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111.
牛肺疫又被称为牛传染性胸膜肺炎,是由肺炎支原体感染引发的急慢性呼吸道疾病,临床上主要表现为呼吸急促,呼吸困难,从鼻腔中流出脓性分泌物,主要对患病牛的肺脏、胸膜和淋巴结造成危害,典型的临床特征是肺小叶浆液性肺炎和肺实质纤维素性肺炎,被国际兽医局划归为A类动物疫病,我国将其划归为一类重大动物疫病,发生流行后,需要执行严格的扑杀、无害化处理制度,逐渐净化牛群,避免疫情进一步扩展蔓延到造成更为严重的经济损失。该文主要论述牛肺疫的临床症状和综合防治措施。  相似文献   
112.
疫病一直是生猪养殖中影响猪群健康的重要因素,受到疾病影响的猪群会给养殖户带来巨大的经济损失,严重阻碍养殖业的发展。该文将简要概述猪丹毒和猪肺疫的病理状况,分析猪丹毒和猪肺疫混合感染的发病特征和临床症状,并研究综合诊治猪丹毒和猪肺疫混合感染的方法,降低猪丹毒和猪肺疫混合感染对生猪养殖的影响。  相似文献   
113.
近年,生猪养殖产业不断向着集约化规模化方向发展,养殖密度增加的同时,各种传染性疾病呈现高发趋势。猪传染性疾病发生后,会造成生长发育不良,行动迟缓,生理指标失衡,甚至引发死亡,带来的经济损失不可估量,某些人畜共患病还会威胁人类的身体健康。在疫病防控过程中,需要从传染源、传播途径和易感群体等角度出发,减少养殖环境病原数量,切断病原传播途径,保护易感群体,确保生猪健康生长。该文主要结合一个乡镇的疫病流行特点,分析切断传染源和传播途径对防治猪病发生流行的重要性。  相似文献   
114.
呼吸道疾病是目前威胁鸡养殖产业健康发展的一类重大动物疫病,呼吸道疾病的病原种类多种多样,且造成的临床症状大致相同,诊断难度较大,如果没有进行妥善有效的鉴别、诊断,易造成整体的治疗方案缺乏针对性,难以在短时间内控制病情,错过最佳的防控时期。鸡呼吸道疾病常常混合感染并发感染,2种以上的病原相互叠加表现的临床症状复杂,诊断难度更大。该文主要论述鸡呼吸道疾病的鉴别诊断和防治措施。  相似文献   
115.
In order to detect the clinical efficacy of oligosaccharide sulfate(DEAE) and dextran sulfate (DS-4000) against bovine mastitis,56 cows with bovine mastitis were divided into 5 groups (DEAE group,DS-4000 group,DEAE+penicillin group,DS-4000+penicillin group and penicillin group),and their breasts were perfusion with different drugs twice one day for 3 days.The effective rates of drugs were observed by clinic symptoms.Milk samples were collected before and after treatment of drugs,and the bacterial negative conversion rate of each group were detected by microbial examination.The results showed that total effective rates of 5 groups were 10.00%,20.00%,58.33%,75.00% and 50.00%,respectively,and the bacterial negative conversion rates were 0,12.50%,50.00%,54.55% and 44.44%,respectively.In conclusion,the curative efficiencies of the polysaccharides against bovine mastitis were weak,but it could be improved by combination with penicillin.  相似文献   
116.
In order to study and analyze L1 gene of bovine papillomavirus(BPV)in Guizhou province,the L1 gene of BPV-GZ01 strain was amplified,cloned and sequenced using bioinformatic softwares and methods,and the secondary structure,tertiary structure,B-cell preponderant epitope,conserved domains analysis, transmembrane domain and signal peptide of L1 gene were predicted.The results showed that the length of L1 gene was 1 494 bp,encoding 497 amino acids.The L1 gene of BPV-GZ01 strain shared an amino acid identities of 98.6%,99.4%,98.4%,94.4% and 91.3%,and a nucleotide identities of 99.1%,99.8%,99.4%,87.6% and 82.8% with those of BPV2,BPV2-SW01,BPV2-AKS01,BPV13 and BPV1 strains,respectively.The results of phylogenetic tree analysis indicated that there was a close relationship between BPV-GZ01 and BPV2-SW01 strains.The prediction of secondary structure of L1 protein indicated that the random coil,extended strand and alphahelix took a higher percentage.The L1 protein was supposed contain 6 potential antigen epitopes.And no transmembrane domains and no signal peptide were found.The tertiary structure of L1 protein was curved spiral structure.These results provided a theoretical basis for immunologic diagnosis and further research of nucleic acid vaccine of BPV.  相似文献   
117.
This experiment was designed to study the complex of Lactobacillus rhamnosus fermented herbal and Bacillus subtilis on White Feather broiler immunity performance and impact of Escherichia coli infection.360 one-day-old broiler chickens were randomly divided into 3 groups with 4 replicates in each group and 30 chickens per replicate.The pretrial period lasted for 7 d,and the experiment lasted for 35 d.The chickens in the group Ⅰ(positive control group) and group Ⅱ(negative control group)were all only fed a basal diet,group Ⅲ was test group,by additive 1% fermented herbal preparations,groups Ⅱ and Ⅲ were intraperitoneal injection of 1 mL E.coli at 35 d,broiler mortality,immune organ index,cecalmicroflora content,immunoglobulin levels,IL-2 and IL-6 content were tested.The results showed that injection of E.coli caused massive death of chickens,group Ⅱtook up to 75.00%,it was significantly higher than groups Ⅰ and Ⅲ (P < 0.05),the mortality in group Ⅲ was significantly lower than group Ⅱ(P < 0.05),was only 23.33%.Injection of E.coli maked spleen index and thymus index of group Ⅱincreased significantly (P < 0.05),the spleen index and thymus index of groups Ⅰ and Ⅲ were no significant difference (P > 0.05).E.coli counts was significantly decreased after injectionin group Ⅲ (P < 0.05),but the number of intestinal Lactobacilli of group Ⅲ was significantly increased (P < 0.05),and inhibited the propagation of E.coli,the counts of E.coli in groups Ⅰ and Ⅲ were no significant difference (P > 0.05).At 42 d,the sIgA of the intestinal fluid in group Ⅲ were higher than that of groups Ⅰ and Ⅱ with 11.99% and 36.56%,respectively(P < 0.05).The serum IgG concentrations of group Ⅲ was higher than that of groupsⅠand Ⅱwith 14.68% and 28.15%,respectively(P < 0.05).At 42 d,the IL-2 content of group Ⅱ was the lowest,it was significantly lower than group Ⅲ(P < 0.05),the IL-6 of group Ⅲ was significantly lower than group Ⅱ(P < 0.05).  相似文献   
118.
To establish a rapid,sensitive and specific assay for the differential detection of Nipah virus (NiV) and highly pathogenic porcine reproductive and respiratory syndrome virus (HP-PRRSV),a duplex Real-time RT-PCR was developed with specific primers and probes targeting to the special sequences of NiV M gene and HP-PRRSV nsp2 gene by optimization of reaction conditions.The performance of the assay was linear ranging from 4.6×101 to 4.6×107 copies/μL for RNA standard control of NiV M (NiV-M-RNA) and from 4.1×101 to 4.1×108 copies/μL for RNA standard control of HP-PRRSV nsp2 (HP-PRRSV-nsp2-RNA),and detection limits of the assay was 46 copies for the NiV-M-RNA and 4.1 copies for the HP-PRRSV-nsp2-RNA,respectively.The coefficients of variation (CVs) of both inter-assay and intra-assay repeatability were less than 2.0%,showing good repeatability.The assay was able to specifically detect NiV and HP-PRRSV simultaneously without cross-reaction with classical swine fever virus (CSFV),porcine epidemic diarrhea virus (PEDV),swine influenza virus (SIV),porcine parvovirus (PPV),pseudorabies virus (PRV) and porcine circovirus type 2 (PCV2).Of the 236 samples from pigs for both NiV and HP-PRRSV detection by the established assay,all the samples were negative for NiV,8 samples were HP-PRRSV positive.In conclusion,this assay offers a useful approach for the differential detection of NiV and HP-PRRSV in clinical specimens from the pigs.  相似文献   
119.
为了实现快速检测猪繁殖与呼吸综合征病毒(PRRSV)并同步鉴别高致病性PRRSV毒株(HPPRRSV),根据PRRSV囊膜蛋白GP2基因保守序列和HP-PRRSV特有的Nsp2基因区保守序列设计特异扩增引物和杂交探针,通过双重一步法RT-PCR不对称扩增和双重微球杂交反应,建立了双重液相基因芯片方法。对12株PRRSV以及其他12种猪病原体的检测显示,该法能特异性检测12株PRRSV毒株并准确鉴别其中7株HP-PRRSV,与其他病原体无交叉反应;对PRRSV、HP-PRRSV病毒液的检测低限均小于每个反应0.5TCID_(50);其组内、组间检测变异系数均10%;检测55份疑似临床样品并与商品化荧光RTPCR试剂盒比较检测结果,符合率达98.2%(54/55)。研究结果为适应临床快速检测PRRSV提供了一种新的分子生物学检测方法。  相似文献   
120.
弓形虫病是一种世界性分布的人兽共患寄生虫病,在人和动物中广泛传播。孕妇感染弓形虫后多表现为隐性感染,无明显的临床表现,但该虫可通过垂直传播影响胎儿发育,造成早产、流产、畸形和死胎等不良妊娠现象。论文对弓形虫病流行病学、感染因素、免疫学、诊断和治疗等方面阐述弓形虫感染对孕妇的影响,为孕妇弓形虫病的防治提供参考。  相似文献   
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