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11.
Transmission of bovine tuberculosis was quantified in three dairy herds located in south Santa Fe Province, Argentina. Using estimates of Mycobacterium bovis transmission (β) and a Reed–Frost simulation model, the prevalence of tuberculosis infection in the study herds over time was investigated. The Reed–Frost model was modified by incorporating randomness in both β and the incubation period () of M. bovis. The mean estimated herd β was 2.2 infective contacts per year and did not differ significantly between the study herds. Modeling as Poisson distributed (mean 24 months) best fit the observed prevalences. Infection was predicted by the model either to spread quickly (<10 years) within a herd and reach a high prevalence (>50%), or to persist at a low prevalence (<5–10%). The model was robust, predictions were realistic and the mean β estimated was consistent with previous studies of bovine tuberculosis.  相似文献   
12.
The commercial LCx amplification assay, usually employed to detect the Myocobacterium tuberculosis complex in respiratory specimens, was evaluated by comparing the results it gave with those obtained using Löwenstein-Jensen solid medium and pathological findings on 55 lymph nodes from cattle with positive and 10 lymph nodes from cattle with negative skin tests for tuberculosis. Fifty-three cultures (51 and 2, respectively) were positive for M. bovis, while the results for the LCx assay and the histological method were positive in 48 (45, 3) and 24 (20, 4) samples, respectively. None of the samples from cattle from certified tuberculosis-free herds were positive by any of the procedures. The results obtained with the LCx assay, compared with the culture procedure, regarded as the gold standard among the diagnostic techniques, gave a specificity of 91.6% and sensitivity of 90.5%. Although the sensitivity of LCx was suboptimal, DNA of M. bovis was detected in 81.8% of the skin test-positive animals. Amplification techniques could provide a rapid and reasonably reliable tool for detecting bovine tuberculosis.  相似文献   
13.
Genotyping of Mycobacterium bovis by geographic location within Mexico   总被引:1,自引:0,他引:1  
The spacer oligonucleotide typing (spoligotyping) method was used to differentiate 62 Mycobacterium bovis isolates obtained from tissues with macroscopic lesions typical of tuberculosis in dairy cattle from different regions of Mexico. Our purpose was to see if a strain from one region was genetically different from those of other regions (with the long-term aim of doing molecular trace back of isolates obtained in the laboratory). Results from the genetic analysis indicate that M. bovis isolates cannot be grouped by geographic location due to a wide range of genetic types involved in dairy cattle infections. Isolates even from the same herd showed different spoligotypes but some isolates from different region had similar genetic patterns. Genetic typing without epidemiologic information does not seem to be a plausible method to trace back animals to source of origin to detect and eliminate sources of infection.  相似文献   
14.
抑制鹿源多药耐药结核菌中药的筛选   总被引:1,自引:0,他引:1  
为了筛选对鹿源多药耐药结核菌有效的中药耐药抑制剂,通过MABA法检测24种中药的水和乙醇提取物对多药耐药结核菌及标准菌H37Rv的体外抗菌效果,将筛选出的抗菌效果好的黄连醇提物和黄连水提物采用紫外分光光度法进行活性成分含量测定,同时以MABA法与标准品比较体外抗结核菌活性。结果显示,黄连、独活和侧柏叶有明显的抗结核活性,其中黄连水粗提物和乙醇粗提物效果最佳,测得它们活性成分即总生物碱含量分别为22.74%和35.23%,并显示二者与小檗碱的体外抗结核作用相同。  相似文献   
15.
对一群经两次检疫均为结核菌素阳性并经临床学、病理解剖学和细菌学证实为结核杆菌感染奶牛,随机选择20头奶,每日按25mg/kg体重投与异烟肼复合剂,连服60日,接着再按上述剂量每隔一天给药一次连服60次。结果感染牛在治疗后的70天转阴率为50%;治疗后165天转阴率为80.1%;未经治疗的7头对照牛仍呈阳性。  相似文献   
16.
以吉林农业大学经济动物疾病实验室保存的鹿体内分离并鉴定的结核病流行株的基因组为模板,应用PCR方法从已构建的鹿结核病野毒株与卡介苗差异基因文库中扩增RD1区的Rv3872、Rv3873、Rv3874、Rv3875和Rv3878 5段目的基因,分别与p MD18-T Simple Vector连接,经PCR、酶切鉴定后的阳性重组克隆质粒与原核表达载体p GEX-4T-1连接并进行原核表达,采用谷胱甘肽琼脂糖亲和层析方法对目的蛋白进行纯化,通过SDS-PAGE和Western blot对表达产物的反应原性进行初步研究。基因测序结果显示差异基因与期望的序列一致,并在大肠杆菌中成功诱导表达,获得以可溶形式表达的目的蛋白,经SDS-PAGE分析目的蛋白的相对分子量与理论值相符,经Western blot鉴定纯化好的目的蛋白能与鹿结核病的阳性血清发生反应,具有良好的反应原性,为其在鹿结核病血清诊断学中的应用奠定了试验基础。  相似文献   
17.
应用变态反应方法诊断鹿结核病的研究   总被引:7,自引:1,他引:7  
利用牛型新,旧结核菌素(PPD,OT),禽型旧结核菌素(OT)为变应原,采用变态反应点眼法进行了鹿结核病的诊断研究。结果表明:变应原以牛型OT为最好,其敏感性高于禽型OT,检出率高于牛型PDD;一次二回点眼的阳性率可达92.33%,且较一次一回的检出率高44.6%;判定最佳时间为3,6,9h。用牛型OT一次二回点眼法抽检了11个鹿场2450余头成年鹿,其阳性率最高者为99.8%,最低者为1.1%,  相似文献   
18.
本文采用牛结核PPD检出阳性牛分离的分枝杆菌(包括有牛分枝杆菌、瘰疬分枝杆菌、乌胞内分枝杆菌2型及9型、副结核分枝杆菌、偶发分枝杆菌以及草分枝杆菌等),制成灭活免疫原进行豚鼠接种,并以各种分枝杆菌PPD进行变态反应检查,以观察其发生交叉反应的情况。试验结果表明:各种分枝杆菌除发生主反应外,均表现出明显的相互交叉的变态反应,尤以瘰疬分枝杆菌、乌胞内分杆菌2型及9型、副结核分枝杆菌以及牛分枝杆菌等交叉严重。提示:在牛结核及副结核的检疫中出现其它分枝杆菌干扰的假阳性反应。  相似文献   
19.
Objective To evaluate the antituberculous activities of Huangkuisu (HISS). Meth-ods lOStandard human strains of mycobacterium tuberculosis (H37RV) and multi-drug resistant TBstrainswere inoculated in different concentrations of HISS, blank control and positive TB drug culture medium[()observe the growth of mycobacterium tuberculosis and evaluate the antibacterial activity in vitro.②Certain number of standard strains of Mycobacterium tuberculosis H37Rv and drug-resistant strains were injected into the tail vein[()establish a mouse model of mycobacterium tuberculosis infection. The mice were randomly divided into treatment group, rifampicin, HISS treatment group treated lasting for 6 weeks; the control group was given normal saline. The antibacterial activity in vivo were evaluated[()compare the treatment results according[()the pathological changes in lung and spleen tissues (HE staining and acid-fast staining) and charging amount of bacteria. Results lOthe bactreial colonies were grew normally in model group, but were not grew in  相似文献   
20.
本研究旨在利用毕赤酵母(Pichia pastoris)系统融合表达结核分枝杆菌(Mycobacterium tuberculosis,MTB)的培养滤液蛋白10(culture filter protein 10,CFP10)和早期分泌抗原靶6蛋白(earlier secreted antigen target 6,ESAT6),并评价其作为牛结核病外周血γ-干扰素(interferon gamma,IFN-γ)体外释放实验特异性刺激剂来诊断牛结核病的应用潜能.通过PCR扩增cfp1 0-esat6融合基因,构建pPICZα A-(cfp10-esat6)重组质粒,电转化毕赤酵母GSll5,添加甲醇至终浓度1.0%,诱导3d,取培养上清进行SDS-PAGE分析,镍离子金属螯合亲和层析柱纯化目的蛋白,Western blot分析重组蛋白的免疫反应性;取纯化的融合蛋白CFP10-ESAT6作为刺激剂用于牛结核病外周血IFN-γ体外释放实验,评价其牛结核病诊断价值.结果表明,目的蛋白(33kD)被成功分泌表达,该融合蛋白与抗CFP10、ESAT6、组氨酸标签和c-Myc4种单抗均发生特异性反应,具有较好的免疫反应性.165份奶牛外周血样品的IFN-γ检测结果表明,CFP 10-ESAT6融合蛋白与结核菌素纯蛋白衍生物(purified protein derivative,PPD)作为刺激剂,二者阳性符合率为82.3%,阴性符合率为78.8%.本研究利用酵母表达系统成功表达CFP10-ESAT6融合蛋白,并表现出更高的生物学活性,在牛结核病外周血IFN-γ体外释放实验中可作为候选刺激剂,并能克服混合感染导致的PPD漏检问题,从而进一步提高检测的敏感性和特异性.  相似文献   
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