Oers, Johanna M. M. van and Adam, Christoph and Denzinger, Stefan and Stoehr, Robert and Bertz, Simone and Zaak, Dirk and Stief, Christian and Hofstaedter, Ferdinand and Zwarthoff, Ellen C. and van der Kwast, Theodorus H. and Knuechel, Ruth and Hartmann, Arndt (2006) Chromosome 9 deletions are more frequent than FGFR3 mutations in flat urothelial hyperplasias of the bladder. International journal of cancer. Journal international du cancer 119 (5), pp. 1212-1215.
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Other URL: http://dx.doi.org/10.1002/ijc.21958
Flat urothelial hyperplasias (FUHs) in patients with papillary bladder tumours frequently show deletions of chromosome 9, suggesting that FUH could be the first neoplastic step in the development of papillary bladder cancer. FGFR3 mutations are frequent in non-invasive papillary tumours with low risk of progression. Our aim was to investigate the frequency of FGFR3 mutations and deletions of ...
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|Date:||1 September 2006|
|Institutions:||Medicine > Lehrstuhl für Pathologie|
|Keywords:||flat urothelial hyperplasia; FGFR3; LOH chromosome 9|
|Dewey Decimal Classification:||600 Technology > 610 Medical sciences Medicine|
|Refereed:||Yes, this version has been refereed|
|Created at the University of Regensburg:||Unknown|
|Deposited On:||29 Mar 2007|
|Last Modified:||13 Mar 2014 10:10|