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排序方式: 共有71条查询结果,搜索用时 15 毫秒
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GU Qing-fang YU Jie-zhong GUO Min-fang WEI Wen-yue XIAO Bao-guo ZHANG Guang-xian MA Cun-gen 《园艺学报》2019,35(12):2227-2234
AIM: To explore the neuroprotective effect of novel Rho kinase inhibitor FSD-C10 on Alzheimer disease (AD) model of APP/PS1 double transgenic (Tg) mice. METHODS: Male APP/PS1 Tg mice (n=20) at 8 months of age were randomly divided into 2 groups:model group and FSD-C10 treatment group. The mice were treated with normal saline or FSD-C10 (25 mg·kg-1·d-1) by intraperitoneal injection, once daily for 2 months. Age-and sex-matched wild-type (WT) mice without treatment were used as the control. The Morris water maze (MWM) test and SMART 3.0 behavioral record system were applied to examine and analyze the spatial cognitive function of the mice. The protein levels and distribution of Aβ, p-tau and synapse-associated proteins such as synaptophysin, α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR) and postsynaptic density protein 95 (PSD-95) were determined by immunofluorescence staining. The protein levels of phosphorylated amyloid precursor protein at Thr668[p-APP(Thr668)], beta-site APP-cleaving enzyme 1 (BACE1) and synapse-associated proteins in the brain were analyzed by Western blot. RESULTS: Compared with model group, FSD-C10 treatment significantly improved the cognitive function of the APP/PS1 Tg mice, accompanied by reduced Aβ deposition and p-tau level, increased protein level of p-APP (Thr668) in the central nervous system, decreased expression of BACE1, and increased expression of synapse-associated proteins in the brain of the mice (P<0.05). CONCLUSION: FSD-C10 has neuroprotective potential in the APP/PS1 Tg mice. The mechanism may be related to enhancing the non-amyloidogenic APP cleavage pathway, reducing the production of Aβ oligomers, the deposition of senile plaques and the amount of tau protein, up-regulating synapse-associated proteins, and increasing synaptic plasticity. 相似文献
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2020年2月份山西某大型规模猪场育肥猪突发呼吸困难,无过多症状表现,即突然死亡,发病率为2%,死亡率1.5%左右。实验室以病死猪为研究对象,综合死亡猪只脏器病变状况观察,无菌采集病死猪的肺脏、肝脏、脾脏病料,进行RT-PCR检测猪蓝耳病原;用含1%NAD和5%胎牛血清的TSA琼脂培养基进行细菌分离培养和纯化,经形态学鉴定、PCR鉴定、16Sr RNA基因序列进化树构建等方法,结果显示:该发病猪群为猪繁殖与呼吸障碍综合征并发猪胸膜肺炎放线杆菌感染。药敏试验结果显示:该猪胸膜肺炎放线杆菌对安普霉素、硫酸黏菌素、替米考星+氟苯尼考、替米考星+阿莫西林、氟苯尼考、头孢噻呋钠+硫酸黏菌素、头孢喹肟、头孢噻呋钠+新霉素、替米考星+头孢噻呋钠、多西环素+氟苯尼考、头孢噻呋钠+阿莫西林、阿莫西林+克拉维酸钾、头孢噻呋钠+恩诺沙星、新霉素、头孢噻呋钠、安普霉素+头孢噻呋钠敏感。对恩诺沙星耐药。本实验室根据临床及检测结果制定治疗方案,为该猪场的猪繁殖与呼吸障碍综合征并发猪胸膜肺炎的临床诊断及用药提供了理论依据。 相似文献
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通过分析衡阳烟区烤烟3414肥效试验数据,获得了衡阳烤烟精准施肥的相关技术参数,筛选出了植烟土壤有效养分校正系数估算的最佳数学模型;并依据斯坦福施肥量计算公式W=(U-Ns)/R,结合烟叶目标产量、植烟土壤速效养分测试值及实际施肥纯量等指标,建立了N、P、K施肥用量(Y)同烟叶产量(X_1)和烟田土壤养分含量(X_2)的二元一次回归数学模型;将最适施肥的数学模型及计算过程置入Excel软件和安卓智能手机APP中,构建了烟草推荐施肥专家系统。该系统能简单方便地指导烟户因地制宜地精准施肥,同时通俗易懂、可行性高,适合基层技术人员及农户使用。 相似文献
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针对青海气象公共服务的现状,研究并实现了一套气象服务移动应用系统。该系统通过将Arc GIS技术、Sqlite.Swift技术、Alamofire、流量压缩、数据加密技术等应用于设计与研发过程,实现了青海气象天气预报、天气实况、灾害预警、卫星云图、公共气象服务产品等实时信息的动态展示、快速查询,将基于互联网+移动APP服务模式应用于气象公众服务领域,丰富了气象服务手段,提高了青海气象公众服务质量。 相似文献
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Asta Tvarijonaviciute 《Research in veterinary science》2011,90(1):31-34
The purpose of the study was to analyse serum concentrations of four different positive acute phase proteins (APPs): C-reactive protein, haptoglobin, serum amyloid A and ceruloplasmin in a model of experimentally short-term developed obesity in Beagle dogs. All APPs were quantified by commercially available ELISA methods and C-reactive protein was also determined by a highly sensitive time-resolved fluorometric assay. There were no significant differences between APPs concentrations at the beginning and the end of the study in groups of dogs that increased their body condition scores. In addition, dogs with body condition scores of 4 and 5 did not shown significant differences for any of the acute phase proteins studied compared with control dogs of BCS of 3, with exception of a decrease in haptoglobin. It was concluded that overweight induced in the experimental conditions of this study does not produce a significant change in acute phase proteins. 相似文献
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参照GenBank中已发表的ApxIV基因序列,以自行分离的App DNA为模板,利用PCR方法扩增出ApxIV3'端,大小为552bp的保守基因序列.将PCR产物克隆到pMD18-T Simple Vector中,获得重组质粒pMD-ApxIV,对其重组质粒pMD-ApxIV进行BamHI、HindIII双酶切,并将酶切产物克隆到原核表达载体pET-32a(+)中,构建了重组表达质粒pET-ApxIV.将表达质粒转化至大肠杆菌BL21中,用IPTG诱导表达,通过SDS-PAGE和Western blot分析,结果表明pET-ApxIV在BL21中成功表达,并能被App阳性血清所识别,具有良好的免疫原性.表达蛋白的分子质量约为39.5KDa.利用HiTrap FF crude columns将表达的蛋白进行了纯化. 相似文献
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