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991.
993.
Diffuse Large B cell lymphomas (DLBCL) are the most prevalent of the non-Hodgkin lymphomas and are currently initially treated fairly successfully, but frequently relapse as refractory disease, resulting in poor salvage therapy options and short survival. The greatest challenge in improving survival of DLBCL patients is overcoming chemo-resistance, whose basis is poorly understood. Among the potential mediators of DLBCL chemo-resistance is the thioredxoin (Trx) family, primarily because Trx family members play critical roles in the regulation of cellular redox homeostasis, and recent studies have indicated that dysregulated redox homeostasis also plays a key role in chemoresistance. In this study, we showed that most of the DLBCL-derived cell lines and primary DLBCL cells express higher basal levels of Trx-1 than normal B cells and that Trx-1 expression level is associated with decreased patients survival. Our functional studies showed that inhibition of Trx-1 by small interfering RNA or a Trx-1 inhibitor (PX-12) inhibited DLBCL cell growth, clonogenicity, and also sensitized DLBCL cells to doxorubicin-induced cell growth inhibition in vitro. These results indicate that Trx-1 plays a key role in cell growth and survival, as well as chemoresistance, and is a potential target to overcome drug resistance in relapsed/refractory DLBCL. 相似文献
994.
目的为了探讨P糖蛋白(P-glycoprotein,P-gp)在不同分型,分期胃癌中的表达及/与预后的关系。方法应用抗鼠抗人P-gp单克隆抗体JSB1对80例胃癌进行免疫组化研究。结果显示P-gp表达与临床分期有关(P<0.05),Ⅰ期表达率53.5%,Ⅱ期表达率63.1%,Ⅲ期66.6%,呈正相关。与胃癌组织分化程度无关(P>0.05)。不同生存年段的P-gp表达率无差异(P>0.05),但P-gp在癌旁正常组织中的阳性表达率与生存期有显著性差异(P<0.05)。结论提示P-gp表达与胃癌的分期相关,与分型和预后无关,但癌旁正常组织中的表达与生存期呈正相关。 相似文献
995.
996.
Purpose
The value of adjuvant radiotherapy for patients with positive lymph nodes after curative resection of oesophageal squamous cell carcinoma is controversial. This study aims to investigate its long-term benefits in a specific cohort.Patients and Methods
The charts between 1990 and 2003 from patients with positive lymph nodes were retrospectively reviewed. Those subjects were divided into adjuvant radiotherapy and surgery alone groups, with two subgroups defined by radiation dose (cutoff value: 50 Gy). Overall survival, disease-free survival and locoregional recurrence-free survival were compared between two groups, with predictive factors of overall survival analysed meanwhile.Results
In sum, 175 matched patients with 1:2 ratios for group balance were enrolled for final analysis. During the follow-up (median: 37.0 months), 143 (81.7%) deaths were recorded, with 70.6% of deaths from cancer progression. The median overall survival time (19.5, 4 to 172 months) was not significantly different between the two groups (18.9 vs. 20.0 months, P = 0.179). However, the disease-free survival time was significantly shorter in the adjuvant radiotherapy group than that in the control group (median, 11.5 vs. 14.9 months; P = 0.001), with the locoregional recurrence-free survival time impressively prolonged (median: 18.3 vs. 16.5 months; P = 0.022). Age (P = 0.030), number (P = 0.005) and ratio (P = 0.002) of positive lymph nodes were associated with overall survival, but radiation dose was not (P = 0.204).Conclusion
Adjuvant radiotherapy with low- or high-dose did not improve survival compared with surgery alone. However, radiotherapy was effective to control locoregional recurrence, and could be applied as salvage therapy when recurrence event occurred. 相似文献997.
目的 为临床提供一种简便、迅速、无损伤的诊断积水型重复肾伴重复输尿管扩张。方法 应用超声常规扫查两肾区.采取多方位、多切面.对11例积水型重复肾伴重复输尿管扩张患进行检查。结果 超声所见与手术或X线造影基本一致。发生于左肾5例,右肾6例;9例位于上肾部,2例位于下肾部;合并结石1例.合并输尿管囊肿3例。结论 总结了6种积水型重复肾伴重复输尿管扩张超声表现形式,凡具备其中表现形式之一即可直接作出积水型重复肾伴重复输尿管扩张的诊断;如能与X线造影相结合,可提高有功能重复肾重重复辅尿管的诊断的准确率。 相似文献
998.
目的探讨普伐他汀对氧化修饰低密度脂蛋白(oxLDL)诱导的人外周血单核细胞(PBMs)粘附功能的影响,揭示其除调脂外的抗炎作用。方法在体外分离培养人PBMs和脐静脉内皮细胞(HUVEC),PBMs经oxLDL诱导后,应用流式细胞仪和β N 乙酰氨基己糖苷酶比色法,检测单核细胞粘附分子CD11b表达及对HUVEC的粘附,以及普伐他汀的作用。结果普伐他汀在50μmol·L-1即可抑制oxLDL诱导的PBMs对HUVEC的粘附以及下调CD11b的表达(P<001),呈浓度依赖方式;甲羟戊酸可对抗此抑制作用。结论普伐他汀除调脂作用外,尚可抑制循环血单核 巨噬细胞至内皮粘附聚集,具有抗炎作用;其机制与普伐他汀抑制胆固醇前体物质甲羟戊酸生成有关。 相似文献
999.
益气活血药,系黄芪(Radix Astragali)、川芎(Rhizoma chuanxiong)复方注射液,本文对该药进行了主要药效学及一般药效学研究。实验结果表明:该药对豚鼠离体心脏的收缩力,心率,兴奋阈值无明显影响。对豚鼠离体气管平滑肌,小剂量使收缩,大剂量使舒张。对小鼠在常压与低压(-380mmHg)缺氧气下,存活时间显著延长(P<0.05)。对家兔血液检测,体外使红细胞压积,血沉,全血粘度,血浆粘度均降低(P<0.05),体内使红细胞压积,血沉下降。能改善小鼠的微循环障碍。对家兔,大鼠引起暂时的心率减慢,血压暂时略降低。对小鼠活动及呼吸改变不大。 相似文献
1000.
Li XG Yan JT Xu XZ Wang JN Cheng LM Wang T Zuo P Wang DW 《Acta pharmacologica Sinica》2007,28(11):1737-1745
Aim:The renin-angiotensin system plays a crucial role in the development and establishment of hypertension, and the pharmacological blockade of the system results in a reduction in blood pressure. In the present study, we investigated whether the effects of a novel, double-stranded, recombinant adeno-associated virus vector (rAAV)-mediated antisense angiotensin Ⅱ receptor 1 (AT1R) gene efficiently prevents the development of hypertension induced by a high-salt diet in adult, male Sprague-Dawley (SD) rats. Methods:A rAAV was prepared with a cassette containing a cytomegalovirus promoter and partial cDNA (660 base pairs) for the AT1R inserted in the antisense direction (rAAV-AT1-AS). A single tail vein injection of the rAAV-AT1-AS or rAAV-GFP (green fluorescent protein, a reporter gene) was performed in adult, male SD rats. Two weeks after injection, the animals were fed a diet containing 8% NaCl, and the systolic blood pressure was measured weekly using the tail-cuff method for 12 weeks. Results: The high-salt diet induced a significant rise in systolic blood pressure in the rAAV-GFP-treated animals; however, the rAAV-AT1-AS treatment attenuated the rise in blood pressure (142.7±4.5 mmHg vs 117±3.8 mmHg, P〈0.01), and the hypotensive effect was maintained until the experiments ended at 12 weeks. In the rAAV-GFP-treated animals AT1 was overexpressed in various tissues, especially in the aorta and kidney at mRNA levels; in contrast, rAAV-AT1-AS treatment markedly attenuated AT1 expression. Furthermore, rAAV-AT1-AS treatment prevented target organ damages from hypertension, including cardiac dysfunction and renal injury compared to the rAAV-GFP group. Conclusion:These results suggest that rAAVmediated anti-AT1 delivery attenuates the development of hypertension and protects against renal injury and cardiac remodeling. 相似文献