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Showing 1 to 4 of 4 for “"Mitochondrial Encephalomyopathies"”.

  1. Identification and Characterization of Mitochondrial DNA Variants in Alzheimer's Disease

    … population regardless of ethnicity or gender. A mitochondrial hypothesis of AD has been proposed based on a number of studies which establish altered oxidative phosphorylation (OXPHOS) and ATP synthesis in AD tissue. ATP demand is most prevalent in the brain; damage to OXPHOS could severely …

    odu Repository record for Identification and Characterization of Mitochondrial DNA Variants in Alzheimer's Disease (opens in a new tab)

  2. Mitochondrial dysfunction in a cell model of thyroid oncocytoma

    The role of mitochondrial dysfunction in cancer has long been a subject of great interest. In this study, such dysfunction has been examined with regards to thyroid oncocytoma, a rare form of cancer, accounting for less than 5% of all thyroid cancers. A peculiar characteristic of thyroid oncocytic …

    bologna Repository record for Mitochondrial dysfunction in a cell model of thyroid oncocytoma (opens in a new tab)

  3. IDENTIFICAZIONE DI UNA NUOVA CAUSA GENETICA IN UN CASO FAMILIARE DI ENCEFALOMIOPATIA MITOCONDRIALE E DEFICIT DI CITOCROMO C OSSIDASI.

    … gene as the cause of an infantile progressive mitochondrial myopathy. The human GFER (growth factor ERV1 homolog), also called ALR (augmenter of liver regeneration), belongs to the ERV1/ALR sulfhydryl oxidase family, which requires flavin adenine dinucleotide (FAD) as a cofactor. The …

    milano Repository record for IDENTIFICAZIONE DI UNA NUOVA CAUSA GENETICA IN UN CASO FAMILIARE DI ENCEFALOMIOPATIA MITOCONDRIALE E DEFICIT DI CITOCROMO C OSSIDASI. (opens in a new tab)