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G340
KKE Pädiatrische OnkologieID | I:(DE-He78)G340-20160331 |
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Contribution to a book
Interdisziplinäre Therapie kindlicher ZNS-Tumoren
Pädiatrische Neurochirurgie / Bächli, Heidi (Editor) ; Berlin, Heidelberg : Springer Berlin Heidelberg, 2018, Chapter 36 ; ISBN: 978-3-662-48699-3 ; doi:10.1007/978-3-662-48700-6
Berlin, Heidelberg : Springer Berlin Heidelberg 395-404 (2018) [10.1007/978-3-662-48700-6_36]
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Journal Article
A kinome-wide RNAi screen identifies ALK as a target to sensitize neuroblastoma cells for HDAC8-inhibitor treatment.
Cell death and differentiation 25(12), 2053 - 2070 (2018) [10.1038/s41418-018-0080-0]
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Journal Article (Editorial)
Klinischer Nutzen der molekularen Diagnostik pädiatrischer Hirntumore
Klinische Pädiatrie 230(6), 289 - 290 (2018) [10.1055/a-0750-8353]
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Dissertation / PhD Thesis
Targeted Therapy of Neuroblastoma with HDAC8 Inhibitor and ALK Inhibitor.
Dissertation, Universität Heidelberg, 2018
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Journal Article
Transcriptome based individualized therapy of refractory pediatric sarcomas: feasibility, tolerability and efficacy.
OncoTarget 9(29), 20747-20760 (2018) [10.18632/oncotarget.25087]
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Journal Article
Molecular Diagnostics in Pediatric Brain Tumors: Impact on Diagnosis and Clinical Decision-Making - A Selected Case Series.
Klinische Pädiatrie 230(6), 305-313 (2018) [10.1055/a-0637-9653]
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Journal Article
Dual role of HDAC10 in lysosomal exocytosis and DNA repair promotes neuroblastoma chemoresistance.
Scientific reports 8(1), 10039 (2018) [10.1038/s41598-018-28265-5]
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Journal Article
The HDAC6/8/10 inhibitor TH34 induces DNA damage-mediated cell death in human high-grade neuroblastoma cell lines.
Archives of toxicology 92(8), 2649 - 2664 (2018) [10.1007/s00204-018-2234-8]
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Journal Article
Primary intracranial spindle cell sarcoma with rhabdomyosarcoma-like features share a highly distinct methylation profile and DICER1 mutations.
Acta neuropathologica 136(2), 327 - 337 (2018) [10.1007/s00401-018-1871-6]
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Journal Article
Molecularly defined diffuse leptomeningeal glioneuronal tumor (DLGNT) comprises two subgroups with distinct clinical and genetic features.
Acta neuropathologica 136(2), 239 - 253 (2018) [10.1007/s00401-018-1865-4]
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