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21.
Bull’s eye rot is a typical quiescent postharvest apple disease in major fruit-growing areas. The susceptibility of different apple cultivars to Neofabraea spp. (N. vagabunda and N. malicorticis) was assessed, with Granny Smith showing the most resistance and Cripps Pink the most susceptibility. To assess the factors involved in conidial germination, Neofabraea spp. were grown on crude protein extracts (CPEs) collected from apple fruits at different storage periods. Fungal germ tube growth rate and pathogenic enzyme (cellulase and xylanase) activity were assessed. Results showed that CPEs collected after 2 and 4 months of storage progressively stimulated conidial germination and germ tube elongation, while a lesser effect was observed from CPEs after 1 month of storage. Xylanase proved to be the main degrading enzyme secreted by all the isolates, while cellulase was produced only by N. vagabunda isolates. Overall, the isolate ID02 was the most virulent, based on more rapid germ tube elongation and greater activity of the lytic enzymes.  相似文献   
22.
水稻温敏型叶色突变体是研究植物光合作用、叶绿体结构和功能以及温度影响叶绿体发育的理想材料。利用甲基磺酸乙酯(EMS)诱变籼型水稻(OryzasativaL.)三系保持系西农1B,从其后代中筛选到一个突变性状稳定遗传的温敏型叶片白化转绿突变体tsa2 (temperature-sensitive green-revertible albino 2)。与野生型相比, tsa2突变表型受温度影响, 22°C条件下萌发的野生型幼苗表型正常,而tsa2幼苗完全白化,且约40%白化苗死亡,存活白化苗的光合色素含量、光合速率均显著降低,成熟期主要农艺性状均显著变劣;在28°C下萌发的tsa2幼苗叶片呈浅绿色并伴有白条纹,其光合色素含量显著降低,光合速率及主要农艺性状差异较小; 32°C下萌发的tsa2幼苗叶片无明显差异。透射电镜观察显示,与野生型相比,tsa2在22°C下叶肉细胞中无叶绿体或存在异常发育叶绿体(尚未分化出基粒和基层),在28°C下部分叶肉细胞含少量发育完整的叶绿体,在32°C下叶肉细胞数量及形态均正常。实时荧光定量PCR(qRT-PCR)分析表明,与野生型相比,tsa2突变体中部分光合色素代谢途径基因、叶绿体发育相关基因及光合作用相关基因的表达水平呈不同程度变化。遗传分析表明, tsa2突变表型受一对隐性核基因控制, TSA2被定位于第5染色体SSR标记S5-57和S5-119之间,物理距离为718 kb。本研究为水稻遗传改良及研究温度影响叶绿体发育机制奠定了基础。  相似文献   
23.
[Objectives]This study aimed to explore the protective effect of Oxalis coriniculata L.on rats with acute liver injury induced by carbon tetrachloride(CCl4)and ...  相似文献   
24.
AIM: To investigate the effect of salvianolate on oxidative damage induced by hydrogen peroxide in human endothelial EA.hy926 cells.METHODS: EA.hy926 cells were cultured in vitro and divided into the following groups:control group, damage group, and anti-damage groups (salvianolate+damage groups). The cell viability was measured by CCK-8 assay. The migration ability of the EA.hy926 cells was detected by Transwell assay. The content of nitric oxide (NO) in the culture supernatant of the EA.hy926 cells was examined. The levels of vascular endothelial growth factor (VEGF) were detected by ELISA. The apoptosis,mitochondrial membrane potential and intracellular superoxide anion content of the EA.hy926 cells were analyzed by flow cytometry. The protein levels of caspase-3, cleaved caspase-3, Bcl-2, Bax, NF-κB and p53 were determined by Western blot. RESULTS: Compared with damage group, the viability of EA.hy926 cells pretreated with salvianolate at different concentrations was significantly increased (P<0.05). The apoptotic rate was significantly decreased (P<0.05). Savianolate enhanced the migration ability of the cells. The levels of VEGF, NO and mitochondrial transmembrane potential were increased (P<0.05), and the intracellular ROS level was significantly decreased (P<0.05). The protein levels of NF-κB, p53, Bax and cleaved caspase-3 were significantly decreased, and the protein level of Bcl-2 was markedly increased(P<0.05). CONCLUSION: Savianolate reduces the damage of EA.hy926 cells by hydrogen peroxide exposure, and its mechanism may be related to the blocking of NF-κB signaling pathway.  相似文献   
25.
海茄砧1 号是以野生茄子自交系HZ09-5 为母本,以从越南引进的茄子品种自交系HZ10-2 为父本育成的高抗青枯 病樱桃番茄砧木品种。植株生长势较强,第1 雌花节位约为第7 节,花为紫色,果实卵圆形,青熟果淡绿紫色或淡绿色,果 萼绿色,果长7~9 cm,果宽4~6 cm,单果质量为50~60 g,种子千粒重为3.2 g 左右,种皮浅黄色,高抗青枯病。海茄砧 1 号与樱桃番茄的嫁接亲和性好,共生性强,嫁接苗成活率高。嫁接后的樱桃番茄果萼开展,果面有光泽,可明显改善果实 VC、可溶性固形物和可滴定酸含量等品质,提高产量。适宜华南地区樱桃番茄的嫁接栽培。  相似文献   
26.
An agglutination test based on colored silica nanoparticles (colored SiNps) was established to detect serotypes of Pseudomonas aeruginosa. Monodisperse colored SiNps were used as agglutination test carriers. The colored SiNps were prepared through reverse microemulsion with reactive dyes, sensitized with 11 kinds of mono-specific antibodies against P. aeruginosa, and denoted as IgG-colored SiNps. Eleven kinds of IgG-colored SiNps were individually mixed with P. aeruginosa on a glass slide. Different serotypes of P. aeruginosa could be identified by agglutination test with evident agglutination. The P. aeruginosa could be detected in a range from 3.6 × 105 to 3.6 × 1012 cfu mL?1. This new agglutination test was confirmed to be a specific, sensitive, fast, easy-to-perform, and cost-efficient tool for the routine diagnosis of P. aeruginosa.  相似文献   
27.
红星302 是以抗病、耐低温弱光材料01-61 为母本,以01-23 为父本育成的串番茄一代杂种,无限生长类型,果实串收,果色亮红,果实椭圆形,酸甜适口,品质佳,VC 含量为364 mg · kg-1,可滴定酸0.44%,可溶性糖4.25%,平均单果质量30.79 g,硬度为11.40×105 Pa。单株结果数约为53个,产量4 900 kg ·( 667 m2-1 左右,高抗蕨叶病毒病、青枯病,适宜河北地区冬季日光温室和早春保护地栽培。  相似文献   
28.
以直立型扁蓿豆[Medicago ruthenica(L.)Sojak.cv.Zhilixing]为材料,于苗期连续干旱处理12 d后复水4 d,研究直立型扁蓿豆幼苗形态结构特征、生理代谢及生物量分配对干旱胁迫及复水的响应,揭示直立型扁蓿豆对干旱胁迫及复水的适应策略。结果表明:随着干旱胁迫时间延长,直立型扁蓿豆叶片气孔开放率逐渐降低,处理9 d后气孔及表皮细胞密度比正常浇水处理(CK)分别增加48.5%和36.6%,形成小而密的表皮细胞和气孔。生理上,除MDA含量随胁迫时间的延长逐渐增加外,其余指标均先升高后降低,干旱胁迫9 d时达最高,SOD、POD、叶绿素、可溶性糖、可溶性蛋白及脯氨酸分别较CK提高88.9%、111.2%、86.7%、140.5%、147.8%和124.6%。同时,生物量随胁迫时间的延长先增大后减小,于干旱胁迫9 d达最大值,比CK增加16.4%,总的分配格局表现出地上生物量投资高于地下,地下生物量投资比例随胁迫时间的延长逐渐增加,而地上生物量变化与其相反。复水后各指标均能恢复至CK水平或超过CK,表现出极强的复水敏感性和潜在恢复能力。该品种扁蓿豆对干旱胁迫及复水的适应主要分为3个时期:主动适应期,其生理参数的可塑性指数为形态参数的1.33倍,主要通过抗氧化及渗透调节来减少水分散失增加水分吸收、缓解氧化伤害以适应干旱逆境;被动适应期,其形态参数的可塑性指数为生理参数的1.31倍,主要采用牺牲生物量的生存策略以及降低色素含量减少光吸收的光保护机制来提高逆境下的生存能力;复水恢复期,根冠比、气孔开放率、气孔及表皮细胞密度比CK分别增加25.9%、29.7%、24.2%和16.3%,其较高的根冠比和叶片较高的气孔开放率及小而密的气孔及表皮细胞特征,保证了直立型扁蓿豆吸水能力以及水分运输效率的迅速恢复。综上,直立型扁蓿豆抗旱能力较强,能够通过形态生理的改变以及调整不同器官的生物量分配来应对与适应干旱逆境及复水,且在不同处理阶段采取不同的适应策略以达到生存目的。  相似文献   
29.
AIM:To explore the effect of pidotimod on the renal function in IgA nephropathy (IgAN) rat model, and to further study whether this effect is related to the inhibition of inflammatory response. METHODS:The SD rats (n=36) were randomly divided into control group, IgAN model group, IgAN with prednisone treatment group and IgAN with pidotimod treatment group, with 9 rats in each group. The IgAN model was induced by consecutive oral administration of bovine gamma globulin (BGG) for 8 weeks followed by injection of BGG through tail vein for 3 d. After the IgAN model was established, the drug was continuously used for 4 weeks. At the end of the treatment, the urine protein, serum creatinine and blood urea nitrogen were examined by an automated analyzer. IgA deposition in the renal tissues was observed by immunofluorescence staining. The mRNA expression levels of renal fibrosis markers transforming growth factor-β1 (TGF-β1) and fibronectin 1 in the renal tissues were detected by RT-qPCR. The mRNA and protein levels of pro-inflammatory cytokines interleukin-1β (IL-1β) and IL-6 in the renal tissues were determined by RT-qPCR and Western blot, respectively. RESULTS:No significant difference of the body weight was observed in different groups. Compared with control group, the content of urine protein, serum creatinine and blood urea nitrogen were significantly increased (P<0.01), whereas those were reversed by pidotimod treatment. The results of immunofluorescence staining showed that pidotimod inhibited IgA deposition in the IgAN rats. Pitomod treatment inhibited the mRNA expression levels of renal fibrosis markers TGF-β1 and fibronectin 1, and the mRNA and protein levels of pro-inflammatory cytokines IL-1β and IL-6 in the renal tissues of IgAN rats. CONCLUSION:Pidotimod alleviates IgAN progression in rats by inhibition of inflammatory response.  相似文献   
30.
AIM: To investigate the effects of astragaloside IV (AS-IV) on chemokine receptor 4 (CXCR4) and stromal cell-derived factor 1α (SDF-1α) in endothelial progenitor cells (EPCs) and its mechanism. METHODS: Rat bone marrow-derived EPCs were cultured in vitro. The proliferation, adhesion, migration, apoptosis and tube formation capacity of EPCs treated with AS-IV and AMD3100, a specific blocker of CXCR4, were observed. The effects of AS-IV on the expression of SDF-1α/CXCR4 at mRNA and protein levels and the protein level of p-CXCR4 in the EPCs were determined. RESULTS: AS-IV significantly enhanced the proliferation, adhesion, migration and tube formation abilities of EPCs, reduced the apoptosis of EPCs, and up-regulated the mRNA and protein expression of SDF-1α and CXCR4 and the p-CXCR4 protein level in the EPCs. On the other hand, AMD3100 blocked the up-regulating effect of AS-IV on the mRNA and protein expression of CXCR4 and the p-CXCR4 protein level in the EPCs, but did not affect the effect of AS-IV on the expression of SDF-1α. CONCLUSION: AS-IV might enhance the biological function of EPCs by regulating the expression of SDF-1α/CXCR in EPCs.  相似文献   
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