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Titlebook: Dipeptidyl Aminopeptidases in Health and Disease; Nathan Back,Irun R. Cohen,Rodolfo Paoletti Book 2003 The Editor(s) (if applicable) and T

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楼主: indulge
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0065-2598 nopeptidases exert a potent modulatory role at an interface between immune mechanisms, metabolic responses and neuroendocrine pathways. Experimental models and clinical studies addressing the role of these enzymes and the effect of specific inhibitors pave the way to novel therapeutic concepts in im
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Dipeptidyl Peptidase IV Gene Familyotential role for DP8 and DP9 in liver disease, T cell activation and immune function. The role of the two novel enzymes DP8 and DP9 and the other non-enzyme member DPL2 in human disease will be the focus of further studies.
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Isolation and Characterization of Attractin-2 insertion of the isoforms 1, 2, 4 and 5 and questioned the predicted Ser 26 as an active site residue..We could not find differences between DP IV and attractin with respect to the specificity of inhibitors or substrates. Attractin is also capable to release dipeptides from higher molecular substrates such as neuropeptide Y.
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Specific Sports-Related Injuriesthink that DPP IV inhibitors have only little or no side effects on chemokines. Such side effects would be the prolongation or increase of inflammatory responses which have, to our knowledge, not yet been reported after in vivo applications in humans.
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Structure-Function Relationship of DPP IV: Insights into its Dimerisation and Gelatinase Activity
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Exploration of the Active Site of Dipeptidyl Peptidase IV From
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