pubmed-article:19568797 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19568797 | lifeskim:mentions | umls-concept:C0035820 | lld:lifeskim |
pubmed-article:19568797 | lifeskim:mentions | umls-concept:C0596901 | lld:lifeskim |
pubmed-article:19568797 | lifeskim:mentions | umls-concept:C0242485 | lld:lifeskim |
pubmed-article:19568797 | lifeskim:mentions | umls-concept:C1704675 | lld:lifeskim |
pubmed-article:19568797 | lifeskim:mentions | umls-concept:C0012222 | lld:lifeskim |
pubmed-article:19568797 | pubmed:issue | 1-4 | lld:pubmed |
pubmed-article:19568797 | pubmed:dateCreated | 2009-7-1 | lld:pubmed |
pubmed-article:19568797 | pubmed:abstractText | The techniques of diffusion analysis based on optical microscopy approaches have revealed a great diversity of the dynamic organisation of cell membranes. For a long period, two frameworks have dominated the way of representing the membrane structure: the membrane skeleton fences and the lipid raft models. Progresses in the methods of data analysis have shed light on the features and consequently the possible origin of membrane domains: Inter-protein interactions play a role in confinement. Innovative developments pushing forward the spatiotemporal resolution limits are currently emerging, which are likely to provide in the future a detailed understanding of the intimate functional dynamic organisation of the cell membrane. | lld:pubmed |
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