Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Katrin Guse"'
Autor:
Laura-Nanna Lohkamp, Maren Schinz, Claire Gehlhaar, Katrin Guse, Ulrich-Wilhelm Thomale, Peter Vajkoczy, Frank L Heppner, Arend Koch
Publikováno v:
PLoS ONE, Vol 11, Iss 6, p e0156422 (2016)
Giant Cell Glioblastoma (gcGBM) and Pleomorphic Xanthoastrocytoma (PXA) are rare astroglial tumors of the central nervous system. Although they share certain histomorphological and immunohistochemical features, they are characterized by different cli
Externí odkaz:
https://doaj.org/article/406c16f00a274f11b5b42d7045bc26c5
Autor:
Frank L. Heppner, Ulrich-Wilhelm Thomale, Maren Schinz, Peter Vajkoczy, Katrin Guse, Laura-Nanna Lohkamp, Arend Koch, Claire Gehlhaar
Publikováno v:
PLoS ONE, Vol 11, Iss 6, p e0156422 (2016)
PLoS ONE
60th Annual Meeting of the German Society for Neuropathology and Neuroanatomy (DGNN); 20150826-20150828; Berlin; DOC15dgnnP53 /20150825/
PLoS ONE
60th Annual Meeting of the German Society for Neuropathology and Neuroanatomy (DGNN); 20150826-20150828; Berlin; DOC15dgnnP53 /20150825/
Giant Cell Glioblastoma (gcGBM) and Pleomorphic Xanthoastrocytoma (PXA) are rare astroglial tumors of the central nervous system. Although they share certain histomorphological and immunohistochemical features, they are characterized by different cli
Autor:
Katrin Guse, Maren Bradtmöller, Hendrik Bläker, Claire Gehlhaar, Arend Koch, Marcus Bahra, Alexander Arnold, Frank L. Heppner, Dido Lenze
Publikováno v:
Experimental and molecular pathology. 99(2)
In order to study molecular similarities and differences of intrahepatic (IH-CCA) and extrahepatic (EH-CCA) cholangiocarcinoma, 24 FFPE tumor samples (13 IH-CCA, 11 EH-CCA) were analyzed for whole genome copy number variations (CNVs) using a new high
Autor:
Sigrid Tinschert, Thomas Harder, Sabrina Titze, Katrin Guse, Hartmut Peters, Anja Harder, Annegret Buske, Sandra Währisch
Neurofibromatosis type 1 (NF1) is caused by NF1 gene mutations. The phenotype is highly variable, with 'modifiers' being discussed as potential determinants. Mismatch repair deficiency was shown to cause NF1 mutations, but constitutional mutation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a48e726a2cda037e5698e18b3171837
https://europepmc.org/articles/PMC2987165/
https://europepmc.org/articles/PMC2987165/
Autor:
Eve-Kristin Wenzl, Arend Koch, Maren Regehly, Katrin Guse, Gabriele Röhn, Ulrich-Wilhelm Thomale, Roland Goldbrunner, Pablo Hernáiz-Driever, Ulrich Schüller, Frank L. Heppner
Publikováno v:
Cancer Research. 71:3452-3452
Medulloblastomas (MBs) represent the most frequent malignant brain tumors of childhood. Previous genetic studies in MBs have identified mutations in genes coding for beta-catenin, AXIN1 and Conductin (AXIN2), which cause activation of the Wnt signali