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TSUYOSHI OHIRA HIDEKAZU KATAYAMA KATSUMI AIDA HIROMICHI NAGASAWA 《Fisheries Science》2003,69(1):95-100
ABSTRACT: Until now, six crustacean hyperglycemic hormones (CHH) designated Pej-SGP-I, -II, -III, -V, -VI and -VII have been characterized in the kuruma prawn Penaeus japonicus . All CHH consist of 72 amino acid residues and have an amidated carboxyl (C)-terminus. In the present study, we expressed Pej-SGP-III in methylotrophic yeast Pichia pastoris in order to obtain a large quantity of recombinant CHH possessing biological activity. A cDNA encoding Pej-SGP-III that had been previously cloned was processed by polymerase chain reaction (PCR) and the resulting product was ligated into an expression vector. Pichia pastoris was transformed with this vector after which a recombinant Pej-SGP-III was expressed having an additional amino acid residue (glycine) at the C-terminus (rPej-SGP-III-Gly), a form considered to be a putative precursor of this hormone. rPej-SGP-III-Gly secreted into the culture medium was purified by reversed-phase HPLC, and amidated using a peptidylglycine alpha-amidating enzyme. The amidated rPej-SGP-III (rPej-SGP-III) showed hyperglycemic activity in in vivo bioassay almost comparable to that of the natural Pej-SGP-III. rPej-SGP-III thus obtained will be a useful tool not only for its physiological study but also for the determination of its 3-D structure. 相似文献
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Evans EW Harmon BG 《Veterinary clinical pathology / American Society for Veterinary Clinical Pathology》1995,24(4):109-116
Cationic antimicrobial peptides are present throughout the plant and animal kingdoms and bear striking structural and functional similarities across species lines. They provide primitive, nonspecific means of combating a variety of bacteria, fungi, enveloped viruses, and protozoa. Some are also cytotoxic against host cells, including neoplastic cells. Cationic antimicrobial peptides may play various roles in inflammation and tissue repair. Antimicrobial peptides are found in epithelial tissues regularly exposed to microbial attack as well as in cells whose primary function is defense against potential pathogens. They constitute an important part of the nonoxidative antimicrobial arsenal of leukocytes. They are preformed and/or readily synthesized when the cells are stimulated by exposure to pathogens. They exert their effects directly by inserting into membranes of target cells and forming ion channels which increase membrane permeability; however, antimicrobial peptides can also act as opsonins to facilitate phagocytosis. Resistance to defensins is a virulence factor for organisms such as Salmonella sp. The study of cationic antimicrobial peptides is increasing our understanding of innate immunity, inflammation, and the pathogenesis of genetic diseases such as specific granule disease in humans. Therapeutic applications of antimicrobial peptides are currently under investigation. 相似文献
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Till Hornbogen Mirko Glinski Rainer Zocher 《European journal of plant pathology / European Foundation for Plant Pathology》2002,108(7):713-718
The cyclic hexadepsipeptide enniatin is known as a phytopathogenic compound from Fusaria causing necrosis and wilt. The molecule consists of three alternating residues each of a branched chain amino acid and D-hydroxyisovaleric acid (D-Hiv). Enniatins are synthesized by a 347kDa multienzyme (enniatin synthetase) via a thiol template mechanism. The corresponding gene esyn1 has an open reading frame of 9393 nucleotides and harbours two modules, one responsible for D-hydroxy acid activation and one for L-amino acid activation with an integrated N-methyltransferase domain. Such methyltransferases build an homologous group among N-methyl peptide synthetases. Enniatins are synthesized by step-wise condensation of dipeptidol building blocks in an iterative manner resembling fatty acid synthesis. A key enzyme in enniatin biosynthesis is the NADPH-dependent D-2-hydroxyisovalerate dehydrogenase, that supplies enniatin synthetase with D-Hiv. Enniatins contribute to the wilt toxic character of Fusaria. Virulence was significantly reduced in F. avenaceum after disruption of the esyn1 gene. 相似文献
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[目的]研究抗菌肽对抗生素耐药菌株的抑菌活性。[方法]利用抗性平板划线法从腹泻病牛血便中筛选分离出1株耐药菌,通过16S rDNA序列进行鉴定,采用琼脂孔穴扩散法通过梯度盐酸壮观霉素(spectinomycin,Spe+)、氨苄青霉素(ampicillin,Amp+)、硫酸卡那霉素(kanamycin,Kan+)和氯霉素(chloramphenicol,Cm+)试验确定该菌药敏特性,并利用1种抗菌肽制剂对该菌株进行药敏试验。[结果]经BLAST比对分析该菌16S rDNA序列,鉴定该耐药菌为科氏葡萄球菌(Staphylococcus cohnii),此菌对Amp+敏感,但对试验中其他抗生素均有耐药性,各梯度抗菌肽对该耐药菌均具有明显的抑菌活性。[结论]抗菌肽能有效抑制耐药科氏葡萄球菌的生长,有望在畜牧生产中代替抗生素使用。 相似文献
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试验旨在探究精料补充料中使用不同比例棕榈粕替代玉米对藏羊母羊肠道组织形态学、消化酶活性、pH、脂多糖以及抗氧化能力的影响。选取初始体重相近且健康的2~3月龄高原型藏羊母羊120只,随机分为4组,每组30只,每组6个重复,每个重复5只母羊,分别饲喂0%、15%、18%和21%水平的棕榈粕替代精料中玉米。试验期97d。结果显示:1)0%组与15%组间小肠各段的绒毛高度、绒毛宽度、隐窝深度、黏膜厚度以及绒毛高度/隐窝深度差异均不显著(P>0.05);2)0%组空肠的α-淀粉酶、纤维素酶、脂肪酶及糜蛋白酶显著或极显著小于15%组(P<0.05或P<0.01);3)0%组空肠的谷胱甘肽过氧化物酶、过氧化氢酶活性显著低于15%组与18%组(P<0.05),相较于21%组差异不显著(P>0.05);4)18%组与21%组空肠的脂多糖含量显著或极显著高于0%组(P<0.05或P<0.01),与15%组相比差异不显著(P>0.05)。由此可见,棕榈粕可替代部分玉米饲喂藏羊母羊,推荐替代玉米的比例为15%。 相似文献
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依据土壤水动力学理论,基于室内一维土柱入渗试验,选用稻壳、玉米秸秆、河沙3种材料作为添加物,分别将添加物以不同掺量与土壤均匀混合对苏打盐碱土进行入渗试验,从累计入渗量、入渗速率、湿润锋运移距离等方面研究苏打盐碱土在不同添加物及不同掺量下水分的入渗特性.结果表明:对照组土壤入渗量为3 mm·d-1,混掺1%稻壳、玉米秸秆... 相似文献
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玉米粗淀粉加酶挤压参数对抗性淀粉含量的影响 总被引:1,自引:0,他引:1
玉米粗淀粉是制作淀粉糖浆的主要原料之一,为探求玉米粗淀粉通过加酶挤压使玉米淀粉糖浆的DE和出品率增加、过滤速度加快、糖化时间缩短的原因,通过试验,用二次正交旋转组合试验设计安排试验,研究挤压蒸煮参数(套筒温度、物料含水率、螺杆转速、膨化中加酶量)对玉米粗淀粉中抗性淀粉含量的影响规律,得出通过挤压蒸煮技术可以使玉米粗淀粉中的抗性淀粉降低约4.5%,从而提高淀粉利用率。 相似文献
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