全文获取类型
收费全文 | 759篇 |
免费 | 145篇 |
国内免费 | 4篇 |
出版年
2020年 | 6篇 |
2018年 | 9篇 |
2017年 | 11篇 |
2016年 | 9篇 |
2015年 | 30篇 |
2014年 | 23篇 |
2013年 | 39篇 |
2012年 | 55篇 |
2011年 | 55篇 |
2010年 | 33篇 |
2009年 | 27篇 |
2008年 | 33篇 |
2007年 | 27篇 |
2006年 | 25篇 |
2005年 | 24篇 |
2004年 | 26篇 |
2003年 | 25篇 |
2002年 | 22篇 |
2001年 | 19篇 |
2000年 | 24篇 |
1999年 | 21篇 |
1998年 | 10篇 |
1997年 | 5篇 |
1996年 | 7篇 |
1995年 | 14篇 |
1994年 | 13篇 |
1993年 | 11篇 |
1992年 | 29篇 |
1991年 | 19篇 |
1990年 | 21篇 |
1989年 | 18篇 |
1988年 | 16篇 |
1987年 | 13篇 |
1986年 | 13篇 |
1985年 | 18篇 |
1984年 | 12篇 |
1983年 | 8篇 |
1982年 | 8篇 |
1981年 | 15篇 |
1980年 | 7篇 |
1979年 | 9篇 |
1978年 | 14篇 |
1977年 | 10篇 |
1976年 | 15篇 |
1975年 | 8篇 |
1974年 | 9篇 |
1973年 | 5篇 |
1972年 | 6篇 |
1971年 | 7篇 |
1967年 | 4篇 |
排序方式: 共有908条查询结果,搜索用时 15 毫秒
1.
Functional and structural conservation in the mechanosensitive channel MscL implicates elements crucial for mechanosensation 总被引:13,自引:5,他引:8
mscL encodes a channel in Escherichia coli that is opened by membrane stretch force, probably serving as an osmotic gauge. Sequences more or less similar to mscL are found in other bacteria, but the degree of conserved function has been unclear. We subcloned and expressed these putative homologues in E . coli and examined their products under patch clamp. Here, we show that each indeed encodes a conserved mechanosensitive channel activity, consistent with the interpretation that this is an important and primary function of the protein in a wide range of bacteria. Although similar, channels of different bacteria differ in kinetics and their degree of mechanosensitivity. Comparison of the primary sequence of these proteins reveals two highly conserved regions, corresponding to domains previously shown to be important for the function of the wild-type E . coli channel, and a C-terminal region that is not conserved in all species. This structural conservation is providing insight into regions of this molecule that are vital to its role as a mechanosensitive channel and may have broader implications for the understanding of other mechanosensitive systems. 相似文献
2.
Molecular cloning and DNA sequence analysis of the human guanine nucleotide-binding protein Go alpha 总被引:4,自引:0,他引:4
S Lavu J Clark R Swarup K Matsushima K Paturu J Moss H F Kung 《Biochemical and biophysical research communications》1988,150(2):811-815
The nucleotide sequence of human Go alpha was determined from a partial human brain cDNA clone and the sequence of the first two 5' coding exons of a human genomic Go alpha clone. Comparison of this sequence with bovine and rat Go alpha shows greater than 90% homology at the nucleotide and deduced amino acid level. There is 100% identity at the amino acid level for the cholera and pertussis toxin-catalyzed ADP ribosylation sites, the putative guanine nucleotide binding, and the GTP hydrolysis sites. 相似文献
3.
Athymic nude CD4+8- T cells produce IL-2 but fail to proliferate in response to mitogenic stimuli 总被引:5,自引:0,他引:5
A comparative study of immune functions of CD4+8- T cells isolated from normal and athymic nude mice by electronic cell sorting was performed. Athymic nude CD4+8- T cells expressed the TCR-associated CD3 molecule but the level of expression was significantly lower than that of normal CD4+8- T cells. Proliferative responses were studied upon stimulation by 1) the T cell mitogen Con A; 2) anti-CD3 mediated cross-linking of the CD3:TCR complex, and 3) the combined action of PMA + ionomycin. All three mitogenic stimuli caused readily detectable cell division in normal (euthymic) CD4+8- T cells. In marked contrast, none of the mitogenic stimuli induced significant proliferation in athymic nude CD4+8- T cells. The failure of athymic nude CD4+8- T cells to proliferate occurred over a wide range of mitogen concentrations and over a 4-day observation period. Neither exogenously supplied rIL-2 or mixed lymphocyte culture supernatant had any effect on the impaired proliferative response by athymic nude CD4+8- T cells. Although IL-2 was produced by athymic nude CD4+8- T cells at a reduced level when compared to normal CD4+8- T cells, it was nevertheless readily detected upon stimulation with either Con A or anti-CD3. Furthermore, stimulation of athymic nude CD4+8- T cells by anti-CD3 induced the expression of the p55 chain of IL-2R on the cell surface. Therefore, despite production of IL-2 and induced expression of IL-2R, athymic nude CD4+8- T cells failed to undergo cell division. 相似文献
4.
5.
6.
7.
M R Smith M Jaramillo P T Tuazon J A Traugh Y L Liu N Sonenberg H F Kung 《The New biologist》1991,3(6):601-607
Eukaryotic initiation factor-4E (eIF-4E) binds to the cap structure of eukaryotic mRNAs and is a component of the cap-binding protein complex eIF-4F. eIF-4E is present in cells in limiting concentrations and is phosphorylated both in vivo and in vitro by protein kinase C (PKC). Recently, eIF-4E has been implicated as an intracellular transducer of extracellular growth signals; microinjection of recombinant eIF-4E into quiescent NIH 3T3 cells induced DNA synthesis. In the present report, the mitogenic activity of eIF-4E was examined after coinjection with PKC. Recombinant eIF-4E was phosphorylated by PKC at the same amino acid that is phosphorylated in cultured cells and reticulocytes in response to phorbol ester. At limiting concentrations of eIF-4E, coinjection with PKC induced a fivefold increase in the mitogenic activity of eIF-4E. Injection of PKC alone or coinjection of eIF-4E with cAMP-dependent protein kinase (PKA) or the Raf protein had no effect. These results suggest that the mitogenic activity of eIF-4E is enhanced by PKC-specific phosphorylation and that phosphate addition is a rate-limiting step in eIF-4E activity. 相似文献
8.
9.
10.