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Showing 1 to 5 of 5 for “"genome-wide scan"”.

  1. Identifikation und Charakterisierung von Suszeptibilitätsloci für Adipositas und Hypercholesterinämie in der NZO-Maus

    … syndrome, suggesting a common pathophysiology. A genome wide scan revealed a susceptibility locus for obesity and hyperinsulinemia (Nob1) on mouse chromosome 5 in the vicinity of the markers D5Mit392 and D5Mit302. Nob1 contributed to higher body weight and insulin resistance (LOD-score for BMI > …

    aachen Repository record for Identifikation und Charakterisierung von Suszeptibilitätsloci für Adipositas und Hypercholesterinämie in der NZO-Maus (opens in a new tab)

  2. Computational methods for the analysis of next generation sequencing data

    … extended the ability to study the human genome and to better understand the biology of genomes, the new technology has required profound changes to the data analysis. There is a substantial need for computational methods that allow a convenient analysis of these overwhelmingly …

    njit Repository record for Computational methods for the analysis of next generation sequencing data (opens in a new tab)

  3. Identifizierung und Charakterisierung von Suszeptibilitätsloci für Typ-2-Diabetes mellitus in einem Mausmodell für das Metabolische Syndrom

    … glucose, serum insulin, serum lipids). In a genome wide scan with more than 100 polymorphic microsatellite markers, a significant susceptibility locus (Nidd/SJL, LOD score >8) for hyperglycemia with hypoinsulinemia was identified on the distal end of chromosome 4. This SJL-derived locus was …

    aachen Repository record for Identifizierung und Charakterisierung von Suszeptibilitätsloci für Typ-2-Diabetes mellitus in einem Mausmodell für das Metabolische Syndrom (opens in a new tab)

  4. Genetic linkage and association studies in celiac disease: discoveries from whole genome analysis

    … adherence to gluten-free diet (GFD). In a Scandinavian genome wide scan, performed by our group and published in 2001, eight chromosomal regions apart from HLA showed nominal significance (p < 0,05), among them 5q31-33. This region was previously suggested as a susceptibility region in …

    goteborg Repository record for Genetic linkage and association studies in celiac disease: discoveries from whole genome analysis (opens in a new tab)

  5. Clinical and genetical aspects of Celiac Disease

    … ered all fi rst-degree relatives of CD patients. Genome-wide linkage scan was performed in the same material. Th is work showed signifi cant evidence of linkage to CD with an interesting region on chromosome 5q31-33 and on chromosome 11q. Simplex CD family material was collected for further …

    goteborg Repository record for Clinical and genetical aspects of Celiac Disease (opens in a new tab)