全文获取类型
收费全文 | 1973篇 |
免费 | 234篇 |
国内免费 | 1篇 |
出版年
2022年 | 22篇 |
2021年 | 31篇 |
2020年 | 19篇 |
2019年 | 19篇 |
2018年 | 26篇 |
2017年 | 17篇 |
2016年 | 30篇 |
2015年 | 74篇 |
2014年 | 69篇 |
2013年 | 89篇 |
2012年 | 103篇 |
2011年 | 112篇 |
2010年 | 49篇 |
2009年 | 62篇 |
2008年 | 84篇 |
2007年 | 81篇 |
2006年 | 71篇 |
2005年 | 68篇 |
2004年 | 59篇 |
2003年 | 49篇 |
2002年 | 60篇 |
2001年 | 68篇 |
2000年 | 70篇 |
1999年 | 48篇 |
1998年 | 35篇 |
1997年 | 32篇 |
1996年 | 29篇 |
1995年 | 23篇 |
1994年 | 20篇 |
1993年 | 26篇 |
1992年 | 50篇 |
1991年 | 35篇 |
1990年 | 31篇 |
1989年 | 46篇 |
1988年 | 39篇 |
1987年 | 24篇 |
1986年 | 30篇 |
1985年 | 18篇 |
1984年 | 32篇 |
1983年 | 22篇 |
1981年 | 25篇 |
1980年 | 18篇 |
1979年 | 17篇 |
1977年 | 20篇 |
1975年 | 24篇 |
1973年 | 23篇 |
1972年 | 18篇 |
1971年 | 16篇 |
1970年 | 20篇 |
1969年 | 21篇 |
排序方式: 共有2208条查询结果,搜索用时 15 毫秒
971.
972.
Protein misfolding is increasingly recognized as a factor in many diseases, including cystic fibrosis, Parkinson's, Alzheimer's and atherosclerosis. Many proteins involved in misfolding-based pathologies are membrane-associated, such that the bilayer may play roles in normal and aberrant folding. It can be argued that the in vivo partitioning of eukaryotic membrane proteins between folding and misfolding pathways is under kinetic control. Moreover, the balance between these pathways can be surprisingly delicate. 相似文献
973.
974.
975.
Despite the wide acceptance of yeast two-hybrid (Y2H) system for protein-protein interaction analysis and discovery, conventional Y2H assays are not well suited for high-throughput screening of the protein interaction network (“interactome”) on a genomic scale due to several limitations, including labor-intensive agar plating and colony selection methods associated with the use of nutrient selection markers, complicated reporter analysis methods associated with the use of LacZ enzyme reporters, and incompatibility of the liquid handling robots. We recently reported a robust liquid culture Y2H system based on quantitative analysis of yeast-enhanced green fluorescent protein (yEGFP) reporters that greatly increased the analysis throughput and compatibility with liquid handling robots. To further advance its utility in high-throughput complementary DNA (cDNA) library screening, we report the development of a novel surface display Y2H (sdY2H) library screening system with uniquely integrated surface display hemagglutination (sdHA) antigen and yEGFP reporters. By introduction of a surface reporter sdHA into the yEGFP-based Y2H system, positive Y2H targets are quickly isolated from library cells by a simple magnetic separation without a large plating effort. Moreover, the simultaneous scoring of multiple reporters, including sdHA, yEGFP, and conventional nutrient markers, greatly increased the specificity of the Y2H assay. The feasibility of the sdY2H assay on large cDNA library screening was demonstrated by the successful recovery of positive P53/T interaction pairs at a target-to-background ratio of 1:1,000,000. Together with the massive parallel DNA sequencing technology, it may provide a powerful proteomic tool for high-throughput interactome mapping on a genomic scale. 相似文献
976.
977.
Stimulation of the β2-adrenergic receptor (β2AR) on a CD40L/interleukin-4-activated B lymphocyte increases the level of immunoglobulin E (IgE) in a protein kinase A (PKA)- and p38 mitogen-activated protein kinase (MAPK)-dependent manner. However, the mechanism by which β2AR stimulation mediates the increase in the level of p38 MAPK activation has remained unclear. Here we show that the β2AR-induced increase in p38 MAPK activation occurred via a hematopoietic protein tyrosine phosphatase (HePTP)-mediated cross talk between PKA and p38 MAPK. β2AR agonists, cAMP-elevating agents, and PKA inhibitors were used to show that β2AR stimulation resulted in a PKA-dependent increase in p38 MAPK phosphorylation. Pharmacological agents and gene-deficient mice revealed that p38 MAPK phosphorylation was regulated by the G-stimulatory (Gs)/cAMP/PKA pathway independently of the G-inhibitory or β-arrestin-2 pathways. Coimmunoprecipitation and Western blot analysis showed that HePTP was phosphorylated in a PKA-dependent manner, which inactivated HePTP and allowed for increased free p38 MAPK to be phosphorylated by the MAPK cascade that was activated by CD40L. HePTP short hairpin RNA confirmed that HePTP played a role in regulating the level of p38 MAPK phosphorylation in a B cell. Thus, β2AR stimulation on a B cell phosphorylates and inactivates HePTP in a Gs/cAMP/PKA-dependent manner to release bound p38 MAPK, making more available for phosphorylation and subsequent IgE regulation. 相似文献
978.
979.
Tresa George Qin Wen Richard Griffiths Anil Ganesh Mark Meuth Cyril M. Sanders 《Nucleic acids research》2009,37(19):6491-6502
Pif-1 proteins are 5′→3′ superfamily 1 (SF1) helicases that in yeast have roles in the maintenance of mitochondrial and nuclear genome stability. The functions and activities of the human enzyme (hPif1) are unclear, but here we describe its DNA binding and DNA remodeling activities. We demonstrate that hPif1 specifically recognizes and unwinds DNA structures resembling putative stalled replication forks. Notably, the enzyme requires both arms of the replication fork-like structure to initiate efficient unwinding of the putative leading replication strand of such substrates. This DNA structure-specific mode of initiation of unwinding is intrinsic to the conserved core helicase domain (hPifHD) that also possesses a strand annealing activity as has been demonstrated for the RecQ family of helicases. The result of hPif1 helicase action at stalled DNA replication forks would generate free 3′ ends and ssDNA that could potentially be used to assist replication restart in conjunction with its strand annealing activity. 相似文献
980.