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991.
Yuan He Deng-ning Xia Qiu-xia Li Jin-song Tao Yong Gan Chi Wang 《Acta pharmacologica Sinica》2015,36(9):1151-1160
Aim:
Saquinavir (SQV) is the first protease inhibitor for the treatment of HIV infection, but with poor solubility. The aim of this study was to prepare a colloidal nanocrystal suspension for improving the oral absorption of SQV.Methods:
SQV nanocrystals were prepared using anti-solvent precipitation–high pressure homogenization method. The nanocrystals were characterized by a Zetasizer and transmission electron microscopy (TEM). Their dissolution, cellular uptake and transport across the human colorectal adenocarcinoma cell line (Caco-2) monolayer were investigated. Bioimaging of ex vivo intestinal sections of rats was conducted with confocal laser scanning microscopy. Pharmacokinetic analysis was performed in rats administered nanocrystal SQV suspension (50 mg/kg, ig), and the plasma SQV concentrations were measured with HPLC.Results:
The SQV nanocrystals were approximately 200 nm in diameter, with a uniform size distribution. The nanocrystals had a rod-like shape under TEM. The dissolution, cellular uptake, and transport across a Caco-2 monolayer of the nanocrystal formulation were significantly improved compared to those of the coarse crystals. The ex vivo intestinal section study revealed that the fluorescently labeled nanocrystals were located in the lamina propria and the epithelium of the duodenum and jejunum. Pharmacokinetic study showed that the maximal plasma concentration (Cmax) was 2.16-fold of that for coarse crystalline SQV suspension, whereas the area under the curve (AUC) of nanocrystal SQV suspension was 1.95-fold of that for coarse crystalline SQV suspension.Conclusion:
The nanocrystal drug delivery system significantly improves the oral absorption of saquinavir. 相似文献992.
Phoebe L. Zarnetske Jessica Gurevitch Janet Franklin Peter M. Groffman Cheryl S. Harrison Jessica J. Hellmann Forrest M. Hoffman Shan Kothari Alan Robock Simone Tilmes Daniele Visioni Jin Wu Lili Xia Cheng-En Yang 《Proceedings of the National Academy of Sciences of the United States of America》2021,118(15)
As the effects of anthropogenic climate change become more severe, several approaches for deliberate climate intervention to reduce or stabilize Earth’s surface temperature have been proposed. Solar radiation modification (SRM) is one potential approach to partially counteract anthropogenic warming by reflecting a small proportion of the incoming solar radiation to increase Earth’s albedo. While climate science research has focused on the predicted climate effects of SRM, almost no studies have investigated the impacts that SRM would have on ecological systems. The impacts and risks posed by SRM would vary by implementation scenario, anthropogenic climate effects, geographic region, and by ecosystem, community, population, and organism. Complex interactions among Earth’s climate system and living systems would further affect SRM impacts and risks. We focus here on stratospheric aerosol intervention (SAI), a well-studied and relatively feasible SRM scheme that is likely to have a large impact on Earth’s surface temperature. We outline current gaps in knowledge about both helpful and harmful predicted effects of SAI on ecological systems. Desired ecological outcomes might also inform development of future SAI implementation scenarios. In addition to filling these knowledge gaps, increased collaboration between ecologists and climate scientists would identify a common set of SAI research goals and improve the communication about potential SAI impacts and risks with the public. Without this collaboration, forecasts of SAI impacts will overlook potential effects on biodiversity and ecosystem services for humanity. 相似文献
993.
994.
目的分析GATA3基因变异导致甲状旁腺功能减退症(hypoparathyroidism, HP)患者的临床特点及分子机制。方法在1975年至2020年间于北京协和医院内分泌科随诊并行靶向基因捕获联合二代测序的198例未成年人(≤18岁)起病的非手术性HP患者中筛查到5例GATA3基因致病/可疑致病性变异, 回顾性收集分析其临床资料, 并对基因检测结果进行生物信息学分析。结果 5例患者HP的起病年龄为0.5(0.1, 1.3)岁, 发病至诊断为HP和甲状旁腺功能减退-耳聋-肾发育不良(hypoparathyroidism-deafness-renal dysplasia, HDR)综合征的时间分别为(7.0±5.2)年和(15.0±5.4)年。临床表现为手足搐搦伴癫痫样发作、颅内钙化各5例, 白内障1例, 听力减退4例, 肾脏畸形或缺如2例。治疗前血钙和血甲状旁腺激素(PTH)分别为(1.65±0.31)mmol/L和(4.64±2.63)ng/L。5例患者GATA3基因的杂合变异, 分别引起无义突变、移码突变和剪接位点突变, 经Clin Var数据库预测及美国医学遗传学和基因组学学会(... 相似文献
995.
Gao Zhen-yu Su Lin-chong Wu Qing-chao Sheng Jiao-e Wang Yun-long Dai Yu-fang Chen An-ping He San-shan Huang Xia Yan Guo-qing 《Clinical rheumatology》2022,41(2):437-452
Clinical Rheumatology - Lupus erythematosus is an autoimmune disease that causes damage to multiple organs ranging from skin lesions to systemic manifestations. Cutaneous lupus erythematosus (CLE)... 相似文献
996.
Chen Yi Zhang Hongzhou Chen Yuxin Li Meng Luo Wei Liu Yue Fu Yang Xia Huasong Xu Cong Jiang Yu Wu Yanqing 《Clinical rheumatology》2022,41(6):1873-1887
Clinical Rheumatology - Colchicine is an ancient anti-inflammatory drug. In recent years, an increasing number of studies have shown that colchicine improves the prognosis of patients with coronary... 相似文献
997.
He Xuxia Wen Yubing Hu Rongrong Wu Haiting Ye Wei Yue Cai Qin Yan Xia Peng Chen Limeng 《Clinical rheumatology》2022,41(11):3551-3563
Clinical Rheumatology - The typical nephrological presentation of antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis (AAV) is rapidly progressive glomerulonephritis.... 相似文献
998.
Qiu Zhen Ming Hao Zhang Yi Yu Yanli Lei Shaoqing Xia Zhong-yuan 《Cardiovascular drugs and therapy / sponsored by the International Society of Cardiovascular Pharmacotherapy》2022,36(2):229-243
Cardiovascular Drugs and Therapy - Histone deacetylase 3 (HDAC3) and silent information regulator 1 (SIRT1) are histone deacetylases that regulate important metabolic pathways and play important... 相似文献
999.
Calley L. Hirsch Zeynep Coban Akdemir Li Wang Gowtham Jayakumaran Dan Trcka Alexander Weiss J. Javier Hernandez Qun Pan Hong Han Xueping Xu Zheng Xia Andrew P. Salinger Marenda Wilson Frederick Vizeacoumar Alessandro Datti Wei Li Austin J. Cooney Michelle C. Barton Benjamin J. Blencowe Jeffrey L. Wrana Sharon Y.R. Dent 《Genes & development》2015,29(12):1341
1000.
目的:探讨香烟提取物(CSE)能否引起小鼠C2C12成肌细胞衰老,并研究成肌细胞衰老与组蛋白去乙酰化酶2(HDAC2)的关系。方法:培养C2C12细胞株,分化为成熟成肌细胞,观察CSE干预对成肌细胞衰老和HDAC2表达的影响,采用real-time PCR和Western blot方法分别检测HDAC2 mRNA和蛋白的表达;β-半乳糖苷酶染色检测衰老细胞的百分率。结果:MTT法测定最佳CSE浓度与干预时间分别为60 m L/L和24 h。CSE干预后β-半乳糖苷酶染色阳性细胞数增加,同时伴有HDAC2 mRNA和蛋白表达的减少。四溴苯三唑(TBB)在促进HDAC2 mRNA和蛋白表达的同时,β-半乳糖苷酶染色阳性细胞数减少;用HDAC2的特异性阻滞剂丙戊酸抑制HDAC2 mRNA和蛋白的表达时,β-半乳糖苷酶染色阳性细胞数增加。结论:香烟提取物可通过减少小鼠C2C12成肌细胞HDAC2的表达促进细胞老化。 相似文献