85 research outputs found

    Pediatric Natural Killer Cell Malignancy

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    Extending Erlang for Safe Mobile Code Execution

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    This paper discusses extensions to the functional language Erlang which provide a secure execution environment for remotely sourced code. This is in contrast to much existing work which has focused on securing procedural languages. Using a language such as Erlang provides a high degree of inherent run-time safety, which means effort can be focused on providing a suitable degree of system safety. We found that the main changes needed were the use of unforgeable (capability) references with access rights to control the use of system resources; the provision of a hierarchy of execution nodes to provide custom views of the resources available and to impose utilisation limits; and support for remote module loading. We then discuss prototype implementations of these changes, used to evaluate their utility and impact on visibility for the users of the language, and mention work in progress using this foundation to specify safety policies by filtering messages to server processes...

    Post-induction MRD by FCM and GATA1-PCR are significant prognostic factors for myeloid leukemia of Down syndrome.

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    Myeloid leukemia of Down syndrome (ML-DS) is associated with good response to chemotherapy, resulting in favorable outcomes. However, no universal prognostic factors have been identified to date. To clarify a subgroup with high risk of relapse, the role of minimal residual disease (MRD) was explored in the AML-D11 trial by the Japanese Pediatric Leukemia/Lymphoma Study Group. MRD was prospectively evaluated at after induction therapy and at the end of all chemotherapy, using flow cytometry (FCM-MRD) and GATA1-targeted deep sequencing (GATA1-MRD). A total of 78 patients were eligible and 76 patients were stratified to the standard risk (SR) group by morphology. In SR patients, FCM-MRD and GATA1-MRD after induction were positive in 5/65 and 7/59 patients, respectively. Three-year event-free survival (EFS) and overall survival (OS) rates were 93.3% and 95.0% in the FCM-MRD-negative population, and 60.0% and 80.0% in the positive population. Three-year EFS and OS rates were both 96.2% in the GATA1-MRD-negative population, and 57.1% and 71.4% in the positive population. Adjusted hazard ratios for associations of FCM-MRD or GATA1-MRD with EFS were 10.98 (p = 0.01) and 27.68 (p < 0.01), respectively. Detection of MRD by either FCM or GATA1 after initial induction therapy represents a significant prognostic factor for predicting ML-DS relapse

    Targeting the glycoproteome

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