Search for dissertations about: "Marie-louise Andersson"

Found 3 swedish dissertations containing the words Marie-louise Andersson.

  2. 1. Human Endogenous Retroviruses: Expression and Evolutionary Relationships

    Author : Marie-Louise Andersson; Avdelningen för medicinsk mikrobiologi; []
    Keywords : MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; Mikrobiologi; mycology; virology; bacteriology; Microbiology; bakteriologi; expression; transcription; reverse transcriptase; HERV; phylogeny; virologi; mykologi;

    Abstract : The human genome contains genetic elements which are more or less similar to infectious retroviruses. These are called human endogenous retroviruses (HERVs) and are thought to be remnants of infections in the primate lineage. READ MORE

  4. 2. A sub-phenotype approach to dissect the genetic control of murine type 1 diabetes

    Author : Marie-Louise Bergman; Leif Andersson; Umeå universitet; []
    Keywords : MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES;

    Abstract : The non-obese diabetic (NOD) mouse is a model for human type 1 diabetes (T1D). The disease in the NOD mouse is polygenic and multifactorial and so far at least 20 insulin dependent diabetes (Idd) susceptibility loci have been identified. However, no etiological mutations have been definitely ascribed to the Idd loci. READ MORE

  5. 3. Genetic and Clinical Investigation of Noonan Spectrum Disorders

    Author : Sara Ekvall; Marie-Louise Bondeson; Göran Andersson; Uppsala universitet; []
    Keywords : MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; RASopathies; Noonan syndrome; neurofibromatosis type 1; neurofibromatosis-Noonan syndrome; RAS-MAPK pathway; mutation; Medical Science; Medicinsk vetenskap;

    Abstract : Noonan spectrum disorders belong to the RASopathies, a group of clinically related developmental disorders caused by dysregulation of the RAS-MAPK pathway. This thesis describes genetic and clinical investigations of six families with Noonan spectrum disorders. READ MORE