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:      
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   606篇
  免费   80篇
  国内免费   15篇
  2023年   14篇
  2022年   12篇
  2021年   29篇
  2020年   35篇
  2019年   52篇
  2018年   27篇
  2017年   29篇
  2016年   36篇
  2015年   27篇
  2014年   48篇
  2013年   63篇
  2012年   17篇
  2011年   28篇
  2010年   13篇
  2009年   23篇
  2008年   24篇
  2007年   18篇
  2006年   25篇
  2005年   15篇
  2004年   10篇
  2003年   13篇
  2002年   16篇
  2001年   8篇
  2000年   2篇
  1999年   5篇
  1998年   2篇
  1997年   6篇
  1996年   4篇
  1995年   2篇
  1994年   5篇
  1993年   7篇
  1992年   9篇
  1991年   2篇
  1990年   2篇
  1989年   4篇
  1988年   5篇
  1987年   10篇
  1985年   6篇
  1984年   6篇
  1983年   5篇
  1982年   5篇
  1981年   2篇
  1980年   4篇
  1979年   6篇
  1978年   2篇
  1977年   2篇
  1976年   4篇
  1975年   4篇
  1974年   2篇
  1973年   3篇
排序方式: 共有701条查询结果,搜索用时 719 毫秒
21.
目的:探究椎间孔镜与开窗术对腰椎间盘突出患者治疗远期效果对比。方法:选择2016年3月至2018年3月于我院接受治疗的腰椎间盘突出患者,按照其接受术式的不同将其分为孔镜组(108例)和开窗组(40例),对比两组手术出血量、术后卧床时间及切口长度,对比两组术前、术后3个月及术后12个月腰椎日本矫形外科学会(Japan Orthopaedic Assoctiation,JOA)评分、Odwestry功能障碍指数(Odwestris ability index, ODI)评分、视觉模拟评分(Visual analog scales,VAS)及生活质量评分,最后对比两组术后12个月椎间隙高度降低数值。结果:(1)孔镜组术中出血量、术后卧床时间及切口长度均小于开窗组,手术时间长于开窗组(P0.05);(2)术前两者JOA及ODI评分对比无统计学意义(P0.05),术后3个月及术后12个月孔镜组JOA及ODI评分优于开窗组(P0.05);(3)术前两组VAS及SF-36量表(the 36-item shot form health survey,SF-36)评分对比无统计学意义(P0.05),术后3个月及12个月两组VAS评分均有明显下降,SF-36评分有明显上升(P0.05),且术后3个月及12个月孔镜组SF-36评分高于开窗组(P0.05),VAS评分对比无统计学意义(P0.05);(4)术后12个月,孔镜组椎间隙高度降低率低于开窗组(P0.05)。结论:椎间孔镜在治疗腰椎间盘突出方面效果较好,相比于开窗术,孔镜术患者术中创伤小、术后恢复快、腰椎功能改善明显,且远期随访显示患者生活质量更高,值得进行临床推广。  相似文献   
22.
23.
24.
BACKGROUNDTo date, there has been no effective treatment for intervertebral disc degeneration (IDD). Nucleus pulposus-derived mesenchymal stem cells (NPMSCs) showed encouraging results in IDD treatment, but the overexpression of reactive oxygen species (ROS) impaired the endogenous repair abilities of NPMSCs. 6-gingerol (6-GIN) is an antioxidant and anti-inflammatory reagent that might protect NPMSCs from injury.AIMTo investigate the effect of 6-GIN on NPMSCs under oxidative conditions and the potential mechanism.METHODSThe cholecystokinin-8 assay was used to evaluate the cytotoxicity of hydrogen peroxide and the protective effects of 6-GIN. ROS levels were measured by 2´7´-dichlorofluorescin diacetate analysis. Matrix metalloproteinase (MMP) was detected by the tetraethylbenzimidazolylcarbocyanine iodide assay. TUNEL assay and Annexin V/PI double-staining were used to determine the apoptosis rate. Additionally, autophagy-related proteins (Beclin-1, LC-3, and p62), apoptosis-associated proteins (Bcl-2, Bax, and caspase-3), and PI3K/Akt signaling pathway-related proteins (PI3K and Akt) were evaluated by Western blot analysis. Autophagosomes were detected by transmission electron microscopy in NPMSCs. LC-3 was also detected by immunofluorescence. The mRNA expression of collagen II and aggrecan was evaluated by real-time polymerase chain reaction (RT-PCR), and the changes in collagen II and MMP-13 expression were verified through an immunofluorescence assay.RESULTS6-GIN exhibited protective effects against hydrogen peroxide-induced injury in NPMSCs, decreased hydrogen peroxide-induced intracellular ROS levels, and inhibited cell apoptosis. 6-GIN could increase Bcl-2 expression and decrease Bax and caspase-3 expression. The MMP, Annexin V-FITC/PI flow cytometry and TUNEL assay results further confirmed that 6-GIN treatment significantly inhibited NPMSC apoptosis induced by hydrogen peroxide. 6-GIN treatment promoted extracellular matrix (ECM) expression by reducing the oxidative stress injury-induced increase in MMP-13 expression. 6-GIN activated autophagy by increasing the expression of autophagy-related markers (Beclin-1 and LC-3) and decreasing the expression of p62. Autophagosomes were visualized by transmission electron microscopy. Pretreatment with 3-MA and BAF further confirmed that 6-GIN-mediated stimulation of autophagy did not reduce autophagosome turnover but increased autophagic flux. The PI3K/Akt pathway was also found to be activated by 6-GIN. 6-GIN inhibited NPMSC apoptosis and ECM degeneration, in which autophagy and the PI3K/Akt pathway were involved.CONCLUSION6-GIN efficiently decreases ROS levels, attenuates hydrogen peroxide-induced NPMSCs apoptosis, and protects the ECM from degeneration. 6-GIN is a promising candidate for treating IDD.  相似文献   
25.
目的:探究经皮椎间孔镜法治疗腰椎间盘突出症的效果。方法:选择我院于2018年1月2020年3月收治的腰椎间盘突出症患者77例为研究对象,根据入院顺序经随机数字表法分成两组,给予对照组39例患者进行开放手术:腰椎后路间盘切除、椎间融合、椎弓根钉内固定术,给予研究组38例患者经皮椎间孔镜法进行治疗。对比两组治疗后腰部功能恢复情况;两组手术时间、术中出血量、住院天数、切口长度等临床指标;两组术前及术后1 d白介素-1β(Inter leukin-1β,IL-1β)及C反应蛋白(C-reactive protein,CRP)水平。结果:研究组的腰部功能恢复总优良率92.11%(35/38)显著高于对照组的腰部功能恢复总优良率66.67%(26/39)(P<0.05);研究组的术中出血量、住院天数、切口长度、手术时间均显著少(短)于对照组(P<0.05);术前,两组的IL-1β、CRP水平对比无显著性差异(P>0.05);术后1 d,两组的IL-1β、CRP水平均比术前显著升高,但研究组显著低于对照组(P<0.05)。结论:经皮椎间孔镜法治疗腰椎间盘突出症的效果显著,可有效改善患者临床指标,且损伤较小,值得推荐至临床广泛应用。  相似文献   
26.
27.
28.
29.
Abstract

With each heartbeat, billions of cardiomyocytes work in concert to propagate the electrical excitation needed to effectively circulate blood. Regulated expression and timely delivery of connexin proteins to form gap junctions at the specialized cell–cell contact region, known as the intercalated disc, is essential to ventricular cardiomyocyte coupling. We focus this review on several regulatory mechanisms that have been recently found to govern the lifecycle of connexin 43 (Cx43), the short-lived and most abundantly expressed connexin in cardiac ventricular muscle. The Cx43 lifecycle begins with gene expression, followed by oligomerization into hexameric channels, and then cytoskeletal-based transport toward the disc region. Once delivered, hemichannels interact with resident disc proteins and are organized to effect intercellular coupling. We highlight recent studies exploring regulation of Cx43 localization to the intercalated disc, with emphasis on alternatively translated Cx43 isoforms and cytoskeletal transport machinery that together regulate Cx43 gap junction coupling between cardiomyocytes.  相似文献   
30.
Abstract

In this issue, guest editors Kathy Green and Mario Delmar, who are leaders in the fields of epidermal desmosomes and heart intercalated discs respectively, have joined forces to collate a two-part series of reviews focused on junctional proteins and genes that are targets of skin and heart diseases.  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