检索结果 - Sahm, Felix

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  1. 1
    INSP-14. Novel approaches to molecular diagnostics

    INSP-14. Novel approaches to molecular diagnostics 由 Sahm, Felix

    出版 2022
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  2. 2
    ID(H)entifying checkpoint inhibitor candidates among diffuse glioma

    ID(H)entifying checkpoint inhibitor candidates among diffuse glioma 由 Sahm, Felix, Wick, Antje

    出版 2017
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  3. 3
    TERT, the target?

    TERT, the target? 由 Sahm, Felix, Kalamarides, Michel

    出版 2018
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  4. 4
    Introduction to the mini‐symposium “molecular neuropathology of meningioma”

    Introduction to the mini‐symposium “molecular neuropathology of meningioma” 由 Sahm, Felix, Mawrin, Christian

    出版 2022
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  5. 5
    DNA methylation profiling as a model for discovery and precision diagnostics in neuro-oncology

    DNA methylation profiling as a model for discovery and precision diagnostics in neuro-oncology 由 Pratt, Drew, Sahm, Felix, Aldape, Kenneth

    出版 2021
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  6. 6
    Mutation specific antibodies: tool or dinosaur?

    Mutation specific antibodies: tool or dinosaur? 由 von Deimling, Andreas, Sahm, Felix, Capper, David

    出版 2012
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  7. 7
    DDIS-07. IDENTIFICATION OF DRUGGABLE MOLECULAR TARGETS IN MENINGIOMA

    DDIS-07. IDENTIFICATION OF DRUGGABLE MOLECULAR TARGETS IN MENINGIOMA 由 Tran, Anh, Zhang, Lyndsee, Sahm, Felix, Scholtens, Denise, Horbinski, Craig

    出版 2019
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  8. 8
    MNGI-13. A DNA METHYLATION-BASED CLASSIFIER FOR ASSESSMENT OF RISK OF RECURRENCE IN MENINGIOMA

    MNGI-13. A DNA METHYLATION-BASED CLASSIFIER FOR ASSESSMENT OF RISK OF RECURRENCE IN MENINGIOMA 由 Sahm, Felix, Schrimpf, Daniel, Sill, Martin, Stichel, Damian, Pfister, Stefan M, von Deimling, Andreas

    出版 2018
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  9. 9
    The Prognostic Value of Methylation Signatures and NF2 Mutations in Atypical Meningiomas

    The Prognostic Value of Methylation Signatures and NF2 Mutations in Atypical Meningiomas 由 Meta, Rahmina, Boldt, Henning B., Kristensen, Bjarne W., Sahm, Felix, Sjursen, Wenche, Torp, Sverre H.

    出版 2021
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  10. 10
    Frequent AKT1(E17K) mutations in skull base meningiomas are associated with mTOR and ERK1/2 activation and reduced time to tumor recurrence

    Frequent AKT1(E17K) mutations in skull base meningiomas are associated with mTOR and ERK1/2 activation and reduced time to tumor recurrence 由 Yesilöz, Ümmügülsüm, Kirches, Elmar, Hartmann, Christian, Scholz, Johannes, Kropf, Siegfried, Sahm, Felix, Nakamura, Makoto, Mawrin, Christian

    出版 2017
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  11. 11
    Diagnostic challenges in meningioma

    Diagnostic challenges in meningioma 由 Nowosielski, Martha, Galldiks, Norbert, Iglseder, Sarah, Kickingereder, Philipp, von Deimling, Andreas, Bendszus, Martin, Wick, Wolfgang, Sahm, Felix

    出版 2017
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  12. 12
    Mutational landscape of primary and recurrent glioblastoma reveals potentially actionable SNVs including WNT pathway variation

    Mutational landscape of primary and recurrent glioblastoma reveals potentially actionable SNVs including WNT pathway variation 由 Ellis, Hayley, Sahm, Felix, Schrimpf, Daniel, Stupnikov, Alexei, Wadsley, Mark, Wragg, Christopher, McArt, Darragh, Kurian, Kathreena

    出版 2018
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  13. 13
    MNGI-28. CORRELATION OF METHYLATION CLASS AND GENETIC ALTERATIONS WITH PROGRESSION FREE SURVIVAL IN MENINGIOMA

    MNGI-28. CORRELATION OF METHYLATION CLASS AND GENETIC ALTERATIONS WITH PROGRESSION FREE SURVIVAL IN MENINGIOMA 由 Berghoff, Anna, Ricken, Gerda, Rajky, Ursula, Marosi, Christine, Hainfellner, Johannes, von Deimling, Andreas, Sahm, Felix, Preusser, Matthias

    出版 2018
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  14. 14
    LGG-13. PAPILLARY GLIONEURONAL TUMOR (PGNT) EXHIBITS A CHARACTERISTIC METHYLATION PROFILE AND MANDATORY FUSIONS INVOLVING PRKCA

    LGG-13. PAPILLARY GLIONEURONAL TUMOR (PGNT) EXHIBITS A CHARACTERISTIC METHYLATION PROFILE AND MANDATORY FUSIONS INVOLVING PRKCA 由 Hou, Yanghao, Pinheiro, Jorge, Sahm, Felix, Pfister, Stefan M, Jones, David T W, Bertero, Luca, von Deimling, Andreas

    出版 2019
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  15. 15
    Clinical Significance of Molecular Diagnosis of Pilocytic Astrocytoma: A Case Report

    Clinical Significance of Molecular Diagnosis of Pilocytic Astrocytoma: A Case Report 由 Ono, Takahiro, Takahashi, Masataka, Hatakeyama, Junya, Oda, Masaya, Sahm, Felix, Nanjo, Hiroshi, von Deimling, Andreas, Shimizu, Hiroaki

    出版 2019
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  16. 16
    PATH-04. AN ENHANCED AI-DRIVEN PLATFORM FOR PRECISION MOLECULAR BRAIN TUMOR DIANOSTICS

    PATH-04. AN ENHANCED AI-DRIVEN PLATFORM FOR PRECISION MOLECULAR BRAIN TUMOR DIANOSTICS 由 Sill, Martin, Sahm, Felix, Schrimpf, Daniel, Capper, David, Pfister, Stefan M, von Deimling, Andreas, Jones, David T W

    出版 2020
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  17. 17
    HGG-56. EXTENSIVE MOLECULAR HETEROGENEITY WITHIN H3-/IDH-WILDTYPE PEDIATRIC GLIOBLASTOMA

    HGG-56. EXTENSIVE MOLECULAR HETEROGENEITY WITHIN H3-/IDH-WILDTYPE PEDIATRIC GLIOBLASTOMA 由 Blattner-Johnson, Mirjam, Sahm, Felix, Sill, Martin, Sturm, Dominik, Kramm, Christof M, Pfister, Stefan M, Jones, David

    出版 2020
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  18. 18
    Intraventricular immune checkpoint inhibition with nivolumab in relapsed primary central nervous system lymphoma

    Intraventricular immune checkpoint inhibition with nivolumab in relapsed primary central nervous system lymphoma 由 Kaulen, Leon D, Gumbinger, Christoph, Hinz, Felix, Kessler, Tobias, Winkler, Frank, Bendszus, Martin, Sahm, Felix, Wick, Wolfgang

    出版 2022
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  19. 19
    The Indoleamine-2,3-Dioxygenase (IDO) Inhibitor 1-Methyl-D-tryptophan Upregulates IDO1 in Human Cancer Cells

    The Indoleamine-2,3-Dioxygenase (IDO) Inhibitor 1-Methyl-D-tryptophan Upregulates IDO1 in Human Cancer Cells 由 Opitz, Christiane A., Litzenburger, Ulrike M., Opitz, Uta, Sahm, Felix, Ochs, Katharina, Lutz, Christian, Wick, Wolfgang, Platten, Michael

    出版 2011
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  20. 20
    Intraventricular meningiomas frequently harbor NF2 mutations but lack common genetic alterations in TRAF7, AKT1, SMO, KLF4, PIK3CA, and TERT

    Intraventricular meningiomas frequently harbor NF2 mutations but lack common genetic alterations in TRAF7, AKT1, SMO, KLF4, PIK3CA, and TERT 由 Jungwirth, Gerhard, Warta, Rolf, Beynon, Christopher, Sahm, Felix, von Deimling, Andreas, Unterberg, Andreas, Herold-Mende, Christel, Jungk, Christine

    出版 2019
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