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991.
目的:探讨CD4^+ CD25^+ T细胞、IL-10在系统性红斑狼疮(SLE)患者外周血的表达及临床意义。方法:入组30例SLE患者和20例正常对照者,其中活动性SLE患者17人,非活动性SLE患者13人。用流式细胞仪检测SLE患者和正常对照者的外周血CD4^+ CD25^+ T细胞阳性率,用酶联免疫吸附试验(ELISA)检测血清中IL-10浓度。结果:活动性和非活动性SLE患者CD4^+ T细胞总数均低于正常对照者;活动性和非活动性SLE患者CD4^+ CD25^+ T细胞阳性率高于正常对照者;活动性SLE患者IL-10浓度显著高于非活动性SLE患者和正常对照者。SLE患者CD4^+ CD25^+ T细胞阳性率和血清IL-10浓度与补体C3、抗DNA抗体水平及SLEDAI积分均无相关性。结论:SLE患者外周血CD4^+ CD25^+ T细胞是活化T细胞的标志,IL-10分泌异常与SLE的发病有关。 相似文献
992.
993.
994.
目的 了解辅酶Q10(CoQ10)对大鼠再生肝细胞线粒体通透性转换(MPT)的影响。方法 雌性SD大鼠120只,用不同剂量CoQ10灌胃后行部分肝切除术(PH),于术后不同时间取肝组织分离线粒体,分光光度计法测定线粒体悬液的A540nm值,之后再加入钙离子诱导并检测A540nm值。结果 PH后6~48h,高剂量(60mg/kg)CoQ10处理组的再生肝线粒体通透性明显低于对照组,而低剂量(6mg/kg)处理组只在48h明显低于对照组,其他时间均无显著差异。用钙离子诱导后,各组各时间点的线粒体通透性随时间延长而不同程度的增强,但PH后6~48 h的CoQ10处理组的再生肝线粒体通透性稍小于对照组。结论 一定剂量的CoQ10能降低大鼠再生肝线粒体通透性,作用主要体现在肝再生的细胞增殖阶段。 相似文献
995.
P.L.M. Dalpiaz A.Z. Lamas I.F. Caliman A.R.S. Medeiros G.R. Abreu M.R. Moysés T.U. Andrade M.F. Alves A.K. Carmona N.S. Bissoli 《Brazilian journal of medical and biological research》2013,46(2):171-177
Sex hormones modulate the action of both cytokines and the renin-angiotensin
system. However, the effects of angiotensin I-converting enzyme (ACE) on the
proinflammatory and anti-inflammatory cytokine levels in male and female
spontaneously hypertensive rats (SHR) are unclear. We determined the
relationship between ACE activity, cytokine levels and sex differences in SHR.
Female (F) and male (M) SHR were divided into 4 experimental groups each (n =
7): sham + vehicle (SV), sham + enalapril (10 mg/kg body weight by gavage),
castrated + vehicle, and castrated + enalapril. Treatment began 21 days after
castration and continued for 30 days. Serum cytokine levels (ELISA) and ACE
activity (fluorimetry) were measured. Male rats exhibited a higher serum ACE
activity than female rats. Castration reduced serum ACE in males but did not
affect it in females. Enalapril reduced serum ACE in all groups. IL-10 (FSV =
16.4 ± 1.1 pg/mL; MSV = 12.8 ± 1.2 pg/mL), TNF-α (FSV = 16.6 ± 1.2 pg/mL; MSV =
12.8 ± 1 pg/mL) and IL-6 (FSV = 10.3 ± 0.2 pg/mL; MSV = 7.2 ± 0.2 pg/mL) levels
were higher in females than in males. Ovariectomy reduced all cytokine levels
and orchiectomy reduced IL-6 but increased IL-10 concentrations in males.
Castration eliminated the differences in all inflammatory cytokine levels (IL-6
and TNF-α) between males and females. Enalapril increased IL-10 in all groups
and reduced IL-6 in SV rats. In conclusion, serum ACE inhibition by enalapril
eliminated the sexual dimorphisms of cytokine levels in SV animals, which
suggests that enalapril exerts systemic anti-inflammatory and anti-hypertensive
effects. 相似文献
996.
Heae Surng Park Hyun Yang Yeo Hee Jin Chang Kyung-Hee Kim Ji Won Park Byung Chang Kim Ji Yeon Baek Sun Young Kim Dae Yong Kim 《Yonsei medical journal》2013,54(6):1362-1369
Purpose
The dipeptidyl peptidase IV (DPPIV) gene family exhibits multiple functions and is involved in the pathogenesis of various diseases. It has attracted pharmaceutical interest in the areas of metabolic disorders as well as cancer. However, clinicopathologic significance of DPPIV family in colorectal cancer is not fully understood.Materials and Methods
The clinical relevance of DPPIV and DPP10 expression was determined by immunohistochemical staining, and by assessing its clinicopathologic correlation in 383 colorectal cancer patients with known clinical outcomes.Results
DPPIV was not expressed in normal colon mucosa, but it showed luminal expression in 52 of the 383 colorectal cancers (13.5%). DPPIV expression in tumors was associated with right-sided location of the colon (p=0.010) and more advanced tumor stage (p=0.045). DPP10 was expressed in normal colonic mucosa, but its expression varied in primary colorectal cancer tissues. Loss of DPP10 expression was found in 11 colorectal cancers (CRCs) (2.9%), and multivariate analysis showed that loss of DPP10 expression was an independent factor for poor patient prognosis (p=0.008).Conclusion
DPP10 may play a role in disease progression of colorectal cancer and loss of DPP10 expression in primary CRC is significantly associated with poor survival outcomes. 相似文献997.
Min Jung Kim Jung Yeon Hong Kyung Eun Lee Kyung Won Kim Myung Hyun Sohn Kyu-Earn Kim 《Allergy, asthma & immunology research》2013,5(6):402-408
Purpose
The lipid entities of cell membranes are components of the immune system and important mediators of inflammation. Despite increasing interest in the function of epithelial cells in inflammation, the role of cholesterol in this process has not been described. Here, we investigated the effect of cholesterol depletion on the inflammatory process in airway epithelial cells via the expression of interleukin (IL)-8 as a marker of inflammation.Methods
A 549 cells were treated with 0.5% methyl-β-cyclodextrin as a selective cholesterol extractor. The IL-8 level was assessed by enzyme-linked immunosorbent assay and reassessed after cholesterol repletion. Mitogen-activated protein kinase (MAPK) inhibitors were used to determine the upstream signaling pathway for IL-8 production in cholesterol-depleted cells.Results
We found a relationship between the amount of cholesterol in A 549 cells and inflammation of the airway. IL-8 production was increased in cholesterol-depleted A 549 cells and restored by cholesterol repletion. IL-8 production was decreased by pretreatment with the extracellular signal-regulated kinase (ERK) inhibitor U0126 but not with JNK inhibitor II or the p38 MAPK inhibitor SB202190.Conclusions
Our findings suggest that inflammatory responses are increased in cholesterol-depleted epithelial cells via the MAPK signaling system, predominantly by the ERK pathway. We conclude that the lipid components of airwayepithelial cells may play a role in the inflammatory process. 相似文献998.
《Immunological investigations》2013,42(2-3):165-175
Previously we demonstrated that endogenously produced Interleukin (IL-)IO suppressed the production of tumor necrosis factor-alpha (TNF-alpha) in CD3 activated T-cells via downregulation of paracfine IL-12 secretion from APC. Here we investigated the effect of endogenous IL-10 on TNF-alpha production in purified lipopolysaccharide (LPS) stimulated monocytes and its mechanism. Similarly to its effects on T-cells, EL-10 inhibited monocyte TNF-alpha production by about half Unlike in T-cells, however, this effect was not mediated via IL-12. While blockade of endogenous IL-10 binding to the IL-10 receptor enhanced the autocrine production of TNF-alpha, IL-12 and IL-1 beta, the neutralization of IL-12 or IL-1 beta did not affect the EL-10 effects on TNF-alpha production. This suggests that despite its inhibitory effects on IL-12 and IL-1 beta, which is quite similarly observed in T-cells, in purified monocytes IL-10 does not effect its TNF-alpha suppression by this mechanism. These findings indicate that IL-10 regulates production of pro-inflammatory cytokines by distinct mechanisms in different cells and tissues. Our study thus adds to the appreciation of the complex cytokine regulation of the immune system. 相似文献
999.
《Autoimmunity》2013,46(7):533-539
Th17 lymphocyte and its relative cytokines have been shown to play an important role in autoimmune thyroid diseases (AITD). The aim of this study was to investigate the association between IL-17A and IL-17F gene polymorphisms and two main types of AITD, Graves' disease (GD) and Hashimoto's thyroiditis (HT). Whole blood specimens and clinical data were collected from 508 AITD patients (326 with GD and 182 with HT) and 224 age- and gender-matched healthy controls, respectively. IL-17A (rs2275913, rs8193037, rs3819025) polymorphism was determined using DNA sequencing method and IL-17F/rs763780 polymorphism was assayed by polymerase chain reaction-restriction fragment length polymorphism (PCR -RFLP). The results indicated that the frequencies of IL-17F/rs763780 genotypes in patients with GD and HT differed significantly from their controls (P = 0.013 and P = 0.005, respectively); the G allele frequencies were also significantly higher in the patient groups than the control groups (P = 0.002 and 0.001, respectively). For IL-17A/rs2275913 and rs8193037 SNP, no significant difference was observed in patients with either GD or HT compared to the control groups (P>0.05). Interestingly, for rs3819025, the frequency of A allele was lower in patients with GD than controls (P = 0.011). The frequencies of haplotype AGGG and GGGG in patients with GD and HT were significantly higher than in controls (P = 0.012, P = 0.019, P = 0.017 and P = 0.029, respectively). In conclusion, the results indicate that IL-17F/rs763780 polymorphisms may affect the susceptibility to AITD, and IL-17A/rs3819025 SNP is likely a protective factor to GD in the Chinese population. 相似文献
1000.