{"title":"多尺度动力学评估","authors":"P. Hemmerich, K. Weißhart","doi":"10.1002/IMIC.200990061","DOIUrl":null,"url":null,"abstract":"Most processes in the eukaryotic cell nucleus are spatially and temporally regulated. To understand the dynamics in the underlying networks in quantitative terms necessitates the employment of technologies that can measure molecular concentrations, interactions and diffusion of proteins with high resolution. Using a combination of the available toolkit offers the potential to get a full picture of the dynamics of nuclear proteins in their most natural setting, the living cell.","PeriodicalId":100658,"journal":{"name":"Imaging & Microscopy","volume":"21 1","pages":"42-45"},"PeriodicalIF":0.0000,"publicationDate":"2009-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Multiscale Dynamics Assessment\",\"authors\":\"P. Hemmerich, K. Weißhart\",\"doi\":\"10.1002/IMIC.200990061\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Most processes in the eukaryotic cell nucleus are spatially and temporally regulated. To understand the dynamics in the underlying networks in quantitative terms necessitates the employment of technologies that can measure molecular concentrations, interactions and diffusion of proteins with high resolution. Using a combination of the available toolkit offers the potential to get a full picture of the dynamics of nuclear proteins in their most natural setting, the living cell.\",\"PeriodicalId\":100658,\"journal\":{\"name\":\"Imaging & Microscopy\",\"volume\":\"21 1\",\"pages\":\"42-45\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2009-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Imaging & Microscopy\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/IMIC.200990061\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Imaging & Microscopy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/IMIC.200990061","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Most processes in the eukaryotic cell nucleus are spatially and temporally regulated. To understand the dynamics in the underlying networks in quantitative terms necessitates the employment of technologies that can measure molecular concentrations, interactions and diffusion of proteins with high resolution. Using a combination of the available toolkit offers the potential to get a full picture of the dynamics of nuclear proteins in their most natural setting, the living cell.
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