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1.
ABSTRACT: To clarify the quantitative changes in the transport of orally intubated protein into the blood circulation as macromolecules in development, immunoglobulin Y (IgY) extracted from chicken eggs was administered orally to juvenile Japanese eel, Anguilla japonica . For the first experiment, which was performed before the commencement of artificial feeding, the oral delivery of 2.0 μg/0.1 g bodyweight of IgY resulted in a rapid increase in plasma IgY to a maximum of 2.30 μg/mL. However, the transport of IgY into the blood decreased significantly in the experiments that followed, which were performed after 12, 25 and 42 days. During this period, bodyweight increased approximately by a factor of eight, and rapid growth of the stomach was observed histologically. Possible contributions for the development of the alimentary canal to the diminishment of intestinal protein assimilation are discussed.  相似文献   
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AIM: To examine the expression and distribution of tumor necrosis factor-α (TNF-α), tumor necrosis factor receptor I (TNFR I) and apoptosis in oral lichen planus, and evaluate their roles and relation in the oral lichen. METHODS: Immunohistochemical technique and TUNEL were employed to study the expression of TNF-α, TNFR I and apoptosis in 50 cases of oral lichen planus and 10 normal oral mucosa specimens. RESULTS: Compared with the normal control group, TNF-α expression was upregulated in mononuclear cells in lamina propria and decreased in keratinocytes in oral lichen planus lesion (P<0.05). On the contrary, TNFR I expression was increased in keratinocytes and decreased in lamina propria in oral lichen planus lesion (P<0.05). The increased apoptosis index in keratinocytes and the decreased apoptosis index in lamina propria were found in oral lichen planus (P<0.05). CONCLUSION: The accelerated apoptosis of keratinocytes and the inhibition of lymphocytes apoptosis may contribute to the formation and progression of oral lichen planus.  相似文献   
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为研究酵母多糖(YP)对环磷酰胺(CTX)所致免疫损伤大鼠的拮抗作用,本实验将80只雄性SD大鼠随机分为YP(50 mg/kg)+CTX组、YP(100 mg/kg)+CTX组、YP(200 mg/kg)+CTX组、CTX对照组和正常对照组。YP+CTX组按剂量灌胃并称重,CTX和正常对照组则灌胃给予等量生理盐水,连续给药10 d;在第8 d、9 d,除正常对照组外,其余4组腹腔注射CTX 100 mg/kg。第11 d采血及对相关的免疫器官组织进行检测。结果显示,YP(100 mg/kg)组平均日增重和饲料报酬比正常对照组显著增加(p<0.05);胸腺指数,血清中IgA、IgG、表皮生长因子(EGF)、碱性磷酸酶(AKP)含量及空肠SIgA水平显著(p<0.05)或极显著(p<0.01)高于CTX对照组;结肠壁中前列腺素E2(PGE2)含量与CTX对照组相比显著降低(p<0.05)。以上结果表明,YP能提高大鼠的生长性能;YP对CTX所致免疫损伤具有一定的拮抗保护作用,其中100 mg/kg剂量的YP效果最为显著。  相似文献   
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利用微量液体组织块贴壁法原代培养分离新生广西巴马小型猪肾成纤维细胞,进行常规传代培养、冷冻和复苏;通过接触抑制和解除抑制研究该类细胞的增殖潜力,免疫荧光进行鉴定;并通过脂质体介导对分离到的新生广西巴马小型猪肾成纤维细胞分别进行EGFP-N1和DsRed-N1基因转染。结果成功分离到新生广西巴马小型猪肾成纤维细胞,体外可以大量传代和冷冻,目前已经传至50代以上,生长良好;冷冻复苏和接触抑制解除后仍可以正常培养和传代;细胞免疫荧光检测,波形蛋白表达阳性,角形蛋白表达阴性;转染48h后荧光显微镜下可以观察到绿色荧光和红色荧光,表明瞬时转染新生广西巴马小型猪肾成纤维细胞可以获得成功,其中转染DsRed-N1基因的新生广西巴马小型猪肾成纤维细胞已经传至60代以上。结果表明,本试验成功建立了新生广西巴马小型猪肾成纤维细胞的体外培养体系,在体外能稳定培养和传代,并可以成功获得转基因的新生广西巴马小型猪肾成纤维细胞。  相似文献   
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目的为开发中药防治畜禽沙门氏菌病,根据沙门氏菌病中兽医辩证进行中药组方,为今后畜禽养殖减抗限抗的替代疗法提供参考。方法采用倍比稀释法检测复方板蓝根口服液对鸡白痢沙门氏菌的最小抑菌质量浓度(minimum inhibitory concentration,MIC)和最小杀菌质量浓度(minimum bactericidal concentration,MBC),扫描电镜观察菌体形态变化。试验选取150羽1日龄雏鸡,随机取出30羽做空白组,其余120羽人工感染鸡白痢沙门氏菌,制备雏鸡感染模型。将感染雏鸡随机分为模型组、中药治疗组、西药治疗组和中药预防组,每组30羽。观察雏鸡的发病率及死亡率。于治疗后1、3和5 d检测血清中IL-1β和TNF-α的含量;实时荧光PCR检测禽β-防御素6 (avian beta-defensin 6,AvBD6) 和鸡Toll样受体15 (chicken toll-like receptor 15,ChTLR15) 在雏鸡小肠中的转录水平。结果体外试验结果显示:MIC和MBC分别为62.5和125 mg/mL;扫描电镜下可见菌体出现溢缩,断裂形成许多残体,形状不规则。中药预防组可降低雏鸡的发病率及死亡率。与模型组相比,中药预防组和中药治疗组均可降低IL-1β和TNF-α含量。而ChTLR15和AvBD6在感染初期表达量高,治疗后期趋于正常。结论复方板蓝根口服液对鸡白痢沙门氏菌有明显的抑制作用,其杀菌机制是通过改变菌体的形态结构使细菌丧失活性。试验证实复方板蓝根口服液可有效预防雏鸡沙门氏菌感染,并能有效降低体内炎性因子水平,减轻炎症反应。  相似文献   
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Oral squamous cell carcinoma (OSCC) is the most common oral epithelial malignancy in dogs. It exhibits locally aggressive biological behaviour with the potential to metastasize, and a reported 1-year survival rate of 0% when left untreated. Expression studies suggest that aberrant MAPK signalling plays a key role in canine OSCC tumorigenesis, which is consistent with BRAF and HRAS MAPK-activating mutations reported in some tumours. Several morphological subtypes of canine OSCC have been described, with papillary, conventional, and basaloid as the most common patterns. We hypothesized that mutational differences may underlie these phenotypic variations. In this study, targeted Sanger sequencing and restriction fragment length polymorphism assays demonstrate that up to 85.7% of canine papillary OSCC (n = 14) harbour a BRAF p.V595E mutation. Assessment of neoplastic epithelial cell proliferation using Ki67 immunolabelling (n = 10) confirmed a relatively high proliferation activity, consistent with their known aggressive clinical behaviour. These findings underscore a consistent genetic feature of canine papillary OSCC and provide a basis for the development of novel diagnostic and targeted therapeutic approaches that can improve the quality of veterinary care.  相似文献   
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利用植物生物反应器生产口服疫苗已成为目前研究的热点。与传统疫苗相比,植物源性疫苗具有安全、稳定、高效和廉价等优点。植物作为生产疫苗的载体可将抗原表达于植物的可食部位。当植物被食用或饲喂时,植物源性疫苗可激发保护性的黏膜免疫应答。综述了植物源性口服疫苗的原理,并对可能出现的问题及解决途径进行了探讨。  相似文献   
10.
AIM To investigate the role of p300 in aging-related atrial fibrosis in human atrial fibroblasts (HAFs) and its potential mechanism. METHODS HAFs were obtained from human left atrial tissue, and the senescence model was established by cell passage. Senescence-associated β-galactosidase (SA-β-Gal) staining was used to detect the cell senescence, and Western blot was used to determine the protein levels of p300, p53, Smad3 and other senescence and fibrosis associated proteins in HAFs. RESULTS Compared to passage 3 HAFs, the proportion of senescent cells, and the protein levels of p300, p53, p-Smad3 and other senescence and fibrosis associated proteins were increased in HAFs at passage 7 and 11 (P<0.05). After treated with curcumin (a p300 inhibitor) or transfection with p300 small-hairpin (sh) RNA plasmid, the protein levels of p300, and the senescence and fibrosis associated proteins were decreased in HAFs at passage 7(P<0.05). Up-regulation of p300 by transfection with p300 over-expression plasmid increased the protein levels of p53, Smad3 and MMP-2 in HAFs at passage 3 (P<0.05). CONCLUSION p300/p53/Smad3 signaling pathway plays an important role in aging-related atrial fibrosis in HAFs.  相似文献   
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