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991.
992.
采用高效液相色谱法测定盐酸氨丙啉的含量及对杂质2-甲基吡啶进行检查.用Waters XTerraTM RP C18色谱柱,以乙腈-甲醇-庚烷磺酸钠溶液(将12 g的1-庚烷磺酸钠溶于1000 mL水中,加24mL冰醋酸,6 mL的三乙胺制得)(5:35:60)为流动相,用紫外检测器于254nm处检测,柱温30℃,流速1.0 mL/min.在该条件下盐酸氨丙啉和2-甲基吡啶的分离度很好,盐酸氨丙啉浓度在0.05~0.50 mg/mL范围内,其色谱峰面积与浓度呈良好的线性关系,回归方程为y=3.07×107x-3.90×104,r=0.999 9,RSD=0.76%.该法适用于盐酸氨丙啉原料药的质量控制. 相似文献
993.
GUO Wen-yi YANG Yong JIA Guo-liang ZHANG Rong-qing ZHANG Qing LI Jing-xia GAO Hao-kao 《园艺学报》2005,21(1):72-76
AIM: To examine the effects of L-carnitine on apoptosis and oxidant injury in cultured neonatal rat cardiomyocytes induced by hypoxia/reoxygenation and its possible mechanism. METHODS: The cultured cardiomyocytes were divided into three groups, control, A/R group (anoxia for 120 min, reoxygenation for 240 min) and L-carnitine treatment group, in which cells were exposed to 20 mg/L, 50 mg/L, 100 mg/L, 200 mg/L L-carnitine respectively at 2 h before anoxia. The superoxide dismutase (SOD), succinate dehydrogenase (SDH) activities and malondialdehyde (MDA) content were examined, and the apoptosis was determined by flow of cytometry (FCM). In addition, the ultrastructure was observed by transmission electron microscopy. RESULTS: In A/R group, SOD and SDH activities were lower, the apoptosis rate and MDA content were higher than those in control group (P<0.05). In L-carnitine treatment group, SOD and SDH activities were higher, the apoptosis rate and MDA content were lower than those in A/R group, a L-carnitine concentration-dependent effect was found. Moreover, impairment of myocardial ultrastructure was more severe in A/R group than L-carnitine treatment group. CONCLUSION: L-carnitine can protect cardiomyocytes against hypoxia/reoxygenation-induced injury in a dose-dependent manner. 相似文献
994.
ZHANG Zhan JIA Li-ting HOU Lei WANG Xue-mei CHANG Cai-hong YANG Ru-jing ZHANG Xi LIU Sheng-hong ZHENG Fang GONG Fei-li 《园艺学报》2005,21(12):2457-2461
AIM: To detect the effects of NK cells on the etiology of severe pre-eclampsia. METHODS: The peripheral blood and umbilical blood from severe pre-eclamptic patients and normal late pregnant women were collected. NK cells were seperated in percoll and counted by SAP. The proliferating ability of NK cells was measured by MTT and killing power of NK cells was determined by [51Cr] releasing test. The immunohistochemistry method was used to detect the quantity of NK cells and the expression of HLA-G in placenta of them. RESULTS: (1) Compared with that in normal late pregnant women, the counts of the NK cells in peripheral blood, umbilical blood and decidua of severe pre-eclamptic patients were significantly higher (all P<0.05). (2) Compared with that in normal late pregnant women, proliferating and killing ability of NK cells in peripheral blood and umbilical blood of severe pre-eclamptic patients were significantly higher. (3) The expression of HLA-G protein in placenta of severe pre-eclampsia group was lower than that in normal group (P<0.05). CONCLUSION: The quantity of NK cells in severe pre-eclamptic patients is increased with stronger biologic function. They may be related with the pathogenesis of severe pre-eclampsia. 相似文献
995.
初生型发光杆菌属(Photorhabdus)及嗜线虫致病杆菌属(Xenorhabdus)细菌分别与异小杆线虫属(Heterorhabdltis)和斯氏线虫属(Steinernema)昆虫病原线虫互惠共生。这类昆虫病原细菌在稳定生长期分别产生两种形态各异的胞内晶体蛋白。本文回顾了这类蛋白的研究历史和最新的研究进展,特别是胞内晶体蛋白的理化性质和生物学功能,同时讨论这种晶体蛋白的研究方法与技术。 相似文献
996.
997.
JIA Zhan-jun YU Xue-qing WANG Xin LI Xiao-yan CHEN Wen-fang PENG Wen-xing DOU Xian-rui HAO Wen-ke SUN Liao ZHENG Zhi-hua YIN Pei-da 《园艺学报》2005,21(7):1298-1304
AIM: To observe the effect of antibiotic treatment on the inflammatory mediator expression in peritoneum and the peritoneal transport function in rats with acute peritonitis, and explore its mechanisms. METHODS: Eighty-six SD rats were randomly divided into three groups. Control group (n=28) were treated with PBS (ip), peritonitis group (n=28) and treatment group (n=28) were challenged with the E.coli (ip), but at 3 h and 9 h gentamicin was given (ip) in treatment group. Seven rats of every group were randomly sacrificed at 24 h, 48 h, 72 h and 7 d. Peritoneal equilibration test (PET) was did before they were killed. Leukocyte count, pathological changes and the expression of CD45, NF-κB, IL-1β, TNF-α in peritoneum were examined. RESULTS: (1)The blood leukocytes in peritonitis group decreased strikingly, but did not change obviously in other two groups. The peritoneal fluid leukocytes in peritonitis group increased significantly from 24 h to 72 h, while in treatment group, it enhanced more strikingly than peritonitis group at 24 h, and recovered earlier. (2) Both in peritonitis group and treatment group, the expression of activated NF-κB, IL-1β, TNF-α and CD45 increased significantly, but the treatment group was lower than model group at 48 h and 72 h. The mRNA level of IL-1β and TNF-α had the same trend as their protein expression. (3) Compared with the control group, UF and D/D0 Glu decreased significantly in model group and treatment group, and D/PTP increased dramatically. The D/P TP in treatment group lowered obviously compared with peritonitis group, while the net UF and D/D0 Glu had not significant difference between treatment group and model group. CONCLUSION: Antibiotic treatment can partly decrease the expression of inflammatory mediators in peritoneum of rats with acute peritonitis and also can improve the protein transport ability to some extent, but can not improve the peritoneal ultrafiltration and the glucose transport function. 相似文献
998.
AIM: To study the effects of intrathymic inoculation of liver specific antigen (LSA) on hepatocyte apoptosis after liver allotransplantation. METHODS: Orthotopic liver transplantation was used in this study. Group Ⅰ: syngenic control (Wistar-to-Wistar); Group Ⅱ: acute rejection (SD-to-Wistar); Group Ⅲ: thymus inoculation of SD rat LSA day 7 before transplantation. The observation of general situation and survival time, hepatocyte apoptosis and LAT expression in liver transplants were used to analyze immune state of animals in different groups. RESULTS: The general situation of group Ⅰ was very well after transplantation. Recipients of groupⅡ lost body weight progressively and all died within day 9 to day 13 post transplantation. As for group Ⅲ, the general situation of recipients was remarkably better than that in group Ⅱ. The positive cells of apoptosis in group Ⅲ detected by TUNEL were not significantly different from that in group Ⅰ, but was significantly lower than that in group Ⅱ. LAT was detected at any time in group Ⅱ with peak expression at day 5 and day 7 post transplantation. In contrast, LAT was not detected in any other groups. CONCLUSION: Intrathymic inoculation of LSA protects hepatocytes from apoptosis after liver allotransplantation. 相似文献
999.
1000.