Rearrangement in the second intron of the RARA gene is present in a large majority of patients with acute promyelocytic leukemia and is used as a molecular marker for retinoic acid-induced leukemic cell differentiation
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Characterization of a novel zinc finger gene disrupted by the t(15;17) in acute promyelocytic leukemia
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Diagnosis of acute promyelocytic leukemia by RT-PCR: Detection of PML-RARα and RAR-PML fusion transcripts
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Reverse transcription polymerase chain reaction for the rearranged retinoic acid receptor alpha clarifies diagnosis and detects minimal residual disease in acute promyelocytic leukemia
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The t(15;17) breakpoint in acute promyelocytic leukemia cluster within two different sites of the myl gene: Targets for the detection of minimal residual disease by the polymerase chain reaction
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Characterization of fusion cDNA (RAR/myl) transcribed from the t(15;17) translocation breakpoint in acute promyelocytic leukemia
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Occurrence of distinct PML-RAR-alpha fusion gene isoform in patients with acute promyelocytic leukemia detected by reverse transcriptase/ polymerase chain reaction
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Molecular evaluation of residual disease as a predictor of relapse in acute promyelocytic leukemia
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Clinical study on all-trans retinoic acid in the treatment of 544 patients with acute promyelocytic leukemia
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