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Showing 1 to 7 of 7 for “"Myelodysplastic Syndromes (MDS)"”.

  1. PU.1-ACTIVATED GENOMIC REGIONS DEFINE LOW-RISK MDS SUBSETS CHARACTERIZED BY IMMUNE DYSREGULATION AND DISEASE PROGRESSION

    Myelodysplastic syndromes (MDS) are heterogeneous myeloid neoplasms with an increased risk of progression to secondary acute myeloid leukemia (sAML). This study investigates the genomic signatures associated to disease progression in MDS. To this end, we profiled active genomic regulatory regions …

    milano Repository record for PU.1-ACTIVATED GENOMIC REGIONS DEFINE LOW-RISK MDS SUBSETS CHARACTERIZED BY IMMUNE DYSREGULATION AND DISEASE PROGRESSION (opens in a new tab)

  2. Dissecting The Mechanisms of Venetoclax Resistance In Myelodysplastic Syndromes

    <p>Myelodysplastic syndromes (MDS) are a class of heterogeneous clonal hematopoietic disorders. The current standard of care for MDS is the hypomethylating agent (HMA)-based therapy. However, only 50 percent of the patients respond, with transient effects and no approved second-line treatment …

    uthsc Repository record for Dissecting The Mechanisms of Venetoclax Resistance In Myelodysplastic Syndromes (opens in a new tab)

  3. Clinical Utility and Impact of Targeted Nucleic Acid Sequencing in Myeloid Malignancies and Precursor Lesions

    … mutated in myeloid malignancies, including myelodysplastic syndromes (MDS), myeloproliferative neoplasms (MPN) and acute myeloid leukemia (AML), with expanding diagnostic and clinical significance. Given the breadth of genetic aberrations required to diagnose these diseases, higher …

    queens Repository record for Clinical Utility and Impact of Targeted Nucleic Acid Sequencing in Myeloid Malignancies and Precursor Lesions (opens in a new tab)

  4. Detection of Aneuploidy for Chromosomes 7 and 8 Using Fluorescence <i>In Situ</i> Hybridization in Patients with Aplastic Anemia and Sequencing of the Mitotic Checkpoint Gene hBUB1

    … by complete bone marrow failure. Progression to myelodysplastic syndromes (MDS) and acute nonlymphocytic leukemia (ANLL) occurs frequently. At the time of transformation, cytogenetic abnormalities are common. Detection of cytogenetic abnormalities prior to leukemic transformation may indicate …

    odu Repository record for Detection of Aneuploidy for Chromosomes 7 and 8 Using Fluorescence <i>In Situ</i> Hybridization in Patients with Aplastic Anemia and Sequencing of the Mitotic Checkpoint Gene hBUB1 (opens in a new tab)

  5. Trisomies in Hematologic Malignancies

    … change in acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS), and on high hyperdiploidy ? gains of multiple chromosomes ? in childhood acute lymphoblastic leukemia (ALL). In the first two articles, AML and MDS cases with +8 as the seemingly sole abnormality were studied with …

    lund Repository record for Trisomies in Hematologic Malignancies (opens in a new tab)

  6. PATTERN OF INNATE IMMUNITY IN PATIENTS AFFECTED BY MYELODYSPLASTIC SYNDROME (MDS) EITHER BEFORE ANDAFTER HEMATOPOIETIC STEM CELL TRANSPLANT (HSCT)

    Myelodysplastic syndromes (MDS) are a heterogenous group of myeloid neoplasms that primarily affect elderly people and, in the context of population aging, MDS incidence is set to increase substantially. MDS patients have a variable risk of progression to acute myeloid leukemia (AML) and are …

    milano Repository record for PATTERN OF INNATE IMMUNITY IN PATIENTS AFFECTED BY MYELODYSPLASTIC SYNDROME (MDS) EITHER BEFORE ANDAFTER HEMATOPOIETIC STEM CELL TRANSPLANT (HSCT) (opens in a new tab)

  7. Mechanisms driving the expansion and progression of splicing factor-mutant clonal haematopoiesis

    … mis-splicing events seen in SF3B1-mutant myelodysplastic syndromes (MDS). We then performed high-throughput drug screening to identify therapeutic vulnerabilities of SF3B1-mutant cells. Alongside this, we developed a pipeline for the collection of bone marrow aspirate samples from …

    cambridge Repository record for Mechanisms driving the expansion and progression of splicing factor-mutant clonal haematopoiesis (opens in a new tab)