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971.
R.R. Lesniewski J.D. Kirsch L.E. Mrozinski D.H. Hellwig J. Kotwica G.L. Williams 《Domestic animal endocrinology》1985,2(3):141-150
Experiments were conducted to evaluate the effects of time and temperature on the potential of bovine whole blood (WB) or plasma (PL) to metabolize the ovarian steroids progesterone, estradiol-17β and testosterone. During a radioimmunoassay study (Experiment 1), we observed a temperature and time-dependent reduction (P<0.001) of plasma progesterone concentrations in samples incubated as WB at 5, 15, 25, or 35C for up to 48 hr. Most notable was the observation that 27% of progesterone present in controls was lost when WB was incubated at 5C for 48 hr and a 17% reduction was observed when PL samples were incubated at 35C for 48 hr. Immunoreactive estradiol-17β concentrations (Experiment 2) in PL and WB incubates were not affected by time or temperature. However, immunoreactive testosterone concentrations increased more than 3-fold by 48 hr in WB incubates held at 35C. To examine the latter observation further, 3H-progesteone was incubated with WB at 35C, followed by extraction and thin-layer chromatography (Experiment 3). Results generally supported RIA findings and revealed the presence of significant 17α-hydroxylase, 17–20 lyase and aromatase activity. Heretofore this has not been considered to occur outside major steroid metabolizing organs. 相似文献
972.
辽宁省不同地区的反枝苋对氯嘧磺隆抗药性研究 总被引:3,自引:0,他引:3
在辽宁省不同地区的大豆田中采集反枝苋种子,在室内通过琼脂法和茎叶处理法,测定辽宁不同地区反枝苋对氯嘧磺隆的抗性水平差异以及对反枝苋幼苗的影响。试验结果表明:铁岭开源地区的反枝苋,相对抗性比为751;锦州北镇和丹东东港的反枝苋,其相对抗性比分别为294.5、167;不同地区反枝苋敏感性种群和抗性种群幼苗的苗高、根长、植株鲜重的相对毒力倍数和抗性指数均存在一定的差异。 相似文献
973.
974.
[目的]提高大叶速生槐种根的繁殖系数和苗木的质量。[方法]对不同直径不同长度的大叶速生槐种根的繁殖方法进行研究。[结果]直径5 mm以上的种苗种根采用直接栽种的方法,直径3~5 mm的种根采用先育苗再移栽的方法,育苗主要采用沙坑密植、营养袋育苗和塑管育苗等方法。[结论]此法不仅提高了大叶速生槐种根的繁殖系数,而且提高了苗木的质量。 相似文献
975.
976.
977.
家蚕品种最适环境片区的划分 总被引:2,自引:0,他引:2
对家蚕品种最适环境片区划分进行了研究,初步得到如下结果:参试的8个地区可以划分为两个环境片区。第一个环境片区包括四川、重庆和浙江;第二个环境片区包括陕西、山东、安徽、湖北和镇江;第一个环境片区的最适基因型是品种B;第二个环境片区的最适基因型是品种C。如果在各环境片区推广相应最适基因型比在所有地区只推广品种C,则全区平均万蚕收茧量可提高2.1%。 相似文献
978.
WANG Leming WANG Yurui ZENG Zixuan RAO Guoshun WU Zhengjiao JIN Weikun WANG Dongying 《中国畜牧兽医》2022,49(2):677-686
【Objective】 This study was intend to obtain cathepsin L1(rFgCat L1) specific monoclonal antibody and construct the double antibody sandwich ELISA.【Method】 Five BALB/c mice were immunized with 1 mg/mL rFgCat L1 protein for four times.Mouse splenocytes were isolated and fused with SP2/0 cells to construct hybridoma cells.Strong positive hybridoma cell lines were screened, 1×106 cells were injected intraperitoneally per mouse to prepare monoclonal antibodies.Antibody titer and antigenic epitope were detected using ELISA method, antibody subtype and specificity were identified using Western blotting method.The double antibody sandwich ELISA was constructed by combining the anti-rFgCat L1 polyclonal antibody, and its sensitivity and specificity were tested.The positive and negative critical value was screened by 20 negative sera with positive control, and the constructed double antibody sandwich ELISA was verified by 47 goat positive sera and 47 dairy cow positive sera.【Result】 After immunization, the antibody titers in serum of 4 mice were all more than 104.After isolated mouse with the highest immune response spleen cells were fused with SP2/0 cells total of 8 of them were positive cell lines were obtained after selective culture.5D5 and 7G6 were identified as strong positive strains with stable antibody secretion.After multiple subcloning screens and subcultures, the antibodies secreted in the cell supernatant were stable, with titers of 29 and 210 respectively, with ascites titers of 107 and 108.Western blotting and antibody subtype identification kits identified that the two antibodies were IgG1 type and the light chain was kappa type, both of which could specifically bind FgESP.According to the same antigen site was recognized by the two kinds of antibodies, the antigen titer of the two monoclonal antibodies were comparied, 7G6 was used as the coating antibody, and anti-rFgCat L1 was used as the enzyme-labeled secondary antibody.The optimized condition of method was that 7G6 was coated at a concentration of 2 μg/mL, the dilution concentration of anti-rFgCat L1 polyclonal antibody was 25 μg/mL, the dilution of Don-HRP-conjugated was 1∶4 000, 5% skimmed milk powder was selected as the blocking solution and the color development time was 25 min.The method was proved that could recognize the lowest antigen concentration of 0.625 μg/mL, also could specifically recognize antigen of Fasciola fasciatus.The constructed sandwich ELISA method was used for antigen detection of 47 dairy cow positive serum and 47 goat positive serum infective samples kept in the laboratory and the positive antigen rate were 72.3% and 78.7%, respectively.【Conclusion】 Anti-rFgCat L1 monoclonal antibody was successfully prepared and the double-sheet sandwich ELISA method for fascioliasis was constructed, which provided a good theoretical basis and material basis for the development of low-cost and rapid diagnostic kits. 相似文献
980.