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991.
芸薹根肿菌严重危害大白菜和其他十字花科作物。由于根肿菌通常以多个生理小种混生状态进行侵染,导致抗病品种的抗性不能持久。以沈阳地区根肿菌为材料,进行了单孢分离技术体系构建,结果表明采取冷冻盒接菌法对两日龄大白菜幼苗进行单孢接种,可将侵染率提高到47.86%;采用基质过渡培养可将大白菜植株成活率提高到67%。利用上述根肿菌单孢分离技术体系对沈阳地区根肿菌进行单孢分离和Williams生理小种鉴定,结果表明沈阳地区根肿菌存在4号、8号、9号、11号生理小种,其中4号生理小种为优势小种。 相似文献
992.
CHEN Xiao-yan DENG Chun-yu KUANG Su-juan YANG Hui RAO Fang SHAN Zhi-xin LIN Qiu-xiong JIANG Li 《园艺学报》2017,33(1):128-132
AIM: To investigate the primary culture method for coronary artery smooth muscle cells (CASMCs), and to establish the endoplasmic reticulum stress (ERS) model in CASMCs of SD rats. METHODS: CASMCs were cultured by tissue explant method. The morphological characteristics were observed under optical microscope. The marker proteins of CASMCs, including α-SMA and SM-MHC, were identified by immunofluorescence technique. The protein expression levels of BiP and CHOP, the marker molecules of ERS, were determined by Western blot. RESULTS: The spindle-shaped CASMCs climbed out from the edge of coronary artery tissues after 6 d, and formed the typical "hill and valley" growth pattern of CASMCs at 9~10 d. The result of immunofluorescence technique showed that α-SMA and SM-MHC were positively expressed. The results of Western blot showed that the protein expression of BiP and CHOP in TG (1 and 2 μmol/L) treatment groups was increased compared with control group. Compared with control group, the protein expression of BiP and CHOP was significantly increased after 1 μmol/L TG treatment for 24 and 48 h. CONCLUSION: CASMCs can be successfully cultured by tissue explant method. ERS model of CASMCs was established by 1 μmol/L TG treatment for 24 h. 相似文献
993.
AIM: To detect the expression of miRNA-363 and SOX4 in osteosarcoma tissues and to investigate the effect of miRNA-363 on the viability and apoptosis of human osteosarcoma cell line MG-63.METHODS: Real-time PCR was used to detect the expression level and the relationship of miRNA-363 and SOX4 mRNA in the osteosarcoma tissues and the corresponding paratumorous tissues collected from 63 patients. The expression levels of miRNA-363 and SOX4 in osteosarcoma cell line MG-63 after transfected with miRNA-363 mimics were measured. The cell viability was measured by CCK-8 assay. Flow cytometry was used to monitor the changes of cell cycle and apoptosis. The changes of SOX4 and miRNA-363 expression levels in the MG-63 cells after transfection with SOX4 siRNA or pcDNA/SOX4 was detect by real-time PCR.RESULTS: The expressed level of miRNA-363 was lower, and the expression level of SOX4 was higher in the osteosarcoma tissues than those in the adjacent normal tissues. A significantly negative correlation between the expression levels of miRNA-363 and SOX4 was observed. The expression of miRNA-363 in the MG-63 cells after transfection with miRNA-363 mimics was significantly up-regulated, while the expression of SOX4 in the MG-63 cells was significantly down-regulated, with significant difference as compared with the cells transfected with miRNA-NC and control cells. The viability of MG-63 cells was inhibited, the cell cycle was arrested in G0/G1 phase, and the cell apoptosis was increased by transfection with miRNA-363 mimics. The relative protein expression levels of SOX4 in SOX4 siRNA group and pcNDA/SOX4 group were significantly different from those in negative control group, but the relative expression levels of miRNA-363 had no significant difference. Over-expression of SOX4 restored the viability of the MG-63 cells reduced by miR-363.CONCLUSION: The expression level of miRNA-363 is low in human osteosarcoma tissue. miRNA-363 may inhibits the viability of osteosarcoma cell line MG-63 and promotes cell apoptosis in vitro via inhibiting the SOX4 expression. 相似文献
994.
CHEN Wei-qian PENG Yan-ping ZHANG Wei-xi YE Le-ping DONG Liang XIA Xiao-dong 《园艺学报》2017,33(8):1481-1486
AIM: To investigate the effect of hypercapnia on hypoxia-induced pulmonary hypertension and the changes of lysyl oxidase (LOX) and extracellular matrix collagen cross-links in the rat. METHODS: Sprague-Dawley rats were randomly divided into 4 groups:normoxia group, hypoxia group, hypercapnia group and hypoxia+hypercapnia group. LOX activity was detected by fluorescence spectrophotometry. LOX protein expression was detected by immunohistochemistry and Western blot. The mRNA expression of LOX in the pulmonary artery was detected by real-time PCR. RESULTS: The levels of mean pulmonary artery pressure (mPAP), RV/(LV+S) and WA/TA in hypoxia group were significantly higher than those in normoxia group (P<0.01). Moreover, the levels of mPAP and RV/(LV+S) in hypoxia+hypercapnia group were significantly lower than those in hypoxia group (P<0.01). However, no significant difference of mPAP and RV/(LV+S) between hypercapnia group and normoxia group was observed. In hypoxia group, the collagen cross-links in the lung tissue was significantly higher than that in normoxia group and hypercapnia group (P<0.01). Importantly, collagen cross-links in the lung tissue of hypoxia+hypercapnia group was significantly lower than that in hypoxia group (P<0.01). There was no significant difference in collagen cross-links between hypercapnia group and normoxia group. The expression of LOX at mRNA and protein levels and its activity in the pulmonary arteries of hypoxia group were significantly increased as compared with normoxia group (P<0.01). Furthermore, the expression of LOX at mRNA and protein levels and its activity in the pulmonary arteries in hypoxia+hypercapnia group were lower than those in hypoxia group (P<0.01). CONCLUSION: Hypoxia not only up-regulates LOX but also promotes collagen cross-linking in the rat lung, which contributes to the development of pulmonary hypertension. Hypercapnia inhibits hypoxia-induced LOX expression and collagen cross-linking, therefore impairing the progress in hypoxia-induced pulmonary hypertension. 相似文献
995.
AIM: To investigate the effects of dexmedetomidine (DEX) on acute alcoholic hepatic injury in mice and to explore the possible mechanisms. METHODS: Kunming mice (n=50) were randomly divided into 5 groups (n=10): normal saline control (NS) group, acute alcoholic hepatic injury model (E) group, low-dose (10 μg/kg) DEX (E+L) group, medium-dose (50 μg/kg) DEX (E+M) group and high-dose (100 μg/kg) DEX (E+H) group. The animals were sacrificed at 6 h after gavage of alcohol or normal saline. The levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), triglyceride (TG), malondialdehyde (MDA), glutathione (GSH) and superoxide dismutase (SOD) were measured. The livers were removed for evaluation of histological characteristics and determining the content of tumor necrosis factor-α (TNF-α) amd interleukin-1β (IL-1β) in the liver tissues by ELISA. The expression levels of cytochrome P450 2E1 (CYP2E1) and nuclear factor-κB (NF-κB) in the liver tissues were evaluated by Western blot. RESULTS: Compared with NS group, the levels of ALT, AST and TG were obviously increased in E group, which were obviously decreased in E+M and E+H groups. Compared with NS group, the levels of TNF-α, IL-1β and MDA were obviously increase in E group, which were obviously decreased in E+M and E+H groups. Compared with NS group, the activity of SOD and the content of GSH were obviously decreased in E group, which were obviously increased in E+M and E+H groups. Compared with NS group, the expression of CYP2E1 and NF-κB was obviously increase in E group, which was obviously decreased in E+M and E+H groups. Compared with NS group, ethanol induced marked liver histological injury, which was less pronounced in E+M and E+H groups. CONCLUSION: DEX has a protective effect on mouse liver with acute alcoholic injury by the involvement in the processes of antioxidation and antiinflammation, and its mechanism may be associated with the inhibition of CYP2E1 and NF-κB expression. 相似文献
996.
AIM:To screen the lentiviral vector carrying siRNA with higher efficiency of suppressing the sphingosine-1-phosphate receptor 2(S1P2) gene expression in the primarily cultured corpus cavernosum smooth muscle cells of spontaneously hypertensive rats (SHR).METHODS:SHR and SD rats (n=5 each) were used for primarily culturing corpus cavernosum smooth muscle cells.The cells were randomly divided into 6 groups:SHR siRNA-1,SHR siRNA-2,SHR siRNA-3,SHR GFP,SHR control (SHR non-transfection group),and SD control (SD rat control group).Each group had 5 samples with 1.0×105 cells of each sample.At 72 h after transfection (MOI=60) with lentiviral vectors carrying S1P2 siRNA into the SHR corpus cavernosum smooth muscle cells,the expression of GFP was observed under fluorescence microscope.The protein expression of S1P2,ROCK1,ROCK2 and eNOS in the corpus cavernosum smooth muscle cells,and the mRNA expression of S1P2,ROCK1 and ROCK2 were determined by by Western blot and RT-PCR.RESULTS:The transfection efficiency of the corpus cavernosum smooth muscle cells in SHR siRNA-1,SHR siRNA-2,SHR siRNA-3 and SHR GFP groups were>80%.Compared with SHR control group,the mRNA levels and the protein expression of S1P2,ROCK1 and ROCK2 in SHR GFP group showed no remarkable changes,while those in SHR siRNA-1,SHR siRNA-2,SHR siRNA-3 and SD control groups were significantly lower than those in SHR control group (P<0.05).The protein expression of eNOS in SHR siRNA-1,SHR siRNA-2,SHR siRNA-3 and SHR GFP groups were not significantly changed as compared with SHR control group,but that in SD control group was significantly higher than that in SHR control group.CONCLUSION:Three groups of siRNA lentiviral vectors targeting S1P2 inhibit the expression of S1P2 in the corpus cavernosum smooth muscle cells of SHR,and by silencing the S1P2 expression,the expression of ROCK1 and ROCK2 is inhibited.Among them,siRNA-1 has the highest inhibitory efficiency. 相似文献
997.
六个猕猴桃品种在六盘水市的品比试验 总被引:1,自引:0,他引:1
以国内外较优6个猕猴桃品种为试材,利用引种技术进行品种的引进及筛选,综合评价各品种的物候期、适应性、果实品质等指标,以优化和调整六盘水猕猴桃品种结构,探明并确定贵州猕猴桃主产区六盘水市适应性较好的品种。结果表明:根据各品种的表现和"合理-满意度"分析,在六盘水表现较好的品种有"红阳",成熟期为8月中下旬,总糖含量为11.90%,口味香甜,果肉为红色,667m~2产量742.8kg,"金艳"成熟期为9月,667m~2产量1 018.6kg、单果质量118.43g、香味浓郁、果肉金黄色,"贵长"成熟期较晚,667m~2产量为1 401.7kg,香味较浓、果肉翠绿色;表现不好的品种有"西选2号""楚红",这2个品种产量均较低,果实口感一般;表现相对较好的品种有‘Hort 16A’口感较好,但抗病性较弱,"和平2号"单果质量156.80g,但667m~2产量仅有953.1kg,"海沃德"667m~2产量仅有703.6kg,表现不稳定。"红阳""金艳""贵长"在六盘水地区表现良好,适宜推广种植。 相似文献
998.
以浅色系厚皮甜瓜品种‘九红瑞’为试材,将有机氯杀菌剂(腐霉利,FML)和杀虫剂(高效氯氟氰菊酯,LJZ)分别配制成1 000倍和2 000倍药液,对开花后第15天的甜瓜果实进行单独喷施处理,在果实污染危害症状显现时,利用叶绿素荧光动力学技术对其污染效应进行分析和评价。结果表明:与对照相比(清水加助剂,CK),甜瓜果实在喷施有机氯农药后的第7天便开始产生明显的污染危害症状,且表现出多位点毒害特征,即不仅破坏原初光化学结构,还降低碳吸收动力学活性,更为重要的是增加光能过量耗散,引起光系统II(PSII)乃至整个光合机构的光抑制甚至光损伤,间接导致甜瓜果实表面组织的热灼伤斑点发生。通过模糊数学的隶属函数法对甜瓜果实受有机氯农药污染的程度进行综合评价,结果发现LJZ污染程度明显高于FML的,且随着喷施浓度的增大而增强。 相似文献
999.
为了解不同砧木对‘绿岭’核桃抗寒性的影响,以"中宁强""中宁异""加州黑"和"核桃"作砧木,嫁接‘绿岭’核桃的2年生幼树为试材,分别在-5、-10、-15、-20、-25、-30℃低温胁迫后,测定其1年生枝条的电解质渗出率、丙二醛含量、保护酶活性、渗透调节物质等指标,分析其耐寒能力。结果表明:随着胁迫温度的下降,4种砧木的‘绿岭’核桃枝条的电解质渗出率呈‘S’型上升趋势,"中宁强""中宁异""加州黑""核桃"砧木‘绿岭’核桃的半致死温度分别为-21.7、-22.3、-25.3、-22.8℃;丙二醛含量、保护酶活性、脯氨酸含量、可溶性糖和可溶性蛋白质含量变化均呈先升后降的趋势,丙二醛含量在-25℃出现峰值;保护酶活性、脯氨酸含量在-20℃出现峰值;可溶性糖和可溶性蛋白质含量峰值出现在-15℃;运用隶属函数法进行抗寒性综合评价,得出4种砧木‘绿岭’核桃抗寒顺序为"加州黑""核桃""中宁强""中宁异",表明在抗寒性方面,"加州黑"是适合‘绿岭’核桃的砧木。 相似文献
1000.