全文获取类型
收费全文 | 1137篇 |
免费 | 76篇 |
出版年
2022年 | 3篇 |
2021年 | 17篇 |
2020年 | 10篇 |
2019年 | 16篇 |
2018年 | 12篇 |
2017年 | 15篇 |
2016年 | 18篇 |
2015年 | 25篇 |
2014年 | 42篇 |
2013年 | 68篇 |
2012年 | 78篇 |
2011年 | 74篇 |
2010年 | 50篇 |
2009年 | 47篇 |
2008年 | 82篇 |
2007年 | 76篇 |
2006年 | 75篇 |
2005年 | 74篇 |
2004年 | 69篇 |
2003年 | 60篇 |
2002年 | 68篇 |
2001年 | 14篇 |
2000年 | 12篇 |
1999年 | 12篇 |
1998年 | 19篇 |
1997年 | 13篇 |
1996年 | 10篇 |
1995年 | 11篇 |
1994年 | 17篇 |
1993年 | 8篇 |
1992年 | 8篇 |
1991年 | 6篇 |
1990年 | 7篇 |
1989年 | 7篇 |
1988年 | 7篇 |
1987年 | 6篇 |
1986年 | 6篇 |
1985年 | 3篇 |
1984年 | 12篇 |
1983年 | 3篇 |
1982年 | 8篇 |
1981年 | 9篇 |
1980年 | 6篇 |
1979年 | 8篇 |
1978年 | 6篇 |
1976年 | 2篇 |
1973年 | 4篇 |
1970年 | 2篇 |
1967年 | 1篇 |
1961年 | 1篇 |
排序方式: 共有1213条查询结果,搜索用时 15 毫秒
1.
2.
3.
Yasuko Koumoto Ryuji Tsugeki Tomoo Shimada Hitoshi Mori Maki Kondo Ikuko Hara-Nishimura Mikio Nishimura 《The Plant journal : for cell and molecular biology》1996,10(6):1119-1125
Chaperonin (Cpn) is one of the molecular chaperones. Cpn10 is a co-factor of Cpn60, which regulates Cpn60-mediated protein folding. It is known that Cpn10 is located in mitochondria and chloroplasts in plant cells. The Escherichia coli homologue of Cpn10 is called GroES. A cDNA for the Cpn10 homologue was isolated from Arabidopsis thaliana by functional complementation of the E. coli groES mutant. The cDNA was 647 bp long and encoded a polypeptide of 98 amino acids. The deduced amino acid sequence showed approximately 50% identity to mammalian mitochondrial Cpn10s and 30% identity to GroES. A Northern blot analysis revealed that the mRNA for the Cpn10 homologue was expressed uniformly in various organs and was markedly induced by heat-shock treatment. The Cpn10 homologue was constitutively expressed in transgenic tobaccos. Immunogold and immunoblot analyses following the subcellular fractionation of leaves from transgenic tobaccos revealed that the Cpn10 homologue was localized in mitochondria and accumulated at a high level in transgenic tobaccos. 相似文献
4.
H. Ueda Takeshi Baba Nobuo Terada Yasuko Kato Shigeo Tsukahara Shinichi Ohno 《Histochemistry and cell biology》1997,108(3):243-248
It is known that the retina contains the protein dystrophin in the ribbon synapse, but the ultrastructural analysis is not
yet fully elucidated. Our previous study reported that dystrophin is localized under the rod cell membranes in rat retinas.
In the present study, we have investigated the relationship between dystrophin-rich regions of rod cell membranes and other
neuronal processes in mouse retinas with a monoclonal antibody raised against the human dystrophin C-terminus. Immunoblotting,
immunofluorescence stainings, and immunoelectron microscopy were employed. Immunoblotting analysis indicated that mouse retinas
possessed some of the dystrophin isoforms of approximately 260 kDa, 140 kDa, and 70 kDa molecular weight. Confocal images
showed a punctate appearance in the outer plexiform layer, as previously described. Immunoelectron microscopy showed that
dystrophin immunoreactive products were always observed at submembranous dense regions of the rod spherule abutting bipolar
processes. These results suggest that retinal dystrophin may be closely involved in signal transmission from rods to bipolar
cells.
Accepted: 7 May 1997 相似文献
5.
6.
Yasuko Nakayama 《Microbiology and immunology》1967,11(2):95-101
The zymogram patterns of esterases and catalases of mycobacterial strains were studied using the thin layer agar electrophoresis. Though there were some variations, Mycobacterium hominis, M. bovis, M. kansasii, M. fortuitum, M. runyonii, M. avium, M. phlei and M. smegmatis seemed to show species-specific patterns consisting of 2 to 6 esterase bands and one or more catalase bands. The patterns of scotochromogens and nonchromogens were rather variable. 相似文献
7.
The frequency of interchromatic exchanges induced by mitomycin C in cultured human lymphocytes was markedly lowered in the presence of caffeine or isonicotinic acid hydrazide (INH) during a post-treatment period. The autoradiographic experiment showed that the decrease in the exchange frequency did not result from delaying or cell-killing effects by the post-treatment with caffeine or INH. Therefore, it may deduced that the exchange formation closely related to a process sensitive to caffeine or INH. 相似文献
8.
Glycoprotein O (gO) is conserved among betaherpesviruses, but little is known about the maturation process of gO in human herpesvirus 6 (HHV-6). We found that HHV-6 gO maturation was accompanied by cleavage of its carboxyl terminus and required coexpression of gH and gL, which promoted the export of gO out of the endoplasmic reticulum (ER). Finally, we also found that gO was not required for HHV-6A growth in T cells. 相似文献
9.
The dynamic behavior of organelles is essential for plant survival under various environmental conditions. Plant organelles, with various functions,migrate along actin filaments and contact other types of organelles, leading to physical interactions at a specific site called the membrane contact site. Recent studies have revealed the importance of physical interactions in maintaining efficient metabolite flow between organelles.In this review, we first summarize peroxisome function under different environmental conditions and growth stages to understand organelle interactions. We then discuss current knowledge regarding the interactions between peroxisome and other organelles, i.e., the oil bodies, chloroplast, and mitochondria from the perspective of metabolic and physiological regulation, with reference to various organelle interactions and techniques for estimating organelle interactions occurring in plant cells. 相似文献