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41.
E.coli产Ampli Taq DNA聚合酶的分离纯化 总被引:1,自引:0,他引:1
将含有Taq DNA聚合酶基因的E.coli经发酵,细胞培养液经破壁裂解,粗蛋白抽提Sephaeryl-s-100,CM-Sephadex C50柱层析等纯化步骤,可获得电泳纯的重组Taq DNA聚合酶,用于科研和检测工作。 相似文献
42.
Pretreatment of rats with the extract of Ginkgo biloba termed EGb761 reduced the behavioral sensitization induced by successive
-amphetamine administrations (0.5 mg/kg) as estimated by increasing values of locomotor activity. EGb761 pretreatment also prevented the reduced density of [3H]dexamethasone binding sites in the dentate gyrus and the CA1 hippocampal regions of
-amphetamine treated animals. These observations suggest that EGb761, by reducing glucocorticoid levels, could modulate the activity of the neuronal systems involved in the expression of the behavioral sensitization. 相似文献
43.
Ian Eastwood Philip J. Forshaw Jeyarajah Jeyeratnam Laszlo Magos 《Archives of toxicology》1977,37(3):237-240
The arrhythmogenic effect of 8 g/kg noradrenaline given i.v. was increased in male rats pretreated 1–2 day s earlier with phenobarbitone and starved from the time of the first phenobarbitone injection (80 mg/kg followed by 50 mg/kg 6 h later). Daily exposure to 4.0 mg/l CS2 (first exposure 24 h after the first phenobarbitone injection) for 4 h prevented the decline in susceptibility on the 3rd and 4th days after phenobarbitone, when the reaction of unexposed rats to noradrenaline returned to normal. 相似文献
44.
目的:观察纯中药制剂银康颗粒剂治疗银屑病的,临床疗效及治疗前后患者血粘度的变化。方法:将382例患者随机分为2组,治疗组252例应用银康颗粒剂治疗,对照组130例应用复方青黛胶囊治疗;对治疗组部分病例(212例)治疗前后血粘度指标进行观察。结果:治疗组治愈148例,好转82例,未愈22例,总有效率为91.12%;对照组治愈51例,好转46例,未愈33例,总有效率为74.62%,2组总有效率比较,差异有非常显著性意义(P<0.01)。治疗组患者治疗前后全血粘度差异无显著性意义(P>0.05),血浆粘度差异有显著性意义(P<0.05)。结论:风邪外袭、血虚生风、气滞血瘀是致病的主要原因。治疗应以清热祛风与养血活血并举。 相似文献
45.
循经穴位推拿治疗肩周炎临床观察 总被引:1,自引:1,他引:1
根据肩周炎局部压痛点的经络所属,运用循经推拿治疗肩周炎88例(治疗组),并与常规推拿治疗肩周炎102例(对照组)比较,疗程为3周.结果两组的总有效率分别为100%、89.2%(P<0.05);复发率分别为12.5%、26.4%(P<0.05). 相似文献
46.
The dopamine D3 receptor antagonist nafadotride inhibits development of locomotor sensitization to amphetamine 总被引:6,自引:0,他引:6
Richtand NM Logue AD Welge JA Perdiue J Tubbs LJ Spitzer RH Sethuraman G Geracioti TD 《Brain research》2000,867(1-2):239-242
Behavioral sensitization is a well-studied model of behavioral plasticity mediated at least in part by dopaminergic systems believed to play an important role in several psychiatric conditions. In the rodent, locomotion is regulated by the opposing balance of D3 and D2 receptors, with D2 activation increasing and D3 stimulation inhibiting locomotion. However, receptor occupancy of D3 dopamine receptors is far greater than D2 or D1 occupancy at typical post-stimulant dopamine concentrations. We therefore hypothesized that tolerance of D3 receptor inhibition of locomotion contributes to the development of sensitization. To test this hypothesis, we examined the effect of the D3 receptor antagonist nafadotride on sensitization. As predicted, nafadotride inhibits augmentation of the locomotion response to repetitive amphetamine. This finding is consistent with the proposed model of adaptive down-regulation of D3 dopamine receptor function contributing to the development of behavioral sensitization. 相似文献
47.
48.
本文介绍He-Ne激光沿经络自动照射仪的结构、特点,分析了激光与组织相互作用的物理效应和生物效应,提出了该仪器在针灸临床中的应用。 相似文献
49.
Wei Zhang Ming Lei Qianwen Wen Dunke Zhang Guangcheng Qin Jiying Zhou Lixue Chen 《The journal of headache and pain》2022,23(1)
BackgroundThe pathogenesis of chronic migraine remains unresolved. Recent studies have affirmed the contribution of GLUA1-containing AMPA receptors to chronic migraine. The dopamine D2 receptor, a member of G protein-coupled receptor superfamily, has been proven to have an analgesic effect on pathological headaches. The present work investigated the exact role of the dopamine D2 receptor in chronic migraine and its effect on GLUA1-containing AMPA receptor trafficking.MethodsA chronic migraine model was established by repeated inflammatory soup stimulation. Mechanical, periorbital, and thermal pain thresholds were assessed by the application of von Frey filaments and radiant heat. The mRNA and protein expression levels of the dopamine D2 receptor were analyzed by qRT‒PCR and western blotting. Colocalization of the dopamine D2 receptor and the GLUA1-containing AMPAR was observed by immunofluorescence. A dopamine D2 receptor agonist (quinpirole) and antagonist (sulpiride), a PI3K inhibitor (LY294002), a PI3K pathway agonist (740YP), and a GLUA1-containing AMPAR antagonist (NASPM) were administered to confirm the effects of the dopamine D2 receptor, the PI3K pathway and GULA1 on central sensitization and the GLUA1-containing AMPAR trafficking. Transmission electron microscopy and Golgi-Cox staining were applied to assess the impact of the dopamine D2 receptor and PI3K pathway on synaptic morphology. Fluo-4-AM was used to clarify the role of the dopamine D2 receptor and PI3K signaling on neuronal calcium influx. The Src family kinase (SFK) inhibitor PP2 was used to explore the effect of Src kinase on GLUA1-containing AMPAR trafficking and the PI3K signaling pathway.ResultsInflammatory soup stimulation significantly reduced pain thresholds in rats, accompanied by an increase in PI3K-P110β subunit expression, loss of dopamine receptor D2 expression, and enhanced GLUA1-containing AMPA receptor trafficking in the trigeminal nucleus caudalis (TNC). The dopamine D2 receptor colocalized with the GLUA1-containing AMPA receptor in the TNC; quinpirole, LY294002, and NASPM alleviated pain hypersensitivity and reduced GLUA1-containing AMPA receptor trafficking in chronic migraine rats. Sulpiride aggravated pain hypersensitivity and enhanced GLUA1 trafficking in CM rats. Importantly, the anti-injury and central sensitization-mitigating effects of quinpirole were reversed by 740YP. Both quinpirole and LY294002 inhibited calcium influx to neurons and modulated the synaptic morphology in the TNC. Additional results suggested that DRD2 may regulate PI3K signaling through Src family kinases.ConclusionModulation of GLUA1-containing AMPA receptor trafficking and central sensitization by the dopamine D2 receptor via the PI3K signaling pathway may contribute to the pathogenesis of chronic migraine in rats, and the dopamine D2 receptor could be a valuable candidate for chronic migraine treatment.Supplementary InformationThe online version contains supplementary material available at 10.1186/s10194-022-01469-x. 相似文献
50.
The purpose of this work was to study the possibility of neutralizing high-calcium fly ash expansion during hydration. The object of the study was the fly ash of Berezovskaya GRES, which is capable of independent setting and hardening. The test in the Le Chatelier molds showed that the divergence of indicator arms was 90–100 mm 1 day after mixing with water. The expansion and cracking of the fly ash could be completely prevented by silica fume addition in an amount of 42.9% by weight of the fly ash. At the same time, the compressive strength of specimens from the fly ash–sand paste in a ratio of 1:5 at the age of 28 days was 1.47 MPa. The isothermal heat release at a temperature of 20 °C for 10 days reached 500 kJ/kg. XRF and DTA results showed that free lime in the fly ash was completely hydrated in 11 days and gave the greatest expansion in the absence of silica fume. The presence of silica fume made the lime hydration incomplete and decreased the expansion. Unslaked free lime remained in the system. Exothermic data showed that silica fume inhibited CaO hydration from the reaction start. 相似文献