全文获取类型
收费全文 | 663965篇 |
免费 | 76374篇 |
国内免费 | 351篇 |
专业分类
740690篇 |
出版年
2016年 | 7586篇 |
2015年 | 10329篇 |
2014年 | 12153篇 |
2013年 | 17070篇 |
2012年 | 19245篇 |
2011年 | 19664篇 |
2010年 | 13501篇 |
2009年 | 12622篇 |
2008年 | 17951篇 |
2007年 | 18617篇 |
2006年 | 17521篇 |
2005年 | 17024篇 |
2004年 | 16846篇 |
2003年 | 16241篇 |
2002年 | 15823篇 |
2001年 | 25981篇 |
2000年 | 26101篇 |
1999年 | 21092篇 |
1998年 | 7961篇 |
1997年 | 8327篇 |
1996年 | 7925篇 |
1995年 | 7431篇 |
1994年 | 7339篇 |
1993年 | 7329篇 |
1992年 | 18121篇 |
1991年 | 17865篇 |
1990年 | 17462篇 |
1989年 | 17091篇 |
1988年 | 16255篇 |
1987年 | 15738篇 |
1986年 | 14712篇 |
1985年 | 14703篇 |
1984年 | 12373篇 |
1983年 | 10925篇 |
1982年 | 8544篇 |
1981年 | 7933篇 |
1980年 | 7461篇 |
1979年 | 12261篇 |
1978年 | 9716篇 |
1977年 | 9085篇 |
1976年 | 8708篇 |
1975年 | 9471篇 |
1974年 | 10493篇 |
1973年 | 10270篇 |
1972年 | 9603篇 |
1971年 | 8694篇 |
1970年 | 7661篇 |
1969年 | 7660篇 |
1968年 | 7139篇 |
1967年 | 6125篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
991.
992.
Eliot C. Bush Anne E. Clark Chris M. DeBoever Lillian E. Haynes Sidra Hussain Singer Ma Matthew M. McDermott Adam M. Novak John S. Wentworth 《PloS one》2012,7(11)
A significant proportion of enzymes display cooperativity in binding ligand molecules, and such effects have an important impact on metabolic regulation. This is easiest to understand in the case of positive cooperativity. Sharp responses to changes in metabolite concentrations can allow organisms to better respond to environmental changes and maintain metabolic homeostasis. However, despite the fact that negative cooperativity is almost as common as positive, it has been harder to imagine what advantages it provides. Here we use computational models to explore the utility of negative cooperativity in one particular context: that of an inhibitor binding to an enzyme. We identify several factors which may contribute, and show that acting together they can make negative cooperativity advantageous. 相似文献
993.
Kainate receptors (KARs) are a class of ionotropic glutamate receptors that are expressed throughout the central nervous system. The function and subcellular localization of KARs are tightly regulated by accessory proteins. We have previously identified the single-pass transmembrane proteins, Neto1 and Neto2, to be associated with native KARs. In the hippocampus, Neto1, but not Neto2, controls the abundance and modulates the kinetics of postsynaptic KARs. Here we evaluated whether Neto2 regulates synaptic KAR levels in the cerebellum where Neto1 expression is limited to the deep cerebellar nuclei. In the cerebellum, where Neto2 is present abundantly, we found a ∼40% decrease in GluK2-KARs at the postsynaptic density (PSD) of Neto2-null mice. No change, however, was observed in total level of GluK2-KARs, thereby suggesting a critical role of Neto2 on the synaptic localization of cerebellar KARs. The presence of a putative class II PDZ binding motif on Neto2 led us to also investigate whether it interacts with PDZ domain-containing proteins previously implicated in regulating synaptic abundance of KARs. We identified a PDZ-dependent interaction between Neto2 and the scaffolding protein GRIP. Furthermore, coexpression of Neto2 significantly increased the amount of GRIP associated with GluK2, suggesting that Neto2 may promote and/or stabilize GluK2:GRIP interactions. Our results demonstrate that Neto2, like Neto1, is an important auxiliary protein for modulating the synaptic levels of KARs. Moreover, we propose that the interactions of Neto1/2 with various scaffolding proteins is a critical mechanism by which KARs are stabilized at diverse synapses. 相似文献
994.
Copper is an essential yet toxic metal ion. To satisfy cellular requirements, while, at the same time, minimizing toxicity,
complex systems of copper trafficking have evolved in all cell types. The best conserved and most widely distributed of these
involve Atx1-like chaperones and P1B-type ATPase transporters. Here, we discuss current understanding of how these chaperones bind Cu(I) and transfer it to the
Atx1-like N-terminal domains of their cognate transporter. 相似文献
995.
996.
A method for separation and visualization of the different apolipoprotein B species using 0.2% sodium dodecyl sulfate-1.5% agarose gel electrophoresis and immunoblotting is described. The method is capable of demonstrating the different forms of apolipoprotein B (apo B) in plasma volumes of 10-50 microliters without prior ultracentrifugation. After ultracentrifugation of samples, estimation of the ratio between apo B 48 and apo B 100 is possible by scanning of Coomassie-stained gels or immunoblots. 相似文献
997.
998.
999.
Estimation of bacterial densities by means of the "most probable number" 总被引:68,自引:0,他引:68
COCHRAN WG 《Biometrics》1950,6(2):105-116
1000.