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Showing 1 to 5 of 5 for “"inherited cancer predisposition"”.

  1. Focused CRISPR-Cas9 screens investigating the DNA damage response

    … cause a spectrum of disorders ranging from inherited cancer predisposition syndromes to developmental disorders. Genetic screens can be used to gain insights into the function of known DDR proteins, identify novel DDR components and highlight potential therapeutic opportunities. We …

    cambridge Repository record for Focused CRISPR-Cas9 screens investigating the DNA damage response (opens in a new tab)

  2. Merlin Regulation of Mouse Spinal Cord Neural Precursor Cell Function

    <p>Cancers of the spinal cord are uncommon neoplasms, the majority of which are glial cell tumors (ependymoma and astrocytoma) thought to arise from multipotent neuroglial progenitor (stem) cells (NPCs) within the spinal cord. Whereas many spinal ependymomas exhibit indolent behavior, the only …

    wustl Repository record for Merlin Regulation of Mouse Spinal Cord Neural Precursor Cell Function (opens in a new tab)

  3. Omics Approaches to Uncover Germline and Somatic Variation Underlying Inherited Sarcomagenesis

    … underlying sarcomagenesis, we leveraged two rare inherited cancer predisposition syndromes, Li-Fraumeni Syndrome (LFS), and LFS-like (LFSL), both with a high incidence of sarcomas. LFS is caused by mutations in the tumor suppressor gene <em>TP53 (p53)</em><em>, </em>but has variable and incomplete …

    uthsc Repository record for Omics Approaches to Uncover Germline and Somatic Variation Underlying Inherited Sarcomagenesis (opens in a new tab)

  4. Somatic mutagenesis in humans with deficient DNA repair

    … in normal cells causes the development of cancer and is implicated as a potential mechanism in the physiological process of ageing. In recent years our ability to interrogate the genome of human cancers and the normal tissues from which they arise has expanded greatly. These studies have …

    cambridge Repository record for Somatic mutagenesis in humans with deficient DNA repair (opens in a new tab)

  5. Ethanol-induced formation of colorectal tumours and precursors in a mouse model of Lynch syndrome

    Lynch Syndrome (LS) confers an inherited cancer predisposition, particularly for colorectal cancer, due to germline mutations in one of the DNA mismatch repair (MMR) genes, such as MSH2. MMR is a DNA damage repair pathway involved in the removal of base mismatches and insertion/deletion loops, …

    edinburgh Repository record for Ethanol-induced formation of colorectal tumours and precursors in a mouse model of Lynch syndrome (opens in a new tab)