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一个山羊Ⅰ型毛角蛋白基因的序列及其在皮肤中的表达 总被引:7,自引:0,他引:7
角蛋白家族包含表皮软角蛋白和毛发硬角蛋白,可以分为酸性Ⅰ型和碱性或中性的Ⅱ型角蛋白亚家族。从构建的成年山羊皮肤cDNA文库和ESTs分析中发现了和与绵羊羊毛角蛋白8C1和人Ⅰ型毛发角蛋白相应cDNA序列高度同源的序列,经序列分析证明是一个山羊毛发特异性角蛋白,命名为山羊Ⅰ型毛角蛋白1(gHa1),Gen Bank序列号为AY510110.1。推导的读码框ORF由413氨基酸组成,与绵羊8C1角蛋白的序列一致性为97.8%。原位杂交显示它在皮肤初级和次级毛囊的皮质层有强烈的表达。 相似文献
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为更好地了解青藏高原高寒草甸区暖季放牧条件下人工草地牧草的生长特点,为制定合理放牧制度提供依据,于2001~2003年开展了暖季放牧牦牛对多年生人工草地影响的试验。结果表明:放牧2年后轮牧人工草地播种牧草比例为95.27%,连续放牧人工草地为86.15%,无放牧人工草地为58.01%。轮牧人工草地牧草月风干重最高值3 198.8 kg/hm2,连续放牧人工草地为3 023.2 kg/hm2。放牧可以提高人工草地牧草生长率,轮牧人工草地的牧草生长率高于连续放牧人工草地。放牧还影响着第2年播种牧草的生长,轮牧能促进种子出苗数,播种牧草的鲜重,风干重和种子产量分别达到了5 088.88 kg/hm2,3 053.33 kg/hm2和480 kg/hm2,均高于连续放牧人工草地和无放牧草地,轮牧人工草地杂草鲜草产量最低,为193.33 kg/hm2。适宜的放牧是保持人工草地可持续利用的手段之一。 相似文献
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AIM:To study the differentiation of embryonic stem cells (ESC) at the subretinal space of C3B mouse whose retina are of normal structure. METHODS:Embryonic bodies (EB) were gained when embryonic stem cells were propagated 1 generation after anabiosis. The digested EB were transplanted into subretinal space of C3B mouse. The eyes were analysed by photo microscopy, electric microscopy and immune assay at 1st week, 3rd week and 2nd month after injection. RESULTS:The thickened retina appeared on the place of injection at 1st week. Teratoma formation was observed in 3 transplant recipients at 3rd week and 2nd month. The ratio of forming tumor was 25% in all eyes received cell transplant. Eye atrophy or scar at injection position was seen in other eyes. The nucleus of tumour cells had apparent strange type under electrical microscopy. The immune assay showed that part of the tumour were microtubule-associated protein 2 (MAP-2) positive;part of the tumour were glial fibrillary acid protein (GFAP) positive;a little cells were nestin positive. CONCLUSION:After transplantation into the subretinal space, ESC were not incorporated into retina or differentiated into retinal cells. The teratoma was formed in part of eyes. The security of application for ESC in eye was considerable. 相似文献
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AIM:To study the expression of telomerase inhibitor Pinx1 in acute leukemia cells and during the differentiation of acute promyelocytic leukemia cells,and to realize its effect on telomerase activity.METHODS:Realtime quantitative PCR with fluorescence probe hybridization was used to measure the expression of Pinx1 and hTERT mRNA in acute leukemia cells and during differentiation of NB4 cells induced by ATRA.The correlations between Pinx1 and hTERT expression were also analyzed.RESULTS:Pinx1 mRNA expression in acute leukemia samples (0.00312,5.42×10-4-0.024) was significantly higher than that in normal bone marrow mononuclear cells (7.89×10-4,0-0.00863,P<0.01).The expression of Pinx1 mRNA had significant positive correlation with hTERT mRNA expression (r=0.296,P<0.05).Pinx1 mRNA expression decreased during differentiation,its expression was positive correlated with hTERT mRNA expression (r=0.900,P<0.05).CONCLUSIONS:As an inhibitor of telomerase,however,Pinx1 also had the same direction of regulation with telomerase activity in acute leukemia cells,suggesting its expression variation may be a subsequent reaction induced by that of hTERT to stabilize telomerase activity.The exact mechanisms remained to be verified. 相似文献
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猪繁殖与呼吸综合征活疫苗(CH-1R株)工厂化生产培养条件的研究 总被引:1,自引:0,他引:1
为提高猪繁殖与呼吸综合征病毒(PRRSV)活疫苗CH-1R株的产量和疫苗的质量,本实验探索了PRRSV活疫苗CH-1R株在MARC-145细胞中大规模生产培养的最佳条件。将CH-1R株分别在3L和10L转瓶培养的MARC-145细胞中进行增殖试验,分析CH-1R株在不同接种病毒量和不同接种病毒时间的TCID50变化规律。结果表明,在3L和10L转瓶中,病毒的TCID50最高可达到107.0TCID50/mL以上。CH-1R株通过转瓶在MARC-145细胞中大规模增殖,为PRRSVCH-1R株的工厂化生产奠定了基础。 相似文献
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