Search for dissertations about: "Hereditary cancer"
Showing result 21 - 25 of 94 swedish dissertations containing the words Hereditary cancer.
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21. Towards improved management of Lynch syndrome; ovarian cancer profiles, risk perception, knowledge and family perspectives
Abstract : Lynch syndrome (hereditary nonpolyposis colorectal cancer) is one of the most common hereditary cancer syndromes and predisposes to several cancer types, including cancer of the colorectum, endometrium and ovaries. Cancer develops at an early age and one third of the individuals are affected by a metachronous cancer. READ MORE
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22. Intrinsic subtypes and prognostic implications in epithelial ovarian cancer
Abstract : Ovarian cancer is the seventh most common cancer in women globally, with approximately 240,000 new cases annually. Although a rare disease, it is the most lethal gynecologic malignancy. Unspecific symptoms result in late diagnosis and a generally poor prognosis. READ MORE
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23. Molecular studies of endocrine tumors : Insights from genetics and epigenetics
Abstract : Endocrine tumors may be benign or malignant and may occur in any of the hormone producing tissues. They share several biological characteristics, including a low mutation-burden, and may co-occur in several hereditary tumor syndromes. The aim of this thesis was to identify genetic and epigenetic aberrations in endocrine tumors. READ MORE
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24. Insights into breast cancer: New familial patterns and identification of a potential predictive marker
Abstract : The last proportion of heredity in breast cancer has proven to be somewhat elusive despite massive attempts to identify the associated factors. Approximately 50 percent of breast cancer caused by familial factors is currently explained. READ MORE
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25. Genetic and epidemiological studies of hereditary colorectal cancer
Abstract : Lynch syndrome (Hereditary Nonpolyposis Colorectal Cancer, HNPCC) is the most common hereditary syndrome predisposing to colorectal cancer, accounting for 1-3% of all colorectal cancer. This multi-organ cancer predisposition syndrome is caused by mutations in the mismatch repair (MMR) genes, especially MLH1 and MSH2, and to lesser extents MSH6 and PMS2, which lead to widespread genetic instability and thus microsatellite instability (MSI). READ MORE