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23个欧美杨无性系苗期叶锈病抗性测定 总被引:2,自引:0,他引:2
以引进23个欧美杨无性系为研究对象,通过对苗木叶锈病感病指数的调查,借助SPSS统计软件对调查数据进行统计分析,结果表明:对叶锈病的抗性表现超过对照品种I108的有19个,其中02-36-1、02-36-4、N177、N197和N195这5个无性系对叶锈病完全免疫;无性系02-34-334对叶锈病表现为高度抗病;02-01-119、324、03-04-111、03-04-97和02-34-278表现为抗病;03-04-141、03-04-170、02-34-347和03-05-184表现为感病;02-01-219、03-04-167、03-04-288和02-34-228表现为高感;对叶锈病的抗性表现不及对照品种I108的有3个,即03-05-206、03-04-171和03-05-156,均表现为高感。 相似文献
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通过对高原植物香芸火绒草超临界CO2萃取的研究,获得了温度45℃、压力18MPa为其相对较佳提取条件,提取产物为黄绿色浸膏,得率为0.87%。将该浸膏精制成净油,其得率为60.2%。进一步通过气相色谱-质谱联用技术(GC—MS)对净油分析,鉴定出其中的15种化学成分,并通过峰面积归一法确定了它们的相对含量。挥发油成分主要为:邻苯二甲酸异辛酯、高良姜素黄烷酮、α-甜没药萜醇、橙花叔醇、胡萝卜醇、棕榈酸等。通过对香芸火绒草挥发油成分的研究,为高原特有植物资源的进一步开发利用提供了试验依据。 相似文献
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AIM: To investigate the effect of estrogen antagonists on the in vitro growth of human prolactinomas. METHODS: RT-PCR was applied to the detection of estrogen receptor (ER) mRNA expressed in a human prolactinomas CH3 cell strain. Estradiol and 4-hydroxytamoxifen (OHTam) were added respectively at different concentrations into the culture medium. Cell number and levels of ER mRNA were examined. RESULTS: The growth of CH3 cells became slower in estrogen-deprived medium than that in nomal culture and was higher in medium containing estrogen(E2) at concentration of 10-8 mol/L than at concentration of 10-6 mol/L. OHTam (10-6mol/L) inhibited the growth of CH3 cell strain treated with E2. The expression of ER mRNA in CH3 cells was observed, the levels of ER mRNA in the E2 (10-8mol/L) group, higher than those in estrogen deprived group. OHTam (10-6mol/L) obviously inhibited the expression of ER mRNA. CONCLUSION: The growth of CH3 cells depends on estrogen, estrogen antagonists inhibits the growth of CH3 cells and decline the levels of ER mRNA. ER levels in human prolactinomas cell lines can be auto-regulated. 相似文献
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LUO Yuan-liang LI Meng-si TENG Jia-shuo DAI Xiao-meng TANG Xiang-xu XING Yun Lü Xiu-xiu 《园艺学报》2000,36(9):1543-1550
AIM To observe the effect of adriamycin/doxorubicin (DOX) on the production of inflammatory cytokines and collagen in cardiac fibroblasts and its mechanism. METHODS Neonatal SD rat cardiac fibroblasts were isolated, cultured, and identified by immunofluorescence staining with monoclonal antibodies against vimentin observed under a confocal laser-scanning microscope. The Cell Counting Kit-8 assay was used to detect the toxicity of DOX on cardiac fibroblasts, and flow cytometry with annexin V-FITC/PI double staining was used to detect apoptosis. ELISA was used to detect the release of inflammatory factors in the supernatant of cultured cells. Immunofluorescence labeling assay was used to detected α-smooth muscle actin (α-SMA) expression and mitochondrial reactive oxygen species (mROS) in the cells. Western blot was used to detect the expression of nucleotide-binding oligomerization domain-like receptor protein 3 (NLRP3) inflammasome-related proteins in cardiac fibroblasts. RESULTS (1) Compared with the control group, DOX inhibited the proliferation of cardiac fibroblasts (P <0.05), but had no significant effect on apoptosis (P >0.05). (2) Treatment with DOX promotes the release of proinflammatory factors interleukin-1β (IL-1β) and IL-6 in cardiac fibroblasts (P <0.05). (3) The expression of α-SMA, collagen type I and transforming growth factor-β in DOX treatment group increased significantly compared with control group (P <0.05). (4) Compared with the control group, the levels of mROS, cellular NLRP3 and cleaved caspase-1 in cardiac fibroblasts increased significantly after DOX treatment. CONCLUSION Doxorubicin promotes cardiac fibroblasts to secrete IL-1β and collagen type I by promoting mROS production and activating NLRP3 inflammasome. 相似文献
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