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1 (formerly YbfM) have increased resistance to duramycin.
2 ox status of the lung tissue whereas (99m)Tc-duramycin, a new marker of cell injury, senses cell deat
4 s) mutant became extremely hypersensitive to duramycin, although the sensitivity to papuamide A was u
5 ven the unique physicochemical properties of duramycin and the availability of PtdE in acute cell dea
6 this study was to develop and evaluate 99mTc-duramycin as a novel molecular probe for imaging PtdE.
7 high-dose radiation exposure, using (99m)Tc-duramycin as a phosphatidylethanolamine-binding radiopha
8 e potential use of (99m)Tc-HMPAO and (99m)Tc-duramycin as redox and cell-death imaging biomarkers, re
9 on, followed by a gradual decline in (99m)Tc-duramycin binding accompanied by extensive thymic atroph
11 motherapy and radiotherapy increased (99m)Tc-duramycin binding to COLO205 cells in a concentration/do
13 enously with either (99m)Tc-HMPAO or (99m)Tc-duramycin (both 37-74 MBq), and planar images were acqui
18 PE-specific cyclic peptide lantibiotic agent Duramycin efficiently inhibits the entry of West Nile, d
21 , our aim was to validate the use of (99m)Tc-duramycin for imaging the early response of tumors to tr
36 onclusion: We have demonstrated that (99m)Tc-duramycin specifically accumulates in apoptotic tumors i
38 response evaluation was assessed by (99m)Tc-duramycin SPECT and (18)F-FDG PET imaging in treatment-s
39 response evaluation was assessed by (99m)Tc-duramycin SPECT and (18)F-FDG PET imaging in treatment-s
41 epatic background, the avid binding of 99mTc-duramycin to the infarcted myocardium quickly becomes co
45 After tumor irradiation with 4.5 Gy, (99m)Tc-duramycin uptake in tumors increased significantly (1.24
46 and 3 wk after receipt of 15 Gy, and (99m)Tc-Duramycin uptake was more than doubled at 2 and 3 wk.
47 Results: COLO205 tumor uptake of (99m)Tc-duramycin was increased 7-fold from baseline in conatumu
53 ve power of cell death imaging using (99m)Tc-duramycin with the current gold standard (18)F-FDG for t