全文获取类型
收费全文 | 146篇 |
免费 | 6篇 |
出版年
2023年 | 1篇 |
2019年 | 2篇 |
2018年 | 4篇 |
2017年 | 1篇 |
2016年 | 8篇 |
2015年 | 7篇 |
2014年 | 11篇 |
2013年 | 6篇 |
2012年 | 9篇 |
2011年 | 15篇 |
2010年 | 7篇 |
2009年 | 11篇 |
2008年 | 9篇 |
2007年 | 7篇 |
2006年 | 8篇 |
2005年 | 6篇 |
2004年 | 5篇 |
2003年 | 6篇 |
2002年 | 7篇 |
2001年 | 1篇 |
2000年 | 2篇 |
1999年 | 3篇 |
1998年 | 1篇 |
1997年 | 4篇 |
1996年 | 2篇 |
1994年 | 1篇 |
1993年 | 1篇 |
1990年 | 1篇 |
1989年 | 1篇 |
1987年 | 1篇 |
1984年 | 1篇 |
1981年 | 1篇 |
1978年 | 1篇 |
1977年 | 1篇 |
排序方式: 共有152条查询结果,搜索用时 0 毫秒
151.
The binding kinetics of the specific dopamine D2 antagonist [3H]raclopride to dopamine D2 receptors in rat neostriatum were studied. The pseudo-first-order rate constants of [3H]raclopride binding with these membranes revealed a hyperbolic dependence upon the antagonist concentration, indicating that the reaction had at least two consecutive and kinetically distinguished steps. The first step was fast binding equilibrium, characterized by the dissociation constant KA = 12 ± 2 nM. The following step corresponded to a slow isomerization of the receptor-antagonist complex, characterized by the isomerization equilibrium constant Ki = 0.11. The dissociation constant Kd = 1.3 nM, calculated from these kinetic data, was similar to Kd = 2.4 nM, determined from equilibrium binding isotherm for the radioligand. Implications of the complex reaction mechanism on dopamine D2 receptor assay by [3H]raclopride were discussed. 相似文献
152.
The carbohydrate-deficient glycoprotein syndromes are a recentlydelineated group of genetic, multisystemic diseases with majornervous system involvement. Three distinct variants have beenrecognized and there are probably many more. They are characterizedby a deficiency of the carbohydrate moiety of secretory glycoproteins,lysosomal enzymes and probably also membranous glycoproteins.The biochemical changes are most readily observed in serum transferrinand the diagnosis is usually made by isoelectric focusing ofthis glycoprotein. The deficiency of sialic acid, in particular,results in a cathodal shift and hence the presence of abnormalisoforms of transferrin with higher isoelectric points thannormal. The basis defects are probably in the processing andsynthesis of the carbohydrate moiety of glycoproteins; thereis indirect evidence for a deficiency of asparagine-N-linkedoligosaccharide transfer in type I (endoplasmic reticulum defect)and for a deficiency of N-acetylglucosaminyltransferase II intype II (Golgi defect). From the large number of patients detectedin only a few years, it is expected that these diseases willbecome as important as, for example, the lysosomal, peroxisomalor mitochondrial disorders. Their study will undoubtedly yielda wealth of new information on the function of glycoproteinsand of their carbohydrate moiety. endoplasmic reticulum glycoproteins glycosylation Golgi sialotransferrins 相似文献