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991.
目的:了解人卵巢癌中P53基因突变的特点及其与临床分期的关系。方法:采用聚合酶链反应单链构像多态性分析及序列分析,对60例卵巢癌组织及癌旁组织P53基因外显子5、6、7进行了筛查。结果:所有癌旁组织均未发现突变,癌组织有9例发生了P53基因的突变,并对其中5例进行了序列分析,证实了其突变的存在。5例测序标本中有4例发生了G∶C→A∶T的转换突变。9例阳性标本分别为临床Ⅰ期2例,临床Ⅲ期6例,临床Ⅳ期1例。结论:人卵巢癌中P53基因的突变是自发性突变的结果。P53基因改变可能发生于卵巢癌早期,并持续存在于肿瘤发展的全过程,是卵巢癌发生发展的危险因素之一。推测245位密码子是我国卵巢癌患者的一个突变热点。 相似文献
992.
目的:观察P16蛋白在肺癌组织的表达情况,了解该基因与肺癌的预后关系。方法:应用SP免疫组织化学方法对76例肺癌中抑癌基因CDKN2P16蛋白表达进行研究。结果:76例肺癌P16蛋白表达阳性率为447%。P16蛋白表达与肺癌的病理分级及预后有显著差异(P<005),与临床分期有一定相关性。结论:P16抑癌基因对肺癌的发生发展起着某种关键作用 相似文献
993.
目的 评价大株红景天注射液治疗心绞痛的疗效和安全性。方法 计算机检索Medline、Embase、The Cochrane Library和CNKI、VIP、万方等文献数据库,按纳入和排除标准纳入合格的随机对照试验文献,并对其进行质量评价和meta分析。结果 符合纳入标准的文献共有14篇,包括1 616例患者,但这些研究的质量普遍不高。Meta分析结果显示,大株红景天注射液与对照组心绞痛临床症状疗效和心电图改善的合并比值比(odd ratio,OR)分别为2.29和2.16,95%的可信区间(CI)分别为(1.78,2.96)和(1.69,2.76);大株红景天注射液治疗心绞痛,临床症状疗效和心电图改善优于对照组,但无可靠证据显示该药的安全性。结论 目前,仅有少量证据支持大株红景天注射液作为西医基础治疗的辅助药物时在改善各类心绞痛症状和心电图表现方面优于单纯西医基础治疗,由于纳入研究的数量少和质量不高,且缺乏一些重要的终点指标和生活质量相关指标,尚不能从本系统评价得出大株红景天注射液治疗心绞痛优于单纯西医基础治疗的结论。 相似文献
994.
Yao H Xu L Han F Che X Dong Y Wei M Guan J Shi X Li S 《International journal of pharmaceutics》2008,364(1):21-26
A novel gastro-mucoadhesive delivery system based on ion-exchange fiber has been developed. Riboflavin-5'-phosphate sodium salt (RF5P), which is site-specifically absorbed from the upper gastrointestinal tract, was used as model drug. A modified dissolution system, which can also be called 'flow through diffusion cell' (FTDC), was used to study the drug release from the drug fibers. Gastrointestinal transit studies of the RF5P fiber complexes in rats and gamma imaging study in volunteer was carried out to evaluate the gastro-retentive behavior of the fiber. The pharmacokinetic profile and parameters of riboflavin via analysis of urinary excretion of riboflavin on man were measured. Study on rat and man provide evidence for the validity of the hypothesis that the drug fiber provided good mucoadhesive properties in vivo and should therefore be of considerable interest for the development of future mucoadhesive oral drug delivery dosage forms. 相似文献
995.
Zhang JS Guan J Yang FQ Liu HG Cheng XJ Li SP 《Journal of pharmaceutical and biomedical analysis》2008,48(3):1024-1028
The rhizomes of Curcuma phaeocaulis, Curcuma kwangsiensis, Curcuma wenyujin and Curcuma longa are used as Ezhu or Jianghuang in traditional Chinese medicine for a long time. Due to their similar morphological characters, it is difficult to distinguish their origins of raw materials used in clinic. In this study, a simple, rapid and reliable twice development TLC method was developed for qualitative and quantitative analysis of the four species of Curcuma rhizomes. The chromatography was performed on silica gel 60F(254) plate with chloroform-methanol-formic acid (80:4:0.8, v/v/v) and petroleum ether-ethyl acetate (90:10, v/v) as mobile phase for twice development. The TLC markers were colorized with 1% vanillin-H(2)SO(4) solution. The four species of Curcuma were easily discriminated based on their characteristic TLC profiles, and simultaneous quantification of eight compounds, including bisdemethoxycurcumin, demethoxycurcumin, curcumine, curcumenol, curcumol, curdione, furanodienone and curzerene, in Curcuma were also performed densitometrically at lambda(scan)=518nm and lambda(reference)=800 nm. The investigated compounds had good linearity (r(2)>0.9905) within test ranges. Therefore, the developed TLC method can be used for quality control of Curcuma rhizomes. 相似文献
996.
Shearman LP Stribling DS Camacho RE Rosko KM Wang J Tong S Feng Y Marsh DJ Yu H Guan X Spann SK Macneil DJ Fong TM Metzger JM Goulet MT Hagmann WK Plummer CW Finke PE Mills SG Shah SK Truong Q Van der Ploeg LH Macintyre DE Strack AM 《European journal of pharmacology》2008,579(1-3):215-224
We document in vitro and in vivo effects of a novel, selective cannabinoid CB(1) receptor inverse agonist, Imidazole 24b (5-(4-chlorophenyl)-N-cyclohexyl-4-(2,4-dichlorophenyl)-1-methyl-imidazole-2-carboxamide). The in vitro binding affinity of Imidazole 24b for recombinant human and rat CB(1) receptor is 4 and 10 nM, respectively. Imidazole 24b binds to human cannabinoid CB(2) receptor with an affinity of 297 nM; in vitro, it is a receptor inverse agonist at both cannabinoid CB(1) and CB(2) receptors as it causes a further increase of forskolin-induced cAMP increase. Oral administration of Imidazole 24b blocked CP-55940-induced hypothermia, demonstrating cannabinoid CB(1) receptor antagonist efficacy in vivo. Using ex vivo autoradiography, Imidazole 24b resulted in dose-dependent increases in brain cannabinoid CB(1) receptor occupancy (RO) at 2h post-dosing in rats, indicating that approximately 50% receptor occupancy is sufficient for attenuation of receptor agonist-induced hypothermia. Imidazole 24b administered to C57Bl/6 mice and to dietary-induced obese (DIO) Sprague-Dawley rats attenuated overnight food intake with a minimal effective dose of 10 mg/kg, p.o. Administration had no effect in cannabinoid CB(1) receptor-deficient mice. DIO rats were dosed orally with vehicle, Imidazole 24b (1, 3 or 10 mg/kg), or dexfenfluramine (3 mg/kg) for 2 weeks. At 3 mg/kg, Imidazole 24b reduced cumulative food intake, leading to a non-significant decrease in weight gain. Imidazole 24b at 10 mg/kg and dexfenfluramine treatment inhibited food intake and attenuated weight gain. These findings suggest that selective cannabinoid CB(1) receptor inverse agonists such as Imidazole 24b have potential for the treatment of obesity. 相似文献
997.
本文报告26例正常人和35例乳腺包块~(99m)Tc-葡聚糖乳内淋巴显像的结果。正常人绝大多数双侧淋巴结数和(或)显影浓淡不对称,并发现左右交叉引流和先天性单链各2例;乳癌乳内淋巴转移者双侧或单侧淋巴链不显影,或一侧淋巴链仅低位淋巴结显影而高位缺如。本法判断淋巴受累的灵敏度为100%,特异性为85.2%,准确性为88.6%,假阳性为14.8%,假阴性为零。 相似文献
998.
本文分析我院33例MDS病例的入院前诊断、病例类型、临床表现、血象及骨髓象资料,其中4例转变为急性白血病。 相似文献
999.
1000.