全文获取类型
收费全文 | 8668篇 |
免费 | 1023篇 |
国内免费 | 1856篇 |
专业分类
11547篇 |
出版年
2024年 | 57篇 |
2023年 | 177篇 |
2022年 | 386篇 |
2021年 | 534篇 |
2020年 | 426篇 |
2019年 | 519篇 |
2018年 | 426篇 |
2017年 | 359篇 |
2016年 | 456篇 |
2015年 | 652篇 |
2014年 | 794篇 |
2013年 | 751篇 |
2012年 | 852篇 |
2011年 | 751篇 |
2010年 | 512篇 |
2009年 | 473篇 |
2008年 | 466篇 |
2007年 | 380篇 |
2006年 | 338篇 |
2005年 | 301篇 |
2004年 | 278篇 |
2003年 | 235篇 |
2002年 | 241篇 |
2001年 | 144篇 |
2000年 | 140篇 |
1999年 | 127篇 |
1998年 | 55篇 |
1997年 | 53篇 |
1996年 | 36篇 |
1995年 | 46篇 |
1994年 | 40篇 |
1993年 | 35篇 |
1992年 | 62篇 |
1991年 | 50篇 |
1990年 | 50篇 |
1989年 | 48篇 |
1988年 | 26篇 |
1987年 | 31篇 |
1986年 | 28篇 |
1985年 | 29篇 |
1984年 | 25篇 |
1983年 | 17篇 |
1982年 | 12篇 |
1981年 | 10篇 |
1980年 | 14篇 |
1977年 | 11篇 |
1972年 | 11篇 |
1971年 | 9篇 |
1970年 | 9篇 |
1969年 | 9篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
11.
新型疫苗佐剂的研究进展 总被引:3,自引:0,他引:3
与传统的灭活或活体疫苗相比,由基因工程重组抗原或化学合成多肽组成的现代疫苗往往存在免疫原性弱等问题,需要新型的免疫佐剂来增强其作用。尽管传统的铝盐佐剂是目前唯一全球公认的人用佐剂,但存在激发细胞免疫应答能力差等不足,因此,需要研发更为安全有效的人用新型佐剂,尤其是安全无毒、能够刺激较强细胞免疫应答的佐剂,以及适合粘膜疫苗、DNA疫苗和癌症疫苗的免疫佐剂。分析阐述了新型佐剂研究状况和佐剂发展方向,并进一步对新型佐剂的临床前和临床试验研究以及已批准上市的新型疫苗佐剂进行了综述。 相似文献
12.
13.
为探讨新的豆类凝集素(Flt3 receptor-interacting lectin,FRIL)体外维持脐血CD34^ 细胞的作用以及维持过程中细胞周期调控基因HTm4及HTm4S mRNA的表达及意义,我们利用FRIL维持培养脐血CD34^ 细胞,对其增殖曲线、细胞周期及集落形成能力进行常规分析,并用半定量RT—PCR法分别测定FRIL体外维持不同时间后脐血CD34^ 细胞中周期调控基因HTm4及HTm4S mRNA的表达变化。结果显示,FRIL培养的CD34^ 造血干/祖细胞的增殖趋势平缓,整个培养期间细胞增殖倍数不超过起始的3倍:14d之前,FRIL培养细胞的高增殖潜能集落形成细胞(HPP—CFC)形成集落数与FL组无差别,其后则维持高于FL的情况。细胞周期分析则显示,在28d的培养过程内,利用FRIL培养的细胞始终有80%以上维持在G0期;而周期调控基因HTm4及HTm4S在刚分离的脐血CD34^ 细胞中的表达水平较高;但培养1d后,几乎检测不到HTm4基因的表达;培养3~14d,该基因的表达回升并持续维持在高水平。而HTm4S基因的表达在第7d达最高水平,其余时间基本呈稳定表达。转染HTm4和HTm4S,亚细胞定位结果显示HTm4主要定位于核周围,而HTm4S则定位于整个胞浆,由此可能导致它们功能的区别。以上结果提示,长期培养体现出FRIL在维持造血干/祖细胞多能性上的优势;细胞周期调控基因HTm4及其新剪接子参与了FRIL体外长期维持脐血造血干/祖细胞处于静息状态的过程。 相似文献
14.
Lee JC Won SJ Chao CL Wu FL Liu HS Ling P Lin CN Su CL 《Biochemical and biophysical research communications》2008,372(1):236-242
Morusin is a pure compound isolated from root bark of Morusaustralis (Moraceae). In this study, we demonstrated that morusin significantly inhibited the growth and clonogenicity of human colorectal cancer HT-29 cells. Apoptosis induced by morusin was characterized by accumulation of cells at the sub-G1 phase, fragmentation of DNA, and condensation of chromatin. Morusin also inhibited the phosphorylation of IKK-α, IKK-β and IκB-α, increased expression of IκB-α, and suppressed nuclear translocation of NF-κB and its DNA binding activity. Dephosphorylation of NF-κB upstream regulators PI3K, Akt and PDK1 was also displayed. In addition, activation of caspase-8, change of mitochondrial membrane potential, release of cytochrome c and Smac/DIABLO, and activation of caspase-9 and -3 were observed at the early time point. Downregulation in the expression of Ku70 and XIAP was exhibited afterward. Caspase-8 or wide-ranging caspase inhibitor suppressed morusin-induced apoptosis. Therefore, the antitumor mechanism of morusin in HT-29 cells may be via activation of caspases and inhibition of NF-κB. 相似文献
15.
Hsu WY Chao YW Tsai YL Lien CC Chang CF Deng MC Ho LT Kwok CF Juan CC 《Journal of cellular physiology》2011,226(8):2181-2188
Resistin, firstly reported as an adipocyte-specific hormone, is suggested to be an important link between obesity and diabetes. Recent studies have suggested an association between resistin and atherogenic processes. The adhesion of circulating monocytes to endothelial cells is a critical step in the early stages of atherosclerosis. The purpose of the present study was to investigate the effect of resistin on the adhesion of THP-1 monocytes to human umbilical vein endothelial cells (HUVECs) and the underlying mechanism. Our results showed that resistin caused a significant increase in monocyte adhesion. In exploring the underlying mechanisms of resistin action, we found that resistin-induced monocyte adhesion was blocked by inhibition of p38MAPK activation using SB203580 and SB202190. Furthermore, resistin increased the expression of intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) by HUVECs and these effects were also p38MAPK-dependent. Resistin-induced monocyte adhesion was also blocked by monoclonal antibodies against ICAM-1 and VCAM-1. Taken together, these results show that resistin increases both the expression of ICAM-1 and VCAM-1 by endothelial cells and monocyte adhesion to HUVECs via p38MAPK-dependent pathways. 相似文献
16.
17.
18.
19.
20.
Decreased methylation of the major mouse long interspersed repeated DNA during aging and in myeloma cells 总被引:2,自引:0,他引:2
Sequences of DNA that hybridize on Southern blots with cloned EcoR1 1.3 kb (ER1) of long interspersed repeated sequence (L1Md) of mouse have been examined in genomic DNA of neonatal mice, livers and brains of adult mice (3, 10, 27, and 30 mo old), and the solid myeloma tumor MOPC-315. The isoschizomers Hpa II (CCGG or mCCGG) and Msp I (CCGG or CmCGG) were used to assess methylation. We found that the L1Md sequence is fully methylated in young animals but demethylated in myeloma. Demethylation of L1Md sequence also occurred in aged animals. By scanning the autoradiogram, we found that approximately 8% of the 10(4)-10(5) copies have been demethylated in 27-mo-old liver. 相似文献