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11.
邓建松  魏柏 《现代肿瘤医学》2020,(20):3511-3516
目的:探讨微小RNA-145(microRNA-145,miR-145)对非小细胞肺癌细胞系吉非替尼耐药的作用及其可能的潜在机制。方法:实时荧光定量PCR(Q-PCR)方法检测正常细胞及非小细胞肺癌细胞中miR-145的表达差异;不同时间5 μmol/L吉非替尼干预肺癌细胞SPC-A-1和A549后,Q-PCR检测miR-145表达变化;miR-145 mimics和miR-145 inhibitors分别转染SPC-A-1和A549肺癌细胞后,CCK8检测细胞活力变化;双荧光素酶报告系统检测miR-145与ADAM19的靶向结合;miR-145 mimics转染SPC-A-1和A549肺癌细胞,Western blot检测ADAM19蛋白表达;Western blot检测5 μmol/L吉非替尼干预后,SPC-A-1和A549肺癌细胞中ADAM19蛋白的表达;miR-145 mimics转染SPC-A-1和A549肺癌细胞,再用5 μmol/L吉非替尼干预,Western blot检测ADAM19蛋白的表达;采用siRNA抑制ADAM19表达,再用5 μmol/L吉非替尼干预,CCK8检测细胞活力;采用BALB/C雌性裸鼠皮下接种肿瘤细胞的方法,观察上述效应。结果:Q-PCR结果显示,与正常肺上皮细胞系BEAS-2B相比较,肺癌细胞SPC-A-1和A549中miR-145表达明显降低;5 μmol/L吉非替尼干预SPC-A-1和A549细胞后,miR-145表达显著上调;转染miR-145 mimics后,CCK8结果显示两种细胞细胞活力下降;双荧光素酶报告系统结果显示,miR-145靶向结合ADAM19基因的3'-UTR区;Western blot结果显示,5 μmol/L吉非替尼诱导SPC-A-1和 A549细胞后,两种细胞中ADAM19蛋白表达均降低;miR-145 mimics转染SPC-A-1和A549细胞,之后给予5 μmol/L吉非替尼治疗,ADAM19蛋白表达下调;siRNA抑制SPC-A-1和A549细胞中ADAM19表达,再给予5 μmol/L吉非替尼治疗,CCK8结果显示,两种细胞的细胞活力显著降低;过表达BALB/C雌性裸鼠的miR-145后,显著抑制皮下肿瘤生长,并且增强吉非替尼的抗肿瘤效果。结论:miR-145显著增强肺癌细胞SPC-A-1和A549对吉非替尼的敏感性,其机制可能是通过靶向结合AMDM19基因的3'-UTR区域,从而抑制其表达。miR-145有可能成为治疗非小细胞肺癌吉非替尼耐药的有效靶点。  相似文献   
12.
Introduction:This work reports a patient with recurrent renal calculi subjected to three surgeries in half a year to be in the same position, and the high-throughput sequencing data showed different species in the renal pus and urine samples, which suggested that partial renal infection or stone formation can be judged by the bacteria in urine.Patient concerns:The female patient aged 43 years was referred to the authors’ department on April 13, 2020, due to left waist pain and fever for 3 days.Diagnosis:Kidney stones and hydronephrosis were determined by a urinary system computed tomography scan.Interventions:On April 20, 2020 and June 15, 2020, the patient was successfully treated with left percutaneous nephrolithotomy twice under general anesthesia. An investigation on the health and eating habits of the patient within 6 months was completed at the last admission. The components of the second renal calculus sample were analyzed with an infrared spectrum analyzer. The third renal stone (renal pus, triplicates) was subjected to microbial metagenome sequencing, and urine samples before and after surgery were subjected to 16S RNA sequencing by SEQHEALTH (Wuhan, China).Outcomes:After percutaneous nephrolithotomy, the left kidney stones were basically cleared, stone analysis revealed that the main components were calcium oxalate monohydrate, silica, and a small amount of calcium oxalate dehydrate. Although the urine samples exhibited differences, the renal pus and urine sample shared a single species.Conclusion:It is not clear that the prospects of partial renal infection or stone formation can be judged by the bacteria in urine.  相似文献   
13.
14.
目的 研究计划镇静应用于高龄低肺功能肺癌术后机械通气患者程序化脱机的临床效果。方法 将60例高龄低肺功能肺癌术后机械通气患者分为对照组和计划镇静组,对照组患者按需镇静,计划镇静组患者实施计划镇静方案。两组患者在镇静过程中Richmond躁动-镇静量表评分的目标分值为-3~-1分,最终均行程序化脱机。结果 两组患者首次计划性气管插管拔除成功率分别为43%和80%,谵妄发生率分别为20%和7%,差异有统计学意义(P<0.05),而已拔管患者48h内再插率分别为7%和3%,差异无统计学意义(P>0.05),两组患者首次计划性气管插管拔除后2h血气分析比较,计划镇静组明显优于对照组(P<0.05)。结论 高龄低肺功能肺癌术后机械通气患者给予计划镇静,可以改善患者的临床转归,提高患者对治疗的依从性,减少气管插管的非计划性拔除率。  相似文献   
15.
The Chinese National Twin Registry (CNTR) currently includes data from 61 566 twin pair from 11 provinces or cities in China. Of these, 31 705, 15 060 and 13 531 pairs are monozygotic, same‐sex dizygotic and opposite‐sex dizygotic pairs, respectively, determined by opposite sex or intrapair similarity. Since its establishment in 2001, the CNTR has provided an important resource for analysing genetic and environmental influences on chronic diseases especially cardiovascular diseases. Recently, the CNTR has focused on collecting biologic specimens from disease‐concordant or disease‐discordant twin pairs or from twin pairs reared apart. More than 8000 pairs of these twins have been registered, and blood samples have been collected from more than 1500 pairs. In this review, we summarize the main findings from univariate and multivariate genetic effects analyses, gene–environment interaction studies, omics studies exploring DNA methylation and metabolomic markers associated with phenotypes. There remains further scope for CNTR research and data mining. The plan for future development of the CNTR is described. The CNTR welcomes worldwide collaboration.  相似文献   
16.
Stellate ganglion (SG) modification has been investigated for arrhythmia treatment. In this study, transesophageal SG imaging and intervention were explored using a homemade 30F integrated focused ultrasonic catheter in healthy mongrel canines in vivo. Anatomic details of SGs were ultrasonically imaged and evaluated. SG had a heterogeneous echoic structure and characteristic profiles sketched by hyper-echoic outlines in an ultrasonogram. Left SGs in the experimental group were successfully ablated through the esophagus under ultrasonic guidance provided by the catheter itself. Two weeks after the ablation, the QT and QTc of the experimental group decreased compared with those of the sham group and at baseline (both p values < 0.001). Histologic examination revealed that left SGs were destroyed. No major complications were observed. This approach may be further explored as a method for ganglia remodeling evaluation and as a strategy of ganglia modification for arrhythmia and for other diseases.  相似文献   
17.
目的 研究活血解毒方对缺氧/复氧(H/R)所致的心肌细胞凋亡的影响。方法 体外培养H9C2心肌细胞并分成正常对照组(Control组)、缺氧复氧组(H/R组)、H/R + 活血解毒中药组、LY294002组和活血解毒中药 + LY294002组,其中正常对照组给予DMEM培养基培养,缺氧复氧组给予缺氧4 h、复氧6 h处理,缺氧复氧 + 活血解毒中药组、LY294002组和活血解毒中药 + LY294002组分别给予活血解毒中药、LY294002、活血解毒中药配合LY294002预处理24 h,然后均给予缺氧4 h、复氧6 h处理。采用CCK8检测各组心肌细胞的存活率,流式细胞术检测各组细胞凋亡水平,电镜观察各组心肌细胞中线粒体、自噬体的变化,Western Blot检测各组细胞凋亡蛋白半胱氨酸天冬氨酸蛋白酶3(Caspase3)、半胱氨酸天冬氨酸蛋白水解酶3(Cleaved caspase3)、β-连环蛋白(β-Catenin)、p-p65、B淋巴细胞瘤-2(B-cell lymphoma-2,Bcl-2)蛋白的表达。结果 活血解毒方预处理显著增加H/R诱导的H9C2心肌细胞凋亡,降低凋亡相关蛋白Cleaved caspase3、β-Catenin、p-p65表达,增加Bcl-2表达。结论 活血解毒方可通过抑制细胞凋亡,降低缺氧/复氧所致的心肌细胞损伤,其作用机制可能与PI3K信号通路相关。  相似文献   
18.
Background:Arteriosclerosis obliterans (ASO) is a major cause of adult limb loss worldwide. Autophagy of vascular endothelial cell (VEC) contributes to the ASO progression. However, the molecular mechanism that controls VEC autophagy remains unclear. In this study, we aimed to explore the role of the GRB2 associated binding protein 1 (GAB1) in regulating VEC autophagy.Methods:In vivo and in vitro studies were applied to determine the loss of adapt protein GAB1 in association with ASO progression. Histological GAB1 expression was measured in sclerotic vascular intima and normal vascular intima. Gain- and loss-of-function of GAB1 were applied in VEC to determine the effect and potential downstream signaling of GAB1.Results:The autophagy repressor p62 was significantly downregulated in ASO intima as compared to that in healthy donor (0.80 vs. 0.20, t = 6.43, P < 0.05). The expression level of GAB1 mRNA (1.00 vs. 0.24, t = 7.41, P < 0.05) and protein (0.72 vs. 0.21, t = 5.97, P < 0.05) was significantly decreased in ASO group as compared with the control group. Loss of GAB1 led to a remarkable decrease in LC3II (1.19 vs. 0.68, t = 5.99, P < 0.05), whereas overexpression of GAB1 significantly led to a decrease in LC3II level (0.41 vs. 0.93, t = 7.12, P < 0.05). Phosphorylation levels of JNK and p38 were significantly associated with gain- and loss-of-function of GAB1 protein.Conclusion:Loss of GAB1 promotes VEC autophagy which is associated with ASO. GAB1 and its downstream signaling might be potential therapeutic targets for ASO treatment.  相似文献   
19.
Ecotoxicology - The concentrations, distribution, and ecological risks of 24 typical antibiotics in Hong Kong rivers and seawater were investigated using high-performance liquid chromatography...  相似文献   
20.
社会力量具备相应的经济基础和技术条件,对于公立互联网医院体系建设具有积极的促进作用。但是实践中仍然存在商业模式不完善、监管制度不健全等问题。基于经济学契约理论要义,提出在坚持激励与约束机制并举、平衡公私益关系的前提下,通过完善医保政策、构建互联网医疗服务价格分类管理机制来促进社会力量向医疗服务公益性目标回归,并通过构建完善的监督体制来约束部分社会力量的盲目逐利性行为。  相似文献   
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