全文获取类型
收费全文 | 53篇 |
免费 | 1篇 |
专业分类
系统科学 | 1篇 |
现状及发展 | 12篇 |
研究方法 | 9篇 |
综合类 | 31篇 |
自然研究 | 1篇 |
出版年
2018年 | 1篇 |
2015年 | 1篇 |
2012年 | 3篇 |
2011年 | 3篇 |
2010年 | 1篇 |
2008年 | 1篇 |
2007年 | 2篇 |
2006年 | 2篇 |
2005年 | 2篇 |
2004年 | 3篇 |
2003年 | 5篇 |
2002年 | 8篇 |
2001年 | 1篇 |
2000年 | 5篇 |
1999年 | 1篇 |
1997年 | 1篇 |
1995年 | 1篇 |
1988年 | 2篇 |
1987年 | 1篇 |
1986年 | 1篇 |
1985年 | 2篇 |
1984年 | 1篇 |
1982年 | 1篇 |
1981年 | 1篇 |
1979年 | 2篇 |
1967年 | 2篇 |
排序方式: 共有54条查询结果,搜索用时 15 毫秒
1.
Onouchi Y Gunji T Burns JC Shimizu C Newburger JW Yashiro M Nakamura Y Yanagawa H Wakui K Fukushima Y Kishi F Hamamoto K Terai M Sato Y Ouchi K Saji T Nariai A Kaburagi Y Yoshikawa T Suzuki K Tanaka T Nagai T Cho H Fujino A Sekine A Nakamichi R Tsunoda T Kawasaki T Nakamura Y Hata A 《Nature genetics》2008,40(1):35-42
Kawasaki disease is a pediatric systemic vasculitis of unknown etiology for which a genetic influence is suspected. We identified a functional SNP (itpkc_3) in the inositol 1,4,5-trisphosphate 3-kinase C (ITPKC) gene on chromosome 19q13.2 that is significantly associated with Kawasaki disease susceptibility and also with an increased risk of coronary artery lesions in both Japanese and US children. Transfection experiments showed that the C allele of itpkc_3 reduces splicing efficiency of the ITPKC mRNA. ITPKC acts as a negative regulator of T-cell activation through the Ca2+/NFAT signaling pathway, and the C allele may contribute to immune hyper-reactivity in Kawasaki disease. This finding provides new insights into the mechanisms of immune activation in Kawasaki disease and emphasizes the importance of activated T cells in the pathogenesis of this vasculitis. 相似文献
2.
Yoshida Y Chiba T Tokunaga F Kawasaki H Iwai K Suzuki T Ito Y Matsuoka K Yoshida M Tanaka K Tai T 《Nature》2002,418(6896):438-442
N-glycosylation of proteins in the endoplasmic reticulum (ER) has a central role in protein quality control. Here we report that N-glycan serves as a signal for degradation by the Skp1-Cullin1-Fbx2-Roc1 (SCF(Fbx2)) ubiquitin ligase complex. The F-box protein Fbx2 (ref. 4) binds specifically to proteins attached to N-linked high-mannose oligosaccharides and subsequently contributes to ubiquitination of N-glycosylated proteins. Pre-integrin beta 1 is a target of Fbx2; these two proteins interact in the cytosol after inhibition of the proteasome. In addition, expression of the mutant Fbx2 Delta F, which lacks the F-box domain that is essential for forming the SCF complex, appreciably blocks degradation of typical substrates of the ER-associated degradation pathway. Our results indicate that SCF(Fbx2) ubiquitinates N-glycosylated proteins that are translocated from the ER to the cytosol by the quality control mechanism. 相似文献
3.
An ordered mesoporous organosilica hybrid material with a crystal-like wall structure 总被引:10,自引:0,他引:10
Surfactant-mediated synthesis strategies are widely used to fabricate ordered mesoporous solids in the form of metal oxides, metals, carbon and hybrid organosilicas. These materials have amorphous pore walls, which could limit their practical utility. In the case of mesoporous metal oxides, efforts to crystallize the framework structure by thermal and hydrothermal treatments have resulted in crystallization of only a fraction of the pore walls. Here we report the surfactant-mediated synthesis of an ordered benzene-silica hybrid material; this material has an hexagonal array of mesopores with a lattice constant of 52.5 A, and crystal-like pore walls that exhibit structural periodicity with a spacing of 7.6 A along the channel direction. The periodic pore surface structure results from alternating hydrophilic and hydrophobic layers, composed of silica and benzene, respectively. We believe that this material is formed as a result of structure-directing interactions between the benzene-silica precursor molecules, and between the precursor molecules and the surfactants. We expect that other organosilicas and organo-metal oxides can be produced in a similar fashion, to yield a range of hierarchically ordered mesoporous solids with molecular-scale pore surface periodicity. 相似文献
4.
5.
An expressed pseudogene regulates the messenger-RNA stability of its homologous coding gene 总被引:40,自引:0,他引:40
Hirotsune S Yoshida N Chen A Garrett L Sugiyama F Takahashi S Yagami K Wynshaw-Boris A Yoshiki A 《Nature》2003,423(6935):91-96
6.
Masayuki Yamashita Yadav Navnath D. Masaki Nagahama Tomoki Inaba Ikuo Kawasaki Shunsaku Ohta 《复旦学报(自然科学版)》2005,44(5):895-896
1 Introduction Small ring size cycloalkanes such as cyclopropanes and cyclobutanes have been found as a basic structural constituent in a wide rang of natural products~([1]). In organic synthesis, their cycloalkanes also play an important role owing to their diversity of reaction.1IntroductionSmall ring size cycloalkanes such as cyclopropanes and cyclobutanes have beenfound as a basic structuralconstituent in a wide rang of natural products[1].In organic synthesis ,their cycloalkanes also pla… 相似文献
7.
Summary Isolated post mortem human coronary arteries developed rhythmic contractions in physiological saline solution without being exposed to vasoactive agents.This study was supported by a Scientific Research Fund (No. 56480181) from the Ministry of Education, Japan. 相似文献
8.
Summary When rats were injected with a thiamine disulfide derivative, the content of thiamine triphosphate (TTP) in the liver doubled within 3 h after a preceeding rise in thiamine pyrophosphate; it then returned to the basal level within the next 3h, indicating a net increase of TTP in vivo and its rapid turnover. 相似文献
9.
Oka T Nishimoto Y Sasagawa T Kanouchi H Kawasaki Y Natori Y 《Cellular and molecular life sciences : CMLS》1999,55(1):131-134
An efficient Escherichia coli expression system for the production of a perchloric acid-soluble protein (PSP) has been constructed. Complementary DNA encoding
PSP was inserted into an inducible bacterial expression vector pGEX-4T-1. After the plasmid introduced into E. coli was expressed by isopropyl 1-thio-β-D-galactopyranoside (IPTG), the recombinant product was purified by glutathione-Sepharose 4B affinity chromatography. The
purified product showed the expected NH2-terminal sequence, but the translation inhibitory activity of this product was 10 times lower compared with that of authentic
PSP isolated from rat liver.
Received 8 October 1998; received after revision 6 November 1998; accepted 6 November 1998 相似文献
10.