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pubmed-article:16570163pubmed:abstractTextRecombinant DNA technology is a useful tool that can be used to create insulin analogues with modified absorption kinetics to improve glycaemic control in patients with type 1 and type 2 diabetes. Among conventional insulin analogues, which are usually created by amino acid exchange, insulin detemir is the first analogue to be acylated with a fatty acid to enable reversible albumin binding. In this study we determined activation of the insulin receptor (IR)-signalling cascade by insulin detemir at the level of IR and IR substrate (Irs) phosphorylation, as well as downstream signalling elements such as phosphatidylinositol 3-kinase and Akt, and performed epidural EEG in vivo.lld:pubmed
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pubmed-article:16570163pubmed:articleTitleTissue selectivity of insulin detemir action in vivo.lld:pubmed
pubmed-article:16570163pubmed:affiliationDepartment of Internal Medicine IV, University of Tübingen, 72076 Tübingen, Germany.lld:pubmed
pubmed-article:16570163pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16570163pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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