Zusammenfassung
Die am häufigsten in menschlichen Tumoren nachgewiesene Mutation betrifft das Tumorsuppressorgen TP53 [1]. Das kodierte p53 Protein kontrolliert zentrale Funktionen des Zellzyklus [2]. Bei Erkennung eines DNA Schadens reguliert p53 die DNA Reparatur, stoppt den Zellzyklus oder induziert eine Apoptose. Bei p53 Funktionsverlust kann daher ein unkontrolliertes Zellwachstum mit Akkumulation von Mutationen resultieren.
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© 1999 Springer-Verlag Berlin Heidelberg
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Fein, M. et al. (1999). Reflux von Duodenalsaft erzeugt Ösophaguskarzinome in Trp53-knockout Mäusen. In: Rühland, D., Rothmund, M., Hartel, W., Beger, H.G. (eds) Chirurgisches Forum ’99 für experimentelle und klinische Forschung. Deutsche Gesellschaft für Chirurgie, vol I/99. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-60133-0_21
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DOI: https://doi.org/10.1007/978-3-642-60133-0_21
Publisher Name: Springer, Berlin, Heidelberg
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