全文获取类型
收费全文 | 573篇 |
免费 | 22篇 |
国内免费 | 55篇 |
专业分类
林业 | 2篇 |
农学 | 18篇 |
15篇 | |
综合类 | 135篇 |
农作物 | 18篇 |
水产渔业 | 43篇 |
畜牧兽医 | 373篇 |
园艺 | 8篇 |
植物保护 | 38篇 |
出版年
2023年 | 5篇 |
2022年 | 11篇 |
2021年 | 16篇 |
2020年 | 6篇 |
2019年 | 19篇 |
2018年 | 8篇 |
2017年 | 15篇 |
2016年 | 11篇 |
2015年 | 22篇 |
2014年 | 23篇 |
2013年 | 25篇 |
2012年 | 34篇 |
2011年 | 40篇 |
2010年 | 30篇 |
2009年 | 28篇 |
2008年 | 28篇 |
2007年 | 42篇 |
2006年 | 37篇 |
2005年 | 28篇 |
2004年 | 23篇 |
2003年 | 10篇 |
2002年 | 14篇 |
2001年 | 23篇 |
2000年 | 9篇 |
1999年 | 12篇 |
1998年 | 25篇 |
1997年 | 13篇 |
1996年 | 9篇 |
1995年 | 9篇 |
1994年 | 5篇 |
1993年 | 8篇 |
1992年 | 13篇 |
1991年 | 4篇 |
1990年 | 3篇 |
1989年 | 7篇 |
1988年 | 4篇 |
1987年 | 1篇 |
1986年 | 4篇 |
1985年 | 2篇 |
1984年 | 2篇 |
1983年 | 2篇 |
1982年 | 3篇 |
1981年 | 2篇 |
1980年 | 3篇 |
1979年 | 3篇 |
1978年 | 2篇 |
1977年 | 3篇 |
1976年 | 1篇 |
1974年 | 2篇 |
1973年 | 1篇 |
排序方式: 共有650条查询结果,搜索用时 15 毫秒
21.
用单克隆抗体结合酶联免疫吸附试验检测棉铃虫幼虫体内的核多角体病毒 总被引:1,自引:0,他引:1
在常规ELISA间接法的基础上,应用单克隆抗体检测感染棉铃虫核型多角体病毒的棉铃虫幼虫体内病毒粒子。3龄幼虫饲喂表层涂有HaNPV人工饲料后9小时,即可在幼虫抽提液中检出病毒粒子抗原,而典型病虫显症需5~6天后才出现。因此本法是一种灵敏、快速、特异性强的检测昆虫杆状病毒的方法。利用单克隆抗体结合ELISA试验分别检测来自江苏和山东不同地区棉田自然死亡的棉铃虫幼虫,表明在江苏和山东不同棉区均可检测到HaNPV病毒粒子,但地区间棉铃虫核型多角体病毒检出频率有显著差异 相似文献
22.
The effect of 2 different oxytetracycline treatments in acute E. phagocytophila infected lambs was investigated. Twenty 5-month-old lambs of the Dala and Rygja breeds were used. Ten lambs were inoculated intravenously with a stabilate of an ovine E. phagocytophila strain. On the third day of fever, 4 lambs were given long-acting oxytetracycline (Terramycin prolongatum vet, Pfizer) (20 mg/kg) intramuscularly and another 4 lambs were given short-acting oxytetracycline (Terramycin vet, Pfizer) (10 mg/kg) intravenously for 5 consecutive days. The lambs were examined for the presence of Ehrlichia infection by blood smear evaluation, polymerase chain reaction (PCR) and antibody titre against E. equi. One month after the last antibiotic treatment, 250 ml citrate blood from each of these lambs were inoculated into each of 10 susceptible lambs, which were observed during the following 6 weeks. The results indicate that oxytetracycline given in the acute stage of the infection may effectively terminate the development of fever, rickettsemia and weight reduction in E. phagocytophila infected lambs. No difference was observed between the 2 treatment groups. However, at least 3 of 8 antibiotic treated lambs (37.5%) were still infected with granulocytic Ehrlichia 3 months after treatment. 相似文献
23.
Van den Bossche P Shumba W Njagu C Shereni W 《Tropical animal health and production》2001,33(5):391-405
Tsetse have been cleared from large areas of Zimbabwe during the past 65 years. In most areas, they are prevented from re-invading cleared areas by barriers of odour-baited, insecticide-treated targets. A trypanosomosis survey was conducted to determine the effectiveness of such barriers against re-invasion and to confirm the absence of tsetse in areas where they had previously been eradicated. Parasitological diagnostic methods and an anti-trypanosomal antibody detection enzyme-linked immunosorbent assay (antibody ELISA) were used. The prevalence of trypanosomal infections in the tsetse-cleared areas was generally low. However, the prevalence of anti-trypanosomal antibodies was unexpectedly high in some areas. This high proportion of cattle with antibodies could, in most cases, be explained by recent or historic information on the distribution and density of tsetse. The results from the survey demonstrated the value of anti-trypanosomal antibody detection as an additional sensitive tool for monitoring the effectiveness of tsetse control operations. 相似文献
24.
Christophe Tastet Florence Val Michel Lesage Lionel Renault Laurent Marché Michel Bossis Didier Mugniéry 《European journal of plant pathology / European Foundation for Plant Pathology》2001,107(8):821-832
Two major proteins, Mcf-A67 and Mcf-B66, were identified by mini two-dimensional polyacrylamide gel electrophoresis in order to distinguish the two European quarantine root-knot nematodes, Meloidogyne chitwoodi and M. fallax, from eight other species. These quarantine proteinic markers have been microsequenced after enzymatic digestion. The internal amino acid sequences exhibit similarities to members of a family of low molecular weight intracellular lipid-binding proteins. Moreover, to explore a simple, rapid, and inexpensive way to identify the two quarantine nematodes, dot blot hybridizations were performed using an antiserum (A67) produced from the longest amino-acid sequence of the protein Mcf-A67. Although several proteins stained on the M. chitwoodi and M. fallax western blot membranes, the two nematodes were easily distinguished from other root-knot nematodes, on dot blot assays with soluble proteins extracted from a single female. Because of its specificity and sensitivity, the use of the A67 antiserum to improve the diagnosis of the two European quarantine root-knot nematodes is discussed. 相似文献
25.
Distribution and properties of geographically distinct isolates of sugar beet yellowing viruses 总被引:1,自引:0,他引:1
M. Stevens N. J. Patron ‡ C. A. Dolby R. Weekes § P. B. Hallsworth O. Lemaire H. G. Smith 《Plant pathology》2005,54(2):100-107
From a total of 261 yellow sugarbeet leaves collected from 10 countries representing three continents, the incidence and distribution of strains of Beet mild yellowing virus (BMYV), Beet chlorosis virus (BChV) and Beet yellows virus (BYV) were analysed using serological and molecular methods. BMYV was found in all countries except Greece, and more frequently in the northern and western areas of Europe, whereas BYV predominated in Turkey, Spain, Greece, the USA and Chile. BChV, originally found in the USA and the UK in 1989, was identified in France, Spain, the Netherlands and Chile. Nine sugar beet poleroviruses, plus a reference isolate of Turnip yellows virus (TuYV, syn. Beet western yellows virus ), were further characterized and compared. Isolates obtained from sugar beet infected this species, but not oilseed rape or lettuce; all isolates except one infected Capsella bursa-pastoris . The coat-protein sequences of these isolates were highly similar, with the consensus sequence representing 89% of nucleotide residues. Within the coat-protein gene, two regions were identified that could represent specific epitopes to which monoclonal antibody BYDV-PAV-IL-1 could bind; this antibody is used to distinguish beet poleroviruses in ELISA. Comparison of the sequences at the 5' end showed that sequence homology existed only between isolates with the same host range. The first sequence data of polerovirus isolates from Chile are presented, showing that the coat protein and the 5' end of their genomes are highly similar to those of BMYV isolates found in Europe. Chilean polerovirus isolates may have been imported from the northern hemisphere in sugar beet breeding material. 相似文献
26.
Stefancíková A Stĕpánová G Derdáková M Pet'ko B Kysel'ová J Cigánek J Strojný L Cisláková L Trávnicek M 《Veterinary research communications》2002,26(8):601-611
In the course of epizootological research on Lyme borreliosis in domestic and farm animals, the serological evidence for the occurrence of this zoonosis in cattle was screened. An ELISA showed that 25.2% of cattle from seven geographical areas in Slovakia were positive for anti-Borrelia IgG antibodies. In particular localities, the seroprevalence ranged from 0.6% to 34.3%. Of 33 cases with clinical signs, 20 ELISA-positive samples were also confirmed in Western blots. The most frequent clinical signs were lameness and swollen joints, but most of the cases were asymptomatic. The occurrence of Borrelia burgdorferi antibodies and suspected clinical signs in cattle of Slovak regions indicates that veterinarians should pay attention to this disease in their clinical practice and include it within the differential diagnosis. 相似文献
27.
将海兰褐蛋雏鸡随机分为对照组、肌肉注射组、刺种Ⅰ组和刺种Ⅱ组,用共表达NDV F和IBDV VP0基因重组鸡痘病毒进行免疫,对照组刺种生理盐水,在免疫后的第7,14,21,28,35,42,49 d和56 d采血,分离血清,用固定病毒稀释血清法测血清中抗FPV,NDV,IBDV的中和抗体效价.经分析,抗FPV中和抗体效价及抗NDV中和抗体效价免疫后14 d达到高峰,28 d后下降幅度不明显,42 d时仍保持一定水平;抗IBDV中和抗体效价免疫后21 d达到高峰, 28 d后下降幅度不明显,42 d时仍保持一定水平. 相似文献
28.
A complete diallel cross involving two rabbit sire lines (C and R) was carried out to estimate the crossbreeding genetic parameters of seminal traits. 2140 ejaculates from 153 males were analyzed. The traits studied were: presence of gel plugs (G), urine (U), and calcium carbonate deposits (CC), number of useful ejaculates (UE), pH, volume (V), mass and individual motility (Mm, Mi), useful Mi (UM), concentration (Cn), number of spermatozoa per ejaculate (TSE), percentage of viable spermatozoa (Vi), spermatozoa with normal apical ridge (NAR), normal spermatozoa (Nr), spermatozoa with morphological abnormalities of head (H), neck-midpiece (Nm), and tail (T), presence of proximal and distal cytoplasmic droplet (Dp, Dd).
Estimates of heterosis, direct and maternal genetic effects were obtained from the solutions of the mixed model. There were major differences in direct genetic effects between lines, which were favourable to line C for Cn and TSE, and unfavourable for CC, Nm and Dp. Smaller differences were also observed in Vi and NAR favourable to line R. Differences between lines with respect to the maternal genetic effects were relevant and favourable to line C for V and to line R for U, UM, Cn, TSE, Nm, Mi, and Mm. Individual heterosis was high for Dp and Dd. 相似文献
29.
30.
Brajesh C. Varshney N.M. Ponnanna Pranati A. Sarkar Pragna Rehman Jigar H. Shah 《Journal of veterinary science (Suw?n-si, Korea)》2007,8(1):57-64
Escherichia coli (E. coli) strains were collected from young diarrheic calves in farms and field. Strains that expressed the K99 (F5) antigen were identified by agglutination tests using reference antibodies to K99 antigen and electron microscopy. The K99 antigen from a selected field strain (SAR-14) was heat-extracted and fractionated on a Sepharose CL-4B column. Further purification was carried out by sodium deoxycholate treatment and/or ion-exchange chromatography. Monoclonal antibodies to purified K99 antigen were produced by the hybridoma technique, and a specific clone, NEK99-5.6.12, was selected for propagation in tissue culture. The antibodies, thus obtained, were affinity-purified, characterized and coated onto Giemsa-stained Cowan-I strain of Staphylococcus aureus (S. aureus). The antibody-coated S. aureus were used in a co-agglutination test to detect K99+ E. coli isolated from feces of diarrheic calves. The specificity of the test was validated against reference monoclonal antibodies used in co-agglutination tests, as well as in ELISA. Specificity of the monoclonal antibodies was also tested against various Gram negative bacteria. The developed antibodies specifically detected purified K99 antigen in immunoblots, as well as K99+ E. coli in ELISA and co-agglutination tests. The co-agglutination test was specific and convenient for large-scale screening of K99+ E. coli isolates. 相似文献