全文获取类型
收费全文 | 47407篇 |
免费 | 3351篇 |
国内免费 | 19篇 |
专业分类
50777篇 |
出版年
2024年 | 52篇 |
2023年 | 175篇 |
2022年 | 565篇 |
2021年 | 912篇 |
2020年 | 568篇 |
2019年 | 683篇 |
2018年 | 1027篇 |
2017年 | 906篇 |
2016年 | 1477篇 |
2015年 | 2320篇 |
2014年 | 2666篇 |
2013年 | 2980篇 |
2012年 | 3942篇 |
2011年 | 3778篇 |
2010年 | 2393篇 |
2009年 | 2184篇 |
2008年 | 3028篇 |
2007年 | 2910篇 |
2006年 | 2540篇 |
2005年 | 2357篇 |
2004年 | 2161篇 |
2003年 | 1864篇 |
2002年 | 1615篇 |
2001年 | 1301篇 |
2000年 | 1228篇 |
1999年 | 990篇 |
1998年 | 393篇 |
1997年 | 338篇 |
1996年 | 245篇 |
1995年 | 209篇 |
1994年 | 207篇 |
1993年 | 172篇 |
1992年 | 326篇 |
1991年 | 295篇 |
1990年 | 266篇 |
1989年 | 226篇 |
1988年 | 173篇 |
1987年 | 163篇 |
1986年 | 131篇 |
1985年 | 105篇 |
1984年 | 78篇 |
1983年 | 84篇 |
1982年 | 63篇 |
1981年 | 53篇 |
1980年 | 54篇 |
1979年 | 69篇 |
1978年 | 51篇 |
1977年 | 50篇 |
1976年 | 43篇 |
1974年 | 63篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
21.
Secretion of Recombinant Pediocin PA-1 by Bifidobacterium longum, Using the Signal Sequence for Bifidobacterial α-Amylase 下载免费PDF全文
Gi-Seong Moon Yu-Ryang Pyun Myeong Soo Park Geun Eog Ji Wang June Kim 《Applied microbiology》2005,71(9):5630-5632
A recombinant DNA, encoding the chimeric protein of the signal sequence for bifidobacterial α-amylase mature pediocin PA-1, was introduced into Bifidobacterium longum MG1. Biologically active pediocin PA-1 was successfully secreted from the strain and showed bactericidal activity against Listeria monocytogenes and the same molecular mass as native pediocin PA-1. 相似文献
22.
23.
24.
25.
26.
27.
Changsung Kim 《BMB reports》2015,48(5):256-265
Cardiovascular and neurodegenerative diseases are major health threats in many
developed countries. Recently, target tissues derived from human embryonic stem
(hES) cells and induced pluripotent stem cells (iPSCs), such as cardiomyocytes
(CMs) or neurons, have been actively mobilized for drug screening. Knowledge of
drug toxicity and efficacy obtained using stem cell-derived tissues could
parallel that obtained from human trials. Furthermore, iPSC disease models could
be advantageous in the development of personalized medicine in various parts of
disease sectors. To obtain the maximum benefit from iPSCs in disease modeling,
researchers are now focusing on aging, maturation, and metabolism to
recapitulate the pathological features seen in patients. Compared to pediatric
disease modeling, adult-onset disease modeling with iPSCs requires proper
maturation for full manifestation of pathological features. Herein, the success
of iPSC technology, focusing on patient-specific drug treatment,
maturation-based disease modeling, and alternative approaches to compensate for
the current limitations of patient iPSC modeling, will be further discussed.
[BMB Reports 2015; 48(5): 256-265] 相似文献
28.
29.
88 rice and 75 soybean samples were collected from 8 provinces of Korea from March through September in 1988. The Fusarium mycotoxins, zearalenone was analyzed by direct competitive enzyme linked immunosorbent assay. 10.2% of rice and 9.3 % of soybean samples contained detectable zearalenone. The average levels of zearalenone of rice and soybean samples were 11.78μg/kg and 7.70μ/kg, respectively. 相似文献
30.
We have previously reported that in vitro HCV infection of cells of hepatocyte origin attenuates complement system at multiple steps, and attenuation also occurs in chronically HCV infected liver, irrespective of the disease stage. However, none of these regulations alone completely impaired complement pathways. Modulation of the upstream proteins involved in proteolytic processing of the complement cascade prior to convertase formation is critical in promoting the function of the complement system in response to infection. Here, we examined the regulation of C2 complement expression in hepatoma cells infected in vitro with cell culture grown virus, and validated our observations using randomly selected chronically HCV infected patient liver biopsy specimens. C2 mRNA expression was significantly inhibited, and classical C3 convertase (C4b2a) decreased. In separate experiments for C3 convertase function, C3b deposition onto bacterial membrane was reduced using HCV infected patient sera as compared to uninfected control, suggesting impaired C3 convertase. Further, iC3b level, a proteolytically inactive form of C3b, was lower in HCV infected patient sera, reflecting impairment of both C3 convertase and Factor I activity. The expression level of Factor I was significantly reduced in HCV infected liver biopsy specimens, while Factor H level remained unchanged or enhanced. Together, these results suggested that inhibition of C3 convertase activity is an additional cumulative effect for attenuation of complement system adopted by HCV for weakening innate immune response. 相似文献