首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
  示例: 沙坡头地区,人工植被区,变化  检索词用空格隔开表示必须包含全部检索词,用“,”隔开表示只需满足任一检索词即可!
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   41638篇
  免费   2103篇
  国内免费   709篇
耳鼻咽喉   105篇
儿科学   596篇
妇产科学   321篇
基础医学   5283篇
口腔科学   670篇
临床医学   2854篇
内科学   4671篇
皮肤病学   242篇
神经病学   3924篇
特种医学   1047篇
外国民族医学   2篇
外科学   1521篇
综合类   3196篇
现状与发展   2篇
预防医学   4201篇
眼科学   160篇
药学   10309篇
  23篇
中国医学   3830篇
肿瘤学   1493篇
  2024年   567篇
  2023年   698篇
  2022年   1187篇
  2021年   1455篇
  2020年   1330篇
  2019年   1313篇
  2018年   1257篇
  2017年   1348篇
  2016年   1261篇
  2015年   1185篇
  2014年   2006篇
  2013年   3233篇
  2012年   1778篇
  2011年   2194篇
  2010年   1469篇
  2009年   1740篇
  2008年   1731篇
  2007年   1701篇
  2006年   1436篇
  2005年   1276篇
  2004年   1124篇
  2003年   1009篇
  2002年   900篇
  2001年   854篇
  2000年   649篇
  1999年   659篇
  1998年   669篇
  1997年   579篇
  1996年   562篇
  1995年   536篇
  1994年   460篇
  1993年   446篇
  1992年   450篇
  1991年   413篇
  1990年   386篇
  1989年   391篇
  1988年   347篇
  1987年   339篇
  1986年   325篇
  1985年   444篇
  1984年   400篇
  1983年   279篇
  1982年   352篇
  1981年   277篇
  1980年   284篇
  1979年   208篇
  1978年   221篇
  1977年   159篇
  1976年   194篇
  1975年   79篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
951.
背景:目前的研究大多为单味中药或单一中药成分对体外培养人牙周膜细胞的影响,而中药组方提取液对体外培养细胞影响的研究较少。目的:观察中药双黄补对体外培养的人牙周膜细胞增殖活性的影响。设计、时间及地点:对比观察实验,于2008-11/2009-02 在河北医科大学第四医院科研中心完成。材料:人牙周膜细胞组织选自河北医科大学第四医院口腔科要求手术拔除的埋伏多生牙者。黄连、黄芩、骨碎补均购自河北医科大学第四医院中药房。方法:采用组织块法体外培养人牙周膜细胞。水提醇沉法制备双黄补提取液。以每 1 mL药液含生药 1 g加入体积分数20%的胎牛血清培养液,稀释成质量浓度为10,25,50,100,150,200,250,500,750,1 000 mg/L,分别作用于体外培养的人牙周膜细胞,以不加双黄补提取液的培养细胞为对照。主要观察指标:采用四甲基偶氮唑蓝法测定培养细胞增殖活性的变化,应用流式细胞术检测100 mg/L的双黄补提取液对牙周膜细胞周期的变化和对成纤维细胞生长因子18水平的影响。结果:双黄补对人牙周膜细胞的增殖活性的影响存在质量浓度和时间效应,各质量浓度双黄补均能促进体外培养人牙周膜细胞的增殖活性,其中以100 mg/L质量浓度促增殖活性作用最明显(P < 0.01),相同质量浓度不同作用时间对细胞促增殖活性作用也不同,以48 h作用最明显(P < 0.05)。与对照组相比,100 mg/L的双黄补促进牙周膜细胞成纤维细胞生长因子18水平增高,S期和G2M期细胞数目增多,在48 h最明显。结论:中药双黄补可增强人牙周膜细胞的增殖活性,具有明显的浓度效应和时间效应。  相似文献   
952.
    
Drosophila adults, when placed into a novel open‐field arena, initially exhibit an elevated level of activity followed by a reduced stable level of spontaneous activity and spend a majority of time near the arena edge, executing motions along the walls. In order to determine the environmental features that are responsible for the initial high activity and wall‐following behavior exhibited during exploration, we examined wild‐type and visually impaired mutants in arenas with different vertical surfaces. These experiments support the conclusion that the wall‐following behavior of Drosophila is best characterized by a preference for the arena boundary, and not thigmotaxis or centrophobicity. In circular arenas, Drosophila mostly move in trajectories with low turn angles. Since the boundary preference could derive from highly linear trajectories, we further developed a simulation program to model the effects of turn angle on the boundary preference. In an hourglass‐shaped arena with convex‐angled walls that forced a straight versus wall‐following choice, the simulation with constrained turn angles predicted general movement across a central gap, whereas Drosophila tend to follow the wall. Hence, low turn angled movement does not drive the boundary preference. Lastly, visually impaired Drosophila demonstrate a defect in attenuation of the elevated initial activity. Interestingly, the visually impaired w1118 activity decay defect can be rescued by increasing the contrast of the arena's edge, suggesting that the activity decay relies on visual detection of the boundary. The arena boundary is, therefore, a primary object of exploration for Drosophila.  相似文献   
953.
    
The hippocampus is involved in segregating memories, an ability that utilizes the neural process of pattern separation and allows for cognitive flexibility. We evaluated a proposed role for adult hippocampal neurogenesis in cognitive flexibility using variants of the active place avoidance task and two independent methods of ablating adult‐born neurons, focal X‐irradiation of the hippocampus, and genetic ablation of glial fibrillary acidic protein positive neural progenitor cells, in mice. We found that ablation of adult neurogenesis did not impair the ability to learn the initial location of a shock zone. However, when conflict was introduced by switching the location of the shock zone to the opposite side of the room, irradiated and transgenic mice entered the new shock zone location significantly more than their respective controls. This impairment was associated with increased upregulation of the immediate early gene Arc in the dorsal dentate gyrus, suggesting a role for adult neurogenesis in modulating network excitability and/or synaptic plasticity. Additional experiments revealed that irradiated mice were also impaired in learning to avoid a rotating shock zone when it was added to an initially learned stationary shock zone, but were unimpaired in learning the identical simultaneous task variant if it was their initial experience with place avoidance. Impaired avoidance could not be attributed to a deficit in extinction or an inability to learn a new shock zone location in a different environment. Together these results demonstrate that adult neurogenesis contributes to cognitive flexibility when it requires changing a learned response to a stimulus‐evoked memory. © 2012 Wiley Periodicals, Inc.  相似文献   
954.
    
  相似文献   
955.
Introduction: Limb‐girdle muscular dystrophy type 2A (LGMD2A) is caused by a deficiency of calpain‐3/p94. Although the symptoms in most LGMD2A patients are generally homogeneous, some variation in the severity and progression of the disease has been reported. Methods: We describe 2 patients who carry the same combination of compound heterozygous mutations (pG222R/pR748Q) and whose symptoms are exceptionally benign compared to homozygotes with each missense mutation. Results: The benign phenotype observed in association with the combined pG222R and pR748Q mutations suggested that it may result from a compensatory effect of compound heterozygosity rather than the individual mutations themselves. Our analyses revealed that these two mutations exert different effects on the protease activity of calpain‐3, suggesting “molecular complementation” in these patients. Conclusion: We propose several hypotheses to explain how this specific combination of mutations may rescue the normal proteolytic activity of calpain‐3, resulting in an exceptionally benign phenotype. Muscle Nerve, 2011  相似文献   
956.
957.
958.
959.
    
Early cognitive deficit characteristic of early Alzheimer's disease seems to be produced by the soluble forms of β‐amyloid protein. Such cognitive deficit correlates with neuronal network dysfunction that is reflected as alterations in the electroencephalogram of both Alzheimer patients and transgenic murine models of such disease. Correspondingly, recent studies have demonstrated that chronic exposure to βAP affects hippocampal oscillatory properties. However, it is still unclear if such neuronal network dysfunction results from a direct action of βAP on the hippocampal circuit or it is secondary to the chronic presence of the protein in the brain. Therefore, we aimed to explore the effect of acute exposure to βAP25–35 on hippocampal network activity both in vitro and in vivo, as well as on intrinsic and synaptic properties of hippocampal neurons. We found that βAP25–35, reversibly, affects spontaneous hippocampal population activity in vitro. Such effect is not produced by the inverse sequence βAP35–25 and is reproduced by the full‐length peptide βAP1–42. Correspondingly βAP25–35, but not the inverse sequence βAP35–25, reduces theta‐like activity recorded from the hippocampus in vivo. The βAP25–35‐induced disruption in hippocampal network activity correlates with a reduction in spontaneous neuronal activity and synaptic transmission, as well as with an inhibition in the subthreshold oscillations produced by pyramidal neurons in vitro. Finally, we studied the involvement of Fyn‐kinase on the βAP25–35‐induced disruption in hippocampal network activity in vitro. Interestingly, we found that such phenomenon is not observed in slices obtained from Fyn‐knockout mice. In conclusion, our data suggest that βAP acutely affects proper hippocampal function through a Fyn‐dependent mechanism. We propose that such alteration might be related to the cognitive impairment observed, at least, during the early phases of Alzheimer's disease. © 2009 Wiley‐Liss, Inc.  相似文献   
960.
    
Previous studies have shown that mental imagery is a suitable tool to study the progression of the effect of practice on brain activation. Nevertheless, there is still poor knowledge of changes in brain activation patterns during the very early stages of physical practice. In this study, early and late practice stages of different kinds of locomotion (i.e., balanced and unbalanced) have been investigated using functional magnetic resonance imaging during mental imagery of locomotion and stance. During the task, cardiac activity was also recorded. The cerebral network comprising supplementary motor area, basal ganglia, bilateral thalamus, and right cerebellum showed a stronger activation during the imagery of locomotion with respect to imagery of stance. The heart beat showed a significant increase in frequency during the imagery of locomotion with respect to the imagery of stance. Moreover, early stages of practice determined an increased activation in basal ganglia and thalamus with respect to late stages. In this way, it is proposed the modulation of the brain network involved in the imagery of locomotion as a function of physical practice time. Hum Brain Mapp, 2010. © 2009 Wiley‐Liss, Inc.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号