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Showing 1 to 5 of 5 for “"Atlastin"”.

  1. Testing roles of Hereditary Spastic Paraplegia genes in axonal endoplasmic reticulum modelling in Drosophila

    … mutations in HSP affect proteins of the spastin, atlastin, REEP and reticulon (RTN) families, which possess hydrophobic hairpin domains in the ER membrane to help confer curvature on tubular ER. Drosophila mutants lacking members of RTN and REEP families exhibit partial ER fragmentation in axons. …

    cambridge Repository record for Testing roles of Hereditary Spastic Paraplegia genes in axonal endoplasmic reticulum modelling in Drosophila (opens in a new tab)

  2. The interconnected roles of spastin and protrudin in endosomal sorting

    … (HSP)- associated proteins, spastin (SPG4) and atlastin-1 (SPG3A), as essential for endosomal tubule fission. I investigated the functional interaction of spastin and protrudin and found that protrudin, an ER-associated adaptor molecule involved in anterograde membrane traffic, is a novel factor …

    cambridge Repository record for The interconnected roles of spastin and protrudin in endosomal sorting (opens in a new tab)

  3. Beyond membrane curvature: Clade 6 reticulons and their role within the plant endoplasmic reticulum

    … formation, and ROOT HAIR DEFECTIVE 3 (RHD3/Atlastin/Sey1p) which is required for 3-way junction formation. The differential expression of these proteins induces changes in ER morphology, and morphological dysregulation has been associated with disruptions in overall cellular function. Within …

    oxford-brookes Repository record for Beyond membrane curvature: Clade 6 reticulons and their role within the plant endoplasmic reticulum (opens in a new tab)

  4. Characterising the roles of mammalian atlastins in the endoplasmic reticulum and beyond

    … focuses on endoplasmic reticulum (ER) proteins atlastins (ATLs), particularly ATL1, as *ATL1* gene mutations cause the most frequent childhood-onset form of HSP. Using CRISPRi, I engineered ATL1 knock-down (KD) into the i<sup>3</sup> human induced pluripotent stem cells (iPSCs) and utilised …

    cambridge Repository record for Characterising the roles of mammalian atlastins in the endoplasmic reticulum and beyond (opens in a new tab)

  5. Testing roles of Hereditary Spastic Paraplegia (HSP) proteins in organization of axonal endoplasmic reticulum (ER) and ER-mitochondria contacts

    … encode ER-shaping proteins: spastin (SPG4), atlastin (SPG3A), Receptor Expression Enhancing Protein 1 (REEP1/SPG31) and reticulon (SPG12). These proteins share a common feature of one or two intramembrane hairpin domains that can recognise or drive curvature of the ER membrane. In Drosophila, …

    cambridge Repository record for Testing roles of Hereditary Spastic Paraplegia (HSP) proteins in organization of axonal endoplasmic reticulum (ER) and ER-mitochondria contacts (opens in a new tab)