Publications by authors named "M De Braekeleer"

Article Synopsis
  • Inv(16)(p13q22) and t(16;16)(p13;q22) are key genetic markers in acute myelomonoblastic leukaemia (FAB AML-M4Eo), often linked to abnormal eosinophils and a better prognosis.
  • These genetic abnormalities typically produce a fusion gene (CBFB-MYH11), but some cases show normal karyotypes despite the presence of the fusion transcript.
  • A case study of a 32-year-old woman with AML-M4Eo revealed unusual genetic details, prompting the need for thorough investigations in patients with conflicting results between cytology and cytogenetics due to potential treatment implications.
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Chromosomal rearrangements of the human MLL/KMT2A gene are associated with infant, pediatric, adult and therapy-induced acute leukemias. Here we present the data obtained from 2345 acute leukemia patients. Genomic breakpoints within the MLL gene and the involved translocation partner genes (TPGs) were determined and 11 novel TPGs were identified.

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Exposure to asbestos results in serious risks of developing mesothelioma and lung cancer. The link between asbestos exposure and lung carcinoma is well established. Nevertheless, precise histopathological data are poorly considered when investigating the asbestos-cancer link in a compensatory approach.

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In the last 10 years, several approaches, including microarrays, have been applied to investigate sperm transcript levels. However, success using microarray profiling is highly dependent of the quality of the RNA obtained. Therefore, the development of methods that deliver highly purified and intact RNA is of utmost importance.

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Malignant melanomas may be difficult to differentiate from benign nevi on the basis of histology. Contrary to nevi, the majority of melanomas harbor chromosomal imbalances. Comparative genomic hybridization-based and fluorescence hybridization (FISH) tests can help differentiating malignant from benign tumors.

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