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Showing 1 to 4 of 4 for “"Myxoid liposarcoma"”.

  1. Myxoid Liposarcoma: Models and Mechanisms of Sarcomagenesis and Response to Radiation Therapy

    <p>Myxoid liposarcoma (MLPS) is a malignant soft tissue sarcoma characterized by a pathognomonic t(12;16)(q13;p11) translocation that produces a fusion oncoprotein, FUS-CHOP. This cancer is remarkably sensitive to radiotherapy and exhibits a unique pattern of extrapulmonary metastasis. However, the …

    duke Repository record for Myxoid Liposarcoma: Models and Mechanisms of Sarcomagenesis and Response to Radiation Therapy (opens in a new tab)

  2. Development of digital PCR probe assays targeting SNPs to monitor co-cultured cell lines

    … single nucleotide polymorphisms (SNPs) of each myxoid liposarcoma (MLS) and a fibrosarcoma human-derived cell line. In his thesis, a method was developed for monitoring co-cultures with up to four different cell lines with reliable quantification using dPCR analysis, proving to be both sensitive …

    chalmers Repository record for Development of digital PCR probe assays targeting SNPs to monitor co-cultured cell lines (opens in a new tab)

  3. Molecular analysis of the FET family fusion oncoprotein FUS-DDIT3

    … initiating and driving factors of tumorigenesis. Myxoid liposarcoma (MLS) is defined by the t(12;16)(q13;p11) that cause the fusion of the FUS and DDIT3 genes and expression of a chimeric FUS-DDIT3 oncoprotein. The aim of this thesis was to functionally characterize the FUS-DDIT3 fusion …

    goteborg Repository record for Molecular analysis of the FET family fusion oncoprotein FUS-DDIT3 (opens in a new tab)

  4. Genotype and phenotype in mitochondrial disorders

    … find a probably causative somatic insertion in a myxoid liposarcoma. Natural history <br>Natural history studies tend to be small and recruit participants from specialist clinics. Working together with the National Congenital Anomalies and Rare Diseases Registration Service (NCARDRS), we have …

    cambridge Repository record for Genotype and phenotype in mitochondrial disorders (opens in a new tab)