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No significant changes in mean heart rate or blood pressure. EMM was associated with transient ventricular ectopic activity, but neither sustained ventricular arrhythmias nor other arrhythmias were observed. In all patients, NOGA maps were reliably reproduced after GTx in terms of the number of points, end-diastolic volume, end-systolic volume, and average loop stability data not shown ; . The LV ejection fraction, calculated on the basis of algorithms incorporated in the NOGA system, increased from 31.3 2.7% before GTx to 36.9 2.3% after GTx P 0.023 ; . Foci of ischemic myocardium, identified by preserved viability associated with impaired LLS, ie, electromechanical uncoupling, were demonstrated in all patients before GTx. Foci of ischemia involved the anterior n 1 ; , anteroseptal n 1 ; , lateral n 1 ; , inferolateral n 2 ; , posterior n 3 ; , posterolateral n 2 ; , septal n 2 ; , and inferoseptal n 1 ; walls. Mean UpV and BpV recordings 5 mV and 2 mV, respectively, defining myocardial viability in the ischemic zone, did not change significantly after GTx Table 2 ; . Mean LLS in areas of myocardial ischemia, however, improved significantly from 9.94 1.53% before phVEGF165 GTx to 15.26 0.98% after phVEGF165 GTx P 0.004 ; . The area of ischemic myocardium was consequently reduced from 6.45 1.37 cm2 before phVEGF165 GTx to 0.95 0.41 cm2 after GTx P 0.001, Table 2 ; . Examples of NOGA maps showing septal, lateral, anterior, and inferior ischemic zones before GTx with improvement after GTx are shown in panel A of Figures 1 through 5.

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By contrast, topo IV relaxes positive and negative supercoils and has evolved as an efficient DNA decatenase with a specialized role in separating daughter chromosomes at cell division 9 ; . In addition to their biological functions, topo IV and gyrase are also targets for the quinolone class of antibacterial drugs 5, 10 ; . Topo IV and gyrase are tetrameric complexes comprising two subunits each of ParC and ParE, and GyrA and GyrB, respectively 5 ; . The ParC and GyrA subunits are homologous in their N-terminal domain that carries the DNA breakage-reunion function, but diverge in their C-terminal regions that also contribute to DNA binding 11 ; . The ParE and GyrB proteins contain the ATPase site involved in energy transduction and are closely homologous, both in primary sequence and.

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