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251.
依照《农作物种质资源整理技术规程》,结合国家种质牧草中期库和多年生牧草圃在牧草种质资源繁殖更新技术方面取得的丰富经验,并针对存在问题制定“牧草种质资源繁殖更新技术规程”,使得牧草种质资源进行更科学的繁殖更新,为遗传完整且稳定的活种质的保存和利用提供依据。  相似文献   
252.
猪瘟病毒基因组及基因工程疫苗研究进展   总被引:4,自引:0,他引:4  
本文着重介绍了猪瘟病毒基因组结构组成、基因组产物和以基因组为研究对象开展的亚单位疫苗、活栽体疫苗、标记疫苗等新型基因工程疫苗的研究现状。  相似文献   
253.
本试验以宁夏地区8个公牛家系的各8头女儿共计64头中国荷斯坦母牛为研究对象.利用AB13730测序仪对DGAT2基因Exon4进行了基因型检测后发现三个突变位点474bp(C/G)、48lbp(G/A)、621bp(C/T),各个位点发现有两种基因型,分别为CC型、GC型,GG型、GA型,CC型和CT型,基因型频率分别为0.484、0.516,0.687、0.313,0.484和0.516。通过SAS软件(8.02)对4个产奶性状与DGAT2基因Exon4的关联分析表明.474bp(C/G)CG型305d产奶量和乳脂率显著高于CC型(P〈0.05),乳蛋白率、体细胞数影响不显著(P〉0.05);481bp(G/A)GA型305d产奶量显著高于GG型,与乳脂率、乳蛋白率、体细胞数无显著的相关性(P〉0.05);621bp(C/T)CT型305d产奶量、乳蛋白率、体细胞数都显著高于CC型(P〈0.05),乳脂率影响不显著(P〉O.05)。  相似文献   
254.
In this study,the CDS sequence of buffalo Keap1 gene was cloned and analyzed,then its expression pattern in different tissues was also investigated.A pair of primers of buffalo Keap1 gene was designed based on the nucleotide sequence of Bos taurus Keap1 gene from GenBank,and then the buffalo Keap1 gene was amplified.Using the bioinformation techniques,the gene sequence and the protein structure were analyzed.The expression level of Keap1 gene in different tissues were detected with Real-time quantitative PCR.The results showed that the length of buffalo Keap1 gene coding sequence was 1 875 bp and encoded 624 amino acids.The multiple sequence alignment results showed that buffalo Keap1 gene shared 99%,96%,92% and 90% of similar nucleotide sequence with that of Bos taurus,Ovis aries,Sus scrofa and Homo sapiens,respectively.And the phyogenetic tree also showed the conservatism between several different species.The second structure of buffalo Keap1 protein was predicted as 24 alpha regions,40 beta regions,38 turn regions and 27 coil regions.In addition,the results of Real-time quantitative PCR showed that Keap1 mRNA exists in all seven tissues,but the most abundant expression was in heart and the minimal expression was in liver and spleen.The results provided an foundation for further study of Keap1-Nrf2-ARE signal pathway,for enhancing the ability of antioxidant of buffalo embryo in vitro culture.  相似文献   
255.
鲁西黄河故道杨树林间作效益的研究   总被引:5,自引:0,他引:5  
时明芝 《林业科技》2003,28(1):16-18
经过6年对鲁西黄河故道杨树人工林进行施肥量、间作物、密度等因素的正交试验,证明只有扩大造林行距为10m左右,造林后立即实行林下间作,并尽量延长间作年限,才能保证树体营养供应和林木正常生长,提高林地的生产力和经济效益。同时,探索出在此类土地上不同林龄的杨树人工林的最佳间作方式。  相似文献   
256.
鱼类运动行为的观察能够为鱼类健康监控提供直观信息,而通过人工标定的方式监测鱼群运动行为耗时长、效率低。文章针对鱼类运动行为的监测问题,提出一种基于图像处理技术的罗非鱼运动监测方法。首先利用计算机、CCD高清摄像机获取鱼群运动视频,再对图像进行滤波去噪、灰度等处理;通过Ostu阈值分割法改进Canny边缘检测算法提取鱼群的边缘轮廓;在建立鱼群运动模型的基础上结合目标关联匹配算法,实现罗非鱼运动行为的跟踪和监测。结果显示鱼群的个体检出率为98.96%,轨迹完整度为97%。提出的算法比卡尔曼滤波的轨迹跟踪监测效果略有提升,能够较好地完成鱼群的运动跟踪和动态监测。  相似文献   
257.
In order to investigate the effect of AIR on inflammatory reaction infected by Brucellamelitensis (16M), the AIR domain of Tecpr1 gene of murine macrophages RAW264.7 were knocked down (I-A), overexpressed (O-A) and reversed (OA-IA). Using the chlorine fluorescein (DCFH-DA) as a probe, we detected the variation of ROS production and mitochondria distribution by confocal laser scanning microscopy. We observed the expression changes of NLRP3, ASC and Caspase-1 by qRT-PCR and the expression changes of IL-18,IL-1β and Caspase-1 in host cells by ELISA. The results showed that 16M could stimulate RAW264.7 cells to produce ROS by time-dependent pathway, and I-A group and O-A group showed more abnormal accumulation of mitochondrial. The results of qRT-PCR and ELISA suggested that it had effect on the expression levels of NLRP3, ASC,Caspase-1 and IL-18, IL-1β and Caspase-1 in cells of different groups. Those results indicated that with AIR gene deletion, the release amount of ROS changed, mitochondrial clustered abnormally, and AIR was closely related to the activation of inflammasomes and induction of inflammatory reactions.  相似文献   
258.
彭展  石岿然 《湖北农业科学》2012,51(20):4671-4676
以期权式合同为分析对象,考察它的基本特点与效果。结果表明,企业与农户签订具有这种期权性质的合同可以有效地降低农户的违约风险。而企业通过收取期权费也使自身承担的市场风险有了一定的补偿,契约双方能够初步形成一种风险共担的机制。但是,期权式合同的履行有赖于企业作出可置信承诺,即对农户进行专用性投资,由此使签约双方能够形成一种有效的自我履约机制。  相似文献   
259.
Somatic cell nuclear transfer (SCNT)-derived piglets have significantly higher stillbirth rate and postnatal mortality rate than artificial insemination (AI)-generated piglets. The question whether the low survival rate of SCNT piglets was related to birth weight, umbilical cord or placenta development was investigated. In this study, stillbirth rate, neonatal death rate, birth weight, umbilical cord status, placental parameters and placental gene expression patterns were compared between SCNT and AI piglets. Results showed that mortality rates at birth and during the neonatal stage of SCNT piglets were significantly higher than those of AI piglets. The incidence of abnormal umbilical cord in SCNT and SCNT-liveborn (SCNT-LB) piglets was significantly higher than in AI and AI-liveborn (AI-LB) piglets. Birth weight, placental weight, placental surface area and placental efficiency in SCNT and SCNT-LB piglets were significantly lower than those of AI and AI-LB piglets. Placental expression profiles of imprinting, angiopoiesis and nutrient transport-related genes were defective in SCNT-LB piglets compared with those in AI-LB piglets. Thus, the low survival rate of SCNT piglets may be associated with abnormal umbilical cord and placenta development. These characteristics may have resulted from aberrant expression of angiogenesis, nutrient transport, and imprinting-related genes in the placentas.  相似文献   
260.
Anliucheng (Citrus sinensis Osbeck), a very seedy and widely spread acidless sweet orange cultivar in south of China, was transformed by the strain of Agrobacterium Tumefaciens EHA105 carrying pTA29-barnase gene, which will induce pollen sterility in transgenic plants. The embryogenic calli of Anliucheng were co-cultivated with Agrobacterium tumefaciens for 3 days, and then transferred to selective medium containing 50 mg L-1 basta (a kind of herbicide) for 5 weeks. The resistant calli were recovered and regenerated 118 embryoids. A total of 13 entire plants were obtained after micro-grafted on trifoliate orange. These regenerated plants were verified by PCR amplification and confirmed by PCR-Southern blotting analysis.  相似文献   
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