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Johannes H. Schulte

Researcher at Charité

Publications -  198
Citations -  11678

Johannes H. Schulte is an academic researcher from Charité. The author has contributed to research in topics: Neuroblastoma & Anaplastic lymphoma kinase. The author has an hindex of 50, co-authored 198 publications receiving 9351 citations. Previous affiliations of Johannes H. Schulte include Humboldt University of Berlin & Boston Children's Hospital.

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Journal ArticleDOI

The landscape of genomic alterations across childhood cancers

Susanne Gröbner, +185 more
- 15 Mar 2018 - 
TL;DR: The data suggest that 7–8% of the children in this cohort carry an unambiguous predisposing germline variant and that nearly 50% of paediatric neoplasms harbour a potentially druggable event, which is highly relevant for the design of future clinical trials.
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Stabilization of N-Myc Is a Critical Function of Aurora A in Human Neuroblastoma

TL;DR: AURKA is identified as a gene that is required for the growth of MYCN-amplified neuroblastoma cells but largely dispensable for cells lacking amplified MYCN, and Aurora A has a critical function in regulating turnover of the N-Myc protein.
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Telomerase activation by genomic rearrangements in high-risk neuroblastoma

TL;DR: It is shown that remodelling of the genomic context abrogates transcriptional silencing of TERT in high-risk neuroblastoma and places telomerase activation in the centre of transformation in a large fraction of these tumours.
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Lysine-Specific Demethylase 1 Is Strongly Expressed in Poorly Differentiated Neuroblastoma: Implications for Therapy

TL;DR: First evidence that a histone demethylase, LSD1, is involved in maintaining the undifferentiated, malignant phenotype of neuroblastoma cells is provided, showing that inhibition of LSD1 reprograms the transcriptome of neuro Blastoma cells and inhibits Neuroblastoma xenograft growth in vivo.
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Relapsed neuroblastomas show frequent RAS-MAPK pathway mutations

TL;DR: It is shown that RAS-MAPK pathway mutations may function as a biomarker for new therapeutic approaches to refractory disease and provide a rationale for genetic characterization of relapse neuroblastomas.