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    <title>Untersuchungen zu pathophysiologischen Merkmalen des Morbus Niemann-Pick Typ C1</title>
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  <abstract type="Summary">Morbus Niemann-Pick Typ C1 (NPC1) ist eine seltene autosomal rezessive, lysosomale Lipidose, die sich durch eine Akkumulation von Cholesterol in den Lysosomen auszeichnet. Ziel der Arbeiten war es, ein humanes neuronales in vitro Zellmodellsystem für NPC1 zu entwickeln. Hierzu wurden NPC1 patientenspezifische Fibroblasten in patientenspezifische IPS-Zellen reprogrammiert. Diese wurden in Neurone und Gliazellen differenziert und hinsichtlich der Ausprägung von pathophysiologischen Merkmalen, als Beleg für die Verwendbarkeit der Zellen als NPC1 in vitro Modellsystem, untersucht.&lt;ger&gt;</abstract>
  <abstract type="Summary">Niemann-Pick type C1 (NPC1) disease is a rare autosomal recessive lysosomal lipidosis, characterized by an accumulation of cholesterol in the lysosomes. The aim of the work was to develop a human neural in vitro cell model system for NPC1. For this purpose NPC1 patient-specific fibroblasts were reprogrammed into patient-specific induced pluirpotent stem cells (IPSCs). These IPSCs were differentiated into neurons and glial cells and examined with regard to the expression of pathophysiological features of NPC1, to evidence the feasibility of the cells as a NPC1 in vitro model system.&lt;eng&gt;</abstract>
  <note type="statement of responsibility">vorgelegt von Moritz Johannes Frech</note>
  <note>GutachterInnen: Andreas Hermann (Universitätsmedizin Rostock) ; Holger Lerche (Universitätsklinikum Tübingen) ; Susanne Petri (Medizinische Hochschule Hannover)</note>
  <note type="thesis">Habilitationsschrift Universität Rostock 2020 Kumulative Habilitationsschrift</note>
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