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Detection and quantitation of Bcr-Abl transcripts using a comprehensive quantitative RT-PCR analysis system for minimal residual disease in CML patients

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Given 1907s higher affinity for FAT (SPR: K D1 = 0.8 M, K D2 = 8.7 M) compared to native LD2 (82.6 M), we expected this interaction to adopt slow-exchange NMR features, where ligand binding induces the disappearance and appearance of specific chemical peaks correlated with unbound and bound conformations, respectively