排序方式: 共有6条查询结果,搜索用时 15 毫秒
1
1.
Linda H. Crabbe A. E. S. Gussin Elizabeth A. Tyrrell 《Cellular and molecular life sciences : CMLS》1969,25(8):793-793
Zusammenfassung Es wird gezeigt, dassBacillus cereus die Disaccharid Trehalose fermentieren kann. Die für diese Fermentwirkung benötigte Trehalase wurde durch das Substrat ermöglicht, während Puromycin den Vorgang verhinderte. Dies beweist die Notwendigkeit einer neuen Proteinsynthese.
Publication No. 1 from the Department of the Biological Sciences of Smith College.
This work was supported in part by National Science Foundation Grants to A.E.S.G. and by an Alfred P. Sloan Foundation Summer Participant Grant to L.H.C. We thank MissJudith G.Arnold for technical assistance. 相似文献
Publication No. 1 from the Department of the Biological Sciences of Smith College.
This work was supported in part by National Science Foundation Grants to A.E.S.G. and by an Alfred P. Sloan Foundation Summer Participant Grant to L.H.C. We thank MissJudith G.Arnold for technical assistance. 相似文献
2.
S. P. Wolff M. J. C. Crabbe P. J. Thornalley 《Cellular and molecular life sciences : CMLS》1984,40(3):244-246
Summary Simple monosaccharides are shown to autoxidize, under physiological conditions, forming dicarbonyl compounds and hydrogen peroxide via reactive intermediates of dioxygen and carbon centred free radicals. The rate of enolisation of the substrate to form an enediol is the rate limiting step of this spontaneous process.Acknowledgments. We should like to thank the NIH, MRC ICI Pharmaceuticals Ltd and the SERC for financial support; Dr D. Earle for helpful conversations, Mr. A.J. Bron for provision of laboratory facilities and Dr. J.V. Bannister for the generous gift of superoxide dismutase. 相似文献
3.
Selected mouse lines, alcohol and behavior 总被引:3,自引:0,他引:3
The technique of selective breeding has been employed to develop a number of mouse lines differing in genetic sensitivity to specific effects of ethanol. Genetic animal models for sensitivity to the hypnotic, thermoregulatory, excitatory, and dependence-producing effects of alcohol have been developed. These genetic animal models have been utilized in numerous studies to assess the bases for those genetic differences, and to determine the specific neurochemical and neurophysiological bases for ethanol's actions. Work with these lines has challenged some long-held beliefs about ethanol's mechanisms of action. For example, lines genetically sensitive to one effect of ethanol are not necessarily sensitive to others, which demonstrates that no single set of genes modulates all ethanol effects. LS mice, selected for sensitivity to ethanol anesthesia, are not similarly sensitive to all anesthetic drugs, which demonstrates that all such drugs cannot have a common mechanism of action. On the other hand, WSP mice, genetically susceptible to the development of severe ethanol withdrawal, show a similar predisposition to diazepam and phenobarbital withdrawal, which suggests that there may be a common set of genes underlying drug dependencies. Studies with these models have also revealed important new directions for future mechanism-oriented research. Several studies implicate brain gamma-aminobutyric acid and dopamine systems as potentially important mediators of susceptibility to alcohol intoxication. The stability of the genetic animal models across laboratories and generations will continue to increase their power as analytic tools. 相似文献
4.
本文证明了公式β(n)=σ(n-1)+1其中α(n-1)是n-1次多项式微分系统的不为直线的最多条数,βn)是n次多项式微分系统的不变直线的不同斜率的最大个数。这里假设所讨论的多项式系统只有限条不变直线。 相似文献
5.
T. J. Phillips D. J. Feller J. C. Crabbe 《Cellular and molecular life sciences : CMLS》1989,45(9):805-827
Summary The technique of selective breeding has been employed to develop a number of mouse lines differing in genetic sensitivity to specific effects of ethanol. Genetic animal models for sensitivity to the hypnotic, thermoregulatory, excitatory, and dependence-producing effects of alcohol have been developed. These genetic animal models have been utilized in numerous studies to assess the bases for those genetic differences, and to determine the specific neurochemical and neurophysiological bases for ethanol's actions. Work with these lines has challenged some long-held beliefs about ethanol's mechanisms of action. For example, lines genetically sensitive to one effect of ethanol are not necessarily sensitive to others, which demonstrates that no single set of genes modulates all ethanol effects. LS mice, selected for sensitivity to ethanol anesthesia, are not similarly sensitive to all anesthetic drugs, which demonstrates that all such drugs cannot have a common mechanism of action. On the other hand, WSP mice, genetically susceptible to the development of severe ethanol withdrawal, show a similar predisposition to diazepam and phenobarbital withdrawal, which suggests that there may be a common set of genes underlying drug dependentcies. Studies with these models have also revealed important new directions for future mechanism-oriented research. Several studies implicate brain gamma-aminobutyric acid and dopamine systems as potentially important mediators of susceptibility to alcohol intoxication. The stability of the genetic animal models across laboratories and generations will continue to increase their power as analytic tools. 相似文献
6.
Churchill GA Airey DC Allayee H Angel JM Attie AD Beatty J Beavis WD Belknap JK Bennett B Berrettini W Bleich A Bogue M Broman KW Buck KJ Buckler E Burmeister M Chesler EJ Cheverud JM Clapcote S Cook MN Cox RD Crabbe JC Crusio WE Darvasi A Deschepper CF Doerge RW Farber CR Forejt J Gaile D Garlow SJ Geiger H Gershenfeld H Gordon T Gu J Gu W de Haan G Hayes NL Heller C Himmelbauer H Hitzemann R Hunter K Hsu HC Iraqi FA Ivandic B Jacob HJ Jansen RC Jepsen KJ Johnson DK Johnson TE Kempermann G 《Nature genetics》2004,36(11):1133-1137
The goal of the Complex Trait Consortium is to promote the development of resources that can be used to understand, treat and ultimately prevent pervasive human diseases. Existing and proposed mouse resources that are optimized to study the actions of isolated genetic loci on a fixed background are less effective for studying intact polygenic networks and interactions among genes, environments, pathogens and other factors. The Collaborative Cross will provide a common reference panel specifically designed for the integrative analysis of complex systems and will change the way we approach human health and disease. 相似文献
1