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排序方式: 共有126条查询结果,搜索用时 388 毫秒
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为研究参麦与黄芪注射液联用对大鼠卡氏肺孢子虫肺炎(PCP)的治疗效果,以地塞米松连续肌肉注射Wistar大鼠6周,建立PCP大鼠模型,用参麦与黄芪注射液皮下注射治疗患病大鼠,同时设复方磺胺甲恶唑(SMZ-TMP)治疗对照组和PCP模型阳性对照组。通过各组大鼠基本情况变化、肺组织印片检查包囊、肺组织病理切片染色观察组织变化,探讨其治疗效果。结果发现,参麦与黄芪注射液联用治疗后,大鼠饮食、饮水增加,活跃程度恢复,体重不同程度增加,肺印片Pc包囊数量比治疗前明显减少,肺组织炎症反应减轻,高剂量组治疗效果接近复方磺胺甲恶唑组。研究结果表明,参麦与黄芪注射液对肺孢子虫有明显的治疗作用。 相似文献
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通过运用HYDSIM液力计算软件模拟电控共轨喷油器的喷射特性,探讨了电控共轨喷油器控制室的进油孔、出油孔和控制活塞直径的变化对喷油器喷嘴针阀升程及喷油规律的影响。分析结果表明,需要选择合适的共轨喷油器控制室进油孔、出油孔及控制活塞直径,以便使柴油机发挥更加良好的工作性能和排放性能。 相似文献
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Rashmi Kumari Hirokazu Ito Masahiro Takatani Miho Uchiyama Tadashi Okamoto 《Journal of Wood Science》2007,53(6):470-480
Although wood/cellulose-plastic composites (WPC) of low wood/cellulose content have been more accepted worldwide and are promoted
as low-maintenance, high-durability building products, composites containing high wood/cellulose content are not yet developed
on an industrial scale. In this study, flow properties, mechanical properties, and water absorption properties of the compounds
of cellulose microfiber/polypropylene (PP) and maleic anhydride-grafted polypropylene (MAPP) were investigated to understand
effects of the high cellulose content and the dimensions of the cellulose microfiber. The molding processes studied included
compression, injection, and extrusion. It was found that fluidity is not only dependent on resin content but also on the dimension
of the filler; fluidity of the compound declined with increased fiber length with the same resin content. Dispersion of the
composite was monitored by charge-coupled device (CCD) microscope. Increasing the plastic content in the cellulose-plastic
formulation improved the strength of mold in addition to the bond development between resin and filler, and the tangle of
fibers. The processing mode affected the physicomechanical properties of the cellulosic plastic. Compression-molded samples
exhibited the lowest modulus of rupture (MOR) and modulus of elasticity (MOE) and the highest water absorption, while samples
that were injection-molded exhibited the highest MOR (70 MPa) and MOE (7 GPa) and low water absorption (2%). 相似文献
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为了研究阿莫西林混悬注射液在猪体内的药代动力学和生物等效性,采用双处理、双周期随机交叉试验设计,将24头健康猪随机分成2组,按15 mg/kg体重肌肉分别单剂量注射受试制剂和参比制剂,采用高效液相色谱法测定血浆中阿莫西林的浓度,利用Win Nonlin6.4软件计算主要药动学参数,并评价两种制剂的生物等效性。结果显示,受试制剂和参比制剂的Tmax分别为(3.45±2.49)h,(1.34±1.74)h;Cmax分别为(6.94±4.73)mg/L,(4.39±2.87)mg/L;AUC0-t分别为(37.00±11.48)mg·h·L-1,(30.02±8.93)mg·h·L-1;AUC0-∞分别为(40.26±13.36)mg·h·L-1,(38.46±15.38)mg·h·L-1。阿莫西林混悬注射液受试制剂和参比制剂的AUC0-t、AUC0-∞、Cmax、Tmax均有显著性差异,双单侧t检验结果显示两种制剂生物不等效,试验为兽医临床给药方案的制定以及合理用药提供参考。 相似文献
7.
Antti Oksanen Kjetil ?sbakk Marja Raekallio Mauri Nieminen 《Acta veterinaria Scandinavica》2014,56(1)
Background
Overwintering (breeding) reindeer (Rangifer tarandus tarandus) are commonly treated with ivermectin against parasitic infestations once yearly in autumn-winter roundups. The only preparations registered to reindeer are those for subcutaneous injection. However, also oral extra-label ivermectin administration is used. Twenty-six, 8-month-old reindeer calves were randomly allocated into three groups. Group 1 (n = 9) received oral ivermectin mixture (Ivomec® vet mixt. 0.8 mg/ml, oral ovine liquid drench formulation), Group 2 (n = 9) oral ivermectin paste (Ivomec® vet 18.7 mg/g equine paste), and Group 3 (n = 8) subcutaneous injection of ivermectin (Ivomec® 10 mg/ml vet inj.), each group at a dose of 200 μg/kg body weight. Blood samples were collected at treatment and at days 1, 2, 3, 6, 9 and 16 post treatment. Plasma concentrations of ivermectin were determined by high-pressure liquid chromatography (HPLC) with fluorescence detection.Results
The peak plasma concentration (Cmax) was reached by 2 days after each treatment. The Cmax and Area Under Curve (AUC) differed significantly between the groups: Cmax was 30.2 ± 3.9, 14.9 ± 5.7 and 63.1 ± 13.1 ng/ml, and AUC∞ was 2881 ± 462, 1299 ± 342 and 6718 ± 1620 ng*h/ml for groups 1, 2 and 3, respectively (mean ± standard deviation).Conclusions
The differences in plasma concentrations of ivermectin are concomitant with earlier observed differences in antiparasitic efficacy, which discounts the use of the equine paste in reindeer in favour of the oral ovine liquid drench formulation, or preferably, the reindeer-registered subcutaneous injection formulation. 相似文献8.
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