Rezultati pretrage - Sahm, Felix
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TERT, the target? od Sahm, Felix, Kalamarides, Michel
Izdano 2018Tekst -
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Frequent AKT1(E17K) mutations in skull base meningiomas are associated with mTOR and ERK1/2 activation and reduced time to tumor recurrence od Yesilöz, Ümmügülsüm, Kirches, Elmar, Hartmann, Christian, Scholz, Johannes, Kropf, Siegfried, Sahm, Felix, Nakamura, Makoto, Mawrin, Christian
Izdano 2017Tekst -
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Mutational landscape of primary and recurrent glioblastoma reveals potentially actionable SNVs including WNT pathway variation od Ellis, Hayley, Sahm, Felix, Schrimpf, Daniel, Stupnikov, Alexei, Wadsley, Mark, Wragg, Christopher, McArt, Darragh, Kurian, Kathreena
Izdano 2018Tekst -
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MNGI-28. CORRELATION OF METHYLATION CLASS AND GENETIC ALTERATIONS WITH PROGRESSION FREE SURVIVAL IN MENINGIOMA od Berghoff, Anna, Ricken, Gerda, Rajky, Ursula, Marosi, Christine, Hainfellner, Johannes, von Deimling, Andreas, Sahm, Felix, Preusser, Matthias
Izdano 2018Tekst -
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LGG-13. PAPILLARY GLIONEURONAL TUMOR (PGNT) EXHIBITS A CHARACTERISTIC METHYLATION PROFILE AND MANDATORY FUSIONS INVOLVING PRKCA od Hou, Yanghao, Pinheiro, Jorge, Sahm, Felix, Pfister, Stefan M, Jones, David T W, Bertero, Luca, von Deimling, Andreas
Izdano 2019Tekst -
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Clinical Significance of Molecular Diagnosis of Pilocytic Astrocytoma: A Case Report od Ono, Takahiro, Takahashi, Masataka, Hatakeyama, Junya, Oda, Masaya, Sahm, Felix, Nanjo, Hiroshi, von Deimling, Andreas, Shimizu, Hiroaki
Izdano 2019Tekst -
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Intraventricular immune checkpoint inhibition with nivolumab in relapsed primary central nervous system lymphoma od Kaulen, Leon D, Gumbinger, Christoph, Hinz, Felix, Kessler, Tobias, Winkler, Frank, Bendszus, Martin, Sahm, Felix, Wick, Wolfgang
Izdano 2022Tekst -
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The Indoleamine-2,3-Dioxygenase (IDO) Inhibitor 1-Methyl-D-tryptophan Upregulates IDO1 in Human Cancer Cells od Opitz, Christiane A., Litzenburger, Ulrike M., Opitz, Uta, Sahm, Felix, Ochs, Katharina, Lutz, Christian, Wick, Wolfgang, Platten, Michael
Izdano 2011Tekst -
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Intraventricular meningiomas frequently harbor NF2 mutations but lack common genetic alterations in TRAF7, AKT1, SMO, KLF4, PIK3CA, and TERT od Jungwirth, Gerhard, Warta, Rolf, Beynon, Christopher, Sahm, Felix, von Deimling, Andreas, Unterberg, Andreas, Herold-Mende, Christel, Jungk, Christine
Izdano 2019Tekst