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排序方式: 共有216条查询结果,搜索用时 15 毫秒
1.
XU Ruo-bing WEN Jian-ming ZHANG Meng LV Chang-hai XIAO Gang ZHANG Wen-min LIANG Hui-zhen 《园艺学报》2004,20(11):1982-1988
AIM: To study effects of urokinase-type plasminogen activator (uPA) signal transduction on expression of matrix metalloproteinase-2 (MMP-2) and tissue inhibitor of matrix metalloproteinase-3 (TIMP-3) in giant cell tumor of bone (GCT). METHODS: Expression of uPAR, MMP-2 and TIMP-3 in GCT tissue was detected by immunohistochemistry. Phosphorylation level of mitogen-activated protein kinase (p44) in uPA/uPAR signal pathway in cultured GCT cells was detected by immunoprecipitation. The expression of MMP-2 and TIMP-3 in cultured cells after treatment with uPA-ATF or anti-uPAR antibody was also detected by Western blotting. RESULTS: 1) Urokinase-type plasminogen activator receptor (uPAR) was positive on the cell membrane and in cytoplasm of some mononuclear stromal cells (MSCs) and multinucleated giant cells (MGCs); 2) MMP-2 was positive in the cytoplasm and on the cell membrane of almost all of MSCs and some of MGCs. The polar distribution of MMP-2 in the cytoplasm of MGCs was especially obvious; 3) The expression of TIMP-3 of some MSCs and MGCs in GCT was much lower than MMP-2. The positive signal also showed a prominent polarity; 4) After treatment with uPA-ATF, the phosphorylation level of p44 in GCT cultured cells was much higher than the control. Addition of anti-uPAR antibody in the cells remarkably down-regulated the phosphorylation level of p44 as compared with the control group, suggesting that uPA-ATF participates cell signal transduction and this reaction can be inhibited by anti-uPAR antibody; 5) uPA-ATF cell signal pathway up-regulated expression of MMP-2 and TIMP-3, while anti-uPAR antibody down-regulated the expression of MMP-2 and TIMP-3. CONCLUSION: These results demonstrate for the first time that uPA-ATF directly regulates the expression of MMP-2 and TIMP-3 by signal transduction pathway, and the over-expression of MMP-2 and TIMP-3 may play an important role in local osteolysis of GCT. 相似文献
2.
大熊猫放归计划框架与操作程序初探 总被引:3,自引:0,他引:3
本文依据IUCN/RSG关于物种放归的标准,借鉴麋鹿、普氏野马和扬子鳄等物种放归的成功经验,提出了大熊猫放归的基本内容和程序,即:足够的生物学和生态学的知识;适宜栖息地的选择;充足的释放动物种源;在实验的基础上,经过有效的工作小组的分析和综合,从潜在的栖息地的评估和选择,到小规模的释放试验性项目,长期监测,发展到正式放归项目实施。 相似文献
3.
野外放归大熊猫肠道菌群变化的研究 总被引:2,自引:0,他引:2
对四川卧龙中国保护大熊猫研究中心的一只野外放归亚成体大熊猫肠道菌群的组成和季节变化规律进行了研究,同时与其圈养双胞胎兄弟的肠道菌群进行了比较。从放归大熊猫粪便中分离出17种肠道菌,优势菌群为肠杆菌、肠球菌和乳杆菌。与圈养大熊猫相比,放归大熊猫肠道菌群中优势菌群的种类未发生改变,但是肠球菌数量增加,肠杆菌和乳杆菌的数量减少。研究发现放归大熊猫肠道菌群中的肠杆菌和肠球菌的数量随季节变化有较大波动,乳杆菌的数量随季节变化波动不大;而圈养大熊猫三种优势菌的数量随季节变化波动都不大。 相似文献
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根据Gen Bank中大鲵虹彩病毒主衣壳蛋白MCP(major capsid protein,MCP)基因序列(序列号:KF512820),设计一对特异性引物,以大鲵虹彩病毒贵州分离株基因组DNA为模板,PCR扩增大鲵虹彩病毒MCP基因并测序,与Gen Bank中大鲵虹彩病毒MCP基因进行比对,然后将其亚克隆到原核表达载体p ET-32a(+)中,转化大肠杆菌BL21(DE3)感受态细胞,经IPTG诱导后进行Western blot分析。结果显示:PCR扩增出长度为1 392 bp的片段,与Gen Bank中大鲵虹彩病毒MCP基因核苷酸序列相似性为99.7%~99.9%,SDSPAGE电泳显示该重组蛋白的相对分子质量约为67×103。免疫原性检测结果表明,该重组蛋白可与兔抗大鲵虹彩病毒阳性血清特异性反应,具有免疫原性。 相似文献
8.
Irena Pípalová 《Aquaculture International》2003,11(4):325-336
The aims of this experiment were (1) toquantify the ability of grass carp to processduckweed and (2) to assess indirect changes inwater chemistry and phytoplankton community,caused by grass carp feeding. Yearling grass carp sized 126 ± 7.7 mm (TL) and19.6 g in weight were kept in 9 laminate tanksof 1 m3 for 14 days. Two stockingdensities (2 and 6 fish per m3) anda control without fish were used. Standard growthrate (SGR) of grass carp fed exclusively onduckweed was 0.70% body weight (BW) d–1and food conversion ratio (FCR) reached 2.0(average water temperature =21.1 ± 3.8 °C). Daily food intakewas 0.2 g of duckweed dry weight (DW), i.e.,1% of average BW of grass carp. SGR ofduckweed growing in 20 × 20 cm floatingenclosures, differed significantly[F(6,2) = 417.9; p = 0.002] between the twostocking densities of grass carp and thecontrol tanks (without fish). Mean SGR ofduckweed was 0.02 g g–1 day–1 and thehighest SGR was recorded in the control tanks.Both decrease in NH4-N and increase inNO2-N concentrations differedsignificantly between the treatments[F(2,2) = 45.3; p = 0.02 and F(2,2) = 19.2; p = 0.04 respectively]. Changes in other nitrogenand phosphorus components (NO3-N, TN, TPand PO4-P) caused by stocking of grasscarp were not significant. Biomass ofphytoplankton, dominated by filamentous algaeand blue-greens, increased proportionately tostocking density of grass carp. Althoughduckweed has a large potential for nutrientremoval, the most common pathway for thenutrients released through grass carp grazingif duckweed cover is loose is theirincorporation into phytoplankton biomass. 相似文献
9.
大鲵虹彩病毒理化及生物学特性研究 总被引:7,自引:1,他引:7
对大鲵虹彩病毒(Giant salamander iridovirus,GSIV)的理化特性及生物学特性进行了研究。结果表明:GSIV对热处理敏感,56℃和65℃处理30 min均可彻底灭活病毒;GSIV经酸(pH3)和碱(pH10)处理,病毒滴度(TCID50)与对照组相比较分别下降了8.58、9.04个对数级,差异极显著(P<0.01);GSIV经有机溶剂氯仿、乙醚以及胰蛋白酶处理,TCID50与对照组相比较分别下降了9.33、7.83、6.49个对数级,差异极显著(P<0.01)。冻融次数对GSIV滴度的影响不显著(P>0.05)。GSIV对细胞培养物的感染性试验结果表明,GSIV可在鲤上皮瘤细胞系(Epithelioma papilloma cyprini,EPC)、斑点叉尾鮰肾脏细胞系(Channel catfish kidney,CCK)、虹鳟鱼性腺细胞系(Rainbow trout gonadal,RTG-2)等细胞中增殖,但在EPC、CCK细胞中增殖速度快,TCID50高;GSIV在EPC细胞中的最适生长温度是25℃。GSIV在EPC细胞中增殖动态试验结果表明,GSIV感染细胞6 h后TCID50开始快速上升,进入对数增长期,72 h时TCID50达到最大值,以后趋于稳定。GSIV感染EPC细胞超薄切片透射电镜观察结果显示,在EPC细胞质中可见大量虹彩病毒样颗粒,呈晶格状排列,直径约140 nm。 相似文献
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