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Showing 1 to 4 of 4 for “"Genetic Predisposition to Disease"”.

  1. Investigation of Rare Genetic Variation in Autism Spectrum Disorder by Genomic Screens

    … ASD is highly heritable, however known genetic factors that contribute to ASD explain ~30% of cases, with each factor contributing to <1% of cases. The genetic and phenotypic heterogeneity of ASD reduces the power to identify causative genes. Furthermore, even with the growing number of …

    utswmed Repository record for Investigation of Rare Genetic Variation in Autism Spectrum Disorder by Genomic Screens (opens in a new tab)

  2. Analysis of Coding Region SNPs and Its Propensity to Cause Disease

    … These variations in individuals are considered to be the cause of diseases, difference in response to treatment, susceptibility to diseases or may have no impact. Association studies aim at correlating an observed disease or a phenotype with these sequence variations. However very few of these …

    utswmed Repository record for Analysis of Coding Region SNPs and Its Propensity to Cause Disease (opens in a new tab)

  3. A Mutation in Alk6b Causes Impaired Germ Cell Differentation and Testicular Germ Cell Tumors in Zebrafish

    … exhibit differentiated and undifferentiated histologies, which vary in their malignant potential and response to treatment. The pathways that determine tumor cell differentiation are not known, impeding the development of new therapies. Thus, the treatment of GCTs has remained static since the …

    utswmed Repository record for A Mutation in Alk6b Causes Impaired Germ Cell Differentation and Testicular Germ Cell Tumors in Zebrafish (opens in a new tab)

  4. Neural Mechanisms and Behaviors in Models of Conditional Nprl2 Loss

    The file named "DENTEL-PRIMARY-2022-1.pdf" is the primary dissertation file. Two (2) supplemental video files are also available and may be viewed individually.

    utswmed Repository record for Neural Mechanisms and Behaviors in Models of Conditional Nprl2 Loss (opens in a new tab)