when IFN-γ production resumed and clearance began. In contrast, IFN-γ was crucial for control throughout the infection in the more resistant C57BL/6 mice and the mice died in its absence by 6 weeks post-infection compared to 12 weeks for the more susceptible mice that relied on additional mechanisms of control. In contrast to the IFN-γ knock-out mice, both β2 microglobulin knock-out C57BL/6 mice, which do not express conventional MHC class I molecules and thus cannot present antigen to CD8 T cells, or perforin knock-out C57BL/6 mice, which have no T cell cytotoxic activity, controlled and cleared the infection as well as normal C57BL/6 mice. The hiatus of IFN-γ production in BALB/c mice correlated with very high levels of total IL-12 and it was postulated that the lack of IFN-γ was a consequence of p40 homodimer blocking activity. However, reduction of p40 IL-12 in vivo through administration of indomethacin reduced the infection without a concomitant measurable increase in IFN-γ. Current studies are aimed at elucidating the mechanism of the IFN-γ hiatus.  相似文献   
43.
Common bunt of wheat, caused by Tilletia laevis and T. tritici, is a major seed and soil-borne disease in West Asia and North Africa. The use of resistant cultivars and chemical seed-treatments are the current control measures used to combat this disease. The aim of this study was to investigate alternative control measures to chemical seed-treatments that are environmentally friendly to support cultivar resistance. Several organic nutrients [skimmed milk powder, hucket (local skimmed milk) and wheat flour] at a concentration of 160g per kg of seeds were used as seed-treatments on two susceptible bread and durum wheat cultivars (Bau and Sebou, respectively) to examine their effectiveness in controlling the disease. Field trials over four years showed that skimmed milk powder, hucket, and wheat flour reduced common bunt infection levels by 96%, 93% and 62%, respectively. In most cases, the effectiveness of the skimmed milk powder and hucket was equal to the chemical seed-treatment; thus, these organic nutrients offer an effective and environmentally safe alternative to chemical treatments. However, a study of their economic value as well as of their effect on seed germination, and field emergence is needed.  相似文献   
44.
采用T4噬菌体表面展示系统,将CCK-33肽四多串联体及八多串联体展示在T4噬菌体表面,并研究其免疫原性。将CCK四串联体和八串联体与SOC基因缺失的、依赖溶菌酶的噬菌体ФT4-Z1重组,获得重组噬菌体CT-4CCK和西T-8CCK。SDS-PAGE和Western Blot检测结果表明,CCK多串联体蛋白已经成功展示在T4噬菌体表面,其融合蛋白分子量约30ku和41ku,能够与CCK标准阳性血清发生特异性反应。以重组噬菌体为免疫原制备油佐剂疫苗主动免疫胡须肉鸡后,抗体浓度显著升高,肉鸡的体重、采食量都有所提高,而料肉比有所下降。结果说明,鸡CCK蛋白展示在T4噬菌体表面具有良好的免疫原性。  相似文献   
45.
应用组织匀浆涂片和酸性α-醋酸萘酯酶(ANAE)染色及细胞培养技术和四甲基偶氮唑盐(MTT)测定法对毒害艾美耳球虫(eimeria necatrix,E.necatrix)初次感染雏鸡免疫器官的T细胞比例、白细胞介素-2(interleukin-2,IL-2)诱生活性、T细胞和B细胞对ConA或PMA的增殖功能的动态变化进行了较全面系统的研究。结果发现,E.necatrix初次感染雏鸡,其胸腺和脾脏T细胞比例分别于感染后7~21d和7~24d明显高于对照雏鸡;IL-2诱生活性分别于感染后16~18d和18~21d较对照雏鸡显著升高;T细胞对ConA的增殖反应分别在感染后14~16d和10~18d明显增加。法氏囊和脾脏B细胞对PMA的增殖反应分别于感染后14~24d和14~21d显著高于对照雏鸡。表明E.necatrix初次感染雏鸡免疫器官的IL-2调节及细胞免疫和体液免疫功能均明显提高。  相似文献   
46.
从豫西山区野生针叶松树皮中提取生物活性物质,研究其对肉仔鸡免疫功能的影响。选取180只1日龄Avian肉仔鸡随机分为4组,每组3个重复,每个重复15只。A组为对照组,饲喂基础日粮,B、C、D组分别添加500、1000、4000mg/kg松科植物提取物。在21、49日龄时分别测定免疫器官重量,49日龄时测定淋巴细胞转化率及平均日增重。结果表明,日粮中添加松科植物提取物,可以显著提高免疫器官重量和淋巴细胞转化率(P<0.05)。  相似文献   
47.
为了探讨啤酒酵母葡聚糖在断奶仔猪日粮中的适宜添加剂量及其对断奶仔猪细胞免疫功能的影响,本研究进行了2个试验。试验1选用100头(28±2)d断奶的二元杂交断奶仔猪,按单因子试验设计随机分为5个处理,分别饲喂含葡聚糖0、25、50、100mg/kg和200mg/kg的日粮。结果表明:随葡聚糖添加剂量的增加,平均日增重在14 ̄28 d及0 ̄28 d呈二次曲线变化(P<0.05)。试验2选用80头(28±2)d断奶的二元杂交断奶仔猪,随机分为2个处理,分别饲喂含葡聚糖0mg/kg和50mg/kg的日粮。在试验的第14天和第28天,每重复取1头仔猪前腔静脉采血,测定外周血淋巴细胞转化率。结果显示,在断奶仔猪日粮中添加50mg/kg葡聚糖提高了仔猪在14 ̄28d及0 ̄28d的日增重(P<0.05)。而且,也提高了仔猪在0 ̄14 d、0 ̄28 d及28 ̄35 d的平均日采食量(P<0.05)。但是对淋巴细胞转化率没有影响。结果表明:在断奶仔猪日粮中添加50mg/kg啤酒酵母葡聚糖,可以提高断奶仔猪的生产性能,而且没有性别差异。  相似文献   
48.
精子受精抗原-1(FA-1) mRNA在绵羊睾丸和附睾中的表达   总被引:1,自引:0,他引:1  
本研究通过RT-PCR检测了该基因在绵羊睾丸和附睾中的表达情况。首先,提取绵羊睾丸组织、附睾头、体、尾部组织总RNA,以此为模板,反转录合成cDNA,自行设计引物,PCR扩增出462 bp的目的DNA。然后,将目的片断克隆入T载体,通过菌液PCR和重组质粒酶切,鉴定重组质粒中的目的DNA。再经序列分析鉴定目的片断。同时,以β-actin为内参照物,进行RT-PCR半定量分析,比较精子受精抗原(FA-1)在睾丸、附睾头、体、尾组织中的表达量。结果表明,FA-1在绵羊睾丸和附睾中均表达。  相似文献   
49.
为建立奶牛附红细胞体和伊氏锥虫两种病原诊断方法并探索二者之间在奶牛感染中的关系,本研究针对两病原分别设计两对特异性引物,建立了奶牛附红细胞体和伊氏锥虫感染的二重PCR诊断方法,其扩增片段大小分别为415bp和237bp。敏感性试验和特异性试验表明,附红细胞体和伊氏锥虫的DNA的最低检测量为0.154pg和0.105pg;与猪肺炎支原体、大肠杆菌、葡萄球菌、鸡艾美耳球虫、牛双芽巴贝斯虫无交叉反应。35份临床血样检测结果为:奶牛附红细胞体阳性率22.89%,伊氏锥虫阳性率8.89%,其中共感染率为2.89%。临床试验表明,该方法可用于奶牛附红细胞体和伊氏锥虫的诊断,特别适用于早期诊断。  相似文献   
50.
AIM:To investigate the effect of protein kinase C on resistin expression in 3T3-L1 adipocytes.METHODS:The differentiated 3T3-L1 adipocytes were incubated with 50 nmol/L phorbol 12-myristate 13-acetate (PMA) or 5 μmol/L Ro-31-8220 for 24 h.Expression of resistin mRNA was detected by RT-PCR and expression of resistin protein was detected by Western blotting.RESULTS:Compared with control,PMA increased the expression of resistin mRNA and protein in 3T3-L1 adipocytes significantly (P<0.01),while Ro-31-8220 decreased the expression of resistin mRNA and protein in 3T3-L1 adipocytes obviously (P<0.01).CONCLUSION:Protein kinase C signal pathway may regulate resistin expression in 3T3-L1 adipocytes.  相似文献   
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