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AIM: To investigate the balance of Treg/Th17 in synovium of collagen-induced arthritis (CIA) and the impact of tumor necrosis factor α(TNF-α) blockage therapy. METHODS: Rat CIA model was established by bovine II collagen injection. The pathological score was evaluated by HE staining and toluidine blue staining. The TNF-α level in plasma was measured by ELISA. The expression of Treg/Th17 in synovium was detected by double staining immunofluorescence. RESULTS: The plasma level of TNF-α in CIA group was significantly higher than that in control group and TNFR-Fc treatment group (P<0.01), whereas no significant difference was found between TNFR-Fc treatment group and control group (P>0.05). No significant difference between CIA group and control group in the ratio of CD4+Foxp3+Treg cells/CD4+ cells in synovium (23.12%±4.93% vs 24.66%±5.82%, P>0.05) was observed, whereas the ratio in TNFR-Fc treatment group was significantly increased(33.07%±5.14%). The ratio of CD4+RORγt+Th17 cells/CD4+ cells in CIA group was significantly higher than that in control group and TNFR-Fc treatment group (9.74%±2.23% vs 1.00%±0.59%, 5.63%±1.76%, P<0.01). CONCLUSION: Differentiation disturbance of Treg/Th17 exists in the synovium of CIA rats. TNFR-Fc may restore the balance of Treg/Th17 by inhibiting Th17 cell differentiation and inducing the production or accumulation of Treg. 相似文献
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粘附素蛋白是金黄色葡萄球菌感染早期最重要的致病因子,研究根据金黄色葡萄球菌聚集因子A(c1fa A)基因,设计合成特异性引物,以国内奶牛乳腺炎临床分离株金黄色葡萄球菌基因组为PCR模板,进行c1fa A基因的克隆,并连接入pMD18-T载体进行测序和序列分析,然后经BamH I和Xba I双酶切后构建真核表达载体并进行鉴定。结果表明,以金黄色葡萄球菌标准株为对照,国内分离株多数在990bp处扩增到特异性条带,经测序鉴定,与Genebank发表的金黄色葡萄球菌c1fa A序列同源性为99%;构建的真核表达质粒通过PCR和双酶切鉴定证明构建成功,为研究核酸疫苗奠定基础。 相似文献
34.
AIM: To investigate the role of miR-181b in the expression of Bcl-2 and SP1 at mRNA and protein levels in the human hepatoma G2 cells (HepG2), and to explore the effect of miR-181b on the regulation of HepG2 cell proliferation. METHODS: The synthetic double-strand complementary DNA based on the sequence of miR-181b was inserted into the vector of miRNASelectTM pEGP-miR. The microRNA high-expression plasmid was cloned, and the sequences were identified. The miR-181b plasmid was transfected into HepG2 cells with liposomes. The stable cell line was screened by puromycin. The mRNA and protein levels of Bcl-2 and SP1 were measured by RT-PCR and Western blotting, respectively. Methyl thiazolyl tetrazolium (MTT) method was used to analyze the proliferation of HepG2 cells. RESULTS: The Western blotting results showed that miR-181b inhibited the protein expression of Bcl-2 and SP1. The result of RT-PCR also indicated that the mRNA expression of Bcl-2 and SP1 was suppressed. Compared with the control, the growth rate of HepG2 with high expression of miR-181b was significantly decreased.CONCLUSION: miR-181b inhibits the proliferation of HepG2, which may be related to the down-regulation of Bcl-2 and SP1. 相似文献
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赵洁 《农业图书情报学刊》2019,31(9):69-74
目的 通过对中国30种科技期刊中外引文的数量及其各种分布情况的调查,揭示引文数量和质量与不同学术水平期刊之间的对应关系以及对中国科技期刊的评价效用。方法 采用统计分析方法,对不同学术水平期刊中外引文的数量和质量指标进行比较和分析。结果 学术期刊的引文数量和质量均高于普通期刊,而普通期刊由于中文引文比例大,对中国科技期刊学术评价的贡献度大于学术期刊,但学术评价效用不高。结论 引文作为论文的重要组成部分和学术质量的保证,应该纳入中国科技期刊综合评价指标体系中的独立指标,中国科学引文数据库来源期刊应进行适当调整,注重质量,可吸收一些相关的国际期刊。 相似文献
36.
AIM: To investigate the effect of shikonin on reversing hepatocyte growth factor(HGF)-induced resistance to gefitinib in lung cancer HCC827 cells, and to explore its possible mechanisms.METHODS: The gefitinib-resistant HCC827 cells induced by HGF were treated with shikonin and gefitinibthe alone or in combination. The inhibition rates of cell viability were determined by MTT assay. The invasive ability of HCC827 cells with HGF-induced resistance to gefitinib was determined by Transwell assay. The protein levels of epithelial-mesenchymal transition (EMT) and related signaling pathway in the HCC827 cells were detected by Western blot.RESULTS: The results of MTT assay showed that the cell activity of HCC827 cells was significantly inhibited by shikonin in a dose dependent manner. The IC50 of shikonin in HCC827 cells was 3.06 μmol/L. And the IC50 of gefitinib in HCC827 cells was 0.51 μmol/L. Under the condition of combined treatment with shikonin and gefitinib in the presence of HGF (20 μg/L), the IC50 of gefitinib was 7.36 μmol/L, significantly lower than that treated with gefitinib alone (P<0.01), so did the result of the cell migration (P<0.01). HGF induced EMT, while shikonin reversed this effect. The protein expression level of p-AKT was significantly up-regulated by HGF, while markedly down-regulated treatment with shikonin and gefitinib compared with gefitinib alone (P<0.01).CONCLUSION: Shikonin reverses HGF-induced resistance to gefitinib in lung cancer HCC827 cells, and the mechanism may be likely related to the preventon of EMT and the inhibition of HGF-induced activation of p-AKT signaling pathway. 相似文献
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本试验旨在研究金雀异黄素(genistein,GEN)对雌性大鼠体内促性腺激素及胰岛素样生长因子表达的影响。选取40只SD雌性大鼠[体重(200±20)g],随机分为5组,分别为阴性对照(NC)组、GEN低(L)、中(M)、高剂量(H)组及阳性对照(PC)组,每组8只,NC组灌胃花生油(其他组灌胃试剂以此为溶剂);L、M、H组分别灌胃15、30、60 mg/(kg BW·d)GEN,PC组灌胃己烯雌酚0.5 mg/(kg BW·d)。试验期30 d。采用酶联免疫吸附试验(ELISA)法检测血清中卵泡刺激素(FSH)、黄体生成素(LH)、胰岛素样生长因子-1(IGF-1)、胰岛素样生长因子结合蛋白-1(IGFBP-1)含量;实时定量PCR法检测卵巢IGF-1、IGFBP-1 mRNA表达水平。结果表明:与NC组比较,试验组血清中FSH、LH含量有升高趋势,但差异不显著(P0.05),作用效果与PC组一致;试验组血清IGF-1含量略有降低,但差异不显著(P0.05),PC组显著降低(P0.05);试验组血清IGFBP-1含量显著或极显著升高(P0.05或P0.01),PC组显著升高(P0.05);试验组卵巢组织中IGF-1、IGFBP-1 mRNA表达水平均升高,其中M、H组显著升高(P0.05),与PC组变化一致。由此可见,GEN能够提高雌性大鼠血清FSH、LH含量、降低血清IGF-1含量、提高血清IGFBP-1含量,同时提高卵巢中IG FBP-1、IG F-1 mRNA的表达水平,这些指标协同作用于卵巢,能够促进卵泡的成熟,调节卵巢功能。 相似文献
39.
陡削以兰州新区的一段陡峭边坡作为试验地点,通过分析在植被重建初期经人工整地后形成的4种微地形(大圆形坑、小圆形坑、条形坑和原状坡面)的植被盖度特征及环境因子(土壤硬度和水分、地表和空气温度、坡位、无纺布)对植被盖度的影响,探寻能有效提高植被盖度的几种工程改造措施。研究表明:①铺设了无纺布坡面的植被盖度显著大于对照坡面;陡峭边坡不同坡位的植被盖度:下坡位>中坡位>上坡位(P<0.05),这与自然坡面植被盖度分布规律一致。②3种微地形的植被盖度均显著大于陡峭坡面,其中条形坑的土壤水分和植被盖度最大,最大盖度维持的时间最长。③微地形和坡面的植被盖度均与土壤水分呈显著正相关,与空气温度、地表温度均呈显著负相关;微地形的土壤硬度(3kg·cm^-2)适宜植物生长,大于该值会对植被生长产生抑制作用;铺设无纺布有利于促进上坡位的植被生长,使坡面植被分布更均匀。研究结果表明,在陡峭边坡坡度、坡位和温度等无法改变的情况下,选择对压实的坡面进行整地翻耕处理,增加长条坑的数量并铺设无纺布等有效的工程改造措施,能显著增加植被盖度,促进植被恢复。 相似文献
40.