The ciliopathy disease protein NPHP9 promotes nuclear delivery and activation of the oncogenic transcriptional regulator TAZ

Nephronophthisis (NPH) is a genetically heterogenous kidney disease and represents the most common genetic cause for end-stage renal disease in children. It is caused by the mutation of genes encoding for the nephrocystin proteins (NPHPs) which localize to primary cilia or centrosomes, classifying t...

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Veröffentlicht in:Human molecular genetics 2012-12, Vol.21 (26), p.5528-5538
Hauptverfasser: HABBIG, Sandra, BARTRAM, Malte P, REINHARDT, H. Christian, BURST, Volker, BENZING, Thomas, SCHERMER, Bernhard, SÄGMÜLLER, Josef G, GRIESSMANN, Anabel, FRANKE, Mareike, MÜLLER, Roman-Ulrich, SCHWARZ, Ricarda, HOEHNE, Martin, BERGMANN, Carsten, TESSMER, Claudia
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